Wang Pei, Shao Xueyan, Bao Yifan, Zhu Junjie, Chen Liming, Zhang Lirong, Ma Xiaochao, Zhong Xiao-Bo
Department of Pharmacology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Department of Pharmaceutical Sciences, School of Pharmacy, University of Connecticut, Storrs, CT 06269, USA.
Acta Pharm Sin B. 2020 Jan;10(1):171-185. doi: 10.1016/j.apsb.2019.10.009. Epub 2019 Nov 28.
The prevalence of obesity-associated conditions raises new challenges in clinical medication. Although altered expression of drug-metabolizing enzymes (DMEs) has been shown in obesity, the impacts of obese levels (overweight, obesity, and severe obesity) on the expression of DMEs have not been elucidated. Especially, limited information is available on whether parental obese levels affect ontogenic expression of DMEs in children. Here, a high-fat diet (HFD) and three feeding durations were used to mimic different obese levels in C57BL/6 mice. The hepatic expression of five nuclear receptors (NRs) and nine DMEs was examined. In general, a trend of induced expression of NRs and DMEs (except for and ) was observed in HFD groups compared to low-fat diet (LFD) groups. Differential effects of HFD on the hepatic expression of DMEs were found in adult mice at different obese levels. Family-based dietary style of an HFD altered the ontogenic expression of DMEs in the offspring older than 15 days. Furthermore, obese levels of parental mice affected the hepatic expression of DMEs in offspring. Overall, the results indicate that obese levels affected expression of the DMEs in adult individuals and that of their children. Drug dosage might need to be optimized based on the obese levels.
肥胖相关疾病的流行给临床用药带来了新的挑战。尽管已有研究表明肥胖状态下药物代谢酶(DMEs)的表达会发生改变,但肥胖程度(超重、肥胖和重度肥胖)对DMEs表达的影响尚未阐明。特别是,关于亲代肥胖程度是否会影响儿童DMEs的个体发育表达的信息有限。在此,采用高脂饮食(HFD)和三种喂养时长来模拟C57BL/6小鼠的不同肥胖程度。检测了五种核受体(NRs)和九种DMEs的肝脏表达。总体而言,与低脂饮食(LFD)组相比,HFD组中观察到NRs和DMEs(除了 和 )表达上调的趋势。在不同肥胖程度的成年小鼠中发现了HFD对DMEs肝脏表达的不同影响。基于家庭的HFD饮食方式改变了15日龄以上子代中DMEs的个体发育表达。此外,亲代小鼠的肥胖程度影响子代中DMEs的肝脏表达。总体而言,结果表明肥胖程度会影响成年个体及其子代中DMEs的表达。可能需要根据肥胖程度优化药物剂量。