• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1016/0021-9150(91)90186-7
PMID:1811554
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。

相似文献

1
Effects of gemfibrozil and ketoconazole on human apolipoprotein AI, B and E levels in two hepatoma cell lines, HepG2 and Hep3B.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。
Atherosclerosis. 1991 Nov;91(1-2):51-61. doi: 10.1016/0021-9150(91)90186-7.
2
Regulation of apolipoprotein A-I gene expression by phenobarbital in the human hepatocarcinoma cell line, Hep3B.苯巴比妥对人肝癌细胞系Hep3B中载脂蛋白A-I基因表达的调控
Atherosclerosis. 1994 Feb;105(2):235-43. doi: 10.1016/0021-9150(94)90054-x.
3
Cell culture conditions determine apolipoprotein CIII secretion and regulation by fibrates in human hepatoma HepG2 cells.细胞培养条件决定人肝癌HepG2细胞中载脂蛋白CIII的分泌及贝特类药物对其的调控。
Cell Physiol Biochem. 1999;9(3):139-49. doi: 10.1159/000016311.
4
Protein-DNA interactions at a drug-responsive element of the human apolipoprotein A-I gene.人类载脂蛋白A-I基因药物反应元件处的蛋白质-DNA相互作用。
J Biol Chem. 1996 Oct 25;271(43):27152-60.
5
Fibrates influence the expression of genes involved in lipoprotein metabolism in a tissue-selective manner in the rat.在大鼠中,贝特类药物以组织选择性方式影响参与脂蛋白代谢的基因的表达。
Arterioscler Thromb. 1992 Mar;12(3):286-94. doi: 10.1161/01.atv.12.3.286.
6
Apolipoprotein gene expression in analbuminemic rats and in rats with Heymann nephritis.无白蛋白血症大鼠和海曼肾炎大鼠载脂蛋白基因的表达
Am J Physiol. 1992 May;262(5 Pt 2):F755-61. doi: 10.1152/ajprenal.1992.262.5.F755.
7
No effect of fibrates on synthesis of apolipoprotein(a) in primary cultures of cynomolgus monkey and human hepatocytes: apolipoprotein A-I synthesis increased.贝特类药物对食蟹猴和人原代肝细胞载脂蛋白(a)合成无影响:载脂蛋白A-I合成增加。
Biochem Biophys Res Commun. 1998 Mar 17;244(2):374-8. doi: 10.1006/bbrc.1998.8279.
8
Apolipoprotein synthesis and secretion in Hep G2 cells: effects of monensin and cycloheximide.载脂蛋白在Hep G2细胞中的合成与分泌:莫能菌素和环己酰亚胺的作用。
Biochem Cell Biol. 1992 Dec;70(12):1339-46. doi: 10.1139/o92-182.
9
Effect of gemfibrozil on apolipoprotein B secretion and diacylglycerol acyltransferase activity in human hepatoblastoma (HepG2) cells.
Atherosclerosis. 2002 Oct;164(2):221-8. doi: 10.1016/s0021-9150(02)00060-6.
10
Butyrate stimulates the secretion of apolipoprotein B-100-containing lipoproteins from HepG2 cells by inhibiting the intracellular degradation.丁酸盐通过抑制细胞内降解来刺激HepG2细胞分泌含载脂蛋白B-100的脂蛋白。
Biochim Biophys Acta. 1994 Aug 4;1213(3):349-56. doi: 10.1016/0005-2760(94)00064-6.

引用本文的文献

1
Cytochrome P450 and gene activation--from pharmacology to cholesterol elimination and regression of atherosclerosis.细胞色素P450与基因激活——从药理学到胆固醇清除及动脉粥样硬化消退
Eur J Clin Pharmacol. 2008 Sep;64(9):841-50. doi: 10.1007/s00228-008-0515-5. Epub 2008 Jul 17.
2
Gemfibrozil. A reappraisal of its pharmacological properties and place in the management of dyslipidaemia.吉非贝齐。对其药理特性及在血脂异常管理中的地位的重新评估。
Drugs. 1996 Jun;51(6):982-1018. doi: 10.2165/00003495-199651060-00009.
3
Triglycerides and disease.
甘油三酯与疾病。
Postgrad Med J. 1993 Sep;69(815):679-95. doi: 10.1136/pgmj.69.815.679.