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抗抑郁药会影响条件性位置偏爱中的动机吗?

Do antidepressants affect motivation in conditioned place preference?

作者信息

Subhan F, Deslandes P N, Pache D M, Sewell R D

机构信息

Neuropharmacology Drug Action Group, Welsh School of Pharmacy, Cardiff University, Redwood Building, King Edward VII Avenue, Cathays Park, CF10 3XF, Cardiff, UK.

出版信息

Eur J Pharmacol. 2000 Nov 24;408(3):257-63. doi: 10.1016/s0014-2999(00)00771-8.

Abstract

The positive motivational effects of a range of antidepressants/neurotransmitter reuptake inhibitor compounds were studied using conditioned place preference. These agents included amitriptyline (2.5-10 mg/kg), venlafaxine (5 and 10 mg/kg), sibutramine (5 and 10 mg/kg), fluoxetine (2.5-10 mg/kg), paroxetine (5-15 mg/kg) and sertraline (2.5-10 mg/kg). Male Wistar rats were place conditioned in a three-compartment box to vehicle or drug alternately for 8 days using a 30-min pretreatment time. Control animals received vehicle only. Cocaine (5 mg/kg) was used as a positive control for the procedure. Significant place preference (P<0.05) was observed with paroxetine (15 mg/kg), fluoxetine (5 and 10 mg/kg), sertraline (2.5-10 mg/kg) and cocaine. Venlafaxine and sibutramine, serotonin/noradrenaline reuptake inhibitors, produced no place conditioning, while the highest dose of the tricyclic antidepressant, amitriptyline (10 mg/kg), produced signs of place aversion. The role of serotonin in reward pathways and differences in serotonin, noradrenaline and dopamine reuptake-inhibiting properties of these compounds may explain why only the serotonin-selective reuptake inhibitors produced place preference in this study.

摘要

使用条件性位置偏爱实验研究了一系列抗抑郁药/神经递质再摄取抑制剂化合物的正向动机效应。这些药物包括阿米替林(2.5 - 10毫克/千克)、文拉法辛(5和10毫克/千克)、西布曲明(5和10毫克/千克)、氟西汀(2.5 - 10毫克/千克)、帕罗西汀(5 - 15毫克/千克)和舍曲林(2.5 - 10毫克/千克)。雄性Wistar大鼠在一个三室箱中进行位置条件化训练,交替给予溶剂或药物,预处理时间为30分钟,共8天。对照动物仅给予溶剂。可卡因(5毫克/千克)用作该实验程序的阳性对照。观察到帕罗西汀(15毫克/千克)、氟西汀(5和10毫克/千克)、舍曲林(2.5 - 10毫克/千克)和可卡因产生了显著的位置偏爱(P<0.05)。5-羟色胺/去甲肾上腺素再摄取抑制剂文拉法辛和西布曲明未产生位置条件化,而三环类抗抑郁药阿米替林的最高剂量(10毫克/千克)产生了位置厌恶的迹象。5-羟色胺在奖赏通路中的作用以及这些化合物在5-羟色胺、去甲肾上腺素和多巴胺再摄取抑制特性上的差异,可能解释了为什么在本研究中只有5-羟色胺选择性再摄取抑制剂产生了位置偏爱。

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