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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Phenylephrine enhances glutamate release in the medial prefrontal cortex through interaction with N-type Ca2+ channels and release machinery
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Phenylephrine enhances glutamate release in the medial prefrontal cortex through interaction with N-type Ca2+ channels and release machinery

机译:苯肾上腺素通过与N型Ca2 +通道和释放机制的相互作用增强前额内侧皮层中的谷氨酸释放

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alpha(1)-adrenoceptors ((1)-ARs) stimulation has been found to enhance excitatory processes in many brain regions. A recent study in our laboratory showed that (1)-ARs stimulation enhances glutamatergic transmission via both pre- and post-synaptic mechanisms in layer V/VI pyramidal cells of the rat medial prefrontal cortex (mPFC). However, a number of pre-synaptic mechanisms may contribute to (1)-ARs-induced enhancement of glutamate release. In this study, we blocked the possible post-synaptic action mediated by (1)-ARs to investigate how (1)-ARs activation regulates pre-synaptic glutamate release in layer V/VI pyramidal neurons of mPFC. We found that the (1)-ARs agonist phenylephrine (Phe) induced a significant enhancement of glutamatergic transmission. The Phe-induced potentiation was mediated by enhancing pre-synaptic glutamate release probability and increasing the number of release vesicles via a protein kinase C-dependent pathway. The mechanisms of Phe-induced potentiation included interaction with both glutamate release machinery and N-type Ca2+ channels, probably via a pre-synaptic G(q)/phospholipase C/protein kinase C pathway. Our results may provide a cellular and molecular mechanism that helps explain (1)-ARs-mediated influence on PFC cognitive functions.
机译:已发现α(1)-肾上腺素能受体((1)-ARs)刺激可增强许多大脑区域的兴奋性过程。我们实验室中的一项最新研究表明,(1)-ARs刺激通过大鼠前额内侧皮层(mPFC)的V / VI层锥体细胞中的突触前和突触后机制增强谷氨酸能传递。但是,许多突触前机制可能有助于(1)-ARs诱导的谷氨酸释放增强。在这项研究中,我们阻止了由(1)-ARs介导的可能的突触后作用,以研究(1)-ARs的活化如何调节mPFC的V / VI锥体神经元中的突触前谷氨酸释放。我们发现(1)-ARs激动剂去氧肾上腺素(Phe)诱导了谷氨酸能传递的显着增强。 Phe诱导的增强作用是通过增强突触前谷氨酸的释放概率和通过蛋白激酶C依赖性途径增加释放小泡的数量来介导的。 Phe诱导的增强作用的机制包括可能通过突触前的G(q)/磷脂酶C /蛋白激酶C途径与谷氨酸释放机制和N型Ca2 +通道相互作用。我们的结果可能提供有助于解释(1)-ARs介导的对PFC认知功能影响的细胞和分子机制。

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