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芦荟多糖对小鼠慢性酒精性肝毒性的肝保护潜力。

Hepatoprotective potential of Aloe vera polysaccharides against chronic alcohol-induced hepatotoxicity in mice.

作者信息

Cui Yan, Ye Qing, Wang Heya, Li Yingchao, Yao Weirong, Qian He

机构信息

State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi, 214122, Jiangsu, China.

出版信息

J Sci Food Agric. 2014 Jul;94(9):1764-71. doi: 10.1002/jsfa.6489. Epub 2014 Jan 2.

Abstract

BACKGROUND

Aloe vera polysaccharides are reported to exhibit multiple biological effects, including anti-oxidation, anti-inflammation and immune enhancement. However, their influence on alcoholic liver disease (ALD) remains unclear. This study was designed to determine the protective effect of extracted A. vera polysaccharides (AVGP) against ALD in a chronic alcohol-feeding mouse model and investigate the possible underlying mechanisms.

RESULTS

Supplementation of AVGP significantly attenuated the levels of serum aminotransferases, lipids and hepatic TG and ameliorated histopathological alterations in the model of ALD. Interestingly, AVGP markedly up-regulated hepatic expression of lipolytic genes (AMPK-α2 and PPAR-α) but had no effect on lipogenic gene expression. AVGP diminished alcohol-dependent oxidative stress partly through a decrease in MDA and increase in GSH and SOD. Alcohol-induced inflammation was also mitigated by AVGP treatment via significant reduction in LPS and TNF-α, down-regulation of TLR-4 and MyD88 and up-regulation of IκB-α.

CONCLUSION

This study clearly showed that AVGP exerts a potent protective effect against chronic alcohol-induced liver injury. Its hepatoprotective effect appears to be associated with its antioxidant capacity and its ability to accelerate lipolysis and inhibit inflammatory response. The results indicate that AVGP could be considered as a potent food supplement in the prevention of ALD.

摘要

背景

据报道,芦荟多糖具有多种生物学效应,包括抗氧化、抗炎和免疫增强作用。然而,它们对酒精性肝病(ALD)的影响仍不清楚。本研究旨在确定提取的芦荟多糖(AVGP)在慢性酒精喂养小鼠模型中对ALD的保护作用,并探讨可能的潜在机制。

结果

补充AVGP可显著降低血清转氨酶、脂质和肝脏甘油三酯水平,并改善ALD模型中的组织病理学改变。有趣的是,AVGP显著上调了肝脏中脂解基因(AMPK-α2和PPAR-α)的表达,但对脂肪生成基因的表达没有影响。AVGP部分通过降低丙二醛(MDA)水平、增加谷胱甘肽(GSH)和超氧化物歧化酶(SOD)来减轻酒精依赖的氧化应激。AVGP治疗还通过显著降低脂多糖(LPS)和肿瘤坏死因子-α(TNF-α)水平、下调Toll样受体4(TLR-4)和髓样分化因子88(MyD88)以及上调核因子κB抑制蛋白α(IκB-α)来减轻酒精诱导的炎症。

结论

本研究清楚地表明,AVGP对慢性酒精诱导的肝损伤具有强大的保护作用。其肝脏保护作用似乎与其抗氧化能力以及加速脂肪分解和抑制炎症反应的能力有关。结果表明,AVGP可被视为预防ALD的一种有效食品补充剂。

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