南美超级胎牛血清999尝鲜特惠
转染试剂低至5折
基质胶阶梯特惠
积分商城,好礼送不停
南美超级胎牛血清999尝鲜特惠
转染试剂低至5折
基质胶阶梯特惠
积分商城,好礼送不停
分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

人乳低聚糖3'-唾液酸乳糖和乳-N-新四糖可通过重塑微生物组-代谢组网络,缓解自然衰老雄性小鼠的肠道功能衰退现象。

Human milk oligosaccharides 3′-sialyllactose and lacto-N-neotetraose ameliorate intestinal decline in naturally aged male mice in association with microbiome-metabolome reprogramming

Haichao Zhang, Fei Yao, Zhihong Lyu, Keqin Xie, Rui Ge, Xinru Zhao, Guocheng Wang, Zijin Yang, Hanxiao Zhang, Boyan Li, Yumei Qin, Jianzhong Han, Yanpei Gu

Journal:FOOD RESEARCH INTERNATIONAL

IF:8.8

DOI:10.1016/j.foodres.2026.120792

PMID:42914466

Published:2026-09-10

research field:分子生物学微生物组研究免疫学胃肠病学营养科学微生物学遗传学与基因组学食品生物活性成分

Abstract

Structurally distinct human milk oligosaccharides differentially regulate intestinal epithelial homeostasis in aged mice. • 3′-Sialyllactose and lacto- N -neotetraose exhibit superior effects on intestinal barrier function and intestinal stem cell function. • Gut microbiota is required for the beneficial effects of human milk oligosaccharides on intestinal epithelial homeostasis in aged mice. Intestinal epithelial homeostasis undergoes progressive functional decline during aging and contributes to systemic age-related dysfunction. Human milk oligosaccharides (HMOs) have well-documented prebiotic and immunomodulatory properties; however, their effects on the aging gut and functional differences among distinct structures remain largely unexplored. Here, we show that structurally distinct HMOs differentially regulate intestinal epithelial homeostasis in naturally aged male mice, with 3′-sialyllactose (3′-SL) and lacto- N -neotetraose (LNnT) showing broader effects than 2′-fucosyllactose (2′-FL). 3′-SL and LNnT supplementation improved barrier-related markers, including Muc2 and ZO-1, and attenuated age-associated epithelial hyperproliferation while maintaining intestinal stem cell (ISC)-related function. Antibiotic-mediated microbiota depletion markedly weakened these effects, supporting an important role of the gut microbiota. Multi-omics analyses further revealed distinct microbiome-metabolome alterations associated with 3′-SL and LNnT supplementation. Specifically, 3′-SL increased the relative abundance of Alistipes and was accompanied by higher levels of metabolites such as spermine. LNnT was associated with increased Allobaculum abundance and elevated acetylcholine levels in colonic contents. Collectively, our findings indicate that specific HMO structures ameliorate age-related decline of the intestinal epithelium in association with alterations in the microbiota–metabolite axis, providing a basis for further investigation of 3′-SL and LNnT as candidate die

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