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This version published online on October 19, 2004
Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2004-0583
A more recent version of this article appeared on January 1, 2005
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Submitted on March 26, 2004
Accepted on October 10, 2004

Expression and activity of 20{alpha}-hydroxysteroid dehydrogenase (AKR1C1) in abdominal subcutaneous and omental adipose tissue in women

Sophie Blanchette, Karine Blouin, Christian Richard, Pierre Dupont, Van Luu-The, and André Tchernof*

Molecular Endocrinology and Oncology Research Center, Department of Nutrition, Gynecology Unit, Laval University Medical Center and Laval University

* To whom correspondence should be addressed.
André Tchernof, E-mail: andre.tchernof{at}crchul.ulaval.ca

We have examined the expression and activity of 20{alpha}-hydroxysteroid dehydrogenase (20{alpha}-HSD) in abdominal adipose tissue in women. This recently-characterized enzyme from the aldoketoreductase 1C family (AKR1C1) is responsible for the conversion of progesterone into 20{alpha}-hydroxyprogesterone. Abdominal sc (SC) and omental (OM) adipose tissue biopsies were obtained from a sample of 32 women aged 47.7 ± 5.9 yr (BMI: 27.6 ± 5.0 kg/m2) undergoing abdominal hysterectomies. Body composition and body fat distribution measurements were performed before the surgery by dual energy x-ray absorptiometry and computed tomography respectively. The expression of 20{alpha}-HSD was determined by real-time RT-PCR, and its activity was measured in whole tissue homogenates. Messenger RNA and activity of the enzyme were detected in both the SC and OM fat depots, the two measures being significantly higher in the SC compartment. Women characterized by a visceral adipose tissue area greater than or equal to 100 cm2 had an increased 20{alpha}-HSD conversion rate in their omental adipose tissue compared with women without visceral obesity (13.99 ± 2.07 vs. 7.92 ± 0.83 fmol/µG protein/24 h, P < 0.05). Accordingly, a positive correlation was found between omental adipose tissue 20{alpha}-HSD activity and computed tomography-measured visceral adipose tissue area (r=0.36, P < 0.05). Significant positive correlations were also found between omental 20{alpha}-HSD activity and omental adipocyte diameter (r=0.49, P < 0.05) and omental adipose tissue LPL activity (r=0.36, P = 0.06). In conclusion, 20{alpha}-HSD activity and mRNA were detected in SC and OM adipose tissue in women, and omental 20{alpha}-hydroxylation of progesterone was highest in women with visceral obesity. Further studies are required to establish whether local conversion of progesterone may impact on the metabolism and function of adipocytes located within the abdominal cavity.


Key words: women • abdominal obesity • omental adipose tissue • computed tomography • progesterone • 20{alpha}-hydroxyprogesterone




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