Pharmacomechanical coupling in vascular smooth muscle cells-an overview.
- 1 January 1991
- journal article
- review article
- Published by Elsevier in The Japanese Journal of Pharmacology
- Vol. 55 (1) , 1-9
- https://doi.org/10.1254/jjp.55.1
Abstract
In vascular smooth muscles, neurotransmitters or autacoids produce contraction through activation of Ca2+-influx and release of Ca2+ from intracellular store sites. These agonists appear to activate Ca2+-influxes in both voltage-dependent and voltage-independent manners. The release of Ca2+ is thought to be linked to the action of inositol 1, 4, 5-trisphosphate. The phosphorylation of myosin light chain may be the mechanism for the Ca2+-induced contraction in smooth muscles. Some agonists only transiently increase cellular Ca2+ and the phosphorylation of myosin, but they produce a sustained contraction in various vascular tissues. Hence, additional high Ca2+-sensitive mechanisms are no doubt involved in the contraction of vascular smooth muscle. In the present article, attention will be directed to the mechanisms and agonist-induced contraction in arterial smooth muscle.Keywords
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