INHIBITION OF HEPATIC LIPOGENESIS BY 2-TETRADECYLGLYCIDIC ACID

被引:33
作者
MCCUNE, SA
NOMURA, T
HARRIS, RA
机构
[1] Department of Biochemistry, Indiana University School of Medicine, Indianapolis, 46223, IN
关键词
D O I
10.1007/BF02534133
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
2-Tetradecylglycidic acid (TDGA), a hypoglycemic agent, has been found to be a very effective inhibitor of de novo fatty acid synthesis by isolated hepatocytes. A comparison was made between the effectiveness of TDGA and 5-(tetradecyloxy)-2-furoic acid (TOFA), a hypolipidemic agent, on the metabolic processes of isolated hepatocytes. These compounds are structurally related and both inhibit fatty acid synthesis; however, they have opposite effects from each other on the oxidation and esterification of fatty acids. TDGA inhibits whereas TOFA stimulates fatty acid oxidation. TDGA stimulates whereas TOFA inhibits fatty acid esterification. © 1979 American Oil Chemists' Society.
引用
收藏
页码:880 / 882
页数:3
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