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
相关论文
共 41 条
  • [1] The pharmacokinetics, pharmacodynamics, safety and tolerability of NN2211, a new long-acting GLP-1 derivative, in healthy men
    Agerso, H
    Jensen, LB
    Elbrond, B
    Rolan, P
    Zdravkovic, M
    [J]. DIABETOLOGIA, 2002, 45 (02) : 195 - 202
  • [2] Bregenholt S, 2001, DIABETES, V50, pA31
  • [3] DEGRADATION OF GLUCAGON-LIKE PEPTIDE-1 BY HUMAN PLASMA IN-VITRO YIELDS AN N-TERMINALLY TRUNCATED PEPTIDE THAT IS A MAJOR ENDOGENOUS METABOLITE IN-VIVO
    DEACON, CF
    JOHNSEN, AH
    HOLST, JJ
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (03) : 952 - 957
  • [4] Glucagon-like peptide 1 undergoes differential tissue-specific metabolism in the anesthetized pig
    Deacon, CF
    Pridal, L
    Klarskov, L
    Olesen, M
    Holst, JJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1996, 271 (03): : E458 - E464
  • [5] Initiation of increased pancreatic islet growth in young normoglycemic mice (Umea +/?)
    Edvell, A
    Lindström, P
    [J]. ENDOCRINOLOGY, 1999, 140 (02) : 778 - 783
  • [6] Exendin-4 reduces fasting and postprandial glucose and decreases energy intake in healthy volunteers
    Edwards, CMB
    Stanley, SA
    Davis, R
    Brynes, AE
    Frost, GS
    Seal, LJ
    Ghatei, MA
    Bloom, SR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2001, 281 (01): : E155 - E161
  • [7] GLUCAGON-LIKE PEPTIDE-1(7-36)AMIDE AND GLUCOSE-DEPENDENT INSULINOTROPIC POLYPEPTIDE SECRETION IN RESPONSE TO NUTRIENT INGESTION IN MAN - ACUTE POSTPRANDIAL AND 24-H SECRETION PATTERNS
    ELLIOTT, RM
    MORGAN, LM
    TREDGER, JA
    DEACON, S
    WRIGHT, J
    MARKS, V
    [J]. JOURNAL OF ENDOCRINOLOGY, 1993, 138 (01) : 159 - 166
  • [8] High glucose causes apoptosis in cultured human pancreatic Islets of Langerhans - A potential role for regulation of specific Bcl family genes toward an apoptotic cell death program
    Federici, M
    Hribal, M
    Perego, L
    Ranalli, M
    Caradonna, Z
    Perego, C
    Usellini, L
    Nano, R
    Bonini, P
    Bertuzzi, F
    Marlier, LNJL
    Davalli, AM
    Carandente, O
    Pontiroli, AE
    Melino, G
    Marchetti, P
    Lauro, R
    Sesti, G
    Folli, F
    [J]. DIABETES, 2001, 50 (06) : 1290 - 1301
  • [9] The effect of physiological levels of glucagon-like peptide-1 on appetite, gastric emptying, energy and substrate metabolism in obesity
    Flint, A
    Raben, A
    Ersboll, AK
    Holst, JJ
    Astrup, A
    [J]. INTERNATIONAL JOURNAL OF OBESITY, 2001, 25 (06) : 781 - 792
  • [10] Glucagon-like peptide 1 promotes satiety and suppresses energy intake in humans
    Flint, A
    Raben, A
    Astrup, A
    Holst, JJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (03) : 515 - 520