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Differential Effects of |[sigma]|1 Receptor Blockade on Self-Administration and Conditioned Reinstatement Motivated by Cocaine vs Natural Reward

机译:|σ| 1受体阻滞对可卡因与自然奖赏动机的自我管理和有条件恢复的差异作用

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Growing evidence suggests a role for sigma1 (1) receptors in cognitive function, anxiety, depression, regulation of stress responses, and, recently, the appetitive effects of cocaine as measured by conditioned place preference. This study was designed to extend understanding of the role of 1 receptors in addiction-relevant conditioned effects of cocaine by testing the effects of a potent and selective 1 receptor antagonist, BD1047, on conditioned reinstatement of cocaine-seeking. To determine whether modification of conditioned reinstatement by BD1047 is selective for drug-directed behavior or reflects general suppressant effects on motivated behavior, BD1047 was tested also on reinstatement induced by stimuli conditioned to a natural reward, sweetened condensed milk (SCM). Additionally, because 1 receptors have been implicated also in processes linked to the acute reinforcing actions of cocaine, tests of the effects of BD1047 on cocaine self-administration—including a comparison with the 1 antagonist effects on SCM self-administration—were conducted as well. Cocaine self-administering male Wistar rats were trained to associate a discriminative stimulus (SD) with the availability of cocaine or SCM, and then subjected to reinstatement tests following extinction of cocaine or SCM-reinforced behavior. BD1047 (1–30mg/kg) reversed response reinstatement induced by the cocaine SD at 20 and 30mg/kg but did not modify SCM SD-induced responding at all but the highest 30mg dose, at which responding was reversed to extinction levels. BD1047 did not modify responding reinforced directly by SCM or cocaine. The findings support a role for 1 receptors in regulating conditioned responses to cocaine-related contextual stimuli and identify this receptor as a potential treatment target for the prevention of craving and relapse.
机译:越来越多的证据表明,sigma1(1)受体在认知功能,焦虑,抑郁,应激反应调节以及最近由可卡因引起的食欲影响中起着作用。这项研究旨在通过测试有效和选择性的1受体拮抗剂BD1047对寻求可卡因的条件恢复的作用,扩展对1受体在与成瘾相关的条件可卡因中的作用的了解。为了确定BD1047对条件恢复的修饰是否对药物定向行为具有选择性或反映了对动机行为的一般抑制作用,还对BD1047对条件适应自然奖励甜炼乳(SCM)的刺激诱导的恢复进行了测试。此外,由于1受体也参与了与可卡因的急性增强作用有关的过程,因此还进行了BD1047对可卡因自我给药作用的测试,包括与1对SCM自我给药拮抗作用的比较。 。对可卡因自我给药的雄性Wistar大鼠进行训练,使其将判别性刺激(SD)与可卡因或SCM的有效性相关联,然后在可卡因或SCM强化行为消失后接受恢复测试。 BD1047(1–30mg / kg)逆转了可卡因SD分别以20和30mg / kg诱导的应答恢复,但没有改变SCM SD诱导的应答,但最高剂量为30mg,在该剂量下应答已消失。 BD1047没有改变直接由SCM或可卡因强化的反应。这些发现支持了1种受体在调节对可卡因相关情境刺激的条件反应中的作用,并将该受体确定为预防渴望和复发的潜在治疗靶标。

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