Allen Daicia C, Ford Matthew M, Grant Kathleen A
Department of Behavioral Neurosciences, Oregon Health & Science University, Portland, OR, 97239, USA.
Division of Neuroscience, Oregon National Primate Research Center, Beaverton, OR, 97006, USA.
Curr Top Behav Neurosci. 2018;39:95-111. doi: 10.1007/7854_2017_2.
The progress on understanding the pharmacological basis of ethanol's discriminative stimulus effects has been substantial, but appears to have plateaued in the past decade. Further, the cross-species translational efforts are clear in laboratory animals, but have been minimal in human subject studies. Research findings clearly demonstrate that ethanol produces a compound stimulus with primary activity through GABA and glutamate receptor systems, particularly ionotropic receptors, with additional contribution from serotonergic mechanisms. Further progress should capitalize on chemogenetic and optogenetic techniques in laboratory animals to identify the neural circuitry involved in mediating the discriminative stimulus effects of ethanol. These infrahuman studies can be guided by in vivo imaging of human brain circuitry mediating ethanol's subjective effects. Ultimately, identifying receptors systems, as well as where they are located within brain circuitry, will transform the use of drug discrimination procedures to help identify possible treatment or prevention strategies for alcohol use disorder.
在理解乙醇辨别性刺激效应的药理学基础方面已取得了重大进展,但在过去十年中似乎已趋于平稳。此外,跨物种转化研究在实验动物中成果显著,但在人体研究中却极为有限。研究结果清楚地表明,乙醇通过γ-氨基丁酸(GABA)和谷氨酸受体系统,特别是离子型受体产生具有主要活性的复合刺激,血清素能机制也有额外作用。未来的进一步进展应利用实验动物中的化学遗传学和光遗传学技术,以确定介导乙醇辨别性刺激效应的神经回路。这些非人类研究可通过对介导乙醇主观效应的人脑回路进行体内成像来指导。最终,确定受体系统及其在脑回路中的位置,将改变药物辨别程序的应用,以帮助确定酒精使用障碍的可能治疗或预防策略。