1. PACAP38/mast-cell-specific receptor axis mediates repetitive stress-induced headache in mice.
- Author
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Son H, Zhang Y, Shannonhouse J, Gomez R, and Kim YS
- Subjects
- Animals, Male, Mice, Receptors, G-Protein-Coupled metabolism, Receptors, G-Protein-Coupled genetics, Trigeminal Ganglion metabolism, Headache etiology, Headache metabolism, Headache physiopathology, Mice, Knockout, Mice, Inbred C57BL, Disease Models, Animal, Pituitary Adenylate Cyclase-Activating Polypeptide metabolism, Mast Cells metabolism, Stress, Psychological complications, Stress, Psychological metabolism
- Abstract
Background: Pain, an evolutionarily conserved warning system, lets us recognize threats and motivates us to adapt to those threats. Headache pain from migraine affects approximately 15% of the global population. However, the identity of any putative threat that migraine or headache warns us to avoid is unknown because migraine pathogenesis is poorly understood. Here, we show that a stress-induced increase in pituitary adenylate cyclase-activating polypeptide-38 (PACAP38), known as an initiator of allosteric load inducing unbalanced homeostasis, causes headache-like behaviour in male mice via mas-related G protein-coupled receptor B2 (MrgprB2) in mast cells., Methods: The repetitive stress model and dural injection of PACAP38 were performed to induce headache behaviours. We assessed headache behaviours using the facial von Frey test and the grimace scale in wild-type and MrgprB2-deficient mice. We further examined the activities of trigeminal ganglion neurons using in vivo Pirt-GCaMP Ca
2+ imaging of intact trigeminal ganglion (TG)., Results: Repetitive stress and dural injection of PACAP38 induced MrgprB2-dependent headache behaviours. Blood levels of PACAP38 were increased after repetitive stress. PACAP38/MrgprB2-induced mast cell degranulation sensitizes the trigeminovascular system in dura mater. Moreover, using in vivo intact TG Pirt-GCaMP Ca2+ imaging, we show that stress or/and elevation of PACAP38 sensitized the TG neurons via MrgprB2. MrgprB2-deficient mice showed no sensitization of TG neurons or mast cell activation. We found that repetitive stress and dural injection of PACAP38 induced headache behaviour through TNF-a and TRPV1 pathways., Conclusions: Our findings highlight the PACAP38-MrgprB2 pathway as a new target for the treatment of stress-related migraine headache. Furthermore, our results pertaining to stress interoception via the MrgprB2/PACAP38 axis suggests that migraine headache warns us of stress-induced homeostatic imbalance., (© 2024. The Author(s).)- Published
- 2024
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