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前额梨状皮层中的 CB1 受体控制气味偏好记忆。

CB1 Receptors in the Anterior Piriform Cortex Control Odor Preference Memory.

机构信息

INSERM, U1215 NeuroCentre Magendie, 146 rue Léo Saignat, 33077 Bordeaux Cedex, France; University of Bordeaux, 146 rue Léo Saignat, 33000 Bordeaux, France.

Department of Neurosciences, University of the Basque Country UPV/EHU, Barrio Sarriena s\n, 48940 Leioa, Spain; Achucarro Basque Center for Neuroscience, Science Park of the UPV/EHU, 48940 Leioa, Spain.

出版信息

Curr Biol. 2019 Aug 5;29(15):2455-2464.e5. doi: 10.1016/j.cub.2019.06.041. Epub 2019 Jul 18.

DOI:10.1016/j.cub.2019.06.041
PMID:31327715
Abstract

The retrieval of odor-related memories shapes animal behavior. The anterior piriform cortex (aPC) is the largest part of the olfactory cortex, and it plays important roles in olfactory processing and memory. However, it is still unclear whether specific cellular mechanisms in the aPC control olfactory memory, depending on the appetitive or aversive nature of the stimuli involved. Cannabinoid-type 1 (CB1) receptors are present in the aPC (aPC-CB1), but their potential impact on olfactory memory was never explored. Here, we used a combination of behavioral, genetic, anatomical, and electrophysiological approaches to characterize the functions of aPC-CB1 receptors in the regulation of appetitive and aversive olfactory memory. Pharmacological blockade or genetic deletion of aPC-CB1 receptors specifically impaired the retrieval of conditioned odor preference (COP). Interestingly, expression of conditioned odor aversion (COA) was unaffected by local CB1 receptor blockade, indicating that the role of aPC endocannabinoid signaling is selective for retrieval of appetitive memory. Anatomical investigations revealed that CB1 receptors are highly expressed on aPC GABAergic interneurons, and ex vivo electrophysiological recordings showed that their pharmacological activation reduces miniature inhibitory post-synaptic currents (mIPSCs) onto aPC semilunar (SL), but not pyramidal principal neurons. COP retrieval, but not COA, was associated with a specific CB1-receptor-dependent decrease of mIPSCs in SL cells. Altogether, these data indicate that aPC-CB1 receptor-dependent mechanisms physiologically control the retrieval of olfactory memory, depending on odor valence and engaging modulation of local inhibitory transmission.

摘要

气味相关记忆的提取塑造了动物行为。前梨状皮层 (aPC) 是嗅觉皮层中最大的部分,它在嗅觉处理和记忆中发挥着重要作用。然而,目前尚不清楚 aPC 中的特定细胞机制是否取决于所涉及刺激的奖赏性或厌恶性来控制嗅觉记忆。大麻素型 1 (CB1) 受体存在于 aPC (aPC-CB1) 中,但它们对嗅觉记忆的潜在影响从未被探索过。在这里,我们使用行为学、遗传学、解剖学和电生理学方法相结合,来描述 aPC-CB1 受体在调节奖赏性和厌恶性嗅觉记忆中的功能。药理学阻断或 aPC-CB1 受体的基因缺失特异性损害了条件性气味偏好 (COP) 的检索。有趣的是,条件性气味厌恶 (COA) 的表达不受局部 CB1 受体阻断的影响,表明 aPC 内源性大麻素信号的作用是选择性地用于检索奖赏性记忆。解剖学研究表明,CB1 受体在 aPC GABA 能中间神经元上高度表达,并且离体电生理记录表明,它们的药理学激活减少了 aPC 半月形 (SL) 上的微小抑制性突触后电流 (mIPSCs),但对 SL 上的锥体神经元没有影响。COP 的检索,但不是 COA,与 SL 细胞中特定的 CB1 受体依赖性 mIPSCs 减少有关。总之,这些数据表明,aPC-CB1 受体依赖性机制依赖于气味效价和参与调节局部抑制性传递,从而在生理上控制嗅觉记忆的检索。

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