The Venture 17 Division Of Education

THE CONSERVATORY OF MEDICAL ARTS AND SCIENCES
XVII
ANATOMY AND PHYSIOLOGY LIBRARY AND COURSE
Below, you will find many resources and reference systems to aid you in your studies of Human Anatomy and Physiology. At the bottom of this page you will find our Library. It consists of six units. An image library with accompanying didactic discussions in slide presentation format; designed to parallel your college coursework in Anatomy and Physiology.
Our library remains dynamic, and is often changed to meet the requirements of different courses at different scopes of knowledge.
CONSERVATORY ACADEMIC PARTNERS:
Get Body Smart
The Conservatory Anatomy Library also partners with Get Body Smart. Just click to gain access. The Get Body Smart anatomy teaching tool is important in that it utilizes not only animation, but offers a detailed interactive cadaver dissection.
Dissection is the best technique for learning anatomy and system relationships.
The Blausen Human Atlas
Thank you, Mr. Blausen.The largest 3-D Animated Anatomy Library in the world, the Blausen Atlas was welcomed on board in 2013.
Designed and produced by Bruce Blausen, a Master of Medical Illustration from Johns Hopkins University, School of Medicine, the atlas is an eloquently rendered work of scientific anamation, also available as a mobile-ap.
Thank you, Mr. Blausen.
The Biodigital Human
The Bio-digital Human is a free 3-D interactive anatomy teaching tool. Just click the image.
The Bio-digital Human requires newer computer platforms and software. You will need to make sure that your computer is compatible with this program.
Human Anatomy, although an extremely visual science, is a discipline initiated through rote memorization. Some students are visual in their studying techniques and some are auditory, and then there are others who must hear it, write it and see it together. All of these techniques work. Find the best one for you. Power Point presentations are available through our library. Visual presentations will be coming soon.
To aid our clients and online users, we offer an online textbook and learning module. This tool allows us to present Anatomy and Physiology as an online didactic resource and course, available at no cost to our students. The rubrics are designed as an assistant to the students we teach on campus, but this online course is also available to anyone wanting to increase their medical knowledge and competitive edge.
For you to be able to utilize the Anatomy Course materials at no cost, you must sign into We Teach College Students, and request the course. You will be assisted through our vetting bridge which interfaces with your current college to confirm student status. We will then add you to our roster and email your access codes within twenty-four hours. This is a self paced programmed course. The course utilizes a large and concise text on anatomy, with case studies, color illustrations of gross and micro-anatomy, color labeling exercises, and flashcards, in addition to a terminology coach. Questions can be addressed on our Academic Questions page.
Our affiliate links are well established, web-sturdy, and safe, in addition to offering vigorous and enterprising content. They can help you take your studies as far as you wish.
The Anatomy Library is a complete image based library with accompanying didactics. Constructed as six units in slide presentation format, each unit screen can be paused, advanced, and reversed at your discretion. You may point and click to manipulate these features.
The units appear in order from top to bottom, with titles as follows:
I. Constituents of the Human Body.
II. Support and Movement.
III. Communication, Control, and Integration.
IV. Transportation and Defense.
V. Respiration, Nutrition, and Excretion. And lastly,
VI. Reproduction and Development.
Unit I. Constituents of the Human Body:
Organization, Chemistry, Cellular Anatomy,Cellular Physiology, Cell Growth and Reproduction, and finally, Tissues.
The Anatomic Position
Nine regions of the abdominopelvic cavity. Only the most superficial structures of the internal organs are shown here.
Only the most superficial structures of the internal organs are shown here.
Homeostasis of blood glucose.
Homeostasis of blood glucose. The range over which a given value, such as the blood glucose concentration, is maintained is accomplished through homeostatic mechanisms. Note that the concentration of glucose fluctuates above and below a normal set point value (90 mg/ml) within a normal set point range (80–100 mg/ml).
The Periodic Chart
The periodic chart of the elements. The major elements found in the body are highlighted in pink. The trace elements, found in very tiny quantities in the body, are highlighted in orange.
Energy Levels
Energy levels. A, Energy levels (electron shells) surrounding the nucleus of an atom. Each concentric shell represents a different electron energy level. Note that nitrogen can accept three more electrons to satisfy the octet rule. B, Energy levels of five common elements. All atoms are balanced with respect to positive and negative charges. In atoms with a single energy level, two electrons are required for stability. Hydrogen with its single electron is reactive, whereas helium with its full energy level is not. In atoms with more than one energy level, eight electrons in the outermost energy level are required for stability (according to the octet rule). Neon is stable because its outer energy level has eight electrons. However, oxygen and carbon, with four and six electrons (respectively) in their outer energy shells, are chemically reactive. Oxygen can accept two more electrons and carbon can accept four more electrons to satisfy the octet rule.
The Hydrogen Bond
Hydrogen bonds between water molecules. Hydrogen bonds serve to weakly attach the negative (oxygen) side of one water molecule to the positive (hydrogen) side of a nearby water molecule. This diagram depicts a few bonded molecules, as one would expect in liquid water. Ice would instead have more hydrogen bonds; steam would have none.
The pH Scale
The pH scale. Note that as the concentration of H+ increases, the solution becomes increasingly acidic and the pH value decreases. As the H+ concentration decreases, the pH value increases, and the solution becomes more and more basic, or alkaline. (The scale on the left side of the diagram shows the actual concentrations of H+ in moles per liter, or molar concentration, as an ordinary number, and expressed as an exponent [logarithm] of 10. You can see that the pH scale is simply the negative exponent of 10.)
Triglyceride
Formation of triglyceride. Glycerol tricaproate is a composite molecule made up of three molecules of caproic acid (a six-carbon fatty acid). The fatty acids are coupled in a dehydration synthesis reaction to a single glycerol backbone. In addition to the triglyceride, this process results in the formation of three molecules of water.
Amino Acids
Basic structural formula for an amino acid. Note relationship of the side chain (R), amine group, and carboxyl group to the alpha carbon. The amine group (NH2) is depicted in the figure as H2N to show that the nitrogen atom of the group bonds to the alpha carbon.
Transfer RNA
Transfer RNA (Ribonucleic Acid). Representation of a transfer RNA (tRNA) molecule, showing an attachment site at one end for a specific amino acid and a site (anticodon) at the other end for attachment to a codon of a copied gene. Gray areas represent slightly altered bases (a characteristic of tRNA).
A Composite Human Cell
Typical, or composite, cell. A, Artist’s interpretation of cell structure. B, Color-enhanced electron micrograph of a cell. Both show the many organelles, including the mitochondria, known as the “power plants of the cell.” Note the innumerable dots bordering the endoplasmic reticulum. These are ribosomes, the cell’s “protein factories.” (B. Courtesy A. Arlan Hinchee.)
The Golgi Apparatus
Golgi apparatus. Sketch of the structure of the Golgi apparatus showing a stack of flattened sacs, or cisternae, and numerous small membranous bubbles, or secretory vesicles.
The Cytoskeleton
The cytoskeleton. Artist’s interpretation of the cell’s internal framework. Notice that the “free” ribosomes and other organelles are not really free at all but are secured by the cytoskeletal elements of the cell.
Cellular Connections
Cell connections. Spot and belt desmosomes, gap junction, and tight junction.
Examples of Cell Types. Gland cells
Functional Anatomy of Cell Membranes.
Functional Anatomy of Cell Membranes. Structure: Receptor molecules that trigger metabolic changes in membrane (or on other side of membrane). Function: Sensitivity to hormones and other regulatory chemicals; involved in signal transduction
Functional Anatomy of Cell Membranes.
Functional Anatomy of Cell Membranes. Structure: Glycoproteins or proteins in the membrane that act as markers. Function: Recognition of cells or organelles
Osmosis
Osmosis. Osmosis is the diffusion of water through a selectively permeable membrane. Because there are relatively more water molecules in 10% albumin than in 20% albumin, more water molecules osmose from the more dilute into the more concentrated solution (as indicated by the larger arrow in the left diagram) than osmose in the opposite direction. The overall direction of osmosis, in other words, is toward the more concentrated solution. Net osmosis produces the following changes in these solutions: (1) their concentrations equilibrate, (2) the volume and pressure of the originally more concentrated solution increase, and (3) the volume and pressure of the other solution decrease proportionately.
Sodium-potassium pump.
Sodium-potassium pump. Three sodium ions (Na+) bind to sodium binding sites on the pump’s inner face. At the same time, an energy-containing adenosine triphosphate (ATP) molecule produced by the cell’s mitochondria binds to the pump. The ATP breaks apart, and its stored energy is transferred to the pump. The pump then changes shape, releases the three Na+ ions to the outside of the cell, and attracts two potassium ions (K+) to its potassium binding sites. The pump then returns to its original shape, and the two K+ ions and the remnant of the ATP molecule are released to the inside of the cell. The pump is now ready for another pumping cycle. ATPase, Adenosine triphosphatase. The small inset is a simplified view of Na+-K+-pump activity. (Adapted from McCance K, Huether S: Pathophysiology, ed 4, St Louis, 2002, Mosby.)
Enzyme regulation of a metabolic pathway.
Enzyme regulation of a metabolic pathway. In a metabolic pathway, the product of one enzyme-regulated reaction becomes the substrate for the next reaction. Thus a whole series of enzymes is required to keep the pathway functioning. Notice that these enzymes are embedded in a cell membrane, whereas other types of enzymes are mobile in the cytosol.
Summary of Cellular Respiration.
Summary of cellular respiration. This simplified outline of cellular respiration represents one of the most important catabolic pathways in the cell. Note that one phase (glycolysis) occurs in the cytosol, but that the two remaining phases (citric acid cycle and electron transport system) occur within a mitochondrion. Note also the divergence of the anaerobic and aerobic pathways of cellular respiration. ADP, Adenosine diphosphate; ATP, adenosine triphosphate; CoA, coenzyme A; FADH2, reduced form of flavin adenine dinucleotide; NADH, reduced form of nicotinamide adenine dinucleotide.
Passive Transport Processes. Osmosis
Active Transport Processes. Phagocytosis (endocytosis)
Genes
Function of genes. Genes copied from DNA are copied to RNA molecules, which use the code to determine a cell’s structural and functional characteristics. There are approximately 24,000 genes in the human genome (all the DNA molecules together).
The Genetic Code.
The genetic code. The first graphic “phrasebook” or “decoder” of the genetic language of the cell was developed in 1966 to summarize the amino acids encoded by various codons (three-base sequences of nucleotides) in RNA. One of the clearest is this version adapted from Ben Fry’s decoder, developed when he was a student at Massachusetts Institute of Technology. To read the decoder, start with any codon (for example, CGA). Find the first base along the top of the decoder to find the correct box to use (C is the third box). The second base is found in each row of that box, labeled on the left (G is the first row). Then use the third base to find the correct column, labeled at the bottom of each box (A is the second column, showing that Arg [arginine] is the amino acid encoded by CGA).
The Major Events of Mitosis
Diagram of loose (areolar) connective tissue.
Diagram of loose (areolar) connective tissue. This artist’s sketch illustrates that loose connective tissue includes a number of different extracellular matrix (ECM) components such as collagenous fibers and elastic fibers, as well as a variety of different cell types.
Types of body membranes.
Types of body membranes. A, Epithelial membranes, including cutaneous membrane (skin), serous membranes (parietal and visceral pleura and peritoneum), and mucous membranes. B, Connective tissue membranes, including synovial membranes.
Connective tissue
Membranous Epithelial Tissues: Simple Epithelium.
Membranous Epithelial Tissues: Simple Epithelium. Simple cuboidal: Photomicrograph of kidney tubules showing the single layer of cuboidal cells touching a basement membrane. (Dennis Strete.)
Membranous Epithelial Tissues: Simple Epithelium.
Membranous Epithelial Tissues: Simple Epithelium. Stratified squamous, nonkeratinized: Photomicrograph of the lining of the esophagus. Each cell in the layer is flattened near the surface and attached to the sheet. (Dennis Strete.)
Structural Classification of Multicellular Exocrine Glands.
Tubular (coiled)
Structural Classification of Multicellular Exocrine Glands.
