日本生理学会大会発表要旨集
日本生理学会大会発表要旨集
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会議情報

心臓におけるCa2+チャネル不活性化モデル
*村上 慎吾河津 俊宏Findlay Ian鈴木 慎悟赤羽 悟美野村 泰伸倉智 嘉久
著者情報
キーワード: ion channel, calmodulin, CaMKII
会議録・要旨集 フリー

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The inactivation of the cardiac L-type Ca2+ current is composed of voltage-dependent and calcium-dependent mechanisms. We modeled physiological modulation of inactivation of the current in cardiac ventricular myocytes. Firstly, we used the recent detailed kinetic data for voltage dependent-inactivation (VDI) and its modulation by β-adrenergic stimulation. We modeled VDI based on the experimental data and calcium dependent-inactivation (CDI) as a function of Ca2+-influx through L-type Ca2+ channels. This model could largely reproduce the behavior of physiological L-type Ca2+ channel current carried by divalent cations in the basal as well as under β-adrenergic stimulation. Next, we constructed microstructure based Ca2+ dynamics models to simulate Ca2+ influx through individual L-type Ca2+ channels and diffusion in the dyadic space which would induce CDI. These models used the agent base Monte Carlo method and they consisted of L-type Ca2+ channels with distal and proximal Ca2+ binding sites, dyadic space, sarcoplasmic reticulum membrane, and free calcium ions. The models reproduced major features of the CDI process which had been measured with single channel recording. The developed models will be useful to estimate the respective roles of VDI and CDI of L-type Ca2+ channels in various physiological and pathological conditions of the heart. [J Physiol Sci. 2008;58 Suppl:S46]
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© 2008 日本生理学会
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