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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Involvement of dopamine receptors in diethylpropion-induced conditioning place preference
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Involvement of dopamine receptors in diethylpropion-induced conditioning place preference

机译:多巴胺受体参与二乙基丙酸诱导的调理位置偏好

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Diethylpropion (DEP) is an amphetamine-like agent used as an anorectic drug. Abuse of DEP has been reported and some restrictions of its use have been recently imposed. The conditioning place preference (CPP) paradigm was used to evaluate the reinforcing properties of DEP in adult male Wistar rats. After initial preferences were determined, animals weighing 250-300 g (N = 7 per group) were conditioned with DEP (10, 15 or 20 mg/kg). Only the dose of 15 mg/kg produced a significant place preference (358 ± 39 vs 565 ± 48 s). Pretreatment with the D1 antagonist SCH 23390 (0.05 mg/kg, sc) 10 min before DEP (15 mg/kg, ip) blocked DEP-induced CPP (418 ± 37 vs 389 ± 31 s) while haloperidol (0.5 mg/kg, ip), a D2 antagonist, 15 min before DEP was ineffective in modifying place conditioning produced by DEP (385 ± 36 vs 536 ± 41 s). These results suggest that dopamine D1 receptors mediate the reinforcing effect of DEP
机译:Diethylpropion(DEP)是一种苯丙胺类药物,用作厌食药。据报道滥用DEP,最近已对其使用施加了一些限制。条件位置偏好(CPP)范式用于评估成年雄性Wistar大鼠DEP的增强特性。确定最初的偏好后,将体重为250-300 g(每组N = 7)的动物用DEP(10、15或20 mg / kg)进行处理。仅15 mg / kg的剂量产生明显的位置偏爱(358±39 vs 565±48 s)。在DEP(15 mg / kg,ip)之前10分钟用D1拮抗剂SCH 23390(0.05 mg / kg,sc)进行预处理,以阻断DEP诱导的CPP(418±37 vs 389±31 s),而氟哌啶醇(0.5 mg / kg, ip),一种D2拮抗剂,DEP前15分钟不能有效改变DEP产生的位置调节效果(385±36 vs 536±41 s)。这些结果表明,多巴胺D1受体介导DEP的增强作用。

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