Caffeine intake may modulate inflammation markers in trained rats

Nutrients. 2014 Apr 21;6(4):1678-90. doi: 10.3390/nu6041678.

Abstract

Caffeine is presented in many commercial products and has been proven to induce ergogenic effects in exercise, mainly related to redox status homeostasis, inflammation and oxidative stress-related adaptation mechanisms. However, most studies have mainly focused on muscle adaptations, and the role of caffeine in different tissues during exercise training has not been fully described. The aim of this study was therefore, to analyze the effects of chronic caffeine intake and exercise training on liver mitochondria functioning and plasma inflammation markers. Rats were divided into control, control/caffeine, exercise, and exercise/caffeine groups. Exercise groups underwent four weeks of swimming training and caffeine groups were supplemented with 6 mg/kg/day. Liver mitochondrial swelling and complex I activity, and plasma myeloperoxidase (MPO) and acetylcholinesterase (AChE) activities were measured. An anti-inflammatory effect of exercise was evidenced by reduced plasma MPO activity. Additionally, caffeine intake alone and combined with exercise decreased the plasma AChE and MPO activities. The per se anti-inflammatory effect of caffeine intake should be highlighted considering its widespread use as an ergogenic aid. Therefore, caffeine seems to interfere on exercise-induced adaptations and could also be used in different exercise-related health treatments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / blood
  • Animals
  • Biomarkers / blood*
  • Caffeine / pharmacology*
  • Inflammation / blood*
  • Inflammation / drug therapy
  • Male
  • Membrane Potentials
  • Mitochondria, Liver / drug effects*
  • Oxidative Stress / drug effects
  • Peroxidase / blood
  • Physical Conditioning, Animal / physiology*
  • Rats
  • Rats, Wistar
  • Reactive Oxygen Species

Substances

  • Biomarkers
  • Reactive Oxygen Species
  • Caffeine
  • Peroxidase
  • Acetylcholinesterase