Charlton M P, Augustine G J
Department of Physiology, University of Toronto, Ont., Canada.
J Neurosci Methods. 1988 Jan;22(3):195-202. doi: 10.1016/0165-0270(88)90040-4.
In voltage clamp experiments at the squid giant synapse anisopotentiality of the presynaptic terminal can distort measurements of synaptic transfer. Local compression of the presynaptic cell, at the point where the terminal joins its axon, appears to reduce this problem by electrically isolating the terminal from the axon. Because compression reduced anisopotentiality in the presynaptic terminal and altered the apparent voltage dependency of transmitter release, this procedure may be a simple way to improve voltage clamp control in this and other long cells. Compression of the presynaptic cell also reduced the diffusion of injected molecules out of the terminal region. This increased the effective concentration of given quantities of tetraethylammonium and Fast green injected into the presynaptic terminal. Thus, compression should also facilitate experiments in which molecules are microinjected into this and other cells because the effective volume of the cell is reduced and less of the injected substance will be required.
在枪乌贼巨大突触的电压钳实验中,突触前终末的各向异性电位会使突触传递的测量结果失真。在突触前终末与其轴突相连处对突触前细胞进行局部挤压,似乎可以通过将终末与轴突进行电隔离来减少这个问题。由于挤压降低了突触前终末的各向异性电位,并改变了递质释放的表观电压依赖性,所以这个方法可能是改善该细胞及其他长细胞电压钳控制的一种简单方式。对突触前细胞的挤压还减少了注入分子从终末区域的扩散。这增加了注入到突触前终末的一定量四乙铵和固绿的有效浓度。因此,挤压也应该便于在将分子显微注射到该细胞及其他细胞中的实验,因为细胞的有效体积减小了,所需的注入物质也会更少。