Brodifacoum does not modulate human cannabinoid receptor-mediated hyperpolarization of AtT20 cells or inhibition of adenylyl cyclase in HEK 293 cells

Synthetic cannabinoids are a commonly used class of recreational drugs that can have significant adverse effects. There have been sporadic reports of co-consumption of illicit drugs with rodenticides such as warfarin and brodifacoum (BFC) over the past 20 years but recently, hundreds of people have...

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Veröffentlicht in:PeerJ (San Francisco, CA) CA), 2019-09, Vol.7, p.e7733, Article e7733
Hauptverfasser: Sachdev, Shivani, Boyd, Rochelle, Grimsey, Natasha L, Santiago, Marina, Connor, Mark
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Sprache:eng
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Zusammenfassung:Synthetic cannabinoids are a commonly used class of recreational drugs that can have significant adverse effects. There have been sporadic reports of co-consumption of illicit drugs with rodenticides such as warfarin and brodifacoum (BFC) over the past 20 years but recently, hundreds of people have been reported to have been poisoned with a mixture of synthetic cannabinoids and BFC. We have sought to establish whether BFC directly affects cannabinoid receptors, or their activation by the synthetic cannabinoid CP55940 or the phytocannabinoid Δ -tetrahydrocannabinol (Δ -THC). The effects of BFC on the hyperpolarization of wild type AtT20 cells, or AtT20 cells stably expressing human CB - or CB - receptors, were studied using a fluorescent assay of membrane potential. The effect of BFC on CB - and CB -mediated inhibition of forskolin-stimulated adenylyl cyclase (AC) activation was measured using a BRET assay of cAMP levels in HEK 293 cells stably expressing human CB or CB . BFC did not activate CB or CB receptors, or affect the hyperpolarization of wild type AtT20 cells produced by somatostatin. BFC (1 µM) did not affect the hyperpolarization of AtT20-CB or AtT20-CB cells produced by CP55940 or Δ -THC. BFC (1 µM) did not affect the inhibition of forskolin-stimulated AC activity by CP55940 in HEK 293 cells expressing CB or CB . BFC (1 µM) also failed to affect the desensitization of CB and CB signaling produced by prolonged (30 min) application of CP55940 or Δ -THC to AtT20 cells. BFC is not a cannabinoid receptor agonist, and appeared not to affect cannabinoid receptor activation. Our data suggests there is no pharmacodynamic rationale for mixing BFC with synthetic cannabinoids; however, it does not speak to whether BFC may affect synthetic cannabinoid metabolism or biodistribution. The reasons underlying the mixing of BFC with synthetic cannabinoids are unknown, and it remains to be established whether the "contamination" was deliberate or accidental. However, the consequences for people who ingested the mixture were often serious, and sometimes fatal, but this seems unlikely to be due to BFC action at cannabinoid receptors.
ISSN:2167-8359
2167-8359
DOI:10.7717/peerj.7733