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2016 Fiscal Year Final Research Report

Dynamics of angiogenesis in ischemic areas of the infarcted heart

Research Project

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Project/Area Number 25461104
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Cardiovascular medicine
Research InstitutionNagoya University

Principal Investigator

Kobayashi Koichi  名古屋大学, 医学部附属病院, 講師 (20567010)

Project Period (FY) 2013-04-01 – 2017-03-31
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.

Free Research Field

虚血性心疾患

URL: 

Published: 2018-03-22  

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