2016 Fiscal Year Final Research Report
Dynamics of angiogenesis in ischemic areas of the infarcted heart
Project/Area Number |
25461104
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Cardiovascular medicine
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Research Institution | Nagoya University |
Principal Investigator |
|
Project Period (FY) |
2013-04-01 – 2017-03-31
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Keywords | 血管新生 / 虚血 / 心筋梗塞 / 血管増殖因子 / アポトーシス |
Outline of Final Research Achievements |
The mechanism and timing for new vessel formation in the mammalian heart following hypoxia are unclear. Identifying targets that benefit from angiogenesis treatment is indispensable for the development of revolutionary therapies. Here, we describe a novel circulatory system wherein new vessels develop from the endocardium of the left ventricle to perfuse the hypoxic area and salvage damaged cardiomyocytes at 3-14 days after MI by activating vascular endothelial growth factor signaling. Moreover, enhanced angiogenesis increased cardiomyocyte survival along the endocardium in the ischemic zone and suppressed ventricular remodeling in infarcted hearts. In contrast, cardiomyocytes in the border zone’s hypoxic area underwent apoptosis within 12 h of MI, and the border area that was amenable to treatment disappeared. These data indicate that the non-perfused area along the endocardium is a site of active angiogenesis and a promising target for MI treatment.
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Free Research Field |
虚血性心疾患
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