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Glucagon-like peptide-2 treatment improves glucose dysmetabolism in mice fed a high-fat diet

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Abstract

Previous studies suggested that endogenous glucagon-like peptide 2 (GLP-2) is dispensable for the regulation of glucose homeostasis under normal conditions, while it can play a beneficial role in obesity conditions. The purpose of the present study was to investigate whether chronic treatment with Gly2-GLP-2, a stable analogue of GLP-2, can have an impact on glycaemic and lipid control in mice fed a high-fat diet (HFD), an animal model of human obesity and insulin resistance. HFD mice were treated once a day with Gly2-GLP-2 for 4 weeks. Body weight, food intake, fasting glucose, intraperitoneal glucose tolerance, insulin-induced glucose clearance, glucose-stimulated insulin secretion, β-cell mass, plasma lipid metabolic profile, and lipid deposition in the liver were examined. In untreated HFD mice, fasting glucose levels, glucose tolerance, glucose-stimulated plasma insulin and sensibility to exogenous insulin were deteriorating with time and β-cell mass increased. In Gly2-GLP-2-treated mice, we found significant increase in glucose tolerance and exogenous insulin sensitivity, reduction in glucose-stimulated plasma insulin and in the increase in β-cell mass in comparison with pair-aged HFD untreated animals. The chronic treatment with the peptide was not associated with remarkable improvements of dyslipidemia and it did not prevent liver fat accumulation and the presence of microvesicular steatosis. In conclusion, the results of the present study suggest, for the first time, that Gly2-GLP-2 may produce glucose metabolic benefits in mice with diet-induced obesity. The mechanisms underlying the beneficial impact of GLP-2 on glucose metabolism remain to be established.

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References

  1. A.S. Al-Goblan, M.A. Al-Alfi, M.Z. Khan, Mechanism linking diabetes mellitus and obesity. Diabetes Metab. Syndr. Obes. 7, 587–591 (2014)

    Article  PubMed  PubMed Central  Google Scholar 

  2. I. Vaněčková, L. Maletínská, M. Behuliak, V. Nagelová, J. Zicha, J. Kuneš, Obesity-related hypertension: possible pathophysiological mechanisms. J. Endocrinol. 223, R63–R78 (2014)

    Article  CAS  PubMed  Google Scholar 

  3. M.K. Badman, J.S. Flier, The gut and energy balance: visceral allies in the obesity wars. Science 307, 1909–1914 (2005)

    Article  CAS  PubMed  Google Scholar 

  4. S. Baldassano, A. Amato, GLP-2: what do we know? What are we going to discover? Regul. Pept. 194–195, 6–10 (2014)

    Article  CAS  PubMed  Google Scholar 

  5. K.J. Rowland, P.L. Brubaker, The “cryptic” mechanism of action of glucagon-like peptide-2. Am. J. Physiol. Gastrointest. Liver Physiol. 301, G1–G8 (2011)

    Article  CAS  PubMed  Google Scholar 

  6. P. Janssen, A. Rotondo, F. Mulé, J. Tack, Review article: a comparison of glucagon-like peptides 1 and 2. Aliment. Pharmacol. Ther. 37, 18–36 (2013)

    Article  CAS  PubMed  Google Scholar 

  7. K. Vipperla, S.J. O’Keefe, Targeted therapy of short-bowel syndrome with teduglutide: the new kid on the block. Clin. Exp. Gastroenterol. 7, 489–495 (2014)

    Article  PubMed  PubMed Central  Google Scholar 

  8. J.F. Marier, M.S. Mouksassi, N.H. Gosselin, M. Beliveau, J. Cyran, J. Wallens, Population pharmacokinetics of teduglutide following repeated subcutaneous administrations in healthy participants and in patients with short bowel syndrome and Crohn’s disease. J. Clin. Pharmacol. 50, 36–49 (2010)

    Article  CAS  PubMed  Google Scholar 

  9. H. Kissow, Glucagon-like peptides 1 and 2: intestinal hormones implicated in the pathophysiology of mucositis. Curr. Opin. Support Palliat. Care 9, 196–202 (2015)

