Pharmacological profile of novel psychoactive benzofurans
British Journal of Pharmacology – March 13, 2015
Source: OpenAlex
Summary
A critical *Pharmacology* finding reveals benzofurans, emerging substances in *Psychedelics and Drug Studies*, activate a *receptor* linked to heart valve fibrosis. This *Neurotransmitter Receptor Influence on Behavior* is a key concern for *Forensic Toxicology and Drug Analysis*. Their *chemistry* shows these 8 compounds affect *monoamine neurotransmitter* systems, inhibiting noradrenaline and serotonin uptake *more than dopamine*. Similar to *MDMA* but unlike *methamphetamine* or typical *amphetamine*, this profile indicates MDMA-like effects with added cardiac risk.
Abstract
Background and Purpose Benzofurans are newly used psychoactive substances, but their pharmacology is unknown. The aim of the present study was to pharmacologically characterize benzofurans in vitro . Experimental Approach We assessed the effects of the benzofurans 5‐ APB , 5‐ APDB , 6‐ APB , 6‐ APDB , 4‐ APB , 7‐ APB , 5‐ EAPB and 5‐ MAPDB and benzodifuran 2 C ‐ B ‐ FLY on the human noradrenaline ( NA ), dopamine and 5‐ HT uptake transporters using HEK 293 cells that express the respective transporters. We also investigated the release of NA , dopamine and 5‐ HT from monoamine‐preloaded cells, monoamine receptor‐binding affinity and 5‐ HT 2A and 5‐ HT 2B receptor activation. Key Results All of the benzofurans inhibited NA and 5‐ HT uptake more than dopamine uptake, similar to methylenedioxymethamphetamine ( MDMA ) and unlike methamphetamine. All of the benzofurans also released monoamines and interacted with trace amine‐associated receptor 1 ( TA 1 receptor), similar to classic amphetamines. Most benzofurans were partial 5‐ HT 2A receptor agonists similar to MDMA , but also 5‐ HT 2B receptor agonists, unlike MDMA and methamphetamine. The benzodifuran 2 C ‐ B ‐ FLY very potently interacted with 5‐ HT 2 receptors and also bound to TA 1 receptors. Conclusions and Implications Despite very similar structures, differences were found in the pharmacological profiles of different benzofurans and compared with their amphetamine analogues. Benzofurans acted as indirect monoamine agonists that interact with transporters similarly to MDMA . The benzofurans also interacted with 5‐HT receptors. This pharmacological profile probably results in MDMA ‐like entactogenic psychoactive properties. However, benzofurans induce 5‐ HT 2B receptor activation associated with heart valve fibrosis. The pharmacology of 2 C ‐ B ‐ FLY indicates predominant hallucinogenic properties and a risk for vasoconstriction.