Ceftezole, a cephem antibiotic, is an alpha-glucosidase inhibitor with in vivo anti-diabetic activity

Int J Mol Med. 2007 Sep;20(3):379-83.

Abstract

Using a high throughput-compatible assay to screen for potential alpha-glucosidase inhibitors, we found that the beta-lactam antibiotic ceftezole exhibited potent alpha-glucosidase inhibitory activity. In in vitro alpha-glucosidase assays, ceftezole was shown to be a reversible, non-competitive inhibitor of yeast alpha-glucosidase with a Ki value of 5.78 x 10(-7) M when the enzyme mixture was pretreated with ceftezole. Using an in vivo streptozotocin-induced mouse model, we confirmed that blood glucose levels decreased by 30% 20 min after ceftezole treatment (10 mg/kg/day). Expression levels of glycogen synthase kinase-3, peroxisome proliferator-activated receptor-gamma, and uncoupling protein-3 mRNA were also slightly decreased compared to controls following ceftezole treatment. Taken together, these in vivo and in vitro results suggest that ceftezole may be a clinically useful anti-diabetic compound.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Base Sequence
  • Blood Glucose / metabolism
  • Cefmenoxime / analogs & derivatives*
  • Cefmenoxime / pharmacology
  • DNA Primers / genetics
  • Diabetes Mellitus, Experimental / blood
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / genetics
  • Drug Evaluation, Preclinical
  • Female
  • Gene Expression / drug effects
  • Glycogen Synthase Kinase 3 / genetics
  • Glycoside Hydrolase Inhibitors*
  • Hypoglycemic Agents / pharmacology*
  • In Vitro Techniques
  • Mice
  • Mice, Inbred C57BL
  • PPAR gamma / genetics
  • RNA, Messenger / blood
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Anti-Bacterial Agents
  • Blood Glucose
  • DNA Primers
  • Glycoside Hydrolase Inhibitors
  • Hypoglycemic Agents
  • PPAR gamma
  • RNA, Messenger
  • cefteram
  • Glycogen Synthase Kinase 3
  • Cefmenoxime