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Am J Physiol Regul Integr Comp Physiol (July 15, 2004). doi:10.1152/ajpregu.00339.2004
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Submitted on May 25, 2004
Accepted on July 8, 2004

Actions of PPAR{gamma} agonism on adipose tissue remodeling, insulin sensitivity and lipemia in absence of glucocorticoids

Magalie Berthiaume1, Henrike Sell1, Josee Lalonde1, Yves Gelinas1, Andre Tchernof2, Denis Richard1, and Yves Deshaies1*

1 Department of Anatomy and Physiology, Laval University, Quebec, Quebec, Canada
2 CHUL Medical Research Center, Laval University, Quebec, Quebec, Canada

* To whom correspondence should be addressed. E-mail: yves.deshaies{at}phs.ulaval.ca.

Peroxisome proliferator-activated receptor {gamma} (PPAR{gamma}) agonists improve insulin sensitivity and lipemia partly through enhancing adipose tissue proliferation and capacity for lipid retention. The agonists also reduce local adipose glucocorticoid production, which may in turn contribute to their metabolic actions. This study assessed the effects of a PPAR{gamma} agonist in absence of glucocorticoids (adrenalectomy, ADX). Intact, ADX, and intact pair-fed (PF) rats were treated with the PPAR{gamma} agonist rosiglitazone (RSG) for 2 weeks. RSG increased inguinal (subcutaneous) white (50%) and brown adipose tissue (6-fold) weight, but not that of retroperitoneal (visceral) white adipose. ADX, but not PF, reduced fat accretion in both inguinal and retroperitoneal adipose depots, but did not affect brown adipose mass. RSG no longer increased inguinal weight in ADX and PF rats, but increased brown adipose mass, albeit less so than in intact rats. RSG increased cell proliferation in white (3-fold) and brown adipose (6-fold), as assessed microscopically and by total DNA, an effect that was attenuated but not abrogated by ADX. RSG reduced the expression of the glucocorticoid-activating enzyme 11{beta}HSD1 in all adipose depots. RSG improved insulin sensitivity (reduction in fasting insulin and HOMA-IR, both -50%) and triacylglycerolemia (-75%) regardless of the glucocorticoid status, these effects being fully additive to those of ADX and PF. In conclusion, RSG partially retained its ability to induce white and brown adipose cell proliferation and brown adipose fat accretion, and further improved insulin sensitivity and lipemia in ADX rats, such effects being therefore independent from the PPAR{gamma}-mediated modulation of glucocorticoids.




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