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Acute Ethanol Exposure Elevates Muscarinic Tone in the Septohippocampal System

机译:急性乙醇暴露会升高海马海马系统中的毒蕈碱度

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摘要

The septohippocampal system has been implicated in the cognitive deficits associated with ethanol consumption, but the cellular basis of ethanol action awaits full elucidation. In the medial septum/diagonal band of Broca (MS/DB), a muscarinic tone, reflective of firing activity of resident cholinergic neurons, regulates that of their noncholinergic, putatively GABAergic, counterparts. Here we tested the hypothesis that ethanol alters this muscarinic tone. The spontaneous firing activity of cholinergic and noncholinergic MS/DB neurons were monitored in acute MS/DB slices from C57Bl/6 mice. Exposing the entire slice to ethanol increased firing in both cholinergic and noncholinergic neurons. However, applying ethanol focally to individual MS/DB neurons increased firing only in cholinergic neurons. The differential outcome suggested different mechanisms of ethanol action on cholinergic and noncholinergic neurons. Indeed, with bath-perfused ethanol, the muscarinic antagonist methyl scopolamine prevented the increase in firing in noncholinergic, but not cholinergic, MS/DB neurons. Thus, the effect on noncholinergic neuronal firing was secondary to ethanol's direct action of acutely increasing muscarinic tone. We propose that the acute ethanol-induced elevation of muscarinic tone in the MS/DB contributes to the altered net flow of neuronal activity in the septohippocampal system that underlies compromised cognitive function.
机译:七海马系统参与了与乙醇消费有关的认知缺陷,但乙醇作用的细胞基础尚待充分阐明。在Broca的中隔/对角带(MS / DB)中,毒蕈碱调反映了常驻胆碱能神经元的放电活动,从而调节了其非胆碱能的,假定为GABA能的对应神经元的放电活动。在这里,我们测试了乙醇改变这种毒蕈碱色调的假设。在来自C57Bl / 6小鼠的急性MS / DB切片中监测胆碱能和非胆碱能MS / DB神经元的自发放电活性。将整个切片暴露于乙醇会增加胆碱能和非胆碱能神经元的放电。但是,将乙醇集中应用于单个MS / DB神经元只会增加胆碱能神经元的放电。不同的结果表明乙醇对胆碱能和非胆碱能神经元的作用机制不同。实际上,使用浴液灌注的乙醇,毒蕈碱拮抗剂甲基东amine碱可阻止非胆碱能(而非胆碱能)MS / DB神经元的放电增加。因此,对非胆碱能神经元放电的影响是继乙醇急剧增加毒蕈碱色调的直接作用之后产生的。我们建议,急性酒精诱导的MS / DB中毒蕈碱色调的升高可导致海马体系统中神经元活动的净流量改变,这是认知功能受损的基础。

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