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Understanding Electrical Signals in Nerves and Muscles: Action and Graded Potentials, Schemes and Mind Maps of Biology

An in-depth exploration of action potentials and graded potentials, the electrical signals used by nerve and muscle cells. Learn about the terms related to these potentials, the events that occur during an action potential, the mechanisms underlying these events, and the restoration of ion gradients. Additionally, discover how action potentials are conducted in neurons and the special properties of action potentials.

Typology: Schemes and Mind Maps

2021/2022

Uploaded on 09/12/2022

albertein
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Download Understanding Electrical Signals in Nerves and Muscles: Action and Graded Potentials and more Schemes and Mind Maps Biology in PDF only on Docsity! Biology 251 Fall 2015 1 TOPIC 4: ACTION POTENTIALS AND GRADED POTENTIALS I. Introduction A. All cells possess a membrane potential related to the non-uniform distribution of, and differential permeability of, Na+, K+ and A-. B. Nerve and muscle are excitable tissue that use this potential by undergoing controlled, transient, rapid changes in membrane potential. Such fluctuations in membrane potential serve as electrical signals. C. Two kinds of such electrical signals 1. Graded potentials are short distance signals 2. Action potentials are long distance signals II. Action Potentials A. Terms (Fig 7.11) 1. Polarization: separation of charges 2. Depolarization: reduction in potential 3. Hyperpolarization: increase in potential 4. Repolarization: return to resting potential B. Events in an Action Potential (Fig 7.16) 1. Occurrence of a triggering event 2. Slow depolarization from -70 mV to -55 mV 3. -55 mV is threshold potential; as soon as it is reached, a very rapid depolarization to +30 mV occurs 4. repolarization then occurs 5. frequently overshoots to -80 mV before repolarizing at -70 mV; this is hyperpolarization 6. in a nerve, this whole process takes 0.001 seconds C. Mechanisms underlying events in Action Potential (Fig 7.16, 7.17) 1. Membrane contains Na+ channels and K+ channels. Both of these are voltage regulated channels, meaning that changes in voltage (i.e., membrane potential) open or close them. 2. At rest (-70 mV) some K+ channels are open, fewer Na+ channels open; the “leaking” of these two ions across membrane balanced by Na-K-ATPase pump (see Topic 3-VI-C-4) 3. As depolarization begins in response to triggering event, the change in voltage causes additional Na+ channels to open 4. Na+ concentration and electrical gradients are INTO cell, so Na+ begins to move into cell 5. This causes more depolarization, which opens more voltage-gated Na+ channels 6. Positive feedback loop established 7. When threshold reached at -55 mV membrane becomes 600 times more permeable to Na+ than K+ because all voltage-gated Na+ channels opened at -55 mV 8. Na+ rushes in, and inside of cell becomes positive (30 mV); note that this is close to the Na+ equilibrium potential 9. Na+ voltage-gated channels close at 30 mV 10. When membrane voltage is 30 mV, K+ voltage gated channels open wide and K+ rushes out of cell down both its concentration and electrical gradient. 11. Positive charges leaving w/ K+ repolarizes the membrane back to resting potential of -70 mV; sometimes a few too many K+ leave and cause hyperpolarization. 12. Relative to the total number of Na+ ions outside neuron very few Na+ ions move into cell during depolarization; likewise, relative to the total number of K+ ions inside neuron, very few K+ ions move out of the cell during repolarization. Biology 251 Fall 2015 2 D. Restoration of Ion Gradients 1. At completion, the resting membrane potential of -70 mV is restored, but concentrations of Na+ and K+ are not. 2. However, very few K+ and Na+ actually cross the membrane during an action potential compared to total amount of these ions available (only about 1 out of every 100,000 ions crosses the membrane) so their overall concentration is not changed much. 3. Eventually the original concentrations restored by Na+-K+ ATPase pump. Without this pump, repeated action potentials would eventually erode separation of Na+ and K+ III. The Neuron and Conduction of Action Potentials A. Neuron Structure (Fig 7.2) 1. Three parts a) cell body (1) nucleus and organelles b) dendrites (1) numerous extensions from cell body c) axon or nerve fiber (1) single elongated tubular extension (2) conducts action potentials away from cell body (3) may give off side branches or collaterals (4) has highly branched endings called axon terminals d) first portion of axon + region of cell body from which it leaves is called axon hillock 2. Can range in length from less 1 mm to over 1 meter (e.g., lower back to big toe) B. Conduction of Action Potential in a neuron (fig 7.22) 1. Initiated in axon hillock 2. Conduction of AP by local current flow down the axon 3. Resting potential in an adjacent inactive area is depolarized to threshold by local current flow in active area 4. First action potential triggers next one in adjacent area 5. This is a self perpetuating cycle down the neuron C. Mylenation (fig 7.7) 1. Myelin: fibers composed of lipids 2. Surrounds portion of axon, like rubber insulation 3. In CNS, myelin forming cells are called oligodendrocytes 4. In Peripheral NS, myelin formed by Schwann cells. 5. Gaps between myelin are called Nodes of Ranvier a) Impulse jumps from node to node; this is called saltatory conduction (fig 7.23) 6. Increases speed of the conduction of action potential 7. Multiple sclerosis is caused by autoimmune destruction of myelin D. Toilets and Guns: Special properties of action potentials 1. Refractory Period of action potentials (Fig 7.20) a) Don’t want action potential moving in both directions on axon, so a refractory period is required to keep APs from bouncing back and forth in a neuron. b) Absolute refractory period: Na+ gates are closed and inactivated; no action potential can occur c) Relative refractory period:action potential can occur, but stimulus must be much
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