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Synaptic potentiation of dual-component excitatory postsynaptic currents in the rat hippocampus.

机译:大鼠海马中双组分兴奋性突触后电流的突触增强。

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摘要

1. Whole-cell patch-clamp recording has been used to study tetanus-induced synaptic potentiation of dual-component excitatory postsynaptic currents (EPSCs) in the CA1 region of rat hippocampal slices, following blockade of GABAA and GABAB receptor-mediated synaptic inhibition. 2. At a holding potential of -60 mV, the initial slope of the EPSC (between 10 and 60% of maximum amplitude) provided an accurate measurement of the AMPA receptor-mediated component, and the amplitude of the EPSC at a latency of 100 ms provided the best estimate of the size of the NMDA receptor-mediated component. 3. Neurons were voltage clamped for at least 45 min prior to delivery of a tetanus (test intensity, 100 Hz, 1 s). Measurements at 10 and 30 min following the tetanus were used as indications of short-term potentiation (STP) and long-term potentiation (LTP), respectively. One set of neurons were voltage clamped at -60 mV throughout. These neurons could be subdivided into two populations on the basis of whether or not there was LTP (n = 9), or only STP (n = 6), of the AMPA receptor-mediated component. A second set of neurons were voltage clamped at -60 mV for 30 min and then at -50 mV for 15 min before, during and for 30 min following tetanization. In these experiments there was STP but not LTP (n = 8). 4. In all neurons (n = 23), the time course of the potentiation of the NMDA receptor-mediated component paralleled that of the AMPA receptor-mediated component. In addition, potentiation of the NMDA and AMPA receptor-mediated components were of a similar magnitude. 5. These data demonstrate that it is possible to induce LTP by high frequency stimulation after 45 min of whole-cell recording. Under these conditions, there is a parallel potentiation of the AMPA and NMDA receptor-mediated components of dual-component EPSCs. This constitutes the first evidence, from studies of dual-component synaptic responses, which is consistent with a presynaptic locus of expression of tetanus-induced STP and LTP in the hippocampus.
机译:1.全细胞膜片钳记录已被用于研究破伤风诱导的大鼠海马切片CA1区双组分兴奋性突触后突触电流(EPSC)的突触增强作用,该阻滞作用是在GABAA和GABAB受体介导的突触抑制受阻后发生的。 2.在-60 mV的保持电势下,EPSC的初始斜率(在最大振幅的10%至60%之间)提供了AMPA受体介导成分的精确测量,以及在100潜伏期的EPSC振幅ms提供了NMDA受体介导的成分大小的最佳估计。 3.在递送破伤风之前,将神经元电压钳制至少45分钟(测试强度,100 Hz,1 s)。破伤风发生后10分钟和30分钟的测量分别用作短期增强(STP)和长期增强(LTP)的指标。整个过程中,一组神经元电压钳位在-60 mV。根据是否存在AMPA受体介导的成分的LTP(n = 9)或仅STP(n = 6),可以将这些神经元细分为两个群体。在钛化之前,期间和之后,将第二组神经元电压钳制在-60 mV电压下30分钟,然后在-50 mV电压下15分钟。在这些实验中,有STP但没有LTP(n = 8)。 4.在所有神经元(n = 23)中,NMDA受体介导的组分的增强作用的时间过程与AMPA受体介导的组分的增强作用的时间过程平行。另外,NMDA和AMPA受体介导的组分的增强作用具有相似的程度。 5.这些数据表明,在全细胞记录45分钟后,可以通过高频刺激诱导LTP。在这些条件下,双组分EPSC的AMPA和NMDA受体介导的组分平行增强。这是双组分突触反应研究的第一个证据,这与破伤风诱导的海马中STP和LTP的突触前表达位点一致。

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