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Intracellular Signaling in Vascular Smooth Muscle

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Interactive Phenomena in the Cardiac System

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 346))

Abstract

The two major modalities of pharmacomechanical coupling, inositol 1,4,5 trisphosphate induced Ca2+ release and modulation of Ca2+-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 Ca2+-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.

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Somlyo, A.V., Somlyo, A.P. (1993). Intracellular Signaling in Vascular Smooth Muscle. In: Sideman, S., Beyar, R. (eds) Interactive Phenomena in the Cardiac System. Advances in Experimental Medicine and Biology, vol 346. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-2946-0_4

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  • DOI: https://doi.org/10.1007/978-1-4615-2946-0_4

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-6280-7

  • Online ISBN: 978-1-4615-2946-0

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