Phase-plane trajectories of atrial cell action potentials: effects of temperature reduction

1974 ◽  
Vol 8 (4) ◽  
pp. 451-459 ◽  
Author(s):  
S. E. FREEMAN ◽  
R. J. TURNER
1976 ◽  
Vol 10 (1) ◽  
pp. 136-138
Author(s):  
E. L. DE BEER ◽  
H. B. K. BOOM ◽  
H. C. SCHAMHARDT

1982 ◽  
Vol 99 (1) ◽  
pp. 207-221
Author(s):  
W. WINLOW ◽  
A. V. HOLDEN ◽  
P. G. HAYDON

1. Phase plane techniques have been used to demonstrate that identifiable neurones of Lymnaea stagnalis may be characterized by their action potential trajectories. 2. These trajectories are consistent from preparation to preparation, but may be altered by strong synaptic inputs or by injection of current into neurones. 3. There is a pronounced hysteresis in the maximum rates of depolarization (V·d) and the maximum rates of repolarization (V·r) of many cells following a period of hyperpolarization. 4. Curves relating V·a and V·r to injected current have been constructed for each neurone type investigated and may be used to identify the neurones. 5. We conclude that phase plane portraits of action potentials together with measures of V·d and V·r are useful in identification of neurones when structural criteria are not available. Note:


2000 ◽  
Vol 83 (6) ◽  
pp. 3462-3472 ◽  
Author(s):  
J. Wang ◽  
G. Chambers ◽  
J. E. Cottrell ◽  
I. S. Kass

Intracellular recordings, ATP and cytosolic calcium measurements from CA1 pyramidal cells in rat hippocampal slices were used to examine the mechanisms by which temperature alters hypoxic damage. Hypothermia (34°C) preserved ATP (1.7 vs. 0.8 nM/mg) and improved electrophysiologic recovery of the CA1 neurons after hypoxia; 58% of the neurons subjected to 10 min of hypoxia (34°C) recovered their resting and action potentials, while none of the neurons at 37°C recovered. Increasing the glucose concentration from 4 to 6 mM during normothermic hypoxia improved ATP (1.3 vs. 0.8 nM/mg) and mimicked the effects of hypothermia; 67% of the neurons recovered their resting and action potentials. Hypothermia attenuated the membrane potential changes and the increase in intracellular Ca2+(212 vs. 384 nM) induced by hypoxia. Changing the glucose concentration in the artificial cerebrospinal fluid primarily affects ATP levels during hypoxia. Decreasing the glucose concentration from 4 to 2 mM during hypothermic hypoxia worsened ATP, cytosolic Ca2+, and electrophysiologic recovery. Ten percent of the neurons subjected to 4 min of hypoxia at 40°C recovered their resting and action potentials; this compared with 60% of the neurons subjected to 4 min of normothermic hypoxia. None of the neurons subjected to 10 min of hypoxia at 40°C recovered their resting and action potentials. Hyperthermia (40°C) worsens the electrophysiologic changes and induced a greater increase in intracellular Ca2+(538 vs. 384 nM) during hypoxia. Increasing the glucose concentration from 4 to 8 mM during 10 min of hyperthermic hypoxia improved ATP (1.4 vs. 0.6 nM/mg), Ca2+(267 vs. 538 nM), and electrophysiologic recovery (90 vs. 0%). Our results indicate that the changes in electrophysiologic recovery with temperature are primarily due to changes in ATP and that the changes in depolarization and Ca2+are secondary to these ATP changes. Both primary and secondary changes are important for explaining the improved electrophysiologic recovery with hypothermia.


1976 ◽  
Vol 230 (2) ◽  
pp. 403-409 ◽  
Author(s):  
HK Jacobs ◽  
FE South

Resting and action potential parameters were measured from papillary muscle isolated from hibernating and control hamsters and from rats. The temperature range of the study was 12-38 degrees C. The decrease in resting membrane potential (Em) with decreasing temperature was significantly less in the hibernation preparations (HH), down to 20 degrees C, than in either the control hamsters or rats. Below 20 degrees C the declines in Em of all preparations were indistinguishable. Action potential magnitude was adequately maintained in HH to 12 degrees C while both control hamster and rat action potentials declined markedly as temperatures were reduced. Both types of hamster preparations showed greatly prolonged action potentials with reduced temperatures as contrasted to a limited prolongation of rat action potentials. The data are suggestive of a membrane modication in hibernation.


1977 ◽  
Vol 233 (1) ◽  
pp. C35-C46 ◽  
Author(s):  
M. Baron ◽  
C. Eyzaguirre

Excised cat carotid bodies and nerves were placed in a Lucite chamber through which saline flowed at different temperatures. Action potentials were recorded with a suction electrode. Glomus cells were impaled with microelectrodes and identified by ejecting Procion navy blue from the micropipette. Membrane potentials (MP) averaged 20 mV and input resistances (R0), 40 Momega. Cooling induced depolarization and decreased R0. This effect had a reversal potential of about -6 mV. [K+]0 did not affect MP, R0, or cooling effects. Lack of sodium increased MP, R0, and depressed cooling effects. Low chloride had opposite effects. Ca2+ and Mg2+ influenced MP and R0 but had little effects on temperature actions. Ouabain decreased MP and R0. Results indicate that glomus cells are exquisitely sensitive to temperature changes; their MP and R0 increase with high temperatures and decrease when temperature is lowered. These effects are mostly dependent on the external concentration of Cl- and Na+. Glomus cells may be the site of the intense metabolism of this tissue and thus contribute to the generation of chemosensory impulses.


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