多组学整合揭示白术少药汤治疗仔猪断奶应激的肠道菌群-胆汁酸串扰机制

IF 4.4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yuanyuan Wei, Chao Han, Zhuo Chen, Cuncai Wang, Mingjie Liu, Yimeng Fan, Jianyu Lv, Zhihui Hao
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引用次数: 0

摘要

腹泻在婴儿中很常见,尤其是2岁以下的儿童。顽固性或持续性婴儿腹泻通常与喂养不耐受和吸收不良有关,这对新生儿来说是致命的。本研究旨在探讨白术少药汤(BSD)对断奶仔猪肠道菌群及相关代谢物的调节作用,从而阐明白术少药汤缓解仔猪断奶应激的机制。将仔猪分为5组,每组分别给予对照组、枣虎散和BSD低、中、高剂量组,每组6头,连续用药14 d。为了确定与腹泻相关的生物标志物,研究人员比较了早期断奶仔猪(对照组)和1.28 g/kg BSD处理仔猪(中剂量BSD组)的微生物群落、功能和代谢物。我们的研究结果显示,中剂量BSD组仔猪的微生物组成、功能和代谢谱发生了显著变化,这与宿主腹泻状态密切相关。此外,与对照组相比,中剂量BSD组仔猪的碳水化合物代谢和生物合成、脂质和氨基酸代谢、聚糖活性和碳水化合物消化酶均出现下调。转录组分析强调了FoxO1/3转录因子在减轻断奶应激中的关键作用,特别是通过增加CD4+/CD8+ T细胞比例。我们的研究结果强调,BSD对断奶应激的治疗作用包括肠屏障恢复、脑肠肽表达的调节和回肠肥大细胞活性的降低。BSD对改善婴幼儿早期断奶腹泻有显著效果。其作用机制是通过提高肠道关键菌群lachnospirace_bacterium的丰度,影响肠道胆汁酸代谢物(如鹅脱氧胆酸、鹅脱氧胆酸)的变化,从而调节肠道黏膜免疫和肠脑肽,达到治疗断奶应激的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multi-Omics Integration Reveals Gut Microbiota-Bile Acid Crosstalk Underlying Baizhu Shaoyao Decoction's Therapeutic Efficacy in Weaning Stress of Piglets

Multi-Omics Integration Reveals Gut Microbiota-Bile Acid Crosstalk Underlying Baizhu Shaoyao Decoction's Therapeutic Efficacy in Weaning Stress of Piglets

Diarrhea is common in infants, particularly children less than 2 years old. Intractable or protracted infancy diarrhea is typically associated with feeding intolerance and malabsorption that is lethal for newborns. The objective of this study is to explore the regulatory effects of baizhu shaoyao decoction (BSD) on the gut microbiota and associated metabolites in weaned piglets, thereby elucidating the mechanism by which BSD mitigates weaning stress in piglets. Piglets were allocated into five groups, with each group receiving designated medication for a continuous 14-day period: control, zaohu powder, as well as low-, medium-, and high-dose BSD groups (n = 6 piglets per group). To identify diarrhea-related biomarkers, microbial communities, functions, and metabolites were compared between the early-weaned piglets (control group) and those treated with 1.28 g/kg BSD (medium-dose BSD group). Our findings revealed significant shifts in microbial composition, function, and metabolic profiles in piglets from the medium-dose BSD group, intricately associated with the host's diarrhea status. Furthermore, carbohydrate metabolism and biosynthesis, lipid and amino acid metabolism, glycan activity, and carbohydrate digestive enzymes exhibited downregulation in piglets of the medium-dose BSD group compared to those in the control group. Transcriptome analysis highlighted the pivotal role of the FoxO1/3 transcription factor in mitigating weaning stress, particularly through the augmentation of CD4+/CD8+ T cell proportions. Our findings underscored that therapeutic effects of BSD on weaning stress involve intestinal barrier restoration, modulation of brain–gut peptide expression, and a reduction in mast-cell activity in the ileum. BSD has a significant effect on improving early weaning diarrhea in infants. Its mechanism of action involves improving the abundance of key intestinal microbiota Lachnospiraceae_bacterium, affecting changes in intestinal bile acid metabolites (such as, chenodeoxyglycocholic acid, glycochenodeoxycholic acid) and thereby regulating intestinal mucosal immunity and gut-brain peptides, achieving the effect of treating weaning stress.

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来源期刊
The FASEB Journal
The FASEB Journal 生物-生化与分子生物学
CiteScore
9.20
自引率
2.10%
发文量
6243
审稿时长
3 months
期刊介绍: The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.
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