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首页> 外文期刊>Environmental Science and Pollution Research >Alleviation of lead acetate-induced nephrotoxicity byMoringa oleiferaextract in rats: highlighting the antioxidant, anti-inflammatory, and anti-apoptotic activities
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Alleviation of lead acetate-induced nephrotoxicity byMoringa oleiferaextract in rats: highlighting the antioxidant, anti-inflammatory, and anti-apoptotic activities

机译:通过Mmoringa Oleiferaextact在大鼠中减轻铅醋酸铅诱导的肾毒性:突出抗氧化剂,抗炎和抗凋亡活动

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摘要

Lead (Pb) is an environmental toxicant; its consumption can induce renal deficits. In this study, we explored the possible protective efficiency ofMoringa oleiferaextract (MOE) against lead acetate (PbAc)-mediated reprotoxicity. Four experimental groups of seven rats each were used: control, PbAc, MOE, and MOE+PbAc groups. All groups were given their respective treatment for 4 weeks. PbAc impaired the oxidative/antioxidative balance in the renal tissue, as shown by the decreased antioxidant proteins (glutathione, glutathione reductase, glutathione peroxidase, catalase, and superoxide dismutase) and increased oxidants (lipid peroxidation and nitric oxide). Additionally, PbAc enhanced the progression of kidney inflammation by increasing tumor necrosis factor-alpha, interleukin-1 beta, and nuclear factor kappa B associated with upregulation of inducible nitric oxide synthase. Moreover, a dysregulation in the apoptotic-regulating proteins (Bax, caspase-3, and Bcl2) were recorded upon PbAc exposure. Remarkably, MOE oral administration restored redox homeostasis, suppressed the inflammatory and apoptotic responses in the kidney tissue. Our findings point out that MOE could be used as an alternative remedy to overcome the adverse effects of Pb exposure, which may be due to its potent antioxidant, anti-inflammatory, and anti-apoptotic effects.
机译:铅(PB)是一种环保毒性;它的消费可以诱导肾脏赤字。在这项研究中,我们探讨了Moversa OleiferaExtract(Moe)的可能的保护效率,对醋酸铅(PBAC)介导的再定毒性。使用七只大鼠的四组七组:对照,PBAC,MOE和MOE + PBAC组。所有群体都被赋予它们各自的治疗4周。 PBAC损害肾组织中的氧化/抗氧化平衡,如下降的抗氧化蛋白(谷胱甘肽,谷胱甘肽),谷胱甘肽过氧化物酶,过氧化氢酶和超氧化物歧化酶)和增加的氧化剂(脂质过氧化和一氧化氮)所示。此外,PBAC通过增加与诱导型一氧化氮合酶的上调相关的肿瘤坏死因子-α,白细胞介素-1β和核因子Kappa B来增强肾炎的进展。此外,在PBAC暴露时记录了凋亡调节蛋白(BAX,Caspase-3和BCl2)中的脱孔调节蛋白(Bax,Caspase-3和Bcl 2)。值得注意的是,Moe口服给药恢复了氧化还原稳态,抑制了肾组织中的炎症和凋亡反应。我们的调查结果指出,MOE可以用作替代补救措施,以克服PB暴露的不良反应,这可能是由于其有效的抗氧化,抗炎和抗凋亡效应。

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