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Serotonergic gene variation in substance use pharmacotherapy: a systematic review

机译:物质使用药物疗法的血清onoReric基因变异:系统审查

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摘要

Drug addiction is a serious disease with damaging effects on the brain and physical health. Despite the increase in the number of affected individuals, there are few effective pharmacological treatment options for substance use disorders. The study of the influence of an individual's genetic features on the treatment response may help to identify more efficacious treatment options. This systematic review focuses on the serotonergic system because of its relevant role in mood and impulse control disorders, and its contribution to the development and maintenance of drug use disorders. In particular, we examine the role of serotonergic genes in the response to pharmacotherapy for alcohol, cocaine and nicotine addiction. Current evidence suggests that genetic variability of the serotonergic biosynthesis enzyme tryptophan hydroxylase 2 (TPH2) and the serotonin transporter (SLC6A4) genes mediates the efficacy of several addiction treatments, such as ondansetron and disulfiram, and the antidepressants bupropion, nortriptyline and sertraline.
机译:吸毒成瘾是一种严重的疾病,对大脑和身体健康有害影响。尽管受影响的个体的数量增加,但物质使用障碍有很少有效的药理学治疗方案。对个体遗传特征对治疗反应的影响的研究可能有助于鉴定更有效的治疗方案。这种系统评论主要集中在Serotonergic系统上,因为其在情绪和冲动控制障碍中的相关作用,以及对药物使用障碍的开发和维护的贡献。特别是,我们研究了血清onOronergic基因在对酒精,可卡因和尼古丁成瘾的药物疗法的反应中的作用。目前的证据表明,Serotonergic生物合成酶色氨酸羟化酶2(TPH2)和血清素转运蛋白(SLC6A4)基因的遗传可变性介导几种成瘾治疗的功效,例如ondansetron和Divulfiram,以及抗抑郁症Bulapion,Nortriptyline和塞拉甲醛。

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