Department of Pharmacology, School of Medicine, Emory University, Atlanta, Georgia (E.T.M., S.M.M.); Department of Pathology, University of Utah, Salt Lake City, Utah (T.J.L.); Department of Pharmacy Practice and Department of Biopharmaceutical Sciences, College of Pharmacy, University of Illinois, Chicago, Illinois (H.J., J.L.D.); Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington (J.L.D., J.Y.C.); and Department of Biomedical and Pharmaceutical Sciences, University of Rhode Island, Kingston, Rhode Island (A.L.S., S.K.)
Department of Pharmacology, School of Medicine, Emory University, Atlanta, Georgia (E.T.M., S.M.M.); Department of Pathology, University of Utah, Salt Lake City, Utah (T.J.L.); Department of Pharmacy Practice and Department of Biopharmaceutical Sciences, College of Pharmacy, University of Illinois, Chicago, Illinois (H.J., J.L.D.); Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington (J.L.D., J.Y.C.); and Department of Biomedical and Pharmaceutical Sciences, University of Rhode Island, Kingston, Rhode Island (A.L.S., S.K.).
Drug Metab Dispos. 2018 May;46(5):503-513. doi: 10.1124/dmd.117.079905. Epub 2018 Mar 7.
This article is a report on a symposium entitled "Physiological Regulation of Drug Metabolism and Transport" sponsored by the American Society for Pharmacology and Experimental Therapeutics and held at the Experimental Biology 2017 meeting in Chicago, IL. The contributions of physiologic and pathophysiological regulation of drug-metabolizing enzymes and transporters to interindividual variability in drug metabolism are increasingly recognized but in many cases are not well understood. The presentations herein discuss the phenomenology, consequences, and mechanism of such regulation. CYP2D6 transgenic mice were used to provide insights into the mechanism of regulation of this enzyme in pregnancy, via hepatocyte nuclear factor 4, small heterodimer partner, and retinoids. Regulation of intestinal and hepatic drug-processing enzymes by the intestinal microbiota via tryptophan and its metabolites was investigated. The potential impact of parasitic infections on human drug metabolism and clearance was assessed in mice infected with or AS, both of which produced widespread and profound effects on murine hepatic drug-metabolizing enzymes. Finally, the induction of Abcc drug efflux transporters by fasting was investigated. This was demonstrated to occur via a cAMP, protein kinase A/nuclear factor-E2-related factor 2/Sirtuin 1 pathway via antioxidant response elements on the Abcc genes.
这是一篇关于题为“药物代谢和转运的生理调节”研讨会的报告,该研讨会由美国药理学和实验治疗学会主办,并在伊利诺伊州芝加哥举行的 2017 年实验生物学会议上举行。生理和病理生理学调节药物代谢酶和转运体对药物代谢个体间差异的贡献越来越受到认可,但在许多情况下,这种调节的机制尚不清楚。本文中的介绍讨论了这种调节的现象学、后果和机制。CYP2D6 转基因小鼠被用于通过肝细胞核因子 4、小异二聚体伴侣和视黄酸提供对妊娠期间该酶调节的机制的深入了解。通过色氨酸及其代谢物研究了肠道微生物群对肠道和肝脏药物处理酶的调节作用。评估了寄生虫感染对人类药物代谢和清除的潜在影响,在感染 或 的小鼠中进行了评估,这两种寄生虫均对小鼠肝脏药物代谢酶产生广泛而深远的影响。最后,研究了禁食诱导 Abcc 药物外排转运体的作用。这被证明是通过 Abcc 基因上的抗氧化反应元件通过 cAMP、蛋白激酶 A/核因子-E2 相关因子 2/Sirtuin 1 途径发生的。