Berberine alleviates intestinal barrier dysfunction in glucolipid metabolism disorder hamsters by modulating gut microbiota and gut‐microbiota‐related tryptophan metabolites

肠道菌群 新陈代谢 小檗碱 化学 势垒函数 生物化学 生物 内分泌学 细胞生物学
作者
Yuting Chen,Zhangsen Hao,Han Zhao,Xiaofeng Duan,Dongsheng Jia,Kaipeng Li,Yuxin Yang,Hongjuan Cui,Mingming Gao,Ding Zhao
出处
期刊:Journal of the Science of Food and Agriculture [Wiley]
卷期号:103 (3): 1464-1473 被引量:23
标识
DOI:10.1002/jsfa.12242
摘要

Abstract BACKGROUND Barberry plants can be considered as useful additives and functional compounds in various industries, especially in the food industry. Berberine (BBR), the most important functional compound in the barberry roots, has recently been used to treat obesity, diabetes, and atherosclerosis. Gut microbiota and the intestinal barrier play an important role in the development of glucolipid metabolism disorders (GLMDs). However, the association of gut microbiota metabolism disorder and the intestinal barrier dysfunction effect of BBR in GLMDs remains elusive. RESULTS The results showed that administration of BBR could increase the number of colonic glands and goblet cell mucus secretion, improve the intestinal barrier function, and reduce the serum glycolipid level in GLMD hamsters. Interestingly, BBR was metabolized into 12 metabolites by gut microbiota, and the main metabolic pathways were oxidation, demethylation, and hydrogenation. In addition, BBR significantly improved the species diversity and uniformity of gut microbiota and promoted the proliferation of beneficial microbiota. Furthermore, the levels of tryptophan metabolites, such as indole, indole‐3‐acetamide, indole‐3‐acetaldehyde, indole‐3‐pyruvic acid, and indole‐3‐acetic acid were significantly altered by BBR. Both the intestinal tight junction proteins and intestinal immune factors were altered by BBR. CONCLUSION BBR could alleviate intestinal barrier dysfunction of GLMDs by modulating gut microbiota and gut‐microbiota‐related tryptophan metabolites, which may be one of the pharmacological mechanisms for the treatment of GLMDs. © 2022 Society of Chemical Industry.
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