Scientific publications

RIP140 Gene and Protein Expression Levels are Downregulated in Visceral Adipose Tissue in Human Morbid Obesity

Victoria Catalán [SP] (1,5), Javier Gómez-Ambrosi [SP] (1,5), Amaia Lizanzu (1), Amaia Rodríguez (1,5), Camilo Silva [SP] (2,5), Fernando Rotellar [SP] (3,5), María J. Gil [SP] (4,5), Javier A. Cienfuegos (3,5), Javier Salvador (2,5) and Gema Frühbeck [SP](1,2,5)
(1) Metabolic Research Laboratory, Clínica Universitaria de Navarra, University of Navarra, Pamplona, Spain
(2) Department of Endocrinology, Clínica Universitaria de Navarra, University of Navarra, Avda. Pío XII, 36, 31008 Pamplona, Spain
(3) Department of Surgery, Clínica Universitaria de Navarra, University of Navarra, Pamplona, Spain
(4) Department of Biochemistry, Clínica Universitaria de Navarra, University of Navarra, Pamplona, Spain
(5) CIBER de Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, Pamplona, Spain

Magazine: Obesity Surgery

Date: Apr 15, 2009

General and Digestive Surgery Obesity Unit Endocrinology and Nutrition [SP]

BACKGROUND
Receptor-interacting protein 140 (RIP140) is a corepressor for nuclear receptors with an important role in the inhibition of energy expenditure. Rip140-knockout mice are lean and resistant to diet-induced obesity due to an increase in mitochondrial biogenesis, fatty acid oxidation, and oxidative phosphorylation. The aim of the present work was to evaluate the effect of morbid obesity on gene and protein expression levels of RIP140 in visceral adipose tissue (VAT).

METHODS
VAT biopsies obtained from 17 subjects were used in the study. Patients were classified as lean (body mass index [BMI] = 21.8 +/- 1.3 kg/m(2)) or obese (BMI = 48.2 +/- 2.6 kg/m(2)). Reverse transcription polymerase chain reaction and Western blot analyses were performed to quantify the expression levels of RIP140 in VAT. We also analyzed glucose and lipid profile as well as some inflammatory factors.

RESULTS
Obese patients exhibited significantly lower RIP140 mRNA expression levels compared to lean subjects (lean = 1.00 +/- 0.17 arbitrary units, obese = 0.65 +/- 0.18 arbitrary units; P < 0.05). Protein expression of RIP140 followed the same trend, being significantly higher in lean volunteers (lean = 1.00 +/- 0.18 arbitrary units, obese = 0.45 +/- 0.11 arbitrary units; P < 0.05). Furthermore, a significant negative correlation was found between RIP140 protein levels and both BMI (rho = -0.85; P < 0.001) and body fat percentage (rho = -0.88; P < 0.001).

CONCLUSIONS
The lower gene and protein expression levels of RIP140 in obese subjects may suggest a compensatory mechanism in order to favor energy expenditure and reduce fat accumulation in obesity states.

CITATION  Obes Surg. 2009 Jun;19(6):771-6

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