Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

Molecular Biology

Gastric ghrelin cells in obese patients are hyperactive

Abstract

Background/objectives

Distribution and activity of ghrelin cells in the stomach of obese subjects are controversial.

Subjects/methods

We examined samples from stomachs removed by sleeve gastrectomy in 49 obese subjects (normoglycemic, hyperglycemic and diabetic) and quantified the density of ghrelin/chromogranin endocrine cells by immunohistochemistry. Data were compared with those from 13 lean subjects evaluated by gastroscopy. In 44 cases (11 controls and 33 obese patients) a gene expression analysis of ghrelin and its activating enzyme ghrelin O-acyl transferase (GOAT) was performed. In 21 cases (4 controls and 17 obese patients) the protein levels of unacylated and acylated-ghrelin were measured by ELISA tests. In 18 cases (4 controls and 14 obese patients) the morphology of ghrelin-producing cells was evaluated by electron microscopy.

Results

The obese group, either considered as total population or divided into subgroups, did not show any significant difference in ghrelin cell density when compared with control subjects. Inter-glandular smooth muscle fibres were increased in obese patients. In line with a positive trend of the desacylated form found by ELISA, Ghrelin and GOAT mRNA expression in obese patients was significantly increased. The unique ghrelin cell ultrastructure was maintained in all obese groups. In the hyperglycemic obese patients, the higher ghrelin expression matched with ultrastructural signs of endocrine hyperactivity, including expanded rough endoplasmic reticulum and reduced density, size and electron-density of endocrine granules. A positive correlation between ghrelin gene expression and glycemic values, body mass index and GOAT was also found. All obese patients with type 2 diabetes recovered from diabetes at follow-up after 5 months with a 16.5% of weight loss.

Conclusions

Given the known inhibitory role on insulin secretion of ghrelin, these results suggest a possible role for gastric ghrelin overproduction in the complex architecture that takes part in the pathogenesis of type 2 diabetes.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Density of ghrelin-producing cells (GPCs) in human stomach.
Fig. 2: Gene expression of ghrelin and its activator ghrelin O-acyltransferase in human stomach.
Fig. 3: Representative electron microscope images showing ghrelin-like cells of obese and control patients.
Fig. 4: Morphometric analysis performed on electron microscope images of ghrelin cells in obese and control groups.
Fig. 5: Correlation between glycaemic values and ghrelin gene expression in obese patients.

Similar content being viewed by others

References

  1. Kojima M, Hosoda H, Date Y, Nakazato M, Matsuo H, Kangawa K. Ghrelin is a growth-hormone-releasing acylated peptide from stomach. Nature. 1999;402(Dec):656–60. 9.

    Article  CAS  PubMed  Google Scholar 

  2. Tschöp M, Smiley DL, Heiman ML. Ghrelin induces adiposity in rodents. Nature. 2000;407(Oct):908–13. 19.

    Article  PubMed  Google Scholar 

  3. Goitein D, Lederfein D, Tzioni R, Berkenstadt H, Venturero M, Rubin M. Mapping of ghrelin gene expression and cell distribution in the stomach of morbidly obese patients-a possible guide for efficient sleeve gastrectomy construction. Obes Surg. 2012;22(Apr):617–22.

    Article  PubMed  Google Scholar 

  4. Müller TD, Nogueiras R, Andermann ML, Andrews ZB, Anker SD, Argente J, et al. Ghrelin. Mol Metab. 2015;4(Jun):437–60.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  5. Moran TH. Gut peptides in the control of food intake. Int J Obes. 2009;33(Apr):S7–10. 2005. Suppl 1.

    Article  CAS  Google Scholar 

  6. Poher A-L, Tschöp MH, Müller TD. Ghrelin regulation of glucose metabolism. Peptides. 2018;100:236–42.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Masuda Y, Tanaka T, Inomata N, Ohnuma N, Tanaka S, Itoh Z, et al. Ghrelin stimulates gastric acid secretion and motility in rats. Biochem Biophys Res Commun. 2000;276(Oct):905–8. 5.

    Article  CAS  PubMed  Google Scholar 

  8. Asakawa A, Inui A, Kaga T, Yuzuriha H, Nagata T, Ueno N, et al. Ghrelin is an appetite-stimulatory signal from stomach with structural resemblance to motilin. Gastroenterology. 2001;120(Feb):337–45.

    Article  CAS  PubMed  Google Scholar 

  9. Reed JA, Benoit SC, Pfluger PT, Tschöp MH, D’Alessio DA, Seeley RJ. Mice with chronically increased circulating ghrelin develop age-related glucose intolerance. Am J Physiol Endocrinol Metab. 2008;294(Apr):E752–760.

