Timing Matters: Late, but Not Early, Exercise Training Ameliorates MASLD in Part by Modulating the Gut‐Liver Axis in Mice

塞德 肠道菌群 毛螺菌科 医学 生理学 内科学 内分泌学 生物 免疫学 16S核糖体RNA 细菌 遗传学 厚壁菌
作者
Artemiy Kovynev,Zhixiong Ying,Sen Zhang,Elena Olgiati,Joost M. Lambooij,C. Visentin,Bruno Guigas,Quinten R. Ducarmon,Patrick C.N. Rensen,Milena Schönke
出处
期刊:Journal of Pineal Research [Wiley]
卷期号:76 (8) 被引量:1
标识
DOI:10.1111/jpi.70003
摘要

ABSTRACT Metabolic dysfunction‐associated steatotic liver disease (MASLD) affects two billion people worldwide and is currently mostly treatable via lifestyle interventions, such as exercise training. However, it is unclear whether the positive effects of exercise are restricted to unique circadian windows. We therefore aimed to study whether the timing of exercise training differentially modulates MASLD development. Twenty weeks old male APOE*3‐Leiden.CETP mice were fed a high fat‐high cholesterol diet to induce MASLD and treadmill‐trained for 1 h five times per week for 12 weeks either early (ZT13; E‐RUN) or late (ZT22; L ‐RUN) in the dark phase while corresponding sedentary groups (E‐SED and L‐SED) did not. Late, but not early exercise training decreased the MASLD score, body weight, fat mass, and liver triglycerides, accompanied by an altered composition of the gut microbiota. Specifically, only late exercise training increased the abundance of short‐chain fatty acid‐producing bacterial families and genera, such as Akkermansia, Lachnospiraceae , and Rikenella . To assess the role of the gut microbiota in training‐induced effects, the study was repeated and trained (ZT22 only, RUN) or sedentary mice (SED) served as fecal donors for sedentary recipient mice (RUN FMT and SED FMT). Fecal microbiota transplantation reduced liver weight and plasma triglycerides in RUN FMT compared to SED FMT and tended to lower the MASLD score and liver triglycerides. Timing of exercise training is a critical factor for the positive effect on MASLD in this preclinical model, and the effect of late exercise is partially mediated via the gut‐liver axis.
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