2014 Fiscal Year Final Research Report
Role for periarterial adipose tissue in atherosclerosis in obesity
Project/Area Number |
24591057
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Circulatory organs internal medicine
|
Research Institution | Kagawa University |
Principal Investigator |
OHMORI Koji 香川大学, 医学部, 准教授 (00263913)
|
Co-Investigator(Kenkyū-buntansha) |
HASAN Arif Ul 香川大学, 医学部, 研究員 (00570368)
KOHNO Masakazu 香川大学, 医学部, 教授 (20153489)
NOMA Takahisa 香川大学, 医学部附属病院, 講師 (20363202)
IMACHI Hitomi 香川大学, 医学部, 准教授 (80380187)
ISHIHARA Yasuhiro 香川大学, 医学部附属病院, 助教 (80532689)
HORII Taiko 香川大学, 医学部, 教授 (90423425)
YAMASHITA Yoichi 香川大学, 医学部, 准教授 (80363208)
|
Project Period (FY) |
2012-04-01 – 2015-03-31
|
Keywords | 動脈硬化 / 肥満 / 脂肪細胞 / 血管内皮成長因子 / アディポサイトカイン / vasa sasorum / 細胞培養 / レポーターアッセイ |
Outline of Final Research Achievements |
It is hypothesized that periarterial adipose tissue releases vascular endothelial growth factor (VEGF) and proinflammatory cytokines into vascular wall from adventitial side to grow the atherosclerotic plaques. In this study employing mature adipocytes, block of constitutive activity of angiotensin II type-1 receptor by valsartan decreased production of interleukin-6 and increased that of adiponectin. However, another putative anti-atherosclerotic fatty acid, eicosapentaenoic acid promoted the production of VEGF through an integrated mechanism including G-protein coupled receptor 120 and peroxisome-proliferator activated receptor-gamma. These findings provide for the comprehensive understanding of the "out-side-in" mechanisms for atherosclerosis.
|
Free Research Field |
循環器内科学
|