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可卡因与诺龙共同给药对雄性大鼠攻击性的影响。

The effects of cocaine and nandrolone co-administration on aggression in male rats.

作者信息

Long S F, Wilson M C, Sufka K J, Davis W M

机构信息

Department of Pharmacology, School of Pharmacy, University of Mississippi, University, USA.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 1996 Jul;20(5):839-56. doi: 10.1016/0278-5846(96)00063-2.

DOI:10.1016/0278-5846(96)00063-2
PMID:8870068
Abstract
  1. Cocaine and anabolic-androgenic steroids are among the more commonly abused substances in selected populations. These agents, when used alone or in combination, have been reported to cause aggressive tendencies in both laboratory-based animal models and in human clinical situations. This project, using a resident-intruder paradigm, examined the effects of co-administration of cocaine and a typical anabolic-androgenic steroid, nandrolone decanoate, on the development of aggression in male Sprague-Dawley rats. 2. Dose response studies demonstrated that low dose cocaine (1 mg/kg) produced more aggression in a greater percentage of animals than for either the controls or groups receiving higher doses (up to 20 mg/kg). Initially, high intermittent doses of nandrolone (20 mg twice weekly) produced more aggression; however, low daily doses of nandrolone (2 mg) produced greater levels of aggression following 4 weeks of treatment. 3. Optimal doses of cocaine and nandrolone, when administered together, resulted in aggression scores that were not significantly different from controls or either drug singly. However, a greater percentage of animals receiving both drugs exhibited aggression than did rats receiving either drug alone. 4. These results support the interpretation that the drugs interact to produce unique effects in the development of aggression. However, the complexity and extent of the interactions is great and remains to be fully elucidated.
摘要
  1. 可卡因和合成代谢雄激素类固醇是特定人群中较常被滥用的物质。据报道,这些药物单独使用或联合使用时,在基于实验室的动物模型和人类临床情况中都会引发攻击倾向。本项目采用 resident-intruder 范式,研究了可卡因与一种典型的合成代谢雄激素类固醇癸酸诺龙联合给药对雄性 Sprague-Dawley 大鼠攻击行为发展的影响。2. 剂量反应研究表明,低剂量可卡因(1毫克/千克)在更大比例的动物中引发的攻击行为比对照组或接受更高剂量(高达20毫克/千克)的组更多。最初,高剂量间歇性使用的诺龙(每周两次,每次20毫克)引发的攻击行为更多;然而,低剂量每日使用的诺龙(2毫克)在治疗4周后引发的攻击水平更高。3. 可卡因和诺龙的最佳剂量联合给药时,攻击得分与对照组或单独使用任何一种药物时无显著差异。然而,同时接受两种药物的动物表现出攻击行为的比例高于单独接受任何一种药物的大鼠。4. 这些结果支持这样的解释,即这些药物相互作用,在攻击行为的发展中产生独特的效果。然而,相互作用的复杂性和程度很大,仍有待充分阐明。

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