首页> 外文期刊>The Journal of Physiology >Activation of M2 muscarinic receptors leads to sustained suppression of hippocampal transmission in the medial prefrontal cortex.
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Activation of M2 muscarinic receptors leads to sustained suppression of hippocampal transmission in the medial prefrontal cortex.

机译:M2毒蕈碱受体的激活导致内侧前额叶皮层中海马传播的持续抑制。

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摘要

Cholinergic innervation of the prefrontal cortex is critically involved in arousal, learning and memory. Dysfunction of muscarinic acetylcholine receptors and their downstream signalling pathways has been identified in mental retardation. To assess the role played by the muscarinic receptors at the hippocampal-frontal cortex synapses, an important relay in information storage, we used a newly developed frontal slice preparation in which hippocampal afferent fibres are preserved. Transient activation of muscarinic receptors by carbachol results in a long-lasting depression of synaptic efficacy at the hippocampal but not cortical pathways or local circuitry. On the basis of a combination of electrophysiological, pharmacological and anatomical results, this input-specific muscarinic modulation can be partially attributed to the M2 subtype of muscarinic receptors, possibly through a combination of pre- and postsynaptic mechanisms.
机译:前额叶皮层的胆碱能神经支配主要涉及唤醒,学习和记忆。毒蕈碱型乙酰胆碱受体及其下游信号通路的功能障碍已在智力低下中得到确认。为了评估毒蕈碱受体在海马-额叶皮层突触(信息存储中的重要中继点)上的作用,我们使用了一种新开发的额叶切片制剂,其中保留了海马传入纤维。卡巴胆碱对毒蕈碱受体的短暂激活会导致海马区的突触效力长期下降,但不会导致皮质途径或局部回路。根据电生理,药理学和解剖学结果的组合,这种输入特定的毒蕈碱调节可以部分归因于毒蕈碱受体的M2亚型,可能是通过突触前和突触后机制的组合。

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