» Articles » PMID: 3826358

Interaction of Two Electrical Pacemakers in Muscularis of Canine Proximal Colon

Overview
Journal Am J Physiol
Specialty Physiology
Date 1987 Mar 1
PMID 3826358
Citations 52
Authors
Affiliations
Soon will be listed here.
Abstract

Experiments were performed to determine the source of the 20 cycles/min electrical oscillation commonly seen in colonic electrical records, the influence of the 20 cycles/min rhythm on the circular and longitudinal muscle layers, and the interactions between the 20 cycles/min rhythm and slow waves in circular muscle cells. Cross-sectional muscle preparations of the canine proximal colon were used to allow impalement of cells at any point through the thickness of the muscularis. Intracellular recordings from circular muscle cells clearly showed the two characteristic pacemaker frequencies in the colon (6 cycles/min slow waves; 20 cycles/min oscillations). The 20 cycles/min oscillations were recorded from longitudinal and circular muscle cells. Their amplitudes were greatest at the myenteric border. In the longitudinal layer the 20 cycles/min events initiated action potentials; in circular muscle the 20 cycles/min events summed with slow waves. Simultaneous recordings from circular and longitudinal cells across the myenteric border demonstrated that events in the two layers were usually in phase, suggesting that the two layers are electrically coupled and are paced by a common pacemaker. The amplitude of the 20 cycles/min events decayed with distance from the myenteric border in both circular and longitudinal muscles. The data demonstrate that two discrete populations of pacemaker cells generate the spontaneous electrical activity in the colon. Both events appear to passively spread through the circular muscle. It is the summation of these events that appears to serve as the signal for excitation-contraction coupling in circular muscle.

Citing Articles

Ca²⁺ signaling in myenteric interstitial cells of Cajal (ICC-MY) and their role as conditional pacemakers in the colon.

Baker S, Karwa M, Lee J, Riar S, Drumm B, Sanders K Cell Calcium. 2025; 125():102990.

PMID: 39755028 PMC: 11737426. DOI: 10.1016/j.ceca.2024.102990.


Insights on gastrointestinal motility through the use of optogenetic sensors and actuators.

Drumm B, Cobine C, Baker S J Physiol. 2022; 600(13):3031-3052.

PMID: 35596741 PMC: 9250614. DOI: 10.1113/JP281930.


Ca signaling driving pacemaker activity in submucosal interstitial cells of Cajal in the murine colon.

Baker S, Leigh W, Del Valle G, De Yturriaga I, Ward S, Cobine C Elife. 2021; 10.

PMID: 33399536 PMC: 7806270. DOI: 10.7554/eLife.64099.


Gastric Biopsies in Gastroparesis: Insights into Gastric Neuromuscular Disorders to Aid Treatment.

Chikkamenahalli L, Pasricha P, Farrugia G, Grover M Gastroenterol Clin North Am. 2020; 49(3):557-570.

PMID: 32718570 PMC: 7387746. DOI: 10.1016/j.gtc.2020.04.009.


Excitatory cholinergic responses in mouse colon intramuscular interstitial cells of Cajal are due to enhanced Ca release via M receptor activation.

Drumm B, Rembetski B, Huynh K, Nizar A, Baker S, Sanders K FASEB J. 2020; 34(8):10073-10095.

PMID: 32539213 PMC: 7790594. DOI: 10.1096/fj.202000672R.