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缰核 CB1 受体控制厌恶性记忆的表达。

Habenular CB1 Receptors Control the Expression of Aversive Memories.

机构信息

INSERM, U862 NeuroCentre Magendie, Group Endocannabinoids and Neuroadaptation, Bordeaux 33077, France; University of Bordeaux, Bordeaux 33077, France.

National Institute of Biological Sciences, Beijing 100875, China.

出版信息

Neuron. 2015 Oct 21;88(2):306-13. doi: 10.1016/j.neuron.2015.08.035. Epub 2015 Sep 24.

Abstract

Expression of aversive memories is key for survival, but the underlying brain mechanisms are not fully understood. Medial habenular (MHb) axons corelease glutamate and acetylcholine onto target postsynaptic interpeduncular (IPN) neurons, but their role in aversive memories has not been addressed so far. We found that cannabinoid type 1 receptors (CB1R), key regulators of aversive responses, are present at presynaptic terminals of MHb neurons in the IPN. Conditional deletion of CB1R from MHb neurons reduces fear-conditioned freezing and abolishes conditioned odor aversion in mice, without affecting neutral or appetitively motivated memories. Interestingly, local inhibition of nicotinic, but not glutamatergic receptors in the target region IPN before retrieval, rescues these phenotypes. Finally, optogenetic electrophysiological recordings of MHb-to-IPN circuitry revealed that blockade of CB1R specifically enhances cholinergic, but not glutamatergic, neurotransmission. Thus, presynaptic CB1R control expression of aversive memories by selectively modulating cholinergic transmission at MHb synapses in the IPN.

摘要

厌恶记忆的表达对生存至关重要,但相关的大脑机制尚不完全清楚。中脑导水管周围灰质(MHb)轴突在投射靶区脚间核(IPN)神经元上共释放谷氨酸和乙酰胆碱,但它们在厌恶记忆中的作用尚未得到解决。我们发现,大麻素 1 型受体(CB1R)是厌恶反应的关键调节因子,存在于 IPN 中 MHb 神经元的突触前末梢。MHb 神经元中 CB1R 的条件性缺失会减少恐惧条件性冻结,并消除小鼠的条件性气味厌恶,而不影响中性或有动机的记忆。有趣的是,在检索前,在靶区 IPN 中局部抑制烟碱型而非谷氨酸型受体,可以挽救这些表型。最后,MHb 到 IPN 回路的光遗传电生理学记录显示,CB1R 的阻断特异性增强了胆碱能,而不是谷氨酸能神经传递。因此,突触前 CB1R 通过选择性调节 IPN 中 MHb 突触的胆碱能传递来控制厌恶记忆的表达。

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