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Gary G. Matthews is the author of Cellular Physiology of Nerve and Muscle, 4th Edition, published by Wiley.
1. Introduction to Electrical Signaling in the Nervous System.
The Patellar Reflex as a Model for Neural Function.
The Cellular Organization of Neurons.
Electrical Signals in Neurons.
Transmission between Neurons.
2. Composition of Intracellular and Extracellular Fluids.
Intracellular and Extracellular Fluids.
The Structure of the Plasma Membrane.
Summary.
3. Maintenance of Cell Volume.
Molarity, Molality, and Diffusion of Water.
Osmotic Balance and Cell Volume.
Answers to the Problem of Osmotic Balance.
Tonicity.
Time-Course of Volume Changes.
4. Membrane Potential: Ionic Equilibrium.
Diffusion Potential.
Equilibrium Potential.
The Nernst Equation.
The Principle of Electrical Neutrality.
The Cell Membrane as an Electrical Capacitor.
Incorporating Osmotic Balance.
Donnan Equilibrium.
A Model Cell That Looks Like a Real Animal Cell.
The Sodium Pump.
5. Membrane Potential: Ionic Steady State.
Equilibrium Potentials for Sodium, Potassium, and Chloride.
Ion Channels in the Plasma Membrane.
Membrane Potential and Ionic Permeability.
The Goldman Equation.
Ionic Steady State.
The Chloride Pump.
Electrical Current and the Movement of Ions Across Membranes.
Factors Affecting Ion Current Across a Cell Membrane.
Membrane Permeability vs. Membrane Conductance.
Behavior of Single Ion Channels.
Part II: Cellular Physiology of Nerve Cells.
6. Generation of Nerve Action Potential.
The Action Potential.
Ionic Permeability and Membrane Potential.
Measuring the Long-Distance Signal in Neurons.
Characteristics of the Action Potential.
Initiation and Propagation of Action Potentials.
Changes in Relative Sodium Permeability During an Action Potential.
Voltage-Dependent Sodium Channels of the Neuron Membrane.
Repolarization.
The Refractory Period.
Propagation of an Action Potential Along a Nerve Fiber.
Factors Affecting the Speed of Action Potential Propagation.
Molecular Properties of the Voltage-Sensitive Sodium Channel.
Molecular Properties of Voltage-Dependent Potassium Channels.
Calcium-Dependent Action Potentials.
7. The Action Potential: Voltage Clamp Experiments.
The Voltage Clamp.
Measuring Changes in Membrane Ionic Conductance Using the Voltage Clamp.
The Squid Giant Axon.
Ionic Currents Across an Axon Membrane Under Voltage Clamp.
The Gated Ion Channel Model.
Membrane Potential and Peak Ionic Conductance.
Kinetics of the Change in Ionic Conductance Following a Step Depolarization.
Sodium Inactivation.
The Temporal Behavior of Sodium and Potassium Conductance.
Gating Currents.
8. Synaptic Transmission at the Neuromuscular Junction.
Chemical and Electrical Synapses.
The Neuromuscular Junction as a Model Chemical Synapse.
Transmission at a Chemical Synapse.
Presynaptic Action Potential and Acetylcholine Release.
Effect of ACh on the Muscle Cell.
Neurotransmitter Release.
The Vesicle Hypothesis of Quantal Transmitter Release.
Mechanism of Vesicle Fusion.
Recycling of Vesicle Membrane.
Inactivation of Released Acetylcholine.
Recording the Electrical Current Flowing Through a Single Acetylcholine-Activated Ion Channel.
Molecular Properties of the Acetylcholine-Activated Channel.
9. Synaptic Transmission in the Central Nervous System.
Excitatory and Inhibitory Synapses.
Excitatory Synaptic Transmission Between Neurons.
Temporal and Spatial Summation of Synaptic Potentials.
Some Possible Excitatory Neurotransmitters.
Conductance-Decrease E.P.S.P.'s.
Inhibitory Synaptic Transmission.
The Synapse Between Sensory Neurons and Antagonist Neurons in the Patellar Reflex.
Characteristics of Inhibitory Synaptic Transmission.
Mechanism of Inhibition in the Postsynaptic Membrane.
Some Possible Inhibitory Neurotransmitters.
The Family of Neurotransmitter-Gated Ion Channels.
Neuronal Integration.
Indirect Actions of Neurotransmitters.
Presynaptic Inhibition and Factilitation.
Synaptic Plasticity.