Alveolar (multiple)
Connective Tissues. Fibrous Tissue.
Adipose (fat): Note the large storage spaces for fat inside the
Connective Tissues. Dense Fibrous Tissue.
Elastic: Note the roughly parallel arrangement of short, darkly stained elastic fibers. (Adapted from Gartner L, Hiatt J: Color textbook of histology, ed 3, Philadelphia, 2006, Saunders.)
Connective Tissues. Cartilage Tissue.
Fibrocartilage: Photomicrograph of the pubic symphysis joint. The strong dense fibers that fill the matrix convey shock-absorbing qualities. (Dennis Strete.)
Muscle and Nervous Tissues. Nervous Tissue.
Smooth (nonstriated, involuntary, or visceral): Photomicrograph, longitudinal section. Note the central placement of nuclei in the spindle-shaped smooth muscle fibers. (Dennis Strete.)
Levels of organization.
The smallest parts of the body are the atoms that make up our molecules. In turn, molecules make up microscopic parts called organelles that fit together to form each cell of the body. Groups of similar cells are called tissues, which combine with other tissues to form organs. Groups of organs that work together are called systems. All the systems of the body together make up an individual organism. Knowledge of the different levels of organization will help you understand the basic concepts of human anatomy and physiology.
Division of the abdomen into four quadrants.
The diagram shows the relationship of internal organs to the four abdominopelvic quadrants.
Internal Environment
Diagram of the body’s internal environment. The human body is like a bag of fluid separated from the external environment. Tubes, such as the digestive tract and respiratory tract, bring the external environment to deeper parts of the bag where substances may be absorbed into the internal fluid environment or excreted into the external environment. All the “accessories” help maintain a constant environment inside the bag, allowing the cells that live there to survive.
Major Elements
Major elements of the body. These elements are found in great quantity in the body (see Figure 2-1). The graph shows the relative abundance of each. Notice that oxygen (O), carbon (C), hydrogen (H), and nitrogen (N) predominate.
The Ionic Bond
Example of an ionic bond. Energy-level models show the steps involved in forming an ionic bond between atoms of sodium and chlorine within the internal fluid environment of the body (water). Sodium “donates” an electron to chlorine, thereby forming a positive sodium ion and a negative chloride ion. The electrical attraction between the now oppositely charged ions forms an ionic bond.
Metabolic Reactions
Metabolic reactions. Hydrolysis is a catabolic reaction that adds water to break down large molecules into smaller molecules, or subunits. Dehydration synthesis is an anabolic reaction that operates in the reverse fashion: small molecules are assembled into large molecules by removing water. Note that a specific example of dehydration synthesis is shown in Figure 2-15.
Glucose
Structure of glucose. A, Straight chain, or linear model, of glucose. B, Ring model representing glucose in solution. C, Three-dimensional, or space-filling, model of glucose.
The Biphospholipid cell membrane
Phospholipid bilayer. A, Orientation of phospholipid molecules when surrounded by water and forming a bilayer. B, Cartoon commonly used to depict a phospholipid bilayer.
Protein Structure
Structural levels of protein. Primary structure: determined by the number, kind, and sequence of amino acids in the chain. Secondary structure: hydrogen bonds stabilize folds or helical spirals. Tertiary structure: globular shape maintained by strong (covalent) intramolecular bonding and by stabilizing hydrogen bonds. Quaternary structure: results from bonding between more than one polypeptide unit.
ATP
Adenosine triphosphate (ATP). A, Structure of ATP. A single adenosine group (A) has three attached phosphate groups (P). High-energy bonds between the phosphate groups can release chemical energy to do cellular work. B, General scheme of the ATP energy cycle. ATP stores energy in its last high-energy phosphate bond. When that bond is later broken, energy is transferred as important intermediate compounds are formed. The adenosine diphosphate (ADP) and phosphate groups that result can be resynthesized into ATP, thereby capturing additional energy from nutrient catabolism. Note that energy is transferred from nutrient catabolism to ADP, thus converting it to ATP. Energy is then transferred from ATP to provide the energy required for anabolic reactions or cellular processes as it reverts back to ADP.
Plasma Membrane (Cell Membrane)
Plasma membrane. The plasma membrane is a fluid mosaic made of a bilayer of phospholipid molecules arranged with their nonpolar “tails” pointing toward each other. Cholesterol molecules help stabilize the flexible bilayer structure. Protein molecules and hybrid molecules (e.g., glycolipids) may be found on the outer or inner surface of the bilayer. They may also extend all the way through the membrane.
Protein Export
The cell’s protein export system. The Golgi apparatus processes and packages protein molecules delivered by small vesicles from the endoplasmic reticulum. After entering the first cisterna of the Golgi apparatus, a protein molecule undergoes a series of chemical modifications, is sent (by means of a vesicle) to the next cisterna for further modification, and so on, until it is ready to exit the last cisterna. When it is ready to exit, a molecule is packaged in a membranous secretory vesicle that migrates to the surface of the cell and “pops open” to release its contents into the space outside the cell. Some vesicles remain inside the cell for some time and serve as storage vessels for the substance to be secreted.
Cell Fibers
A, Microfilaments are thin, twisted strands of protein molecules. B, Intermediate filaments are thicker, twisted protein strands. C, Microtubules are hollow fibers that consist of a spiral arrangement of protein subunits.
Examples of Cell Types. Nerve cells
Examples of Cell Types. Immune cells
Functional Anatomy of Cell Membranes.
Functional Anatomy of Cell Membranes. Structure: Enzyme molecules that catalyze specific chemical reactions. Function: Regulation of metabolic reactions
Diffusion
Diffusion. The molecules of sugar are very densely packed when they enter the coffee. As sugar molecules collide frequently in the area of high concentration, they gradually spread away from each other—toward the area of lower concentration. Eventually, the sugar molecules become evenly distributed. That is, they reach an equilibrium of concentration.
Effects of Osmosis on Cells
Effects of osmosis on cells. A, Normal red blood cells placed in a hypotonic solution may swell (as the scanning electron micrograph shows) or even burst (as the drawing shows). This change results from the inward diffusion of water (osmosis). B, Cells placed in an isotonic solution maintain constant volume and pressure because the potential osmotic pressure of the intracellular fluid matches that of the extracellular fluid. C, Cells placed in a solution that is hypertonic to the intracellular fluid lose volume and pressure as water osmoses out of the cell into the hypertonic solution. The “spikes” seen in the scanning electron micrograph are rigid microtubules of the cytoskeleton. These supports become visible as the cell “deflates.”
Bulk Transport
Bulk transport by vesicles. This sketch summarizes the essential difference between endocytosis, which moves substances into the cell by means of a vesicle, and exocytosis, which moves substances out of the cell by means of a vesicle. The type of endocytosis shown here is phagocytosis, in which the endocytic vesicle fuses with a lysosome to allow digestive enzymes to break down the ingested material.
Glycolysis
Glycolysis. This diagram of the reactions involved in glycolysis represents a classic example of a catabolic pathway. Note that each of the chemical reactions in this pathway cannot proceed until the previous step has occurred. Recall from our discussion that each step also requires the presence of one or more specific enzymes. ADP, Adenosine diphosphate; ATP, adenosine triphosphate; NAD+ and NADH, oxidized and reduced forms of nicotinamide adenine dinucleotide; Pi, inorganic phosphate.
Dialysis
Dialysis. A, Dialysis. A dialysis bag containing glucose, water, and albumin (protein) molecules is suspended in pure water. Over time, the smaller solute molecules (glucose) diffuse out of the bag. The larger solute molecules (albumin) remain trapped in the bag because the bag is impermeable to them. Thus dialysis is diffusion that results in separation of small and large solute particles. B, Hemodialysis. In hemodialysis, the patient’s blood is pumped through a dialysis cartridge, which has a semipermeable membrane that separates the blood from the clean dialysis fluid. As dialysis occurs, some of the urea and other small solutes in the blood diffuse into the dialysis fluid, whereas the larger solutes (plasma proteins) and blood cells remain in the blood. (B. From Goldman L, Ausiello D, Cecil textbook of medicine, ed 22, Philadelphia, 2004, Saunders.)
Passive Transport Processes. Channel-mediated passive transport (facilitated diffusion)
Active Transport Processes.Pinocytosis (endocytosis)
Transcription
Transcription of messenger RNA (mRNA). A DNA molecule “unzips” in the region of the gene to be transcribed. RNA nucleotides already present in the nucleus temporarily attach themselves to exposed DNA bases along one strand of the unzipped DNA molecule according to the principle of complementary pairing. As the RNA nucleotides attach to the exposed DNA, they bind to each other and form a chainlike RNA strand called a messenger RNA (mRNA) molecule. Notice that the new mRNA strand is an exact copy of the base sequence on the opposite side of the DNA molecule, with the exception of U (uracil) on the mRNA replacing T (thymine) on the DNA. As in all metabolic processes, the formation of mRNA is controlled by an enzyme—in this case, the enzyme is called RNA polymerase.
Life Cycle of the Cell.
Life cycle of the cell. The processes of growth and reproduction of successive generations of cells exhibit a cyclic pattern. Newly formed cells grow to maturity by synthesizing new molecules and organelles (G1 and G2 phases), including the replication of an extra set of DNA molecules (S phase) in anticipation of reproduction. Mature cells reproduce (M phase) by first distributing the two identical sets of DNA (produced during the S phase) in the orderly process of mitosis, then splitting the plasma membrane, cytoplasm, and organelles of the parent cell into two distinct daughter cells (cytokinesis). Daughter cells that do not go on to reproduce are in a maintenance phase (G0).
Classification of epithelial tissues.
Classification of epithelial tissues. The tissues are classified according to the shape and arrangement of cells. The color scheme of these drawings is based on a common staining technique used by histologists called hematoxylin and eosin (H&E) staining. H&E staining usually renders the cytoplasm pink and the chromatin inside the nucleus a purplish color. The cellular membranes, including the plasma membrane and nuclear envelope, do not generally pick up any stain and are thus transparent.
Types of muscle tissue.
Health Matters: Hay Fever and Asthma.
Health Matters: Hay Fever and Asthma. Some allergies cause itchiness and watering of the eyes, which may trigger frequent rubbing of the eyes that produces these reddened features. (From Zitelli B, Davis H: Atlas of pediatric physical diagnosis, ed 3, Philadelphia, 1997, Mosby.)
Muscle tissue
Membranous Epithelial Tissues: Simple Epithelium.
Membranous Epithelial Tissues: Simple Epithelium. Simple columnar: Photomicrograph of simple columnar epithelium. (Adapted from Gartner L, Hiatt J: Color textbook of histology, ed 3, Philadelphia, 2006, Saunders.)
Membranous Epithelial Tissues: Simple Epithelium.
Membranous Epithelial Tissues: Simple Epithelium. Stratified cuboidal (and columnar): Photomicrograph of the excretory duct of a gland. Note the double layer of cuboidal cells. (Adapted from Young B, Lowe J, Stevens A, et al: Wheater’s functional histology, ed 5, Philadelphia, 2006, Churchill Livingstone.)
Structural Classification of Multicellular Exocrine Glands.
Tubular (multiple)
Structural Classification of Multicellular Exocrine Glands.
Tubular (multiple)
Connective Tissues. Fibrous Tissue.
Reticular: The supporting framework of reticular fibers are stained black in this section of lymph node. (Dennis Strete.)
Connective Tissues. Bone Tissue.
Compact bone: Photomicrograph of ground compact bone. Many wheel-like structural units of bone, known as osteons or haversian systems, are apparent in this section. (Dennis Strete.)
Connective Tissues. Cartilage Tissue.
Elastic: Photomicrograph of the voice box (larynx). Note the cartilage cells in the lacunae surrounded by matrix and dark-staining elastic fibers. (Dennis Strete.)
Muscle and Nervous Tissues. Nervous Tissue.
Cardiac (striated involuntary): The dark bands, called intercalated disks, which are characteristic of cardiac muscle, are easily identified in this tissue section. (From Gartner L, Hiatt J: Color Textbook of Histology, ed 3, Philadelphia, 2006, Saunders.)
