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大鼠海马CA1区对河豚毒素敏感的钙传导通道

Tetrodotoxin-sensitive calcium-conducting channels in the rat hippocampal CA1 region.

作者信息

Akaike N, Takahashi K

机构信息

Department of Neurophysiology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

J Physiol. 1992 May;450:529-46. doi: 10.1113/jphysiol.1992.sp019141.

DOI:10.1113/jphysiol.1992.sp019141
PMID:1331428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1176136/
Abstract
  1. Tetrodotoxin (TTX)-sensitive Ca2+ conducting channels which produce a transient inward current were investigated in pyramidal neurones freshly dissociated from the dorsal part of rat hippocampal CA1 region by the use of the suction-pipette technique, which allows for intracellular perfusion under a single-electrode voltage clamp. 2. In all cells superfused with Na(+)- and K(+)-free external solution containing 10 mM-Ca2+ and 10(-5) M-La3+, a transient inward Ca2+ current was evoked by a step depolarization to potentials more positive than about -50 mV from a holding potential (VH) of -100 mV. This current was inhibited by either removing the extracellular Ca2+ or adding TTX (termed as 'TTX-ICa'). 3. Activation and inactivation processes of the TTX-ICa were highly potential dependent at 20-22 degrees C, and the latter was fitted by a double exponential function. The time to peak of the current decreased from 5.0 to 2.3 ms at a test potential change from -50 to 0 mV. The time constants of the current decay decreased from 2.8 to 2.2 ms for fast component (tau if) and from 16.0 to 8.2 ms for slow component (tau is) at a potential change from -35 to -10 mV. 4. The TTX-ICa was activated at threshold potential of about -55 mV and reached full activation at -30 mV. The steady-state inactivation of TTX-ICa could be fitted by a Boltzmann equation with a slope factor of 6.0 mV and a half-inactivation voltage of -72.5 mV. 5. Biphasic recovery (reactivation) from the complete inactivation of TTX-ICa was observed. The time constant of the major component (78.8 to 91.6% of total) of the reactivation was 13.1 ms, and that of the minor one was 120 to 240 ms. Therefore, TTX-ICa remained fairly constant at a train of stimulation up to 3 Hz. However, the inhibition of current amplitude occurred as the repetitive stimulation increased more than 10 Hz, and considerable tonic inhibition occurred with increasing stimulation frequency. 6. When the peak amplitudes in the individual current-voltage (I-V) relationships of TTX-ICa at various extracellular Ca2+ concentrations ([Ca2+]o) were plotted as a function of [Ca2+]o, the current amplitude increased linearly without showing any saturation. 7. The ratio of peak amplitude in the individual I-V relationships of Ca2+, Sr2+ and Ba2+ currents passing through the TTX-sensitive Ca2+ conducting channel was 1:0.33:0.05, although the current kinetics were much the same.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 运用吸液管技术,对从大鼠海马CA1区背侧新鲜分离的锥体神经元中产生瞬态内向电流的河豚毒素(TTX)敏感型Ca2+传导通道进行了研究,该技术可在单电极电压钳制下进行细胞内灌注。2. 在所有用含10 mM - Ca2+和10(-5) M - La3+的无Na+和无K+的细胞外溶液灌流的细胞中,从 - 100 mV的钳制电位(VH)进行阶跃去极化至比约 - 50 mV更正的电位时,可诱发瞬态内向Ca2+电流。去除细胞外Ca2+或添加TTX(称为“TTX - ICa”)均可抑制该电流。3. 在20 - 22℃时,TTX - ICa的激活和失活过程高度依赖电位,后者可用双指数函数拟合。在测试电位从 - 50 mV变为0 mV时,电流峰值时间从5.0 ms降至2.3 ms。在电位从 - 35 mV变为 - 10 mV时,电流衰减的快成分(tau if)时间常数从2.8 ms降至2.2 ms,慢成分(tau is)从16.0 ms降至8.2 ms。4. TTX - ICa在约 - 55 mV的阈值电位处被激活,在 - 30 mV时达到完全激活。TTX - ICa的稳态失活可用玻尔兹曼方程拟合,斜率因子为6.0 mV,半失活电压为 - 72.5 mV。5. 观察到TTX - ICa从完全失活的双相恢复(再激活)。再激活的主要成分(占总量的78.8%至91.6%)的时间常数为13.1 ms,次要成分的时间常数为120至240 ms。因此,在高达3 Hz的一串刺激下,TTX - ICa保持相当稳定。然而,当重复刺激增加超过10 Hz时,电流幅度出现抑制,且随着刺激频率增加出现相当大的强直抑制。6. 将TTX - ICa在不同细胞外Ca2+浓度([Ca2+]o)下的单个电流 - 电压(I - V)关系中的峰值幅度绘制为[Ca2+]o的函数时,电流幅度呈线性增加,未显示任何饱和。7. 通过TTX敏感型Ca2+传导通道的Ca2+、Sr2+和Ba2+电流的单个I - V关系中的峰值幅度之比为1:0.33:0.05,尽管电流动力学大致相同。(摘要截于400字)

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