首页> 外文期刊>Phytomedicine : >Effects of aqueous extracts of Halimeda incrassata (Ellis) Lamouroux and Bryothamnion triquetrum (S.G.Gmelim) Howe on hydrogen peroxide and methyl mercury-induced oxidative stress in GT1-7 mouse hypothalamic immortalized cells.
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Effects of aqueous extracts of Halimeda incrassata (Ellis) Lamouroux and Bryothamnion triquetrum (S.G.Gmelim) Howe on hydrogen peroxide and methyl mercury-induced oxidative stress in GT1-7 mouse hypothalamic immortalized cells.

机译:Halimeda incrassata(Ellis)Lamouroux和Bryothamnion triquetrum(S.G. Gmelim)Howe的水提物对GT1-7小鼠下丘脑永生化细胞中过氧化氢和甲基汞诱导的氧化应激的影响。

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摘要

The current investigation focuses attention on the neuroprotective and antioxidant properties of aqueous extracts from Halimeda incrassata (Hi) and Bryothamniom triquetrum (Bt) in the mouse immortalized hypothalamic GT1-7 cell line. Under basal oxidative conditions, Hi extract reduces intracellular reactive oxygen species production, as assessed by 2',7'-dichlorofluorescein fluorescence, while Bt extract does not contribute to basal ROS generation. Both extracts, at concentrations higher than 0.20 mg/ml, exert protection against hydrogen peroxide-mediated cell death, although only Hi extract can additionally prevent hydrogen peroxide-induced ROS production. The two seaweed aqueous extracts, at concentrations higher than 0.05 mg/ml, also display protection against neuronal death induced by methyl mercury chloride, as well as against methyl mercury chloride-mediated ROS generation. None of the extracts increase GSH intracellular pools, in basal conditions, after depleting its levels with either hydrogen peroxide or methyl mercury chloride. Some comments on the probable targets of the neuroprotection exerted by these two extracts are included in this paper.
机译:目前的研究集中在小鼠永生化的下丘脑GT1-7细胞系中,来自Halimeda incrassata(Hi)和Bryothamniom triquetrum(Bt)的水提取物的神经保护和抗氧化特性。在基础氧化条件下,Hi提取物可降低细胞内活性氧的产生,如2',7'-dichlorofluorescein荧光所评估的那样,而Bt提取物不会促进基础ROS的产生。两种提取物的浓度均高于0.20 mg / ml,对过氧化氢介导的细胞死亡具有保护作用,尽管只有Hi提取物才能另外防止过氧化氢诱导的ROS产生。两种浓度高于0.05 mg / ml的海藻水提取物还显示出针对甲基汞氯化物诱导的神经元死亡以及甲基汞氯化物介导的ROS生成的保护作用。在基础条件下,用过氧化氢或甲基汞氯化物耗尽GSH的含量后,没有一种提取物能增加GSH的细胞内池。本文包括对这两种提取物可能发挥的神经保护作用的一些评论。

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