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高脂饮食破坏肠道微生物群-结肠细胞相互作用导致外周色氨酸-犬尿氨酸代谢失调。

High-fat diet-disturbed gut microbiota-colonocyte interactions contribute to dysregulating peripheral tryptophan-kynurenine metabolism.

机构信息

College of Veterinary Medicine, Northwest A&F University, Yangling, 712100, Shaanxi, China.

Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, Guangdong, China.

出版信息

Microbiome. 2023 Jul 19;11(1):154. doi: 10.1186/s40168-023-01606-x.

Abstract

BACKGROUND

Aberrant tryptophan (Trp)-kynurenine (Kyn) metabolism has been implicated in the pathogenesis of human disease. In particular, populations with long-term western-style diets are characterized by an excess of Kyn in the plasma. Host-gut microbiota interactions are dominated by diet and are essential for maintaining host metabolic homeostasis. However, the role of western diet-disturbed gut microbiota-colonocyte interactions in Trp metabolism remains to be elucidated.

RESULTS

Here, 4-week-old mice were fed with a high-fat diet (HFD), representing a typical western diet, for 4 weeks, and multi-omics approaches were adopted to determine the mechanism by which HFD disrupted gut microbiota-colonocyte interplay causing serum Trp-Kyn metabolism dysfunction. Our results showed that colonocyte-microbiota interactions dominated the peripheral Kyn pathway in HFD mice. Mechanistically, persistent HFD-impaired mitochondrial bioenergetics increased colonic epithelial oxygenation and caused metabolic reprogramming in colonites to support the expansion of Proteobacteria in the colon lumen. Phylum Proteobacteria-derived lipopolysaccharide (LPS) stimulated colonic immune responses to upregulate the indoleamine 2,3-dioxygenase 1 (IDO1)-mediated Kyn pathway, leading to Trp depletion and Kyn accumulation in the circulation, which was further confirmed by transplantation of Escherichia coli (E.coli) indicator strains and colonic IDO1 depletion. Butyrate supplementation promoted mitochondrial functions in colonocytes to remodel the gut microbiota in HFD mice, consequently ameliorating serum Kyn accumulation.

CONCLUSIONS

Our results highlighted that HFD disrupted the peripheral Kyn pathway in a gut microbiota-dependent manner and that the continuous homeostasis of gut bacteria-colonocytes interplay played a central role in the regulation of host peripheral Trp metabolism. Meanwhile, this study provided new insights into therapies against western diet-related metabolic disorders. Video Abstract.

摘要

背景

色氨酸(Trp)-犬尿氨酸(Kyn)代谢异常与人类疾病的发病机制有关。特别是,长期采用西方饮食的人群,其血浆中的 Kyn 含量过高。宿主-肠道微生物群相互作用受饮食影响,并对维持宿主代谢稳态至关重要。然而,西方饮食扰乱的肠道微生物群-结肠细胞相互作用在 Trp 代谢中的作用仍有待阐明。

结果

本研究中,4 周龄的小鼠接受高脂饮食(HFD)喂养 4 周,代表典型的西方饮食,采用多组学方法确定 HFD 破坏肠道微生物群-结肠细胞相互作用导致血清 Trp-Kyn 代谢功能障碍的机制。我们的研究结果表明,结肠细胞-微生物群相互作用主导 HFD 小鼠的外周 Kyn 途径。从机制上讲,持续的 HFD 损害线粒体生物能学增加结肠上皮的氧合作用,并导致结肠细胞的代谢重编程,以支持肠腔中变形菌的扩张。厚壁菌门来源的脂多糖(LPS)刺激结肠免疫反应,上调吲哚胺 2,3-双加氧酶 1(IDO1)介导的 Kyn 途径,导致循环中 Trp 耗竭和 Kyn 积累,这通过移植大肠杆菌(E.coli)指示株和结肠 IDO1 耗竭得到进一步证实。丁酸盐补充促进结肠细胞中线粒体功能,重塑 HFD 小鼠的肠道微生物群,从而改善血清 Kyn 积累。

结论

本研究结果强调,HFD 以依赖肠道微生物群的方式破坏外周 Kyn 途径,而肠道细菌-结肠细胞相互作用的持续稳态在调节宿主外周 Trp 代谢中起着核心作用。同时,本研究为针对西方饮食相关代谢紊乱的治疗提供了新的见解。视频摘要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6929/10355067/993105988445/40168_2023_1606_Fig1_HTML.jpg

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