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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Inhibition of UVB-induced skin phototoxicity by a grape seed extract as modulator of nitrosative stress, ERK/NF-kB signaling pathway and apoptosis, in SKH-1 mice
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Inhibition of UVB-induced skin phototoxicity by a grape seed extract as modulator of nitrosative stress, ERK/NF-kB signaling pathway and apoptosis, in SKH-1 mice

机译:葡萄籽提取物对SKH-1小鼠亚硝化应激,ERK / NF-kB信号传导途径和细胞凋亡的调节剂对UVB诱导的皮肤光毒性的抑制

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摘要

Molecular mechanisms concerning the modulation of nitrosative stress, signal transduction and proliferation/apoptosis by a grape seed extract, Burgund Mare variety (BM), in SKH-1 mice exposed to UVB, were investigated. The animals were irradiated with single and multiple doses of UVB in 10 consecutive days. In each experiment were used five groups of animals: control, vehicle, UVB irradiated, vehicle+UVB, BM+UVB. The extract was applied topically, 30min before each UVB exposure, in a dose of 4mg total polyphenols/cm2. BM remarkably inhibited UVB-induced activation of inducible nitric oxide synthase (iNOS) and therefore generation of nitric oxide (NO) and nitrotyrosine, in a UVB single dose regimen. BM also suppressed NF-kB activation by UVB but did not affect the activity of total ERK 1/2. In multiple UVB irradiations, BM increased NO formation and total ERK 1/2 activity and reduced iNOS activity and nitrotyrosine levels, inhibited cell proliferation, diminished p53 and caspase-3 immunoreactivities and increased the percentage of Bcl-2 positive cells. We concluded that BM modulates the apoptotic response of SKH-1 mice skin in UVB irradiation by the inhibition of p53, caspase-3, Bax/Bcl-2 and proliferating cell nuclear antigen expressions, as well as by reducing the activation of iNOS and NF-kB.
机译:研究了在暴露于UVB的SKH-1小鼠中,葡萄籽提取物Burgund Mare变种(BM)对亚硝化胁迫的调节,信号转导和增殖/凋亡的分子机制。在连续10天中用单剂量和多剂量的UVB照射动物。在每个实验中,使用五组动物:对照,媒介物,UVB照射,媒介物+ UVB,BM + UVB。在每次UVB暴露前30分钟,以4mg总多酚/ cm2的剂量局部应用​​提取物。在UVB单剂量方案中,BM显着抑制UVB诱导的可诱导型一氧化氮合酶(iNOS)的活化,因此抑制一氧化氮(NO)和亚硝基酪氨酸的生成。 BM还抑制UVB激活NF-kB,但不影响总ERK 1/2的活性。在多次UVB照射中,BM增加NO形成和总ERK 1/2活性,降低iNOS活性和硝基酪氨酸水平,抑制细胞增殖,降低p53和caspase-3免疫反应性,并增加Bcl-2阳性细胞的百分比。我们得出的结论是,BM通过抑制p53,caspase-3,Bax / Bcl-2和增殖细胞核抗原的表达以及减少iNOS和NF的激活来调节UVB照射下SKH-1小鼠皮肤的凋亡反应。 -kB。

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