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Silkworm pupa oil attenuates acetaminophen‐induced acute liver injury by inhibiting oxidative stress‐mediated NF‐κB signaling

机译:蚕蛹油通过抑制氧化应激介导的NF-κB信号传导来衰减乙酰氨基酚诱导的急性肝损伤

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Acetaminophen (APAP) overdose causes severe hepatotoxicity and acute liver failure. The current study aims to investigate the protection effects of silkworm pupa oil (SPO) against acute hepatic injury in APAP‐exposed Kunming mice. Our results showed that the liver index and the levels of serum alanine transaminase (ALT) and aspartate transaminase (AST) in mice subjected to APAP treatment were decreased by SPO. Supplement of SPO also restored hepatic histopathological alterations induced by APAP. The APAP‐induced increase in proinflammatory cytokines, including TNF‐α, IL‐6, and IL‐12, was reversed by SPO, which was mediated by the reduction of nuclear factor (NF)‐κB p65 expression and the increase in the expression of IκB‐α in liver tissue. Moreover, SPO inhibited APAP‐triggered oxidative stress by decreasing MDA level and increasing the activities of SOD and GSH‐Px. Collectively, SPO attenuated hepatic injury induced by APAP, which attributed to the suppression of oxidative stress‐mediated NF‐κB signaling. Our findings suggest that SPO supplementation may be potential strategy against acute hepatic injury.
机译:乙酰氨基酚(APAP)过量导致严重的肝毒性和急性肝衰竭。目前的研究旨在探讨家蚕蛹油(SPO)对APAP暴露昆明小鼠急性肝损伤的保护效果。我们的研究结果表明,通过孢子减少了对APAP处理进行APAP处理的小鼠中血清丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)的肝脏指数和水平。 SPO的补充还恢复了APAP诱导的肝组织病理学改变。通过SPO反转的促炎细胞因子(包括TNF-α,IL-6和IL-12)的APAP诱导的促炎细胞因子增加,其被核因子(NF)-κBp65表达的减少和表达的增加介导肝组织IκB-α的影响。此外,SPO通过降低MDA水平并增加SOD和GSH-PX的活性来抑制APAP触发的氧化应激。通过APAP统计,SPO减毒肝损伤,其归因于抑制氧化应激介导的NF-κB信号传导。我们的研究结果表明,SPO补充可能是针对急性肝损伤的潜在策略。

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