Novel halogenated derivates of JWH-018: Behavioral and binding studies in mice.
A Vigolo, Andrea Ossato, Claudio Trapella, Fabrizio Vincenzi, Claudia Rimondo, C Seri, Katia Varani, Giovanni Serpelloni, Matteo Marti
Neuropharmacology August 2015 DOI: 10.1016/j.neuropharm.2015.02.008 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Preclinical in vitro and in vivo animal study Peer reviewed |
|---|---|
| Population | Mice; mouse and human CB1 receptors in vitro |
| Interventions | JWH-018 Cl JWH-018 Br JWH-018 Δ(9)-THC AM 251 |
| Dose | 0.01-6 mg/kg i.p. |
| Keywords | Cb1 receptor Jwh-018 pubchem cid Jwh-018 br Jwh-018 cl Synthetic cannabinoids δ9-THC Pubchem Cid |
| Key points | JWH-018 Cl and JWH-018 Br bind mouse and human CB1 receptors with high affinity and, in mice, impair motor activity, induce catalepsy, raise pain thresholds, and cause hypothermia more severely than Δ(9)-THC. Unlike high-dose JWH-018, the halogenated compounds, particularly JWH-018 Br, produce fewer seizures, myoclonia, and hyperreflexia. The authors argue these compounds may have been introduced to the market to mimic JWH-018's intoxicating effects with fewer side effects. |
Abstract
JWH-018 is a synthetic CB1 and CB2 agonist illegally marketed as products named "Spice" or "herbal blend" for its psychoactive effects which are much higher than those produced by cannabis. In the last year, the European Monitoring Centre for Drugs and Drug Addiction reported to the Italian National Early Warning System the seizure of plant material containing new halogenated derivatives of JWH-018 (JWH-018 Cl and JWH-018 Br). The present study aimed to investigate the in vitro and in vivo activity of these two new synthetic cannabinoids in mice. In vitro competition binding experiments performed on mouse and human CB1 receptors revealed a high affinity and potency of the halogenated compounds. Synthetic cannabinoids (0.01-6 mg/kg i.p.) impaired motor activity and induced catalepsy in mice and their effects were more severe with respect to those evoked by Δ(9)-THC. Moreover, they increased the mechanical and thermal pain threshold and induced a marked hypothermia. It is interesting to note that whereas high doses of JWH-018 cause seizures, myoclonia and hyperreflexia, the halogenated compounds, in particular JWH-018Br, were less effective. Behavioral and neurological changes were prevented by the selective CB1 receptor antagonist AM 251. These data demonstrate for the first time that JWH-018 Cl and JWH-018 Br act similarly to JWH-018 while inducing less convulsive episodes and myoclonias. These data support the hypothesis that the halogenated compounds may have been introduced onto market to produce similar intoxicating effects as JWH-018 while causing less side effects.
Citations in the library
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- Effect fingerprinting of new psychoactive substances (NPS): What can we learn from in vitro data? Pharmacology & Therapeutics February 1, 2018
- Sex and Gender Differences in the Effects of Novel Psychoactive Substances. Brain Sciences September 3, 2020
- Neurocognition and subjective experience following acute doses of the synthetic cannabinoid JWH‐018: a phase 1, placebo‐controlled, pilot study British Journal of Pharmacology November 22, 2017
- Effect of -NBOMe Compounds on Sensorimotor, Motor, and Prepulse Inhibition Responses in Mice in Comparison With the 2C Analogs and Lysergic Acid Diethylamide: From Preclinical Evidence to Forensic Implication in Driving Under the Influence of Drugs. Frontiers in Psychiatry 2022
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Cites 2
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- Phase I hydroxylated metabolites of the K2 synthetic cannabinoid JWH-018 retain in vitro and in vivo cannabinoid 1 receptor affinity and activity. PLoS One 2011