Prevention of spiral wave formation and breakup bycontmlof intracellular calcium dynamics
| Project/Area Number |
18590767
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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 |
Circulatory organs internal medicine
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| Research Institution | Nagoya University |
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Principal Investigator |
HONJO Haruo Nagoya University, Research Institute of Environmental Medicine, Associate Professor (70262912)
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| Co-Investigator(Kenkyū-buntansha) |
KAMIYA Kaichiro Nagoya University, Research Institute of Environmental Medicine, Professor (50194973)
KODAMA Itsuo Nagoya University, ResearchInstitute ofEnvironmental Medicine, Professor (30124720)
SAKUMA Ichiro The University of Tokyo, Graduate School ofEngineering, Professor (50178597)
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| Project Period (FY) |
2006 – 2007
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| Project Status |
Completed (Fiscal Year 2007)
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| Budget Amount *help |
¥3,890,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥390,000)
Fiscal Year 2007: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2006: ¥2,200,000 (Direct Cost: ¥2,200,000)
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| Keywords | Arrhythmia / Action potential / Calcium dynamics / Optical mapping / Reentry / Elecronhvsioloey / 致死性不整脈 / 蛍光プローブ / カルシウム / 蛍光色素 |
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| Research Abstract |
Recent theoretical studies using computer simulation has suggested that intercellular Can dynamics plays an important role in the initiation and maintenance of spiral wave reentry, which is a principal mechanism underlying ventricular tachyarrhythmias such as ventricular fibrillation/tachycardia. In this study, we have developed 2 types of dual optical mapping systems to record action potential/intracellular Ca^2+ fluorescence images simultaneously from isolated heart preparations of experimental animals: the first system has a dicrotic mirror to separate fluorescence signals and 2 high-speed CMOS video cameras, and the second system includes a high-speed switching apparatus of excitation LEDs combined with rotating optical filters fir fluorescence. A series of fluorescence images for action potentials and intracellular Ca^2+ were recorded simultaneously from the left ventricular epicardial myocardium Langendorff-perfused rabbit hearts with reasonable spatiotemporal resolution. In the firmer system, however, an additional development of image processing software to adjust the dual fluorescence images will be required, and in the latter system, an improvement of time resolution (20 frames/s) will be needed for precise analysis of relationship between action potentials and intracellular Ca^2+ dynamics to elucidate the roles of intracellular Ca^2+ dynamics on spiral wave reentry.
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Report
(3 results)
Research Products
(28 results)
