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首页> 外文期刊>Environmental Science and Pollution Research >The protective efficacy of soursop fruit extract against hepatic injury associated with acetaminophen exposure is mediated through antioxidant, anti-inflammatory, and anti-apoptotic activities
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The protective efficacy of soursop fruit extract against hepatic injury associated with acetaminophen exposure is mediated through antioxidant, anti-inflammatory, and anti-apoptotic activities

机译:Soursop果提取物对肝损伤与对乙酰氨基酚暴露相关的肝损伤的保护效果通过抗氧化剂,抗炎和抗凋亡活性介导

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摘要

In the current report, we examined the potential beneficial role of soursop fruit extract (SSFE) on liver injury induced by a single paracetamol (APAP) overdose (2000mg/kg). Thirty-five Wistar albino rats were randomly divided into five groups as follows: control, SSFE, APAP, SSFE+APAP, and silymarin (SIL)+APAP. APAP intoxication was found to elevate alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, and total bilirubin levels. Moreover, it increased the levels of malondialdehyde, nitrites, and nitrates and depleted glutathione, superoxide dismutase, catalase, glutathione reductase, and glutathione peroxidase. APAP intoxication inactivated the nuclear factor erythroid 2-related factor 2 (Nrf2) defense pathway and upregulated the expression of heme oxygenase-1 (HO-1). APAP administration enhanced the activation of nuclear factor-kappa B (NF-B), the elevation of tumor necrosis factor-alpha and interleukin 1-beta levels, and the upregulation of inducible nitric oxide synthase mRNA expression. In addition, APAP activated the overexpression of Bax protein, increased release of cytochrome c, and the downregulation of Bcl-2 protein. Finally, APAP-induced overexpression of transforming growth factor-beta (TGF-) further suggested enhanced liver damage. On the other hand, SSFE pretreatment attenuated these biochemical, molecular, and histopathological alterations in the liver, which might be partially due to the regulation of hepatic Nrf2/HO-1 and downregulation of NF-B and TGF-.
机译:在目前的报告中,我们研究了Soursop水果提取物(SSFE)对由单对旁邻旁邻戊酰胺(APAP)过量(2000mg / kg)诱导的肝损伤的潜在有益作用。将35只Wistar白化大鼠随机分为五组,如下:对照,SSFE,APAP,SSFE + APAP和Silymarin(SIL)+ APAP。发现APAP中毒升高丙氨酸氨基转移酶,天冬氨酸氨基转移酶,碱性磷酸酶和总胆红素水平。此外,它增加了丙二醛,亚硝酸盐和硝酸盐和贫谷叶,超氧化物歧化酶,过氧化氢酶,谷胱甘肽还原酶和谷胱甘肽过氧化物酶的水平。 APAP中毒灭活了核因子红外2相关系数2(NRF2)防御途径,并上调血红素氧酶-1(HO-1)的表达。 APAP管理增强了核因子-Kappa(NF-B)的激活,肿瘤坏死因子-α和白细胞介素1-β水平的升高,以及诱导型一氧化氮合酶mRNA表达的上调。此外,APAP活化了Bax蛋白的过表达,增加了细胞色素C的释放,以及Bcl-2蛋白的下调。最后,APAP诱导的转化生长因子-β(TGF-)的过表达进一步提高了增强的肝损伤。另一方面,SSFE预处理衰减了肝脏中的这些生化,分子和组织病理学改变,这可能部分是由于肝NRF2 / HO-1的调节和NF-B和TGF的下调。

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