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新型第三代氟化合成大麻素5F-ADBINACA、AB-FUBINACA和STS-135对小鼠的药物毒理学作用。体外和体内研究。

Pharmaco-toxicological effects of the novel third-generation fluorinate synthetic cannabinoids, 5F-ADBINACA, AB-FUBINACA, and STS-135 in mice. In vitro and in vivo studies.

作者信息

Canazza Isabella, Ossato Andrea, Vincenzi Fabrizio, Gregori Adolfo, Di Rosa Fabiana, Nigro Federica, Rimessi Alessandro, Pinton Paolo, Varani Katia, Borea Pier Andrea, Marti Matteo

机构信息

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

Institute of Public Health, Section of Legal Medicine, Catholic University of Rome, Rome, Italy.

出版信息

Hum Psychopharmacol. 2017 May;32(3). doi: 10.1002/hup.2601. Epub 2017 Jun 9.

Abstract

INTRODUCTION

5F-ADBINACA, AB-FUBINACA, and STS-135 are 3 novel third-generation fluorinate synthetic cannabinoids that are illegally marketed as incense, herbal preparations, or research chemicals for their psychoactive cannabis-like effects.

METHODS

The present study aims at investigating the in vitro and in vivo pharmacological activity of 5F-ADBINACA, AB-FUBINACA, and STS-135 in male CD-1 mice, comparing their in vivo effects with those caused by the administration of Δ -THC and JWH-018. In vitro competition binding experiments revealed a nanomolar affinity and potency of the 5F-ADBINACA, AB-FUBINACA, and STS-135 on mouse and human CB and CB receptors. Moreover, these synthetic cannabinoids induced neurotoxicity in murine neuro-2a cells.

RESULTS

In vivo studies showed that 5F-ADBINACA, AB-FUBINACA, and STS-135 induced hypothermia; increased pain threshold to both noxious mechanical and thermal stimuli; caused catalepsy; reduced motor activity; impaired sensorimotor responses (visual, acoustic, and tactile); caused seizures, myoclonia, and hyperreflexia; and promoted aggressiveness in mice. Behavioral and neurological effects were fully prevented by the selective CB receptor antagonist/inverse agonist AM 251. Differently, the visual sensory response induced by STS-135 was only partly prevented by the AM 251, suggesting a CB -independent mechanism.

CONCLUSIONS

For the first time, the present study demonstrates the pharmaco-toxicological effects induced by the administration of 5F-ADBINACA, AB-FUBINACA, and STS-135 in mice and suggests their possible detrimental effects on human health.

摘要

引言

5F-ADBINACA、AB-FUBINACA和STS-135是三种新型的第三代氟化合成大麻素,因其具有类似大麻的精神活性作用而被非法作为熏香、草药制剂或研究化学品进行销售。

方法

本研究旨在调查5F-ADBINACA、AB-FUBINACA和STS-135在雄性CD-1小鼠体内和体外的药理活性,将它们的体内效应与给予Δ-THC和JWH-018所产生的效应进行比较。体外竞争结合实验显示,5F-ADBINACA、AB-FUBINACA和STS-135对小鼠和人类的CB1和CB2受体具有纳摩尔级的亲和力和效力。此外,这些合成大麻素在小鼠神经母细胞瘤-2a细胞中诱导了神经毒性。

结果

体内研究表明,5F-ADBINACA、AB-FUBINACA和STS-135可导致体温过低;提高对有害机械刺激和热刺激的疼痛阈值;引起僵住症;降低运动活性;损害感觉运动反应(视觉、听觉和触觉);引发癫痫、肌阵挛和反射亢进;并增强小鼠的攻击性。选择性CB1受体拮抗剂/反向激动剂AM 251可完全预防行为和神经学效应。不同的是,AM 251只能部分预防STS-135诱导的视觉感觉反应,这表明存在一种不依赖CB1的机制。

结论

本研究首次证明了给予5F-ADBINACA、AB-FUBINACA和STS-135在小鼠体内产生的药物毒理学效应,并提示它们可能对人类健康产生有害影响。

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