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右美沙芬在MPTP帕金森病模型中的神经保护作用:NADPH氧化酶的作用

Neuroprotective effect of dextromethorphan in the MPTP Parkinson's disease model: role of NADPH oxidase.

作者信息

Zhang Wei, Wang Tongguang, Qin Liya, Gao Hui-Ming, Wilson Belinda, Ali Syed F, Zhang Wanqin, Hong Jau-Shyong, Liu Bin

机构信息

Laboratory of Pharmacology and Chemistry, National Institute of Environmental Health Science, Research Triangle Park, North Carolina, USA.

出版信息

FASEB J. 2004 Mar;18(3):589-91. doi: 10.1096/fj.03-0983fje. Epub 2004 Jan 20.

Abstract

Parkinson's disease (PD) is a neurodegenerative movement disorder characterized by a progressive loss of dopaminergic neurons in the substantia nigra and depletion of the neurotransmitter dopamine in the striatum. Progress in the search for effective therapeutic strategies that can halt this degenerative process remains limited. Mechanistic studies using animal systems such as the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) rodent PD model have revealed the involvement of the brain's immune cells and free radical-generating processes. We recently reported that dextromethorphan (DM), a widely used anti-tussive agent, attenuated endotoxin-induced dopaminergic neurodegeneration in vitro. In the current study, we investigated the potential neuroprotective effect of DM and the underlying mechanism of action in the MPTP rodent PD model. Mice (C57BL/6J) that received daily MPTP injections (15 mg free base/kg body weight, s.c.) for 6 consecutive days exhibited significant degeneration of the nigrostriatal dopaminergic pathway. However, the MPTP-induced loss of nigral dopaminergic neurons was significantly attenuated in those mice receiving DM (10 mg/kg body weight, s.c.). In mesencephalic neuron-glia cultures, DM significantly reduced the MPTP-induced production of both extracellular superoxide free radicals and intracellular reactive oxygen species (ROS). Because NADPH oxidase is the primary source of extracellular superoxide and intracellular ROS, we investigated the involvement of NADPH oxidase in the neuroprotective effect of DM. Indeed, the neuroprotective effect of DM was only observed in the wild-type but not in the NADPH oxidase-deficient mice, indicating that NADPH oxidase is a critical mediator of the neuroprotective activity of DM. More importantly, due to its proven safety record of long-term clinical use in humans, DM may be a promising agent for the treatment of degenerative neurological disorders such as PD.

摘要

帕金森病(PD)是一种神经退行性运动障碍,其特征是黑质中多巴胺能神经元逐渐丧失以及纹状体中神经递质多巴胺耗竭。在寻找能够阻止这种退行性过程的有效治疗策略方面,进展仍然有限。使用动物模型(如1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)啮齿动物PD模型)进行的机制研究揭示了大脑免疫细胞和自由基生成过程的参与。我们最近报道,右美沙芬(DM),一种广泛使用的止咳药,在体外可减轻内毒素诱导的多巴胺能神经退行性变。在本研究中,我们研究了DM在MPTP啮齿动物PD模型中的潜在神经保护作用及其潜在作用机制。连续6天每天接受MPTP注射(15mg游离碱/ kg体重,皮下注射)的小鼠(C57BL / 6J)表现出黑质纹状体多巴胺能通路的明显退化。然而,在接受DM(10mg / kg体重,皮下注射)的那些小鼠中,MPTP诱导的黑质多巴胺能神经元损失明显减轻。在中脑神经元-胶质细胞培养物中,DM显著降低了MPTP诱导的细胞外超氧自由基和细胞内活性氧(ROS)的产生。因为NADPH氧化酶是细胞外超氧化物和细胞内ROS的主要来源,我们研究了NADPH氧化酶在DM神经保护作用中的参与情况。事实上,仅在野生型小鼠中观察到DM的神经保护作用,而在NADPH氧化酶缺陷小鼠中未观察到,这表明NADPH氧化酶是DM神经保护活性的关键介质。更重要的是,由于其在人类长期临床使用中已被证实的安全记录,DM可能是治疗诸如PD等退行性神经疾病的有前景的药物。

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