Literature DB >> 22555471

The incretin hormones: from scientific discovery to practical therapeutics.

S Mudaliar1, R R Henry.   

Abstract

The incretins are gut hormones secreted in response to nutrient/carbohydrate ingestion and act on the pancreatic beta cell to amplify glucose-stimulated insulin secretion. Incretin hormone-based treatments for patients with type 2 diabetes represent a major advance in diabetes therapeutics. The ability of the incretin agents (glucagon-like peptide 1 [GLP-1] agonists and dipeptidyl peptidase IV [DPP-4] inhibitors) to improve glycaemia with a low associated risk of hypoglycaemia, together with beneficial/neutral effects on body weight, offers a significant advantage for both patients and treating clinicians. In this edition of 'Then and Now,' it is useful to look back 25 years and reflect upon the developments in this field since Nauck and colleagues published two seminal papers. In 1986 they first documented a reduced incretin effect in patients with type 2 diabetes (Diabetologia 29:46-52), and then in 1993 they demonstrated that, in patients with poorly controlled type 2 diabetes, a single exogenous infusion of an incretin (GLP-1) increased insulin levels in a glucose-dependent manner and normalised fasting hyperglycaemia (Diabetologia 36:741-744). In the ensuing 26 years, progress in the field of incretin hormones has resulted in a greater understanding of the relative roles of GLP-1 and glucose-dependent insulinotropic polypeptide secretion and activity in the pathogenesis of type 2 diabetes and the important recognition that native GLP-1 is quickly degraded by the ubiquitous protease DPP-4. This has led to the development of GLP-1 agonists that are resistant to degradation by DPP-4 and of selective inhibitors of DPP-4 activity as therapeutic agents. GLP-1 agonists (exenatide and liraglutide) and DPP-4 inhibitors (sitagliptin, vildagliptin, saxagliptin and linagliptin) currently represent effective treatment options for patients with type 2 diabetes. Several additional agents are in the pipeline, including longer acting DPP-4-resistant GLP-1 agonists. More exciting, however, is the increasing recognition that the incretin agents have numerous extra-glycaemic effects that could translate into potential cardiovascular and other benefits.

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Year:  2012        PMID: 22555471     DOI: 10.1007/s00125-012-2561-x

Source DB:  PubMed          Journal:  Diabetologia        ISSN: 0012-186X            Impact factor:   10.122


  18 in total

1.  Release of glucagon-like peptide 1 (GLP-1 [7-36 amide]), gastric inhibitory polypeptide (GIP) and insulin in response to oral glucose after upper and lower intestinal resections.

Authors:  M A Nauck; J Siemsglüss; C Orskov; J J Holst
Journal:  Z Gastroenterol       Date:  1996-03       Impact factor: 2.000

2.  Physiological and pharmacological mechanisms through which the DPP-4 inhibitor sitagliptin regulates glycemia in mice.

Authors:  Aurélie Waget; Cendrine Cabou; Myriam Masseboeuf; Pierre Cattan; Mattieu Armanet; Mélis Karaca; Julien Castel; Celine Garret; Gaëlle Payros; Adriano Maida; Thierry Sulpice; Jens J Holst; Daniel J Drucker; Christophe Magnan; Rémy Burcelin
Journal:  Endocrinology       Date:  2011-06-14       Impact factor: 4.736

Review 3.  Incretin-based therapies for type 2 diabetes mellitus: properties, functions, and clinical implications.

Authors:  Michael A Nauck
Journal:  Am J Med       Date:  2011-01       Impact factor: 4.965

4.  GLP-1 receptor stimulation reduces amyloid-beta peptide accumulation and cytotoxicity in cellular and animal models of Alzheimer's disease.

Authors:  Yazhou Li; Kara B Duffy; Mary Ann Ottinger; Balmiki Ray; Jason A Bailey; Harold W Holloway; David Tweedie; Tracyann Perry; Mark P Mattson; Dimitrios Kapogiannis; Kumar Sambamurti; Debomoy K Lahiri; Nigel H Greig
Journal:  J Alzheimers Dis       Date:  2010       Impact factor: 4.472

5.  GLP-1 and GIP are colocalized in a subset of endocrine cells in the small intestine.

Authors:  Kristine Mortensen; Louise Lundby Christensen; Jens Juul Holst; Cathrine Orskov
Journal:  Regul Pept       Date:  2003-07-15

Review 6.  Incretin-based therapies in type 2 diabetes mellitus.

Authors:  Chee W Chia; Josephine M Egan
Journal:  J Clin Endocrinol Metab       Date:  2008-07-15       Impact factor: 5.958

7.  Cardioprotective and vasodilatory actions of glucagon-like peptide 1 receptor are mediated through both glucagon-like peptide 1 receptor-dependent and -independent pathways.

