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Moringa oleifera stem extract protect skin keratinocytes against oxidative stress injury by enhancement of antioxidant defense systems and activation of PPAR alpha

机译:Moringa Oleifera茎提取物通过增强抗氧化防御系统和PPARα激活来保护皮肤角蛋白酶免受氧化胁迫损伤

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摘要

Oxidative stress is an important cause of skin injury induced by UVB radiation. Moringa oleifera also known as horseradish tree or drumstick tree, have multiple nutraceutical or pharmacological functions. However, whether Moringa oleifera protects skin against oxidative stress injury remains unknown. To investigate the effects of the ethanol extract of Moringa oleifera stem (MSE) on skin oxidative stress injury and its molecular mechanism, we first determined the effect of MSE on epidermal oxidative stress injury induced by H2O2 in keratinocytes (HaCaT cells) and by UVB-radiation in mice. Then we investigated the effect of MSE on the enhancement of antioxidant system and activation of PPAR alpha in vitro and in vivo. Furthermore, the flavonoids compositions in MSE were assayed by high-performance liquid chromatography (HPLC), and then molecular docking study was used to assess the major component in MSE to activate PPAR alpha. Our results indicate that MSE (100-400 mu g/mL) protected the epidemic cell against oxidative stress injury in vitro and topical treatment with MSE cream (6%) inhibit UVB-induced oxidative stress injury in the epidermis of the mouse skin. PPAR alpha activation is involved in the protective effect of MSE. HPLC assay and molecular docking study indicated that rutin might be the main component in MSE to activate PPAR alpha. These results confirm that MSE exerts the protective effect on oxidative stress induced skin keratinocytes injury. Moreover, the protective effect of MSE is mediated by enhancement of antioxidant defense systems and activation of PPAR alpha in skin keratinocytes.
机译:氧化应激是UVB辐射诱导皮肤损伤的重要原因。 Moringa Oleifera又称辣根树或鼓槌树,有多种营养素或药理功能。但是,辣木oleifera是否保护皮肤免受氧化应激损伤仍然未知。为了探讨辣木醇溶液(MSE)对皮肤氧化胁迫损伤及其分子机制的乙醇提取物的影响,首先确定了MSE对角蛋白酶细胞(HACAT细胞)和UVB-的表皮氧化胁迫损伤的影响。小鼠的辐射。然后我们调查了MSE对抗氧化系统增强的影响,体内和体内PPARα激活。此外,通过高效液相色谱(HPLC)测定MSE中的类黄酮组合物,然后使用分子对接研究来评估MSE中的主要组分以激活PPARα。我们的结果表明,MSE(100-400 mu g / ml)保护抗氧化胁迫损伤的氧化胁迫损伤,并用MSE乳膏(6%)抑制了小鼠皮肤表皮中的UVB诱导的氧化应激损伤。 PPARα激活参与了MSE的保护作用。 HPLC测定和分子对接研究表明,芦丁可能是MSE中的主要成分,以激活PPARα。这些结果证实,MSE对氧化应激诱导的皮肤角蛋白损伤施加保护作用。此外,MSE的保护作用是通过增强抗氧化剂防御系统和皮肤角蛋白酶细胞的PPARα的激活介导的。

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