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Study on the antiatherogenic factor in vivo : Inhibitory mechanism of ACAT by heparinoid

Research Project

Project/Area Number 08671168
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field 内分泌・代謝学
Research InstitutionKyushu University

Principal Investigator

YOSHINARI Mototaka  Kyushu University, Faculty of Medicine, Lecturer, 医学部, 講師 (00191627)

Project Period (FY) 1996 – 1997
Project Status Completed (Fiscal Year 1997)
Budget Amount *help
¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 1997: ¥400,000 (Direct Cost: ¥400,000)
Fiscal Year 1996: ¥900,000 (Direct Cost: ¥900,000)
KeywordsACAT / macrophaqe / atherosclerosis / heparin / prostacyclin / diabetes mellitus / LDL / アセチルLPL
Research Abstract

As an antiatherogenic factor, heparinoid is thought to have a very important role in vivo, since AcylCoA acetyl transferase (ACAT) inmacrophages is inhibited by heparin. ACAT activity in diabetic macrophages was not inhibited by heparin. The 6keto-PGF1a, which is a stable metabolite of PGI2, was reduced in diabetic rats, macrophages. PGI2 attenuated heparin to inhibit ACAT through the activation of cholesteryl ester hydlase. Thromboxane A2 synthase inhibitor, ozagrel Na, inhibited the reesterification of cholesterol in diabetic rats. The inhibition of cyclooxiganase with acetylsalicylate decreased cholesterol reesterification in non-diabetic macrophages, but increased that in diabetic ones. On the other hand, the inhibitory effect of heparin for ACAT was enhanced by acetylsalicylate in rats with and without diabetes. Therefore, heparin is thought to have a direct inhibitory effect on ACAT,independent to prostaglandines. Oxidized LDL which is known to inhibit the synthesis of heparinoid induced the accumulation of cholesteryl ester in macrophages, which was inhibited by heparin. The synthesis of heparin seemed to be stimulated with prostacyclin. Therefore, heparinoid is thought to have an important role in the regulation of ACAT,and participates in the accumulation of cholesterol metabolism in macrophages.

Report

(3 results)
  • 1997 Annual Research Report   Final Research Report Summary
  • 1996 Annual Research Report

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Published: 1996-04-01   Modified: 2016-04-21  

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