    Article  PubMed  Google Scholar 

  10. M. Wøjdemann, A. Wettergren, B. Hartmann, J.J. Holst, Glucagon-like peptide-2 inhibits centrally induced antral motility in pigs. Scand. J. Gastroenterol. 33, 828–832 (1998)

    PubMed  Google Scholar 

  11. A. Amato, S. Baldassano, R. Serio, F. Mulè, Glucagon-like peptide-2 relaxes mouse stomach through vasoactive intestinal peptide release. Am. J. Physiol. Gastrointest. Liver Physiol. 296, G678–G684 (2009)

    Article  CAS  PubMed  Google Scholar 

  12. A. Amato, A. Rotondo, L. Cinci, S. Baldassano, M.G. Vannucchi, F. Mulè, Role of cholinergic neurons in the motor effects of glucagon-like peptide-2 in mouse colon. Am. J. Physiol. Gastrointest. Liver Physiol. 299, G1038–G1044 (2010)

    Article  CAS  PubMed  Google Scholar 

  13. L. Cinci, M.S. Faussone-Pellegrini, A. Rotondo, F. Mulè, M.G. Vannucchi, GLP-2 receptor expression in excitatory and inhibitory enteric neurons and its role in mouse duodenum contractility. Neurogastroenterol. Motil. 23, e383–e392 (2011)

    Article  CAS  PubMed  Google Scholar 

  14. S. Baldassano, S. Liu, M.H. Qu, F. Mulè, J.D. Wood, Glucagon-like peptide-2 modulates neurally evoked mucosal chloride secretion in guinea pig small intestine in vitro. Am. J. Physiol. Gastrointest. Liver Physiol. 297, G800–G805 (2009)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. A. Rotondo, A. Amato, S. Baldassano, L. Lentini, F. Mulè, Gastric relaxation induced by glucagon-like peptide-2 in mice fed a high-fat diet or fasted. Peptides 32, 1587–1592 (2011)

    Article  CAS  PubMed  Google Scholar 

  16. S. Baldassano, A.L. Bellanca, R. Serio, F. Mulè, Food intake in lean and obese mice after peripheral administration of glucagon-like peptide 2. J. Endocrinol. 213, 277–284 (2012)

    Article  CAS  PubMed  Google Scholar 

  17. M. Tang-Christensen, P.J. Larsen, J. Thulesen, J. Romer, N. Vrang, The proglucagon-derived peptide, glucagon-like peptide-2, is a neurotransmitter involved in the regulation of food intake. Nat. Med. 6, 802–807 (2000)

    Article  CAS  PubMed  Google Scholar 

  18. X. Shi, F. Zhou, X. Li, B. Chang, D. Li, Y. Wang, Q. Tong, Y. Xu, M. Fukuda, J.J. Zhao, D. Li, D.G. Burrin, L. Chan, X. Guan, Central GLP-2 enhances hepatic insulin sensitivity via activating PI3K signaling in POMC neurons. Cell Metab. 18, 86–98 (2013)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. X. Guan, The CNS glucagon-like peptide-2 receptor in the control of energy balance and glucose homeostasis. Am. J. Physiol. Regul. Integr. Comp. Physiol. 307, R585–R596 (2014)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. J. Hsieh, C. Longuet, A. Maida, J. Bahrami, E. Xu, C.L. Baker, P.L. Brubaker, D.J. Drucker, K. Adeli, Glucagon-like peptide-2 increases intestinal lipid absorption and chylomicron production via CD36. Gastroenterology 137, 997–1005 (2009)

    Article  CAS  PubMed  Google Scholar 

  21. G.F. Watts, D.C. Chan, Novel insights into the regulation of postprandial lipemia by glucagon-like peptides: significance for diabetes. Diabetes 62, 336–338 (2013)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. S. Dash, C. Xiao, C. Morgantini, P.W. Connelly, B.W. Patterson, G.F. Lewis, Glucagon-like peptide-2 regulates release of chylomicrons from the intestine. Gastroenterology 147, 1275–1284 (2014)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. P.D. Cani, S. Possemiers, T. Van de Wiele, Y. Guiot, A. Everard, O. Rottier, L. Geurts, D. Naslain, A. Neyrinck, D.M. Lambert, G.G. Muccioli, N.M. Delzenne, Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2-driven improvement of gut permeability. Gut 58, 1091–1103 (2009)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. J. Bahrami, C. Longuet, L.L. Baggio, K. Li, D.J. Drucker, Glucagon-like peptide-2 receptor modulates islet adaptation to metabolic stress in the ob/ob mouse. Gastroenterology 139, 857–868 (2010)

