Center for Health Sciences, SRI International, Menlo Park, CA.
University of Vermont Medical Center Neurology, Burlington, VT.
Nicotine Tob Res. 2019 Feb 18;21(3):357-369. doi: 10.1093/ntr/nty063.
Emerging studies indicate that striatal cholinergic interneurons play an important role in synaptic plasticity and motor control under normal physiological conditions, while their disruption may lead to movement disorders. Here we discuss the involvement of the cholinergic system in motor dysfunction, with a focus on the role of the nicotinic cholinergic system in Parkinson's disease and drug-induced dyskinesias. Evidence for a role for the striatal nicotinic cholinergic system stems from studies showing that administration of nicotine or nicotinic receptor drugs protects against nigrostriatal degeneration and decreases L-dopa-induced dyskinesias. In addition, nicotinic receptor drugs may ameliorate tardive dyskinesia, Tourette's syndrome and ataxia, although further study is required to understand their full potential in the treatment of these disorders. A role for the striatal muscarinic cholinergic system in movement disorders stems from studies showing that muscarinic receptor drugs acutely improve Parkinson's disease motor symptoms, and may reduce dyskinesias and dystonia. Selective stimulation or lesioning of striatal cholinergic interneurons suggests they are primary players in this regulation, although multiple central nervous systems appear to be involved.
Accumulating data from preclinical studies and clinical trials suggest that drugs targeting CNS cholinergic systems may be useful for symptomatic treatment of movement disorders. Nicotinic cholinergic drugs, including nicotine and selective nAChR receptor agonists, reduce L-dopa-induced dyskinesias, as well as antipsychotic-induced tardive dyskinesia, and may be useful in Tourette's syndrome and ataxia. Subtype selective muscarinic cholinergic drugs may also provide effective therapies for Parkinson's disease, dyskinesias and dystonia. Continued studies/trials will help address this important issue.
新兴研究表明,纹状体胆碱能中间神经元在正常生理条件下的突触可塑性和运动控制中发挥重要作用,而其破坏可能导致运动障碍。在这里,我们讨论了胆碱能系统在运动功能障碍中的作用,重点是烟碱型胆碱能系统在帕金森病和药物诱导的运动障碍中的作用。纹状体烟碱型胆碱能系统发挥作用的证据来自于研究表明,给予尼古丁或烟碱受体药物可预防黑质纹状体变性并减少左旋多巴诱导的运动障碍。此外,烟碱受体药物可能改善迟发性运动障碍、妥瑞氏综合征和共济失调,尽管需要进一步研究才能了解它们在治疗这些疾病中的全部潜力。纹状体毒蕈碱型胆碱能系统在运动障碍中的作用源自研究表明毒蕈碱受体药物可急性改善帕金森病运动症状,并可能减少运动障碍和肌张力障碍。纹状体胆碱能中间神经元的选择性刺激或损伤表明它们是这种调节的主要参与者,尽管多个中枢神经系统似乎都参与其中。
来自临床前研究和临床试验的累积数据表明,靶向中枢神经系统胆碱能系统的药物可能对运动障碍的症状治疗有用。烟碱型胆碱能药物,包括尼古丁和选择性 nAChR 受体激动剂,可减少左旋多巴诱导的运动障碍,以及抗精神病药引起的迟发性运动障碍,并且可能对妥瑞氏综合征和共济失调有用。亚型选择性毒蕈碱型胆碱能药物也可能为帕金森病、运动障碍和肌张力障碍提供有效的治疗方法。持续的研究/试验将有助于解决这个重要问题。