Body Cavities
Major body cavities. The dorsal body cavities are in the dorsal (back) part of the body. They include a cranial cavity above and a spinal cavity below. The ventral body cavities are on the ventral (front) side of the trunk. They include the thoracic cavity above the diaphragm and the abdominopelvic cavity below the diaphragm. The thoracic cavity is subdivided into the mediastinum in the center and pleural cavities to the sides. The abdominopelvic cavity is subdivided into the abdominal cavity above the pelvis and the pelvic cavity within the pelvis.
Dissectional Planes
Directions and planes of the body.
Homeostatic Control
Basic components of homeostatic control mechanisms. A, Heat regulation by a furnace controlled by a thermostat. B, Homeostasis of body temperature. Note that in both examples A and B, a stimulus (drop in temperature) activates a sensor mechanism (sensor in the thermostat or body temperature receptor) that sends input to an integrating, or control, center (on-off switch or hypothalamus), which then sends input to an effector mechanism (furnace or contracting muscle). The resulting heat that is produced maintains the temperature within the “normal range.” Feedback of effector activity to the sensor mechanism completes the control loop. Both are examples of negative feedback loops.
The Atom
Models of the atom. The nucleus—protons (+) and neutrons—is at the core. Electrons inhabit outer regions called electron shells or energy levels.
The Covalent Bond
Types of covalent bonds. A, A single covalent bond formed by the sharing of one electron pair between two atoms of hydrogen results in a molecule of hydrogen gas. B, A double covalent bond (double bond) forms by the sharing of two pairs of electrons between two atoms. In this case, two double bonds form—one between carbon and each of the two oxygen atoms.
Chemical Groups
The principal functional chemical groups. Each functional group confers specific chemical properties on the molecules that possess them.
Sucrose
Formation of sucrose. Glucose and fructose are joined in a synthesis reaction that involves the removal of water.
Steroids
Steroid compounds. The steroid nucleus—highlighted in yellow—found in cholesterol A, forms the basis for many other important compounds such as cortisol B, estradiol (an estrogen) C, and testosterone D.
Denatured Protein
Denatured protein. When a protein loses its normal folded organization and thus loses its functional shape, it is called a denatured protein. Denatured proteins are not able to function normally. However, if the protein shape is restored, the renatured protein may resume its normal function.
Blood Lipoproteins: Structure of a lipoprotein
Blood Lipoproteins: Structure of a lipoprotein
The Endoplasmic Reticulum
Endoplasmic reticulum (ER). In both the drawing A, and the transmission electron micrograph B, the rough ER (RER) is distinguished by the presence of tiny ribosomes dotting the boundary of flattened membrane sacs. The smooth ER (SER) is more tubular in structure and lacks ribosomes on its surface. Note also that the ER is continuous with the outer membrane of the nuclear envelope.
A Mitochondrion
Mitochondrion. Cutaway sketch showing outer and inner membranes. Note the many folds (cristae) of the inner membrane. Although some mitochondria have the capsule shape shown here, many are round or oval.
The Centrosome
Centrosome. Sketch showing the structure of a centrosome, which acts as a microtubule-organizing center for the cell’s cytoskeleton.
Examples of Cell Types. Muscle cells
Functional Anatomy of Cell Membranes.
Functional Anatomy of Cell Membranes. Structure: Sheet (bilayer) of phospholipids stabilized by cholesterol. Function: Maintains boundary (integrity) of a cell or membranous organelle
Functional Anatomy of Cell Membranes.
Functional Anatomy of Cell Membranes. Structure: Membrane proteins that bind to molecules outside the cell. Function: Form connections between one cell and another
Diffusion through a membrane
Diffusion through a membrane. Note that the membrane allows solute (a dissolved particle) and water to pass and that it separates a 10% solution from a 20% solution. The container on the left (A) shows the two solutions separated by the membrane at the start of diffusion. The container on the right (B) shows the result of diffusion after time.
Membrane channels
Membrane channels. Gated channel proteins form tunnels through which only specific molecules may pass—as long as the “gates” are open. Molecules that do not have a specific shape and charge are never permitted to pass through the channel. Notice that the transported molecules move from an area of high concentration to an area of low concentration. The cell membrane is said to be permeable to the type of molecule in question.
Receptor-mediated endocytosis.
Receptor-mediated endocytosis. An artist’s interpretation (left) and transmission electron micrographs (right) show the basic steps of receptor-mediated endocytosis. A, Membrane receptors bind to specific molecules in the extracellular fluid. B, A portion of the plasma membrane is pulled inward by the cytoskeleton and forms a small pocket around the material to be moved into the cell. C, The edges of the pocket eventually fuse and form a vesicle. D, The vesicle is then pulled inward—away from the plasma membrane—by the cytoskeleton. In this example, only the receptor-bound molecules enter the cell. In some cases, some free molecules or even entire cells may also be trapped within the vesicle and transported inward. (Electron micrographs: Courtesy M.M. Perry and A.B. Gilbert, Edinburgh Research Center.)
Citric acid cycle. KREBS
Citric acid cycle. The citric acid cycle is a circular metabolic pathway that breaks down an acetyl molecule with the release of CO2 molecules and energized electrons (which along with their protons [H+], are shuttled away by the coenzymes nicotinamide adenine dinucleotide [NAD] and flavin adenine dinucleotide [FAD]). ATP, Adenosine triphosphate
Filtration
Filtration. Particles small enough to fit through the pores in the filtration membrane move from the area of high hydrostatic pressure to the area of low hydrostatic pressure. This results in separation of small particles from larger ones.
Passive Transport Processes. Carrier-mediated passive transport (facilitated diffusion)
Active Transport Processes. Exocytosis
Protein Synthesis
Protein synthesis. Each of the numbered steps in the figure is further summarized in Table 5-2. Protein synthesis begins with transcription, a process in which an mRNA molecule forms along one gene sequence of a DNA molecule within the cell’s nucleus (1-3). As it is formed, the mRNA molecule separates from the DNA molecule (4), is edited (5), and leaves the nucleus through the large nuclear pores (6). Outside the nucleus, ribosome subunits attach to the beginning of the mRNA molecule and begin the process of translation (7). In translation, transfer RNA (tRNA) molecules bring specific amino acids—encoded by each mRNA codon—into place at the ribosome site (8). As the amino acids are brought into the proper sequence, they are joined together by peptide bonds (9) to form long strands called polypeptides (10). Several polypeptide chains may be needed to make a complete protein molecule.
DNA Replication
DNA replication. When a DNA molecule makes a copy of itself, it “unzips” to expose its nucleotide bases. Through the mechanism of obligatory base pairing, coordinated by the enzyme DNA polymerase, new DNA nucleotides bind to the exposed bases. This forms a new “other half” to each half of the original molecule. After all the bases have new nucleotides bound to them, two identical DNA molecules will be ready for distribution to the two daughter cells. Refer to Table 5-4 for numbered steps.
Exocrine Glands
Three types of exocrine glands. Exocrine glands may be classified by the method of secretion.
Nervous tissue.
Sports & Fitness: Tissues and Fitness. (From Linsley D: Wardlaw’s perspectives in nutrition, ed 2, St Louis, 1993, Mosby–Year Book.)
Nervous tissue
Membranous Epithelial Tissues: Simple Epithelium.
Membranous Epithelial Tissues: Simple Epithelium. Pseudostratified columnar: This photomicrograph from the respiratory system shows that each irregularly shaped columnar cell touches the underlying basement membrane. Placement of cell nuclei at irregular levels in the cells gives a false (pseudo) impression of stratification. This tissue is ciliated—note the “fuzz” along the outer edge of the cells. (Dennis Strete.)
Membranous Epithelial Tissues: Simple Epithelium.
Membranous Epithelial Tissues: Simple Epithelium. Transitional: Photomicrograph from the urethra showing that its cell shape is variable, from cuboidal to squamous. Several layers of cells are present. (Dennis Strete.)
Structural Classification of Multicellular Exocrine Glands.
Alveolar (single)
Structural Classification of Multicellular Exocrine Glands.
Some tubular; some alveolar
Connective Tissues. Dense Fibrous Tissue.
Irregular: Section of skin (dermis) showing arrangements of collagenous fibers (pink) and purple-staining fibroblast cell nuclei. (Dennis Strete.)
Connective Tissues. Bone Tissue.
Cancellous (spongy) bone: Photomicrograph of cancellous (spongy or trabecular) bone. The pink-stained mineralized bone tissue forms a lattice of irregular beams, or trabeculae, that support the softer reticular tissue of the bone marrow. The darkly stained nuclei of osteocytes (OC) are visible, as well as the dark boundaries (arrows) of mineralized bone layers or lamellae. (From Kerr J: Atlas of functional histology, London, 1999, Mosby.)
Connective Tissues. Cartilage Tissue.
Blood: Photomicrograph of a human blood smear (×270) showing three white blood cells (leukocytes), surrounded by numerous smaller red blood cells (erythrocytes) and platelets. (Adapted from Gartner L, Hiatt J: Color textbook of histology, ed 3, Philadelphia, 2006, Saunders.)
Muscle and Nervous Tissues. Nervous Tissue.
Nervous Tissue. Photomicrograph showing multipolar neurons surrounded by smaller neuroglia in a smear of spinal cord tissue. All of the large neurons in this photomicrograph show cell bodies and multiple cell processes. (Dennis Strete.)
Body Regions
Specific body regions. Note that the body as a whole can be subdivided into two major portions: axial (along the middle, or axis, of the body) and appendicular (the arms and legs, or appendages). Names of specific body regions follow the Latin form, with the English equivalent in parentheses.
Transverse section of the abdomen.
A transverse, or horizontal, plane through the abdomen shows the position of various organs within the body. This is a view from below, looking in a direction toward the head.
Levels of control.
The many complex processes of the body are coordinated at many levels: intracellular (within cells), intrinsic (within tissues/organs), and extrinsic (organ to organ).
Hydrogen
Structure of hydrogen and two of its isotopes. A, The most common form of hydrogen. B, An isotope of hydrogen called deuterium. C, The hydrogen isotope tritium. Note that isotopes of an element differ only in the number of their neutrons.
Water
Water—example of a polar molecule. The polar nature of water is represented in an energy-level model (A) and a spacefilling model (B). The two hydrogen atoms are nearer to one end of the molecule and give that end a partial positive charge. The “oxygen end” of the molecule attracts the electrons more strongly and thus has a partial negative charge.
Water as a Solvent
Water as a solvent. The polar nature of water (blue) favors ionization of substances in solution. Sodium (Na+) ions (pink) and chloride (Cl-) ions (green) dissociate in the solution.
Fatty Acids
Types of fatty acids. A, Palmitic acid, a saturated fatty acid. Note that it contains no double bonds; its hydrocarbon chain is filled with hydrogen atoms. The lower three-dimensional model shows three molecules of palmitic acid joined to a molecule of glycerol to form a triglyceride. B, The upper structural formula shows the unsaturated fatty acid linolenic acid. The lower three-dimensional model shows triglyceride exhibiting “kinks” caused by the presence of double bonds in the fatty acids.
Prostaglandin
Prostaglandin. Prostaglandins such as this example of prostaglandin E (PGE) are 20-carbon unsaturated fatty acids with a 5-carbon ring. Prostaglandins act as local regulators in the body.
DNA; Deoxyribonucleic Acid
The DNA molecule. Representation of the DNA double helix showing the general structure of a nucleotide and the two kinds of “base pairs”: adenine (A) (blue) with thymine (T) (yellow), and guanine (G) (purple) with cytosine (C) (red). Note that the G–C base pair has three hydrogen bonds and an A–T base pair has two. Hydrogen bonds are extremely important in maintaining the structure of this molecule.
Visualizing Proteins
Visualizing Proteins. Three ways to visualize the same folded protein molecule. (From National Institute of General Medical Sciences, The structures of life, July 2007,
The Ribosome
Ribosome. A ribosome is composed of a small subunit and a large subunit, shown here from two different perspectives. After the small subunit attaches to an mRNA strand containing the genetic “recipe” for a polypeptide strand, the subunits come together to form a complete ribosome. tRNA brings amino acids into the cavity between subunits, where they are assembled into a strand according to the mRNA code. As the polypeptide strand elongates, it moves out through a tunnel and a tiny exit hole in the large subunit.
