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培养的小鼠海马神经元之间兴奋性突触处的Sr2+与量子事件

Sr2+ and quantal events at excitatory synapses between mouse hippocampal neurons in culture.

作者信息

Abdul-Ghani M A, Valiante T A, Pennefather P S

机构信息

MRC Nerve Cell and Synapse Group, Faculty of Pharmacy, University of Toronto, Ontario, Canada.

出版信息

J Physiol. 1996 Aug 15;495 ( Pt 1)(Pt 1):113-25. doi: 10.1113/jphysiol.1996.sp021578.

Abstract
  1. Whole-cell recording from pairs of adjacent mouse hippocampal neurons in culture was used to study the quantal properties of action potential-evoked excitatory synaptic transmission and to demonstrate the use of Sr2+ in quantifying those properties. 2. In the presence of extracellular Sr2+, excitatory postsynaptic currents (EPSCs) were followed by an after-discharge of miniature excitatory postsynaptic currents (mEPSCs) lasting 1-2 s and generated by evoked asynchronous release of presynaptic quanta of transmitter. Like the EPSC of which it is thought to be an extension, the after-discharge was modulated by procedures expected to modulate Sr2+ influx into the nerve terminal. The number of mEPSCs in the after-discharge was decreased by increasing extracellular [Mg2+], and increased by increasing extracellular [Sr2+] or increasing the number of action potentials used to evoke the after-discharge. 3. EPSCs recorded in media containing either 1 mM Ca2+ or 6 mM Sr2+ were of similar amplitude. Adding Sr2+ to low-Ca2+ media increased EPSC amplitude, while adding Sr2+ to high-Ca2+ media lowered EPSC amplitude. These results suggest that extracellular Sr2+ is less effective than Ca2+ in supporting quantal release. 4. The levels of extracellular Ca2+, Mg2+ and Sr2+ were adjusted so that most after-discharge mEPSCs were discrete and comparable in numbers to the quantal events that contributed to the corresponding evoked EPSCs. In a series of twenty-five pairs of neurons, the mean amplitude of mEPSCs recorded at -80 mV was 35 +/- 10 pA and the mean coefficient of variation was 0.50 +/- 0.10 (range, 0.26-0.62). The mEPSC amplitude histogram was positively skewed. 5. In ten pairs of neurons, the mean and variance of EPSCs and mEPSCs and quantal content were determined from samples of more than 100 evoked events (in superfusion solutions containing (mM): 0.5 Ca2+, 2 Sr2+ and 10 Mg2+) and mean quantal content was determined from the ratio of amplitudes of the mean EPSC and mEPSC. A binomial quantal analysis produced values of 2-12 for Napp (apparent number of independent synapses) and 0.25-0.75 for Papp (apparent probability of releasing a quantum at one of those synapses). These parameters predicted the number of observed failures. The observed coefficient of variation for quantal content predicted the observed coefficient of variation of the EPSC amplitude when the coefficient of variability of quantal amplitude of after-discharge mEPSCs was taken into account. 6. In six pairs of neurons, where more than 250 evoked events were recorded, the observed amplitude histogram for EPSCs could be approximated by a predicted amplitude distribution generated from the estimated binomial parameters and an empirical function describing the amplitude distribution of after-discharge mEPSCs. 7. The observation that parameters derived from mEPSCs that contribute to the Sr(2+)-generated after-discharge can predict the shape of the EPSC amplitude distribution and a quantal content consistent with the observed failure rate and EPSC amplitude variance, suggests that this subset of mEPSCs has the same properties as the quantal events released around the time of the peak of the corresponding EPSCs. The use of Sr2+ to evoke after-discharges of mEPSCs should allow unambiguous determination of the extent to which modification of synaptic strength is pre- or postsynaptic.
摘要
  1. 采用培养的相邻小鼠海马神经元对的全细胞记录,研究动作电位诱发的兴奋性突触传递的量子特性,并证明 Sr2+ 在量化这些特性中的应用。2. 在细胞外 Sr2+ 存在的情况下,兴奋性突触后电流(EPSCs)之后会有持续 1 - 2 秒的微小兴奋性突触后电流(mEPSCs)的后放电,这是由突触前递质量子的诱发异步释放产生的。与被认为是其延伸的 EPSC 一样,后放电受到预期会调节 Sr2+ 流入神经末梢的程序的调制。增加细胞外 [Mg2+] 会减少后放电中 mEPSCs 的数量,增加细胞外 [Sr2+] 或增加用于诱发后放电的动作电位数量会增加其数量。3. 在含有 1 mM Ca2+ 或 6 mM Sr2+ 的培养基中记录的 EPSCs 幅度相似。向低 Ca2+ 培养基中添加 Sr2+ 会增加 EPSC 幅度,而向高 Ca2+ 培养基中添加 Sr2+ 会降低 EPSC 幅度。这些结果表明,细胞外 Sr2+ 在支持量子释放方面比 Ca2+ 效果更差。4. 调整细胞外 Ca2+、Mg2+ 和 Sr2+ 的水平,以使大多数后放电 mEPSCs 是离散的,并且数量与构成相应诱发 EPSCs 的量子事件相当。在一系列 25 对神经元中,在 -80 mV 记录的 mEPSCs 的平均幅度为 35 ± 10 pA,平均变异系数为 0.50 ± 0.10(范围为 0.26 - 0.6)。mEPSC 幅度直方图呈正偏态。5. 在 10 对神经元中,从超过 100 个诱发事件的样本(在含有(mM):0.5 Ca2+、2 Sr2+ 和 10 Mg2+ 的灌注溶液中)确定 EPSCs 和 mEPSCs 的平均值、方差以及量子含量,并根据平均 EPSC 和 mEPSC 的幅度比确定平均量子含量。二项式量子分析得出 Napp(表观独立突触数)的值为 2 - 12,Papp(在其中一个突触释放一个量子的表观概率)的值为 0.25 - 0.75。这些参数预测了观察到的失败次数。当考虑后放电 mEPSCs 的量子幅度变异系数时,观察到的量子含量变异系数预测了观察到的 EPSC 幅度变异系数。6. 在记录了超过 250 个诱发事件的 6 对神经元中,观察到的 EPSCs 的幅度直方图可以由根据估计的二项式参数和描述后放电 mEPSCs 幅度分布的经验函数生成的预测幅度分布近似。7. 从导致 Sr(2+) 产生后放电的 mEPSCs 得出的参数能够预测 EPSC 幅度分布的形状以及与观察到的失败率和 EPSC 幅度方差一致的量子含量,这一观察结果表明,该 mEPSCs 子集与相应 EPSCs 峰值附近释放的量子事件具有相同的特性。利用 Sr2+ 诱发 mEPSCs 的后放电应该能够明确确定突触强度改变是突触前还是突触后的程度。

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