Galactooligosaccharides ameliorate dietary advanced glycation end product-induced intestinal barrier damage in C57BL/6 mice by modulation of the intestinal microbiome

封堵器 阿克曼西亚 糖基化 粘蛋白 微生物群 粘液 杯状细胞 化学 免疫学 内科学 内分泌学 男科 生物 医学 紧密连接 生物化学 上皮 生物信息学 病理 糖尿病 乳酸菌 发酵 生态学
作者
Chenxi Nie,Xiaoqing Xie,Huicui Liu,Xiaojin Yuan,Qingyu Ma,Aobai Tu,Min Zhang,Zhifei Chen,Juxiu Li
出处
期刊:Food & Function [Royal Society of Chemistry]
卷期号:14 (2): 845-856 被引量:6
标识
DOI:10.1039/d2fo02959f
摘要

Advanced glycation end products (AGEs) are increasingly recognized as potentially pathogenic components of processed foods, and long-term consumption of dietary AGEs triggers disruption of the intestinal barrier integrity and increases the risk of chronic diseases. Galactooligosaccharides (GOS) as prebiotics can modulate the intestinal microbiota and improve the intestinal barrier integrity. In this study, we aimed to investigate whether GOS could ameliorate the intestinal barrier damage induced by AGEs. The results showed an increased number of goblet cells (AGEs vs. H-GOS, 133.4 vs. 174.7, p < 0.05) and neutral mucin area (PAS positive area, 7.29% vs. 10.05%, p < 0.05). Upregulated expressions of occludin and claudin-1 and improved intestinal barrier integrity were observed in the H-GOS group. Using 16S rRNA sequencing analysis, we found that GOS significantly reduced the high enrichment of Akkermansia (16.95% vs. 1.29%, p < 0.05) induced by dietary AGEs while increasing the content of short-chain fatty acids. Fecal microbiota transplantation (FMT) showed that AGE-induced damage to the intestinal mucus barrier was reversed in the H-GOS transplanted group. Collectively, GOS ameliorated dietary AGE-induced intestinal barrier damage by reversing the dysregulated state of the intestinal microbiota. Our study lays the foundation for further research on dietary guidelines for populations with high AGE diets.
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