The psychoactive cannabinoid THC inhibits peripheral nociceptors by targeting NaV1.7 and NaV1.8 nociceptive sodium channels

Δ⁹-Tetrahydrocannabinol (THC), the primary psychoactive compound in cannabis, is widely recognized for its central effects mediated by cannabinoid receptors. Here, we uncover a distinct peripheral mechanism by which THC inhibits the excitability of nociceptive neurons. We show that THC directly targets the nociceptive voltage-gated sodium channels Na<sub>V</sub>1.7 and Na<sub>V</sub>1.8 through the conserved local anesthetic binding site. This interaction reduces sodium currents and suppresses action potential generation in peripheral sensory neurons. Our findings demonstrate that, beyond its central psychoactivity, THC exerts direct peripheral nociceptor inhibition via modulation of Na<sub>V</sub>1.7 and Na<sub>V</sub>1.8, offering new insight into cannabinoid-based analgesia independent of cannabinoid receptor signaling.

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Publication Details

Journal
Neuropsychopharmacology
Published
2026-01-21
DOI
https://doi.org/10.1038/s41386-026-02355-9
Citations
1
Primary Topic
Cannabis and Cannabinoid Research
Type
article
Field-Weighted Citation Impact
32.57

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article

The psychoactive cannabinoid THC inhibits peripheral nociceptors by targeting NaV1.7 and NaV1.8 nociceptive sodium channels

Alexander M. Binshtok, Yossef Maatuf, Avi Priel, Ariel Iskimov
1 citations
Neuropsychopharmacology
Cannabis and Cannabinoid Research
32.57
article

The psychoactive cannabinoid THC inhibits peripheral nociceptors by targeting NaV1.7 and NaV1.8 nociceptive sodium channels

Alexander M. Binshtok, Yossef Maatuf, Avi Priel, Ariel Iskimov
article en
1 citations

Abstract

Δ⁹-Tetrahydrocannabinol (THC), the primary psychoactive compound in cannabis, is widely recognized for its central effects mediated by cannabinoid receptors. Here, we uncover a distinct peripheral mechanism by which THC inhibits the excitability of nociceptive neurons. We show that THC directly targets the nociceptive voltage-gated sodium channels Na<sub>V</sub>1.7 and Na<sub>V</sub>1.8 through the conserved local anesthetic binding site. This interaction reduces sodium currents and suppresses action potential generation in peripheral sensory neurons. Our findings demonstrate that, beyond its central psychoactivity, THC exerts direct peripheral nociceptor inhibition via modulation of Na<sub>V</sub>1.7 and Na<sub>V</sub>1.8, offering new insight into cannabinoid-based analgesia independent of cannabinoid receptor signaling.

Neuropsychopharmacology
Hebrew University of Jerusalem (IL)
Israel Cancer Research Fund, Hebrew University of Jerusalem, Israel Science Foundation
Openalex Percentile: Top 2%
Cannabis and Cannabinoid Research
32.57
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