    Article  CAS  PubMed  Google Scholar 

  10. Gray SM, Page LC, Tong J. Ghrelin regulation of glucose metabolism. J Neuroendocrinol. 2019;31(Jul):e12705.

    PubMed  PubMed Central  Google Scholar 

  11. Shiiya T, Nakazato M, Mizuta M, Date Y, Mondal MS, Tanaka M, et al. Plasma ghrelin levels in lean and obese humans and the effect of glucose on ghrelin secretion. J Clin Endocrinol Metab. 2002;87(Jan):240–4.

    Article  CAS  PubMed  Google Scholar 

  12. English PJ, Ghatei MA, Malik IA, Bloom SR, Wilding JPH. Food fails to suppress ghrelin levels in obese humans. J Clin Endocrinol Metab. 2002;87(Jun):2984.

    Article  CAS  PubMed  Google Scholar 

  13. Churm R, Davies JS, Stephens JW, Prior SL. Ghrelin function in human obesity and type 2 diabetes: a concise review. Obes Rev Off J Int Assoc Study Obes. 2017;18:140–8.

    Article  CAS  Google Scholar 

  14. Basso N, Soricelli E, Castagneto-Gissey L, Casella G, Albanese D, Fava F, et al. Insulin resistance, microbiota, and fat distribution changes by a new model of vertical sleeve gastrectomy in obese rats. Diabetes. 2016;65:2990–3001.

    Article  CAS  PubMed  Google Scholar 

  15. Mani BK, Shankar K, Zigman JM. Ghrelin’s Relationship to Blood Glucose. Endocrinology. 2019;160:1247–61. 01.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Bray GA, Frühbeck G, Ryan DH, Wilding JPH. Management of obesity. Lancet Lond Engl. 2016;387(May):1947–56. 7.

    Article  Google Scholar 

  17. González-Muniesa P, Mártinez-González M-A, Hu FB, Després J-P, Matsuzawa Y, Loos RJF. et al.Obesity.Nat Rev Dis Primer.2017;3(Jun):17034 . 15.

    Article  Google Scholar 

  18. Bray GA, Kim KK, Wilding JPH, World Obesity Federation. Obesity: a chronic relapsing progressive disease process. A position statement of the World Obesity Federation. Obes Rev Off J Int Assoc Study Obes. 2017;18:715–23.

  19. Cummings DE, Rubino F. Metabolic surgery for the treatment of type 2 diabetes in obese individuals. Diabetologia. 2018;61:257–64.

    Article  PubMed  Google Scholar 

  20. Miyazaki Y, Takiguchi S, Seki Y, Kasama K, Takahashi T, Kurokawa Y, et al. Clinical significance of ghrelin expression in the gastric mucosa of morbidly obese patients. World J Surg. 2013;37(Dec):2883–90.

    Article  PubMed  Google Scholar 

  21. Ritze Y, Schollenberger A, Hamze Sinno M, Bühler N, Böhle M, Bárdos G, et al. Gastric ghrelin, GOAT, leptin, and leptinR expression as well as peripheral serotonin are dysregulated in humans with obesity. Neurogastroenterol Motil Off J Eur Gastrointest Motil Soc. 2016;28:806–15.

    Article  CAS  Google Scholar 

  22. Maksud FAN, Alves JS, Diniz MTC, Barbosa AJA. Density of ghrelin-producing cells is higher in the gastric mucosa of morbidly obese patients. Eur J Endocrinol. 2011;165(Jul):57–62.

    Article  CAS  PubMed  Google Scholar 

  23. Musella M, Di Capua F, D’Armiento M, Velotti N, Bocchetti A, Di KL. et al. No Difference in Ghrelin-Producing Cell Expression in Obese Versus Non-obese Stomach: a Prospective Histopathological Case-Control Study. Obes Surg. 2018;28(Nov):3604–10.

    Article  PubMed  Google Scholar 

  24. Abdemur A, Slone J, Berho M, Gianos M, Szomstein S, Rosenthal RJ. Morphology, localization, and patterns of ghrelin-producing cells in stomachs of a morbidly obese population. Surg Laparosc Endosc Percutan Tech. 2014;24(Apr):122–6.

    Article  PubMed  Google Scholar 

  25. Gagner M. Obesity: sleeve gastrectomy-the ideal choice for weight-loss surgery. Nat Rev Endocrinol. 2013;9(Jul):382–4.

