Institute of Medical Science, University of Toronto, Terrence Donnelly Centre for Cellular and Biomolecular Research, Toronto, Ontario, Canada M5S 3E1.
Department of Molecular Genetics, Neurobiology Research Group, University of Toronto, Terrence Donnelly Centre for Cellular and Biomolecular Research, Toronto, Ontario, Canada M5S 3E1.
Behav Brain Res. 2013 Jun 15;247:174-177. doi: 10.1016/j.bbr.2013.03.026. Epub 2013 Mar 26.
Although D1 receptor knockout mice demonstrate normal morphine place preferences, antagonism of basolateral amygdala (BLA) D1 receptors only during drug-naive rat conditioning has been reported to inhibit the expression of a morphine place preference. One possible explanation for this result is state-dependent learning. That is, the omission of the intra-BLA infusion cue during testing - which acts as a potent discriminative stimulus - may have prevented the recall of a morphine-environment association and therefore, the consequent expression of a morphine place preference. To examine this possibility, we tested whether intra-BLA infusion of the D1-receptor antagonist SCH23390 during both training and testing might reveal a morphine place preference. Our results suggest that in previously drug-naive animals, D1 receptor antagonism during testing restores the opiate conditioned place preference that is normally absent when D1 receptors are blocked only during training, suggesting that BLA D1 receptors can mediate state-dependent memory retrieval.
尽管 D1 受体敲除小鼠表现出正常的吗啡位置偏好,但据报道,仅在药物-naive 大鼠条件作用期间拮抗杏仁核基底外侧核(BLA)D1 受体可抑制吗啡位置偏好的表达。这种结果的一个可能解释是状态依赖性学习。也就是说,在测试期间省略 BLA 内输注线索 - 作为一种有效的鉴别性刺激 - 可能阻止了吗啡环境关联的回忆,因此,随后表达了吗啡位置偏好。为了检验这种可能性,我们测试了在训练和测试期间是否将 D1 受体拮抗剂 SCH23390 输注到 BLA 内是否可能揭示出吗啡位置偏好。我们的结果表明,在以前药物-naive 的动物中,在测试期间 D1 受体拮抗作用恢复了鸦片类药物条件位置偏好,而当仅在训练期间阻断 D1 受体时,通常不存在这种位置偏好,这表明 BLA D1 受体可以介导状态依赖性记忆检索。