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首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Inhibition effect of Gynura procumbens extract on UV-B-induced matrix-metalloproteinase expression in human dermal fibroblasts.
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Inhibition effect of Gynura procumbens extract on UV-B-induced matrix-metalloproteinase expression in human dermal fibroblasts.

机译:绞股蓝提取物对人皮肤成纤维细胞中UV-B诱导的基质金属蛋白酶表达的抑制作用。

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摘要

ETHNOPHARMACOLOGICAL RELEVANCE: Gynura procumbens Merr. (Asteraceae) has been used as a traditional remedy for various skin diseases in certain areas of Southeast Asia. AIM OF THE STUDY: In order to evaluate the protective activity of Gynura procumbens extract on skin photoaging and elucidate its mode of action. MATERIALS AND METHODS: Matrix-metalloproteinase (MMP)-1 and -9 expressions were induced by UV-B irradiation in human primary dermal fibroblasts. MMP-1 expression level was measured by enzyme-linked immunosorbent assay (ELISA) and Western blot analysis. Zymography was employed for evaluating the enzymatic activity of MMP-9. Anti-inflammatory activity and anti-oxidative capacity of the extract were evaluated by ELISA and dichlorodihydrofluorescein diacetate (DCF-DA) assay. RESULTS: The ethanolic extract of Gynura procumbens inhibited MMP-1 expression up to 70% compare to negative control group. The enzymatic activity of MMP-9 was inhibited around 73% by the treatment of 20mug/mL of the extract. The extract markedly reduced the production of reactive oxygen species (ROS). Gynura procumbens extract showed an inhibitory effect on releasing pro-inflammatory cytokines (IL-6 and IL-8) in human HaCat keratinocyte. CONCLUSION: The ethanolic extract of Gynura procumbens inhibited MMP-1 and MMP-9 expressions induced by UV-B irradiation via inhibition of pro-inflammatory cytokine mediator release and ROS production.
机译:人类药理学相关性:Gynura procumbens Merr。 (菊科)已被用作东南亚某些地区各种皮肤疾病的传统疗法。研究目的:为了评估绞股蓝提取物对皮肤光老化的保护活性,并阐明其作用方式。材料与方法:紫外线-B辐射诱导人原代皮肤成纤维细胞基质金属蛋白酶(MMP)-1和-9的表达。通过酶联免疫吸附测定(ELISA)和蛋白质印迹分析测量MMP-1表达水平。浸染法用于评估MMP-9的酶活性。提取物的抗炎活性和抗氧化能力通过ELISA和二乙酸二氯二氢荧光素(DCF-DA)分析进行评估。结果:与阴性对照组相比,绞股蓝乙醇提取物抑制MMP-1表达达70%。通过处理20mug / mL的提取物,MMP-9的酶活性被抑制了约73%。提取物显着减少了活性氧(ROS)的产生。 Gynura procumbens提取物对人HaCat角质形成细胞中促炎性细胞因子(IL-6和IL-8)的释放具有抑制作用。结论:绞股蓝乙醇提取物通过抑制促炎性细胞因子的释放和ROS的产生,抑制了UV-B辐射诱导的MMP-1和MMP-9的表达。

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