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α-生育酚和γ-生育三烯酚对过氧化氢诱导原代培养星形胶质细胞凋亡的比较作用

Comparative effects of alpha-tocopherol and gamma-tocotrienol against hydrogen peroxide induced apoptosis on primary-cultured astrocytes.

作者信息

Mazlan Musalmah, Sue Mian Then, Mat Top Gapor, Zurinah Wan Ngah Wan

机构信息

Department of Biochemistry, Medical Faculty, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.

出版信息

J Neurol Sci. 2006 Apr 15;243(1-2):5-12. doi: 10.1016/j.jns.2005.10.006. Epub 2006 Jan 27.

Abstract

Oxidative stress is thought to be one of the factors that cause neurodegeneration and that this can be inhibited by antioxidants. Since astrocytes support the survival of central nervous system (CNS) neurons, we compared the effect of alpha-tocopherol and gamma-tocotrienol in minimizing the cytotoxic damage induced by H(2)O(2), a pro-oxidant. Primary astrocyte cultures were pretreated with either alpha-tocopherol or gamma-tocotrienol for 1 h before incubation with 100 microM H(2)O(2) for 24 h. Cell viability was then assessed using the MTS assay while apoptosis was determined using a commercial ELISA kit as well as by fluorescent staining of live and apoptotic cells. The uptake of alpha-tocopherol and gamma-tocotrienol by astrocytes were also determined using HPLC. Results showed that gamma-tocotrienol is toxic at concentrations >200 microM but protects against H(2)O(2) induced cell loss and apoptosis in a dose dependent manner up to 100 microM. alpha-Tocopherol was not cytotoxic in the concentration range tested (up to 750 microM), reduced apoptosis to the same degree as that of gamma-tocotrienol but was less effective in maintaining the viable cell number. Since the uptake of alpha-tocopherol and gamma-tocotrienol by astrocytes is similar, this may reflect the roles of these 2 vitamin E subfamilies in inhibiting apoptosis and stimulating proliferation in astrocytes.

摘要

氧化应激被认为是导致神经退行性变的因素之一,而抗氧化剂可以抑制这种情况。由于星形胶质细胞支持中枢神经系统(CNS)神经元的存活,我们比较了α-生育酚和γ-生育三烯酚在最小化由促氧化剂H₂O₂诱导的细胞毒性损伤方面的作用。原代星形胶质细胞培养物在与100μM H₂O₂孵育24小时之前,先用α-生育酚或γ-生育三烯酚预处理1小时。然后使用MTS法评估细胞活力,同时使用商业ELISA试剂盒以及通过对活细胞和凋亡细胞进行荧光染色来确定细胞凋亡情况。还使用高效液相色谱法测定星形胶质细胞对α-生育酚和γ-生育三烯酚的摄取。结果表明,γ-生育三烯酚在浓度>200μM时具有毒性,但在高达100μM的浓度范围内以剂量依赖的方式保护细胞免受H₂O₂诱导的细胞损失和凋亡。α-生育酚在所测试的浓度范围内(高达750μM)没有细胞毒性,将细胞凋亡减少到与γ-生育三烯酚相同的程度,但在维持活细胞数量方面效果较差。由于星形胶质细胞对α-生育酚和γ-生育三烯酚的摄取相似,这可能反映了这两个维生素E亚家族在抑制星形胶质细胞凋亡和刺激其增殖方面的作用。

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