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新型卤代合成大麻素损害小鼠的感觉运动功能。

Novel halogenated synthetic cannabinoids impair sensorimotor functions in mice.

机构信息

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

Department of Morphology, Experimental Medicine and Surgery, Section of Legal Medicine, University of Ferrara, Ferrara, Italy.

出版信息

Neurotoxicology. 2020 Jan;76:17-32. doi: 10.1016/j.neuro.2019.10.002. Epub 2019 Oct 11.

Abstract

JWH-018-Cl, JWH-018-Br and AM-2201 (JWH-018 halogenated-derivatives; JWH-018-R compounds) are synthetic cannabinoid agonists illegally marketed as "Spice", "K2", "herbal blend" and research chemicals for their cannabis-like psychoactive effects. In rodents, JWH-018 and its halogenated derivatives reproduce the typical effects of Δ-tetrahydrocannabinol (Δ-THC), i.e. hypothermia, analgesia, hypolocomotion and akinesia. Yet, the effects of JWH-018-R compounds on sensorimotor functions are still unknown. This study was designed to investigate the effect of an acute intraperitoneal (i.p.) administration of JWH-018-R compounds (0.01-6 mg/kg) on sensorimotor functions in mice and to compare them to those caused by the reference compound JWH-018 and Δ-THC. A well validated battery of behavioral tests was used to investigate the effects of these synthetic cannabinoids on the visual, auditory and tactile responses in mice, while the pre-pulse inhibition (PPI) test was used to investigate their effect on sensorimotor gating. The effect of the synthetic cannabinoids on spontaneous locomotion was also measured by a video tracking analysis to assess potential cannabinoid-induced motor impairment. Results showed that, similarly to JWH-018, systemic administration of JWH-018-R compounds inhibits sensorimotor and PPI responses at lower doses (0.01-0.1 mg/kg) and reduced spontaneous locomotion at intermediate/high doses (1-6 mg/kg). All effects were prevented by the administration of the selective cannabinoid CB receptor antagonist/inverse agonist AM-251 thus confirming a CB receptor-mediated action. Finding that lower doses of JWH-018-R compounds selectively impair sensorimotor and PPI responses without affecting locomotion should be carefully considered to better understand the potential danger that halogenated-derivatives of JWH-018 may pose to public health, with particular reference to decreased performance in driving and hazardous works.

摘要

JWH-018-Cl、JWH-018-Br 和 AM-2201(JWH-018 的卤代衍生物;JWH-018-R 化合物)是作为“香料”、“K2”、“草药混合物”和研究化学品非法销售的合成大麻素激动剂,因其具有类似大麻的致幻作用。在啮齿动物中,JWH-018 及其卤代衍生物再现了 Δ-四氢大麻酚(Δ-THC)的典型作用,即体温过低、镇痛、运动减少和运动不能。然而,JWH-018-R 化合物对感觉运动功能的影响尚不清楚。本研究旨在研究急性腹腔内(i.p.)给予 JWH-018-R 化合物(0.01-6mg/kg)对小鼠感觉运动功能的影响,并将其与参考化合物 JWH-018 和 Δ-THC 进行比较。使用经过充分验证的行为测试组合来研究这些合成大麻素对小鼠视觉、听觉和触觉反应的影响,同时使用预脉冲抑制(PPI)测试来研究它们对感觉运动门控的影响。通过视频跟踪分析测量合成大麻素对自发运动的影响,以评估潜在的大麻素引起的运动障碍。结果表明,与 JWH-018 相似,较低剂量(0.01-0.1mg/kg)的 JWH-018-R 化合物全身给药会抑制感觉运动和 PPI 反应,并在中/高剂量(1-6mg/kg)时降低自发运动。所有作用均被选择性大麻素 CB 受体拮抗剂/反向激动剂 AM-251 的给药所预防,从而证实了 CB 受体介导的作用。发现 JWH-018-R 化合物的较低剂量选择性地损害感觉运动和 PPI 反应而不影响运动,这应该引起谨慎考虑,以更好地了解 JWH-018 的卤代衍生物可能对公共健康构成的潜在危险,特别是在驾驶和危险工作中的表现下降。

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