Liraglutide, but not vildagliptin, restores normoglycaemia and insulin content in the animal model of type 2 diabetes, Psammomys obesus

被引:12
作者
Vedtofte, Louise [1 ]
Bodvarsdottir, Thora B. [2 ]
Gotfredsen, Carsten F. [2 ]
Karlsen, Allan E. [2 ]
Knudsen, Lotte B. [2 ]
Heller, R. Scott [1 ]
机构
[1] Hagedorn Res Inst, Dept Beta Cell Regenerat, Gentofte, Denmark
[2] Novo Nordisk AS, Diabet Res Unit, Malov, Denmark
关键词
GLP-1; Pancreas; Insulin; Liraglutide; Vildagliptin; Psammomys obesus; Diabetes; GLUCAGON-LIKE PEPTIDE-1; BETA-CELL MASS; IV INHIBITOR LAF237; GLP-1; 7-36; AMIDE; DIPEPTIDYL PEPTIDASE-4; GLUCOSE-TOLERANCE; RAT; EXPRESSION; NEOGENESIS; REPLICATION;
D O I
10.1016/j.regpep.2009.12.005
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
In order to investigate the effect and mechanism of liraglutide and vildagliptin in diabetic Psammomys obesus, we examined proliferation and apoptosis of beta-cells, beta-cell mass (BCM), and pancreatic insulin content after zero, six and fourteen days of treatment compared to control groups. One group of animals was kept on low-energy diet and seven groups were given high-energy diet (HED) that induced diabetes over a four week period. Non-fasting morning blood glucose, body weight, HbA(1C) and pancreatic insulin content were measured and beta cell mass (BCM), proliferation and apoptosis frequencies were determined using stereological point counting. Liraglutide significantly reduced blood glucose and even normalized it in all animals treated for six days and in I I out of 17 animals treated for fourteen days. HED increased BCM and treatment with liraglutide did not change this. However, compared to the vehicle-treated animals pancreatic insulin content was normalized in animals treated for six and fourteen days with liraglutide. In contrast, vildagliptin, in doses causing full inhibition of plasma DPP-IV activity, neither reduced blood glucose nor altered HED-induced increases in BCM or pancreatic insulin content. These results suggest that liraglutide restores normoglycaemia and improves glycaemic control in P. obesus by increasing their insulin content and improving the function of the beta-cells. In contrast, vildagliptin does not improve glycaemic control in P. obesus nor affect beta-cell insulin content. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:106 / 114
页数:9
相关论文
共 57 条
[1]
Beta-cell expression of a dominant-negative HNF-1α compromises the ability of inhibition of dipeptidyl peptidase-4 to elicit a long-term augmentation of insulin secretion in mice [J].
Ahrén, B ;
Winzell, MS ;
Burkey, B ;
Hughes, TE .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2005, 521 (1-3) :164-168
[2]
Inhibition of dipeptidyl peptidase-4 reduces glycemia, sustains insulin levels, and reduces glucagon levels in type 2 diabetes [J].
Ahrén, B ;
Landin-Olsson, M ;
Jansson, PA ;
Svensson, M ;
Holmes, D ;
Schweizer, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (05) :2078-2084
[3]
Twelve- and 52-week efficacy of the dipeptidyl peptidase IV inhibitor LAF237 in metformin-treated patients with type 2 diabetes [J].
Ahrén, B ;
Gomis, R ;
Standl, E ;
Mills, D ;
Schweizer, A .
DIABETES CARE, 2004, 27 (12) :2874-2880
[4]
DPP-4 inhibition improves glucose tolerance and increases insulin and GLP-1 responses to gastric glucose in association with non-nalized islet topography in mice with β-cell-specific overexpression of human islet amylold polypeptide [J].
Ahren, Bo ;
Winzell, Maria Sorhede ;
Wierup, Nils ;
Sundler, Frank ;
Burkey, Bryan ;
Hughes, Thomas E. .
REGULATORY PEPTIDES, 2007, 143 (1-3) :97-103
[5]
BARILLA D, 2004, 64 SCI SESS AM DIAB
[6]
The endocrine pancreas in non-diabetic rats after short-term and long-term treatment with the long-acting GLP-1 derivative NN2211 [J].
Bock, T ;
Pakkenberg, B ;
Buschard, K .
APMIS, 2003, 111 (12) :1117-1124
[7]
BODVARSDOTTIR TB, 2005, 65 SCI SESS AM DIAB
[8]
The long-acting glucagon-like peptide-1 analogue, liraglutide, inhibits β-cell apoptosis in vitro [J].
Bregenbolt, S ;
Moldrup, A ;
Blume, N ;
Karlsen, AE ;
Friedrichsen, BN ;
Tornhave, D ;
Knudsen, LB ;
Petersen, JS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 330 (02) :577-584
[9]
Acute and chronic effects of the incretin enhancer vildagliptin in insulin-resistant rats [J].
Burkey, BF ;
Li, X ;
Bolognese, L ;
Balkan, B ;
Mone, M ;
Russell, M ;
Hughes, TE ;
Wang, PR .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 315 (02) :688-695
[10]
Combination of the Dipeptidyl Peptidase IV Inhibitor LAF237 [(S)-1-[(3-Hydroxy-1-adamantyl)ammo]acetyl-2-cyano-pyrrolidine] with the Angiotensin II Type 1 Receptor Antagonist Valsartan [N-(1-Oxopentyl)-N-[[2′-(1H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl]methyl]-L-valine] Enhances Pancreatic Islet Morphology and Function in a Mouse Model of Type 2 Diabetes [J].
Cheng, Qianni ;
Law, Pui Ki ;
de Gasparo, Marc ;
Leung, Po Sing .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2008, 327 (03) :683-691