Hutcheson D M, Tzavara E T, Smadja C, Valjent E, Roques B P, Hanoune J, Maldonado R
Département de Pharmacologie Moléculaire et Structurale, U266 INSERM, URA D1500 CNRS, Université René Descartes, Paris, France.
Br J Pharmacol. 1998 Dec;125(7):1567-77. doi: 10.1038/sj.bjp.0702228.
Tolerance and dependence induced by chronic delta-9-tetrahydrocannabinol (THC) administration were investigated in mice. The effects on body weight, analgesia and hypothermia were measured during 6 days of treatment (10 or 20 mg kg(-1) THC twice daily). A rapid tolerance to the acute effects was observed from the second THC administration. The selective CB-1 receptor antagonist SR 141716A (10 mg kg(-1)) was administered at the end of the treatment, and somatic and vegetative manifestations of abstinence were evaluated. SR 141716A administration precipitated several somatic signs that included wet dog shakes, frontpaw tremor, ataxia, hunched posture, tremor, ptosis, piloerection, decreased locomotor activity and mastication, which can be interpreted as being part of a withdrawal syndrome. Brains were removed immediately after the behavioural measures and assayed for adenylyl cyclase activity. An increase in basal, forskolin and calcium/calmodulin stimulated adenylyl cyclase activities was specifically observed in the cerebellum of these mice. The motivational effects of THC administration and withdrawal were evaluated by using the place conditioning paradigm. No conditioned change in preference to withdrawal associated environment was observed. In contrast, a conditioned place aversion was produced by the repeated pairing of THC (20 mg kg(-1)), without observing place preference at any of the doses used. This study constitutes a clear behavioural and biochemical model of physical THC withdrawal with no motivational aversive consequences. This model permits an easy quantification of THC abstinence in mice and can be useful for the elucidation of the molecular mechanisms involved in cannabinoid dependence.
在小鼠中研究了长期给予δ-9-四氢大麻酚(THC)所诱导的耐受性和依赖性。在为期6天的治疗期间(每天两次给予10或20 mg kg(-1) THC),测量了对体重、镇痛和体温过低的影响。从第二次给予THC开始,观察到对急性效应的快速耐受性。在治疗结束时给予选择性CB-1受体拮抗剂SR 141716A(10 mg kg(-1)),并评估戒断的躯体和植物性表现。给予SR 141716A引发了几种躯体症状,包括湿狗样抖动、前爪震颤、共济失调、弓背姿势、震颤、眼睑下垂、竖毛、运动活动减少和咀嚼,这些可被解释为戒断综合征的一部分。在行为测量后立即取出大脑,测定腺苷酸环化酶活性。在这些小鼠的小脑中特别观察到基础、福斯高林和钙/钙调蛋白刺激的腺苷酸环化酶活性增加。通过使用条件性位置偏爱范式评估了给予THC和戒断的动机效应。未观察到对与戒断相关环境的偏好的条件性变化。相反,通过将THC(20 mg kg(-1))重复配对产生了条件性位置厌恶,在所使用的任何剂量下均未观察到位置偏爱。这项研究构成了一个明确的THC身体戒断的行为和生化模型,没有动机性厌恶后果。该模型允许轻松量化小鼠中的THC戒断,并且可用于阐明大麻素依赖性所涉及的分子机制。