| Project/Area Number |
20590220
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
General physiology
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| Research Institution | Kanazawa Medical University |
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Principal Investigator |
KURATA Yasutaka Kanazawa Medical University, 医学部, 准教授 (00267725)
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| Co-Investigator(Kenkyū-buntansha) |
SHIBAMOTO Toshishige 金沢医科大学, 医学部, 教授 (90178921)
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| Project Period (FY) |
2008 – 2010
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| Project Status |
Completed (Fiscal Year 2010)
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| Budget Amount *help |
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2010: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2009: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2008: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
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| Keywords | 非線形力学 / 生物・生体工学 / 生物物理 / 生理学 / 再生医学 |
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| Research Abstract |
The aim of this study was to elucidate the dynamical mechanisms of generation and regulation of pacemaker activity during differentiation of mouse ES-cell derived cardiomyocytes. We have constructed nonlinear dynamical systems (nonlinear ordinary differential equations) of the ES-cell derived cardiomyocytes (sinoatrial node-type, atrial-type, and ventricular-type) on the basis of electrophysiological data. Analyzing the bifurcation structures (ways of generating or abolishing pacemaker activity) of these model systems, we have clarified that the emergence and abolition of pacemaker activity during differentiation of the cardiomyocytes are bifurcation phenomena, and that both sarcolemmal ionic channel currents and intracellular Ca^<2+> dynamics are involved in occurrence of the bifurcations.
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