Distinct role of adiposity and insulin resistance in glucose intolerance: Studies in ventromedial hypothalamic-lesioned obese rats

• Published in: Metabolism, clinical and experimental Vol. 51; no. 6; pp. 716 - 723
• Main Authors: Kageyama, Asako, Hirano, Tsutomu, Kageyama, Haruaki, Osaka, Toshimasa, Namba, Yoshio, Tsuji, Masatomi, Adachi, Mitsuru, Inoue, Shuji
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 2002; Elsevier
• Subjects: Animals; Area Under Curve; Biological and medical sciences; Blood Glucose - drug effects; Body Weight - drug effects; Diabetes. Impaired glucose tolerance; Dietary Supplements; Disease Models, Animal; Eating - drug effects; Endocrine pancreas. Apud cells (diseases); Endocrinopathies; Etiopathogenesis. Screening. Investigations. Target tissue resistance; Fatty Acids, Nonesterified - blood; Female; Fructose - administration & dosage; Glucose Intolerance - physiopathology; Glucose Tolerance Test; Insulin - blood; Insulin Resistance - physiology; Leptin - blood; Medical sciences; Metabolic diseases; Obesity; Obesity - physiopathology; Rats; Triglycerides - blood; Ventromedial Hypothalamic Nucleus - physiopathology; Endocrinopathy; Animal model; Obesity; Pancreatic hormone; Rat; Pathogenesis; Rodentia; Nutrition disorder; Insulin; Blood plasma; Target tissue resistance; Vertebrata; Concomitant disease; Mammalia; Animal; Leptin; Hormonal investigation; Impaired glucose tolerance; Nutritional status
• ISSN: 0026-0495; 1532-8600
• DOI: 10.1053/meta.2002.32728

It remains unclear whether adiposity plays an important role in glucose intolerance independently of insulin resistance. We investigated whether adiposity and insulin resistance had distinct roles in glucose intolerance in rats. We examined glucose tolerance and insulin resistance using ventromedial hypothalamic (VMH)-lesioned rats in the dynamic and the static phases of obesity (2 and 14 weeks after lesioning, respectively). Rats were fed either normal chow or a fructose-enriched diet (60% of total calories). The intravenous glucose tolerance test (IVGTT) was performed by bolus injection of glucose solution (1 g/kg) and blood sampling after 0, 5 10, 30, and 60 minutes. Insulin resistance was evaluated from the steady-state plasma glucose (SSPG) value during continuous infusion of glucose, insulin, and somatostatin. SSPG was not increased in VMH-lesioned rats in the dynamic phase of obesity, but increased markedly in the static phase. The area under the glucose curve (glucose AUC) during IVGTT was increased in VMH-lesioned rats in the static phase, but not in the dynamic phase, when compared with their sham-operated counterparts. A fructose-enriched diet for 2 or 14 weeks increased SSPG values to a similar extent in both sham-operated and VMH-lesioned rats without inducing excess adiposity, but glucose intolerance was only developed in the obese rats. The plasma leptin level, an excellent indicator of adiposity, was significantly related to the glucose AUC independently of the insulin level. Insulin resistance or increased adiposity alone is not sufficient to impair glucose tolerance, but increased adiposity plays an important role in the development of glucose intolerance in an insulin-resistant state.