Center for Molecular and Behavioral Neuroscience, Rutgers, the State University of New Jersey, Newark, NJ, USA.
Eur J Neurosci. 2021 Apr;53(8):2421-2442. doi: 10.1111/ejn.15135. Epub 2021 Apr 26.
The critical role of acetylcholine (ACh) in the basal ganglia is evident from the effect of cholinergic agents in patients suffering from several related neurological disorders, such as Parkinson's disease, Tourette syndrome, or dystonia. The striatum possesses the highest density of ACh markers in the basal ganglia underlying the importance of ACh in this structure. Striatal cholinergic interneurons (CINs) are responsible for the bulk of striatal ACh, although extrinsic cholinergic afferents from brainstem structures may also play a role. CINs are tonically active, and synchronized pause in their activity occurs following the presentation of salient stimuli during behavioral conditioning. However, the synaptic mechanisms involved are not fully understood in this physiological response. ACh modulates striatal circuits by acting on muscarinic and nicotinic receptors existing in several combinations both presynaptically and postsynaptically. While the effects of ACh in the striatum through muscarinic receptors have received particular attention, nicotinic receptors function has been less studied. Here, after briefly reviewing relevant results regarding muscarinic receptors expression and function, I will focus on striatal nicotinic receptor expressed presynaptically on glutamatergic and dopaminergic afferents and postsynaptically on diverse striatal interneurons populations. I will also review recent evidence suggesting the involvement of different GABAergic sources in two distinct nicotinic-receptor-mediated striatal circuits: the disynaptic inhibition of striatal projection neurons and the recurrent inhibition among CINs. A better understanding of striatal nicotinic receptors expression and function may help to develop targeted pharmacological interventions to treat brain disorders such as Parkinson's disease, Tourette syndrome, dystonia, or nicotine addiction.
乙酰胆碱 (ACh) 在基底神经节中的关键作用,从接受几种相关神经障碍治疗的患者中,如帕金森病、妥瑞氏综合征或肌张力障碍的患者中,使用胆碱能药物的效果就可以明显看出。基底神经节中纹状体含有最高密度的 ACh 标志物,这表明 ACh 在该结构中的重要性。纹状体胆碱能中间神经元(CINs)负责大部分纹状体 ACh,尽管来自脑干结构的外在胆碱能传入也可能发挥作用。CINs 是紧张性活跃的,在行为条件反射过程中呈现显著刺激后,其活动会同步暂停。然而,这种生理反应中的突触机制尚未完全了解。ACh 通过作用于存在于几个组合中的毒蕈碱和烟碱受体,调制纹状体回路,这些受体存在于突触前和突触后。虽然 ACh 通过毒蕈碱受体在纹状体中的作用受到了特别关注,但烟碱受体的功能研究较少。在这里,在简要回顾了关于毒蕈碱受体表达和功能的相关结果之后,我将重点介绍纹状体烟碱受体在谷氨酸能和多巴胺能传入物上的突触前表达,以及在各种纹状体中间神经元群体上的突触后表达。我还将回顾最近的证据,这些证据表明不同的 GABA 能来源参与了两个不同的烟碱受体介导的纹状体回路:纹状体投射神经元的双突触抑制和 CIN 之间的回返抑制。对纹状体烟碱受体表达和功能的更好理解,可能有助于开发针对治疗帕金森病、妥瑞氏综合征、肌张力障碍或尼古丁成瘾等脑部疾病的靶向药理学干预措施。