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Δ⁹-四氢大麻酚与大麻模拟剂CP 55,940、WIN 55,212-2和花生四烯酸乙醇胺之间的交叉耐受性。

Cross-tolerance between delta-9-tetrahydrocannabinol and the cannabimimetic agents, CP 55,940, WIN 55,212-2 and anandamide.

作者信息

Pertwee R G, Stevenson L A, Griffin G

机构信息

Department of Biomedical Sciences, Marischal College, University of Aberdeen.

出版信息

Br J Pharmacol. 1993 Dec;110(4):1483-90. doi: 10.1111/j.1476-5381.1993.tb13989.x.

Abstract
  1. Mice pretreated intraperitoneally for 2 days with delta-9-tetrahydrocannabinol (delta-9-THC) at a dose of 20 mg kg-1 day-1 and then challenged intravenously with this drug, 24 h after the second pretreatment, showed a 6 fold tolerance to the hypothermic effect of delta-9-THC. This pretreatment also induced tolerance to the hypothermic effects of the cannabimimetic agents, CP 55,940 (4.6 fold) and WIN 55,212-2 (4.9 fold), but not to the hypothermic effect of the putative endogenous cannabinoid, anandamide. 2. Vasa deferentia removed from mice pretreated intraperitoneally with delta-9-THC twice at a dose of 20 mg kg-1 day-1 were less sensitive to its inhibitory effect on electrically-evoked contractions than vasa deferentia obtained from control animals. The cannabinoid pretreatment induced a 30 fold parallel rightward shift in the lower part of the concentration-response curve of delta-9-THC and a marked reduction in the maximal inhibitory effect of the drug. It also induced tolerance to the inhibitory effects on the twitch response of CP 55,940 (8.7 fold), WIN 55,212-2 (9.6 fold) and anandamide (12.3 fold). 3. The results confirm that cannabinoid tolerance can be rapid in onset and support the hypothesis that it is mainly pharmacodynamic in nature. The finding that in vivo pretreatment with delta-9-THC can produce tolerance not only to its own inhibitory effect on the vas deferens but also to that of three other cannabimimetic agents, suggests that this tissue would be suitable as an experimental model for investigating the mechanisms responsible for cannabinoid tolerance. 4. Further experiments are required to establish why tolerance to anandamide-induced hypothermia was not produced by a pretreatment with delta-9-THC that did induce tolerance to the hypothermic effects of delta-9-THC, CP 55,940 and WIN 55,212-2 and to the inhibitory effects of delta-9-THC,CP 55,940, WIN 55,212-2 and anandamide on the twitch response of the vas deferens.
摘要
  1. 小鼠以20毫克/千克/天的剂量腹腔注射δ-9-四氢大麻酚(δ-9-THC)预处理2天,然后在第二次预处理后24小时静脉注射该药物,结果显示对δ-9-THC的降温作用产生了6倍的耐受性。这种预处理还诱导了对大麻素模拟剂CP 55,940(4.6倍)和WIN 55,212-2(4.9倍)降温作用的耐受性,但对假定的内源性大麻素花生四烯乙醇胺的降温作用没有诱导耐受性。2. 从以20毫克/千克/天的剂量腹腔注射δ-9-THC两次预处理的小鼠身上取出的输精管,与从对照动物身上取出的输精管相比,对其对电诱发收缩的抑制作用不太敏感。大麻素预处理使δ-9-THC浓度-反应曲线下部出现30倍的平行右移,并使该药物的最大抑制作用显著降低。它还诱导了对CP 55,940(8.7倍)、WIN 55,212-2(9.6倍)和花生四烯乙醇胺(12.3倍)对抽搐反应抑制作用的耐受性。3. 结果证实大麻素耐受性起效迅速,并支持其本质上主要是药效学的假说。体内用δ-9-THC预处理不仅能产生对其自身对输精管抑制作用的耐受性,还能产生对其他三种大麻素模拟剂抑制作用的耐受性,这一发现表明该组织将适合作为研究大麻素耐受性机制的实验模型。4. 需要进一步实验来确定为什么用能诱导对δ-9-THC、CP 55,940和WIN 55,212-2降温作用以及对δ-9-THC、CP 55,940、WIN 55,212-2和花生四烯乙醇胺对输精管抽搐反应抑制作用产生耐受性的δ-9-THC预处理,却没有产生对花生四烯乙醇胺诱导的低温的耐受性。

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