Comparison of changes in markers of muscle damage induced by eccentric exercise and ischemia/reperfusion

Scand J Med Sci Sports. 2010 Oct;20(5):748-56. doi: 10.1111/j.1600-0838.2009.01015.x.

Abstract

To examine the effects of eccentric exercise (EE) and ischemia/reperfusion (I/R) on the markers of muscle damage, 72 rats were randomly assigned to the EE group, I/R group and control group (C), respectively. The rats in EE ran downhill on a treadmill with a 16 ° inclination at a constant speed for 90 min, and the rats in the I/R group underwent 90 min of four-limb ischemia, followed by 24, 48 and 72 h of reperfusion. Blood and tissue samples were collected immediately, 24, 48 and 72 h after exercise or reperfusion. Quantitative analyses showed that the I/R group had a significantly larger mitochondrial volume at 24 h after reperfusion compared with the C, and there were more disrupted Z-lines in the EE group and more disrupted mitochondria in the I/R group at 24 h after exercise or reperfusion. When compared with the C, a significantly lower total antioxidant capacity and higher interleukin-6 value were observed after exercise or reperfusion. Our data suggest that although EE and I/R result in some similar changes in the muscle damage markers, there are still some differences. The EE- and I/R-induced muscle damage may be due to different mechanisms.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Biomarkers / metabolism*
  • Creatine Kinase / blood
  • Creatine Kinase, MM Form / blood
  • Female
  • Interleukin-6 / blood
  • L-Lactate Dehydrogenase / blood
  • Mitochondria, Muscle / ultrastructure*
  • Muscles / injuries*
  • Muscles / metabolism
  • Muscles / ultrastructure
  • Oxidative Stress
  • Physical Conditioning, Animal / adverse effects*
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury / metabolism*
  • Reperfusion Injury / pathology*
  • Superoxide Dismutase / blood

Substances

  • Biomarkers
  • Interleukin-6
  • L-Lactate Dehydrogenase
  • Superoxide Dismutase
  • Creatine Kinase
  • Creatine Kinase, MM Form