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首页> 外文期刊>Pharmacological research: The official journal of The Italian Pharmacological Society >Repeated administration of phytocannabinoid Delta(9)-THC or synthetic cannabinoids JWH-018 and JWH-073 induces tolerance to hypothermia but not locomotor suppression in mice, and reduces CB1 receptor expression and function in a brain region-specific manner
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Repeated administration of phytocannabinoid Delta(9)-THC or synthetic cannabinoids JWH-018 and JWH-073 induces tolerance to hypothermia but not locomotor suppression in mice, and reduces CB1 receptor expression and function in a brain region-specific manner

机译:重复施用植物大麻素Delta(9)-THC或合成大麻素JWH-018和JWH-073可以诱导小鼠对体温过低的耐受性,而不是运动抑制,并以脑区域特异性方式降低CB1受体的表达和功能

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摘要

These studies probed the relationship between intrinsic efficacy and tolerance/cross-tolerance between Delta(9)-THC and synthetic cannabinoid drugs of abuse (SCBs) by examining in vivo effects and cellular changes concomitant with their repeated administration in mice. Dose-effect relationships for hypothermic effects were determined in order to confirm that SCBs JWH-018 and JWH-073 are higher efficacy agonists than Delta(9)-THC in mice. Separate groups of mice were treated with saline, sub-maximal hypothermic doses of JWH-018 or JWH-073 (3.0 mg/kg or 10.0 mg/kg, respectively) or a maximally hypothermic dose of 30.0 mg/kg Delta(9)-THC once per day for 5 consecutive days while core temperature and locomotor activity were monitored via biotelemetry. Repeated administration of all drugs resulted in tolerance to hypothermic effects, but not locomotor effects, and this tolerance was still evident 14 days after the last drug administration. Further studies treated mice with 30.0 mg/kg Delta(9)-THC once per day for 4 days, then tested with SCBs on day 5. Mice with a Delta(9)-THC history were cross-tolerant to both SCBs, and this cross-tolerance also persisted 14 days after testing. Select brain regions from chronically treated mice were examined for changes in CB1 receptor expression and function. Expression and function of hypothalamic CB1Rs were reduced in mice receiving chronic drugs, but cortical CB1R expression and function were not altered. Collectively, these data demonstrate that repeated Delta(9)-THC, JWH-018 and JWH-073 can induce long-lasting tolerance to some in vivo effects, which is likely mediated by region-specific downregulation and desensitization of CB1Rs. (C) 2015 Elsevier Ltd. All rights reserved.
机译:这些研究通过检查体内效应和伴随小鼠反复给药的细胞变化,探讨了Delta(9)-THC与合成大麻类滥用药物(SCB)之间的内在功效与耐受/交叉耐受之间的关系。为了确定SCB JWH-018和JWH-073是在小鼠中比Delta(9)-THC更高的激动剂,确定了低温效应的剂量效应关系。单独的小鼠组接受生理盐水,次最大低温剂量的JWH-018或JWH-073(分别为3.0 mg / kg或10.0 mg / kg)或最大低温剂量的30.0 mg / kg Delta(9)-每天连续5天进行一次THC,同时通过生物遥测法监测核心温度和运动活动。重复给药所有药物都会导致对体温降低的耐受性,但对运动效应没有耐受性,这种耐受性在最后一次给药后14天仍然很明显。进一步的研究每天用30.0 mg / kg Delta(9)-THC小鼠处理一次,共4天,然后在第5天用SCB进行测试。具有Delta(9)-THC历史的小鼠对两种SCB都具有交叉耐受性,因此测试后14天,交叉耐受性也持续存在。检查了来自慢性治疗小鼠的选定大脑区域中CB1受体表达和功能的变化。下丘脑CB1Rs的表达和功能在接受慢性药物的小鼠中降低,但皮质CB1R的表达和功能未改变。总的来说,这些数据表明重复的Delta(9)-THC,JWH-018和JWH-073可以诱导对某些体内效应的持久耐受,这可能是由CB1Rs的区域特异性下调和脱敏介导的。 (C)2015 Elsevier Ltd.保留所有权利。

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