The Cell Nucleus
Nucleus. An artist’s rendering A, and an electron micrograph B, show that the nuclear envelope is composed of two separate membranes and is perforated by large openings, or nuclear pores. (B. Courtesy Charles Flickinger, University of Virginia.)
Movement Patterns
Movement patterns. A flagellum (left) produces wavelike movements, which propel a sperm cell forward—like the tail of an eel. In humans, cilia (middle and right) found in groups on stationary cells beat in a coordinated oarlike pattern to push fluid and particles in the extracellular fluid along the outer cell surface.
Examples of Cell Types. Red blood cells
Functional Anatomy of Cell Membranes.
Functional Anatomy of Cell Membranes. Structure: Membrane proteins that act as channels or carriers of molecules. Function: Controlled transport of water-soluble molecules from one compartment to another
Functional Anatomy of Cell Membranes.
Functional Anatomy of Cell Membranes. Structure: Membrane proteins that bind to support structures. Function: Support and maintain the shape of a cell or membranous organelle; participate in cell movement; bind to fibers of the extracellular matrix (ECM)
Simple diffusion through a phospholipid bilayer
Simple diffusion through a phospholipid bilayer. Some small, uncharged molecules can easily pass through the phospholipid membrane, but water and urea (a waste product of protein catabolism) rarely get through the membrane. Larger uncharged molecules and ions (charged molecules) may not pass through the phospholipid membrane at all.
Membrane Carrier
Membrane carrier. In carrier-mediated transport, a membrane-bound carrier protein attracts a solute molecule to a binding site (A) and changes shape in a manner that allows the solute to move to the other side of the membrane (B). Passive carriers may transport molecules in either direction, depending on the concentration gradient.
Enzyme Action
Model of enzyme action. Enzymes are functional proteins whose molecular shape allows them to catalyze chemical reactions. Substrate molecule AB is acted on by a digestive enzyme to yield simpler molecules A and B as products of the reaction. Notice how the active site of the enzyme chemically fits the substrate—the lock-and-key model of biochemical interaction. Notice also how the enzyme molecule bends its shape in performing its function.
The Electron Transport Chain.
Electron transport system (ETS). 1, Pairs of high-energy electrons (e-) and their protons (H+) are shuttled from the citric acid cycle by coenzymes NAD and FAD to protein complexes (I, II, III, IV) embedded in the inner membrane of the mitochondrion. 2, As the electrons are transported from molecule to molecule (red path), their energy is used to pump the protons (H+) to the intermembrane space. 3, As the proton gradient increases, passive movement of protons back across the membrane (through the ATP synthase carrier) provides the energy needed to “recharge” ADP and Pi to form ATP. Notice that oxygen (from O2) is required as the final acceptor of the electrons and protons transported through the system, thus forming H2O as a by-product. ADP, Adenosine diphosphate; ATP, adenosine triphosphate; FAD, flavin adenine dinucleotide; NAD, nicotinamide adenine dinucleotide.
Passive Transport Processes. Simple diffusion
Active Transport Processes. Pumping
DNA
Watson-Crick model of the DNA molecule. The DNA structure illustrated here is based on that published by James Watson (photograph, left) and Francis Crick (photograph, right) in 1953. Note that each side of the DNA molecule consists of alternating sugar and phosphate groups. Each sugar group is united to the sugar group opposite it by a pair of nitrogenous bases (adenine-thymine or cytosine-guanine). The sequence of these pairs constitutes a genetic code that determines the structure and function of a cell. (Cold Spring Harbor Laboratory.)
The Genetic Code
The genetic code. The first graphic “phrasebook” or “decoder” of the genetic language of the cell was developed in 1966 to summarize the amino acids encoded by various codons (three-base sequences of nucleotides) in RNA. One of the clearest is this version adapted from Ben Fry’s decoder, developed when he was a student at Massachusetts Institute of Technology. To read the decoder, start with any codon (for example, CGA). Find the first base along the top of the decoder to find the correct box to use (C is the third box). The second base is found in each row of that box, labeled on the left (G is the first row). Then use the third base to find the correct column, labeled at the bottom of each box (A is the second column, showing that Arg [arginine] is the amino acid encoded by CGA).
Meiosis.
Meiosis. Meiotic cell division takes place in two steps: meiosis I and meiosis II. Meiosis I is called reduction division because the number of chromosomes is reduced by half (from the diploid number to the haploid number). More detailed diagrams of meiosis are presented in Chapters 24 and 25. Only four sets of chromosomes were used in this figure for the sake of simplicity.
Classification of connective tissues.
Healing of a minor wound.
Healing of a minor wound. When a minor injury damages a layer of epithelium and the underlying connective tissue (as in a minor skin cut), the epithelial tissue and the connective tissue can repair itself.
Epithelial tissue
Membranous Epithelial Tissues: Simple Epithelium.
Membranous Epithelial Tissues: Simple Epithelium. Simple squamous: Photomicrograph of the Bowman capsule of the kidney showing thin simple squamous epithelium. (Dennis Strete.)
Membranous Epithelial Tissues: Simple Epithelium.
Membranous Epithelial Tissues: Simple Epithelium. Stratified squamous, keratinized: Photomicrograph of the thick skin showing cells becoming progressively flattened and scalelike as they approach the surface and are lost. The outer surface of this epithelial sheet contains many flattened cells that have lost their nuclei. (Dennis Strete.)
Structural Classification of Multicellular Exocrine Glands.
Tubular (single, straight)
Structural Classification of Multicellular Exocrine Glands.
Alveolar (multiple)
Connective Tissues. Fibrous Tissue. Loose (areolar)
Connective Tissues. Fibrous Tissue Loose (areolar): Notice that the bundles of collagen fibers are a pinkish color and the elastin fibers and cell nuclei are a darker, purplish color. (Adapted from Gartner L, Hiatt J: Color textbook of histology, ed 3, Philadelphia, 2006, Saunders.)
Connective Tissues. Dense Fibrous Tissue.
Regular collagenous: Photomicrograph of tissue in a tendon. Note the multiple (regular) bundles of collagenous fibers arranged in parallel rows. (Dennis Strete.)
Connective Tissues. Cartilage Tissue.
Hyaline: Photomicrograph of the trachea. Note the many spaces, or lacunae, in the gel-like matrix. (Dennis Strete.)
Muscle and Nervous Tissues. Nervous Tissue.
Skeletal (striated voluntary): Note the striations of the skeletal muscle cell fibers in longitudinal section. (Dennis Strete.)
Unit II. Support and Movement: The integument, Skeletal Tissues, The Axial Skeleton, The Appendicular Skeleton, Joint Systems, and The Muscular System.
The Skin
Photomicrograph of the skin. The staining of this cross section of skin clearly shows the red superficial epidermis and the bluish dermis below it. This photograph has been cropped; the dermis is actually quite thick in comparison to the epidermis. (Ed Reschke. Barbara Cousins.)
Lines of Stress
Cleavage lines. A, If an incision "cuts across" cleavage lines (Langer’s lines), stress tends to pull the cut edges apart and may retard healing. B, Surgical incisions parallel to cleavage lines are subjected to less stress and tend to heal more rapidly.
Color changes in a bruise.
Color changes in a bruise. In this light-skinned individual, different colors appear in the skin as hemoglobin becomes unoxygenated and turns bluish (see Figure 6-12) and perhaps even black as the blood clots. As macrophages consume the hemoglobin, it is broken down into brownish, greenish, and yellowish pigments—sometimes producing a rainbow of skin colors. (From McCance K, Huether S: Pathophysiology, ed 5, St Louis, 2005, Mosby.)
Male pattern baldness.
An x linked gene.
Tinea infection
Tinea infection (ringworm). Note that the lesions heal in the center, with inflamed rings left on the skin’s surface. (From Shah B, Laude T: Atlas of pediatric clinical diagnosis, Philadelphia, 2000, Saunders.)
Classification of burns.
Classification of burns. Partial-thickness burns include first- and second-degree burns. Full-thickness burns include third-degree burns. Fourth-degree burns involve tissues under the skin, such as muscle or bone.
Structure of the Skin
Compact and cancellous bone in a flat bone.
Compact and cancellous bone in a flat bone. A, Section of a flat bone. (See also Figure 7-4.) Outer layers of compact bone surround cancellous bone. Note the fine structure of compact (B) and cancellous (C) bone. (B: Dennis Strete.)
Endochondral bone formation.
Endochondral bone formation. A, Cartilage model. B, Subperiosteal bone collar formation. C, Development of the primary ossification center and entrance of a blood vessel. D, Prominent medullary cavity with thickening and lengthening of the collar. E, Development of secondary ossification centers in epiphyseal cartilage. F, Enlargement of secondary ossification centers, with bone growth proceeding toward the diaphysis from each end. G, With cessation of bone growth, the lower, then upper epiphyseal plates disappear (only the epiphyseal lines remain).
Bone remodeling.
Bone remodeling. Bone formation on the outside of the shaft coupled with bone reabsorption on the inside increases the bone’s diameter. Endochondral growth during bone remodeling increases the length of the diaphyses and causes the epiphysis to enlarge.
Skeleton. A Anterior view.
Skeleton. A Anterior view.
Left half of the skull viewed from within.
Bones of the skull.
Bones of the skull. G, Vomer. G1, Anterior view; G2, lateral view.
Bones of the nasal cavity.
Bones of the nasal cavity.
Vertebrae.
Vertebrae. E, Lateral and superior views of a thoracic vertebra, T10. F, Lateral and superior views of a lumbar vertebra, L3. (From Gosling J, Harris P, Whitmore I, Willan P: Human anatomy, ed 4, Philadelphia, 2002, Mosby.)
Bones of the arm (right arm, posterior view)
Bones of the arm (right arm, posterior view). A, Humerus (upper part of the arm). B, Radius and ulna (forearm). C, Elbow joint, showing how the distal end of the humerus joins the proximal ends of the radius and ulna. (The inset shows the relative position of the right arm bones within the entire skeleton.) (C: Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
Arches of the foot.
Arches of the foot. A, Longitudinal arch. The medial portion is formed by the calcaneus, talus, navicular, cuneiforms, and three metatarsal bones; the lateral portion is formed by the calcaneus, cuboid, and two lateral metatarsal bones. B, "Flatfoot" results when the tendons and ligaments attached to the tarsal bones are weakened. Downward pressure by the weight of the body gradually flattens out the normal arch of the bones. The photo shows the clinical appearance of a flatfoot. C, Transverse arch in the metatarsal region of the left foot. D, High heels throw the weight forward and cause the heads of the metatarsal bones to bear most of the body's weight. (Arrows show direction of force.) (From Yvonne Wylie Walston. From Seidel HM, Ball JW, Dains JE, Benedict GW: Mosby's guide to physical examination, ed 5, St Louis, 2003, Mosby.)
Fibrous joints
Fibrous joints. Examples of the types of fibrous joints.
Joints of the wrist.
Joints of the wrist. A, Coronal section of the hand showing the joints of the wrist. Note that the thumb and little finger are not in the plane of section. B, Radiograph of an adolescent hand and wrist. Note that the epiphyseal plates are present. C, Major synovial spaces of the wrist: 1, proximal; 2, intermediate; 3, distal. (A-B: From Gosling J, Harris P, Whitmore I, Willan P: Human anatomy, ed 4, Philadelphia, 2002, Mosby. C: From Heylings D, Spence R, Kelly B: Integrated anatomy, Edinburgh, 2007, Churchill Livingstone.)
Vertebrae.
Vertebrae. Sagittal section of vertebrae showing normal (A) and herniated (B) disks.
Movements and ROM of the shoulder.
Movements and ROM of the shoulder. A, Forward flexion, extension (back to the anatomical position of 0 degrees), and backward hyperextension up to 50 degrees. B, Abduction and adduction. (From Barkauskas V, Baumann L, Stoltenberg-Allen K, Darling-Fisher C: Health and physical assessment, ed 2, St Louis, 1998, Mosby.)
Movements and ROM of the foot and ankle.
