Ishida A T, Neyton J
Proc Natl Acad Sci U S A. 1985 Mar;82(6):1837-41. doi: 10.1073/pnas.82.6.1837.
Currents elicited by L-glutamate and the related agonists quisqualate and kainate were analyzed under voltage clamp in isolated goldfish horizontal cells, using the whole-cell recording configuration of the patch-clamp method [Hamill, O.P., Marty, A., Neher, E., Sakmann, B. & Sigworth, F. J. (1981) Pflügers Arch. 391, 85-100]. These currents resulted from an increase in cationic conductance and were indistinguishable from one another in terms of reversal potential (approximately equal to 0 mV) and apparent elementary conductance (2-3 pS). The power-density spectra of the noise increases produced by each agonist were fit by the sum of two Lorentzian curves having similar cutoff frequencies (tau 1 approximately equal to 5 msec, tau 2 approximately equal to 1 msec), but the relative power of these components were different for quisqualate and glutamate than for kainate. Moreover, the responses to high doses of either quisqualate or glutamate rapidly faded, whereas the responses to kainate did not. Finally, quisqualate and glutamate produced an inhibition of responses to kainate which appeared to be uncompetitive. Kainate, quisqualate, and in our preparation, glutamate appear to activate channels different than those activated by N-methyl-D-aspartate in other preparations. At least some of the effects of quisqualate and glutamate appear to be mediated by receptors bound by kainate.
利用膜片钳技术的全细胞记录模式,在电压钳条件下分析了L-谷氨酸以及相关激动剂quisqualate和海人酸在离体金鱼水平细胞中引发的电流[哈米尔,O.P.,马蒂,A.,内尔,E.,萨克曼,B.和西格沃思,F.J.(1981年)《普弗吕格尔氏学报》391卷,85 - 100页]。这些电流是由阳离子电导增加引起的,就反转电位(约等于0 mV)和表观单通道电导(2 - 3 pS)而言,它们彼此无法区分。每种激动剂产生的噪声增加的功率密度谱由两条具有相似截止频率(τ1约等于5毫秒,τ2约等于1毫秒)的洛伦兹曲线之和拟合,但quisqualate和谷氨酸的这些成分的相对功率与海人酸不同。此外,对高剂量的quisqualate或谷氨酸的反应迅速消退,而对海人酸的反应则不然。最后,quisqualate和谷氨酸对海人酸的反应产生了抑制作用,这种抑制作用似乎是非竞争性的。在我们的实验准备中,quisqualate、谷氨酸和海人酸似乎激活了与其他实验准备中由N - 甲基 - D - 天冬氨酸激活的通道不同的通道。quisqualate和谷氨酸的至少一些作用似乎是由与海人酸结合的受体介导的。