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The pharmacogenetics of analgesia

机译:镇痛药的药理学

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摘要

Genomic variations influencing response to pharmacotherapy of pain are under investigation. Candidate genes such as (opioid)-receptors, transporters and other molecules important for pharmacotherapy are discussed. Drug metabolising enzymes represent a further major target of ongoing research in order to identify associations between an individual's genetic profile and drug response (pharmacogenetics). Polymorphisms of the cytochrome P450 enzymes influence analgesic efficacy of codeine, tramadol and tricyclic antidepressants (CYP2D6). Blood levels of some NSAIDs are dependent on CYP2C9 activity, whereas opioid-receptor polymorphisms are discussed for differences in opioid mediated analgesia and side effects. Pharmacogenetics as a diagnostic tool has the potential to improve patient therapy and care, and it is hoped that pharmacogenetics will individualise drug treatment to a greater extent in the near future. Copyright 2007 Informa UK Ltd.
机译:影响疼痛药物治疗反应的基因组变异正在研究中。讨论了候选基因,如(阿片类)受体,转运蛋白和其他对药物治疗重要的分子。药物代谢酶是正在进行的研究的另一个主要目标,目的是鉴定个体的遗传特征与药物反应(药物遗传学)之间的关联。细胞色素P450酶的多态性影响可待因,曲马多和三环类抗抑郁药(CYP2D6)的镇痛效果。某些NSAID的血药浓度取决于CYP2C9活性,而阿片受体多态性因阿片介导的镇痛作用和副作用的差异而被讨论。药物遗传学作为诊断工具具有改善患者治疗和护理的潜力,希望药物遗传学将在不久的将来更大程度地个性化药物治疗。版权所有2007 Informa UK Ltd.

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