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衰老调节饮食血糖指数对小鼠肠道微生物组成的影响。

Aging Modulates the Effect of Dietary Glycemic Index on Gut Microbiota Composition in Mice.

机构信息

JM-USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, United States; Division of Biochemical and Molecular Nutrition, Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA, United States.

Division of Biochemical and Molecular Nutrition, Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA, United States; Department of Integrative Physiology, University of Colorado Boulder, Boulder, CO, United States.

出版信息

J Nutr. 2024 Sep;154(9):2852-2861. doi: 10.1016/j.tjnut.2024.07.014. Epub 2024 Jul 15.

Abstract

BACKGROUND

Gut microbiome composition profoundly impacts host physiology and is modulated by several environmental factors, most prominently diet. The composition of gut microbiota changes over the lifespan, particularly during the earliest and latest stages. However, we know less about diet-aging interactions on the gut microbiome. We previously showed that diets with different glycemic indices, based on the ratio of rapidly digested amylopectin to slowly digested amylose, led to altered composition of gut microbiota in male C57BL/6J mice.

OBJECTIVES

Here, we examined the role of aging in influencing dietary effects on gut microbiota composition and aimed to identify gut bacterial taxa that respond to diet and aging.

METHODS

We studied 3 age groups of male C57BL/6J wild-type mice: young (4 mo), middle-aged (13.5 mo), and old (22 mo), all fed either high glycemic (HG) or low glycemic (LG) diets matched for caloric content and macronutrient composition. Fecal microbiome composition was determined by 16S rDNA metagenomic sequencing and was evaluated for changes in α- and β-diversity and bacterial taxa that change by age, diet, or both.

RESULTS

Young mice displayed lower α-diversity scores than middle-aged counterparts but exhibited more pronounced differences in β-diversity between diets. In contrast, old mice had slightly lower α-diversity scores than middle-aged mice, with significantly higher β-diversity distances. Within-group variance was lowest in young, LG-fed mice and highest in old, HG-fed mice. Differential abundance analysis revealed taxa associated with both aging and diet. Most differential taxa demonstrated significant interactions between diet and aging. Notably, several members of the Lachnospiraceae family increased with aging and HG diet, whereas taxa from the Bacteroides_H genus increased with the LG diet. Akkermansia muciniphila decreased with aging.

CONCLUSIONS

These findings illustrate the complex interplay between diet and aging in shaping the gut microbiota, potentially contributing to age-related disease.

摘要

背景

肠道微生物组的组成对宿主生理学有深远影响,并受到多种环境因素的调节,其中最主要的是饮食。肠道微生物组的组成会随时间而变化,尤其是在生命的最早和最晚阶段。然而,我们对饮食与衰老对肠道微生物组的相互作用知之甚少。我们之前的研究表明,基于快速消化的支链淀粉与缓慢消化的直链淀粉的比例,不同血糖指数的饮食会导致雄性 C57BL/6J 小鼠肠道微生物组组成发生改变。

目的

本研究旨在探究衰老在影响饮食对肠道微生物组组成的影响中的作用,并确定对饮食和衰老有反应的肠道细菌分类群。

方法

我们研究了 3 组雄性 C57BL/6J 野生型小鼠:年轻(4 个月)、中年(13.5 个月)和老年(22 个月),它们均喂食高血糖(HG)或低血糖(LG)饮食,这些饮食的热量和宏量营养素组成相匹配。通过 16S rDNA 宏基因组测序确定粪便微生物组组成,并评估 α-多样性和β-多样性的变化,以及因年龄、饮食或两者兼而有之而发生变化的细菌分类群。

结果

年轻小鼠的α-多样性评分低于中年小鼠,但饮食之间的β-多样性差异更为明显。相反,老年小鼠的α-多样性评分略低于中年小鼠,但β-多样性距离显著增加。在年轻、LG 喂养的小鼠中,组内变异最低,而在年老、HG 喂养的小鼠中,组内变异最高。差异丰度分析揭示了与衰老和饮食均相关的分类群。大多数差异分类群表现出饮食和衰老之间的显著相互作用。值得注意的是,几个lachnospiraceae 家族的成员随着衰老和 HG 饮食而增加,而属 Bacteroides_H 的分类群随着 LG 饮食而增加。 Akkermansia muciniphila 随着衰老而减少。

结论

这些发现说明了饮食和衰老在塑造肠道微生物组方面的复杂相互作用,这可能导致与年龄相关的疾病。

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