C. The Resting Membrane Potential (pp. 396–398; Figs. 11.7–11.8)
1. The neuron cell membrane is polarized, being more negatively charged inside than outside. The degree of this difference in electrical charge is the resting membrane potential.
2. The resting membrane potential is generated by differences in ionic makeup of intracellular and extracellular fluids, and differential membrane permeability to solutes.
D. Membrane Potentials That Act as Signals (pp. 398–404; Figs. 11.9–11.14)
1. Neurons use changes in membrane potential as communication signals. These can be brought on by changes in membrane permeability to any ion, or alteration of ion concentrations on the two sides of the membrane.
2. Changes in membrane potential relative to resting membrane potential can either be depolarizations, in which the interior of the cell becomes less negative, or hyperpolarizations, in which the interior of the cell becomes more negatively charged.
3. Graded potentials are short-lived, local changes in membrane potentials. They can either be depolarizations or hyperpolarizations, and are critical to the generation of action potentials.
4. Action potentials, or nerve impulses, occur on axons and are the principle way neurons communicate.
a. Generation of an action potential involves a transient increase in Na+ permeability, followed by restoration of Na+ impermeability, and then a short-lived increase in K+ permeability.
b. Propagation, or transmission, of an action potential occurs as the local currents of an area undergoing depolarization cause depolarization of the forward adjacent area.
c. Repolarization, which restores resting membrane potential, follows depolarization along the membrane.
5. A critical minimum, or threshold, depolarization is defined by the amount of influx of Na+ that at least equals the amount of efflux of K+.
6. Action potentials are all-or-none phenomena: they either happen completely, in the case of a threshold stimulus, or not at all, in the event of a subthreshold stimulus.
7. Stimulus intensity is coded in the frequency of action potentials.
8. The refractory period of an axon is related to the period of time required so that a neuron can generate another action potential.
E. Conduction Velocity (pp. 404–406; Fig. 11.15)
1. Axons with larger diameters conduct impulses faster than axons with smaller diameters.
2. Unmyelinated axons conduct impulses relatively slowly, while myelinated axons have a high conduction velocity.
The Synapse (pp. 406–413; Figs. 11.16–11.19; Table 11.2)
A. A synapse is a junction that mediates information transfer between neurons or between a neuron and an effector cell (p. 406; Fig. 11.16).
B. Neurons conducting impulses toward the synapse are presynaptic cells, and neurons carrying impulses away from the synapse are postsynaptic cells (p. 406).
C. Electrical synapses have neurons that are electrically coupled via protein channels and allow direct exchange of ions from cell to cell (p. 406).
D. Chemical synapses are specialized for release and reception of chemical neurotransmitters (pp. 407–408; Fig. 11.17).
E. Neurotransmitter effects are terminated in three ways: degradation by enzymes from the postsynaptic cell or within the synaptic cleft; reuptake by astrocytes or the presynaptic cell; or diffusion away from the synapse (p. 408).
F. Synaptic delay is related to the period of time required for release and binding of neurotransmitters (p. 408).
G. Postsynaptic Potentials and Synaptic Integration (pp. 408–413; Figs. 11.18–11.19; Table 11.2)
1. Neurotransmitters mediate graded potentials on the postsynaptic cell that may be excitatory or inhibitory.
2. Summation by the postsynaptic neuron is accomplished in two ways: temporal summation, which occurs in response to several successive releases of neurotransmitter, and spatial summation, which occurs when the postsynaptic cell is stimulated at the same time by multiple terminals.
3. Synaptic potentiation results when a presynaptic cell is stimulated repeatedly or continuously, resulting in an enhanced release of neurotransmitter.
4. Presynaptic inhibition results when another neuron inhibits the release of excitatory neurotransmitter from a presynaptic cell.
5. Neuromodulation occurs when a neurotransmitter acts via slow changes in target cell metabolism, or when chemicals other than neurotransmitter modify neuronal activity.
Additional information on topics covered in Chapter 11 can be found in the chapters listed below.
