Weight loss with exercise improves muscle architecture and progenitor cell populations compared with weight loss alone in mice with preneoplastic colorectal lesions

Appl Physiol Nutr Metab. 2021 Jul;46(7):837-845. doi: 10.1139/apnm-2020-0956. Epub 2021 Feb 12.

Abstract

Weight loss and exercise reduce colorectal cancer (CRC) risk in persons with obesity. Whether weight loss and exercise effect myofiber characteristics and muscle stem/progenitor cell populations in mice with preneoplastic colorectal lesions, a model of CRC risk, is unknown. To address this gap, male C57Bl/6J mice were fed a high-fat diet (HFD) to induce obesity or a control (CON) diet prior to azoxymethane injection to induce preneoplastic colorectal lesions. The HFD group was then randomized to weight loss conditions that included (1) switching to the CON diet only (HFD-SED) or switching to the CON diet with treadmill exercise training (HFD-EX). Average myofiber cross-sectional area was not different between groups. There were more smaller-sized fibres in HFD-EX (p < 0.05 vs. CON), and more fibrosis in HFD-SED (p < 0.05 vs. HFD-EX and CON). There was a trend for more committed (Pax7+MyoD+) myoblasts (p = 0.059) and more fibro-adipogenic progenitors in HFD-EX (p < 0.05 vs. CON). Additionally, the canonical pro-inflammatory marker p-NF-κB was markedly reduced in the interstitium of HFD-EX (p < 0.05 vs. CON and HFD-SED). Our findings suggest that in mice with preneoplastic colorectal lesions, HFD followed by weight loss with exercise reduces muscle fibrosis and results in a higher content of muscle stem/progenitor cells. Novelty: Exercise improves muscle architecture in mice with preneoplastic colorectal lesion Exercise increases fibro/adipogenic progenitors and reduces inflammatory signaling in mice with preneoplastic colorectal lesions.

Keywords: activité physique; adiposity; adiposité; cachexia; cachexie; cancer colorectal; cellules satellites; colorectal cancer; fibroadipogenic progenitors; fibrose; fibrosis; physical activity; progéniteurs fibroadipogéniques; satellite cells.

MeSH terms

  • Animals
  • Azoxymethane
  • Body Fat Distribution
  • Colorectal Neoplasms / physiopathology*
  • Colorectal Neoplasms / prevention & control
  • Diet, High-Fat
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Muscle, Skeletal / anatomy & histology*
  • Muscle, Skeletal / cytology*
  • NF-kappa B / metabolism
  • Obesity / etiology
  • Obesity / physiopathology
  • Physical Conditioning, Animal / physiology*
  • Precancerous Conditions / physiopathology*
  • Precancerous Conditions / prevention & control
  • Risk Factors
  • Satellite Cells, Skeletal Muscle / cytology
  • Stem Cells / physiology*
  • Weight Loss*

Substances

  • NF-kappa B
  • Azoxymethane