The trigeminovascular system (TVS) refers to neurons and their axonal projections within the trigeminal nerve that project to the cranial meninges and meningeal blood vessels[1][2] residing on the brain's surface.[3] The term, introduced in 1983[4] denotes also the neuropeptides contained within axons that are released into the meninges[5][6] to target vessels and surrounding cells (e.g., mast cells, macrophages, Schwann cells).

The major drugs used to treat migraine in the 19th and 20th century (ergot alkaloids, triptans) were found by Moskowitz and colleagues[7][6] to inhibit neuropeptide release from TV axons as their major mechanism of action. Because drugs that block the release of neuropeptides from trigeminovascular fibres are therapeutically relevant for relieving migraine headaches (especially CGRP to date), hence, It has been hypothesized that the trigeminovascular system may be involved in migraine headaches.[3][8][9] Studies of the TVS have helped to identify therapeutic targets for migraine including onabotulinum toxin, 5-HT1F receptor agonist (lasmiditan),5-HT1B,D[10] as well as CGRP and its receptor system[11] including both small molecule drugs and biologicals. Numerous experimental studies have established that cortical spreading depolarization, the biological substrate for migraine aura, can discharge trigeminovascular afferents as a cause of head pain and by extension unilateral headache overlying the dysfunctional hemisphere in migraineurs with aura.[12] Hence, the TVS has provided a template for migraine pathophysiology and target for drug discovery.

The history of some discoveries re the TV System are summarised in Ashina, et al.[13]

The Brain Prize for 2021 was awarded to 4 investigators studying the trigeminovascular system and its implications for migraine pathophysiology and treatments.

See also

References

  1. ^ Moskowitz, MichaelA.; Romero, Jorge; Reinhard, JohnF.; Melamed, Eldad; Pettibone, DouglasJ. (October 1979). "NEUROTRANSMITTERS AND THE FIFTH CRANIAL NERVE: IS THERE A RELATION TO THE HEADACHE PHASE OF MIGRAINE?". The Lancet. 314 (8148): 883–885. doi:10.1016/s0140-6736(79)92692-8. ISSN 0140-6736.
  2. ^ Moskowitz, Michael A. (August 1984). "The neurobiology of vascular head pain". Annals of Neurology. 16 (2): 157–168. doi:10.1002/ana.410160202. ISSN 0364-5134.
  3. ^ a b May, A.; Goadsby, P. J. (1999). "The Trigeminovascular System in Humans: Pathophysiologic Implications for Primary Headache Syndromes of the Neural Influences on the Cerebral Circulation". Journal of Cerebral Blood Flow & Metabolism: 115. doi:10.1097/00004647-199902000-00001.
  4. ^ Liu-Chen, Lee-Yuan; Mayberg, Marc R.; Moskowitz, Michael A. (May 1983). "Immunohistochemical evidence for a substance P-containing trigeminovascular pathway to pial arteries in cats". Brain Research. 268 (1): 162–166. doi:10.1016/0006-8993(83)90402-x. ISSN 0006-8993.
  5. ^ Moskowitz, M.A.; Brody, M.; Liu-Chen, L.-Y. (August 1983). "In vitro release of immunoreactive substance P from putative afferent nerve endings in bovine pia arachnoid". Neuroscience. 9 (4): 809–814. doi:10.1016/0306-4522(83)90269-5. ISSN 0306-4522.
  6. ^ a b Buzzi, M (November 1991). "Dihydroergotamine and sumatriptan attenuate levels of CGRP in plasma in rat superior sagittal sinus during electrical stimulation of the trigeminal ganglion". Neuropharmacology. 30 (11): 1193–1200. doi:10.1016/0028-3908(91)90165-8. ISSN 0028-3908.
  7. ^ Buzzi, M. Gabriella; Moskowitz, Midiael A. (January 1990). "The antimigraine drug, sumatriptan (GR43175), selectively blocks neurogenic plasma extravasation from blood vessels in dura mater". British Journal of Pharmacology. 99 (1): 202–206. doi:10.1111/j.1476-5381.1990.tb14679.x. ISSN 0007-1188. PMC 1917483.
  8. ^ Fanciullacci, M.; Alessandri, M.; Sicuteri, R.; Marabini, S. (1997). "Responsiveness of the trigeminovascular system to nitroglycerine in cluster headache patients". Brain. 120 (2): 283. doi:10.1093/brain/120.2.283.
  9. ^ Noseda, R.; Jakubowski, M.; Kainz, V.; Borsook, D.; Burstein, R. (2011). "Cortical Projections of Functionally Identified Thalamic Trigeminovascular Neurons: Implications for Migraine Headache and Its Associated Symptoms". Journal of Neuroscience. 31 (40): 14204–14217. doi:10.1523/JNEUROSCI.3285-11.2011. PMC 3501387. PMID 21976505.
  10. ^ Moskowitz, MA; et al. (November 2022). "Migraine research comes of age in the 21st century". Lancet Neurology. 21 (11): 955–958. doi:10.1016/S1474-4422(22)00398-2.
  11. ^ Warfvinge, Karin; Edvinsson, Lars (2013-05-13). "Pearls and pitfalls in neural CGRP immunohistochemistry". Cephalalgia. 33 (8): 593–603. doi:10.1177/0333102412472072. ISSN 0333-1024.
  12. ^ Bolay, Hayrunnisa; Reuter, Uwe; Dunn, Andrew K.; Huang, Zhihong; Boas, David A.; Moskowitz, Michael A. (February 2002). "Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model". Nature Medicine. 8 (2): 136–142. doi:10.1038/nm0202-136. ISSN 1078-8956.
  13. ^ Ashina, Messoud; Hansen, Jakob Møller; Do, Thien Phu; Melo-Carrillo, Agustin; Burstein, Rami; Moskowitz, Michael A (August 2019). "Migraine and the trigeminovascular system—40 years and counting". Lancet Neurology. 18 (8): 795–804. doi:10.1016/s1474-4422(19)30185-1. ISSN 1474-4422. PMC 7164539.

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