Suppr超能文献

[遗传学、疼痛与镇痛]

[Genetics, pain and analgesia].

作者信息

Stamer U, Bayerer B, Stüber F

机构信息

Klinik und Poliklinik für Anästhesiologie und Operative Intensivmedizin, Rheinische Friedrich-Wilhelms-Universität, Sigmund-Freud-Str. 25, 53105, Bonn.

出版信息

Anaesthesist. 2006 Jul;55(7):746-52. doi: 10.1007/s00101-006-1017-4.

Abstract

Genomic variations influencing nociceptive sensitivity and susceptibility to pain conditions, as well as responses to pharmacotherapy of pain are currently under investigation. Candidate genes involved in pain perception, pain processing and pain management such as (opioid) receptors, transporters and other targets of pharmacotherapy are discussed. Drug metabolizing 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 P 450 enzymes influence analgesic efficacy of codeine, tramadol and tricyclic antidepressants (CYP2D6). Blood levels of some non-steroidal anti-inflammatory drugs (NSAIDs) are dependent on CYP2C9 activity, whereas opioid receptor polymorphisms are discussed with respect to differences in opioid-mediated analgesia and side-effects. Pharmacogenetics is seen as a potential diagnostic tool for improving patient therapy and care and will contribute to a more individualized drug treatment in the future.

摘要

目前正在研究影响伤害性感受敏感性、疼痛病症易感性以及疼痛药物治疗反应的基因组变异。文中讨论了参与疼痛感知、疼痛处理及疼痛管理的候选基因,如(阿片类)受体、转运体以及其他药物治疗靶点。药物代谢酶是当前研究的另一个主要靶点,旨在确定个体基因谱与药物反应(药物遗传学)之间的关联。细胞色素P450酶的多态性会影响可待因、曲马多和三环类抗抑郁药(CYP2D6)的镇痛效果。一些非甾体抗炎药(NSAIDs)的血药浓度取决于CYP2C9活性,而阿片受体多态性则与阿片介导的镇痛作用及副作用差异有关。药物遗传学被视为改善患者治疗和护理的潜在诊断工具,未来将有助于实现更个体化的药物治疗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验