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Voluntary exercise fails to prevent metabolic dysfunction-associated steatotic liver disease progression in male rats fed a high-fat high-cholesterol diet

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posted on 2024-04-18, 14:24 authored by Clément Besqueut-Rougerie, Vivien Chavanelle, Arnaud Michaux, Yolanda Otero, Pascal Sirvent, James KingJames King, Gael Ennequin

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a major public health issue with a worldwide prevalence of 30%–32%. In animal models, voluntary exercise may be an alternative to forced physical activity, avoiding stress, potential injuries, and being logistically simpler. Here, we assessed voluntary exercise (Vex) in Sprague–Dawley rats fed a high-fat, high-cholesterol diet for 18 weeks to induce MASLD. We quantified workload (speed and distance) using exercise wheels and evaluated energy expenditure using calorimetric cages. MASLD progression was assessed using circulating and hepatic biochemical and gene markers of steatosis, inflammation, and fibrosis. The animals ran an average of 301 km during the study period, with the average daily distance peaking at 4937 m/day during Weeks 3–4 before decreasing to 757 m/day by the end of the study. Rats exposed to Vex showed no improvement in any of the MASLD-associated features, such as steatosis, inflammation, or fibrosis. Rats exposed to Vex exhibited a higher total energy expenditure during the night phase (+0.35 kcal/h; p = 0.003) without resulting in any effect on body composition. We conclude that, in our experimental conditions, Vex failed to prevent MASLD progression in male Sprague–Dawley rats exposed to a high-fat high-cholesterol diet for 18 weeks.

Funding

Agence Nationale de la Recherche (ANR). Grant Number: 21-PRRD-0009-01

History

School

  • Sport, Exercise and Health Sciences

Published in

Physiological Reports

Volume

12

Issue

8

Publisher

Wiley Periodicals LLC

Version

  • VoR (Version of Record)

Rights holder

© The Authors

Publisher statement

This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

Acceptance date

2024-03-20

Publication date

2024-04-16

Copyright date

2024

ISSN

2051-817X

eISSN

2051-817X

Language

  • en

Depositor

Dr James King. Deposit date: 21 March 2024

Article number

e15993

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