» Articles » PMID: 1362333

Desensitization to Acetylcholine in Single Sinoatrial Node Cells Isolated from Rabbit Hearts

Overview
Journal Am J Physiol
Specialty Physiology
Date 1992 Dec 1
PMID 1362333
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

The negative chronotropic effect of acetylcholine (ACh) on the sinoatrial node fades in the continuous presence of ACh as a result of desensitization. We have investigated the mechanism underlying desensitization in single rabbit sinoatrial node cells using the whole cell patch clamp technique. The negative chronotropic effect resulting from the injection of a constant hyperpolarizing current faded. ACh activated an inwardly rectifying potassium current (iK,ACh), which faded in the continuous presence of ACh. ACh had no effect on "basal" L-type calcium current (iCa), but ACh decreased iCa, which had been potentiated by isoprenaline. This effect did not fade during a 2-min exposure to ACh. ACh decreased the hyperpolarization-activated current (i(f)). This effect again did not fade. These results suggest that desensitization of the negative chronotropic response to ACh is, in part, the result of the membrane hyperpolarization and, in part, the result of the fade of iK,ACh. These results also suggest that, whereas the activation of potassium current by ACh rapidly fades, the effects resulting from the inhibition of adenylate cyclase do not.

Citing Articles

Acute desensitization of acetylcholine and endothelin-1 activated inward rectifier K+ current in myocytes from the cardiac atrioventricular node.

Choisy S, James A, Hancox J Biochem Biophys Res Commun. 2012; 423(3):496-502.

PMID: 22683635 PMC: 3400056. DOI: 10.1016/j.bbrc.2012.05.148.


Modulation by endothelin-1 of spontaneous activity and membrane currents of atrioventricular node myocytes from the rabbit heart.

Choisy S, Cheng H, Smith G, James A, Hancox J PLoS One. 2012; 7(3):e33448.

PMID: 22479400 PMC: 3315568. DOI: 10.1371/journal.pone.0033448.


A model of cellular cardiac-neural coupling that captures the sympathetic control of sinoatrial node excitability in normotensive and hypertensive rats.

Tao T, Paterson D, Smith N Biophys J. 2011; 101(3):594-602.

PMID: 21806927 PMC: 3145287. DOI: 10.1016/j.bpj.2011.05.069.


Conformational changes in the M2 muscarinic receptor induced by membrane voltage and agonist binding.

Navarro-Polanco R, Moreno Galindo E, Ferrer-Villada T, Arias M, Rigby J, Sanchez-Chapula J J Physiol. 2011; 589(Pt 7):1741-53.

PMID: 21282291 PMC: 3099027. DOI: 10.1113/jphysiol.2010.204107.


A novel quantitative explanation for the autonomic modulation of cardiac pacemaker cell automaticity via a dynamic system of sarcolemmal and intracellular proteins.

Maltsev V, Lakatta E Am J Physiol Heart Circ Physiol. 2010; 298(6):H2010-23.

PMID: 20228256 PMC: 2886657. DOI: 10.1152/ajpheart.00783.2009.