Yoshinari Kouichi, Takagi Shunsuke, Yoshimasa Teruyasu, Sugatani Junko, Miwa Masao
Department of Pharmaco-Biochemistry, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka, 422-8526, Japan.
Pharm Res. 2006 Jun;23(6):1188-200. doi: 10.1007/s11095-006-0071-6. Epub 2006 May 25.
Changes in physiological, pathophysiological, and/or nutritional conditions often alter the expression of drug-metabolizing enzymes. In this study, we investigated obesity-induced changes in hepatic cytochrome P450 (P450) levels using nutritionally obese mice.
To induce obesity, mice were fed a high-fat diet or treated with gold thioglucose, which impairs ventromedial hypothalamus. Total RNAs and microsomal and nuclear proteins were prepared from the liver of these mice, and mRNA and protein levels of P450s and transcription factors were determined.
Among P450s examined, the constitutive expression of CYP3As was drastically reduced at both mRNA and protein levels by nutrition-induced obesity. One-week administration of a high-fat diet also reduced hepatic CYP3As. However, changes in nuclear receptors involved in the transcriptional regulation of CYP3A genes were not correlated with that of CYP3As. Obese mice induced by gold thioglucose exhibited a different expression profile of hepatic P450s with no significant change in CYP3As.
High-fat diet-induced changes in energy metabolism, which eventually result in obesity, modulate the hepatic expression profile of P450s, particularly CYP3As. Alternatively, the accumulation of a certain component in a high-fat diet may directly attenuate the CYP3A expression, suggesting a clinically important drug-diet interaction.
生理、病理生理和/或营养状况的改变常常会改变药物代谢酶的表达。在本研究中,我们使用营养性肥胖小鼠研究肥胖诱导的肝脏细胞色素P450(P450)水平的变化。
为诱导肥胖,给小鼠喂食高脂饮食或用硫代葡萄糖金处理,后者会损害腹内侧下丘脑。从这些小鼠的肝脏中制备总RNA、微粒体和核蛋白,并测定P450和转录因子的mRNA和蛋白水平。
在所检测的P450中,营养诱导的肥胖使CYP3A的组成型表达在mRNA和蛋白水平均显著降低。高脂饮食喂养一周也会降低肝脏CYP3A水平。然而,参与CYP3A基因转录调控的核受体的变化与CYP3A的变化不相关。硫代葡萄糖金诱导的肥胖小鼠表现出不同的肝脏P450表达谱,CYP3A无显著变化。
高脂饮食诱导的能量代谢变化最终导致肥胖,调节肝脏P450的表达谱,尤其是CYP3A。或者,高脂饮食中某种成分的积累可能直接减弱CYP3A的表达,提示临床上重要的药物-饮食相互作用。