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吉非贝齐和酮康唑对两种肝癌细胞系HepG2和Hep3B中人载脂蛋白AI、B和E水平的影响。

Effects of gemfibrozil and ketoconazole on human apolipoprotein AI, B and E levels in two hepatoma cell lines, HepG2 and Hep3B.

作者信息

Tam S P

机构信息

Department of Biochemistry, Queen's University, Kingston, Ontario, Canada.

出版信息

Atherosclerosis. 1991 Nov;91(1-2):51-61. doi: 10.1016/0021-9150(91)90186-7.

Abstract

Exposure of HepG2 and Hep3B cells to gemfibrozil (40 micrograms/ml), a hypolipidemic drug, resulted in a 2-fold induction of apo AI mRNA and, a one-third reduction in apo B mRNA but had no significant effect on apo E mRNA levels. The hypothesis that the mechanism of action of gemfibrozil involved the cytochrome P-450 system was tested by using ketoconazole, a P-450 inhibitor, which blocks the formation of endogenous polar sterols. When the cells were treated with ketoconazole at a concentration of greater than or equal to 15 microM, the levels of apo AI, and apo B mRNAs decreased by 50% and 35%, respectively, compared to the basal level. No significant effect on apo E mRNA level was observed during ketoconazole treatment. The effects of gemfibrozil and ketoconazole on various apolipoprotein secretion were studied using pulse-chase experiments. It was observed that the selective alterations in the rates of apo AI and apo B production were occurring at the level of synthesis. This observation is consistent with the findings indicating a strong direct correlation between hepatic apolipoprotein mRNA concentration and secreted apolipoprotein levels. The induction of apo AI mRNA by gemfibrozil was not apparent when the cells were simultaneously treated with ketoconazole. However, the level of apo B mRNA was reduced further to less than 55% of the control level suggesting that there might be an additive effect of these two drugs on apo B synthesis.

摘要

将HepG2和Hep3B细胞暴露于降血脂药物吉非贝齐(40微克/毫升)中,可使载脂蛋白AI mRNA诱导增加2倍,载脂蛋白B mRNA减少三分之一,但对载脂蛋白E mRNA水平无显著影响。通过使用酮康唑(一种P-450抑制剂,可阻断内源性极性固醇的形成)来检验吉非贝齐作用机制涉及细胞色素P-450系统这一假说。当细胞用浓度大于或等于15微摩尔的酮康唑处理时,与基础水平相比,载脂蛋白AI和载脂蛋白B mRNA水平分别下降了50%和35%。在酮康唑处理期间,未观察到对载脂蛋白E mRNA水平有显著影响。使用脉冲追踪实验研究了吉非贝齐和酮康唑对各种载脂蛋白分泌的影响。观察到载脂蛋白AI和载脂蛋白B产生速率的选择性改变发生在合成水平。这一观察结果与表明肝脏载脂蛋白mRNA浓度与分泌的载脂蛋白水平之间存在强直接相关性的研究结果一致。当细胞同时用酮康唑处理时,吉非贝齐对载脂蛋白AI mRNA的诱导作用不明显。然而,载脂蛋白B mRNA水平进一步降至对照水平的55%以下,这表明这两种药物对载脂蛋白B合成可能有相加作用。

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