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大鼠梯形体内侧核的突触前和突触后全细胞记录。

Pre- and postsynaptic whole-cell recordings in the medial nucleus of the trapezoid body of the rat.

作者信息

Borst J G, Helmchen F, Sakmann B

机构信息

Abteilung Zellphysiologie, Max-Planck-Institut für medizinische Forschung, Heidelberg, Germany.

出版信息

J Physiol. 1995 Dec 15;489 ( Pt 3)(Pt 3):825-40. doi: 10.1113/jphysiol.1995.sp021095.

Abstract
  1. Simultaneous whole-cell recordings in a rat brain slice preparation are described from presynaptic terminals (calyces of Held) and postsynaptic somata which form an axosomatic synapse in the medial nucleus of the trapezoid body (MNTB). 2. Presynaptic action potentials evoked suprathreshold excitatory postsynaptic potentials (EPSPs). The minimum synaptic delay was around 0.4 ms at 36 degrees C and 0.9 ms at 23-24 degrees C. The amplitude of the L-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) receptor-mediated component of the excitatory postsynaptic currents (EPSCs) was 2-13 nA (at -80 mV). 3. Current-voltage relations showed that presynaptic Ca2+ channels were of the high voltage-activated type. 4. A single action potential evoked a presynaptic fluorescence transient that decayed with a time constant of 0.3-0.7 s, depending on the concentration (60-200 microM) of the Ca2+ indicator Calcium Green-5N (CG-5N). The peak amplitude of the [Ca2+]i transient was severalfold larger in the terminal than in the preterminal axon. 5. EPSC peak amplitudes were stable for more than 30 min after establishing the whole-cell configuration in the presynaptic terminal when the pipette contained 50 microM BAPTA. In contrast, with 1 mM BAPTA, peak amplitudes of EPSCs were reduced to one-third. 6. Trains of presynaptic action potentials evoked EPSCs with progressively smaller amplitudes. Little change was observed in the depression when the terminals were dialysed with 50 microM BAPTA, whereas depression was reduced with 1 mM BAPTA. 7. In low (1 mM) [Ca2+]o, facilitation instead of depression of EPSCs was observed. 8. The effects of presynaptic BAPTA suggest that the endogenous mobile Ca2+ buffer capacity of giant presynaptic terminals in the MNTB is lower than in other terminals of fast transmitting synapses.
摘要
  1. 本文描述了在大鼠脑片制备中,对内侧橄榄耳蜗核(MNTB)中形成轴体突触的突触前终末(Held壶腹)和突触后胞体进行的同步全细胞记录。2. 突触前动作电位诱发阈上兴奋性突触后电位(EPSP)。在36℃时最小突触延迟约为0.4毫秒,在23 - 24℃时为0.9毫秒。兴奋性突触后电流(EPSC)中由L-α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体介导的成分的幅度为2 - 13纳安(在-80毫伏时)。3. 电流-电压关系表明突触前Ca²⁺通道为高电压激活型。4. 单个动作电位诱发突触前荧光瞬变,其衰减时间常数为0.3 - 0.7秒,这取决于Ca²⁺指示剂钙绿-5N(CG-5N)的浓度(60 - 200微摩尔)。终末中[Ca²⁺]i瞬变的峰值幅度比终末前轴突中的大几倍。5. 当移液管中含有50微摩尔BAPTA时,在突触前终末建立全细胞配置后,EPSC峰值幅度在30多分钟内保持稳定。相比之下,当使用1毫摩尔BAPTA时,EPSC峰值幅度降至三分之一。6. 一串突触前动作电位诱发的EPSC幅度逐渐减小。当终末用50微摩尔BAPTA透析时,在抑制方面几乎没有变化,而当使用1毫摩尔BAPTA时抑制作用减弱。7. 在低(1毫摩尔)[Ca²⁺]o时,观察到EPSC出现易化而非抑制。8. 突触前BAPTA的作用表明,MNTB中巨大突触前终末的内源性可移动Ca²⁺缓冲能力低于快速传递突触的其他终末。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ee6/1156851/e85070868b48/jphysiol00306-0206-a.jpg

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