Migraine-linked protein exhibits sex-specific pain effects

Migraine-linked protein exhibits sex-specific pain effects
Dr. Greg Dussor is the corresponding author of the study and an associate professor of neuroscience in the UT Dallas School of Behavioral and Brain Sciences. Credit: UT Dallas / Ricardo Castrillón

A new preclinical study from University of Texas at Dallas researchers may help explain why migraine is three times more common in women than men.

In research published online April 8 in the Journal of Neuroscience, a protein implicated in the development of symptoms caused pain responses in female rodents, but not in males, when introduced into the meninges, the protective tissue layers surrounding the brain.

Most previous preclinical investigations of migraine and the protein, called calcitonin gene-related peptide (CGRP), used only male animals, leaving the question of neurobiological sex differences unanswered, said Dr. Greg Dussor, the corresponding author of the study and an associate professor of neuroscience in the UT Dallas School of Behavioral and Brain Sciences.

"This is the first study to show that CGRP might act differently between sexes," said Dussor, Fellow, Eugene McDermott Professor. "It also shows that CGRP can have a pain-related effect in the meninges, which is something that has been questioned in the literature previously."

Migraine—a condition defined by severe periodic headaches often accompanied by nausea, vision disturbances and light or sound sensitivity—is the most common neurological disorder worldwide and the second-leading cause of disability. Despite CGRP's well-established role in migraine, it is unknown where in the body it contributes to the condition.

"We already know CGRP has a prominent role in migraine. It's been investigated for more than 30 years," Dussor said. "CGRP is produced both in the —the brain and spinal cord—and in the peripheral nervous system, which goes everywhere else, including the meninges. But it can't move between the two; it's too large to cross the that shields the central nervous system."

The neurons that innervate the meninges signal the pain of a headache. However, because of the full range of symptoms and phases involved in migraine, the condition is believed to start in the brain.

The experiment involved injecting small doses of CGRP into the dura mater, the outermost layer of the meninges. Only the female animals experienced headache symptoms. The researchers observed a similar pain response in the female animals' paws when injected there.

Migraine neurobiology linked to prevalence in females
Dural administration of CGRP produces facial hypersensitivity and priming in female but not in male rats. Credit: Avona et al., JNeurosci (2019)

"That response shows that females may be more sensitive to CGRP throughout the body, not just the meninges," Dussor said. "But we don't know what that means for other types of pain yet."

The reasons for migraine's prevalence in females are likely complex. Because the male rodents were unaffected by introducing CGRP into the meninges, Dussor said the study does suggest that CGRP-based signaling from the meninges may contribute to the female-biased nature of this disorder.

In the wake of CGRP gaining more attention in migraine prevention research, the Food and Drug Administration has recently approved three therapeutic drugs that block the protein.

"Although CGRP plays a clear role in migraine, this does not imply that migraine is exclusively a CGRP-based disorder," Dussor said. "This is just the beginning of demonstrations showing that CGRP might act differently in women."

More information: Dural calcitonin gene-related peptide produces female-specific responses in rodent migraine models, Journal of Neuroscience (2019). DOI: 10.1523/JNEUROSCI.0364-19.2019

Journal information: Journal of Neuroscience

Citation: Migraine-linked protein exhibits sex-specific pain effects (2019, April 8) retrieved 22 September 2023 from https://medicalxpress.com/news/2019-04-migraine-linked-protein-sex-specific-pain-effects.html
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