Clonazepam activates the transient receptor potential melastatin 8 (TRPM8) ion channel

Benzodiazepines represent a major class of drugs prescribed as treatments for anxiety, insomnia and seizures. They act by engaging GABA<sub>A</sub> receptors in the central nervous system to depress neuronal excitability. Here, the polypharmacology of benzodiazepines was explored by studying their engagement of human TRP channels revealing clonazepam acts as a robust and selective activator of the TRPM8 ion channel. Clonazepam-evoked Ca<sup>2+</sup> signals were observed in cells expressing human TRPM8 channels, and in mouse trigeminal neurons. These responses were completely blocked by pharmacological or genetic inhibition of TRPM8 function. This discovery likely explains why clonazepam is an effective treatment for the painful oral condition known as burning mouth disorder, where local activation of TRPM8 channels in sensory neurons mitigates the painful symptoms of this disease.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-22
DOI
https://doi.org/10.64898/2026.01.19.700423
Primary Topic
Ion Channels and Receptors
Type
article
Field-Weighted Citation Impact
0.00
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article

Clonazepam activates the transient receptor potential melastatin 8 (TRPM8) ion channel

Evgeny G. Chulkov, Jonathan Enders, Jonathan S. Marchant, Anthony D. Menzel et al.
bioRxiv (Cold Spring Harbor Laboratory)
Ion Channels and Receptors
article

Clonazepam activates the transient receptor potential melastatin 8 (TRPM8) ion channel

Evgeny G. Chulkov, Jonathan Enders, Jonathan S. Marchant, Anthony D. Menzel, Logan Elkin, Sang-Kyu Park, Cheryl L Stucky
article en

Abstract

Benzodiazepines represent a major class of drugs prescribed as treatments for anxiety, insomnia and seizures. They act by engaging GABA<sub>A</sub> receptors in the central nervous system to depress neuronal excitability. Here, the polypharmacology of benzodiazepines was explored by studying their engagement of human TRP channels revealing clonazepam acts as a robust and selective activator of the TRPM8 ion channel. Clonazepam-evoked Ca<sup>2+</sup> signals were observed in cells expressing human TRPM8 channels, and in mouse trigeminal neurons. These responses were completely blocked by pharmacological or genetic inhibition of TRPM8 function. This discovery likely explains why clonazepam is an effective treatment for the painful oral condition known as burning mouth disorder, where local activation of TRPM8 channels in sensory neurons mitigates the painful symptoms of this disease.

bioRxiv (Cold Spring Harbor Laboratory)
Medical College of Wisconsin (US)
Good health and well-being
Openalex Percentile: Top 78%
Ion Channels and Receptors
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