Hosseinzadeh Sahafi Oveis, Sardari Maryam, Alijanpour Sakineh, Rezayof Ameneh
Department of Animal Biology, School of Biology, College of Science, University of Tehran, Tehran 14155-6465, Iran.
Department of Neurophysiology, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan.
Brain Sci. 2023 May 17;13(5):815. doi: 10.3390/brainsci13050815.
The functional interplay between the corticolimbic GABAergic and opioidergic systems plays a crucial role in regulating the reward system and cognitive aspects of motivational behaviors leading to the development of addictive behaviors and disorders. This review provides a summary of the shared mechanisms of GABAergic and opioidergic transmission, which modulate the activity of dopaminergic neurons located in the ventral tegmental area (VTA), the central hub of the reward mechanisms. This review comprehensively covers the neuroanatomical and neurobiological aspects of corticolimbic inhibitory neurons that express opioid receptors, which act as modulators of corticolimbic GABAergic transmission. The presence of opioid and GABA receptors on the same neurons allows for the modulation of the activity of dopaminergic neurons in the ventral tegmental area, which plays a key role in the reward mechanisms of the brain. This colocalization of receptors and their immunochemical markers can provide a comprehensive understanding for clinicians and researchers, revealing the neuronal circuits that contribute to the reward system. Moreover, this review highlights the importance of GABAergic transmission-induced neuroplasticity under the modulation of opioid receptors. It discusses their interactive role in reinforcement learning, network oscillation, aversive behaviors, and local feedback or feedforward inhibitions in reward mechanisms. Understanding the shared mechanisms of these systems may lead to the development of new therapeutic approaches for addiction, reward-related disorders, and drug-induced cognitive impairment.
皮质边缘GABA能系统与阿片肽能系统之间的功能相互作用在调节奖赏系统以及导致成瘾行为和障碍发展的动机行为的认知方面起着关键作用。本综述总结了GABA能和阿片肽能传递的共同机制,这些机制调节位于腹侧被盖区(VTA)的多巴胺能神经元的活动,VTA是奖赏机制的核心枢纽。本综述全面涵盖了表达阿片受体的皮质边缘抑制性神经元的神经解剖学和神经生物学方面,这些神经元充当皮质边缘GABA能传递的调节因子。同一神经元上阿片受体和GABA受体的存在使得腹侧被盖区多巴胺能神经元的活动能够被调节,这在大脑的奖赏机制中起关键作用。受体及其免疫化学标记物的这种共定位可为临床医生和研究人员提供全面的理解,揭示对奖赏系统有贡献的神经回路。此外,本综述强调了在阿片受体调节下GABA能传递诱导的神经可塑性的重要性。它讨论了它们在强化学习、网络振荡、厌恶行为以及奖赏机制中的局部反馈或前馈抑制中的相互作用。了解这些系统的共同机制可能会促成针对成瘾、奖赏相关障碍和药物诱导的认知障碍的新治疗方法的开发。