Expression of Peroxisome Proliferator-Activated Receptor-γ1 and Peroxisome Proliferator-Activated Receptor-γ2 in Visceral and Subcutaneous Adipose Tissue of Obese Women
- Vittorio Giusti1,
- Chantal Verdumo1,
- Michel Suter2,
- Rolf Christian Gaillard3,
- Peter Burckhardt1 and
- Francois Pralong3
- 1Department of Internal Medicine, Diabetology and Metabolism Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland
- 2Department of Surgery, Diabetology and Metabolism Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland
- 3Division of Endocrinology, Diabetology and Metabolism Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland
- Address correspondence and reprint requests to Vittorio Giusti, MD, Department of Internal Medicine, Centre Hospitalier Universitaire, Vaudois, 1011 Lausanne, Switzerland. E-mail: vittorio.giusti{at}chuv.hospvd.ch
Abstract
Data regarding the expression of peroxisome proliferator-activated receptor (PPAR)-γ1 and PPAR-γ2 in human visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT) are conflicting. To clarify this issue, we studied 50 women who had a BMI >35 kg/m2 were undergoing gastric reduction surgery. Phenotyping included recording of anthropometric parameters and of a biological profile. Quantification of the expression of PPAR-γ1 and PPAR-γ2 in samples of VAT and SAT was performed by real-time RT-PCR. In both SAT and VAT, the level of expression of PPAR-γ2 were >20-fold that of PPAR-γ1 (P < 0.001 for both). However, only PPAR-γ1 was differentially expressed, its levels in SAT being 216 ± 34% those in VAT (P < 0.001). In a stepwise, multivariate regression analysis, the levels of PPAR-γ1 in both SAT and VAT were the major determinants of waist circumference (R2 = 21% for both; P < 0.01). Finally, leptin but not PPARs appeared as the single parameter explaining the largest part of the variability of BMI in our cohort of patients (R2 = 22%, P < 0.001). These results are consistent with the putative roles of PPAR-γ1 and PPAR-γ2 in carbohydrate metabolism and energy homeostasis, respectively. As such, they constitute an important step toward the identification of potential targets for novel therapeutic strategies in the fields of obesity.
- PPAR, peroxisome proliferator-activated receptor
- SAT, subcutaneous adipose tissue
- VAT, visceral adipose tissue
Footnotes
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- Accepted February 21, 2003.
- Received December 17, 2002.
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