Quik Maryka, Kulak Jennifer M
The Parkinson's Institute, Sunnyvale, CA 94089, USA.
Neurotoxicology. 2002 Oct;23(4-5):581-94. doi: 10.1016/s0161-813x(02)00036-0.
The development of nicotinic agonists for therapy in neurodegenerative disorders such as Parkinson's disease is an area currently receiving considerable attention. The rationale for such work stems from findings that reveal a loss of nicotinic receptors in Parkinson's disease brains. These results, coupled with reports that nicotine treatment relieves some of the symptoms of this disorder, provides support for the contention that nicotine and/or nicotinic agonists may be beneficial for acute symptomatic treatment. Moreover, the observation that there is a decreased incidence of Parkinson's disease with tobacco use, possibly due to the nicotine in tobacco products, may imply that such drugs are useful for long-term neuroprotection. However, there are multiple nicotinic receptor populations in the brain with different functional properties. Identification of the subtypes involved in nigrostriatal dopaminergic activity is therefore critical for the rational use of selective therapeutic agents for symptomatic treatment and/or neuroprotection. Accumulating evidence, both in rodents and nonhuman primates now indicate that alpha6* nicotinic receptors are present on nigrostriatal dopaminergic neurons, and furthermore, that receptors containing this subunit may be most vulnerable to nigrostriatal damage, at least in nonhuman primates. These data suggest that nicotinic receptor ligands directed to alpha6* nicotinic receptors might be particularly relevant for Parkinson's disease therapeutics.
开发用于治疗帕金森病等神经退行性疾病的烟碱类激动剂是目前备受关注的领域。开展此类研究的理论依据源于帕金森病患者大脑中烟碱受体缺失的研究发现。这些结果,再加上尼古丁治疗可缓解该疾病某些症状的报道,为尼古丁和/或烟碱类激动剂可能有助于急性症状治疗的观点提供了支持。此外,观察到吸烟人群中帕金森病发病率降低,可能是由于烟草制品中的尼古丁,这意味着此类药物对长期神经保护有用。然而,大脑中有多种具有不同功能特性的烟碱受体群体。因此,确定参与黑质纹状体多巴胺能活动的亚型对于合理使用选择性治疗药物进行症状治疗和/或神经保护至关重要。目前在啮齿动物和非人类灵长类动物中积累的证据均表明,黑质纹状体多巴胺能神经元上存在α6烟碱受体,此外,至少在非人类灵长类动物中,含有该亚基的受体可能最易受到黑质纹状体损伤。这些数据表明,针对α6烟碱受体的烟碱受体配体可能与帕金森病治疗特别相关。