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首页> 外文期刊>Psychopharmacology >Transient inactivation of the paraventricular nucleus of the thalamus enhances cue-induced reinstatement in goal-trackers, but not sign-trackers
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Transient inactivation of the paraventricular nucleus of the thalamus enhances cue-induced reinstatement in goal-trackers, but not sign-trackers

机译:丘脑盆腔的瞬时失活增强了目标跟踪器中的提示急剧恢复,但不是签名者

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Abstract Rationale The paraventricular nucleus of the thalamus (PVT) has been shown to mediate cue-motivated behaviors, such as sign- and goal-tracking, as well as reinstatement of drug-seeking behavior. However, the role of the PVT in mediating individual variation in cue-induced drug-seeking behavior remains unknown. Objectives This study aimed to determine if inactivation of the PVT differentially mediates cue-induced drug-seeking behavior in sign-trackers and goal-trackers. Methods Rats were characterized as sign-trackers (STs) or goal-trackers (GTs) based on their Pavlovian conditioned approach behavior. Rats were then exposed to 15?days of cocaine self-administration, followed by a 2-week forced abstinence period and then extinction training. Rats then underwent tests for cue-induced reinstatement and general locomotor activity, prior to which they received an infusion of either saline (control) or baclofen/muscimol (B/M) to inactivate the PVT. Results Relative to control animals of the same phenotype, GTs show a robust increase in cue-induced drug-seeking behavior following PVT inactivation, whereas the behavior of STs was not affected. PVT inactivation did not affect locomotor activity in either phenotype. Conclusion In GTs, the PVT appears to inhibit the expression of drug-seeking, presumably by attenuating the incentive value of the drug cue. Thus, inactivation of the PVT releases this inhibition in GTs, resulting in an increase in cue-induced drug-seeking behavior. PVT inactivation did not affect cue-induced drug-seeking behavior in STs, suggesting that the role of the PVT in encoding the incentive motivational value of drug cues differs between STs and GTs.
机译:摘要丘脑(PVT)的基本基础已被证明介导提示激励行为,例如签署和目标跟踪,以及恢复药物寻求行为。然而,PVT在介导提示诱导的药物寻找行为中的个体变异中的作用仍然未知。目的本研究旨在确定PVT的灭活差异地介导在符号跟踪器和目标跟踪器中介绍提示诱导的药物寻求行为。方法基于其Pavlovian条件的方法行为,大鼠表征为标志跟踪器(STS)或目标跟踪器(GTS)。然后将大鼠接触到15°的可卡因自我管理,然后强迫禁欲期,然后灭绝培训。然后在其接受恢复和通用运动活性的大鼠进行测试,它们接受了盐水(对照)或Baclofen / muscimol(B / M)的输注以使PVT灭活。结果相对于相同表型的对照动物,GTS显示PVT灭活后的提示诱导的药物寻求行为的稳健增加,而STS的行为不受影响。 PVT失活在任何一种表型中都不会影响运动活性。结论在GTS中,PVT似乎抑制了药物寻求的表达,大概通过减轻药物提示的激励价值。因此,PVT的失活释放在GTS中的这种抑制,导致提示诱导的药物寻求行为增加。 PVT灭活并未影响STS中的提示诱导的药物行为,这表明PVT在编码药物线索的激励动力值中的作用在STS和GTS之间不同。

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