Wu L G, Saggau P
Division of Neuroscience, Baylor College of Medicine, Houston, Texas 77030.
J Neurosci. 1994 Sep;14(9):5613-22. doi: 10.1523/JNEUROSCI.14-09-05613.1994.
The effects of voltage-dependent Ca channel (VDCC) antagonists on synaptic transmission were investigated at CA3-CA1 synapses of guinea pig hippocampal slices. After selectively loading presynaptic structures in area CA1 with the calcium indicator fura-2, we simultaneously recorded a presynaptic calcium transient ([Ca]t) and the corresponding field excitatory postsynaptic potential (fEPSP) evoked by a single stimulus given to the Schaffer collateral-commissural (SCC) pathway. Application of nifedipine did not reduce either the [Ca]t of the fEPSP, suggesting that nifedipine-sensitive Ca channels do not significantly contribute to evoked synaptic transmission at low stimulation frequency. Application of omega-conotoxin GVIA (omega-CgTX) or omega-agatoxin-IVA (omega-Aga-IVA) dose-dependently blocked both the [Ca]t and the fEPSP. The time course of the block of the [Ca]t was similar to that of the fEPSP. About 40% of the total [Ca]t was omega-CgTX sensitive, and more than 20% was omega-Aga-IVA sensitive. Combined application of these two blockers showed no overlap of the omega-CgTX-sensitive with the omega-Aga-IVA-sensitive [Ca]t. These results suggest that there are at least two types of presynaptic VDCCs at CA3-CA1 synapses of the hippocampus: omega-CgTX-sensitive and omega-Aga-IVA-sensitive Ca channels. Our results also suggest that these two types of Ca channels are colocalized at a single presynaptic terminal. During application of omega-CgTX or omega-Aga-IVA, the initial slope of the fEPSP varied approximately as the fourth power of the amplitude of the [Ca]t, suggesting that omega-CgTX-sensitive and omega-Aga-IVA-sensitive Ca channels have about equal efficacy in triggering transmitter release. These results in combination with similar findings at the squid giant synapse suggest that the nonlinear relationship between transmitter release and the Ca influx is well conserved from the molluscan to the mammalian nervous system.
在豚鼠海马切片的CA3-CA1突触处研究了电压依赖性钙通道(VDCC)拮抗剂对突触传递的影响。在用钙指示剂fura-2选择性加载CA1区的突触前结构后,我们同时记录了突触前钙瞬变([Ca]t)以及给予海马联合纤维-连合纤维(SCC)通路单个刺激所诱发的相应场兴奋性突触后电位(fEPSP)。硝苯地平的应用并未降低fEPSP的[Ca]t,这表明对硝苯地平敏感的钙通道在低刺激频率下对诱发的突触传递没有显著贡献。ω-芋螺毒素GVIA(ω-CgTX)或ω-阿加毒素-IVA(ω-Aga-IVA)的应用剂量依赖性地阻断了[Ca]t和fEPSP。[Ca]t阻断的时间进程与fEPSP相似。约40%的总[Ca]t对ω-CgTX敏感,超过20%对ω-Aga-IVA敏感。这两种阻断剂的联合应用表明ω-CgTX敏感的[Ca]t与ω-Aga-IVA敏感的[Ca]t没有重叠。这些结果表明,海马CA3-CA1突触处至少存在两种类型的突触前VDCC:对ω-CgTX敏感和对ω-Aga-IVA敏感的钙通道。我们的结果还表明,这两种类型的钙通道共定位于单个突触前终末。在应用ω-CgTX或ω-Aga-IVA期间,fEPSP 的初始斜率大约随[Ca]t振幅的四次方变化,这表明对ω-CgTX敏感和对ω-Aga-IVA敏感的钙通道在触发递质释放方面具有大致相同的效能。这些结果与在枪乌贼巨大突触处的类似发现相结合,表明从软体动物到哺乳动物神经系统,递质释放与钙内流之间的非线性关系得到了很好的保留。