    Article  PubMed  Google Scholar 

  26. Barresi V, Valenti G, Spampinato G, Musso N, Castorina S, Rizzarelli E, et al. Transcriptome analysis reveals an altered expression profile of zinc transporters in colorectal cancer. J Cell Biochem. 2018;119:9707–19.

    Article  CAS  PubMed  Google Scholar 

  27. Cinti F, Bouchi R, Kim-Muller JY, Ohmura Y, Sandoval PR, Masini M, et al. Evidence of β-Cell Dedifferentiation in Human Type 2 Diabetes. J Clin Endocrinol Metab. 2016;101(Mar):1044–54.

    Article  CAS  PubMed  Google Scholar 

  28. Wickham H. Intrauterine contraception: a look at devices and systems. Community Nurse. 2000;6(Oct):41–2,45.

    CAS  PubMed  Google Scholar 

  29. Miettinen M. Modern soft tissue pathology: tumors and non-neoplastic conditions. Cambridge University Press; Cambridge 2010. 1117 p.

  30. Yanagi S, Sato T, Kangawa K, Nakazato M. The Homeostatic Force of Ghrelin. Cell Metab. 2018;27:786–804. 03.

    Article  CAS  PubMed  Google Scholar 

  31. Ishii N, Tsubouchi H, Miura A, Yanagi S, Ueno H, Shiomi K, et al. Ghrelin alleviates paclitaxel-induced peripheral neuropathy by reducing oxidative stress and enhancing mitochondrial anti-oxidant functions in mice. Eur J Pharmacol. 2018;819(Jan):35–42. 15.

    Article  CAS  PubMed  Google Scholar 

  32. Sakata I, Nakamura K, Yamazaki M, Matsubara M, Hayashi Y, Kangawa K, et al. Ghrelin-producing cells exist as two types of cells, closed- and opened-type cells, in the rat gastrointestinal tract. Peptides. 2002;23(Mar):531–6.

    Article  CAS  PubMed  Google Scholar 

  33. Fakhry J, Stebbing MJ, Hunne B, Bayguinov Y, Ward SM, Sasse KC, et al. Relationships of endocrine cells to each other and to other cell types in the human gastric fundus and corpus. Cell Tissue Res. 2019;376(Apr):37–49. 1.

    Article  CAS  PubMed  Google Scholar 

  34. Ozkan Y, Timurkan ES, Aydin S, Sahin İ, Timurkan M, Citil C, et al. Acylated and Desacylated Ghrelin, Preptin, Leptin, and Nesfatin-1 Peptide Changes Related to the Body Mass Index [Internet]. Vol. 2013, International Journal of Endocrinology. Hindawi; 2013 [cited 2020 Jul 7]. p. e236085. https://www.hindawi.com/journals/ije/2013/236085/.

  35. Rindi G, Necchi V, Savio A, Torsello A, Zoli M, Locatelli V, et al. Characterisation of gastric ghrelin cells in man and other mammals: studies in adult and fetal tissues. Histochem Cell Biol. 2002;117(Jun):511–9.

    Article  CAS  PubMed  Google Scholar 

  36. Sjöström L. Review of the key results from the Swedish Obese Subjects (SOS) trial - a prospective controlled intervention study of bariatric surgery. J Intern Med. 2013;273(Mar):219–34.

    Article  PubMed  Google Scholar 

  37. Gagner M, Hutchinson C, Rosenthal R. Fifth International Consensus Conference: current status of sleeve gastrectomy. Surg Obes Relat Dis Off J Am Soc Bariatr Surg. 2016;12(May):750–6.

    Article  Google Scholar 

  38. Mihalache L, Arhire LI, Giuşcă SE, Gherasim A, Niţă O, Constantinescu D, et al. Ghrelin-producing cells distribution in the stomach and the relation with Helicobacter pylori in obese patients. Rom J Morphol Embryol. 2019;60:219–25.

    PubMed  Google Scholar 

  39. Gündoğan M, Çalli Demırkan N, Tekın K, Aybek H. Gastric histopathological findings and ghrelin expression in morbid obesity. Turk Patoloji Derg. 2013;29:19–26.

    PubMed  Google Scholar 

  40. Veedfald S, Plamboeck A, Hartmann B, Vilsbøll T, Knop FK, Deacon CF, et al. Ghrelin secretion in humans - a role for the vagus nerve? Neurogastroenterol Motil Off J Eur Gastrointest Motil Soc. 2018;30:e13295.

