Low-carbohydrate diet disrupts the association between insulin resistance and weight gain

• Published in: Metabolism, clinical and experimental Vol. 58; no. 8; pp. 1116 - 1122
• Main Authors: Leite, Jose O, DeOgburn, Ryan, Ratliff, Joseph C, Su, Randy, Volek, Jeff S, McGrane, Mary M, Dardik, Alan, Fernandez, Maria Luz
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01.08.2009; Elsevier
• Subjects: Animals; Biological and medical sciences; Blood Glucose - metabolism; Body Weight; Diet, Carbohydrate-Restricted; Diet, Fat-Restricted; Dietary Carbohydrates - administration & dosage; Dietary Carbohydrates - metabolism; Dietary Fats - administration & dosage; Dietary Fats - metabolism; Dietary Proteins - administration & dosage; Dietary Proteins - metabolism; Eating; Endocrinology & Metabolism; Energy Intake; Fasting; Feeding. Feeding behavior; Fundamental and applied biological sciences. Psychology; Glucagon-Like Peptide 1 - blood; Gluconeogenesis; Guinea Pigs; Insulin - blood; Insulin Resistance; Linear Models; Male; Satiation; Vertebrates: anatomy and physiology, studies on body, several organs or systems; Weight Gain; Endocrinopathy; Target tissue resistance; Association; Diet; Metabolic diseases; Insulin resistance; Carbohydrate; Weight gain; Endocrinology; Feeding
• ISSN: 0026-0495; 1532-8600
• DOI: 10.1016/j.metabol.2009.04.004

Abstract The cornerstone to treat metabolic syndrome and insulin resistance is dietary intervention. Both low-carbohydrate diet (LCD) and low-fat diet (LFD) have been reported to induce weight loss and improve these conditions. One of the factors associated with a subject's adherence to the diet is satiety. The aim of this study was to evaluate the effects of LCD and LFD on body weight, appetite hormones, and insulin resistance. Twenty guinea pigs were randomly assigned to LCD or LFD (60%:10%:30% or 20%:55%:25% of energy from fat/carbohydrate/protein, respectively) for 12 weeks. Weight and food intake were recorded every week. After this period, animals were killed and plasma was obtained to measure plasma glucose and insulin, appetite hormones, and ketone bodies. Guinea pigs fed LCD gained more weight than those fed LFD. The daily amount of food intake in grams was not different between groups, suggesting that food density and gastric distension played a role in satiety. There was no difference in leptin levels, which excludes the hypothesis of leptin resistance in the LCD group. However, plasma glucagon-like peptide–1 was 47.1% lower in animals fed LCD ( P < .05). Plasma glucose, plasma insulin, and insulin sensitivity were not different between groups. However, the heavier animals that were fed LFD had impairment in insulin sensitivity, which was not observed in those fed LCD. These findings suggest that satiety was dependent on the amount of food ingested. The weight gain in animals fed LCD may be related to their greater caloric intake, lower levels of glucagon-like peptide–1, and higher protein consumption. The adoption of LCD promotes a unique metabolic state that prevents insulin resistance, even in guinea pigs that gained more weight. The association between weight gain and insulin resistance seems to be dependent on high carbohydrate intake.