Section on Behavioral Science and Genetics, Laboratory for Integrative Neuroscience, National Institute on Alcoholism and Alcohol Abuse, NIH, Bethesda, MD 20852, USA.
Trends Pharmacol Sci. 2010 Jan;31(1):2-7. doi: 10.1016/j.tips.2009.10.003. Epub 2009 Dec 28.
There is current interest in identifying drugs that facilitate fear extinction, as this form of learning is the basis of certain cognitive therapies for anxiety disorders. Following an initial report several years ago that the alpha2-adrenoreceptor antagonist yohimbine facilitated extinction in mice, more recent studies have shown mixed effects or even impairment. It has become clear that the effect of yohimbine on extinction depends on a number of factors, including genetic background, contextual variables and the presence of competing behaviors. To what extent theses effects of yohimbine are mediated through the alpha2-adrenoreceptor, as opposed to other sites of action, is also uncertain. More work is needed before this drug can be approved as a pharmacological adjunct for extinction-based therapies. More generally, the case of yohimbine may serve as a model for the development of other extinction facilitators.
目前人们对寻找能够促进恐惧消退的药物很感兴趣,因为这种形式的学习是某些焦虑障碍认知疗法的基础。几年前,有报道称α2-肾上腺素受体拮抗剂育亨宾促进了小鼠的消退,最近的研究显示出了混合的效果,甚至是损伤。很明显,育亨宾对消退的影响取决于许多因素,包括遗传背景、环境变量和竞争行为的存在。这种育亨宾的作用在多大程度上是通过α2-肾上腺素受体介导的,而不是通过其他作用部位介导的,也不确定。在这种药物被批准作为基于消退的治疗的药理学辅助药物之前,还需要做更多的工作。更一般地说,育亨宾的案例可以作为开发其他消退促进剂的模型。