    Article  CAS  Google Scholar 

  41. Xing J, Chen JDZ. Alterations of gastrointestinal motility in obesity. Obes Res. 2004;12(Nov):1723–32.

    Article  PubMed  Google Scholar 

  42. Peiris M, Aktar R, Raynel S, Hao Z, Mumphrey MB, Berthoud H-R, et al. Effects of obesity and gastric bypass surgery on nutrient sensors, endocrine cells, and mucosal innervation of the mouse colon. Nutrients. 2018;10:1529–42.

  43. Selim MM, Wendelschafer-Crabb G, Redmon JB, Khoruts A, Hodges JS, Koch K, et al. Gastric mucosal nerve density: a biomarker for diabetic autonomic neuropathy? Neurology. 2010;75(Sep):973–81. 14.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Kitazawa T, Kaiya H. Regulation of Gastrointestinal Motility by Motilin and Ghrelin in Vertebrates. Front Endocrinol. 2019;10:278.

    Article  Google Scholar 

  45. Porporato PE, Filigheddu N, Reano S, Ferrara M, Angelino E, Gnocchi VF, et al. Acylated and unacylated ghrelin impair skeletal muscle atrophy in mice. J Clin Investig. 2013;123(Feb):611–22.

    CAS  PubMed  PubMed Central  Google Scholar 

  46. Pradhan G, Samson SL, Sun Y. Ghrelin: much more than a hunger hormone. Curr Opin Clin Nutr Metab Care. 2013;16(Nov):619–24.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Crivellato E, Nico B, Bertelli E, Nussdorfer GG, Ribatti D. Dense-core granules in neuroendocrine cells and neurons release their secretory constituents by piecemeal degranulation (review). Int J Mol Med. 2006;18(Dec):1037–46.

    CAS  PubMed  Google Scholar 

  48. Rindi G, Torsello A, Locatelli V, Solcia E. Ghrelin expression and actions: a novel peptide for an old cell type of the diffuse endocrine system. Exp Biol Med Maywood NJ. 2004;229(Nov):1007–16.

    Article  CAS  Google Scholar 

  49. Muscogiuri G, Balercia G, Barrea L, Cignarelli A, Giorgino F, Holst JJ, et al. Gut: a key player in the pathogenesis of type 2 diabetes? Crit Rev Food Sci Nutr. 2018;58(May):1294–309. 24.

    Article  CAS  PubMed  Google Scholar 

  50. Malin S, Samat A, Wolski K, Abood B, Pothier C, Bhatt D, et al. Improved acylated ghrelin suppression at 2 years in obese patients with type 2 diabetes: effects of bariatric surgery vs standard medical therapy. Int J Obes. 2014;38(Mar):364–70. 2005.

    Article  CAS  Google Scholar 

  51. Hotamisligil GS. Inflammation, metaflammation and immunometabolic disorders. Nature. 2017;542:177–85. 08.

    Article  CAS  PubMed  Google Scholar 

  52. Camastra S, Vitali A, Anselmino M, Gastaldelli A, Bellini R, Berta R, et al. Muscle and adipose tissue morphology, insulin sensitivity and beta-cell function in diabetic and nondiabetic obese patients: effects of bariatric surgery. Sci Rep. 2017;7:9007. 21.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  53. Alemán JO, Iyengar NM, Walker JM, Milne GL, Da Rosa JC, Liang Y, et al. Effects of rapid weight loss on systemic and adipose tissue inflammation and metabolism in obese postmenopausal women. J Endocr Soc. 2017;1(Apr):625–37. 25

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  54. Nannipieri M, Baldi S, Mari A, Colligiani D, Guarino D, Camastra S, et al. Roux-en-Y gastric bypass and sleeve gastrectomy: mechanisms of diabetes remission and role of gut hormones. J Clin Endocrinol Metab. 2013;98(Nov):4391–9.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We thank Prof Filippo Palermo (Catania) and Prof Daniela Morale (Milano) for their assistance in evaluating the statistical data, Dr Giuseppe Grasso (Catania), Dr Valentina Merendino (Catania) and Dr Maria Cristina Zingaretti (Ancona) for their excellent technical support and Prof Riccarda Granata (Torino) for the critical reading of the paper.

Funding

PRIN 2017 to Saverio Cinti; FIR Unict 2014 and Mediterranean Foundation “G.B. Morgagni” Catania to Sergio Castorina. The sources of funding had no involvement in the study design; in the collection, analysis and interpretation of data; in the writing of the report; and in the decision to submit the article for publication.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Saverio Cinti.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Castorina, S., Barresi, V., Luca, T. et al. Gastric ghrelin cells in obese patients are hyperactive. Int J Obes 45, 184–194 (2021). https://doi.org/10.1038/s41366-020-00711-3

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41366-020-00711-3

Search

Quick links