Kraszewski K, Grantyn R
Department of Neurophysiology, Max Planck Institute for Psychiatry, Martinsried, F.R.G.
Neuroscience. 1992;47(3):555-70. doi: 10.1016/0306-4522(92)90165-x.
The aim of this study was to identify the conductance change induced by one quantum of gamma-aminobutyric acid from axonal release sites on cultured superior colliculus neurons. Unitary (single cell-activated) inhibitory postsynaptic currents and spontaneous synaptic activity were recorded with patch clamp techniques in the whole cell configuration while superfusing the entire neuron with normal saline. Miniature inhibitory postsynaptic currents were recorded in the presence of tetrodotoxin and in reduced [Ca2+]o/[Mg2+]o. In addition, the membrane area contributing to synaptic activity was limited to a narrow window of 50 microns. Smaller neurons were chosen for recording to render a standard deviation of the "instrumental" noise of less than 1.5 pA at a holding voltage of -80 mV. After two weeks in vitro, the percentage of synaptically connected tectal neurons exceeded 50%. At holding voltages of -80 mV (Cl- equilibrium potential -12 mV) minimal amplitudes of unitary inhibitory postsynaptic currents were as low as 7-10 pA, while maximal amplitudes exceeded 500 pA. The mean time to peak and time constant of decay were 3.0 and 34.4 ms, respectively (n = 31). Fluctuating unitary inhibitory postsynaptic currents were deemed to be compound postsynaptic responses. Multiple Gaussian equations could be fitted to the amplitude histograms of unitary postsynaptic currents. This procedure rendered a quantal size between 5.0 and 10.9 pA (mean 7.1 pA; S.D. 1.78 pA) in five neurons from mature cultures. The amplitudes of statistically determined quantal inhibitory postsynaptic currents were slightly smaller than the independent estimate from somatic miniature inhibitory postsynaptic currents. The latter had a mean amplitude of 9.1 pA (S.D. 3.3 pA, n = 23), a mean time to peak of 1.65 ms (n = 9), and a mean time constant of decay of 16.2 ms (n = 9). Single channel recording from outside-out patches showed three to four main conductance states ranging from 9 to 22 pS. Single channel closures at the 21-24 pS level were occasionally observed during relaxation of miniature currents. The small size of whole cell quantal inhibitory postsynaptic currents and somatic miniature currents indicates that one GABA quantum opened only 5-15 single Cl- channels.
本研究的目的是确定培养的上丘神经元轴突释放位点释放一个γ-氨基丁酸量子所引起的电导变化。采用膜片钳技术在全细胞模式下记录单位(单细胞激活)抑制性突触后电流和自发突触活动,同时用生理盐水灌注整个神经元。在存在河豚毒素和降低的细胞外钙浓度/细胞外镁浓度的情况下记录微小抑制性突触后电流。此外,参与突触活动的膜面积被限制在50微米的狭窄范围内。选择较小的神经元进行记录,以使在-80 mV的钳制电压下“仪器”噪声的标准差小于1.5 pA。体外培养两周后,突触连接的顶盖神经元百分比超过50%。在-80 mV的钳制电压(氯离子平衡电位为-12 mV)下,单位抑制性突触后电流的最小幅度低至7-10 pA,而最大幅度超过500 pA。平均峰值时间和衰减时间常数分别为3.0和34.4毫秒(n = 31)。波动的单位抑制性突触后电流被认为是复合突触后反应。多个高斯方程可拟合到单位突触后电流的幅度直方图。该程序在来自成熟培养物的五个神经元中得出量子大小在5.0至10.9 pA之间(平均7.1 pA;标准差1.78 pA)。统计学确定的量子抑制性突触后电流的幅度略小于来自体细胞微小抑制性突触后电流的独立估计值。后者的平均幅度为9.1 pA(标准差3.3 pA,n = 23),平均峰值时间为1.65毫秒(n = 9),平均衰减时间常数为16.2毫秒(n = 9)。从外向内膜片的单通道记录显示三到四个主要电导状态,范围从9到22 pS。在微小电流松弛期间偶尔观察到21-24 pS水平的单通道关闭。全细胞量子抑制性突触后电流和体细胞微小电流的小尺寸表明一个GABA量子仅打开5-15个单氯离子通道。