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藤黄酸对胚胎大鼠皮质神经元和星形胶质细胞自由基生成及一氧化氮产生的影响。

Effects of garcinol on free radical generation and NO production in embryonic rat cortical neurons and astrocytes.

作者信息

Liao Chiung-Ho, Ho Chi-Tang, Lin Jen-Kun

机构信息

Institute of Biochemistry and Molecular Biology, College of Medicine, National Taiwan University, Taipei, Taiwan.

出版信息

Biochem Biophys Res Commun. 2005 Apr 22;329(4):1306-14. doi: 10.1016/j.bbrc.2005.02.110.

Abstract

Garcinol (camboginol) is a polyisoprenylated benzophenone derivative isolated from fruit rind of Garcinia indica. This study was to elucidate the anti-oxidative and neuroprotective properties of garcinol in rat cortical neuron cultures. First, garcinol protects DNA from Fenton reaction-induced breakage in a dose-dependent manner, with an IC(50) value of 0.32 microM. Garcinol also inhibits xanthine oxidase activity with an IC(50) value of 52 microM and exhibits competitive inhibition. To further ascertain the neuroprotective effects of garcinol in inflammatory-mediated neurotoxicity, we utilized primary neuron/astrocyte co-cultures treated with LPS or cytokine. Our data implicate that treatment with garcinol (5 microM) for 7 days promotes neuronal attachment and neurite extension. The formation of nitric oxide (NO) by LPS in rat astrocytes has been suggested to correlate with the neurodegenerative process. In identifying the effect of neuroprotection, we found that garcinol prevented NO accumulation in LPS-treated astrocytes. Garcinol significantly reduced the expression of LPS-induced inflammatory mediators, such as iNOS and COX-2. Consequently, our results suggest that the neuroprotective effects of garcinol are associated with anti-oxidation and inhibition of iNOS induction in astrocytic cells. Garcinol may exert a similar anti-inflammatory effect and may be neuroprotective against brain injury.

摘要

藤黄脂素(藤黄果醇)是一种从藤黄果的果皮中分离出来的多异戊烯基化二苯甲酮衍生物。本研究旨在阐明藤黄脂素在大鼠皮质神经元培养物中的抗氧化和神经保护特性。首先,藤黄脂素以剂量依赖的方式保护DNA免受芬顿反应诱导的断裂,IC50值为0.32微摩尔。藤黄脂素还抑制黄嘌呤氧化酶活性,IC50值为52微摩尔,并表现出竞争性抑制作用。为了进一步确定藤黄脂素在炎症介导的神经毒性中的神经保护作用,我们使用了用脂多糖(LPS)或细胞因子处理的原代神经元/星形胶质细胞共培养物。我们的数据表明,用5微摩尔藤黄脂素处理7天可促进神经元附着和神经突延伸。有人提出,LPS在大鼠星形胶质细胞中形成一氧化氮(NO)与神经退行性过程相关。在确定神经保护作用时,我们发现藤黄脂素可防止LPS处理的星形胶质细胞中NO的积累。藤黄脂素显著降低了LPS诱导的炎症介质如诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的表达。因此,我们的结果表明,藤黄脂素的神经保护作用与抗氧化以及抑制星形胶质细胞中iNOS的诱导有关。藤黄脂素可能发挥类似的抗炎作用,并且可能对脑损伤具有神经保护作用。

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