    Article  CAS  PubMed  Google Scholar 

  25. S. Baldassano, F. Rappa, A. Amato, F. Cappello, F. Mulè, GLP-2 as beneficial factor in the glucose homeostasis in mice fed a high fat diet. J. Cell. Physiol. 230, 3029–3036 (2015)

    Article  CAS  PubMed  Google Scholar 

  26. I. Hadjiyanni, K.K. Li, D.J. Drucker, Glucagon-like peptide-2 reduces intestinal permeability but does not modify the onset of type 1 diabetes in the nonobese diabetic mouse. Endocrinology 150, 529–592 (2009)

    Article  CAS  Google Scholar 

  27. R. Iakoubov, L.M. Lauffer, S. Trivedi, Y.I. Kim, P.L. Brubaker, Carcinogenic effects of exogenous and endogenous glucagon-like peptide-2 in azoxymethane-treated mice. Endocrinology 150, 4033–4043 (2009)

    Article  CAS  PubMed  Google Scholar 

  28. J. Folch, M. Lees, G.H. Sloane Stanley, A simple method for the isolation and purification of total lipides from animal tissues. J. Biol. Chem. 226, 497–509 (1957)

    CAS  PubMed  Google Scholar 

  29. A.M. Johnson, J.M. Olefsky, The origins and drives of insulin resistance. Cell 152, 673–684 (2013)

    Article  CAS  PubMed  Google Scholar 

  30. L. Prasad-Reddy, D. Isaacs, A clinical review of GLP-1 receptor agonists: efficacy and safety in diabetes and beyond. Drugs Context 4, 212283 (2015)

    Article  PubMed  PubMed Central  Google Scholar 

  31. L.L. Baggio, D.J. Drucker, Biology of incretins: GLP-1 and GIP. Gastroenterology 132, 2131–2157 (2007)

    Article  CAS  PubMed  Google Scholar 

  32. A.M. Deane, N.Q. Nguyen, J.E. Stevens, R.J.L. Fraser, R.H. Holloway, L.K. Besanko, C. Burgstad, K.L. Jones, M.J. Chapman, C.K. Rayner, M. Horowitz, Endogenous glucagon-like peptide-1 slows gastric emptying in healthy subjects, attenuating postprandial glycemia. J. Clin. Endocrinol. Metabol. 95, 215–221 (2010)

    Article  CAS  Google Scholar 

  33. A. Rotondo, A. Amato, L. Lentini, S. Baldassano, F. Mulè, Glucagon-like peptide-1 relaxes gastric antrum through nitric oxide in mice. Peptides 32, 60–64 (2011)

    Article  CAS  PubMed  Google Scholar 

  34. J. Hsieh, C. Longuet, C.L. Baker, B. Qin, L.M. Federico, D.J. Drucker, K. Adeli, The glucagon-like peptide 1 receptor is essential for postprandial lipoprotein synthesis and secretion in hamsters and mice. Diabetologia 53, 552–561 (2010)

    Article  CAS  PubMed  Google Scholar 

  35. J.P. Gutzwiller, B. Goke, J. Drewe, P. Hildebrand, S. Ketterer, D. Handschin, R. Winterhalder, D. Conen, C. Beglinger, Glucagon-like peptide-1: a potent regulator of food intake in humans. Gut 44, 81–86 (1999)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. A. Amato, L. Cinci, A. Rotondo, R. Serio, M.S. Faussone-Pellegrini, M.G. Vannucchi, F. Mulè, Peripheral motor action of glucagon-like peptide-1 through enteric neuronal receptors. Neurogastroenterol. Motil. 22, 664–e203 (2010)

