» Articles » PMID: 13718006

Effects of Temperature on the Generator and Action Potentials of a Sense Organ

Overview
Journal J Gen Physiol
Specialty Physiology
Date 1961 Sep 1
PMID 13718006
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Charge transfer through the receptor membrane of the nonmyelinated ending of Pacinian corpuscles is markedly affected by temperature. The rate of rise and the amplitude of the generator potential in response to a constant mechanical stimulus increase with temperature coefficients of 2.5 and 2.0 respectively. The duration of the falling phase, presumably a purely passive component, and the rise time of the generator potential are but little affected by temperature. The following interpretation is offered: Mechanical stimulation causes the conductance of the receptor membrane to increase and ions to flow along their electrochemical gradients. An energy barrier of about 16,000 cal/mole limits the conductance change. The latter increases, thus, steeply with temperature, causing both the rate of rise and the intensity of the generator current to increase. The membrane of the adjacent Ranvier node behaves in a distinctly different manner. The amplitude of the nodal action potential is little changed over a wide range of temperature, while the durations of its rising and falling phases increase markedly. The electrical threshold of the nodal membrane is rather constant between 40 and 12 degrees C. Below 12 degrees C the threshold rises, and the mechanically elicited generator current fails to meet the threshold requirements of the first node. Cold block of nerve impulse initiation then ensues, although the receptor membrane still continues to produce generator potentials in response to mechanical stimulation.

Citing Articles

Thermal effects and ephaptic entrainment in Hodgkin-Huxley model.

Brasil de Sousa M, Moreno Cunha G, Corso G, Dos Santos Lima G Sci Rep. 2024; 14(1):20075.

PMID: 39209942 PMC: 11362309. DOI: 10.1038/s41598-024-70655-5.


Effects of active and passive warming of the foot sole on vibration perception thresholds.

Schmidt D, Germano A, Milani T Clin Neurophysiol Pract. 2018; 2:38-43.

PMID: 30214969 PMC: 6123895. DOI: 10.1016/j.cnp.2016.12.005.


Mechanical sensibility of nociceptive and non-nociceptive fast-conducting afferents is modulated by skin temperature.

Boada M, Eisenach J, Ririe D J Neurophysiol. 2015; 115(1):546-53.

PMID: 26581873 PMC: 4760509. DOI: 10.1152/jn.00796.2015.


Vascularization of Air Sinuses and Fat Bodies in the Head of the Bottlenose Dolphin (Tursiops truncatus): Morphological Implications on Physiology.

Costidis A, Rommel S Front Physiol. 2012; 3:243.

PMID: 22969724 PMC: 3431794. DOI: 10.3389/fphys.2012.00243.


Temperature dependence of rapidly adapting mechanically activated currents in rat dorsal root ganglion neurons.

Jia Z, Ling J, Gu J Neurosci Lett. 2012; 522(2):79-84.

PMID: 22743298 PMC: 4862582. DOI: 10.1016/j.neulet.2012.06.024.


References
1.
Gray J, Sato M . Properties of the receptor potential in Pacinian corpuscles. J Physiol. 1953; 122(3):610-36. PMC: 1366145. DOI: 10.1113/jphysiol.1953.sp005025. View

2.
Ling G, WOODBURY J . Effect of temperature on the membrane potential of frog muscle fibers. J Cell Comp Physiol. 1949; 34(3):407-12. DOI: 10.1002/jcp.1030340306. View

3.
FATT P, Katz B . An analysis of the end-plate potential recorded with an intracellular electrode. J Physiol. 1951; 115(3):320-70. PMC: 1392060. DOI: 10.1113/jphysiol.1951.sp004675. View

4.
CORABOEUF E, Weidmann S . Temperature effects on the electrical activity of Purkinje fibres. Helv Physiol Pharmacol Acta. 1954; 12(1):32-41. View

5.
Burkhardt D . Effect of temperature on isolated stretch-receptor organ of the crayfish. Science. 1959; 129(3346):392-3. DOI: 10.1126/science.129.3346.392. View