Isaacson J S, Nicoll R A
Physiology Graduate Program, University of California, San Francisco 94143-0450.
Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10936-40. doi: 10.1073/pnas.88.23.10936.
Aniracetam is a nootropic drug that has been shown to selectively enhance quisqualate receptor-mediated responses in Xenopus oocytes injected with brain mRNA and in hippocampal pyramidal cells [Ito, I., Tanabe, S., Kohda, A. & Sugiyama, H. (1990) J. Physiol. (London) 424, 533-544]. We have used patch clamp recording techniques in hippocampal slices to elucidate the mechanism for this selective action. We find that aniracetam enhances glutamate-evoked currents in whole-cell recordings and, in outside-out patches, strongly reduces glutamate receptor desensitization. In addition, aniracetam selectively prolongs the time course and increases the peak amplitude of fast synaptic currents. These findings indicate that aniracetam slows the kinetics of fast synaptic transmission and are consistent with the proposal [Trussell, L. O. & Fischbach, G. D. (1989) Neuron 3, 209-218; Tang, C.-M., Dichter, M. & Morad, M. (1989) Science 243, 1474-1477] that receptor desensitization governs the strength of fast excitatory synaptic transmission in the brain.
茴拉西坦是一种促智药,已被证明能选择性增强注射脑信使核糖核酸的非洲爪蟾卵母细胞和海马锥体细胞中由喹啉酸受体介导的反应[伊藤,I.,田边,S.,小田,A. & 杉山,H.(1990年)《生理学杂志》(伦敦)424,533 - 544]。我们利用海马切片中的膜片钳记录技术来阐明这种选择性作用的机制。我们发现,在全细胞记录中,茴拉西坦增强谷氨酸诱发的电流,而在外侧向外膜片中,茴拉西坦强烈减少谷氨酸受体脱敏。此外,茴拉西坦选择性地延长快速突触电流的时间进程并增加其峰值幅度。这些发现表明茴拉西坦减缓了快速突触传递的动力学,并且与以下观点一致[特拉塞尔,L. O. & 菲施巴赫,G. D.(1989年)《神经元》3,209 - 218;唐,C.-M.,迪希特,M. & 莫拉德,M.(1989年)《科学》243,1474 - 1477],即受体脱敏决定了大脑中快速兴奋性突触传递的强度。