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Endocrinology-informed neuroimaging in eating disorders: GLP1, orexins, and psilocybin.

Trevor Steward

Trends in molecular medicine April 1, 2024 DOI: 10.1016/j.molmed.2023.12.001 (opens in new tab) via PubMed

Summary

AI-generated from the abstract

Neuroimaging combined with peripheral endocrine measures can reveal the neurobiological drivers of eating disorders such as anorexia nervosa, bulimia nervosa, and binge eating disorder. Orexins/hypocretins, glucagon-like peptide-1 receptor (GLP1R) agonists, and psilocybin are highlighted as promising avenues for future investigation into the underlying mechanisms and potential treatments.

Study at a glance

Characteristics Review Peer reviewed
Topics Psilocybin
Keywords Glp1 Eating disorders FMRI Orexin
Key finding Neuroimaging combined with peripheral endocrine measures can provide insights into the neurobiological drivers of eating disorders, and orexins/hypocretins, GLP1R agonists, and psilocybin are highlighted as avenues for investigation.

Abstract

The neurobiology of eating disorders [EDs; anorexia nervosa (AN), bulimia nervosa (BN), and binge eating disorder (BED)] remains poorly understood. Here, I describe how neuroimaging, accompanied by peripheral endocrine measures, can provide insights into the neurobiological drivers of eating disorders. Orexins/hypocretins, glucagon-like peptide-1 receptor (GLP1R) agonists, and psilocybin are highlighted as avenues for investigation.

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