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首页> 外文期刊>Behavioural Brain Research: An International Journal >NMDA antagonist MK 801 in nucleus accumbens core but not shell disrupts the restraint stress-induced reinstatement of extinguished cocaine-conditioned place preference in rats
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NMDA antagonist MK 801 in nucleus accumbens core but not shell disrupts the restraint stress-induced reinstatement of extinguished cocaine-conditioned place preference in rats

机译:NMDA拮抗剂MK 801位于伏隔核的核心,但不破坏壳层,从而抑制了限制性应激诱导的可卡因条件下熄灭的位置偏好的恢复

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摘要

Relapse is a common feature of cocaine addiction. In rodents, it can be elicited by cues, stress or the drug. Restraint stress-induced reinstatement of cocaine-conditioned place preference (CPP) is a useful model to study the mechanisms involved in stress-induced relapse of drug-seeking behavior. There is evidence that the glutamate NMDA receptors are critically involved in drug- and cue-induced reinstatement of seeking behavior and drug-CPP responses. The aim of this study was to investigate the contribution of NMDA receptors within core vs. shell nucleus accumbens (NAc) subregions to restraint stress-induced reinstatement of extinguished cocaine-CPP. After extinction of cocaine-conditioned preference, animals were administered MK 801 systemically or directly into intra-core or intra-shell, and restrained for 30 min or left undisturbed in their home-cages. First, we demonstrated that restraint stress-induced reinstatement of extinguished cocaine-CPP depends on the duration of restraint as well as on the context in which it is applied. Second, this effect was blocked by systemic MK 801 administration either before or after restraint. Third, intra-core but not intra-shell administration abrogated the restraint stress-induced reinstatement. These findings show that NMDA receptors within NAc core, but not shell, play a critical role in restraint stress-induced reinstatement of cocaine-CPP. (C) 2016 Elsevier B.V. All rights reserved.
机译:复发是可卡因成瘾的普遍特征。在啮齿动物中,它可能是由线索,压力或药物引起的。抑制应激诱导的可卡因条件位置偏爱(CPP)恢复是研究应激诱导的药物寻求行为复发机制的有用模型。有证据表明,谷氨酸NMDA受体与药物和提示诱导的寻求行为和药物CPP反应的恢复密切相关。这项研究的目的是调查核心与壳伏伏核(NAc)子区域内的NMDA受体对抑制应激诱导的可卡因-CPP的恢复的作用。在可卡因限制的条件消失后,将MK 801全身或直接给药于核内或壳内,并限制30分钟或使其笼中不受干扰。首先,我们证明了抑制应激引起的可卡因-CPP的消失取决于抑制的持续时间以及应用抑制的背景。第二,在约束之前或之后,全身性MK 801的给药可阻断这种作用。第三,核心内给药而不是壳内给药取消了束缚应激诱导的恢复。这些发现表明,NAc核心而不是壳中的NMDA受体在抑制应激诱导的可卡因-CPP的恢复中起关键作用。 (C)2016 Elsevier B.V.保留所有权利。

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