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首页> 外文期刊>Inflammopharmacology >Ziziphus spina-christi leaf extract pretreatment inhibits liver and spleen injury in a mouse model of sepsis via anti-oxidant and anti-inflammatory effects
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Ziziphus spina-christi leaf extract pretreatment inhibits liver and spleen injury in a mouse model of sepsis via anti-oxidant and anti-inflammatory effects

机译:Ziziphus Spina-Christi Lead提取物预处理通过抗氧化剂和抗炎作用抑制肝脏小鼠模型中的肝脏和脾损伤

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摘要

Sepsis is a systemic response to infection that can result in acute hepatic and splenic damage. Ziziphus spina-christi (L.) is a wild tree used as a medicinal plant by ancient Egyptians. However, little is known about the mechanism underlying its effects on sepsis. The current study investigated the protective effects of a Z. spina-christi leaf extract (ZSCLE) on liver and spleen damage in a male C57BL/6 mouse model of sepsis, induced by cecal ligation and puncture (CLP). Prior to CLP, ZSCLE was administered daily for five consecutive days via oral gavage at doses of 100, 200, or 300 mg/kg. The mice were euthanized 9 h after CLP, and oxidative stress markers were measured (myeloperoxidase, lipid peroxidation, nitric oxide, and reduced glutathione). In addition, we investigated histological changes, anti-oxidant enzyme activities (superoxide dismutase, catalase, glutathione peroxidase, and glutathione reductase), cytokine levels, protein expression of nuclear factor-kappa B and inducible nitric oxide synthase (iNOS), and mRNA levels of mitogen-activated protein kinase (8, 9, and 14), iNOS, tumor necrosis factor-alpha, and interleukin-1 beta. Our results indicated that ZSCLE significantly and dose-dependently inhibited sepsis-induced liver and spleen injury. These results suggest that ZSCLE could provide a therapeutic agent for sepsis by inducing anti-inflammatory and anti-oxidant effects.
机译:败血症是对感染的系统反应,可能导致急性肝脾和脾损坏。 Ziziphus Spina-Christi(L.)是古埃及人用作药用植物的野生树。然而,关于其对败血症影响的机制很少。目前的研究研究了Z.Spina-Christi叶提取物(Zscle)对败血症雄性C57BL / 6小鼠模型中肝脏和脾损伤的保护作用,通过盲肠连接和穿刺(CLP)诱导。在CLP之前,每天通过100,200或300mg / kg的剂量连续5天每天施用Zscle。在CLP之后将小鼠安乐死,并测量氧化应激标记物(髓过氧化物酶,脂质过氧化,一氧化氮和降低的谷胱甘肽)。此外,我们研究了组织学变化,抗氧化酶活性(超氧化物歧化酶,过氧化氢酶,谷胱甘肽还原酶和谷胱甘肽),细胞因子水平,核因子-κB和诱导型一氧化氮合酶(Inos)的蛋白表达,和mRNA水平丝裂原激活蛋白激酶(8,9和14),InOS,肿瘤坏死因子-α和白细胞介素-1β。我们的结果表明,Zscle显着和剂量依赖性抑制败血症诱导的肝脏和脾损伤。这些结果表明,Zscle可以通过诱导抗炎和抗氧化效果来提供脓毒症的治疗剂。

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