Movements and ROM of the foot and ankle. A, Dorsiflexion and plantar flexion. B, Inversion and eversion. C, Abduction and adduction.
Sports and Fitness. Knee arthrogram.
Sports and Fitness. Knee arthrogram A, Normal medial meniscus. Spot film showing the normal triangular shape of the meniscus (arrows). B, Linear tear of the medial meniscus.
Muscle actions.
Muscle actions. A, The flexor muscle (biceps brachii) is the prime mover in flexing the elbow. The extensor muscle (triceps brachii) is the antagonist, which in this case must relax to permit easy flexion of the elbow. The pronator teres muscle acts as a synergist by also flexing the elbow. B, Here the biceps brachii is again the prime mover of flexion of the elbow. The pronator teres muscle acts as a synergist by also flexing the elbow. To prevent the biceps from also moving the shoulder while straining against a heavy weight, the posterior portion of the deltoid muscle tenses to stabilize the shoulder joint—thus acting as a fixator muscle in this action. (Adapted from Muscolino J: Kinesiology, St Louis, 2006, Mosby.)
Muscles of mastication.
Muscles of mastication. A, Muscles of the tongue and pharynx. B, Right lateral dissection view showing the insertion of the temporalis muscle on the mandible—the masseter muscle is cut and part of the zygomatic arch has been removed. C, View of the pterygoids in a posterior dissection view. D, Lateral and medial pterygoid muscles viewed from the right side after removal of the zygomatic arch.
Muscles of the back.
Muscles of the back. B, Deep muscle dissection of the back—posterior view. The superficial and intermediate muscles have been removed. The muscles in the gluteal region have been removed to expose the pelvic insertion of the multifidus.
Muscles acting on the forearm.
Muscles acting on the forearm. A, Lateral view of the right shoulder and arm. B, Anterior view of the right shoulder and arm (deep). The deltoid and pectoralis major muscles have been removed to reveal deeper structures.
Cross sections (proximal to distal) through the lower extremity.
Cross sections (proximal to distal) through the lower extremity. A, Section through the middle of the femur. B, Section about 4 cm above the adductor tubercle of the femur. C, Section about 10 cm distal to the knee joint. D, Section about 6 cm above the medial malleolus. In each section you are viewing the superior (proximal) aspect of the specimen.
Superficial muscles of the leg. A, Anterior view. B, Posterior view. C, Lateral view.
Unique features of the skeletal muscle cell.
Unique features of the skeletal muscle cell. Notice especially the T tubules, which are extensions of the plasma membrane, or sarcolemma, and the sarcoplasmic reticulum (SR), a type of smooth endoplasmic reticulum that forms networks of tubular canals and sacs containing stored calcium ions. A triad is a triplet of adjacent tubules: a terminal (end) sac of the SR, a T tubule, and another terminal sac of the SR.
Effects of excitation on a muscle fiber.
Effects of excitation on a muscle fiber. Excitation of the sarcolemma by a nerve impulse initiates an impulse in the sarcolemma. The impulse travels across the sarcolemma and through the T tubules, where it triggers adjacent sacs of the sarcoplasmic reticulum to release a flood of calcium ions (Ca++) into the sarcoplasm. Ca++ is then free to bind to troponin molecules in the thin filaments. This binding, in turn, initiates the chemical reactions that produce a contraction.
Energy sources for muscle contraction.
Energy sources for muscle contraction. A, The basic structure of two high-energy molecules in the sarcoplasm: adenosine triphosphate (ATP) and creatine phosphate (CP). B, This diagram shows how energy released during the catabolism of nutrients can be transferred to the high-energy bonds of ATP directly or, instead, stored temporarily in the high-energy bond of CP. During contraction, ATP is hydrolyzed and the energy of the broken bond is transferred to a myosin head.
The twitch contraction.
The twitch contraction. Three distinct phases are apparent: (1) the latent period, (2) the contraction phase, and (3) the relaxation phase.
Factors that influence the strength of muscle contraction.
Muscle strain.
Muscle strain. Severe strain of the biceps brachii muscle. In a severe muscle strain, a muscle may break in two pieces and result in a visible gap in muscle tissue under the skin. Notice how the broken ends of the muscle reflexively contract (spasm) to form a knot of tissue. (Courtesy Rob Williams, from Booher JM, Thibodeau GA: Athletic injury assessment, ed 2, St Louis, 1989, Mosby.)
Effects of Exercise on Skeletal Muscles.
Effects of Exercise on Skeletal Muscles. B, Effects of aerobic training. The graph shows that aerobic training increases the metabolic condition of muscles mainly by increasing levels of enzymes and the availability of oxygen. Only moderate increases in muscle fiber size occur.
Skin Structure
Diagram of skin structure. A, Thick skin, found on surfaces of the palms and soles of the feet. B, Thin skin, found on most surface areas of the body. In each diagram, the epidermis is raised at one corner to reveal the papillae of the dermis.
Melanin
Melanin production. Melanin is produced by melanocytes in the stratum basale. Melanocytes have long projections that reach between the keratinocytes and release packets of pigment called melanosomes. By endocytosis, the melanosomes are brought into the keratinocytes, where they are arranged as a cap over the nucleus—protecting it from UV radiation from above.
Vitamin D production.
Vitamin D production. The essential first step in producing the active form of vitamin D in the body occurs in the presence of ultraviolet (UV) light in the skin.
Structure of nails.
Structure of nails. A, Fingernail viewed from above. B, Sagittal section of a fingernail and associated structures. (Courtesy Christine Olekyk.)
Decubitus ulcer.
Decubitus ulcer. The skin forms craterlike lesions when the blood supply is diminished and skin tissue cannot be maintained in the area of reduced blood flow. (From Potter P, Perry A: Basic nursing: essentials for practice, ed 5, St Louis, 2003, Mosby.)
Vitiligo.
The skeleton.
Orientation of trabeculae.
Orientation of trabeculae. Longitudinal section of a long bone showing trabeculae oriented along lines of stress.
Fetal ossification centers.
Fetal ossification centers. Photograph of a specially prepared fetal hand specimen showing primary ossification centers in the bones of the hand (metacarpal bones) and fingers (phalanges). Note that none of the wrist (carpal) bones show any evidence of ossification. (From Williams P: Gray’s anatomy, ed 38, Philadelphia, 1996, Churchill Livingstone.)
Primary osteon formation.
Primary osteon formation. First, a tubelike passage in the woven bone surrounding a blood vessel is demineralized by osteoblasts. Osteoblasts then begin laying down one layer (lamella) after another along the endosteal lining of the tube. As layers build up, they eventually fill most of the demineralized tube—thus forming the concentric lamellae around a central canal that characterize an osteon.
Skeleton. B, Posterior view. C, Lateral view.
Skeleton. B, Posterior view. C, Lateral view.
Bones of the left orbit and signs of fracture.
Bones of the left orbit and signs of fracture. A, Skull showing an area of enlargement. B, Diagram showing detail of the orbital bones.
Bones of the skull.
Bones of the skull. H, Right maxilla. H1, Medial view; H2, lateral view.
Skull at birth.
Skull at birth. A, Skull showing an area of enlargement. B, Diagram showing detail of the orbital bones. C, Viewed from behind. D, Viewed from above. (B-D: From Abrahams P, Marks S, Hutchings R: McMinn's color atlas of human anatomy, ed 5, Philadelphia, 2003, Mosby.)
Vertebrae.
Vertebrae. G, Lumbar vertebra L5 and the upper portion of the sacrum in an expanded anterior view. H, Oblique view of the sacrum, coccyx, and right hip bone. (From Gosling J, Harris P, Whitmore I, Willan P: Human anatomy, ed 4, Philadelphia, 2002, Mosby.)
Bones of the hand and wrist.
Bones of the hand and wrist. A, Dorsal view of the right hand and wrist. B, Palmar view of the right hand and wrist. (Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
Comparison of the bony pelvis of the male and female skeletons.
Comparison of the bony pelvis of the male and female skeletons. A and C, Diagrams showing components of the bony pelvis of the male and female. B and D, Photographs showing the bony pelvis of the male and female from in front and above. (B-D: From Abrahams P, Marks S, Hutchings R: McMinn's color atlas of human anatomy, ed 5, Philadelphia, 2003, Mosby.)
Cartilaginous joints
Cartilaginous joints. Examples of the types of cartilaginous joints.
Joints of the hand and fingers.
Joints of the hand and fingers. Radiograph of an adult hand shows the absence of epiphyseal plates. All the phalanges and metacarpal bones are easily seen. The inset shows a dissected specimen in a coronal section through the second metacarpophalangeal joint. The collateral ligaments are simply thickenings of the walls of the joint capsule. (From Gosling J, Harris P, Whitmore I, Willan P: Human anatomy, ed 4, Philadelphia, 2002, Mosby.)
Vertebrae and their ligaments.
Vertebrae and their ligaments. Sagittal section of two lumbar vertebrae and their ligaments.
ROM of elbow.
Movements and ROM of the elbow. A, Flexion and extension of the elbow. B, Supination and pronation. (From Barkauskas V, Baumann L, Stoltenberg-Allen K, Darling-Fisher C: Health and physical assessment, ed 2, St Louis, 1998, Mosby.)
Olecranon bursitis.
Olecranon bursitis. Pain, inflammation, and swelling of the bursa may limit motion, although the elbow joint itself may not be affected. (From Seidel HM, Ball JW, Dains JE, Benedict GW: Mosby's guide to physical examination, ed 5, St Louis, 2003, Mosby.)
Sports and Fitness. Joint replacement.
Lever classes.
Lever classes. A, Class I: fulcrum (F) between the load (L) and force or pull (P). B, Class II: load (L) between the fulcrum (F) and force or pull (P). C, Class III: force or pull (P) between the fulcrum (F) and the load (L). The lever rod is yellow in each.
Muscles that move the head. Posterior view of muscles of the neck and the back.
Muscles of the pelvic floor. A, Male, inferior view. B, Female, inferior view.
Muscles acting on the forearm.
Muscles acting on the forearm. A, Biceps brachii. B, Coracobrachialis and pronator teres. C, Triceps brachii. D, Brachialis. O, Origin; I, insertion.
Muscles of the anterior aspect of the thigh.
Muscles of the anterior aspect of the thigh. A, Anterior view of the right thigh. B, Adductor region of the right thigh. The tensor fasciae latae, sartorius, and quadriceps muscles have been removed.
Intrinsic muscles of the foot. Inferior (plantar) view.
Storage and release of calcium ions.
Storage and release of calcium ions. At rest (left), calcium ion pumps in the sarcoplasmic reticulum (SR) membrane actively pull Ca++ into the SR—thus creating a concentration gradient with very little Ca++ left in the sarcoplasm. Note that the Ca++ is sequestered by protein filaments (calsequestrin) in "bunches" just inside the closed Ca++ channels. When the fiber is stimulated (right), an electrical impulse travels from the sarcolemma and down the T tubule, where the voltage fluctuation triggers the opening of voltage-gated calcium channels. This allows passive diffusion of the Ca++ inside the SR out to the sarcoplasm, where it will trigger the contraction process. Almost immediately after stimulation, the calcium channels close and the Ca++ is once again pumped into the sacs of the SR (left). ATP, Adenosine triphosphate.
The molecular basis of muscle contraction.
Blood supply of muscle fibers.
Blood supply of muscle fibers. Tiny "exchange" vessels called capillaries branch out longitudinally (L) from small arteries (arrow) to form a network that supplies muscle fibers with glucose and oxygen and removes carbon dioxide and lactic acid. In this micrograph, the muscle fibers appear translucent and the blood vessels appear reddish. (From Lodish H: Molecular cell biology, ed 4, New York, 2000, WH Freeman.)
Myograms
Myograms of various types of muscle contractions. A, A single twitch contraction. B, The treppe phenomenon, or "staircase effect," is a steplike increase in the force of contraction over the first few in a series of twitches. C, Incomplete tetanus occurs when a rapid succession of stimuli produces "twitches" that seem to add together (wave summation) to produce a rather sustained contraction. D, Complete tetanus is a smoother sustained contraction produced by the summation of "twitches" that occur so close together that the muscle cannot relax at all.
Isotonic and isometric contraction.
