EA 3502 and Institut National de la Santé et de la Recherche Médicale (INSERM) Avenir and Paris VI University, Department of Nutrition (Y.-M.L., C.P., V.P., B.G.-G., A.B., K.C.), Department of Medical Biochemistry (J.-M.L., C.C.), Hôtel-Dieu, 75004 Paris, France; and Obesity Research Unit 586 (N.V., D.L.), INSERM, Louis Bugnard Institute, Paul Sabatier University, 31403 Toulouse, France
Address all correspondence and requests for reprints to: Karine Clément, M.D., Ph.D., Service de Nutrition, Hôtel-Dieu, place du Parvis Notre-Dame, 75004 Paris, France. E-mail: karine.clement{at}htd ap-hop-paris.fr.
Adiponectin is an adipocyte-derived protein suggested to beinvolved in energy homeostasis and in lipid and glucose metabolism.Little is known regarding the consequence of acute changes inenergy balance on adiponectin mRNA expression in human adiposetissue. Using a real-time RT-PCR assay, we investigated theeffects of 2-d very low calorie diet (VLCD) and subsequent refeedingon adiponectin mRNA expression in sc adipose tissue of morbidlyobese women. Basal adiponectin mRNA abundance of the obese womenshowed a wide distribution (2.614.3 mRNA/18S rRNA; coefficientof variation, 51.2%) and was significantly lower than that oflean controls (P < 0.001). In the obese group, the VLCD causeda 33% rise (P < 0.01) in the average level of mRNA, whereasrefeeding caused a 32.8% fall (P < 0.05). In contrast, thechange in leptin mRNA expression with either VLCD or refeedingwas not statistically significant. The obese subjects who showedan acute adiponectin mRNA response to the changes in energyintake had a higher basal level of adiponectin mRNA (P = 0.02)and a borderline-significantly lower body mass index comparedwith the subjects who showed no or weak adiponectin mRNA response.Insulin sensitivity of the responder subgroup significantlyincreased by 89% (P = 0.008) after the VLCD, whereas insulinsensitivity of the nonresponder subgroup only increased by 24%(P = 1.56). This study indicates that adiponectin mRNA in scadipose tissue can acutely respond to short-term energy changesin some obese subjects. Both the levels of adiposity and insulinsensitivity may contribute to the variation in adiponectin geneexpression in response to acute energy changes.
This work was supported by the Direction de la Recherche Clinique/AssistancePublique-Hopitaux de Paris, the Programme Hospitalier de RechercheClinique (AOM 96088 and CRC 97123), and grants from the FrenchFondation pour la Recherche Médicale (2001/2002) andthe Claude Bernard Association (to Y.-M.L.). Funding of theEA 502 (2002/2003) team was provided by Servier Research Instituteand French Association for the Study of Obesity (AFERO).
Abbreviations: BMI, Body mass index; CV, coefficient of variation;GAPDH, glyceraldehyde-3-phosphate dehydrogenase; HOMA, homeostasismodel assessment; VLCD, very low calorie diet.
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