Oxytocin does not acutely improve glucose tolerance in men with type 2 diabetes

Author:

Goll Nina1,Moszka Nina12,Kantartzis Konstantinos345,Preissl Hubert456,Gruber Tim478,Fritsche Louise345,Jumpertz‐von Schwarzenberg Reiner345,García‐Cáceres Cristina479,Fritsche Andreas345,Hallschmid Manfred1456ORCID

Affiliation:

1. Department of Medical Psychology and Behavioural Neurobiology University of Tübingen Tübingen Germany

2. Department of Periodontics, Preventive and Restorative Dentistry, Center for Dental and Oral Medicine University Medical Center Hamburg Eppendorf Hamburg Germany

3. Department of Internal Medicine IV University Hospital Tübingen Tübingen Germany

4. German Center for Diabetes Research (DZD) Tübingen Germany

5. Institute for Diabetes Research and Metabolic Diseases of the Helmholtz Center Munich at the University of Tübingen Tübingen Germany

6. German Center for Mental Health (DZPG) Tübingen Germany

7. Institute for Diabetes and Obesity Helmholtz Diabetes Center, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg Germany

8. Van Andel Institute Grand Rapids Michigan USA

9. Medizinische Klinik und Poliklinik IV Klinikum der Universität, Ludwig‐Maximilians‐Universität München Munich Germany

Abstract

AbstractAimTo assess oxytocin's acute glucoregulatory impact in men with type 2 diabetes in the context of our previous findings that oxytocin improves β‐cell responsivity in healthy men.MethodsIn a double‐blind, crossover comparison, intranasal oxytocin (24 IU) and placebo, respectively, were administered to 25 fasted men with non‐insulin–treated type 2 diabetes (age ± standard error of the mean, 63.40 ± 1.36 years; body mass index, 27.77 ± 0.66 kg/m2; HbA1c, 6.86% ± 0.08%; Homeostatic Model Assessment of Insulin Resistance (HOMA‐IR, 3.44 ± 0.39) 60 minutes before an oral glucose tolerance test (oGTT). Key outcomes were compared with previous results in men with normal weight or obesity.ResultsOxytocin compared with placebo increased plasma oxytocin concentrations and reduced the heart rate, but did not alter glucose metabolism in the 3 hours after oGTT onset (area under the curve, glucose, 2240 ± 80.5 vs. 2190 ± 69.5 mmol/L × min; insulin, 45 663 ± 4538 vs. 44 343 ± 4269 pmol/L × min; C‐peptide, 235 ± 5.1 vs. 231 ± 15.9 nmol/L × min).ConclusionsThis outcome contrasts with the oxytocin‐induced attenuation of early postprandial glucose excursions in normal‐weight individuals, but is in line with the absence of respective effects in men with obesity. We conclude that insulin resistance in type 2 diabetes is associated with decreased sensitivity to the acute glucoregulatory effect of oxytocin in male individuals.

Funder

Deutsche Forschungsgemeinschaft

Bundesministerium für Bildung und Forschung

Publisher

Wiley

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