Anti-CGRP monoclonal antibodies counteract establishment of food aversive memories and chemotherapy-induced anorexia and weight loss.
Pharmacol Res · 2025
Last updated 2026-05-28In a rat study, anti-CGRP monoclonal antibodies—drugs approved for migraine prevention—reduced food aversive memories and counteracted chemotherapy-induced loss of appetite and weight loss. However, these antibodies did not prevent appetite loss caused by the GLP-1 drug liraglutide.
AI summary of the abstract below.
| Journal | Pharmacol Res, 2025 |
|---|---|
| Citations | 1 |
| Molecules | — |
| Conditions studied | Obesity |
Abstract
Glutamatergic neurons of external lateral parabrachial nucleus co-expressing calcitonin gene related peptide (elPB) negatively regulate food intake and establish food aversive memories. They also promote malaise-dependent anorexia, sickness behavior and tumor cachexia. In spite of the pathogenetic potential of elPB neurons in numerous human disorders, whether they can be targeted with drugs inhibiting CGRP-dependent neuromodulation remains unknown. We report that systemically administered anti-CGRP mAbs recently approved for migraine prevention reach the rat brain and counteract CGRP-regulated food aversive memories as well as chemotherapy-induced anorexia and weight loss. Anti-CGRP antibodies also partially reduce fear responses, but are unable to prevent anorexia by the GLP-1 agonist liraglutide. Data disclose the therapeutic potential of anti-CGRP monoclonals to treatment of eating disorders, including tumor treatment-associated syndromes such as chemotherapy induced nausea and vomiting or cachexia.
Verbatim abstract via PubMed 40490094 ↗