Key result
Three weeks of exercise training induced depot-specific adaptations in genes involved in mitochondrial activity, glucose metabolism, and fatty acid uptake and oxidation across 14 adipose tissue depots in mice.
Why the study?
Prior studies focused only on select adipose tissue depots accounting for ~50% of mouse adipose mass, leaving adaptations across all depots unknown.
Answers are grounded in this paper and cite their sources.
Comprehensive mapping of exercise effects across all 14 adipose depots in mice; extends prior limited analyses and leaves open human translation.
Exercise affects whole-body metabolism through adaptations to various tissues, including adipose tissue (AT). Recent studies investigated exercise-induced adaptations to AT, focusing on inguinal white adipose tissue (WAT), perigonadal WAT, and interscapular brown adipose tissue (iBAT). Although these AT depots play important roles in metabolism, they account for only ∼50% of the AT mass in a mouse. Here, we investigated the effects of 3 weeks of exercise training on all 14 AT depots. Exercise induced depot-specific effects in genes involved in mitochondrial activity, glucose metabolism, and fatty acid uptake and oxidation in each adipose tissue (AT) depot. These data demonstrate that exercise training results in unique responses in each AT depot; identifying the depot-specific adaptations to AT in response to exercise is essential to determine how AT contributes to the overall beneficial effect of exercise.
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Lehnig et al. (2019) studied this question. Exercise training was evaluated on Depot-specific effects in genes involved in mitochondrial activity, glucose metabolism, and fatty acid uptake and oxidation. Three weeks of exercise training induced depot-specific adaptations in genes involved in mitochondrial activity, glucose metabolism, and fatty acid uptake and oxidation across 14 adipose tissue depots in mice.
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