Authors:  Kiwon Ban; M Hossein Noyan-Ashraf; Judith Hoefer; Steffen-Sebastian Bolz; Daniel J Drucker; Mansoor Husain
Journal:  Circulation       Date:  2008-04-21       Impact factor: 29.690

8.  Glucagon-like peptide-1 7-36: a physiological incretin in man.

Authors:  B Kreymann; G Williams; M A Ghatei; S R Bloom
Journal:  Lancet       Date:  1987-12-05       Impact factor: 79.321

9.  Preserved incretin activity of glucagon-like peptide 1 [7-36 amide] but not of synthetic human gastric inhibitory polypeptide in patients with type-2 diabetes mellitus.

Authors:  M A Nauck; M M Heimesaat; C Orskov; J J Holst; R Ebert; W Creutzfeldt
Journal:  J Clin Invest       Date:  1993-01       Impact factor: 14.808

10.  GIP does not potentiate the antidiabetic effects of GLP-1 in hyperglycemic patients with type 2 diabetes.

Authors:  Nikolaos Mentis; Irfan Vardarli; Lars D Köthe; Jens J Holst; Carolyn F Deacon; Michael Theodorakis; Juris J Meier; Michael A Nauck
Journal:  Diabetes       Date:  2011-02-17       Impact factor: 9.461

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  8 in total

1.  Exendin-4 protects pancreatic beta cells from palmitate-induced apoptosis by interfering with GPR40 and the MKK4/7 stress kinase signalling pathway.

Authors:  Annalisa Natalicchio; Rossella Labarbuta; Federica Tortosa; Giuseppina Biondi; Nicola Marrano; Alessandro Peschechera; Emanuele Carchia; Maura Roberta Orlando; Anna Leonardini; Angelo Cignarelli; Piero Marchetti; Sebastio Perrini; Luigi Laviola; Francesco Giorgino
Journal:  Diabetologia       Date:  2013-08-31       Impact factor: 10.122

2.  Efficacy and safety over 26 weeks of an oral treatment strategy including sitagliptin compared with an injectable treatment strategy with liraglutide in patients with type 2 diabetes mellitus inadequately controlled on metformin: a randomised clinical trial.

Authors:  B Charbonnel; H Steinberg; E Eymard; L Xu; P Thakkar; V Prabhu; M J Davies; S S Engel
Journal:  Diabetologia       Date:  2013-04-19       Impact factor: 10.122

3.  No Association of Proton Pump Inhibitor Use with Fasting or Postload Glycaemia in Patients with Cardiovascular Disease: A Cross-Sectional Retrospective Study.

Authors:  Olga Kruszelnicka; Marcin Kuźma; Iwona Z Pena; Ian B Perera; Bernadeta Chyrchel; Ewa Wieczorek-Surdacka; Andrzej Surdacki
Journal:  Int J Med Sci       Date:  2017-09-02       Impact factor: 3.738

4.  Mechanisms of glucose lowering of dipeptidyl peptidase-4 inhibitor sitagliptin when used alone or with metformin in type 2 diabetes: a double-tracer study.

Authors:  Carolina Solis-Herrera; Curtis Triplitt; Jose de Jesús Garduno-Garcia; John Adams; Ralph A DeFronzo; Eugenio Cersosimo
Journal:  Diabetes Care       Date:  2013-04-11       Impact factor: 19.112

5.  Sitagliptin reduces cardiac apoptosis, hypertrophy and fibrosis primarily by insulin-dependent mechanisms in experimental type-II diabetes. Potential roles of GLP-1 isoforms.

Authors:  Belén Picatoste; Elisa Ramírez; Alicia Caro-Vadillo; Cristian Iborra; Sara Ares-Carrasco; Jesús Egido; José Tuñón; Oscar Lorenzo
Journal:  PLoS One       Date:  2013-10-21       Impact factor: 3.240

Review 6.  Glucagon-like peptide-1 receptor agonists in the treatment of type 2 diabetes: Past, present, and future.

Authors:  Sanjay Kalra; Manash P Baruah; Rakesh K Sahay; Ambika Gopalakrishnan Unnikrishnan; Shweta Uppal; Omolara Adetunji
Journal:  Indian J Endocrinol Metab       Date:  2016 Mar-Apr

7.  Intestinal organoids for assessing nutrient transport, sensing and incretin secretion.

Authors:  Tamara Zietek; Eva Rath; Dirk Haller; Hannelore Daniel
Journal:  Sci Rep       Date:  2015-11-19       Impact factor: 4.379

8.  Serum Glucose-Dependent Insulinotropic Polypeptide (GIP) and Glucagon-Like Peptide-1 (GLP-1) in association with the Risk of Gestational Diabetes: A Prospective Case-Control Study.

Authors:  Maryam Mosavat; Siti Zawiah Omar; Sajad Jamalpour; Peng Chiong Tan
Journal:  J Diabetes Res       Date:  2020-01-29       Impact factor: 4.011

  8 in total

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