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Neurogliaform cells of amygdala: A source of slow phasic inhibition in the basolateral complex

机译:杏仁核的神经胶质细胞:基底外侧复合体的缓慢阶段性抑制源

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Synaptic inhibition in the amygdala actively participates in processing emotional information. To improve the understanding of interneurons in amygdala networks it is necessary to characterize the GABAergic cell types, their connectivity and physiological roles. We used a mouse line expressing a green fluorescent protein (GFP) under the neuropeptide Y (NPY) promoter. Paired recordings between presynaptic NPY-GFP-expressing (+) cells and postsynaptic principal neurons (PNs) of the basolateral amygdala (BLA) were performed. The NPY-GFP+ neurons displayed small somata and short dendrites embedded in a cloud of highly arborized axon, suggesting a neurogliaform cell (NGFC) type. We discovered that a NPY-GFP+ cell evoked a GABA A receptor-mediated slow inhibitory postsynaptic current (IPSC) in a PN and an autaptic IPSC. The slow kinetics of these IPSCs was likely caused by the low concentration and spillover of extracellular GABA. We also report that NGFCs of the BLA fired action potentials phase-locked to hippocampal theta oscillations in anaesthetized rats. When this firing was re-played in NPY+-NGFCs in vitro, it evoked a transient depression of the IPSCs. Presynaptic GABA B receptors and functional depletion of synaptic vesicles determined this short-term plasticity. Synaptic contacts made by recorded NGFCs showed close appositions, and rarely identifiable classical synaptic structures. Thus, we report here a novel interneuron type of the amygdala that generates volume transmission of GABA. The peculiar functional mode of NGFCs makes them unique amongst all GABAergic cell types of the amygdala identified so far.
机译:杏仁核中的突触抑制积极参与处理情绪信息。为了更好地了解杏仁核网络中的中间神经元,必须表征GABA能细胞的类型,它们的连通性和生理作用。我们使用了在神经肽Y(NPY)启动子下表达绿色荧光蛋白(GFP)的小鼠品系。进行了突触前表达NPY-GFP的(+)细胞与基底外侧杏仁核(BLA)的突触后主要神经元(PNs)之间的配对记录。 NPY-GFP +神经元在高度乔化的轴突的云中显示出小的躯体和短树突,表明是神经胶质细胞(NGFC)类型。我们发现,NPY-GFP +细胞在PN和自闭性IPSC中诱发了GABA A受体介导的缓慢抑制突触后电流(IPSC)。这些IPSC的动力学缓慢可能是由于细胞外GABA浓度低和溢出所致。我们还报告说,BLA的NGFC激发了被麻醉大鼠海马theta振荡相位锁定的动作电位。当这种射击在NPY + -NGFCs体外重播时,引起了IPSC的短暂抑制。突触前GABA B受体和突触小泡的功能耗竭决定了这种短期可塑性。记录的NGFC产生的突触接触显示出亲密的位置,并且很少可识别的经典突触结构。因此,我们在此报告了一种新型的杏仁核中间神经元类型,它可以生成GABA的体积传输。 NGFCs独特的功能模式使它们在迄今为止鉴定出的杏仁体的所有GABA能细胞类型中都是独一无二的。

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