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Mitochondrial fission contributes to heat‐induced oxidative stress in skeletal muscle but not hyperthermia in mice

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Aims: We have previously demonstrated in vitro that heat‐induced skeletal muscle damage is associated with an increase in dynamin‐related protein 1 (Drp1)‐mediated mitochondrial fission and no change in mitochondrial fusion.… Click to show full abstract

Aims: We have previously demonstrated in vitro that heat‐induced skeletal muscle damage is associated with an increase in dynamin‐related protein 1 (Drp1)‐mediated mitochondrial fission and no change in mitochondrial fusion. In this study, we investigated the in vivo effects of mitochondrial fission inhibition on heat‐induced oxidative skeletal muscle injury and hyperthermic response in mice. Main methods: Core body temperatures of mice pre‐treated with vehicle or Mdivi‐1 were recorded by radio telemetry during heat exposure. Tissue samples were obtained immediately following heat exposure. Key findings: We found that heat exposure caused increased mitochondrial fragmentation and mitochondrial fission protein Drp1 expression, whereas had no effect on the mitochondrial fusion‐related proteins mitofusin 1, mitofusin 2 and OPA1 in mouse gastrocnemius muscles. Two groups of mice with a similar high level of heat‐induced hyperthermia were allowed to recover for at least one week and subsequently treated with Mdivi‐1 and vehicle, respectively. Neither Mdivi‐1 nor vehicle altered the hyperthermic responses of mice during heat exposure. However, Mdivi‐1 significantly reduced mitochondrial fragmentation and Drp1, reactive oxygen species levels and apoptotic responses in mouse gastrocnemius muscles following heat exposure compared with vehicle. Significance: These results suggest that Drp1‐mediated mitochondrial fission plays a role in heat‐induced oxidative stress in skeletal muscle, but not in hyperthermic response in mice.

Keywords: heat; skeletal muscle; heat induced; mitochondrial fission

Journal Title: Life Sciences
Year Published: 2018

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