AI Article Synopsis

  • Local cryotherapy is a prevalent method for treating sports-related muscle injuries, but its underlying molecular mechanisms are not well understood.
  • Research conducted through in vitro, ex vivo, and in vivo experiments showed that repeated cold stimulations significantly enhance the phosphorylation of CREB1 and recruitment of CREB-binding proteins, indicating an activation of specific pathways.
  • Additionally, the studies revealed that cold exposure upregulates genes related to mitochondrial function and biogenesis, suggesting that the frequency and duration of cryotherapy sessions play a crucial role in its effectiveness as a treatment strategy.

Article Abstract

Local cryotherapy is widely used as a treatment for sports-related skeletal muscle injuries. The molecular mechanisms are unknown. To clarify these mechanisms, we applied one to three 15-min cold stimulations at 4 °C to various cell lines (in vitro), the tibialis anterior (TA) muscle (ex vivo), and mouse limbs (in vivo). In the in vitro assay, cyclic AMP (cAMP) response element binding protein 1 (CREB1) was markedly phosphorylated (p-CREB1), and the CREB-binding protein (CBP) was recruited to p-CREB-1 in response to two or three cold stimulations. In a reporter assay with the cAMP-responsive element, the signals significantly increased after two to three cold stimulations at 4 °C. In the ex vivo study, CREB-targeting genes were significantly upregulated following two or three cold stimulations. The in vivo experiment disclosed that cold stimulation of a mouse limb for 9 days significantly increased mitochondrial DNA copy number and upregulated genes involved in mitochondrial biogenesis. The results suggest that local cryotherapy increases CREB transcription and upregulates CREB-targeting genes, in a manner dependent on cold stimulation frequency and duration. This information will inform further investigations into local cryotherapy as a treatment for sports-related skeletal muscle trauma.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370117PMC
http://dx.doi.org/10.3390/ijms21134588DOI Listing

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