Effect of the antiobesity agent sibutramine in obese-diabetic ob/ob mice

Int J Obes Relat Metab Disord. 1998 Jul;22(7):619-23. doi: 10.1038/sj.ijo.0800636.

Abstract

Background: Sibutramine is a reuptake inhibitor of 5-hydroxytryptamine and noradrenaline, being developed as a treatment for obesity.

Objective: To investigate the effect of sibutramine on glucose homeostasis in obese-hyperglycaemic insulin-resistant ob/ob mice.

Design: Sibutramine 5 mg/kg once daily was administered orally to ob/ob mice for six weeks.

Results: Sibutramine treatment decreased body weight gain by 12% without a significant overall change in daily food intake. Sibutramine reduced the hyperinsulinaemia by 31%, and lowered plasma non-esterified fatty acids (NEFA) by 17%. Basal plasma glucose concentrations were not significantly altered by sibutramine, but glucose concentrations fell more rapidly after an i.p. glucose challenge, despite lower insulin concentrations. The rate of insulin-induced glucose disappearance was increased by 10% during sibutramine treatment. First administration of sibutramine, 5 mg/kg, did not acutely alter basal plasma glucose, insulin or NEFA concentrations in ob/ob mice, although NEFA concentrations were raised after 24 h.

Conclusion: The results indicate that chronic administration of sibutramine can reduce weight gain, lower NEFA concentrations, decrease hyperinsulinaemia and ameliorate the insulin resistance of ob/ob mice.

MeSH terms

  • Animals
  • Appetite Depressants / therapeutic use*
  • Blood Glucose / metabolism
  • Cyclobutanes / therapeutic use*
  • Diabetes Mellitus / drug therapy*
  • Fatty Acids, Nonesterified / blood
  • Homeostasis
  • Insulin / blood
  • Insulin Resistance
  • Mice
  • Mice, Obese
  • Obesity*
  • Weight Gain

Substances

  • Appetite Depressants
  • Blood Glucose
  • Cyclobutanes
  • Fatty Acids, Nonesterified
  • Insulin
  • sibutramine