George Blessy, You Dahea, Joy Melanie S, Aleksunes Lauren M
Department of Pharmacology and Toxicology, Rutgers University Ernest Mario School of Pharmacy, 170 Frelinghuysen Road, Piscataway, NJ 08854, USA.
Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado, Aurora, CO 80045, USA; Division of Renal Diseases and Hypertension, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Adv Drug Deliv Rev. 2017 Jul 1;116:73-91. doi: 10.1016/j.addr.2017.01.005. Epub 2017 Jan 20.
Renal proximal tubules are targets for toxicity due in part to the expression of transporters that mediate the secretion and reabsorption of xenobiotics. Alterations in transporter expression and/or function can enhance the accumulation of toxicants and sensitize the kidneys to injury. This can be observed when xenobiotic uptake by carrier proteins is increased or efflux of toxicants and their metabolites is reduced. Nephrotoxic chemicals include environmental contaminants (halogenated hydrocarbon solvents, the herbicide paraquat, the fungal toxin ochratoxin, and heavy metals) as well as pharmaceuticals (certain beta-lactam antibiotics, antiviral drugs, and chemotherapeutic drugs). This review explores the mechanisms by which transporters mediate the entry and exit of toxicants from renal tubule cells and influence the degree of kidney injury. Delineating how transport proteins regulate the renal accumulation of toxicants is critical for understanding the likelihood of nephrotoxicity resulting from competition for excretion or genetic polymorphisms that affect transporter function.
肾近端小管是毒性作用的靶器官,部分原因是介导外源性物质分泌和重吸收的转运蛋白的表达。转运蛋白表达和/或功能的改变可增强毒物的蓄积,并使肾脏对损伤敏感。当载体蛋白对外源性物质的摄取增加或毒物及其代谢产物的外排减少时,就会出现这种情况。肾毒性化学物质包括环境污染物(卤代烃溶剂、除草剂百草枯、真菌毒素赭曲霉毒素和重金属)以及药物(某些β-内酰胺抗生素、抗病毒药物和化疗药物)。本综述探讨了转运蛋白介导毒物进出肾小管细胞并影响肾损伤程度的机制。阐明转运蛋白如何调节毒物在肾脏中的蓄积,对于理解因排泄竞争或影响转运蛋白功能的基因多态性导致肾毒性的可能性至关重要。