Short-Term Changes in Synaptic Strength.
Long-Term Changes in Synaptic Strength.
Part III: Cellular Physiology of Muscle Cells.
10. Excitation-Contraction Coupling in Skeletal Muscle.
The Three Types of Muscle.
Structure of Skeletal Muscle.
Changes in Striation Pattern on Contraction.
Molecular Composition of Filaments.
Interaction Between Myosin and Actin.
Regulation of Contraction.
The Sarcoplasmic Reticulum.
The Transverse Tubule System.
11. Neural Control of Muscle Contraction.
The Motor Unit.
The Mechanics of Contraction.
The Relationship Between Isometric Tension and Muscle Length.
Control of Muscle Tension by the Nervous System.
Recruitment of Motor Neurons.
Fast and Slow Muscle Fibers.
Temporal Summation of Contractions Within a Single Motor Unit.
Asynchronous Activation of Motor Units During Maintained Contraction.
12. Cardiac Muscle: The Autonomic Nervous System.
Autonomic Control of the Heart.
The Pattern of Cardiac Contraction.
Coordination of Contraction Across Cardiac Muscle Fibers.
Generation of Rhythmic Contractions.
The Cardiac Action Potential.
The Pacemaker Potential.
Actions of Acetylcholine and Norepinephrine on Cardiac Muscle Cells.
Appendix A: Derivation of the Nernst Equation.
Appendix B: Derivation of the Goldman Equation.
Appendix C: Electrical Properties of Cells.
Suggested Readings
To set the stage for discussing the generation and transmission of signals in the nervous system, it will be useful to describe the characteristics of those signals using a simple example: the patellar reflex, also known as the knee-jerk reflex. Figure 1-1 shows the neural circuitry underlying the patellar reflex. Tapping the patellar tendon, which connects the knee cap (patella) to the bones of the lower leg, pulls the knee cap down and stretches the quadriceps muscle at the front of the thigh. Specialized nerve cells (sensory neurons) sense the stretch of the muscle and send a signal that travels along the thin fibers of the sensory neurons from the muscle to the spinal cord. In the spinal cord, the sensory signal is received by other neurons, called motor neurons. The motor neurons send nerve fibers back to the quadriceps muscle and command the muscle to contract, which causes the knee joint to extend.
Figure 1-1 A schematic representation of the patellar reflex. The sensory neuron is activated by stretching the thigh muscle. The incoming (afferent) signal is carried to the spinal cord along the nerve fiber of the sensory neuron. In the spinal cord, the sensory neuron activates motor neurons, which in turn send outgoing (efferent) signals along the nerve back to the thigh muscle, causing it to contract.
The reflex loop exemplified by the patellar reflex embodies in a particularly simple way all of the general features that characterize the operation of the nervous system. A sensory stimulus (muscle stretch) is detected, the signal is transmitted rapidly over long distance (to and from the spinal cord), and the information is focally and specifically directed to appropriate targets (the quadriceps motor neurons, in the case of the sensory neurons, and the quadriceps muscle cells, in the case of the motor neurons). The sensory pathway, which carries information into the nervous system, is called the afferent pathway, and the motor output constitutes the efferent pathway. Much of the nervous system is devoted to processing afferent sensory information and then making the proper connections with efferent pathways to ensure that an appropriate response occurs. In the case of the patellar reflex, the reflex loop ensures that passive stretch of the muscle will be automatically opposed by an active contraction, so that muscle length remains constant.
Neurons are structurally complex cells, with long fibrous extensions that are specialized to receive and transmit information. This complexity can be appreciated by examining the structure of a motor neuron, shown schematically in Figure 1-2a. The cell body, or soma, of the motor neuron-where the nucleus resides-is only about 20-30 µm in diameter in the case of motor neurons involved in the patellar reflex. The soma is only a small part of the neuron, however, and it gives rise to a tangle of profusely branching processes called dendrites, which can spread out for several millimeters within the spinal cord. The dendrites are specialized to receive signals passed along as the result of the activity of other neurons, such as the sensory neurons of the patellar reflex, and to funnel those signals to the soma. The soma also gives rise to a thin fiber, the axon, that is specialized to transmit signals over long distances. In the case of the motor neuron in the patellar reflex, the axon extends all the way from the spinal cord to the quadriceps muscle, a distance of approximately 1 meter. As shown in Figure 1-2b, the sensory neuron of the patellar reflex is structurally simpler than the motor neuron. Its soma, which is located just outside the spinal cord in the dorsal root ganglion, gives rise to only a single nerve fiber, the axon. The axon splits into two branches shortly after it exits the dorsal root ganglion: one branch extends away from the spinal cord to contact the muscle cells of the quadriceps muscle, and the other branch passes into the spinal cord to contact the quadriceps motor neurons. The axon of the sensory neuron carries the signal generated by muscle stretch from the muscle into the spinal cord. Because the sensory neuron receives its input signal from the sensory stimulus (muscle stretch) at the peripheral end of the axon instead of from other neurons, it lacks the den-drites seen in the motor neuron.