Isotonic and isometric contraction. A, In isotonic contraction the muscle shortens and produces movement. Concentric contractions occur when the muscle shortens during the movement. Eccentric contractions occur when the contracting muscle lengthens. B, In isometric contraction the muscle pulls forcefully against a load but does not shorten because it cannot overcome the resistance.
A More Detailed Look at the Sarcomere.
Thin Skin
Thick and thin skin. A, The surface of thick skin is hairless and features regular, deep sulci and friction ridges, which form the "prints" of the palmar and plantar surfaces of the hands and feet. B, The surface of thin skin features irregular sulci (grooves) and hairs. (Copyright Kevin Patton, Lion Den Inc, Weldon Spring, MO.)
Skin Color
How genes affect skin color. Genes determine an individual’s basic skin color by controlling the amount and type of melanin synthesized and deposited in the epidermis. However, as the diagram shows, other factors may modify the basic skin color.
The skin as a thermoregulatory organ.
The skin as a thermoregulatory organ. When homeostasis requires that the body conserve heat, blood flow in the warm organs of the body’s core increases. A, When heat must be lost to maintain stability of the internal environment, flow of warm blood to the skin increases. B, Heat can be lost from the blood and skin by means of radiation, conduction, convection, and evaporation. The head, hands, and feet are major areas of heat loss.
Pigmented nails.
Pigmented nails. In light-skinned individuals, the nail bed is usually free of pigmentation. In very dark-skinned individuals, yellowish or brown pigmented bands (seen in the photograph) are common. (From Habif TP: Clinical dermatology, ed 4, St Louis, Mosby, 2004.)
Psoriasis.
Psoriasis. Inflammation and scaling are characteristic of this skin disorder. (From James WD, Berger TG, Elston DM: Andrew’s diseases of the skin: clinical dermatology, ed 10, London, 2000, Saunders.)
Blisters
Vesicular inflammation
Types of bones.
Types of bones. Examples of bone types include A, long bones (humerus); B, short bones (carpal bone); C, irregular bones (vertebra); D, flat bones (sternum); and E, sesamoid bones (patella and sesamoid of thumb).
Osteoblasts and Osteoclasts
Bone-forming and bone-eroding cells. Note the large multinucleate osteoclast cell (Oc) dissolving bone on the upper surface of a developing branch of bone while smaller osteoblast cells (Ob) on the undersurface of the bone are secreting new osteoid. (From Williams P: Gray’s anatomy, ed 38, Philadelphia, 1996, Churchill Livingstone.)
Endochondral ossification of the hand and wrist.
Endochondral ossification of the hand and wrist. Radiographs showing increasing numbers of ossification centers becoming visible in the wrist with increasing age. (From Zitelli B, Davis H: Atlas of pediatric physical diagnosis, ed 4, Philadelphia, Mosby, 2002.)
Bone fracture healing.
Bone fracture healing. A, Fracture of the femur. B, Formation of a fracture hematoma. C, Formation of internal and external bony callus. D, Bone remodeling complete.
Anterior view of the skull. (Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
Anterior view of the skull. (Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
Bones of the skull.
Bones of the skull. A, Right parietal bone viewed from the lateral side. B, Right temporal bone viewed from the lateral side.
Bones of the skull.
Bones of the skull. I, Right zygomatic bone viewed from the lateral side. J, Right palatine bone. J1, Medial view; J2, anterior view.
Hyoid bone
Hyoid bone. The photo insert (radiograph) shows the relationship of the hyoid bone to the base of the skull and cervical spine. Note that the hyoid does not articulate with any other bony structure.
Thoracic cage
Thoracic cage. Note the costal cartilages and their articulations with the body of the sternum.
The female pelvis.
The female pelvis. A, Pelvis viewed from above. Note that the brim of the true pelvis (dotted line) marks the boundary between the superior false pelvis (pelvis major) and the inferior true pelvis (pelvis minor). B and C, Pelvis viewed from below. A comparison of the male pelvis and female pelvis is shown in Figure 8-26. (C: Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
Bone fractures.
Bone fractures. A, Open. B, Closed. C, Incomplete and complete. D, Linear, transverse, and oblique.
Structure of synovial joints.
Structure of synovial joints. A, Artist's interpretation (composite drawing) of a typical synovial joint. B, Dissection photo showing the articular surface of a typical synovial joint—the distal radiocarpal joint (the joint capsule has been cut). See pp. 271-272 for a description of this joint. (B: From Gosling J, Harris P, Whitmore I, Willan P: Human anatomy, ed 4, Philadelphia, 2002, Mosby.)
The hip joint.
The hip joint. A, Artist's diagram, and B, dissection photo (anterior views). C, Artist's diagram, and D, dissection photo (frontal section). (B-D: Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
The Goniometer.
Use of a goniometer. Using a goniometer to measure ROM at the elbow. (From Barkauskas V, Baumann L, Stoltenberg-Allen K, Darling-Fisher C: Health and physical assessment, ed 2, St Louis, 1998, Mosby.)
ROM of hand and wrist.
Movements and ROM of hand and wrist. A, Metacarpophalangeal flexion and hyperextension. B, Wrist radial and ulnar movement. C, Wrist flexion and hyperextension. D, Finger abduction and adduction. (From Seidel HM, Ball JW, Dains JE, Benedict GW: Mosby's guide to physical examination, ed 5, St Louis
Types of arthritis.
Types of arthritis. A, Osteoarthritis. Note Heberden nodes (H) on the distal interphalangeal joints and Bouchard nodes (B) on the proximal interphalangeal joints. B, Rheumatoid arthritis. Note the marked ulnar deviation of the fingers. C, Gouty arthritis. Note the tophi filled with sodium urate crystals. (From Swartz MH: Textbook of physical diagnosis, ed 4, Philadelphia, 2002, Saunders.)
Classification of Synovial Joints
General overview of the body's musculature.
General overview of the body's musculature. A, Anterior view. B, Posterior view.
Muscles of the thorax.
Muscles of the thorax. Anterior view. Note the relationship of the internal and external intercostal muscles and placement of the diaphragm.
Muscles acting on the shoulder girdle.
Muscles acting on the shoulder girdle. A, Posterior view. The trapezius has been removed on the right to reveal the deeper muscles. B, Anterior view. The pectoralis major has been removed on both sides. The pectoralis minor has also been removed on the right side.
Muscles of the forearm.
Muscles of the forearm. A, Anterior view showing the right forearm (superficial). The brachioradialis muscle has been removed. B, Anterior view showing the right forearm (deeper than A). The pronator teres, flexor carpi radialis and ulnaris, and palmaris longus muscles have been removed. C, Anterior view showing the right forearm (deeper than A or B). The brachioradialis, pronator teres, flexor carpi radialis and ulnaris, palmaris longus, and flexor digitorum superficialis muscles have been removed. D, Posterior view showing the deep muscles of the right forearm. The extensor digitorum, extensor digiti minimi, and extensor carpi ulnaris muscles have been cut to reveal deeper muscles.
Muscles that adduct the thigh. O, Origin; I, insertion.
Sports and Fitness. The rotator cuff stabilizes the shoulder during athletic activities.
Skeletal muscle striations.
Skeletal muscle striations. Color-enhanced scanning electron micrographs (SEMs) showing longitudinal views of skeletal muscle fibers. B shows detail of A at greater magnification. Note that the myofilaments of each myofibril form a pattern that when viewed together, produces the striated (striped) pattern typical of skeletal muscle. (A: Courtesy Dr. J.H. Venable, Department of Anatomy, Colorado State University, Fort Collins, CO. B: Courtesy Dr. H.E. Huxley.)
Role of calcium in muscle contraction.
Role of calcium in muscle contraction. Color-enhanced scanning electron micrograph (SEM) of a thin filament. When calcium is absent, the active myosin binding sites on actin are covered by tropomyosin. However, after calcium becomes available and binds to troponin, the tropomyosin is pulled out of its blocking position and reveals the active binding sites on actin. (From Lodish H: Molecular cell biology, ed 4, New York, 2000, WH Freeman.)
Aerobic and anaerobic respiration during muscular activity.
Aerobic and anaerobic respiration during muscular activity. A, Aerobic respiration (purple bars) can supply energy for muscle contraction for a longer time than can anaerobic respiration (purple). B, The lines show that 100% of the energy used at the beginning of maximal exercise comes from anaerobic processes. However, the muscles soon switch to aerobic sources of energy so after 1 hour of maximal exercise, nearly 100% of the energy comes from aerobic respiration in the muscle fibers. More information on aerobic and anaerobic respiration is found in Chapter 27.
Role of calcium in twitch and tetanus.
Role of calcium in twitch and tetanus. A, A single, sudden increase in calcium (Ca++) availability triggers the twitch contraction. B, Repeated stimuli maintain a high level of calcium, permitting sustained (tetanic) contraction. (Adapted from Pollard T, Earnshaw W: Cell biology, ed 2, Philadelphia, 2008, Saunders.)
Cardiac muscle fiber.
Cardiac muscle fiber. Unlike other types of muscle fibers, cardiac muscle fiber is typically branched and forms junctions, called intercalated disks, with adjacent cardiac muscle fibers. Like skeletal muscle fibers, cardiac muscle fibers contain sarcoplasmic reticula and T tubules—although these structures are not as highly organized as in skeletal muscle fibers.
Sports and Fitness. A, Types of muscle fibers.
Sports and Fitness. A, Types of muscle fibers. Using a special staining technique, this micrograph of a cross section of skeletal muscle tissue shows a mix of fiber types: R, red (slow) fibers; W, white (fast) fibers; and I, intermediate fibers.
The Epidermis
Epidermal cell types. Keratinocytes, most of the cells seen here, begin their life in the deepest layer of the epidermis and are pushed upward as more keratinocytes are formed. Melanocytes produce pigments. Epidermal dendritic cells (DCs) function in immunity. Tactile epithelial cells (Merkel cells) attach to sensory nerve endings to form "light touch" receptors.
Tanning
Tanning effects in skin. Photos showing skin effects of ultraviolet (UV) radiation on day 8 after exposure to increasing doses (1 through 7) in three skin types. Notice that the Caucasian skin involves more redness (from burning) than the darker skin types, which become even darker in response to higher doses of UV radiation. (From Rouzaud F, Kadekaro A, Abdel-Malek ZA, Hearing VJ: MC1R and the response of melanocytes to ultraviolet radiation,
Role of skin in homeostasis of body temperature.
Role of skin in homeostasis of body temperature. Body temperature is continually monitored by nerve receptors in the skin and other parts of the body. These receptors feed information back to the hypothalamus of the brain, which compares the actual temperature with the set point temperature and then sends out an appropriate correction signal to effectors. If actual body temperature is above the set point temperature, sweat glands in the skin are signaled to increase their secretion and thus promote evaporation and cooling. At the same time, blood vessels in the dermis are signaled to dilate and thus promote radiation of heat away from the skin’s surface.
Onycholysis.
Onycholysis. Note that separation of this nail from the nail bed begins at the free edge. Minor trauma to long fingernails is the most common cause. (From Habif TP: Clinical dermatology, ed 2, St Louis, 1990, Mosby.)
Skin cancers.
Skin cancers. (A: From Goldman L, Ausiello D, Cecil textbook of medicine, ed 23, Philadelphia, 2003, Saunders. B: From Noble J: Textbook of primary care medicine, ed 3, Philadelphia, 2001, Mosby. C: From Townsend C, Beauchamp RD, Evers BM, Mattox K: Sabiston textbook of surgery, ed 18, Philadelphia, 2008, Saunders. D: From Rakel R: Textbook of family medicine, ed 7, Philadelphia, 2007, Saunders.)
Subcutaneous and intradermal injections.
The Long Bone
Long bone. A, Partial frontal section of a long bone (tibia) showing cancellous and compact bone. B, Frontal section of a long bone. (B: From White T, Human osteology, ed 2, Philadelphia, 2000, Academic Press.)
