Sarcolipin and uncoupling protein 1 play distinct roles in diet‐induced thermogenesis and do not compensate for one another
Objective It is well known that uncoupling protein 1 (UCP1) in brown adipose tissue plays an
important role in diet‐induced thermogenesis. In this study, whether sarcolipin (SLN), a
regulator of sarco/endoplasmic reticulum Ca2+‐ATPase pump in muscle, is also an
important player of diet‐induced thermogenesis was investigated, as well as whether loss of
SLN could be compensated by increased UCP1 expression and vice versa. Methods Age‐
and sex‐matched UCP1−/−, SLN−/−, and double knockout for both UCP1 and SLN mice …
important role in diet‐induced thermogenesis. In this study, whether sarcolipin (SLN), a
regulator of sarco/endoplasmic reticulum Ca2+‐ATPase pump in muscle, is also an
important player of diet‐induced thermogenesis was investigated, as well as whether loss of
SLN could be compensated by increased UCP1 expression and vice versa. Methods Age‐
and sex‐matched UCP1−/−, SLN−/−, and double knockout for both UCP1 and SLN mice …
Objective
It is well known that uncoupling protein 1 (UCP1) in brown adipose tissue plays an important role in diet‐induced thermogenesis. In this study, whether sarcolipin (SLN), a regulator of sarco/endoplasmic reticulum Ca2+‐ATPase pump in muscle, is also an important player of diet‐induced thermogenesis was investigated, as well as whether loss of SLN could be compensated by increased UCP1 expression and vice versa.
Methods
Age‐ and sex‐matched UCP1−/−, SLN−/−, and double knockout for both UCP1 and SLN mice maintained in C57Bl/6J background were challenged to high‐fat diet for 12 weeks and then analyzed for weight gain, alterations in serum metabolites, and changes in thermogenic protein expression.
Results
Loss of either SLN or UCP1 alone was sufficient to cause diet‐induced obesity. No compensatory upregulation of UCP1 in SLN−/− mice or vice versa was found. Paradoxically, loss of both mechanisms failed to exacerbate the obesity phenotype.
Conclusions
Data suggest that both SLN‐ and UCP1‐based adaptive thermogenic mechanisms were essential for achieving maximal diet‐induced thermogenesis. When both mechanisms were absent, less efficient thermogenic mechanisms were activated to counter energy imbalance.
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