Figure 1-2 Structures of single neurons involved in the patellar reflex.
To transmit information rapidly over long distances, neurons produce active electrical signals, which travel along the axons that make up the transmission paths. The electrical signal arises from changes in the electrical voltage difference across the cell membrane, which is called the membrane potential.Although this transmembrane voltage is small-typically less than a tenth of a volt-it is central to the functioning of the nervous system. Information is transmitted and processed by neurons by means of changes in the membrane potential.
What does the electrical signal that carries the message along the sensory nerve fiber in the patellar reflex look like? To answer this question, we must measure the membrane potential of the sensory neuron by placing an ultrafine voltage-sensing probe, called an intracellular microelectrode, inside the sensory nerve fiber, as illustrated in Figure 1-3. A voltmeter is connected to measure the voltage difference between the tip of the intracellular microelectrode (point a in the figure) and a reference point in the extracellular space (point b). When the microelectrode is located outside the sensory neuron, both points a and b are in the extracellular space, and the voltmeter therefore records no voltage difference (Figure 1-3b). When the tip of the probe is inserted inside the sensory neuron, however, the voltmeter measures an electrical potential between points a and b, representing the voltage difference between the inside and the outside of the neuron-that is, the membrane potential of the neuron. As shown in Figure 1-3b, the inside of the sensory nerve fiber is negative with respect to the outside by about seventy-thousandths of a volt (1 millivolt, abbreviated mV, equals one-thousandth of a volt). Because the potential outside the cell is our reference point and the inside is negative with respect to the outside, the membrane potential is represented as a negative number, i.e., -70 mV.
As long as the sensory neuron is not stimulated by stretching the muscle, the membrane potential remains constant at this resting value. For this reason, the unstimulated membrane potential is known as the resting potential of the cell. When the muscle is stretched, however, the membrane potential of the sensory neuron undergoes a dramatic change, as shown in Figure 1-3b. After a delay that depends on the distance of the recording site from the muscle, the membrane potential suddenly moves in the positive direction, transiently reverses sign for a brief period, and then returns to the resting negative level. This transient jump in membrane potential is the action potential-the long-distance signal that carries information in the nervous system.
What happens when the action potential reaches the end of the neuron, and the signal must be transmitted to the next cell? In the patellar reflex, signals are relayed from one cell to another at two locations: from the sensory neuron to the motor neuron in the spinal cord, and from the motor neuron to the muscle cells in the quadriceps muscle. The point of contact where signals are transmitted from one neuron to another is called a synapse. In the patellar reflex, both the synapse between the sensory neuron and the motor neuron and the synapse between the motor neuron and the muscle cells are chemical synapses, in which an action potential in the input cell (the presynaptic cell) causes it to release a chemical substance, called a neurotransmitter. The molecules of neuro-transmitter then diffuse through the extracellular space and change the membrane potential of the target cell (the postsynaptic cell). The change in membrane potential of the target then affects the firing of action potentials Neurotransmitter changes electrica potential of postsynaptic cell by the postsynaptic cell. This sequence of events during synaptic transmission is summarized in Figure 1-4.
Figure 1-3 Recording the action potential in the nerve fiber of the sensory neuron in the patellar stretch reflex. (a) A diagram of the recording configuration. A tiny microelectrode is inserted into the sensory nerve fiber, and a voltmeter is connected to measure the voltage difference (E) between the inside (a) and the outside (b) of the nerve fiber. (b) When the microelectrode penetrates the fiber, the resting membrane potential of the nerve fiber is measured. When the sensory neuron is activated by stretching the muscle, an action potential occurs and is recorded as a rapid shift in the recorded membrane potential of the sensory nerve fiber.
Figure 1-4 Chemical transmission mediates synaptic communication between cells in the patellar reflex. The flow diagram shows the sequence of events involved in the release of chemical neurotransmitter from the synaptic terminal.
Because signaling both within and between cells in the nervous...
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