The long-acting GLP-1 derivative NN2211 ameliorates glycemia and increases beta-cell mass in diabetic mice

Am J Physiol Endocrinol Metab. 2002 Oct;283(4):E745-52. doi: 10.1152/ajpendo.00030.2002.

Abstract

NN2211 is a long-acting, metabolically stable glucagon-like peptide-1 (GLP-1) derivative designed for once daily administration in humans. NN2211 dose dependently reduced the glycemic levels in ob/ob mice, with antihyperglycemic activity still evident 24 h postdose. Apart from an initial reduction in food intake, there were no significant differences between NN2211 and vehicle treatment, and body weight was not affected. Histological examination revealed that beta-cell proliferation and mass were not increased significantly in ob/ob mice with NN2211, although there was a strong tendency for increased proliferation. In db/db mice, exendin-4 and NN2211 decreased blood glucose compared with vehicle, but NN2211 had a longer duration of action. Food intake was lowered only on day 1 with both compounds, and body weight was unaffected. beta-Cell proliferation rate and mass were significantly increased with NN2211, but with exendin-4, only the beta-cell proliferation rate was significantly increased. In conclusion, NN2211 reduced blood glucose after acute and chronic treatment in ob/ob and db/db mice and was associated with increased beta-cell mass and proliferation in db/db mice. NN2211 is currently in phase 2 clinical development.

MeSH terms

  • Animals
  • Blood Glucose / drug effects
  • Body Weight / drug effects
  • Cell Division / drug effects
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Eating / drug effects
  • Exenatide
  • Female
  • Glucagon / analogs & derivatives
  • Glucagon / metabolism
  • Glucagon / pharmacology*
  • Glucagon-Like Peptide 1
  • Hyperglycemia / drug therapy*
  • Insulin / blood
  • Islets of Langerhans / cytology*
  • Liraglutide
  • Mice
  • Mice, Inbred C57BL
  • Mice, Obese
  • Peptide Fragments / metabolism
  • Peptides / pharmacology
  • Protein Precursors / metabolism
  • Venoms*

Substances

  • Blood Glucose
  • Insulin
  • Peptide Fragments
  • Peptides
  • Protein Precursors
  • Venoms
  • Liraglutide
  • Glucagon-Like Peptide 1
  • Glucagon
  • Exenatide