INHIBITION OF HEPATIC CHOLESTEROL-BIOSYNTHESIS BY A 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A SYNTHASE INHIBITOR, 1233A, IN MICE

被引:11
作者
NAGASHIMA, H
KUMAGAI, H
TOMODA, H
OMURA, S
机构
[1] KITASATO INST,BIOL FUNCT RES CTR,MINATO KU,TOKYO 108,JAPAN
[2] KITASATO UNIV,SCH PHARMACEUT SCI,MINATO KU,TOKYO 108,JAPAN
关键词
D O I
10.1016/0024-3205(93)90060-G
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We have studied the in vivo inhibition of hepatic sterol biosynthesis by 1233A, a specific inhibitor of the enzyme 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase. Administration of the compound orally to mice resulted in a dose-dependent inhibition of [C-14]acetate incorporation into sterols in liver, but did not exert any significant effect on [C-14]mevalonate incorporation. The results indicate that the in vivo inhibition of sterol synthesis occurs only at pre-mevalonate enzymatic steps in the sterol biosynthetic pathway, thus being compatible with the presumed site of inhibition, HMG-CoA synthase. Moreover, owing to irreversible inactivation of the enzyme by 1233A, it was possible to detect in vivo effect on the enzyme by assays of its activity in cell-free extracts from livers; the drug-treatment also resulted in a similarly dose-dependent inhibition of HMG-CoA synthase activity. In contrast, acetoacetyl-CoA thiolase and HMG-CoA reductase, the enzymes also responsible for mevalonate synthesis in the pathway, did not show any significant change in activity. These results clearly demonstrate that the inhibition of hepatic sterol synthesis caused by 1233A is indeed due to selective inhibition of HMG-CoA synthase in the tissues.
引用
收藏
页码:1595 / 1600
页数:6
相关论文
共 16 条
[1]   DISCOVERY, BIOCHEMISTRY AND BIOLOGY OF LOVASTATIN [J].
ALBERTS, AW .
AMERICAN JOURNAL OF CARDIOLOGY, 1988, 62 (15) :J10-J15
[2]  
CLINKENBEARD KD, 1975, J BIOL CHEM, V250, P3124
[3]  
CLINKENBEARD KD, 1975, J BIOL CHEM, V250, P3108
[4]  
CLINKENBEARD KD, 1973, J BIOL CHEM, V248, P2275
[6]   INHIBITION OF CHOLESTEROL-SYNTHESIS INVITRO AND INVIVO BY ML-236A AND ML-236B, COMPETITIVE INHIBITORS OF 3-HYDROXY-3-METHYLGLUTARYL-COENZYME-A REDUCTASE [J].
ENDO, A ;
TSUJITA, Y ;
KURODA, M ;
TANZAWA, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1977, 77 (01) :31-36
[7]  
GOLDSTEIN JL, 1983, METHOD ENZYMOL, V98, P241
[8]   INHIBITION OF HYDROXYMETHYLGLUTARYL-COENZYME-A SYNTHASE BY L-659,699 [J].
GREENSPAN, MD ;
YUDKOVITZ, JB ;
LO, CYL ;
CHEN, JS ;
ALBERTS, AW ;
HUNT, VM ;
CHANG, MN ;
YANG, SS ;
THOMPSON, KL ;
CHIANG, YCP ;
CHABALA, JC ;
MONAGHAN, RL ;
SCHWARTZ, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7488-7492
[9]   TISSUE-SELECTIVE INHIBITION OF CHOLESTEROL-SYNTHESIS INVIVO BY PRAVASTATIN SODIUM, A 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A REDUCTASE INHIBITOR [J].
KOGA, T ;
SHIMADA, Y ;
KURODA, M ;
TSUJITA, Y ;
HASEGAWA, K ;
YAMAZAKI, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1045 (02) :115-120
[10]   ANTIBIOTICS FROM BASIDIOMYCETES .37. NEW INHIBITORS OF CHOLESTEROL-BIOSYNTHESIS FROM CULTURES OF XERULA-MELANOTRICHA DORFELT [J].
KUHNT, D ;
ANKE, T ;
BESL, H ;
BROSS, M ;
HERRMANN, R ;
MOCEK, U ;
STEFFAN, B ;
STEGLICH, W .
JOURNAL OF ANTIBIOTICS, 1990, 43 (11) :1413-1420