首页> 美国卫生研究院文献>The Journal of Neuroscience >Opioid Receptors in the Midbrain Periaqueductal Gray Regulate Extinction of Pavlovian Fear Conditioning
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Opioid Receptors in the Midbrain Periaqueductal Gray Regulate Extinction of Pavlovian Fear Conditioning

机译:阿片样受体在中脑水管周围灰色调节巴甫洛夫恐惧条件的灭绝。

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摘要

Four experiments studied the role of opioid receptors in the midbrain periaqueductal gray matter (PAG), an important structure eliciting conditioned fear responses, in the extinction of Pavlovian fear. Rats received pairings of an auditory conditioned stimulus (CS) with a foot shock unconditioned stimulus (US). The freezing conditioned response (CR) elicited by the CS was then extinguished via nonreinforced presentations of the CS. Microinjection of the opioid receptor antagonist naloxone into the ventrolateral PAG (vlPAG) before nonrein-forced CS presentations impaired development of extinction, but such microinjections at the end of extinction did not reinstate an already extinguished freezing CR. This role for opioid receptors in fear extinction was specific to the vlPAG because infusions of naloxone into the dorsal PAG did not impair fear extinction. Finally, the impairment of fear extinction produced by vlPAG infusions of naloxone was dose-dependent. These results show for the first time that the midbrain PAG contributes to fear extinction and specifically identify a role for vlPAG opioid receptors in the acquisition but not the expression of such extinction. Taken together with our previous findings, we suggest that, during fear conditioning, activation of vlPAG opioid receptors contributes to detection of the discrepancy between the actual and expected outcome of the conditioning trial. vlPAG opioid receptors regulate the learning that accrues to the CS and other stimuli present on a trial because they instantiate an associative error correction process influencing US information reaching the site of CS-US convergence in the amygdala. During nonreinforcement, this vlPAG opioid receptor contribution signals extinction.
机译:四个实验研究了阿片样物质受体在巴甫洛夫恐惧症灭绝中的作用,该物质在中脑导水管周围灰质(PAG)中是一种引发条件性恐惧反应的重要结构。大鼠接受了听觉条件刺激(CS)和脚震非条件刺激(US)的配对。然后通过CS的非增强表现消除CS引起的冻结条件反应(CR)。在非强化CS表现之前,将阿片受体拮抗剂纳洛酮微注射入腹侧PAG(vlPAG)会危害灭绝的发展,但是在灭绝结束时进行此类显微注射并不能恢复已经灭绝的冰冻CR。阿片受体在恐惧消退中的这种作用是vlPAG特有的,因为将纳洛酮注入背侧PAG不会损害恐惧消退。最后,由vlPAG输注纳洛酮产生的恐惧消退障碍与剂量有关。这些结果首次表明中脑PAG有助于恐惧的灭绝,并特别确定了vlPAG阿片样物质受体在获得性灭绝中的作用,而不是在这种灭绝的表达中的作用。结合我们以前的发现,我们建议在恐惧调节期间,vlPAG阿片样物质受体的激活有助于检测调节试验的实际结果与预期结果之间的差异。 vlPAG阿片样物质受体可调节试验中CS和其他刺激物产生的学习效果,因为它们会实例化一个错误校正过程,从而影响到达杏仁核中CS-US融合点的美国信息。在非增强过程中,这种vPAG阿片受体的贡献表明灭绝。

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