[HTML][HTML] Mitochondrial remodeling in adipose tissue associated with obesity and treatment with rosiglitazone

L Wilson-Fritch, S Nicoloro… - The Journal of …, 2004 - Am Soc Clin Investig
L Wilson-Fritch, S Nicoloro, M Chouinard, MA Lazar, PC Chui, J Leszyk, J Straubhaar…
The Journal of clinical investigation, 2004Am Soc Clin Investig
Adipose tissue plays a central role in the control of energy homeostasis through the storage
and turnover of triglycerides and through the secretion of factors that affect satiety and fuel
utilization. Agents that enhance insulin sensitivity, such as rosiglitazone, appear to exert
their therapeutic effect through adipose tissue, but the precise mechanisms of their actions
are unclear. Rosiglitazone changes the morphological features and protein profiles of
mitochondria in 3T3-L1 adipocytes. To examine the relevance of these effects in vivo, we …
Adipose tissue plays a central role in the control of energy homeostasis through the storage and turnover of triglycerides and through the secretion of factors that affect satiety and fuel utilization. Agents that enhance insulin sensitivity, such as rosiglitazone, appear to exert their therapeutic effect through adipose tissue, but the precise mechanisms of their actions are unclear. Rosiglitazone changes the morphological features and protein profiles of mitochondria in 3T3-L1 adipocytes. To examine the relevance of these effects in vivo, we studied white adipocytes from ob/ob mice during the development of obesity and after treatment with rosiglitazone. The levels of approximately 50% of gene transcripts encoding mitochondrial proteins were decreased with the onset of obesity. About half of those genes were upregulated after treatment with rosiglitazone, and this was accompanied by an increase in mitochondrial mass and changes in mitochondrial structure. Functionally, adipocytes from rosiglitazone-treated mice displayed markedly enhanced oxygen consumption and significantly increased palmitate oxidation. These data reveal mitochondrial remodeling and increased energy expenditure in white fat in response to rosiglitazone treatment in vivo and suggest that enhanced lipid utilization in this tissue may affect whole-body energy homeostasis and insulin sensitivity.
The Journal of Clinical Investigation