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 language | English |
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Pages (from-to) | 1-11 |
Journal | The Journal of Physiology |
Early online date | 4 Nov 2024 |
DOIs | |
Publication status | Published 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