Campbell Biology in Focus
Campbell Biology in Focus
3rd Edition
ISBN: 9780134710679
Author: Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Rebecca Orr
Publisher: PEARSON
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Chapter 37, Problem 9TYU

DRAW IT Suppose a researcher inserts a pair of electrodes at two different positions along the middle of an axon dissected out of a squid. By applying a depolarizing stimulus, the researcher brings the plasma membrane at both positions to threshold. Using the drawing below as a model, create one or more drawings that illustrate where each action potential would terminate.

Chapter 37, Problem 9TYU, DRAW IT Suppose a researcher inserts a pair of electrodes at two different positions along the

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The graph shows a tracing of membrane potential change during the course of an action potential in a typical neuron. Predict the effect of exposure to the following neurotoxins. Briefly explain how you would expect the action potential to change in the presence of each toxin and why. A toxin produced by puffer fish which specifically binds to voltage-gated sodium channels and blocks the flow of sodium ions through the channel.  A toxin found in scoprion venom which slows the closure of voltage-gated sodium channel inactivation gates.  Assume that the cell is normally brought to threshold by an electrical stimulus applied to it, so that any change is due only to the presence of the toxin Precise values for voltage and duration are not important, just a general trend in how the action potential may differ from the typical trace shown is expected.
Three currents are produced by a 56 mV depolarization leading to an action potential in a squid axon membrane during a voltage clamp experiment as shown. What is the mechanism underlying the capacitive current? 56 mV Depolarization Capacitative current Late current Early current Time (ms) Opening of Na* channels Current due to the Na/K* pump O Neutralization of the charge on the membrane Opening of K channels Membrane Membeane current imA/cm potential (mV)
You are obtaining extracellular recordings from the latetal axons of the earth worm. The distance from the stimulating cathode to the first recording electrode is 60mm and 85mm to the second recording electrode. The time from stimulation to arrival of the action potential at the first recording electrode is 5msec and to the second recording electrode is 10msec. The conduction velocity of this axon would be meters per second. 05 0.2 Ⓒ10 3
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