Harnessing the weight-regulating properties of glucagon-like peptide-1 in the treatment of type 2 diabetes

被引:4
作者
Sesti, G. [1 ]
机构
[1] Univ Magna Graecia Catazaro, Dept Clin & Expt Med, I-86100 Catanzaro, Italy
关键词
glucagon-like peptide-1; incretin; obesity; type; 2; diabetes; HUMAN GLP-1 ANALOG; GLYCEMIC CONTROL; EXENATIDE EXENDIN-4; ENERGY-INTAKE; FOOD-INTAKE; POSTPRANDIAL GLUCOSE; TREATED PATIENTS; BODY-WEIGHT; LIRAGLUTIDE; METFORMIN;
D O I
10.1111/j.1463-1326.2009.01072.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Obesity is associated with increased insulin resistance and is a well-recognized factor for the development of type 2 diabetes. Unfortunately, most diabetes therapies are associated with further weight gain, a most unwelcome characteristic, given the association of weight gain with deteriorating metabolic control, worsening cardiovascular profiles and decreased adherence to treatment. Therapies that effectively control glycaemia without weight gain or with concomitant weight loss are needed. The aim of this article was to review the existing preclinical and clinical evidences, showing that the family of glucagon-like peptide-1 (GLP-1)-based therapies fulfils these criteria by harnessing the beneficial properties of GLP-1, a naturally occurring incretin hormone with a strong blood glucose-lowering action and the ability to induce weight loss.
引用
收藏
页码:4 / 10
页数:7
相关论文
共 47 条
  • [11] The incretin system: glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes
    Drucker, Daniel J.
    Nauck, Michael A.
    [J]. LANCET, 2006, 368 (9548) : 1696 - 1705
  • [12] Glucagon-like peptide-1 receptor is involved in learning and neuroprotection
    During, MJ
    Cao, L
    Zuzga, DS
    Francis, JS
    Fitzsimons, HL
    Jiao, XY
    Bland, RJ
    Klugmann, M
    Banks, WA
    Drucker, DJ
    Haile, CN
    [J]. NATURE MEDICINE, 2003, 9 (09) : 1173 - 1179
  • [13] 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
  • [14] 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
  • [15] FLINT A, 2008, DIABETES S1, V57, pA165
  • [16] Fruhbeck Gema, 2008, V456, P1, DOI 10.1007/978-1-59745-245-8_1
  • [17] Liraglutide versus glimepiride monotherapy for type 2 diabetes (LEAD-3 Mono): a randomised, 52-week, phase III, double-blind, parallel-treatment trial
    Garber, Alan
    Henry, Robert
    Ratner, Robert
    Garcia-Hernandez, Pedro A.
    Rodriguez-Pattzi, Hiromi
    Olvera-Alvarez, Israel
    Hale, Paula M.
    Zdravkovic, Milan
    Bode, Bruce
    [J]. LANCET, 2009, 373 (9662) : 473 - 481
  • [18] Physiology of incretins (GIP and GLP-1) and abnormalities in type 2 diabetes
    Gautier, J. -F.
    Choukem, S. -P.
    Girard, J.
    [J]. DIABETES & METABOLISM, 2008, 34 : S65 - S72
  • [19] Glucagon-like peptide-1 promotes satiety and reduces food intake in patients with diabetes mellitus type 2
    Gutzwiller, JP
    Drewe, J
    Göke, B
    Schmidt, H
    Rohrer, B
    Lareida, J
    Beglinger, C
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 276 (05) : R1541 - R1544
  • [20] Oral antihyperglycemic therapy for type 2 diabetes - Scientific review
    Inzucchi, SE
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (03): : 360 - 372