Osteocyte
Osteocyte. A, Sketch showing osteocytes trapped inside hollow lacunae within hard bone matrix. B, Scanning electron micrograph showing an osteocyte within a lacuna. Note the cytoplasmic process (arrow) extending into a canaliculus below. The cell is surrounded by collagen fibers and mineralized bone. (A: From Muscolino J: Kinesiology, St Louis, 2006, Mosby. B: From Erlandsen SL, Magney J: Color atlas of histology, St Louis, 1992, Mosby.)
Epiphyseal plate structure.
Epiphyseal plate structure. An epiphyseal plate between the epiphyses and diaphyses of a long bone. Photograph shows the zones of the epiphyseal plate. (Ed Reschke.)
Types of cartilage.
Types of cartilage. A, Hyaline cartilage of the trachea. B, Elastic cartilage of the epiglottis. Note the black elastic fibers in the cartilage matrix and the perichondrium layers on both surfaces. C, Fibrocartilage of an intervertebral disk. (A-B: Dennis Strete.)
Skull viewed from the right side.
Bones of the skull.
Bones of the skull. C, Frontal bone viewed from the front and slightly above. D, Occipital bone viewed from below.
Bones of the skull.
Bones of the skull. K, Right lacrimal bone viewed from the lateral side. L, Right nasal bone viewed from the lateral side.
The vertebral column.
The vertebral column. A, Right lateral view. B, Anterior view. C, Posterior view. The photo inset shows a midline sagittal magnetic resonance image (MRI) of the vertebral column. (From Williams P: Gray's anatomy, ed 38, Philadelphia, Churchill Livingstone, 1996.)
Articulation of a rib and vertebra.
Articulation of a rib and vertebra. A, Note the head of the rib articulating with the vertebral body and the tubercle of the rib articulating with the transverse process of the vertebra. B, Anatomical components of a typical rib (fifth rib) viewed from behind. (B: From Abrahams P, Marks S, Hutchings R: McMinn's color atlas of human anatomy, ed 5, Philadelphia, 2003, Mosby.)
Left coxal (hip) bone.
Left coxal (hip) bone. The left coxal bone is disarticulated from the bony pelvis and viewed from the side. (From Abrahams P, Marks S, Hutchings R: McMinn's color atlas of human anatomy, ed 5, Philadelphia, 2003, Mosby.)
Mastoiditis.
Mastoiditis. Note redness and swelling over the mastoid process of the temporal bone. (Courtesy Dr. N. Blevins, New England Medical Center, Boston.)
Types of synovial joints.
Types of synovial joints. Uniaxial: A, hinge, and B, pivot. Biaxial: C, saddle, and D, condyloid. Multiaxial: E, ball and socket, and F, gliding.
The right knee joint.
The right knee joint. A and B, Labeled dissection of the right knee viewed from in front. C and D, Viewed from behind. (B-D: Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
Range of motion.
Movements and ROM. A, Flexion and extension. Extension beyond the anatomical position is sometimes called hyperextension. B, Lateral bending. C, Rotation (supine position). D, Rotation (standing position). (A-C: From Barkauskas V, Baumann L, Stoltenberg-Allen K, Darling-Fisher C: Health and physical assessment, ed 2, St Louis, 1998, Mosby.)
Movements of the fingers and thumb.
Movements of the fingers and thumb. A, Flexion of the metacarpophalangeal joints and flexion of the interphalangeal joints. B, Extension of the metacarpophalangeal joints and flexion of the interphalangeal joints. C, Extension of the metacarpophalangeal and interphalangeal joints. D, Opposition of the thumb. E, Flexion of the thumb. (From Abrahams P, Marks S, Hutchings R: McMinn's color atlas of human anatomy, ed 5, Philadelphia, 2003, Mosby.)
Arthroscopy.
Arthroscopy. A, Fiberoptic light source inserted into a joint. B, Internal view of the joint. (Courtesy Lanny L. Johnson, MD, East Lansing, MI.)
Structure of a muscle organ.
Structure of a muscle organ. A, Note that the connective tissue coverings, the epimysium, perimysium, and endomysium, are continuous with each other and with the tendon. Note also that muscle fibers are held together by the perimysium in groups called fascicles. B, Diagram showing the arm in cross section. Note the relationships of superficial and deep fascia to individual muscles and other structures in the plane of section.
General overview of the body's musculature. C, Lateral view.
Muscles of the trunk and abdominal wall.
Muscles of the trunk and abdominal wall. A, Superficial muscles are visible on the right side of the body and deeper muscles on the left side of the body. B, Transverse section of the anterior wall above the umbilicus (see inset for location).
Muscles that move the upper part of the arm. A, Anterior view. B, Posterior
Muscles of the anterior aspect of the right forearm.
Gluteal muscles. A, Gluteus maximus. B, Gluteus minimus. C, Gluteus medius. O, Origin; I, insertion.
The carpal tunnel.
Health Matters. The carpal tunnel. The median nerve and muscles that flex the fingers pass through a concavity in the wrist called the carpal tunnel.
Structure of myofilaments.
Structure of myofilaments. A, Thin myofilament. B, Thick myofilament. C, Cross section of several thick and thin myofilaments showing the relative positions of myofilaments and the myosin heads that will form cross bridges between them.
Cross bridges.
Cross bridges. Color-enhanced scanning electron micrograph (SEM) showing the myosin heads functioning as cross bridges that connect the thick filaments to the thin filaments, pulling on the thin filaments and causing them to slide. (From Lodish H: Molecular cell biology, ed 4, New York, 2000, WH Freeman.)
The role of skeletal muscle tissues in maintaining a constant body temperature.
The role of skeletal muscle tissues in maintaining a constant body temperature. This diagram shows that a drop in body temperature caused by cold weather can be corrected by a negative feedback mechanism that triggers shivering (muscle contraction), which in turn produces enough heat to warm the body.
Strength
The strength of muscle contraction compared with the strength of the stimulus. After the threshold stimulus is reached, a continued increase in stimulus strength produces a proportional increase in muscle strength until the maximal level of contraction strength is reached.
Cardiac and skeletal muscle contractions compared.
Cardiac and skeletal muscle contractions compared. A brief nerve impulse triggers a brief twitch contraction in skeletal muscle (blue), but a prolonged impulse in the heart tissue produces a rather slow, drawn out contraction in cardiac muscle (red).
Three styles of twitch contraction
Sports and Fitness. B, Three styles of twitch contraction. Different muscle organs have different proportions of slow, fast, and intermediate fibers and thus produce different styles of twitch contractions in a myogram.
Arrector Pili
Arrector pili muscle. When the arrector pili muscle contracts, it pulls the follicle and hair into a more perpendicular position, thus "fluffing up" the hair. Notice how a "goose bump" is raised around the hair shaft.
Age Spots
Age spots. Hyperpigmentations from the cumulative effects of UV exposure over the years are often called "age spots" or "liver spots." (From Regezi JA, Sciubba JJ, Jordan RCK: Oral pathology: clinical pathologic correlations, ed 5, St Louis, 2008, Saunders.)
Hair Follicle
Hair follicle. A, Relationship of a hair follicle and related structures to the epidermal and dermal layers of the skin. B, Enlargement of a hair follicle wall and hair bulb. C, Scanning electron micrograph showing shafts of hair extending from their follicles. (C: Copyright © by David Scharf, 1986, 1993.)
Skin glands.
Skin glands. Several types of exocrine glands occur in the skin.
Body temperature.
Body temperature. This diagram, modeled after a thermometer, shows some physiological consequences of abnormal body temperature. The inset shows a range of body temperatures at which normal function is possible. Ideally, body temperature should be near 37° C (98.6° F), but the body can operate normally within the range shown if conditions are not ideal. (Barbara Cousins.)
Jaundice
Jaundice. Yellowish discoloration of the skin and other tissues by bile pigments was, in the case seen here, caused by a liver infection. The patient was infected with hepatitis B by a contaminated tattoo needle. The yellow tinge of the skin can be best seen by comparing the patient's skin color with that of the physician's hand.
The Flat Bone
Flat bone. A, Horizontal section of a flat bone of the skull (frontal bone) showing cancellous and compact bone. B, Photograph of a frontal bone cut in horizontal section. (B: From Moses K, Nava P, Banks J, Petersen D: Moses atlas of clinical gross anatomy, Philadelphia, 2005, Mosby.)
Calcium Regulation
Calcium homeostasis. Calcitonin and parathyroid hormones have antagonistic (opposing) effects that help to maintain a homeostatic balance of calcium in the blood.
Growth of epiphyseal plate.
Growth of epiphyseal plate. Diagrams showing steps in ossification on either side of the epiphyseal plate.
Osteoporosis.
Osteoporosis. A, Compare the normal vertebral body (left) with the osteoporotic specimen (right). Note that the osteoporotic vertebral body has been shortened by compression fractures. B, Scanning electron micrograph (SEM) of normal bone. C, SEM of osteoporotic bone. Note the loss of trabeculae and appearance of enlarged pores caused by osteoporosis. (From Kumar V, Abbas A, Fausto N: Robbins and Cotran pathologic basis of disease, ed 7, Philadelphia, 2005, Saunders.)
Floor of the cranial cavity viewed from above.
Bones of the skull.
Bones of the skull. E, Sphenoid bone. E1, Superior view; E2, posterior view.
Bones of the skull.
Bones of the skull. M, Right half of the mandible. M1, Medial view; M2, lateral view.
Vertebrae.
Vertebrae. A, Lateral and superior views of C1, the atlas. B, Lateral and superior views of C2, the axis. C, Base of the skull showing C1 (atlas) and C2 (axis) in posterior view. (From Gosling J, Harris P, Whitmore I, Willan P: Human anatomy, ed 4, Philadelphia, 2002, Mosby.)
Right scapula.
Right scapula. A, Anterior view. B, Posterior view. C, Lateral view. D, Posterior view showing articulation of the right scapula with the clavicle. (The inset shows the relative position of the right scapula within the entire skeleton.) (D: Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
Bones of the thigh and leg.
Bones of the thigh and leg. A, Right femur, anterior surface. B, Right femur, posterior view. C, Right tibia and fibula, anterior surface. D, Anterior aspect of the right knee skeleton. E, Right tibia and fibula, posterior aspect. (The inset shows the relative position of the bones of the thigh and leg within the entire skeleton.) (D-E: Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
Abnormal spine curvatures.
Abnormal spine curvatures. A, Lordosis. B, Kyphosis. C, Scoliosis. Black arrows highlight areas of abnormal curvature.
The shoulder joint.
The shoulder joint. A, Artist's diagram, and B, dissection photo (anterior views). C, Artist's diagram, and D, dissection photo (viewed from behind through shoulder joint). (B-D: Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
Knee Joint.
Knee joint (sagittal section). Cadaver dissection showing the articular surfaces and related structures. (From Gosling J, Harris P, Whitmore I, Willan P: Human anatomy, ed 4, Philadelphia, 2002, Mosby.)
Movements of the jaw.
Movements of the jaw. A, Retraction and protraction. B, Elevation and depression.
Movements and ROM of the hip.
Movements and ROM of the hip. A, Hip flexion, knee extended. B, Hip flexion, knee flexed. C, Internal rotation. D, Abduction and adduction. (From Seidel HM, Ball JW, Dains JE, Benedict GW: Mosby's guide to physical examination, ed 5, St Louis, 2003, Mosby.)
Sports and Fitness. Knee injury.
Muscle shape and fiber arrangement.
Muscles of facial expression and mastication. Lateral view.
Dissection photo of the abdominal wall.
Dissection photo of the abdominal wall. The covering rectus sheaths, the left oblique muscles, and part of the left rectus have been removed. (From Gosling J, Harris P, Whitmore I, Willan P: Human anatomy, ed 4, Philadelphia, 2002, Mosby.)
Rotator cuff muscles.
Rotator cuff muscles. Note the tendons of the teres minor, infraspinatus, supraspinatus, and subscapularis muscles surrounding the head of the humerus.
Intrinsic muscles of the hand—anterior (palmar) view.
Quadriceps
Quadriceps femoris group of thigh muscles. A, Vastus medialis. B, Rectus femoris. C, Vastus intermedius. D, Vastus lateralis. O, Origin; I, insertion.
Health Matters. Intramuscular injections.
Cross section of myofibrils.
