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高脂饮食诱导肥胖大鼠中大豆异黄酮对结肠免疫功能的改善作用。

Improvement of Colonic Immune Function with Soy Isoflavones in High-Fat Diet-Induced Obese Rats.

机构信息

Laboratory of Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, Sichuan, China.

Key Laboratory of Animal Disease and Human Health of Sichuan Province, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, Sichuan, China.

出版信息

Molecules. 2019 Mar 22;24(6):1139. doi: 10.3390/molecules24061139.

Abstract

: The damage to intestinal barrier function plays an important role in the development of obesity and associated diseases. Soy isoflavones are effective natural active components for controlling obesity and reducing the level of blood lipid. Here, we explored whether these effects of soy isoflavones were associated with the intestinal barrier function. : The obese rat models were established by high fat diet feeding. Then, those obese rats were supplemented with soy isoflavones at different doses for 4 weeks. Our results showed that obesity induced the expressions of pro-inflammatory cytokines, decreased the anti-inflammatory cytokine (IL-10) expression, elevated intestinal permeability, altered gut microbiota and exacerbated oxidative damages in colon. The administration of soy isoflavones reversed these changes in obese rats, presenting as the improvement of intestinal immune function and permeability, attenuation of oxidative damage, increase in the fraction of beneficial bacteria producing short-chain fatty acids and short-chain fatty acid production, and reduction in harmful bacteria. Furthermore, soy isoflavones blocked the expressions of TLR4 and NF-κB in the colons of the obese rats. : Soy isoflavones could improve obesity through the attenuation of intestinal oxidative stress, recovery of immune and mucosal barrier, as well as re-balance of intestinal gut microbiota.

摘要

肠道屏障功能损伤在肥胖及其相关疾病的发生发展中起着重要作用。大豆异黄酮是控制肥胖和降低血脂水平的有效天然活性成分。在这里,我们探讨了大豆异黄酮的这些作用是否与肠道屏障功能有关。

通过高脂饮食喂养建立肥胖大鼠模型。然后,用不同剂量的大豆异黄酮对肥胖大鼠进行补充,为期 4 周。结果表明,肥胖诱导促炎细胞因子的表达,降低抗炎细胞因子(IL-10)的表达,增加肠道通透性,改变肠道微生物群,并加重结肠的氧化损伤。大豆异黄酮可逆转肥胖大鼠的这些变化,表现为改善肠道免疫功能和通透性,减轻氧化损伤,增加产生短链脂肪酸的有益细菌的比例和短链脂肪酸的产生,减少有害细菌。此外,大豆异黄酮可阻断肥胖大鼠结肠中 TLR4 和 NF-κB 的表达。

大豆异黄酮可通过减轻肠道氧化应激、恢复免疫和黏膜屏障以及重新平衡肠道菌群来改善肥胖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a2a/6470843/abbf0f057c2e/molecules-24-01139-g001a.jpg

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