首页> 外文期刊>The Journal of Physiology >Action potential propagation into the presynaptic dendrites of rat mitral cells.
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Action potential propagation into the presynaptic dendrites of rat mitral cells.

机译:动作电位传播到大鼠二尖瓣细胞的突触前树突中。

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1. Dendritic patch-clamp recordings were obtained from mitral cells in rat olfactory bulb slices, up to 350 microns from the soma. Simultaneous dendritic and somatic whole-cell recordings indicated that action potentials (APs) evoked by somatic or dendritic current injection were initiated near the soma. Both the large amplitude (100.7 +/- 1.1 mV) and the short duration (1.38 +/- 0.07 ms) of the AP were maintained as the AP propagated back into the primary mitral cell dendrites. 2. Outside-out patches isolated from mitral cell dendrites contained voltage-gated Na+ channels (peak conductance density, 90 pS micron-2 at -10 mV). When an AP was used as a somatic voltage-clamp command in the presence of 1 microM tetrodotoxin (TTX), the amplitude of the dendritic potential was attenuated to 48 +/- 14 mV. This shows that dendritic Na+ channels support the active back-propagation of APs. 3. Dendritic patches contained voltage-gated K+ channels with high density (conductance density, 513 pS micron-2 at 30 mV). Dendritic K+ currents were reduced to 35% by 1 mM external tetraethylammonium chloride (TEACl). When an AP was used as a somatic voltage-clamp command in the presence of TEACl, the dendritic potential was markedly prolonged. This indicates that dendritic K+ channels mediate the fast repolarization of dendritic APs. 4. We conclude that voltage-gated Na+ and K+ channels support dendritic APs with large amplitudes and short durations that may trigger fast transmitter release at dendrodendritic synapses in the olfactory bulb.
机译:1.树突状膜片钳记录是从大鼠嗅球切片中的二尖瓣细胞获得的,距体细胞最远为350微米。同时的树突状细胞和体细胞全细胞记录表明,由体细胞或树突状电流注入引起的动作电位(AP)是在体细胞附近引发的。随着AP传播回到原代二尖瓣细胞树突中,AP的大振幅(100.7 +/- 1.1 mV)和短持续时间(1.38 +/- 0.07 ms)都得以维持。 2.从二尖瓣细胞树突中分离出来的外向贴片包含电压门控的Na +通道(峰值电导密度,-10 mV时为90 pS micron-2)。当在存在1 microM河豚毒素(TTX)的情况下将AP用作体电压钳命令时,树突电位的振幅会衰减至48 +/- 14 mV。这表明树突状的Na +通道支持AP的主动反向传播。 3.树突状斑块包含高密度的电压门控K +通道(电导密度,在30 mV时为513 pS micron-2)。 1 mM外部四乙基氯化铵(TEACl)将树状K +电流降低至35%。当在TEAC1存在下将AP用作体电压钳位命令时,树突电位显着延长。这表明树突状K +通道介导了树突状AP的快速复极化。 4.我们得出结论,电压门控的Na +和K +通道支持具有大幅度和短持续时间的树状AP,这可能会触发嗅球中树突状突触的快速释放。

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