Bluesky Facebook Reddit Email

New brain-to-nerve signaling mechanism reveals potential path to migraine pain

07.04.24 | American Association for the Advancement of Science (AAAS)

Aranet4 Home CO2 Monitor

Aranet4 Home CO2 Monitor tracks ventilation quality in labs, classrooms, and conference rooms with long battery life and clear e-ink readouts.

The rapid influx of cerebral spinal fluid (CSF) and protein solutes released during cortical spreading depression (CSD) in the brain activates neurons to trigger aural migraine headaches, according to a new mouse study. The findings identify a novel non-synaptic signaling mechanism between the brain and peripheral sensory system important for migraine. They also suggest potential pharmacological targets for treating the painful disorder. Migraine with aura, or an aural migraine, is a distinct headache disorder that can include sensory disturbances, such as hearing- or vision-related symptoms that precede onset of headache pain. During the aura phase, it is believed that waves of CSD are spontaneously triggered in the cerebral cortex or cerebellum, which, in turn, lead to activation of pain receptors (nociceptors) in the peripheral nervous system (PNS). Previous research has suggested that CSD events release small molecules through the CSF that activate sensory nerve endings in the external tissues of the CNS (central nervous system), “outside” of the blood-brain barrier. These nerve endings are not exposed to CSF. How pathological CSD events in the cortex trigger the activation of peripheral nociceptors outside the brain remains poorly understood. Using a combination of proteomic, histological, imaging, and functional approaches in a mouse model of classical migraine, Martin Rasmussen and colleagues identified a signaling pathway between the CNS and PNS at the trigeminal ganglion. Unlike more distal parts of the CNS, the proximal zone of the trigeminal ganglion lacks a tight nerve barrier, allowing CSF and the signaling molecules released during CSD events to enter and interact with trigeminal cells. Rasmussen et al. found that CSD alters 11% of the CSF proteome, with up-regulation of proteins that directly activate receptors in the trigeminal ganglion, including calcitonin gene-related peptide (CGRP). “Although this work provides some of the strongest data to date for a role of the glymphatic system in migraine, there is much to discover about the foundational role that fluid and solute transport play in neurobiological processes, suggesting that the journey toward understanding the role that glymphatic function and dysfunction play in a wide range of neurological and psychiatric conditions has only just begun,” write Andrew Russo and Jeffery Iliff in a related Perspective.

Science

10.1126/science.adl0544

Trigeminal ganglion neurons are directly activated by influx of CSF solutes in a migraine model

5-Jul-2024

Keywords

Article Information

Contact Information

Science Press Package Team
American Association for the Advancement of Science/AAAS
scipak@aaas.org

How to Cite This Article

APA:
American Association for the Advancement of Science (AAAS). (2024, July 4). New brain-to-nerve signaling mechanism reveals potential path to migraine pain. Brightsurf News. https://www.brightsurf.com/news/8Y43O9KL/new-brain-to-nerve-signaling-mechanism-reveals-potential-path-to-migraine-pain.html
MLA:
"New brain-to-nerve signaling mechanism reveals potential path to migraine pain." Brightsurf News, Jul. 4 2024, https://www.brightsurf.com/news/8Y43O9KL/new-brain-to-nerve-signaling-mechanism-reveals-potential-path-to-migraine-pain.html.