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Stimulation of 5-HT(1B) receptors enhances cocaine reinforcement yet reduces cocaine-seeking behavior.

机译:5-HT(1B)受体的刺激增强可卡因的加强,但减少了可卡因的寻找行为。

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Paradoxically, stimulation of 5-HT(1B) receptors (5-HT(1B)Rs) enhances sensitivity to the reinforcing effects of cocaine but attenuates incentive motivation for cocaine as measured using the extinction/reinstatement model. We revisited this issue by examining the effects of a 5-HT(1B)R agonist, CP94253, on cocaine reinforcement and cocaine-primed reinstatement, predicting that CP94253 would enhance cocaine-seeking behavior reinstated by a low priming dose, similar to its effect on cocaine reinforcement. Rats were trained to self-administer cocaine (0.75 mg/kg, i.v.) paired with light and tone cues. For reinstatement experiments, they then underwent daily extinction training to reduce cocaine-seeking behavior (operant responses without cocaine reinforcement). Next, they were pre-treated with CP94253 (3-10 mg/kg, s.c.) and either tested for cocaine-primed (10 or 2.5 mg/kg, i.p.) or cue-elicited reinstatement of extinguished cocaine-seeking behavior. For reinforcement, effects of CP94253 (5.6 mg/kg) across a range of self-administered cocaine doses (0-1.5 mg/kg, i.v.) were examined. Cocaine dose-dependently reinstated cocaine-seeking behavior, but contrary to our prediction, CP94253 reduced reinstatement with both priming doses. Similarly, CP94253 reduced cue-elicited reinstatement. In contrast, CP94253 shifted the self-administration dose-effect curve leftward, consistent with enhanced cocaine reinforcement. When saline was substituted for cocaine, CP94253 reduced response rates (i.e. cocaine-seeking behavior). In subsequent control experiments, CP94253 decreased open-arm exploration in an elevated plus-maze suggesting an anxiogenic effect, but had no effect on locomotion or sucrose reinforcement. These results provide strong evidence that stimulation of 5-HT(1B)Rs produces opposite effects on cocaine reinforcement and cocaine-seeking behavior, and further suggest that 5-HT(1B)Rs may be a novel target for developing medications for cocaine dependence.
机译:矛盾的是,对5-HT(1B)受体(5-HT(1B)Rs)的刺激增强了对可卡因增强作用的敏感性,但减弱了使用消光/恢复模型测得的可卡因的激励动机。我们通过研究5-HT(1B)R激动剂CP94253对可卡因增强和可卡因引发的恢复的作用来重新审视此问题,并预测CP94253将增强低引发剂量所恢复的可卡因寻找行为,与其作用相似加强可卡因。训练大鼠自给可卡因(0.75 mg / kg,静脉内)与光和音调提示配对。为了进行恢复实验,他们每天接受灭绝训练,以减少寻找可卡因的行为(无需加强可卡因的行动响应)。接下来,将它们用CP94253(3-10 mg / kg,s.c.)进行预处理,并测试可卡因引发的剂量(10或2.5 mg / kg,腹腔注射)或通过提示引起的扑灭可卡因寻求行为的恢复。为了增强效果,检查了CP94253(5.6 mg / kg)在一系列自用可卡因剂量(0-1.5 mg / kg,静脉内)中的作用。可卡因可剂量依赖性地恢复可卡因的寻找行为,但与我们的预测相反,CP94253降低了两种启动剂量的恢复时间。同样,CP94253减少了提示引起的恢复。相反,CP94253将自我给药的剂量效应曲线向左移动,与可卡因强化作用增强一致。当用盐水代替可卡因时,CP94253降低了响应率(即可卡因寻求行为)。在随后的对照实验中,CP94253在高迷宫中减少了张开双臂的探查,提示其具有抗焦虑作用,但对运动或蔗糖增强没有影响。这些结果提供了有力的证据表明,对5-HT(1B)Rs的刺激对可卡因增强和可卡因寻求行为产生相反的影响,并且进一步表明5-HT(1B)Rs可能是开发可卡因依赖性药物的新靶标。

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