Effects of diabetes on disposition and hepatic handling of cefmetazole in rats

Clin Exp Pharmacol Physiol. 1993 Jun;20(6):399-404. doi: 10.1111/j.1440-1681.1993.tb01716.x.

Abstract

1. The effects of streptozotocin-induced diabetes on disposition and hepatic handling of cefmetazole, a broad-spectrum cephalosporin, were investigated in rats. 2. Male Wistar rats were pretreated with streptozotocin (60 mg/kg, i.p.) to induce uncontrolled diabetes. Fourteen days later bile flow was significantly reduced (12%) and bile acid secretion was significantly enhanced (87%) when compared with control animals. 3. Following intravenous injection of cefmetazole at a dose of 200 mumol/kg, maximal and cumulative biliary excretion of the antibiotic were significantly impaired in streptozotocin-treated animals (27 and 22%, respectively). 4. Cefmetazole excretion into bile was accompanied by marked choleresis. The magnitude of bile flow increase was larger in control animals. 5. Total systemic clearance of the antibiotic was reduced (36%) and mean half-life for the fast and slow phases of disposition increased (136 and 48%, respectively) in diabetic rats. 6. These changes were probably due to the diabetic condition of the animals because insulin treatment resulted in almost complete correction.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Bile / metabolism
  • Bile Acids and Salts / metabolism
  • Blood Glucose / analysis
  • Cefmetazole / pharmacokinetics*
  • Cefmetazole / pharmacology
  • Diabetes Mellitus, Experimental / metabolism*
  • Half-Life
  • Insulin / pharmacology
  • Liver / metabolism*
  • Male
  • Rats
  • Rats, Wistar
  • Tissue Distribution

Substances

  • Bile Acids and Salts
  • Blood Glucose
  • Insulin
  • Cefmetazole