Effects of exercise in a cold environment on gene expression for mitochondrial biogenesis and mitophagy

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Abstract

Cold exposure during cycling and recovery enhances PGC-1α transcription, but aspects of mitophagy and a more intense cold exposure without recovery occurring in the cold have not been explored. Purpose: Determine the expression of genes related to mitochondrial biogenesis and mitophagy following an acute cycling bout at a temperature below freezing compared to that of room temperature. Methods: Eleven male participants cycled at 65% Wmax for 1 h at −2 °C and 20 °C and then recovered at room temperature for 6 h. A muscle biopsy was taken from the vastus lateralis before exercise, 3 h, and 6 h post-exercise for gene expression analysis. Results: Exercising heart rate and skin temperature were lower in the cold (p < 0.001; p = 0.004), while core temperature was higher (p = 0.016). Temperature had no effect on gene expression (p > 0.05). BNIP3 and BNIP3L mRNA were not influenced by exercise (p = 0.329; p 0.233). PGC-1α and VEGF were higher after cycling (p < 0.001), but the extent of PGC-1α upregulation was reduced 6 h post-exercise (p 0.006). TFAM increased 6 h post-exercise (p = 0.001). NRF2, ERRα, PINK1, and PARK2 decreased 3 h post-exercise (p 0.035; p = 0.005; p = 0.002; p = 0.001), but this downregulation was diminished after 6 h of recovery (p = 0.017; p 0.006; p = 0.043; p = 0.047). NRF1 was marginally attenuated with exercise (p = 0.001). Conclusions: Exercise induced alterations in gene expression for mitochondrial biogenesis and mitophagy, but these effects were independent of temperature.

Original languageEnglish
Pages (from-to)47-53
Number of pages7
JournalCryobiology
Volume90
DOIs
StatePublished - Oct 2019

Funding

This work was supported by the National Institute of General Medical Sciences [ NIGMS P20GM103427 ], Nebraska IDeA Networks of Biomedical Research Excellence [INBRE] , and a Graduate Research and Creative Activity Grant. This work was supported by the National Institute of General Medical Sciences [NIGMS P20GM103427], Nebraska IDeA Networks of Biomedical Research Excellence [INBRE], and a Graduate Research and Creative Activity Grant.

Funder number
P20GM103427

    Keywords

    • Cycling
    • Human
    • PGC-1α
    • Skeletal muscle
    • Temperature
    • mRNA

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