» Articles » PMID: 5965887

Rebound Excitation of the Smooth Muscle Cells of the Guinea-pig Taenia Coli After Stimulation of Intramural Inhibitory Nerves

Overview
Journal J Physiol
Specialty Physiology
Date 1966 Jul 1
PMID 5965887
Citations 41
Authors
Affiliations
Soon will be listed here.
Abstract

1. A study has been made of the increase in the rate of action potential firing in spontaneously active cells and of the initiation of action potential firing in quiescent cells of the taenia coli after stimulation of the intramural inhibitory nerves.2. In the majority of cells which fired action potentials spontaneously at intervals of about 1 sec, stimulation of the intramural inhibitory nerves with single pulses gave an inhibitory junction potential (I.J.P.) which was followed by action potentials which occurred at intervals as small as 0.5 sec. The increased rate of firing lasted up to 30 sec.3. A small number of cells were either not spontaneously active or only fired action potentials at intervals greater than 5 sec. After stimulation of the intramural inhibitory nerves with either single or repetitive pulses, the quiescent cells gave I.J.P.S which were followed by either a single action potential or a burst of action potentials.4. The rate of firing of action potentials after an I.J.P., and the duration of this enhanced rate of firing increased with an increase in the mean amplitude of the hyperpolarization during the I.J.P. As the amplitude of the I.J.P. increases with an increase in frequency of stimulation of the nerves, the rebound excitation increases with an increase in the frequency of stimulation of the inhibitory nerves.

Citing Articles

Propulsive colonic contractions are mediated by inhibition-driven poststimulus responses that originate in interstitial cells of Cajal.

Koh S, Drumm B, Lu H, Kim H, Ryoo S, Kim H Proc Natl Acad Sci U S A. 2022; 119(18):e2123020119.

PMID: 35446689 PMC: 9170151. DOI: 10.1073/pnas.2123020119.


Pacemaker function and neural responsiveness of subserosal interstitial cells of Cajal in the mouse colon.

Drumm B, Rembetski B, Messersmith K, Manierka M, Baker S, Sanders K J Physiol. 2019; 598(4):651-681.

PMID: 31811726 PMC: 7024031. DOI: 10.1113/JP279102.


Hypothalamic Projections to the Optic Tectum in Larval Zebrafish.

Heap L, Vanwalleghem G, Thompson A, Favre-Bulle I, Rubinsztein-Dunlop H, Scott E Front Neuroanat. 2018; 11:135.

PMID: 29403362 PMC: 5777135. DOI: 10.3389/fnana.2017.00135.


Regulation of gastrointestinal motility--insights from smooth muscle biology.

Sanders K, Koh S, Ro S, Ward S Nat Rev Gastroenterol Hepatol. 2012; 9(11):633-45.

PMID: 22965426 PMC: 4793911. DOI: 10.1038/nrgastro.2012.168.


Effects of autonomic nerve stimulation on colorectal motility in rats.

Tong W, Ridolfi T, Kosinski L, Ludwig K, Takahashi T Neurogastroenterol Motil. 2010; 22(6):688-93.

PMID: 20067587 PMC: 2952396. DOI: 10.1111/j.1365-2982.2009.01461.x.


References
1.
Bennett M . Transmission from intramural excitatory nerves to the smooth muscle cells of the guinea-pig taenia coli. J Physiol. 1966; 185(1):132-47. PMC: 1395870. DOI: 10.1113/jphysiol.1966.sp007976. View

2.
Campbell G . Nerve-mediated excitation of the taenia of the guinea-pig caecum. J Physiol. 1966; 185(1):148-59. PMC: 1395874. DOI: 10.1113/jphysiol.1966.sp007977. View

3.
HODGKIN A, HUXLEY A . A quantitative description of membrane current and its application to conduction and excitation in nerve. J Physiol. 1952; 117(4):500-44. PMC: 1392413. DOI: 10.1113/jphysiol.1952.sp004764. View

4.
KUFFLER S, Eyzaguirre C . Synaptic inhibition in an isolated nerve cell. J Gen Physiol. 1955; 39(1):155-84. PMC: 2147519. DOI: 10.1085/jgp.39.1.155. View

5.
Ito M . The electrical activity of spinal ganglion cells investigated with intracellular microelectrodes. Jpn J Physiol. 1957; 7(4):297-323. DOI: 10.2170/jjphysiol.7.297. View