首页> 美国卫生研究院文献>Acta Pharmaceutica Sinica. B >Schisandra sphenanthera extract (Wuzhi Tablet) protects against chronic-binge and acute alcohol-induced liver injury by regulating the NRF2-ARE pathway in mice
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Schisandra sphenanthera extract (Wuzhi Tablet) protects against chronic-binge and acute alcohol-induced liver injury by regulating the NRF2-ARE pathway in mice

机译:五味子五味子提取物(五指片)可通过调节小鼠的NRF2-ARE途径来预防慢性糖和急性酒精引起的肝损伤

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摘要

Alcohol abuse leads to alcoholic liver disease and no effective therapy is currently available. Wuzhi Tablet (WZ), a preparation of extract from Schisandra sphenanthera that is a traditional hepato-protective herb, exerted a significant protective effect against acetaminophen-induced liver injury in our recent studies, but whether WZ can alleviate alcohol-induced toxicity remains unclear. This study aimed to investigate the contribution of WZ to alcohol-induced liver injury by using chronic-binge and acute models of alcohol feeding. The activities of ALT and AST in serum were assessed as well as the level of GSH and the activity of SOD in the liver. The expression of CYP2E1 and proteins in the NRF2-ARE signaling pathway including NRF2, GCLC, GCLM, HO-1 were measured, and the effect of WZ on NRF2 transcriptional activity was determined. We found that both models resulted in liver steatosis accompanied by increased transaminase activities, but that liver injury was significantly attenuated by WZ. WZ administration also inhibited CYP2E1 expression induced by alcohol, and elevated the level of GSH and the activity of SOD in the liver. Moreover, the NRF2-ARE signaling pathway was activated by WZ and the target genes were all upregulated. Furthermore, WZ significantly activated NRF2 transcriptional activity. Collectively, our study demonstrates that WZ protected against alcohol-induced liver injury by reducing oxidative stress and improving antioxidant defense, possibly by activating the NRF2-ARE pathway.
机译:酗酒会导致酒精性肝病,目前尚无有效的治疗方法。五味片(WZ)是五味子五味子的提取物,是一种传统的保护肝的草药,在我们的近期研究中对乙酰氨基酚引起的肝损伤具有显着的保护作用,但是WZ是否可以减轻酒精引起的毒性尚不清楚。本研究旨在通过慢性酒精摄入和急性饮酒模型研究WZ对酒精引起的肝损伤的贡献。评估血清中ALT和AST的活性以及肝脏中GSH的水平和SOD的活性。 CYP2E1和蛋白在NRF2-ARE信号通路(包括NRF2,GCLC,GCLM,HO-1)中的表达,测定了WZ对NRF2转录活性的影响。我们发现这两种模型均导致肝脏脂肪变性,并伴有转氨酶活性的增加,但是WZ明显减轻了肝脏的损伤。 WZ给药还抑制酒精诱导的CYP2E1表达,并提高肝脏中GSH的水平和SOD的活性。此外,NRF2-ARE信号转导途径被WZ激活,靶基因均被上调。此外,WZ显着激活NRF2转录活性。总体而言,我们的研究表明WZ可以通过减少氧化应激和改善抗氧化防御(可能是通过激活NRF2-ARE途径)来防止酒精引起的肝损伤。

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