Muscles Susceptibility to Ischemia-Reperfusion Injuries Depends on Fiber Type Specific Antioxidant Level

作者：Charles Anne Laure; Guilbert Anne Sophie; Guillot Max; Talha Samy; Lejay Anne; Meyer Alain; Kindo Michel; Wolff Valerie; Bouitbir Jamal; Zoll Joffrey; Geny Bernard

来源：Frontiers in Physiology, 2017, 8: 52.

DOI：10.3389/fphys.2017.00052

• antioxidant
• ischemia-reperfusion
• metabolic phenotype
• mitochondria
• muscle
• sarcopenia
• oxidative stress
• peripheral arterial disease (PAD)

Muscle injury resulting from ischemia-reperfusion largely aggravates patient prognosis but whether and how muscle phenotype modulates ischemia-reperfusion-induced mitochondrial dysfunction remains to be investigated. We challenged the hypothesis that glycolytic muscles are more prone to ischemia-reperfusion-induced injury than oxidative skeletal muscles. We therefore determined simultaneously the effect of 3 h of ischemia induced by aortic clamping followed by 2 h of reperfusion (IR, n = 11) on both gastrocnemius and soleus muscles, as compared to control animals (C, n = 11). Further, we investigated whether tempol, an antioxidant mimicking superoxide dismutase, might compensate a reduced defense system, likely characterizing glycolytic muscles (IR-Tempol, n = 7). In the glycolytic gastrocnemius muscle, as compared to control, ischemia-reperfusion significantly decreased mitochondrial respiration (-30.28 +/- 6.16%, p = 0.003), increased reactive oxygen species production (+79.15 +/- 28.72%, p = 0.04), and decreased reduced glutathione (-28.19 +/- 6.80%, p = 0.011). Less deleterious effects were observed in the oxidative soleus muscle (-6.44 +/- 6.30%, +4.32 +/- 16.84%, and -8.07 +/- 10.84%, respectively), characterized by enhanced antioxidant defenses (0.63 +/- 0.05 in gastrocnemius vs. 1.24 +/- 0.08 mol L-1 g-1 in soleus). Further, when previously treated with tempol, glycolytic muscle was largely protected against the deleterious effects of ischemia-reperfusion. Thus, oxidative skeletal muscles are more protected than glycolytic ones against ischemia-reperfusion, thanks to their antioxidant pool. Such pivotal data support that susceptibility to ischemia-reperfusion-induced injury differs between organs, depending on their metabolic phenotypes. This suggests a need to adapt therapeutic strategies to the specific antioxidant power of the target organ to be protected.

• 出版日期2017-2-6