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Synthetic cannabinoid JWH-073 alters both acute behavior and in vivo/vitro electrophysiological responses in mice

Bibliographic Data

ID15519977
AuthorsMario Barbieri (0000-0003-3501-4034, University of Ferrara), Micaela Tirri (0000-0001-9337-9184, University of Ferrara), Sabrine Bilel (0000-0003-1515-980X, University of Ferrara), Raffaella Arfè (0000-0003-2614-2368, University of Ferrara), Giorgia Corli (0000-0002-2973-2446, University of Ferrara), Beatrice Marchetti (University of Ferrara), Lorenzo Caruso (0000-0001-9895-3990, University of Ferrara), Marie Soukupovà (0000-0002-0489-1977, University of Ferrara), Virginia Cristofori (0000-0002-6837-6042, University of Ferrara), Giovanni Serpelloni (0000-0003-2616-5762, University of Verona), Matteo Marti (0000-0001-8751-2882, University of Ferrara, corresponding author)
Year2022
Volume13
Pages953909-953909
Publication date2022-10-21
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2022.953909
PMID36339851
OpenAlexW4307052013
LanguageEN
References cited76

JWH-073 is a synthetic cannabinoid (SCB) that is illegally marketed within an "herbal blend", causing psychoactive effects more intense than those produced by Cannabis. Users report that JWH-073 causes less harmful effects than other SCBs, misrepresenting it as a "safe JWH-018 alternative", which in turn prompts its recreational use. The present study is aimed to investigate the in vivo pharmacological activity on physiological and neurobehavioral parameters in male CD-1 mice after acute 1 mg/kg JWH-073 administration. To this aim we investigate its effect on sensorimotor (visual, acoustic, and tactile), motor (spontaneous motor activity and catalepsy), and memory functions (novel object recognition; NOR) in mice coupling behavioral and EEG data. Moreover, to clarify how memory function is affected by JWH-073, we performed in vitro electrophysiological studies in hippocampal preparations using a Long-Term Potentiation (LTP) stimulation paradigm. We demonstrated that acute administration of JWH-073 transiently decreased motor activity for up to 25 min and visual sensorimotor responses for up to 105 min, with the highest effects at 25 min (~48 and ~38%, respectively), while the memory function was altered up to 24 h (~33%) in treated-mice as compared to the vehicle. EEG in the somatosensory cortex showed a maximal decrease of α (~23%) and γ (~26%) bands at 15 min, β (~26%) band at 25 min, a maximal increase of θ (~14%) band at 25 min and δ (~35%) band at 2 h, and a significant decrease of θ (~18%), α (~26%), and β (~10%) bands during 24 h. On the other hand, EEG in the hippocampus showed a significant decrease of all bands from 10 min to 2 h, with the maximal effect at 30 min for θ (~34%) and γ (~26%) bands and 2 h for α (~36%), β (~29%), and δ (~15%) bands. Notably, the δ band significant increase both at 5 min (~12%) and 24 h (~19%). Moreover, in vitro results support cognitive function impairment (~60% of decrease) by interfering with hippocampal synaptic transmission and LTP generation. Our results suggest that JWH-073 deeply alters brain electrical responsiveness with minor behavioral symptoms. Thus, it poses a subtle threat to consumers who mistakenly consider it safer than other SCBs

Cannabinoid · Catalepsy · Electrophysiology · Excitatory postsynaptic potential · Hippocampal formation · Inhibitory postsynaptic potential · Long-term potentiation · Somatosensory system · Stimulation · Cannabis and Cannabinoid Research · Chemistry · Forensic Toxicology and Drug Analysis · Medicine · Neuroscience · Neuroscience and Neuropharmacology Research · Psychology · Internal Medicine · Pharmacology

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