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新型JWH-018卤代衍生物:小鼠行为学及结合研究

Novel halogenated derivates of JWH-018: Behavioral and binding studies in mice.

作者信息

Vigolo A, Ossato A, Trapella C, Vincenzi F, Rimondo C, Seri C, Varani K, Serpelloni G, Marti M

机构信息

Department of Life Sciences and Biotechnology (SVeB), University of Ferrara, Italy.

Collaborative Center for the Italian National Early Warning System, Drug Policies Department, Presidency of the Council of Ministers, Italy; Department of Chemistry and Pharmaceutical Sciences, University of Ferrara, Italy.

出版信息

Neuropharmacology. 2015 Aug;95:68-82. doi: 10.1016/j.neuropharm.2015.02.008. Epub 2015 Mar 11.

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.

摘要

JWH-018是一种合成的CB1和CB2激动剂,因其精神活性作用而被非法作为名为“香料”或“草药混合物”的产品销售,其精神活性作用比大麻产生的作用要强得多。去年,欧洲药物和药物成瘾监测中心向意大利国家早期预警系统报告了含有JWH-018新卤代衍生物(JWH-018 Cl和JWH-018 Br)的植物材料的查获情况。本研究旨在调查这两种新的合成大麻素在小鼠体内的体外和体内活性。对小鼠和人CB1受体进行的体外竞争结合实验显示,这些卤代化合物具有高亲和力和高效能。合成大麻素(腹腔注射0.01 - 6毫克/千克)损害小鼠的运动活性并诱发僵住症,并且它们的作用相对于Δ(9)-四氢大麻酚(Δ(9)-THC)引起的作用更严重。此外,它们提高了机械性和热痛阈值并诱发明显的体温过低。有趣的是,虽然高剂量的JWH-018会导致癫痫发作、肌阵挛和反射亢进,但卤代化合物,特别是JWH-018Br,效果较差。行为和神经学变化可被选择性CB1受体拮抗剂AM 251预防。这些数据首次证明JWH-018 Cl和JWH-018 Br的作用与JWH-018相似,但诱发的惊厥发作和肌阵挛较少。这些数据支持这样的假设,即卤代化合物可能已被投放市场以产生与JWH-018相似的中毒作用,同时引起较少的副作用。

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