[Stimulant and non-stimulant medication in current and future therapy for ADHD].

Fortschritte der Neurologie · Psychiatrie Pub Date : 2012-03-01 Epub Date: 2011-05-24 DOI:10.1055/s-0031-1273223
A G Franke, A Konrad, K Lieb, M Huss
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引用次数: 3

Abstract

! The current pharmacotherapy for attention-deficit hyperactivity disorder (ADHD) is mainly based on the stimulant methylphenidate and to a small extent on amphetamines which are not approved in Germany. The only approved non-stimulant so far is atomoxetin (Strattera ® ), a norepinephrine reuptake inhibitor. There is no approved pharmacotherapy for adults. The aim of the available medication is a reduction of impulsivity, hyperactivity, and attention deficits. Neu-robiological correlates of these effects are still not fully understood, however, a functional implication of dopaminergic and noradrenergic systems is known. To date there is no disease-modifying therapy. The currently available substances have limitations due to the short half-life of stimulants, the unknown pathomechanisms, and the use of stimulants in developing brains with possible long-term side-effects. Moreover, the abuse potential of stimulants is still controversially discussed. The recently developed Lisdexamfetamin and SPD-465 have stimulant effects, too. A number of different developmental substances in preclinical and clinical phases show other mechanisms: SPD-503 represents an α 2 A-adrenozeptoragonist, ABT-089 and ABT-418 have partial agonistic effects to the α 4 β 2 -subtype of nicotinic acetylcholinre-ceptors, CX-717, -1739, -1942 and -1796 are glutamatergic α -amino-3-hydroxy-5-methyl-4- isoxazolepropionic acid (AMPA)-receptor agonists and PF-3654746 exhibits antagonistic properties to histaminergic
[兴奋剂和非兴奋剂药物在当前和未来治疗多动症中的应用]。
目前对注意力缺陷多动障碍(ADHD)的药物治疗主要基于兴奋剂哌甲酯和少量安非他明,而安非他明在德国尚未获得批准。迄今为止,唯一被批准的非兴奋剂是阿托莫西汀(Strattera®),一种去甲肾上腺素再摄取抑制剂。目前尚无批准的成人药物治疗方法。现有药物的目的是减少冲动、多动和注意力缺陷。这些影响的神经生物学相关性仍未完全了解,然而,多巴胺能和去甲肾上腺素能系统的功能含义是已知的。到目前为止,还没有治疗疾病的方法。由于兴奋剂的半衰期短、未知的病理机制以及在发育中的大脑中使用兴奋剂可能产生长期副作用,目前可用的物质存在局限性。此外,兴奋剂的滥用潜力仍然是有争议的讨论。最近开发的利地安非他明和SPD-465也有刺激作用。许多不同的发育物质在临床前和临床阶段表现出其他机制:SPD-503代表α(2)A-肾上腺素激动剂,ABT-089和ABT-418对α(4)β(2)-烟碱受体亚型具有部分激动作用,CX-717, -1739, -1942和-1796是谷氨酸能α-氨基-3-羟基-5-甲基-4-异氧唑丙酸(AMPA)受体激动剂,而f -3 654 746对组胺能H(3)-受体具有拮抗作用。α(2) a -肾上腺素受体激动剂Guanfacine (Intuniv®)和肝代谢安非他明前药Lisdexamfetamin (Vyvanse®)尚未在美国被批准用于ADHD治疗。本综述的目的是总结现有的药物治疗方案和即将出现的症状性兴奋剂和非兴奋剂药物在ADHD治疗中的发展阶段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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