1. Chapter 2: Enzymes and enzyme function
2. Chapter 3: Passive and active membrane transport processes; membrane potential; cytoskeletal elements; cell cycle
8. Chapter 16: Nervous system modulation of endocrine function
9. Chapter 18: Membrane potential and the electrical activity of the heart
10. Chapter 19: Baroreceptors and chemoreceptors in blood pressure and flow regulation
11. Chapter 22: Chemoreceptors and stretch receptors related to respiratory function
12. Chapter 23: Sensory receptors and control of digestive processes
13. Chapter 24: Examples of receptors
Multimedia in the Classroom and Lab
Online Resources for Students
The following shows the organization of the Chapter Guide page in myA&P™. The Chapter Guide organizes all the chapter-specific online media resources for Chapter 11 in one convenient location, with e-book links to each section of the textbook. Students can also access A&P Flix animations, MP3 Tutor Sessions, Interactive Physiology® 10-System Suite, Practice Anatomy Lab™ 2.0, PhysioEx™ 8.0, and much more.
Section 11.1 Functions and Divisions of the Nervous System (pp. 386–387)
Interactive Physiology® 10-System Suite: Nervous System I: Orientation
Section 11.2 Histology of Nervous Tissue (pp. 388–395)
Interactive Physiology® 10-System Suite: Nervous System I: Anatomy Review (Neurons)
Memory Game: Neural System
Section 11.3 Membrane Potentials (pp. 395–406)
MP3 Tutor Session: Generation of an Action Potential
Interactive Physiology® 10-System Suite: Nervous I: Ion Channels
A&P Flix animation: Neurophysiology of Nerve Impulses
Interactive Physiology® 10-System Suite: Nervous System II: Anatomy Review (Synapses)
Interactive Physiology® 10-System Suite: Nervous System II: Ion Channels
Interactive Physiology® 10-System Suite: Nervous System II: Synaptic Transmission
Interactive Physiology® 10-System Suite: Nervous System II: Synaptic Potentials and Cellular Integration
Section 11.5 Neurotransmitters and Their Receptors (pp. 413–421)
Section 11.6 Basic Concepts of Neural Integration (pp. 421–423)
Section 11.7 Developmental Aspects of Neurons (pp. 423–424)
Case Study: Congenital Defect
Crossword Puzzle 11.1
Crossword Puzzle 11.2
Crossword Puzzle 11.3
Crossword Puzzle 11.4
Crossword Puzzle 11.5
Art Labeling Quiz
Chapter Practice Test
Answers to End-of-Chapter Questions
Multiple-Choice and Matching Question answers appear in Appendix G of the main text.
Short Answer Essay Questions
13. Anatomical division includes the CNS (brain and spinal cord) and the PNS (nerves and ganglia). Functional division includes the somatic and autonomic motor divisions of the PNS. The autonomic division is divided into sympathetic and parasympathetic subdivisions. (pp. 386–387)
14. a. The cell body is the biosynthetic and metabolic center of a neuron. It contains the usual organelles, but lacks centrioles. (pp. 389–390)
b. Dendrites and axons both function to carry electrical current. Dendrites differ in that they are short, transmit toward the cell body, and function as receptor sites. Axons are typically long, are myelinated, and transmit away from the cell body. Only axons can generate action potentials, the long-distance signals. (pp. 390–391)
15. a. Myelin is a whitish, fatty, phospholipid-insulating material (essentially the wrapped plasma membranes of oligodendrocytes or Schwann cells).
