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Compartment-Specific Gene Regulation of the CAR Inducer Efavirenz In Vivo

机译:在CaR诱导剂依法韦仑体内的车厢特定基因调控

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摘要

Nuclear receptors such as the constitutive androstane receptor (CAR) are central factors that link drug exposure to the activities of drug metabolism and elimination. In order to determine the in vivo effects of efavirenz, a CAR activator, the expression of target genes was determined in duodenal biopsies obtained from 12 healthy volunteers before treatment and after 10 days of treatment with efavirenz; concomitant administration of the cholesterol inhibitor ezetimibe produced no significant difference. However, in in vitro studies, efavirenz significantly increased CYP2B6 expression in several cell types, suggesting that the drug transactivates CAR. This hypothesis is supported by our findings that there is significant induction of CAR target genes in in vivo peripheral blood mononuclear cells (PBMCs) isolated from healthy volunteers treated with multiple doses of efavirenz. The impact of efavirenz on hepatic metabolism in vivo was confirmed by significant changes in plasma 4β-hydroxycholesterol and bilirubin levels and the area under the curve (AUC) of efavirenz. induction of CYP2B6 mRNA expression correlated with the decrease in the AUC of efavirenz (r = 0.61; P = 0.036). Taken together, our results provide evidence that efavirenz exerts compartment-specific inductive capacity in vivo.
机译:核受体如本构androstane受体(汽车)是将药物暴露于药物代谢和消除活动的中央因素。为了确定eFaviraenz的体内效果,一种轿车活化剂,在治疗前的12个健康志愿者中获得的十二指肠活组织检查中测定靶基因的表达,并在efaviraenz治疗10天后;伴随胆固醇抑制剂ezetimibe没有产生显着差异。然而,在体外研究中,EFavirazenz在几种细胞类型中显着增加了CYP2B6表达,这表明药物反式激活汽车。我们的发现支持了我们的发现,即在用多剂量efaviraend治疗的健康志愿者中分离的体内外周血单核细胞(PBMC)中存在显着诱导轿车靶基因。通过血浆4β-羟基胆固醇和胆红素水平的显着变化和培养物(AUC)曲线(AUC)的显着变化,确认了efaviraenz对体内肝脏代谢的影响。 CYP2B6 mRNA表达的诱导与EFAVIRENZ AUC的减少相关(r = 0.61; p = 0.036)。在一起,我们的结果提供了证据表明Efavirenz在体内施加了特定的隔间归纳能力。

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