Llinás R, Joyner R W, Nicholson C
J Gen Physiol. 1974 Nov;64(5):519-35. doi: 10.1085/jgp.64.5.519.
The reversal potential for the EPSP in the squid giant synapse has been studied by means of an intracellular, double oil gap technique. This method allows the electrical isolation of a portion of the axon from the rest of the fiber and generates a quasi-isopotential segment. In order to make the input resistance of this nerve segment as constant as possible, the electroresponsive properties of the nerve membrane were blocked by intracellular injection of tetraethylammonium (TEA) and local extracellular application of tetrodotoxin (TTX). Thus, EPSP's could be evoked in the isolated segment with a minimal amount of electroresponsive properties. The reversal potential for the EPSP (EEPSP) was measured by recording the synaptic potential or the synaptic current during voltage clamping. The results indicate that EEPSP may vary from +15 to +25 mV, which is more positive than would be expected for a 1:1 conductance change for Na(+) and K(+) (approximately -15 mV) and too negative for a pure Na(+) conductance ((+)40 mV). This latter value (E(Na)) was directly determined in the voltage clamp experiments. The results suggest that the synaptic potential is probably produced by a permeability change to Na(+) to K(+) in a 4:1 ratio. No change in time-course was observed in the synaptic current at clamp levels of -100 and +90 mV. The implications of a variable ratio for Na(+)-K(+) permeability in subsynaptic-postsynaptic membranes are discussed.
利用细胞内双油隙技术研究了枪乌贼巨大突触中兴奋性突触后电位(EPSP)的反转电位。该方法可将轴突的一部分与纤维其余部分进行电隔离,并产生一个准等电位段。为了使该神经段的输入电阻尽可能恒定,通过细胞内注射四乙铵(TEA)和局部细胞外应用河豚毒素(TTX)来阻断神经膜的电反应特性。因此,可在具有最小电反应特性的分离段诱发EPSP。通过在电压钳制期间记录突触电位或突触电流来测量EPSP的反转电位(EEPSP)。结果表明,EEPSP可能在+15至+25 mV之间变化,这比Na(+)和K(+) 1:1电导变化预期的值(约 -15 mV)更正,而对于纯Na(+)电导((+)40 mV)又太负。后一个值(E(Na))在电压钳制实验中直接测定。结果表明,突触电位可能是由Na(+)与K(+)以4:1的比例发生通透性变化产生的。在钳制水平为 -100和 +90 mV时,突触电流的时程未观察到变化。讨论了突触后膜中Na(+)-K(+)通透性可变比例的意义。