Iarkov Alexandre, Mendoza Cristhian, Echeverria Valentina
Laboratorio de Neurobiología, Facultad de Ciencias de la Salud, Universidad San Sebastián, Concepción, Chile.
Research & Development Service, Bay Pines VA Healthcare System, Bay Pines, FL, United States.
Front Neurosci. 2021 Sep 20;15:665820. doi: 10.3389/fnins.2021.665820. eCollection 2021.
Parkinson's disease (PD) is a neurodegenerative condition characterized by the loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc) in the midbrain resulting in progressive impairment in cognitive and motor abilities. The physiological and molecular mechanisms triggering dopaminergic neuronal loss are not entirely defined. PD occurrence is associated with various genetic and environmental factors causing inflammation and mitochondrial dysfunction in the brain, leading to oxidative stress, proteinopathy, and reduced viability of dopaminergic neurons. Oxidative stress affects the conformation and function of ions, proteins, and lipids, provoking mitochondrial DNA (mtDNA) mutation and dysfunction. The disruption of protein homeostasis induces the aggregation of alpha-synuclein (α-SYN) and parkin and a deficit in proteasome degradation. Also, oxidative stress affects dopamine release by activating ATP-sensitive potassium channels. The cholinergic system is essential in modulating the striatal cells regulating cognitive and motor functions. Several muscarinic acetylcholine receptors (mAChR) and nicotinic acetylcholine receptors (nAChRs) are expressed in the striatum. The nAChRs signaling reduces neuroinflammation and facilitates neuronal survival, neurotransmitter release, and synaptic plasticity. Since there is a deficit in the nAChRs in PD, inhibiting nAChRs loss in the striatum may help prevent dopaminergic neurons loss in the striatum and its pathological consequences. The nAChRs can also stimulate other brain cells supporting cognitive and motor functions. This review discusses the cholinergic system as a therapeutic target of cotinine to prevent cognitive symptoms and transition to dementia in PD.
帕金森病(PD)是一种神经退行性疾病,其特征是中脑黑质致密部(SNpc)中的多巴胺能神经元丧失,导致认知和运动能力逐渐受损。引发多巴胺能神经元丧失的生理和分子机制尚未完全明确。PD的发生与多种遗传和环境因素有关,这些因素会导致大脑炎症和线粒体功能障碍,进而引发氧化应激、蛋白病以及多巴胺能神经元活力降低。氧化应激会影响离子、蛋白质和脂质的构象与功能,引发线粒体DNA(mtDNA)突变和功能障碍。蛋白质稳态的破坏会诱导α-突触核蛋白(α-SYN)和帕金蛋白聚集以及蛋白酶体降解功能缺陷。此外,氧化应激通过激活ATP敏感性钾通道影响多巴胺释放。胆碱能系统在调节纹状体细胞以控制认知和运动功能方面至关重要。纹状体中表达了多种毒蕈碱型乙酰胆碱受体(mAChR)和烟碱型乙酰胆碱受体(nAChR)。nAChR信号传导可减轻神经炎症并促进神经元存活、神经递质释放和突触可塑性。由于PD患者的nAChR存在缺陷,抑制纹状体中nAChR的丧失可能有助于预防纹状体中多巴胺能神经元的丧失及其病理后果。nAChR还可以刺激支持认知和运动功能的其他脑细胞。本综述讨论了胆碱能系统作为可替宁的治疗靶点,以预防PD的认知症状并向痴呆转变。