Neuropharmacology Section, Laboratory of Toxicology and Pharmacology, National Institute of Environmental Health Sciences/National Institutes of Health, Research Triangle Park, North Carolina 27709, USA.
Mol Pharmacol. 2010 Sep;78(3):466-77. doi: 10.1124/mol.110.064535. Epub 2010 Jun 16.
Parkinson's disease (PD) is the second most common neurodegenerative disease characterized by a progressive loss of dopamine (DA) neurons in the substantia nigra. Accumulating evidence indicates that inhibition of microglia-mediated neuroinflammation may become a reliable protective strategy for PD. Resveratrol, a nonflavonoid polyphenol naturally found in red wine and grapes, has been known to possess antioxidant, anticancer, and anti-inflammatory properties. Although recent studies have shown that resveratrol provided neuroprotective effects against ischemia, seizure, and neurodegenerative disorders, the mechanisms underlying its beneficial effects on dopaminergic neurodegeneration are poorly defined. In this study, rat primary midbrain neuron-glia cultures were used to elucidate the molecular mechanisms underlying resveratrol-mediated neuroprotection. The results clearly demonstrated that resveratrol protected DA neurons against lipopolysaccharide (LPS)-induced neurotoxicity in concentration- and time-dependent manners through the inhibition of microglial activation and the subsequent reduction of proinflammatory factor release. Mechanistically, resveratrol-mediated neuroprotection was attributed to the inhibition of NADPH oxidase. This conclusion is supported by the following observations. First, resveratrol reduced NADPH oxidase-mediated generation of reactive oxygen species. Second, LPS-induced translocation of NADPH oxidase cytosolic subunit p47 to the cell membrane was significantly attenuated by resveratrol. Third and most importantly, resveratrol failed to exhibit neuroprotection in cultures from NADPH oxidase-deficient mice. Furthermore, this neuroprotection was also related to an attenuation of the activation of mitogen-activated protein kinases and nuclear factor-kappaB signaling pathways in microglia. These findings suggest that resveratrol exerts neuroprotection against LPS-induced dopaminergic neurodegeneration, and NADPH oxidase may be a major player in resveratrol-mediated neuroprotection.
帕金森病(PD)是第二常见的神经退行性疾病,其特征是黑质中多巴胺(DA)神经元进行性丧失。越来越多的证据表明,抑制小胶质细胞介导的神经炎症可能成为 PD 的可靠保护策略。白藜芦醇是一种天然存在于红酒和葡萄中的非类黄酮多酚,具有抗氧化、抗癌和抗炎特性。尽管最近的研究表明,白藜芦醇对缺血、癫痫和神经退行性疾病具有神经保护作用,但它对多巴胺能神经退行性变的有益作用的机制尚不清楚。在这项研究中,使用大鼠原代中脑细胞-神经胶质培养物来阐明白藜芦醇介导的神经保护的分子机制。结果清楚地表明,白藜芦醇通过抑制小胶质细胞激活和随后减少促炎因子的释放,以浓度和时间依赖的方式保护 DA 神经元免受脂多糖(LPS)诱导的神经毒性。从机制上讲,白藜芦醇介导的神经保护归因于 NADPH 氧化酶的抑制。这一结论得到了以下观察结果的支持。首先,白藜芦醇减少了 NADPH 氧化酶介导的活性氧的产生。其次,白藜芦醇显著减弱了 LPS 诱导的 NADPH 氧化酶胞浆亚基 p47 向细胞膜的易位。第三也是最重要的一点是,白藜芦醇在 NADPH 氧化酶缺陷型小鼠的培养物中未能表现出神经保护作用。此外,这种神经保护还与小胶质细胞中丝裂原活化蛋白激酶和核因子-κB 信号通路的激活减弱有关。这些发现表明,白藜芦醇对 LPS 诱导的多巴胺能神经退行性变具有神经保护作用,而 NADPH 氧化酶可能是白藜芦醇介导的神经保护的主要参与者。