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. 1984 Jul;46(1):35–44. doi: 10.1016/S0006-3495(84)83996-X

Kinetic model for isometric contraction in smooth muscle on the basis of myosin phosphorylation hypothesis.

S Kato, T Osa, T Ogasawara
PMCID: PMC1434938  PMID: 6547623

Abstract

A kinetic model was proposed to simulate an isometric contraction curve in smooth muscle on the basis of the myosin phosphorylation hypothesis. The Ca2+-calmodulin-dependent activation of myosin light-chain kinase and the phosphorylation-dephosphorylation reaction of myosin were mathematically treated. Solving the kinetic equations at a steady state, we could calculate the relationship between the Ca2+ concentration and the myosin phosphorylation. Assuming that two-head-phosphorylated myosin has an actin-activated Mg2+-ATPase activity and that this state corresponds to an active state, we computed the time courses of the myosin phosphorylation and the active state for various Ca2+ transients. The time course of the active state was converted into that of isometric tension by use of Sandow's model composed of a contractile element and a series elastic component. The model could simulate not only the isometric contraction curves for any given Ca2+ transient but also the following experimental results: the calmodulin-dependent shift of the Ca2+ sensitivity of isometric tension observed in skinned muscle fibers, the disagreement between the Ca2+ sensitivity of myosin phosphorylation and that of isometric tension at a steady state, and the disagreement between the time course of myosin phosphorylation and that of isometric tension development.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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