Nutrition and Calcitonin Gene Related Peptide (CGRP) in Migraine.
Michal FilaJan ChojnackiPiotr SobczukCezary ChojnackiJanusz BlasiakPublished in: Nutrients (2023)
Targeting calcitonin gene-related peptide (CGRP) and its receptor by antibodies and antagonists was a breakthrough in migraine prevention and treatment. However, not all migraine patients respond to CGRP-based therapy and a fraction of those who respond complain of aliments mainly in the gastrointestinal tract. In addition, CGRP and migraine are associated with obesity and metabolic diseases, including diabetes. Therefore, CGRP may play an important role in the functioning of the gut-brain-microflora axis. CGRP secretion may be modulated by dietary compounds associated with the disruption of calcium signaling and upregulation of mitogen-activated kinase phosphatases 1 and 3. CGRP may display anorexigenic properties through induction of anorexigenic neuropeptides, such as cholecystokinin and/or inhibit orexigenic neuropeptides, such as neuropeptide Y and melanin-concentrating hormone CH, resulting in the suppression of food intake, functionally coupled to the activation of the hypothalamic 3',5'-cyclic adenosine monophosphate. The anorexigenic action of CGRP observed in animal studies may reflect its general potential to control appetite/satiety or general food intake. Therefore, dietary nutrients may modulate CGRP, and CGRP may modulate their intake. Therefore, anti-CGRP therapy should consider this mutual dependence to increase the efficacy of the therapy and reduce its unwanted side effects. This narrative review presents information on molecular aspects of the interaction between dietary nutrients and CGRP and their reported and prospective use to improve anti-CGRP therapy in migraine.
Keyphrases
- type diabetes
- cardiovascular disease
- ejection fraction
- metabolic syndrome
- end stage renal disease
- body mass index
- protein kinase
- signaling pathway
- newly diagnosed
- risk assessment
- cell proliferation
- immune response
- drug delivery
- inflammatory response
- stem cells
- replacement therapy
- white matter
- skeletal muscle
- poor prognosis
- genome wide identification
- combination therapy
- glycemic control
- health information
- blood brain barrier