2018
DOI: 10.1016/j.psychres.2018.08.012
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Psychosis and synthetic cannabinoids

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Cited by 51 publications
(30 citation statements)
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References 123 publications
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“…The in vitro activity of compounds 4 and 7-17 at CB 1 and CB 2 were compared to known agonist CP 55,940 (3) using a FLIPR assay (summary of results displayed in Table 1, n = 5 or more independent experiments) following the same methodology as that previously reported [5][6][7][8]. Previously identified SCs APICA (4) and APINACA (7) showed moderate potency at both hCB 1 (EC 50 = 109 and 142 nM, respectively) and hCB 2 (EC 50 = 56 and 141 nM, respectively), with 4 showing a similar preference for activating CB 2 , as previously reported [29].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The in vitro activity of compounds 4 and 7-17 at CB 1 and CB 2 were compared to known agonist CP 55,940 (3) using a FLIPR assay (summary of results displayed in Table 1, n = 5 or more independent experiments) following the same methodology as that previously reported [5][6][7][8]. Previously identified SCs APICA (4) and APINACA (7) showed moderate potency at both hCB 1 (EC 50 = 109 and 142 nM, respectively) and hCB 2 (EC 50 = 56 and 141 nM, respectively), with 4 showing a similar preference for activating CB 2 , as previously reported [29].…”
Section: Resultsmentioning
confidence: 99%
“…As a result, SCs have become one of the most prominent classes of novel psychoactive substances (NPS) [1]. Because of the limited understanding of their pharmacological effects, these compounds have caused a number of unpredictable adverse events, posing a major risk to public health [2][3][4][5][6][7][8][9]. The rate at which new chemical entities are appearing, along with the plethora of potential substitution patterns, has made it virtually impossible for law enforcement agencies to stay ahead of newly appearing SCs (Fig.…”
Section: Introductionmentioning
confidence: 99%
“…However, similar proportions of young people perceived daily use of synthetic cannabis and daily cannabis smoking to be “high risk”. This is a concern given the serious acute health effects of synthetic cannabis use, particularly given their “legal” status in many jurisdictions and widespread consumer confusion about these products [ 29 31 , 60 , 61 ]. Focused attention should be given to highlighting and detailing the risks associated with synthetic cannabinoid that dwarf existing known risks associated with combusted cannabis.…”
Section: Discussionmentioning
confidence: 99%
“…Synthetic cannabis is the term given to mixtures of synthetic compounds marketed as “herbal” mixtures (e.g., Spice, K2m, Mamba, Afghan Incense) that activate cannabinoid receptors. They are the largest, fastest-growing, and most diversified new psychoactive substances which have been observed to precipitate acute psychotic symptoms, fatal poisonings, acute myocardial infarction, delusions, renal dysfunction, among other effects [ 29 31 ]. Synthetic cannabinoid use among youth is an emerging phenomenon in North America, approximately 3% of young Canadians in Grades 7 to 12 have reported its use, and 12% of their American counterparts have reported the same; the Canadian Centre for Substance Abuse identified this as a substance of concern as early as 2014 [ 2 , 32 , 33 ].…”
Section: Introductionmentioning
confidence: 99%
“…After confirming first mentions of specific compounds, we then cataloged all 79 compounds into common classifications guided by previous publications and government reports. Specifically, we ensured that every drug examined had previously been classified into one of the following classes: 2C‐x (King, Nutt, & Independent Scientific Committee on Drugs, ; Shulgin & Shulgin, ; U.S. Drug Enforcement Administration Diversion Control Division, ; Yu et al, ), DOx (Shulgin & Shulgin, ), NBOMe (U.S. Drug Enforcement Administration Diversion Control Division, ), other phenethylamines (Greene, ; King et al, ; Shulgin & Shulgin, ), synthetic cathinones (McGraw & McGraw, ; Power et al, ; Prosser & Nelson, ; U.S. Drug Enforcement Administration Diversion Control Division, ), tryptamines (Glennon et al, ; Shulgin & Shulgin, ; U.S. Drug Enforcement Administration Diversion Control Division, ; van Hout & Hearne, ), synthetic cannabinoids (Deng, Verrico, Kosten, & Nielsen, ; U.S. Drug Enforcement Administration Diversion Control Division, ), dissociatives (arylcyclohexylamines; Berquist et al, ; De Paoli, Brandt, Wallach, Archer, & Pounder, ), lysergamides (Brandt et al, ; Brandt et al, ; Brandt et al, ; Klinke, Muller, Steffenrud, & Dahl‐Sørensen, ), and piperazines (U.S. Drug Enforcement Administration Diversion Control Division, ). 2C, DOx, NBOMe, and other phenethylamines were further classified into an overall phenethylamine class as per the cited studies.…”
Section: Drug Use Variablesmentioning
confidence: 99%