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首页> 外文期刊>The Journal of Physiology >Kainate receptor-mediated presynaptic inhibition at the mouse hippocampal mossy fibre synapse.
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Kainate receptor-mediated presynaptic inhibition at the mouse hippocampal mossy fibre synapse.

机译:海藻酸盐受体介导的小鼠海马苔藓纤维突触的突触前抑制。

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摘要

1. The presynaptic action of kainate (KA) receptor activation at the mossy fibre-CA3 synapse was examined using fluorescence measurement of presynaptic Ca2+ influx as well as electrophysiological recordings in mouse hippocampal slices. 2. Bath application of a low concentration (0.2 microM) of KA reversibly increased the amplitude of presynaptic volley evoked by stimulation of mossy fibres to 146 +/- 6 % of control (n = 6), whereas it reduced the field excitatory postsynaptic potential (EPSPs) to 30 +/- 4 %. 3. The potentiating effect of KA on the presynaptic volleys was also observed in Ca2+-free solution, and was partly antagonized by (2S, 4R)-4-methylglutamic acid (SYM 2081, 1 microM), which selectively desensitizes KA receptors. 4. The antidromic population spike of dentate granule cells evoked by stimulation of mossy fibres was increased by application of 0.2 microM KA to 160 +/- 10 % of control (n = 6). Whole-cell current-clamp recordings revealed that the stimulus threshold for generating antidromic spikes recorded from a single granule cell was lowered by KA application. 5. Application of KA (0.2 microM) suppressed presynaptic Ca2+ influx to 78 +/- 4 % of control (n = 6), whereas the amplitude of the presynaptic volley was increased. 6. KA at 0.2 microM reversibly suppressed excitatory postsynaptic currents (EPSCs) evoked by mossy fibre simulation to 38 +/- 9 % of control (n = 5). 7. These results suggest that KA receptor activation enhances the excitability of mossy fibres, probably via axonal depolarization, and reduces action potential-induced Ca2+ influx, thereby inhibiting mossy fibre EPSCs presynaptically. This novel presynaptic inhibitory action of KA at the mossy fibre-CA3 synapse may regulate the excitability of highly interconnected CA3 networks.
机译:1.使用突触前Ca2 +内流的荧光测量以及小鼠海马切片中的电生理记录,检查了藻酸酯纤维-CA3突触中的海藻酸盐(KA)受体激活的突触前作用。 2.浴液中低浓度(0.2 microM)KA的应用可逆地将苔藓纤维刺激引起的突触前截击幅度提高至对照组的146 +/- 6%(n = 6),而这会降低野外兴奋性突触后突触电位(EPSPs)为30 +/- 4%。 3.在不含Ca2 +的溶液中也观察到KA对突触前​​截纹的增强作用,部分被(2S,4R)-4-甲基谷氨酸(SYM 2081,1 microM)拮抗,选择性地使KA受体脱敏。 4.通过施加0.2 microM KA达到对照的160 +/- 10%(n = 6),增加了通过生苔纤维刺激而引起的齿状颗粒细胞的抗峰种群峰值。全细胞电流钳记录显示,通过应用KA降低了从单个颗粒细胞记录的产生反峰尖峰的刺激阈值。 5.施用KA(0.2 microM)抑制突触前Ca2 +流入,达到对照的78 +/- 4%(n = 6),而突触前截击的幅度增加。 6.在0.2 microM的KA可逆地将苔藓纤维模拟引起的兴奋性突触后突触电流(EPSC)抑制为对照的38 +/- 9%(n = 5)。 7.这些结果表明,KA受体活化可能通过轴突去极化增强了苔藓纤维的兴奋性,并减少了动作电位诱导的Ca2 +内流,从而预先突触抑制了苔藓纤维EPSC。 KA在长满苔藓的纤维CA3突触中的这种新的突触前抑制作用可能调节高度互连的CA3网络的兴奋性。

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