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首页> 外文期刊>Chemico-biological interactions >Cytoprotection against hydrogen peroxide-induced cell death in cultured mouse mesangial cells by erigeroflavanone, a novel compound from the flowers of Erigeron annuus.
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Cytoprotection against hydrogen peroxide-induced cell death in cultured mouse mesangial cells by erigeroflavanone, a novel compound from the flowers of Erigeron annuus.

机译:Erigeroflavanone,一种来自黄rig花的新型化合物,对培养的小鼠系膜细胞中的过氧化氢诱导的细胞死亡具有细胞保护作用。

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摘要

Hyperglycemia-induced oxidative stress has been suggested as a mechanism underlying diabetic complications. Oxidative stress triggers cell death in various cell types, including glomerular mesangial cells which play important roles in diabetic nephropathy. In the present study, we investigated the potential cytoprotective effect of erigeroflavanone, a novel flavanone derivative from the flowers of Erigeron annuus, in cultured mouse mesangial cells using hydrogen peroxide (H2O2) as an oxidative stress inducer. Our data show that hydrogen peroxide induced a decrease in cell viability that was attenuated by erigeroflavanone. Hydrogen peroxide treatment increased formation of dichlorofluorescein (DCF)-sensitive intracellular reactive oxygen species (ROS). This enhanced ROS formation was significantly reduced by pretreatment with erigeroflavanone in a dose-dependent manner. Hydrogen peroxide treatment also induced phosphorylation of the mitogen-activated protein kinases (MAPKs), c-Jun terminal kinase (JNK), extracellular-regulated kinase (ERK) and p38, and activated caspase-3. Pretreatment with erigeroflavanone inhibited hydrogen peroxide-induced activation of MAPKs and caspase-3. From these data we conclude that erigeroflavanone provides a protective effect against oxidative stress-induced cell death in mesangial cells that is associated with its antioxidant action and inhibition of MAPKs and caspase-3. These results suggest that erigeroflavanone has potential as a therapeutic agent in the treatment of renal diabetic complications.
机译:高血糖诱导的氧化应激已被认为是糖尿病并发症的潜在机制。氧化应激触发各种细胞类型的细胞死亡,包括在糖尿病性肾病中起重要作用的肾小球系膜细胞。在本研究中,我们研究了过氧化氢黄酮(H2O2)作为氧化应激诱导物对培养的小鼠系膜细胞中黄曲黄酮(一种来自黄rig花的新黄烷酮衍生物)的潜在细胞保护作用。我们的数据表明,过氧化氢诱导了细胞活力的降低,并被三氯乙黄酮减弱。过氧化氢处理增加了对二氯荧光素(DCF)敏感的细胞内活性氧(ROS)的形成。通过用依瑞黄烷酮预处理以剂量依赖性方式显着减少了这种增强的ROS形成。过氧化氢处理还诱导有丝分裂原激活的蛋白激酶(MAPK),c-Jun末端激酶(JNK),细胞外调节的激酶(ERK)和p38磷酸化,以及激活的caspase-3。 Erigeroflavanone预处理可抑制过氧化氢诱导的MAPKs和caspase-3活化。从这些数据中我们得出结论,乙三黄酮对肾小球系膜细胞的氧化应激诱导的细胞死亡具有保护作用,这与其抗氧化作用以及对MAPKs和caspase-3的抑制有关。这些结果表明,三黄酮黄酮具有作为治疗糖尿病糖尿病并发症的治疗剂的潜力。

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