    Article  CAS  PubMed  Google Scholar 

  37. A. Amato, S. Baldassano, R. Liotta, R. Serio, F. Mulè, Exogenous glucagon-like peptide 1 reduces contractions in human colon circular muscle. J. Endocrinol. 221, 29–37 (2014)

    Article  CAS  PubMed  Google Scholar 

  38. S. Baldassano, G.D. Wang, F. Mulè, J.D. Wood, Glucagon-like peptide-1 modulates neurally evoked mucosal chloride secretion in guinea pig small intestine in vitro. Am. J. Physiol. Gastrointest. Liver Physiol. 302, G352–G358 (2012)

    Article  CAS  PubMed  Google Scholar 

  39. C.Y. Shan, J.H. Yang, Y. Kong, X.Y. Wang, M.Y. Zheng, Y.G. Xu, Y. Wang, H.Z. Ren, B.C. Chang, L.M. Chen, Alteration of the intestinal barrier and GLP2 secretion in Berberine-treated type 2 diabetic rats. J. Endocrinol. 218, 255–262 (2013)

    Article  CAS  PubMed  Google Scholar 

  40. R.S. Surwit, C.M. Kuhn, C. Cochrane, J.A. McCubbin, M.N. Feinglos, Diet-induced type II diabetes in C57BL/6J mice. Diabetes 37, 1163–1167 (1988)

    Article  CAS  PubMed  Google Scholar 

  41. M.S. Winzell, B. Ahren, The high-fat diet–fed mouse: a model for studying mechanisms and treatment of impaired glucose tolerance and type 2 diabetes. Diabetes 53, S215–S219 (2004)

    Article  PubMed  Google Scholar 

  42. M. He, H. Su, W. Gao, S.M. Johansson, Q. Liu, X. Wu, J. Liao, A.A. Young, T. Bartfai, M.W. Wang, Reversal of obesity and insulin resistance by a non-peptidic glucagon-like peptide-1 receptor agonist in diet-induced obese mice. PLoS One 5, e14205 (2010)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. R.E. Stamateris, R.B. Sharma, D.A. Hollern, L.C. Alonso, Adaptive β-cell proliferation increases early in high-fat feeding in mice, concurrent with metabolic changes, with induction of islet cyclin D2 expression. Am. J. Physiol. Endocrinol. Metab. 305, E149–E159 (2013)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. A.E. Butler, J. Janson, S. Bonner-Weir, R. Ritzel, R.A. Rizza, P.C. Butler, Beta cell deficit and increased beta cell apoptosis in humans with type 2 diabetes. Diabetes 52, 102–110 (2003)

    Article  CAS  PubMed  Google Scholar 

  45. J. Ahren, B. Ahren, N. Wierup, Increased beta cell volume in mice fed a high-fat diet: a dynamic study over 12 months. Islets 2, 353–356 (2010)

    Article  PubMed  Google Scholar 

  46. B.A. Omar, J. Vikman, M.S. Winzell, U. Voss, E. Ekblad, J.E. Foley, B. Ahrén, Enhanced beta cell function and anti-inflammatory effect after chronic treatment with the dipeptidyl peptidase-4 inhibitor vildagliptin in an advanced-aged diet-induced obesity mouse model. Diabetologia 56, 1752–1760 (2013)

    Article  CAS  PubMed  Google Scholar 

  47. T. Okada, C.W. Liew, J. Hu, C. Hinault, M.D. Michael, J. Krtzfeldt, C. Yin, M. Holzenberger, M. Stoffel, R.N. Kulkarni, Insulin receptors in beta-cells are critical for islet compensatory growth response to insulin resistance. Proc. Natl. Acad. Sci. USA. 104, 8977–8982 (2007)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. M.M. Sachdeva, D.A. Stoffers, Minireview: meeting the demand for insulin: molecular mechanisms of adaptive postnatal beta-cell mass expansion. Mol. Endocrinol. 23, 747–758 (2009)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. B.R. Gedulin, S.E. Nikoulina, P.A. Smith, G. Gedulin, L.L. Nielsen, A.D. Baron, D.G. Parkes, A.A. Young, Exenatide (exendin-4) improves insulin sensitivity and β-cell mass in insulin-resistant obese fa/fa Zucker rats independent of glycemia and body weight. Endocrinology 146, 2069–2076 (2005)

