Mitochondria play a key role in (and are modulated by) exercise physiology, response to hypoxia and to cellular damage. Consequently, hypobaric hypoxia and exercise could play an important role in muscle damage and recovery through mitochondrial regulation. PURPOSE: To analyze the mitochondrial biogenesis and dynamics in eccentric-exercise induced muscle damage (EEIMD) and its recovery with intermittent hypobaric hypoxia (IHH), alone or combined with light exercise. METHODS: Muscle injury was induced by downhill running to forty-eight Sprague-Dawley trained rats. They were divided into three groups: (1) Ctrl (passive recovery); (2) HYP (exposed to IHH: 4-hour session per day, at 4,000 m); and (3) EHYP (IHH + light aerobic exercise). Each group was analyzed 1, 3, 7 and 14 days after the muscle damage. The following proteins were determined by Western Blotting: PGC-1α, TFAM, TOM20 (proteins related to biogenesis), Mfn1, OPA-1 and DRP-1 (proteins related to mitochondrial fusion and fission) and Sirt3 (protein related to biogenesis and oxidative stress). All results were normalised to the Ctrl group. RESULTS: 7 days after the damage induction, both HYP and EHYP groups showed significant increased levels of biogenesis markers PGC-1α (161 and 159%, respectively) and TOM20 (156 and 147%) compared with the Ctrl group, while only EHYP had a significant increase of TFAM. At t14 only EHYP rats had increased levels of PGC-1α (128%), but both HYP and EHYP groups showed increased TFAM (153 and 155%) and TOM20 (145 and 144%). Sirt3 was significantly increased in HYP t03 (200%) and in the EHYP group at t07 (127%). Regarding to the mitochondrial fusion proteins, HYP and EHYP rats had increased levels of OPA-1 at t07 (171% both) and t14 (136 and 128%), while Mfn1 was only increased at t14 in EHYP (158%). On the other hand, DRP-1 appeared elevated in HYP t07 (133%) and EHYP t14 (162%) groups. These differences had a p-value <0.05. CONCLUSIONS: after an EEIMD protocol, IHH exposure increased mitochondrial biogenesis and dynamics, as well as Sirt3 protein. When combined with light aerobic exercise, these increments were more consistent and took place in a later stage of the recovery. Taking into account the important role of the mitochondria in the muscle cell, the results suggest that these protocols can improve the muscle damage recovery.
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