Herz A
Max-Planck-Institut für Psychiatrie, Martinsried bei München.
Nervenarzt. 1995 Jan;66(1):3-14.
New insights into the neurobiological mechanisms underlying drug addition have become available with recent advances in experimental research. This is particularly true for the opioids and psychostimulants: behavioural and biochemical studies have revealed that activation of the mesolimbic "reward pathways", involving the release of dopamine, which acts upon D1 receptors, plays a critical part in the development of addictive behaviour. In the case of the opioids, the differentiation of various types of receptors (and of the corresponding endogenous ligands, the endorphins) revealed a bidirectional role of opioid receptors in this process: stimulation of the reward system, mediated by mu- and delta-opioid receptors, and inhibition of the reward pathways, mediated by the activation of chi-receptors. Thus, a functional equilibrium between these tonically active opioidergic systems appears to provide a neutral motivational state. During drug withdrawal, the decrease in dopamine release most probably reflects a disturbance of this equilibrium. There is increasing evidence that endogenous opioidergic mechanisms also modulate addictive behaviour caused by psychostimulants and other drugs of abuse. This article discusses the implications of these new findings in the context of pharmacotherapeutic strategies in the treatment of addictive behaviours.
随着实验研究的最新进展,人们对药物成瘾背后的神经生物学机制有了新的认识。对于阿片类药物和精神兴奋剂来说尤其如此:行为和生化研究表明,中脑边缘“奖赏通路”的激活,涉及多巴胺的释放,多巴胺作用于D1受体,在成瘾行为的发展中起着关键作用。就阿片类药物而言,各种类型受体(以及相应的内源性配体,即内啡肽)的分化揭示了阿片受体在这一过程中的双向作用:由μ-和δ-阿片受体介导的奖赏系统刺激,以及由κ-受体激活介导的奖赏通路抑制。因此,这些持续活跃的阿片能系统之间的功能平衡似乎提供了一种中性的动机状态。在药物戒断期间,多巴胺释放的减少很可能反映了这种平衡的紊乱。越来越多的证据表明,内源性阿片能机制也调节由精神兴奋剂和其他滥用药物引起的成瘾行为。本文在治疗成瘾行为的药物治疗策略背景下讨论了这些新发现的意义。