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小鼠肠道微生物组和宿主血清代谢组的年龄依赖性重塑。

Age-dependent remodeling of gut microbiome and host serum metabolome in mice.

机构信息

Department of Nutrition, Texas A&M University, College Station, TX 77843, USA.

USDA/ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Aging (Albany NY). 2021 Feb 17;13(5):6330-6345. doi: 10.18632/aging.202525.

DOI:10.18632/aging.202525
PMID:33612480
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7993679/
Abstract

The interplay between microbiota and host metabolism plays an important role in health. Here, we examined the relationship between age, gut microbiome and host serum metabolites in male C57BL/6J mice. Fecal microbiome analysis of 3, 6, 18, and 28 months (M) old mice showed that the / ratio was highest in the 6M group; the decrease of in the older age groups suggests a reduced capacity of gut microflora to harvest energy from food. We found age-dependent increase in , which may lead to altered mucus structure more susceptible to bacteria penetration and ultimately increased intestinal inflammation. Metabolomic profiling of polar serum metabolites at fed state in 3, 12, 18 and 28M mice revealed age-associated changes in metabolic cascades involved in tryptophan, purine, amino acids, and nicotinamide metabolism. Correlation analyses showed that nicotinamide decreased with age, while allantoin and guanosine, metabolites in purine metabolism, increased with age. Notably, tryptophan and its microbially derived compounds indole and indole-3-lactic acid significantly decreased with age, while kynurenine increased with age. Together, these results suggest a significant interplay between bacterial and host metabolism, and gut dysbiosis and altered microbial metabolism contribute to aging.

摘要

微生物群与宿主代谢之间的相互作用在健康中起着重要作用。在这里,我们研究了雄性 C57BL/6J 小鼠的年龄、肠道微生物群和宿主血清代谢物之间的关系。对 3、6、18 和 28 个月(M)龄小鼠的粪便微生物组分析表明,6M 组的 / 比值最高;在年龄较大的组中, 的减少表明肠道微生物群从食物中获取能量的能力降低。我们发现, 随年龄增长而增加,这可能导致粘液结构发生改变,更容易被细菌穿透,最终导致肠道炎症增加。在 3、12、18 和 28M 小鼠的进食状态下对极性血清代谢物进行代谢组学分析,揭示了参与色氨酸、嘌呤、氨基酸和烟酰胺代谢的代谢级联的年龄相关变化。相关性分析表明,烟酰胺随年龄增长而减少,而嘌呤代谢产物尿囊素和鸟苷随年龄增长而增加。值得注意的是,色氨酸及其微生物衍生化合物吲哚和吲哚-3-乳酸随年龄显著减少,而犬尿氨酸随年龄增加。总之,这些结果表明细菌和宿主代谢之间存在显著的相互作用,肠道菌群失调和微生物代谢改变导致衰老。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ec/7993679/b73ffa9326c5/aging-13-202525-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ec/7993679/4506b7e87e8b/aging-13-202525-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ec/7993679/44c5514a1ffe/aging-13-202525-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ec/7993679/1401c3ab291c/aging-13-202525-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ec/7993679/6f1cc9c74efa/aging-13-202525-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ec/7993679/b73ffa9326c5/aging-13-202525-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ec/7993679/4506b7e87e8b/aging-13-202525-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ec/7993679/44c5514a1ffe/aging-13-202525-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ec/7993679/1401c3ab291c/aging-13-202525-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ec/7993679/6f1cc9c74efa/aging-13-202525-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ec/7993679/b73ffa9326c5/aging-13-202525-g005.jpg

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