Ebrahimi Mohammad Navid, Banazadeh Mohammad, Alitaneh Zahra, Jaafari Suha Ali, Esmaeili Ali, Hasannejad-Asl Behnam, Siahposht-Khachaki Ali, Hassanshahi Amin, Bagheri-Mohammadi Saeid
Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.
Pharmaceutical Sciences and Cosmetic Products Research Center, Kerman University of Medical Sciences, Kerman, Iran.
Physiol Behav. 2024 Oct 1;284:114639. doi: 10.1016/j.physbeh.2024.114639. Epub 2024 Jul 14.
Understanding the central nervous system (CNS) circuitry and its different neurotransmitters that underlie reward is essential to improve treatment for many common health issues, such as addiction. Here, we concentrate on understanding how the mesolimbic circuitry and neurotransmitters are organized and function, and how drug exposure affects synaptic and structural changes in this circuitry. While the role of some reward circuits, like the cerebral dopamine (DA)/glutamate (Glu)/gamma aminobutyric acid (GABA)ergic pathways, in drug reward, is well known, new research using molecular-based methods has shown functional alterations throughout the reward circuitry that contribute to various aspects of addiction, including craving and relapse. A new understanding of the fundamental connections between brain regions as well as the molecular alterations within these particular microcircuits, such as neurotrophic factor and molecular signaling or distinct receptor function, that underlie synaptic and structural plasticity evoked by drugs of abuse has been made possible by the ability to observe and manipulate neuronal activity within specific cell types and circuits. It is exciting that these discoveries from preclinical animal research are now being applied in the clinic, where therapies for human drug dependence, such as deep brain stimulation and transcranial magnetic stimulation, are being tested. Therefore, this chapter seeks to summarize the current understanding of the important brain regions (especially, mesolimbic circuitry) and neurotransmitters implicated in drug-related behaviors and the molecular mechanisms that contribute to altered connectivity between these areas, with the postulation that increased knowledge of the plasticity within the drug reward circuit will lead to new and improved treatments for addiction.
了解中枢神经系统(CNS)中构成奖赏基础的神经回路及其不同的神经递质,对于改善许多常见健康问题(如成瘾)的治疗至关重要。在此,我们专注于了解中脑边缘神经回路和神经递质是如何组织和发挥功能的,以及药物暴露如何影响该神经回路中的突触和结构变化。虽然一些奖赏回路,如脑多巴胺(DA)/谷氨酸(Glu)/γ-氨基丁酸(GABA)能通路在药物奖赏中的作用已为人所知,但使用基于分子的方法进行的新研究表明,整个奖赏回路存在功能改变,这些改变导致成瘾的各个方面,包括渴望和复发。通过观察和操纵特定细胞类型和回路中的神经元活动,人们得以重新认识脑区之间的基本连接以及这些特定微回路中的分子变化,如神经营养因子和分子信号传导或独特的受体功能,这些变化构成了滥用药物诱发的突触和结构可塑性的基础。令人兴奋的是,临床前动物研究的这些发现目前正在临床中得到应用,人类药物依赖的治疗方法,如深部脑刺激和经颅磁刺激,正在接受测试。因此,本章旨在总结目前对与药物相关行为有关的重要脑区(特别是中脑边缘神经回路)和神经递质以及导致这些区域之间连接改变的分子机制的理解,并假定对药物奖赏回路内可塑性的更多了解将带来新的、更好的成瘾治疗方法。