首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Rewarding effects of 3,4-methylenedioxymethamphetamine ('Ecstasy') in dominant and subordinate OF-1 mice in the place preference conditioning paradigm.
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Rewarding effects of 3,4-methylenedioxymethamphetamine ('Ecstasy') in dominant and subordinate OF-1 mice in the place preference conditioning paradigm.

机译:3,4-亚甲二氧基甲基苯丙胺(“迷魂药”)在位置偏好条件范式中对优势和下属OF-1小鼠的奖励作用。

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We tested the ability of 3,4-methylenedioxymethamphetamine (MDMA) to induce conditioned place preference (CPP) in dominant and subordinate OF-1 mice subjected to cohabitation and repeated sessions of agonistic confrontation, as well as in non-confronted mice. We selected doses of MDMA (2, 6, 10 mg/kg) previously reported to induce CPP in mice and we measured expression of c-Fos evoked by the treatments in non-confronted mice. MDMA induced c-Fos protein in several corticolimbic regions involved in drug-induced reward. Mice were exposed to brief sessions of agonistic confrontation on 5 consecutive days. Determinations of circulating hormones and drug conditioning tests were carried out on completion of the encounters. The results of hormone assays indicated that dominant mice had higher serum concentrations of testosterone, but lower levels of corticosterone, than submissive mice. Post-conditioning tests after drug conditioning (4 injections of MDMA or saline on alternate days) showed that MDMA significantly produced CPP at doses of 2 and 6 mg/kg, but not at 10 mg/kg, an inverted U-shaped pattern of conditioning that was invariable in non-confronted, dominant and subordinate mice. These results demonstrate that the endocrine and behavioural correlates linked to social status and social stress in mice are not paralleled by significant changes in the rewarding efficacy of MDMA in the CPP paradigm under the specific conditions tested.
机译:我们测试了3,4-亚甲二氧基甲基苯丙胺(MDMA)诱导条件性位置偏爱(CPP)在主要和从属的OF-1小鼠经历同居和重复的激动对抗的会话以及非面对小鼠中的能力。我们选择了先前报道的在小鼠中诱导CPP的MDMA剂量(2、6、10 mg / kg),并且我们测量了非对抗小鼠中通过治疗诱发的c-Fos表达。 MDMA诱导参与药物诱导奖赏的几个皮质区域的c-Fos蛋白。小鼠连续5天暴露于短暂的激动对抗中。接触完成后进行循环激素的测定和药物调理测试。激素测定的结果表明,与顺从小鼠相比,优势小鼠的睾丸激素水平较高,而皮质酮水平较低。药物调理后的调理后测试(隔天注射4次MDMA或盐水)表明,MDMA在2和6 mg / kg的剂量下能显着产生CPP,但在10 mg / kg时却不能产生CPP,呈倒U形调理在非面对,优势和从属小鼠中这是不变的。这些结果表明,在特定条件下,与小鼠社交状态和社交压力相关的内分泌和行为相关性与CPP范式中MDMA奖励功效的显着变化不相上下。

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