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Molecular basis of ethnic differences in drug disposition and response.

机译:药物处置和反应中种族差异的分子基础。

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摘要

Ethnicity is an important demographic variable contributing to interindividual variability in drug metabolism and response. In this rapidly expanding research area many genetic factors that account for the effects of ethnicity on pharmacokinetics, pharmacodynamics, and drug safety have been identified. This review focuses on recent developments that have improved understanding of the molecular mechanisms responsible for such interethnic differences. Genetic variations that may provide a molecular basis for ethnic differences in drug metabolizing enzymes (CYP 2C9, 2C19, 2D6, and 3A4), drug transporter (P-glycoprotein), drug receptors (adrenoceptors), and other functionally important proteins (eNOS and G proteins) are discussed. A better understanding of the molecular basis underlying ethnic differences in drug metabolism, transport, and response will contribute to improved individualization of drug therapy.
机译:种族是一个重要的人口统计学变量,它导致药物代谢和反应的个体差异。在这个迅速扩展的研究领域中,已经确定了许多遗传因素,这些遗传因素说明了种族对药代动力学,药效学和药物安全性的影响。这篇综述的重点是最近的发展,这些发展已加深了对造成这种种族差异的分子机制的理解。遗传变异可能为药物代谢酶(CYP 2C9、2C19、2D6和3A4),药物转运蛋白(P-糖蛋白),药物受体(肾上腺素受体)和其他功能上重要的蛋白质(eNOS和G)的种族差异提供分子基础蛋白质)进行了讨论。更好地理解药物代谢,转运和反应中种族差异背后的分子基础,将有助于改善药物治疗的个体化。

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