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注意缺陷多动障碍:当前及未来的治疗方法

ADHD: current and future therapeutics.

作者信息

Heal David J, Smith Sharon L, Findling Robert L

机构信息

RenaSci Consultancy Ltd, BioCity, Nottingham, NG1 1GF, UK,

出版信息

Curr Top Behav Neurosci. 2012;9:361-90. doi: 10.1007/7854_2011_125.

Abstract

The stimulants, amphetamine and methylphenidate, have long been the mainstay of attention-deficit hyperactivity disorder (ADHD) therapy. They are rapidly effective and are generally the first medications selected by physicians. In the development of alternative pharmacological approaches, drug candidates have been evaluated with a wide diversity of mechanisms. All of these developments have contributed real progress in the field, but there is still much room for improvement and unmet clinical need in ADHD pharmacotherapy. The availability of a wide range of compounds with a high degree of specificity for individual monoamines (dopamine and noradrenaline) and/or different pharmacological mechanisms has refined our understanding of the essential elements for optimum pharmacological effect in managing ADHD. In this chapter, we review the pharmacology of the different classes of drug used to treat ADHD and provide a neurochemical rationale, predominantly from the use of in vivo microdialysis experiments, to explain their relative efficacy and potential to elicit side effects. In addition, we will consider how predictions based on results from animal models translate into clinical outcomes. The treatment of ADHD is also described from the perspective of the physician. Finally, the new research development for drugs to treat ADHD is discussed.

摘要

兴奋剂,如苯丙胺和哌甲酯,长期以来一直是治疗注意力缺陷多动障碍(ADHD)的主要药物。它们起效迅速,通常是医生首选的药物。在替代药物治疗方法的研发过程中,候选药物经过了多种作用机制的评估。所有这些进展都为该领域带来了实际的进步,但ADHD药物治疗仍有很大的改进空间和未满足的临床需求。一系列对单胺类物质(多巴胺和去甲肾上腺素)具有高度特异性和/或不同药理机制的化合物的出现,深化了我们对ADHD最佳药理效应关键要素的理解。在本章中,我们回顾了用于治疗ADHD的不同类别药物的药理学,并主要基于体内微透析实验的结果,提供一个神经化学原理,以解释它们的相对疗效和引发副作用的可能性。此外,我们将探讨基于动物模型结果的预测如何转化为临床疗效。本文还从医生的角度描述了ADHD的治疗。最后,讨论了治疗ADHD药物的新研究进展。

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