The effect of cilostazol on glucose tolerance and insulin resistance in a rat model of non-insulin dependent diabetes mellitus

Korean J Intern Med. 2001 Jun;16(2):87-92. doi: 10.3904/kjim.2001.16.2.87.

Abstract

Background: It has been reported that many peripheral vasodilating drugs might improve insulin resistance. Cilostazol, a antithrombotic agent, increases peripheral blood flow in non-insulin dependent diabetic patients. The effect of cilostazol treatment on insulin resistance in streptozotocin (STZ)-induced non-insulin dependent diabetic Wistar rats was examined.

Methods: About a half of two-day old neonate siblings were injected intraperitoneally with STZ and maintained for six months, at which time they were compared with age-matched control rats for intraperitoneal glucose tolerance test (IPGTT) and for glucose infusion rate (GINF) in a euglycemic hyperinsulinemic glucose-clamp study. After that, these studies were also performed after feeding rat chow containing cilostazol (100 mg/kg/day) to rats with STZ-induced non-insulin dependent diabetes mellitus for four-weeks and compared with those of age-matched control rats.

Results: In the intraperitoneal glucose tolerance test studies, plasma glucose levels of STZ-induced non-insulin dependent diabetic rats were significantly higher and plasma insulin levels significantly lower than those of age-matched control rats in the age of six months. Glucose infusion rate was lower in STZ-induced non-insulin dependent diabetic rats than those of age-matched control rats. However, after a four-week cilostazol treatment, glucose infusion rate of STZ-induced non-insulin dependent diabetic rats was not significantly different from that of control rats.

Conclusion: These findings suggested that cilostazol may improve insulin resistance in STZ-induced non-insulin dependent diabetic rats.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Animals, Newborn
  • Blood Glucose / drug effects*
  • Cilostazol
  • Diabetes Mellitus, Type 2 / chemically induced
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Disease Models, Animal
  • Glucose Tolerance Test
  • Insulin Resistance*
  • Male
  • Probability
  • Rats
  • Rats, Wistar
  • Reference Values
  • Sensitivity and Specificity
  • Streptozocin
  • Tetrazoles / pharmacology*
  • Vasodilator Agents / pharmacology*

Substances

  • Blood Glucose
  • Tetrazoles
  • Vasodilator Agents
  • Streptozocin
  • Cilostazol