Suppr超能文献

阿魏酸通过改变高脂肪饮食诱导的小鼠肠道微生物组成来改善肠道屏障功能。

Ferulic acid improves intestinal barrier function through altering gut microbiota composition in high-fat diet-induced mice.

机构信息

College of Food Science and Technology, Zhejiang University of Technology, Chaowang Road 18, Hangzhou, 310014, People's Republic of China.

Zhejiang Institute of Modern TCM and Natural Medicine Co., Ltd., Hangzhou, 310052, People's Republic of China.

出版信息

Eur J Nutr. 2022 Oct;61(7):3767-3783. doi: 10.1007/s00394-022-02927-7. Epub 2022 Jun 22.

Abstract

PURPOSE

A high-fat diet (HFD) induces gut microbiota (GM) disorders, leading to intestinal barrier dysfunction and inflammation. Ferulic acid (FA) has shown anti-obesity effects, e.g., reducing body weight and food intake. However, the mechanism linking the anti-obesity effects of FA and GM modulation remains obscure. The present study aimed to clarify the mechanism underlying the anti-obesity effects of FA and modulation of the GM.

METHODS

C57BL/6 J mice were fed by a low-fat diet (LFD) and HFD with or without FA at a dose of 100 mg/kg of body weight by oral gavage for 12 weeks. Using high-throughput sequencing, gas chromatography, real-time fluorescence quantitative PCR and immunohistochemical staining, the attenuation of obesity by FA were assessed via intestinal barrier integrity, inflammation, and the GM.

RESULTS

FA reduced weight gain, improved HFD-induced GM imbalance, significantly enhanced intestinal short-chain fatty acid (SCFA)-producing bacteria (e.g., Olsenella, Eisenbergiella, Dubosiella, Clostridiales_unclassified, and Faecalibaculum) along with SCFA accumulation and its receptors' expression, decreased endotoxin-producing bacteria or obesity-related bacterial genera, and serum endotoxin (lipopolysaccharides), and inhibited the colonic TLR4/NF-κB pathway. Thus, FA can mitigate colonic barrier dysfunction and intestinal inflammation, induce the production of SCFAs and inhibit endotoxins by modulating the GM.

CONCLUSION

These results indicate that enhancement of intestinal barrier by altering the GM may be an anti-obesity target of FA and that FA can be used as a functional compound with great developmental values.

摘要

目的

高脂肪饮食(HFD)可诱导肠道菌群(GM)紊乱,导致肠道屏障功能障碍和炎症。阿魏酸(FA)已显示出抗肥胖作用,例如降低体重和食物摄入。然而,FA 调节 GM 与抗肥胖作用之间的联系机制尚不清楚。本研究旨在阐明 FA 的抗肥胖作用及其对 GM 调节的作用机制。

方法

12 周内,通过口服灌胃,将 C57BL/6J 小鼠分别用低脂肪饮食(LFD)和高脂肪饮食(HFD)加或不加 100mg/kg 体重的 FA 喂养。采用高通量测序、气相色谱、实时荧光定量 PCR 和免疫组织化学染色,通过肠道屏障完整性、炎症和 GM 评估 FA 对肥胖的抑制作用。

结果

FA 降低了体重增加,改善了 HFD 诱导的 GM 失衡,显著增强了肠道短链脂肪酸(SCFA)产生菌(如 Olsenella、Eisenbergiella、Dubosiella、Clostridiales_unclassified 和 Faecalibaculum)以及 SCFA 积累和其受体表达,减少了内毒素产生菌或肥胖相关细菌属,以及血清内毒素(脂多糖),并抑制了结肠 TLR4/NF-κB 途径。因此,FA 可以减轻结肠屏障功能障碍和肠道炎症,通过调节 GM 来诱导 SCFAs 的产生并抑制内毒素。

结论

这些结果表明,通过改变 GM 增强肠道屏障可能是 FA 的抗肥胖作用靶点,FA 可用作具有巨大开发价值的功能性化合物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验