首页> 美国卫生研究院文献>Frontiers in Pharmacology >The Lipid Mediator Resolvin D1 Reduces the Skin Inflammation and Oxidative Stress Induced by UV Irradiation in Hairless Mice
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The Lipid Mediator Resolvin D1 Reduces the Skin Inflammation and Oxidative Stress Induced by UV Irradiation in Hairless Mice

机译:脂质介体Resolvin D1减少了无毛小鼠紫外线照射引起的皮肤炎症和氧化应激。

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摘要

UV irradiation-induced oxidative stress and inflammation contribute to the development of skin diseases. Therefore, targeting oxidative stress and inflammation might contribute to reduce skin diseases. Resolvin D1 (RvD1) is a bioactive metabolite generated during inflammation to actively orchestrate the resolution of inflammation. However, the therapeutic potential of RvD1 in UVB skin inflammation remains undetermined, which was, therefore, the aim of the present study. The intraperitoneal treatment with RvD1 (3-100 ng/mouse) reduced UVB irradiation-induced skin edema, myeloperoxidase activity, matrix metalloproteinase 9 activity, and reduced glutathione depletion with consistent effects observed with the dose of 30 ng/mouse, which was selected to the following experiments. RvD1 inhibited UVB reduction of catalase activity, and hydroperoxide formation, superoxide anion production, and gp91phox mRNA expression. RvD1 also increased the Nrf2 and its downstream targets NQO1 and HO-1 mRNA expression. Regarding cytokines, RvD1 inhibited UVB-induced production of IL-1β, IL-6, IL-33, TNF-α, TGF-β, and IL-10. These immuno-biochemical alterations by RvD1 treatment had as consequence the reduction of UVB-induced epidermal thickness, sunburn and mast cell counts, and collagen degradation. Therefore, RvD1 inhibited UVB-induced skin oxidative stress and inflammation, rendering this resolving lipid mediator as a promising therapeutic agent.
机译:紫外线辐射引起的氧化应激和炎症有助于皮肤疾病的发展。因此,针对氧化应激和炎症可能有助于减少皮肤疾病。 Resolvin D1(RvD1)是在炎症过程中产生的具有生物活性的代谢产物,可主动协调炎症的消退。然而,RvD1在UVB皮肤炎症中的治疗潜力仍未确定,因此,这是本研究的目的。 RvD1(3-100 ng /小鼠)的腹膜内治疗减少了UVB辐射诱导的皮肤水肿,髓过氧化物酶活性,基质金属蛋白酶9活性,并减少了谷胱甘肽耗竭,并以30 ng /小鼠的剂量观察到了一致的效果。以下实验。 RvD1抑制UVB降低过氧化氢酶活性,过氧化氢形成,超氧阴离子生成和gp91phox mRNA表达。 RvD1还增加了Nrf2及其下游靶标NQO1和HO-1 mRNA的表达。关于细胞因子,RvD1抑制UVB诱导的IL-1β,IL-6,IL-33,TNF-α,TGF-β和IL-10的产生。因此,通过RvD1处理的这些免疫生化改变降低了UVB诱导的表皮厚度,晒伤和肥大细胞数量以及胶原蛋白降解。因此,RvD1抑制UVB诱导的皮肤氧化应激和炎症,使这种可分解的脂质介质成为有前途的治疗剂。

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