THE EFFECTS OF PROBUCOL ON LIPOPROTEIN METABOLISM IN THE RAT

被引:8
作者
STAELS, B
VANTOL, A
JANSEN, H
AUWERX, J
机构
[1] CATHOLIC UNIV LEUVEN,EXPTL GENEESKUNDE & ENDOCRINOL LAB,B-3000 LOUVAIN,BELGIUM
[2] ERASMUS UNIV,FAC MED,DEPT BIOCHEM 1,3000 DR ROTTERDAM,NETHERLANDS
关键词
GENE EXPRESSION; HYPERLIPIDEMIA; ATHEROSCLEROSIS; APOLIPOPROTEIN; LDL-RECEPTOR; HYPOLIPIDEMIC DRUG; PROBUCOL;
D O I
10.1016/0005-2760(91)90241-9
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
The effects of probucol on liver and intestinal apolipoprotein, LDL-receptor and hepatic lipase gene expression, as well as plasma lipid and apolipoprotein levels and liver lipase activity were evaluated in male rats. Administration of probucol decreased plasma triacylglycerols, without affecting plasma cholesterol. Plasma apo E and apo B concentrations increased after probucol. Since liver and intestinal apo B and apo E mRNA levels remained unchanged, this increase could be attributed to a delayed clearance by the LDL-receptor, whose mRNA levels dropped by 50% in the liver. For the HDL-apolipoproteins, only liver apo A-IV mRNA levels decreased after probucol, which was reflected by a fall of plasma apo A-IV. Neither hepatic lipase activity nor mRNA levels were significantly influenced by probucol.
引用
收藏
页码:131 / 135
页数:5
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