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Development of Human Membrane Transporters: Drug Disposition and Pharmacogenetics

机译:人膜​​转运蛋白的发展:药物处置和药物遗传学。

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摘要

Membrane transporters play an essential role in the transport of endogenous and exogenous compounds, and consequently they mediate the uptake, distribution, and excretion of many drugs. The clinical relevance of transporters in drug disposition and their effect in adults have been shown in drug-drug interaction and pharmacogenomic studies. Little is known, however, about the ontogeny of human membrane transporters and their roles in pediatric pharmacotherapy. As they are involved in the transport of endogenous substrates, growth and development may be important determinants of their expression and activity. This review presents an overview of our current knowledge on human membrane transporters in pediatric drug disposition and effect. Existing pharmacokinetic and pharmacogenetic data on membrane substrate drugs frequently used in children are presented and related, where possible, to existing ex vivo data, providing a basis for developmental patterns for individual human membrane transporters. As data for individual transporters are currently still scarce, there is a striking information gap regarding the role of human membrane transporters in drug therapy in children.
机译:膜转运蛋白在转运内源性和外源性化合物中起着至关重要的作用,因此它们介导了许多药物的吸收,分布和排泄。药物相互作用和药物基因组学研究表明转运蛋白在药物中的临床相关性及其在成人中的作用。然而,关于人膜转运蛋白的个体发育及其在儿科药物治疗中的作用知之甚少。由于它们参与内源性底物的运输,因此生长和发育可能是其表达和活性的重要决定因素。这篇综述介绍了我们目前在儿科药物处置和效果方面对人类膜转运蛋白的认识。介绍了有关儿童中常用的膜底物药物的现有药代动力学和药物遗传学数据,并在可能的情况下与现有的离体数据相关,为单个人膜转运蛋白的发育模式提供了基础。由于目前仍缺乏单个转运蛋白的数据,因此关于人膜转运蛋白在儿童药物治疗中的作用存在巨大的信息空白。

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