Defective expression of cytochrome P450 proteins in the liver of the genetically obese Zucker rat

Amaia Irizar , Christopher R. Barnett , Peter R. Flatt , Costas Ioannides
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引用次数: 44

Abstract

The hepatic expression of xenobiotic-metabolising cytochrome P450 isoforms in the genetically obese Zucker rat, a model of obesity, was compared to that of its lean littermate. Cytochrome P450 (CYP) levels were determined using diagnostic substrates and/or immunologically in Western blot analyses. When compared with the lean Zucker rat, the obese animal exhibited hyperglycaemia, hypercholesterolaemia, marked hyperinsulinaemia and hypertriglyceridaemia but was normoketonaemic. CYP3A and CYP1A2 levels were higher in the obese Zucker rat when compared with the lean littermate but, in contrast, a protein recognised by human CYP2D6 and, to a lesser extent, CYP2C11 levels were lower. Pretreatment with acetone, dexamethasone and clofibrate resulted in enhanced p-nitrophenol hydroxylase (CYP2E), erythromycin N-demethylase (CYP3A) and lauric acid hydroxylase (CYP4A) activities respectively in the liver of the lean Zucker rat but, in contrast, the obese Zucker rat was refractive to such treatment; similarly, hepatic apoprotein levels of the CYP2E and CYP4A subfamilies were increased markedly only in the lean Zucker rat. It is concluded that CYP2E, CYP3A and CYP4A subfamilies are poorly expressed in the obese Zucker rat, and this rat strain may serve as a good model for elucidating the molecular mechanisms of induction of these cytochrome P450 proteins.

遗传性肥胖Zucker大鼠肝脏细胞色素P450蛋白表达缺陷
在遗传肥胖的Zucker大鼠(肥胖模型)中,异种代谢细胞色素P450亚型的肝脏表达与它的瘦同伴进行了比较。细胞色素P450 (CYP)水平检测采用诊断底物和/或免疫Western blot分析。与瘦Zucker大鼠相比,肥胖大鼠表现出高血糖、高胆固醇血症、明显的高胰岛素血症和高甘油三酯血症,但正常酮血症。肥胖的Zucker大鼠的CYP3A和CYP1A2水平高于瘦弱的同伴,但相比之下,人类CYP2D6和CYP2C11识别的蛋白质水平较低,在较小程度上。丙酮、地塞米松和氯贝特预处理分别增强了瘦型Zucker大鼠肝脏中对硝基酚羟化酶(CYP2E)、红霉素n -去甲基化酶(CYP3A)和月桂酸羟化酶(CYP4A)的活性,而肥胖型Zucker大鼠对丙酮、地塞米松和氯贝特预处理的肝脏中对硝基酚羟化酶(CYP2E)、红霉素n -去甲基化酶(CYP3A)活性;同样,CYP2E和CYP4A亚家族的肝载脂蛋白水平仅在瘦Zucker大鼠中显著升高。综上所述,CYP2E、CYP3A和CYP4A亚家族在肥胖Zucker大鼠中表达较低,该大鼠品系可能为阐明这些细胞色素P450蛋白诱导的分子机制提供了良好的模型。
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