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This version published online on November 3, 2009
Endocrinology, doi:10.1210/en.2009-0647
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Submitted on June 25, 2009
Accepted on October 1, 2009

Circadian Expression of Adiponectin and Its Receptors in Human Adipose Tissue

P. Gómez-Abellán, C. Gómez-Santos, J. A. Madrid, F. I. Milagro, J. Campion, J. A. Martínez, J. M. Ordovás, and M. Garaulet*

Department of Physiology (P.G.-A., C.G.-S., J.A.Mad., M.G.), Faculty of Biology, University of Murcia, 30100 Murcia, Spain; Department of Nutrition and Food Sciences, Physiology, and Toxicology (F.I.M., J.C., J.A.Mar.), University of Navarra, 31080 Pamplona, Spain; Nutrition and Genomics Laboratory (J.M.O.), Jean Mayer United States. Department of Agriculture Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts 02111; and Department of Epidemiology (J.M.O.), Centro Nacional Investigaciones Cardiovasculares, 28029 Madrid, Spain

* To whom correspondence should be addressed. E-mail: garaulet{at}um.es.

Adiponectin is one of the most clinically relevant cytokines associated with obesity. However, circadian rhythmicity of adiponectin in human adipose tissue (AT) has not been analyzed. To assess whether the mRNA levels of adiponectin and its receptors (ADIPOR1 and ADIPOR2) might show daily circadian rhythms in visceral and sc fat explants obtained from morbid obese women, visceral and sc abdominal AT biopsies (n = 6) were obtained from morbidly obese women (body mass index ≥40 kg/m2). Anthropometric variables were measured and fasting plasma glucose, lipid, and lipoprotein concentrations were analyzed. To investigate rhythmic expression pattern, AT explants were cultured during 24 h, and gene expression was analyzed at the following times: 0800, 1400, 2000, and 0200 h, using quantitative real-time PCR. All genes investigated showed a circadian rhythmicity and oscillated accurately and independently of the suprachiasmatic nucleus in both AT explants (P < 0.05). Adiponectin gene expression fluctuated in the same phase as its receptors. Correlation analyses between the genetic circadian oscillation and components of the metabolic syndrome revealed that adiposity and abdominal obesity correlated with a decrease in adiponectin and adiponectin receptors ADIPOR1 and ADIPOR2 amplitude (P < 0.05). Visceral fat showed a trend toward a phase delay and dampening of the mRNA amplitude of adiponectin as compared with sc fat. The mRNA expression of adiponectin and its receptors showed 24-h rhythmicity in human AT from morbidly obese patients.







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