Plasma levels and adipose tissue messenger ribonucleic acid expression of retinol-binding protein 4 are reduced during calorie restriction in obese subjects but are not related to diet-induced changes in insulin sensitivity

Autor: Dominique Langin, Vladimir Stich, Michaela Vitkova, Nathalie Viguerie, Cedric Moro, Jiri Hanacek, Eva Klimcakova, Magda Bajzova, Jan Polak, Carine Valle, Frédéric Capel, Michaela Kovacikova, Blanka Richterova, Jindra Hejnova
Přispěvatelé: Simon, Marie Francoise, Hepatic and adipose tissue and functions in the metabolic syndrome - HEPADIP - 32591 - OLD, Franco-Czech Laboratory for Clinical Research on Obesity, Charles University [Prague] (CU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut de médecine moléculaire de Rangueil (I2MR), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées- Institut Fédératif de Recherche Bio-médicale Institution (IFR150)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institute for Mother and Child Care, Laboratoire de Biochimie [CHU Toulouse], Institut Fédératif de Biologie (IFB), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Pôle Biologie [CHU Toulouse], Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), The authors' work is supported by Institut National de la Sante' et de la Recherche Me'dicale, Grant GACR 303/04/0158 of the Grant Agency of the Czech Republic, research project of the Ministry of Education of Czech Republic MSM 0021620814, RIOMA project of the Agence Nationale de la Recherche and the project 'Hepatic and adipose tissue and functions in the metabolic syndrome' (HEPADIP, see http://www.hepadip.org/), which is supported by the European Commission as an Integrated Project under the 6th Framework Programe (Contract LSHM-CT-2005-018734), European Project: 32591,HEPADIP, Université de Toulouse (UT)-Université de Toulouse (UT)- Institut Fédératif de Recherche Bio-médicale Institution (IFR150)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-IFR150-Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire de Biochimie [Purpan], Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-CHU Toulouse [Toulouse]-Institut Fédératif de Biologie (IFB) - Hôpital Purpan, Hôpital Purpan [Toulouse], CHU Toulouse [Toulouse]-CHU Toulouse [Toulouse]-Hôpital Purpan [Toulouse], CHU Toulouse [Toulouse]
Rok vydání: 2007
Předmět:
Endocrinology
Diabetes and Metabolism

medicine.medical_treatment
Clinical Biochemistry
RNA
Messenger/metabolism

Adipose tissue
Gene Expression
Retinol-Binding Proteins/*genetics/*metabolism
MESH: Glucose Clamp Technique
Biochemistry
Glucose Transporter Type 4/genetics
0302 clinical medicine
Endocrinology
Weight loss
MESH: Obesity
Insulin
Gene Expression/physiology
MESH: Diet
Reducing

2. Zero hunger
0303 health sciences
MESH: Middle Aged
Glucose Transporter Type 4
Middle Aged
Very low calorie diet
MESH: Insulin Resistance
Adipose Tissue
Female
medicine.symptom
MESH: Retinol-Binding Proteins
Plasma

MESH: Adipose Tissue
Adult
medicine.medical_specialty
MESH: Gene Expression
Diet
Reducing

Diet therapy
food.diet
Calorie restriction
030209 endocrinology & metabolism
MESH: Insulin
Biology
Obesity/*diet therapy/*physiopathology
Caloric Restriction
MESH: Weight Loss
03 medical and health sciences
food
Insulin resistance
Internal medicine
Weight Loss
[SDV.BBM] Life Sciences [q-bio]/Biochemistry
Molecular Biology

medicine
Humans
[SDV.BBM]Life Sciences [q-bio]/Biochemistry
Molecular Biology

Obesity
RNA
Messenger

MESH: RNA
Messenger

030304 developmental biology
MESH: Caloric Restriction
Retinol binding protein 4
MESH: Humans
Biochemistry (medical)
Adipose Tissue/*physiology
MESH: Adult
MESH: Retinol-Binding Proteins
medicine.disease
Retinol-Binding Proteins
biology.protein
Glucose Clamp Technique
Weight Loss/physiology
MESH: Glucose Transporter Type 4
Insulin Resistance
Insulin/blood
MESH: Female
Retinol-Binding Proteins
Plasma
Zdroj: Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, 2007, 92 (6), pp.2330-5. ⟨10.1210/jc.2006-2668⟩
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2007, 92 (6), pp.2330-5. ⟨10.1210/jc.2006-2668⟩
ISSN: 0021-972X
1945-7197
DOI: 10.1210/jc.2006-2668⟩
Popis: 0021-972X (Print) 0021-972X (Linking) Journal Article Research Support, Non-U.S. Gov't; International audience; CONTEXT: Retinol-binding protein 4 (RBP4) may play a role in the development of insulin resistance. OBJECTIVE: We investigated whether RBP4 adipose tissue mRNA expression and plasma level are related to insulin sensitivity during a diet-induced weight loss. DESIGN, SETTING, PATIENTS, AND INTERVENTION: Obese women followed a dietary intervention composed of a 4-wk very low-calorie diet (VLCD), a 2-month low-calorie diet, and 3-4 months of a weight maintenance (WM) phase. MAIN OUTCOME MEASURES: Clinical investigation was performed before and at the end of each phase. Insulin sensitivity was assessed with the euglycemic hyperinsulinemic clamp. Adipose tissue mRNA and plasma levels of RBP4 were determined using reverse transcription-quantitative PCR and ELISA, respectively. RESULTS: Weight and fat mass decreased during VLCD and were stabilized during WM. Glucose disposal rate increased during VLCD and remained elevated thereafter. Plasma levels of RBP4 decreased after VLCD and, although increasing at subsequent phases, remained lower than prediet values. Adipose tissue mRNA levels were diminished after VLCD, and increased during low-calorie diet and WM to reach basal values. Basal RBP4 levels or diet-induced variations of RBP4 were not different in lean women and two groups of obese women with high- and low-insulin sensitivity. CONCLUSIONS: Severe calorie restriction promotes a reduction in adipose tissue and plasma levels of RBP4. The study does not bring evidence for a role for RBP4 in the regulation of diet-induced changes in insulin sensitivity.
Databáze: OpenAIRE