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首页> 外文期刊>Behavioural pharmacology >Stimulation of 5-HT2C receptors attenuates cue and cocaine-primed reinstatement of cocaine-seeking behavior in rats.
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Stimulation of 5-HT2C receptors attenuates cue and cocaine-primed reinstatement of cocaine-seeking behavior in rats.

机译:5-HT2C受体的刺激减弱了大鼠的提示和可卡因引发的可卡因寻找行为的恢复。

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摘要

The extinction/reinstatement model has been used in this study to examine the role of 5-HT2C receptors in cocaine-seeking behavior elicited by cocaine-associated cues and cocaine-priming injections. Rats that had been trained to press a lever for cocaine (0.75 mg/kg/0.1 ml, intravenously) paired with light and tone cues underwent daily extinction sessions, during which responding had no consequences. After responding diminished, rats were tested for reinstatement of responding by either response-contingent presentations of the cues or a cocaine-priming injection (10 mg/kg, intraperitoneal, i.p.), with and without pretreatment with the 5-HT2C/2B receptor agonist, MK 212 (0.0-1.0 mg/kg, i.p.). MK 212 attenuated cue and cocaine-primed reinstatement, as well as spontaneous and cocaine-induced locomotion at all doses tested. These effects were reversed by coadministration of the 5-HT2C-selective receptor antagonist, SB 242 084 (3.0 mg/kg, i.p.), suggesting they are 5-HT2C receptor-mediated. Although we cannot rule out the possibility that motor impairment might have been involved in the MK 212 effects on cocaine-seeking behavior, some aspects of the data favor the explanation that MK 212 decreases the motivational effects of cocaine and cocaine cues. The latter interpretation is consistent with a growing body of literature suggesting that 5-HT2C receptors play a role in motivated behaviors in general.
机译:灭绝/恢复模型已用于本研究中,以研究5-HT2C受体在可卡因相关提示和可卡因引发注射引起的可卡因寻求行为中的作用。训练过的大鼠按可卡因杠杆(0.75 mg / kg / 0.1 ml,静脉内)并与灯光和音调提示配对,每天进行灭绝,在此期间反应没有任何后果。应答减弱后,通过提示或可卡因引发注射(10 mg / kg,腹膜内,腹膜内)腹腔注射(ip)或不使用5-HT2C / 2B受体激动剂进行预处理,测试大鼠是否恢复应答,MK 212(0.0-1.0mg / kg,ip)。 MK 212在所有测试剂量下均减弱了提示和可卡因引发的恢复,以及自发和可卡因诱导的运动。通过共同施用5-HT2C选择性受体拮抗剂SB 242 084(3.0 mg / kg,i.p.)可逆转这些作用,表明它们是5-HT2C受体介导的。尽管我们不能排除运动障碍可能参与了MK 212对可卡因寻求行为的影响,但数据的某些方面支持MK 212降低可卡因和可卡因提示的动机影响的解释。后一种解释与越来越多的文献一致,表明5-HT2C受体通常在动机行为中起作用。

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