High intensity interval training promotes total and visceral fat mass loss in obese Zucker rats without modulating gut microbiota

PLoS One. 2019 Apr 9;14(4):e0214660. doi: 10.1371/journal.pone.0214660. eCollection 2019.

Abstract

Aims: Increased visceral adipose tissue and dysbiosis in the overweight and obese promote chronic inflammation. The aim of this study was to compare the effects of moderate-intensity continuous training (MICT) and high-intensity interval training (HIIT) on the gut-adipose tissue cross-talk in obese Zucker rats.

Methods: Obese male Zucker rats (n = 36) were divided in three groups: MICT (12m.min-1 for 51min), HIIT (6 sets at 18 m.min-1 for 4min followed by 3min at 10m.min-1) and controls (CONT; no exercise). The animals ran on a treadmill 5 days/week for 10 weeks. Body composition, glycaemic control, lipid profile, inflammation, lipolysis signalling in subcutaneous and visceral adipose tissue, intestinal permeability (tight junctions and plasma lipopolysaccharide binding protein; LBP), and gut microbiota composition were assessed in the three groups.

Results: After 10 weeks of exercise, total and epididymal fat mass decreased only in the HIIT group. The α/β adrenergic receptor RNA ratio in subcutaneous adipose tissue increased only in the HIIT group. The expression level of phosphorylated hormone-sensitive lipase was not modified by training. Both HIIT and MICT decreased inflammation (plasma myeloperoxidase and keratinocyte-derived chemokine secretion in adipose tissue) and improved glucose metabolism. Zonula occludens-1 and occludin were upregulated in the HIIT group. Plasma LBP was similarly reduced in both training groups. HIIT and MICT did not affect gut microbiota composition.

Conclusion: In obese Zucker rats, HIIT and MICT improved inflammation and glucose metabolism. In contrast, only HIIT decreased total and visceral fat mass. These adaptations were not associated with modifications in gut microbiota composition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins
  • Animals
  • Body Composition
  • Carrier Proteins / blood
  • Energy Metabolism
  • Gastrointestinal Microbiome
  • Gene Expression Regulation
  • Glucose / metabolism
  • Intra-Abdominal Fat / metabolism*
  • Male
  • Membrane Glycoproteins / blood
  • Occludin / genetics
  • Occludin / metabolism
  • Physical Conditioning, Animal*
  • Rats
  • Rats, Zucker
  • Receptors, Adrenergic, alpha / metabolism
  • Receptors, Adrenergic, beta / metabolism
  • Zonula Occludens-1 Protein / genetics
  • Zonula Occludens-1 Protein / metabolism

Substances

  • Acute-Phase Proteins
  • Carrier Proteins
  • Membrane Glycoproteins
  • Occludin
  • Receptors, Adrenergic, alpha
  • Receptors, Adrenergic, beta
  • Zonula Occludens-1 Protein
  • lipopolysaccharide-binding protein
  • Glucose

Grants and funding

This study was supported by the “Region Auvergne-Rhône-Alpes” (PREVAMIC project) and I-SITE project (CAP 2025). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.