Objective To assess the functional effects of a variant, c.89 G > A (p.Arg30Gln), in the transient receptor potential melastatin 8 (TRPM8) cold-sensing, nonselective cation channel, which we have previously identified in a patient with familial trigeminal neuralgia. Methods We carried out Ca2+ imaging and whole-cell patch-clamp recording. Results The TRPM8 mutation enhances channel activation, increases basal current amplitude and intracellular [Ca2+] in cells carrying the mutant channel, and enhances the response to menthol. Conclusions We propose that Arg30Gln confers gain-of-function attributes on TRPM8, which contribute to pathogenesis of trigeminal neuralgia in patients carrying this mutation.

Trigeminal neuralgia TRPM8 mutation: Enhanced activation, basal [Ca2+]i and menthol response / Gualdani, R.; Yuan, J. -H.; Effraim, P. R.; Di Stefano, G.; Truini, A.; Cruccu, G.; Dib-Hajj, S. D.; Gailly, P.; Waxman, S. G.. - In: NEUROLOGY. GENETICS. - ISSN 2376-7839. - 7:1(2021). [10.1212/NXG.0000000000000550]

Trigeminal neuralgia TRPM8 mutation: Enhanced activation, basal [Ca2+]i and menthol response

Di Stefano G.;Truini A.;Cruccu G.;
2021

Abstract

Objective To assess the functional effects of a variant, c.89 G > A (p.Arg30Gln), in the transient receptor potential melastatin 8 (TRPM8) cold-sensing, nonselective cation channel, which we have previously identified in a patient with familial trigeminal neuralgia. Methods We carried out Ca2+ imaging and whole-cell patch-clamp recording. Results The TRPM8 mutation enhances channel activation, increases basal current amplitude and intracellular [Ca2+] in cells carrying the mutant channel, and enhances the response to menthol. Conclusions We propose that Arg30Gln confers gain-of-function attributes on TRPM8, which contribute to pathogenesis of trigeminal neuralgia in patients carrying this mutation.
2021
pain; trigeminal neuralgia
01 Pubblicazione su rivista::01a Articolo in rivista
Trigeminal neuralgia TRPM8 mutation: Enhanced activation, basal [Ca2+]i and menthol response / Gualdani, R.; Yuan, J. -H.; Effraim, P. R.; Di Stefano, G.; Truini, A.; Cruccu, G.; Dib-Hajj, S. D.; Gailly, P.; Waxman, S. G.. - In: NEUROLOGY. GENETICS. - ISSN 2376-7839. - 7:1(2021). [10.1212/NXG.0000000000000550]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1572538
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