Cross section of myofibrils. Color-enhanced scanning electron micrographs (SEMs) showing a cross section from a skeletal muscle fiber. Note the dense arrangement of thick and thin filaments, seen here in cross section as mere dots. Note also the dark glycogen granules and sarcoplasmic reticulum tubules sandwiched between the myofibrils. (From Leeson CR, Leeson T, Paparo A: Text/atlas of histology, St Louis, 1988, Saunders.)
Sliding-filament model.
Sliding-filament model. A, During contraction, myosin cross bridges pull the thin filaments toward the center of each sarcomere, thus shortening the myofibril and the entire muscle fiber. B, Color-enhanced transmission electron micrographs (TEMs) showing the shortening of a sarcomere caused by the sliding of filaments during muscle contraction. (B: Courtesy H.E. Huxley, Brandeis University, Waltham, MA.)
Motor unit.
Motor unit. A motor unit consists of one somatic motor neuron and the muscle fibers supplied by its branches. A, Photomicrograph showing a nerve (black) branching to supply several dozen individual muscle fibers (red). B, Sketch showing a single motor unit. C, Diagram showing several motor units within the same muscle organ. (B: Courtesy Dr. Paul C. Letourneau, Department of Anatomy, Medical School, University of Minnesota, MN.)
The length- tension relationship.
The length- tension relationship. As this graph of muscle tension shows, the maximum strength that a muscle can develop is directly related to the initial length of its fibers. At a short initial length, the sarcomeres are already compressed, and thus the muscle cannot develop much tension (position A). Conversely, the thick and thin myofilaments are too far apart in an overstretched muscle to generate much tension (position C). Maximum tension can be generated only when the muscle has been stretched to a moderate, optimal length (position B).
Smooth muscle fiber.
Smooth muscle fiber. A, Thin bundles of myofilaments span the diameter of a relaxed fiber. The scanning electron micrograph (above) shows that the surface of the cell is rather flat when the fiber is relaxed. B, During contraction, sliding of the myofilaments causes the fiber to shorten by "balling up." The micrograph (above) shows that the fiber becomes shorter and thicker and exhibits "dimples" where the myofilament bundles are pulling on the plasma membrane. (Courtesy Dr. Frederic S. Fay, Department of Physiology, University of Massachusetts, Worcester, MA.)
Sports and Fitness. C, Proportions of fiber types in muscle tissue.
Sports and Fitness. C, Proportions of fiber types in muscle tissue. A person with a spinal cord injury eventually loses nearly all of the postural slow fibers while retaining mostly intermediate and fast fibers. In an extreme endurance athlete, on the other hand, the slow fibers develop so much that they greatly dominate the faster fiber types.
Touch
Skin receptors. Receptors are sensitive nerve endings that make it possible for the skin to act as a sense organ. A, This tactile (Meissner) corpuscle is capable of detecting light touch (slight pressure). B, Another skin receptor is the lamellar corpuscle, also called a Pacini corpuscle, which detects sensations of deep pressure. (Barbara Cousins.)
Cyanosis
The blue discoloration of the fingers of this light-skinned individual is caused by the diffusion of light reflected off dark, unoxygenated hemoglobin in the blood vessels of the skin. The fingertips have an especially high volume of blood and thus look bluer than other regions of the skin. (From Epstein O, Perkin GD, Cookson J, de Bono D: Clinical examination, ed 3, St Louis, 2003, Mosby.)
Gray Hair
Gray hair. Gray hair results from a scattered arrangement of both white (pigmentless) hairs and darker (pigmented) hairs. (Copyright Kevin Patton, Lion Den Inc, Weldon Spring, MO.)
Aged skin.
Aged skin. In late adulthood, wrinkles in the skin often develop—especially in areas of frequent movement such as on the hands, around the mouth, and around the eyelids. (From Habif TP: Clinical dermatology, ed 4, St Louis, Mosby, 2004.)
"Rule of nines."
"Rule of nines." The "rule of nines" is one method used to estimate amount of skin surface burned in an adult.
Acne
Compact and Cancellous Bone
Compact and cancellous bone in a long bone. A, Longitudinal section of a long bone showing both cancellous and compact bone. B, Magnified view of compact bone.
Bone development.
Bone development. Diagram showing osseous development at birth.
Epiphyseal fracture.
Epiphyseal fracture. Radiograph showing an epiphyseal fracture of the distal end of the femur in a young athlete. Note the separation of the diaphysis and epiphysis at the level of the growth plate. (From Booher JM, Thibodeau GA: Athletic injury assessment, St Louis, 1985, Mosby.)
Rickets.
Rickets. Bowing of legs in this toddler is due to poorly mineralized bones from rickets. (From Kumar V, Abbas A, Fausto N: Robbins and Cotran pathologic basis of disease, ed 7, Philadelphia, 2005, Saunders.)
Skull viewed from below.
Bones of the skull.
Bones of the skull. F, Ethmoid bone. F1, Superior view; F2, lateral view; F3, anterior view.
The paranasal sinuses. A, Lateral view. B, Frontal view.
The paranasal sinuses. A, Lateral view. B, Frontal view.
Vertebrae.
Vertebrae. D, Lateral and superior views of a cervical vertebra, C7 (note the prominent spinous process). (From Gosling J, Harris P, Whitmore I, Willan P: Human anatomy, ed 4, Philadelphia, 2002, Mosby.)
Bones of the arm (right arm, anterior view).
Bones of the arm (right arm, anterior view). A, Humerus (upper part of the arm). B, Radius and ulna (forearm). C, Elbow joint, showing how the distal end of the humerus joins the proximal ends of the radius and ulna. (The inset shows the relative position of the right arm bones within the entire skeleton.) (C: Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
The foot.
The foot. A, Bones of the right foot viewed from above. The tarsal bones consist of the cuneiforms, navicular, talus, cuboid, and calcaneus. B, Posterior aspect of the right ankle skeleton and inferior aspect of the right foot skeleton. C, X-ray film of the left foot showing prominent sesamoid bones (arrows) near the distal end (head) of the first metatarsal bone of the great toe. (B: Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
Palpable bony landmarks.
The elbow joint.
The elbow joint. A, Sagittal section through the elbow joint. B, Dissection photo showing the anterior view of the proximal end of the ulna with attached annular ligament. (From Gosling J, Harris P, Whitmore I, Willan P: Human anatomy, ed 4, Philadelphia, 2002, Mosby.)
Ankle joint.
Ankle joint. A, Dorsum of the ankle and foot showing surface relationships to underlying bones. B, Dissection photo of the ankle joint. (A: From Lumley J: Surface anatomy, ed 3, Edinburgh, 2002, Churchill Livingstone. B: Courtesy Vidic B, Suarez FR: Photographic atlas of the human body, St Louis, 1984, Mosby.)
Range of motion in the spine
Movements and ROM of the thoracic and lumbar spine. A, Flexion. B, Hyperextension. C, Lateral bending. D, Rotation of the upper part of the trunk. (From Seidel HM, Ball JW, Dains JE, Benedict GW: Mosby's guide to physical examination, ed 5, St Louis, 2003, Mosby.)
Movements and ROM of the knee.
Movements and ROM of the knee. Flexion may reach 130 degrees. Extension occurs with movement from a 130-degree flexed position back to the 0-degree position. Hyperextension of 0 degrees to 15 degrees is possible in many individuals. (From Barkauskas V, Baumann L, Stoltenberg-Allen K, Darling-Fisher C: Health and physical assessment, ed 2, St Louis, 1998, Mosby.)
Sports and Fitness. Torn ligaments.
Attachments of a skeletal muscle.
Attachments of a skeletal muscle. A, Origin and insertion of a skeletal muscle. A muscle originates at a relatively stable part of the skeleton (origin) and inserts at the skeletal part that is moved when the muscle contracts (insertion). B, Movement of the forearm during weightlifting. Muscle contraction moves bones, which serve as levers, and by acting on joints, which serve as fulcrums for those levers. See the text for discussion and review Figure 10-4, which illustrates types of levers.
Muscles of facial expression and mastication. Anterior view.
Muscles of the back.
Muscles of the back. A, Superficial (left) and intermediate (right) muscle dissection of the back—posterior view. The illustration shows a two-stage dissection. Superficial muscles of the neck and back are shown on the left side and an intermediate-depth dissection is shown on the right.
Cross sections (proximal to distal) through the upper extremity.
Cross sections (proximal to distal) through the upper extremity. A, Section at the junction of the proximal and middle thirds of the humerus. B, Section just proximal to the medial epicondyle of the humerus. C, Section at the level of the radial tuberosity. D, Section at the middle of the forearm. In each section you are viewing the superior (proximal) aspect of the specimen.
Iliopsoas muscle (iliacus, psoas major, and psoas minor muscles). O, Origin; I, insertion.
Hamstrings
Hamstring group of thigh muscles. A, Biceps femoris. B, Semitendinosus. C, Semimembranosus. O, Origin; I, insertion.
Structure of skeletal muscle.
Structure of skeletal muscle. A, Skeletal muscle organ composed of bundles of contractile muscle fibers held together by connective tissue. B, Greater magnification of a single fiber showing smaller fibers—myofibrils—in the sarcoplasm. Note the sarcoplasmic reticulum and T tubules forming a three-part structure called a triad. C, Myofibril magnified further to show a sarcomere between successive Z disks (Z lines). Cross striae are visible. D, Molecular structure of a myofibril showing thick myofilaments and thin myofilaments.
Neuromuscular junction (NMJ).
Neuromuscular junction (NMJ). A, Micrograph showing four neuromuscular junctions (NMJs). Three are surface views (arrows) and one is a side view (arrowhead). N, Nerve fibers; M, muscle fibers. B, This sketch shows a side view of the NMJ. Note how the distal end of a motor neuron fiber forms a synapse, or "chemical junction," with an adjacent muscle fiber. Neurotransmitter molecules (specifically, acetylcholine, or Ach) are released from the neuron's synaptic vesicles and diffuse across the synaptic cleft. There they stimulate receptors in the motor endplate region of the sarcolemma. (A: From Leeson CR, Leeson T, Paparo A: Text/atlas of histology, St Louis, 1988, Saunders.)
Simplified contracting sarcomere.
Simplified contracting sarcomere. This diagram illustrates the concept of muscle contraction as a sort of tug-of-war game in which the myosin heads (shown here as little people) hold onto thin filament "ropes"—thus forming cross bridges. As the myosin heads pull on the thin filaments, the Z disks (Z lines) get closer together—thus shortening the sarcomere. Likewise, the short length of a sarcomere may be held in position by the continued effort of the myosin heads.
Myography.
Myography. This classic type of myograph, called a kymograph, records muscle contractions as graphs showing changes in length. An isolated muscle moves the pen upward during contraction, and the weight pulls the muscle and pen downward as the muscle relaxes. A change in tension produces this change in length. Electrical voltage simulates a nerve impulse to stimulate the fibers in the muscle. Modern myography often uses computer-based systems that record similar muscle tension graphs.
The stretch reflex.
The stretch reflex. The strength of a muscle organ can be matched to the load imposed on it by a negative feedback response centered in the spinal cord. Increased stretch (caused by increased load) is detected by a sensory nerve fiber attached to a muscle cell (called a muscle spindle). The information is integrated in the spinal cord and a correction signal is relayed through motor neurons back to the same muscle, which increases tension to return to the set point muscle length.
Types of smooth muscle.
Types of smooth muscle. A, Single-unit (visceral) smooth muscle. Neurotransmitters released from varicosities (bulges) in the nerve fiber trigger impulses in the smooth muscle membranes—an event that is transmitted to adjacent muscle fibers through gap junctions. Thus a large mass of muscle fibers acts as a single unit. B, Multiunit smooth muscle. Each muscle fiber is triggered independently by nerve stimulation.
Effects of Exercise on Skeletal Muscles.
Effects of Exercise on Skeletal Muscles. A, Disuse atrophy. The arrow points to a group of muscle fibers that have atrophied from disuse (in this case from nerve damage). Notice how much smaller they are than the surrounding, normal fibers.
Unit III. Communication, Control, and Integration: Cells of the Nervous
System, The Central Nervous System, The Peripheral Nervous System, The Sense Organs, and The Endocrine System.