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PMID: 3177686 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Hyperpolarization and increased free calcium in acetylcholine-stimulated endothelial cells.

The American journal of physiology ·Vol. 255 ·No. 4 Pt 2 ·1988-10-00 ·Pages H965-9

Busse R, Fichtner H, Lückhoff A, Kohlhardt M

Abstract

In freshly harvested aortic endothelial cells from rabbits, some cellular events associated with stimulation by acetylcholine (ACh) were analyzed. ACh (3 microM) induced a transient hyperpolarization of 8.3 +/- 2.5 mV, which peaked within 3-5 s and subsequently declined with a similar time course. Hyperpolarization was caused by a transient Ca2+-dependent outward current (IoACh), which was mainly carried by K+. ACh (3 and 10 microM) also evoked transient dose-dependent increases in the intracellular free Ca2+ concentration (Ca2+i). Pretreatment with atropine (1 and 3 microM) abolished both responses to ACh, the increase in Ca2+i as well as the transient outward current. It is concluded that IoACh and the rise in Ca2+i are two manifestations of muscarinic receptor stimulation. The rise in Ca2+i might be the primary event, leading to secondary membrane hyperpolarization.

MeSH Terms
Acetylcholine/pharmacology Animals Calcium/metabolism Cells, Cultured Endothelium, Vascular/drug effects,physiology Female In Vitro Techniques Male Membrane Potentials/drug effects Rabbits
Chemicals
Acetylcholine Calcium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Busse R
Department of Applied Physiology, University of Freiburg, Federal Republic of Germany.
Fichtner H
Lückhoff A
Kohlhardt M
Article Info
Journal
The American journal of physiology
Abbr.
Am J Physiol
ISSN
0002-9513
Published
1988-10-00
Pages
H965-9
Language
English
Region
United States
NLM ID
0370511
Subset
IM
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