Intracellular signaling in vascular smooth muscle.

Abstract:

:The two major modalities of pharmacomechanical coupling, inositol 1,4,5, trisphosphate induced Ca2+ release and modulation of Ca(2+)-sensitivity, are reviewed. Recent studies show that although changes in cytoplasmic Ca2+ play the major role in regulating smooth muscle contraction, agonists can also significantly affect the contractile state by modifying Ca(2+)-sensitivity. Inhibition of myosin light chain kinase or myosin light chain phosphatase leads to, respectively, desensitization or sensitization of the contractile apparatus to Ca2+. G-protein linked inhibition of myosin light chain phosphatase and Ca2+ release mediated by the phosphatidylinol cascade are the two major pharmacomechanical coupling mechanisms.

journal_name

Adv Exp Med Biol

authors

Somlyo AV,Somlyo AP

doi

10.1007/978-1-4615-2946-0_4

subject

Has Abstract

pub_date

1993-01-01 00:00:00

pages

31-8

eissn

0065-2598

issn

2214-8019

journal_volume

346

pub_type

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