b. CNS myelin sheaths are formed by flaplike extensions of oligodendrocytes and lack a neurilemma. Each oligodendrocyte can help to myelinate several fibers. PNS myelin is formed by Schwann cells; the wrapping of each Schwann cell forms the internode region. The sheaths have a neurilemma, and the fibers they protect are capable of regeneration. (pp. 391–392)
16. Multipolar neurons have many dendrites, one axon, and are found in the CNS (and autonomic ganglia). Bipolar neurons have one axon and one dendrite, and are found in receptor end organs of the special senses such as the retina of the eye and olfactory mucosa. Unipolar neurons have one process that divides into an axon and a dendrite and is a sensory neuron with the cell body found in a dorsal root ganglion or cranial nerve ganglion. (pp. 392–393; Table 11.1)
17. A polarized membrane possesses a net positive charge outside, and a net negative charge inside, with the voltage across the membrane being at –70 mv. Diffusion of Na+ and K+ across the membrane establishes the resting potential because the membrane is slightly more permeable to K+. The Na+-K+ pump, an active transport mechanism, maintains this polarized state by maintaining the diffusion gradient for Na+ and K+. (p. 396)
18. a. The generation of an action potential involves: (1) an increase in sodium permeability and reversal of the membrane potential; (2) a decrease in sodium permeability; and (3) an increase in potassium permeability and repolarization. (pp. 399–402)
b. The ionic gates are controlled by changes in the membrane potential and activated by local currents.
c. The all-or-none phenomenon means that the local depolarizing current must reach a critical “firing” or threshold point before it will respond, and when it responds, it will respond completely by conducting the action potential along the entire length of its axon. (pp. 403–404)
19. The CNS “knows” a stimulus is strong when the frequency or rate of action potential generation is high. (p. 404)
20. a. An EPSP is an excitatory (depolarizing) postsynaptic potential that increases the chance of a depolarization event. An IPSP is an inhibitory (hyperpolarizing) postsynaptic potential that decreases the chance of a depolarization event. (pp. 411–412)
b. It is determined by the type and amount of neurotransmitter that binds at the postsynaptic neuron and the specific receptor subtype it binds to. (pp. 411–413)
21. Each neuron’s axon hillock keeps a “running account” of all signals it receives via temporal and spatial summation. (p. 412)
22. The neurotransmitter is quickly removed by enzymatic degradation or reuptake into the presynaptic axon. This ensures discrete limited responses. (p. 408)
23. a. A fibers have the largest diameter and thick myelin sheaths and conduct impulses quickly; B fibers are lightly myelinated, have intermediate diameters, and are slower conductors. (p. 406)
b. Absolute refractory period is when the neuron is incapable of responding to another stimulus because the sodium gates are still open or are inactivated. (p. 404)
c. A node of Ranvier is an interruption of the myelin sheath between the wrappings of individual Schwann cells or of the oligodendrocyte processes. (p. 391)
24. In serial processing, the pathway is constant and occurs through a definite sequence of neurons; the response is predictable and stereotyped. In parallel processing, impulses reach the final CNS target by multiple pathways. Parallel processing allows for a variety of responses. (p. 423)
25. First, they proliferate; second, they migrate to proper position; third, they differentiate. (pp. 423–424)
26. Development of the axon is due to the chemical signals neurotropin and NGF that interact with receptors on the developing axon to support and direct its growth. (p. 424)
Critical Thinking and Clinical Application Questions
1. The resting potential would decrease, that is, become less negative, because the concentration gradient causing net diffusion of K+ out of the cell would be smaller. Action potentials would be fired more easily, that is, in response to smaller stimuli, because the resting potential would be closer to threshold. Repolarization would occur more slowly because repolarization depends on net K+ diffusion from the cell and the concentration gradient driving this diffusion is lower. Also, the subsequent hyperpolarization would be smaller. (pp. 396–398)
2. Local anesthetics such as novocaine and sedatives affect the neural processes usually at the nodes of Ranvier, by reducing the membrane permeability to sodium ions. (p. 402)
3. The bacteria remain in the wound; however, the toxin produced travels via axonal transport to reach the cell body. (p. 391)
4. In MS, the myelin sheaths are destroyed. Loss of this insulating sheath results in shunting of current and eventual cessation of neurotransmission. (pp. 405–406)
5. Glycine is an inhibitory neurotransmitter that is used to modulate spinal cord transmission. Strychnine blocks glycine receptors in the spinal cord, leading to unregulated stimulation of muscles, and spastic contraction to the point where the muscles cannot relax. (p. 417; Table 11.3)