Oxyntomodulin physiology and its therapeutic development in obesity and associated complications

Martin T. W. Kueh, Ming Chuen Chong, Alexander D. Miras, Carel W. le Roux

Research output: Contribution to journalReview articlepeer-review

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Abstract

Incretins, such as glucagon-like peptide-1 (GLP1) and glucose-dependent insulinotropic polypeptide (GIP), have advanced the treatment landscape of obesity to a new pinnacle. As opposed to singular incretin effects, oxyntomodulin (OXM) activates glucagon receptors (GCGR) and glucagon-like peptide-1 receptors (GLP1R), demonstrating a more dynamic range of effects that are more likely to align with evolving ‘health gains’ goals in obesity care. Here, we will review the molecular insights from their inception to recent developments and challenges. This review will discuss the physiological actions of OXM, primarily appetite regulation, energy expenditure, and glucose homeostasis. Finally, we will shed light on the development of OXM-based therapies for obesity and associated complications, and outline important considerations for more translational efforts. (Figure presented.).

Original languageEnglish
Pages (from-to)1-11
JournalThe Journal of Physiology
Early online date4 Nov 2024
DOIs
Publication statusPublished online - 4 Nov 2024

Bibliographical note

Publisher Copyright:
© 2024 The Author(s). The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society.

Keywords

  • gut‐brain axis
  • glucose metabolism
  • obesity
  • oxyntomodulin
  • energy expenditure
  • gut-brain axis

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