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合成代谢雄激素类固醇诺龙对大麻素依赖的影响。

Influence of the anabolic-androgenic steroid nandrolone on cannabinoid dependence.

作者信息

Célérier Evelyne, Ahdepil Therese, Wikander Helena, Berrendero Fernando, Nyberg Fred, Maldonado Rafael

机构信息

Laboratori of Neurofarmacologia, Facultat de Ciéncies de la Salut i de la Vida, Universitat Pompeu Fabra, C/Doctor Aiguader 80, 08003 Barcelona, Spain.

出版信息

Neuropharmacology. 2006 Jun;50(7):788-806. doi: 10.1016/j.neuropharm.2005.11.017. Epub 2006 Jan 27.

Abstract

The identification of the possible factors that might enhance the risk of developing drug addiction and related motivational disorders is crucial to reduce the prevalence of these problems. Here, we examined in mice whether the exposure to the anabolic-androgenic steroid nandrolone would affect the pharmacological and motivational effects induced by Delta(9)-tetrahydrocannabinol (THC), the principal psychoactive component of Cannabis sativa. Mice received nandrolone using pre-exposure (during 14days before THC treatment) or co-administration (1h before each THC injection) procedures. Both nandrolone treatments did not modify the acute antinociceptive, hypothermic and hypolocomotor effects of THC or the development of tolerance after chronic THC administration. Nandrolone pre-exposure blocked THC- and food-induced conditioned place preference and increased the somatic manifestations of THC withdrawal precipitated by the CB1 cannabinoid antagonist rimonabant (SR141617A). The aversive effects of THC were not changed by nandrolone. Furthermore, nandrolone pre-exposure attenuated the anxiolytic-like effects of a low dose of THC without altering the anxiogenic-like effects of a high dose in the lit/dark box, open field and elevated plus-maze. Biochemical experiments showed that chronic nandrolone treatment did not modify CB1 receptor binding and GTP-binding protein activation in the caudate-putamen and cerebellum. Taken together, our results suggest that chronic nandrolone treatment alters behavioural responses related to cannabinoid addictive properties.

摘要

识别可能增加药物成瘾及相关动机障碍风险的因素对于降低这些问题的发生率至关重要。在此,我们在小鼠中研究了合成代谢雄激素类固醇诺龙的暴露是否会影响由大麻主要精神活性成分Δ⁹-四氢大麻酚(THC)诱导的药理和动机效应。小鼠通过预暴露(在THC治疗前14天)或共同给药(每次THC注射前1小时)程序接受诺龙。两种诺龙治疗均未改变THC的急性抗伤害感受、体温过低和运动减少效应或慢性THC给药后的耐受性发展。诺龙预暴露阻断了THC和食物诱导的条件性位置偏爱,并增加了由CB1大麻素拮抗剂利莫那班(SR141617A)引发的THC戒断的躯体表现。诺龙未改变THC的厌恶效应。此外,诺龙预暴露减弱了低剂量THC的抗焦虑样效应,而在明暗箱、旷场和高架十字迷宫中未改变高剂量THC的致焦虑样效应。生化实验表明,慢性诺龙治疗未改变尾状核-壳核和小脑中CB1受体结合及GTP结合蛋白激活。综上所述,我们的结果表明慢性诺龙治疗会改变与大麻素成瘾特性相关的行为反应。

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