Deciphering in silico the Role of Mutated NaV1.1 Sodium Channels in Enhancing Trigeminal Nociception in Familial Hemiplegic Migraine Type 3

Familial hemiplegic migraine type 3 (FHM3) is caused by gain-of-function mutations in the SCN1A gene that encodes the α1 subunit of voltage-gated NaV1.1 sodium channels. The high level of expression of NaV1.1 channels in peripheral trigeminal neurons may lead to abnormal nociceptive signaling thus c...

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Bibliographic Details
Main Authors: Alina Suleimanova, Max Talanov, Arn M. J. M. van den Maagdenberg, Rashid Giniatullin
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Cellular Neuroscience
Subjects:
NaV
ATP
Online Access:https://www.frontiersin.org/articles/10.3389/fncel.2021.644047/full