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2015 Fiscal Year Final Research Report

Downregulation of cPLA2 suppress atherosclerotic lesion formation in apolipoprotein-E deficient mice.

Research Project

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Project/Area Number 25461374
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Metabolomics
Research InstitutionKumamoto University

Principal Investigator

Matsumura Takeshi  熊本大学, 医学部附属病院, 講師 (20398192)

Co-Investigator(Kenkyū-buntansha) SENOKUCHI Takafumi  熊本大学, 大学院生命科学研究部, 助教 (00530320)
Co-Investigator(Renkei-kenkyūsha) MOTOSHIMA Hiroyuki  熊本大学, 医学部附属病院, 助教 (40398201)
Project Period (FY) 2013-04-01 – 2016-03-31
Keywords動脈硬化症
Outline of Final Research Achievements

We investigated the anti-atherogenic effects on cPLA2 and apoE double knockout mice (cPLA2/apoE KO mice). PPARgannma activity was increased in peritoneal macrophage of cPLA2/apoE KO mice. LPS-induced mRNA expression of TNF-alpha and MCP-1 was decreased, and mRNA expression ABCA1/G1 was increased in peritoneal macrophage of cPLA2/apoE KO mice. Moreover, atherosclerotic lesion formation on cPLA2/apoE KO mice was lower than that on control apoE KO mice. These results suggest that cPLA2 is involved in atherosclerotic lesion formation in apoE KO mice, and that may be therapeutic target for diabetic macrovascular complications.

Free Research Field

代謝学

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Published: 2017-05-10  

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