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恐惧条件反射后,对伏隔核进行药理学刺激有助于随后的恐惧消退。

Pharmacological stimulation of infralimbic cortex after fear conditioning facilitates subsequent fear extinction.

机构信息

Department of Psychological and Brain Sciences, Texas A&M University, College Station, USA.

Department of Pharmacology, São Paulo University, São Paulo, Brazil.

出版信息

Neuropsychopharmacology. 2024 Dec;49(13):1951-1957. doi: 10.1038/s41386-024-01961-9. Epub 2024 Aug 13.

Abstract

The infralimbic (IL) division of the medial prefrontal cortex (mPFC) is a crucial site for the extinction of conditioned fear memories in rodents. Recent work suggests that neuronal plasticity in the IL that occurs during (or soon after) fear conditioning enables subsequent IL-dependent extinction learning. We therefore hypothesized that pharmacological activation of the IL after fear conditioning would promote the extinction of conditioned fear. To test this hypothesis, we characterized the effects of post-conditioning infusions of the GABA receptor antagonist, picrotoxin, into the IL on the extinction of auditory conditioned freezing in male and female rats. In four experiments, we found that picrotoxin injections performed immediately, 24 h, or 13 days after fear conditioning reduced conditioned freezing to the auditory conditioned stimulus (CS) during both extinction training and extinction retrieval; this effect was observed up to two weeks after picrotoxin infusions. Interestingly, inhibiting protein synthesis inhibition in the IL immediately after fear conditioning prevented the inhibition of freezing by picrotoxin injected 24 h later. Our data suggest that the IL encodes an inhibitory memory during the consolidation of fear conditioning that is necessary for future fear suppression.

摘要

边缘下区(IL)是内侧前额叶皮层(mPFC)的一个分支,在啮齿类动物中是条件性恐惧记忆消退的关键部位。最近的研究表明,在恐惧条件作用期间或之后发生的 IL 中的神经元可塑性使随后的 IL 依赖性消退学习成为可能。因此,我们假设在恐惧条件作用后对 IL 进行药理学激活会促进条件性恐惧的消退。为了验证这一假设,我们研究了恐惧条件作用后将 GABA 受体拮抗剂,印防己毒素,输注到 IL 中对雄性和雌性大鼠的听觉条件性冻结的消退的影响。在四个实验中,我们发现,印防己毒素注射立即、24 小时或恐惧条件作用后 13 天进行,可减少在消退训练和消退检索期间对听觉条件刺激(CS)的条件性冻结;这种效应可观察到印防己毒素注射后两周。有趣的是,在恐惧条件作用后立即抑制 IL 中的蛋白质合成抑制,可防止 24 小时后注射印防己毒素引起的冻结抑制。我们的数据表明,IL 在恐惧条件作用的巩固过程中编码了一种抑制性记忆,这对于未来的恐惧抑制是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798f/11480363/8cb0e285f05a/41386_2024_1961_Fig1_HTML.jpg

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