Influence of endurance exercise training on antioxidant enzymes, tight junction proteins, and inflammatory markers in the rat ileum

BMC Res Notes. 2015 Sep 30:8:514. doi: 10.1186/s13104-015-1500-6.

Abstract

Background: This study investigated the effects of endurance exercise training on ileum antioxidant status, as well as tight junction, inflammatory, and nutrient transporter gene expression.

Methods: Sprague-Dawley rats (4 month old) were assigned to sedentary (SED) or endurance exercise-training (EXE) groups (n = 8/group). EXE animals were trained on the treadmill for 10 days at a speed of 30 m/min at 0° incline for 60 min/day. SED and EXE animals were sacrificed (24 h after the final training bout) and the ileum was stored for analyses.

Results: The ileum of EXE had higher (p < 0.05) antioxidant protein levels of manganese superoxide dismutase and catalase compared to SED with no change (p > 0.05) in the lipid peroxidation biomarker 4-hydroxynonenal. Ileum mRNA expression of the tight junction gene zonulin increased (p < 0.05) and claudin 1 decreased (p < 0.05) in EXE compared to SED, but occludin and zonula occluden 1 were not different (p > 0.05) between SED and EXE. The ileum mRNA expressions of seven nutrient transporters (SLC5A8, SLC7A6, SLC6A19, SLC7A7, SLC27A2, SLC16A10, and SLC15A1) were not different between the two groups (p > 0.05). EXE had lower ileum TNFα mRNA expression (p < 0.05) compared to SED. No changes (p > 0.05) were found in the other inflammatory mRNAs including NFκB, IFNγ, IL6, CCL2, TLR4, and IL10. In addition, no changes in p-p65:p65 were detected.

Conclusions: These findings suggest that 10 days of endurance exercise training up-regulates key endogenous antioxidant enzymes, decreases select inflammation markers, and alters select markers of tight junction permeability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / metabolism
  • Amino Acid Transport Systems, Neutral / genetics
  • Amino Acid Transport Systems, Neutral / metabolism
  • Animals
  • Antioxidants / metabolism*
  • Catalase / genetics*
  • Catalase / metabolism
  • Chemotactic Factors / genetics
  • Chemotactic Factors / metabolism
  • Cholera Toxin / genetics
  • Cholera Toxin / metabolism
  • Claudin-1 / genetics
  • Claudin-1 / metabolism
  • Gene Expression Regulation
  • Haptoglobins
  • Ileum / metabolism*
  • Lipid Peroxidation
  • Male
  • Monocarboxylic Acid Transporters / genetics
  • Monocarboxylic Acid Transporters / metabolism
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Occludin / genetics
  • Occludin / metabolism
  • Oxidative Stress
  • Physical Conditioning, Animal*
  • Physical Endurance / genetics*
  • Protein Precursors
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Superoxide Dismutase / genetics*
  • Superoxide Dismutase / metabolism
  • Symporters / genetics
  • Symporters / metabolism
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism
  • Zonula Occludens-1 Protein / genetics
  • Zonula Occludens-1 Protein / metabolism

Substances

  • Aldehydes
  • Amino Acid Transport Systems, Neutral
  • Antioxidants
  • Chemotactic Factors
  • Claudin-1
  • Cldn1 protein, rat
  • Haptoglobins
  • Monocarboxylic Acid Transporters
  • NF-kappa B
  • Occludin
  • Ocln protein, rat
  • Protein Precursors
  • RNA, Messenger
  • Symporters
  • Tumor Necrosis Factor-alpha
  • Zonula Occludens-1 Protein
  • zonulin
  • Cholera Toxin
  • Catalase
  • Superoxide Dismutase
  • 4-hydroxy-2-nonenal