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

被引:243
作者
Rolin, B
Larsen, MO
Gotfredsen, CF
Deacon, CF
Carr, RD
Wilken, M
Knudsen, LB
机构
[1] Novo Nordisk AS, Res & Dev, Pharmacol Res 1, DK-2880 Bagsvaerd, Denmark
[2] Univ Copenhagen, Panum Inst, DK-2200 Copenhagen, Denmark
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2002年 / 283卷 / 04期
关键词
incretin hormones; diabetes; animal models; glucagon-like peptide-1;
D O I
10.1152/ajpendo.00030.2002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:E745 / E752
页数:8
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