    Article  CAS  PubMed  Google Scholar 

  50. Y. Matsuzawa, T. Funahashi, T. Nakamura, Molecular mechanism of metabolic syndrome X: contribution of adipocytokines adipocyte-derived bioactive substances. Ann. NY Acad. Sci. 892, 146–154 (1999)

    Article  CAS  PubMed  Google Scholar 

  51. M.W. Rajala, S. Obici, P.E. Scherer, L. Rossetti, Adipose-derived resistin and gut-derived resistin-like molecule-beta selectively impair insulin action on glucose production. J. Clin. Invest. 111, 225–230 (2003)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. H. Yki-Järvinen, J. Westerbacka, The fatty liver and insulin resistance. Curr. Mol. Med. 5, 287–295 (2005)

    Article  PubMed  Google Scholar 

  53. M. Asrih, F.R. Jornayvaz, Inflammation as a potential link between nonalcoholic fatty liver disease and insulin resistance. J. Endocrinol. 218, R25–R36 (2013)

    Article  CAS  PubMed  Google Scholar 

  54. V.E. de Meijer, H.D. Le, J.A. Meisel, M.R. Akhavan Sharif, A. Pan, V. Nosé, M. Puder, Dietary fat intake promotes the development of hepatic steatosis independently from excess caloric consumption in a murine model. Metabolism 59, 1092–10105 (2010)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. J.C. Fraulob, R. Ogg-Diamantino, C. Fernandes-Santos, M.B. Aguila, C.A. Mandarim-de-Lacerda, A mouse model of metabolic syndrome: insulin resistance, fatty liver and non-alcoholic fatty pancreas disease (NAFPD) in C57BL/6 mice fed a high fat diet. J. Clin. Biochem. Nutr. 46, 212–223 (2010)

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  56. N. El-Jamal, E. Erdual, M. Neunlist, D. Koriche, C. Dubuquoy, F. Maggiotto, J. Chevalier, D. Berrebi, L. Dubuquoy, E. Boulanger, A. Cortot, P. Desreumaux, Glugacon-like peptide-2: broad receptor expression, limited therapeutic effect on intestinal inflammation and novel role in liver regeneration. Am. J. Physiol. Gastrointest. Liver Physiol. 307, G274–G285 (2014)

    Article  CAS  PubMed  Google Scholar 

  57. B.A. Moore, N. Peffer, A. Pirone, A. Bassiri, S. Sague, J.M. Palmer, D.L. Johnson, T. Nesspor, C. Kliwinski, P.J. Hornby, GLP-2 receptor agonism ameliorates inflammation and gastrointestinal stasis in murine postoperative ileus. J. Pharmacol. Exp. Ther. 333, 574–583 (2010)

    Article  CAS  PubMed  Google Scholar 

  58. G.W. Moran, C. O’Neill, J.T. McLaughlin, GLP-2 enhances barrier formation and attenuates TNFα-induced changes in a Caco-2 cell model of the intestinal barrier. Regul. Pept. 178, 95–101 (2012)

    Article  CAS  PubMed  Google Scholar 

  59. S. Baldassano, A. Amato, F. Cappello, F. Rappa, F. Mulè, Glucagon-like peptide-2 and mouse intestinal adaptation to a high-fat diet. J. Endocrinol. 217, 11–20 (2013)

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

This work was supported by a Grant from Ministero dell’Istruzione, dell’Università e della Ricerca, Italy (FFR 2012, University of Palermo).

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  1. Dipartimento di Scienze e Tecnologie Biologiche Chimiche e Farmaceutiche (STEBICEF), Laboratorio di Fisiologia generale, Università di Palermo, Viale delle Scienze, 90128, Palermo, Italy

    Sara Baldassano, Antonella Amato, Gaetano Felice Caldara & Flavia Mulè

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Baldassano, S., Amato, A., Caldara, G.F. et al. Glucagon-like peptide-2 treatment improves glucose dysmetabolism in mice fed a high-fat diet. Endocrine 54, 648–656 (2016). https://doi.org/10.1007/s12020-016-0871-3

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