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甘氨酸拮抗剂可阻断大鼠海马切片CA1区的长时程增强的诱导。

Glycine antagonists block the induction of long-term potentiation in CA1 of rat hippocampal slices.

作者信息

Izumi Y, Clifford D B, Zorumski C F

机构信息

Department of Psychiatry, Washington University School of Medicine, St. Louis, MO 63110.

出版信息

Neurosci Lett. 1990 May 4;112(2-3):251-6. doi: 10.1016/0304-3940(90)90212-r.

Abstract

The effects of the strychnine-insensitive glycine receptor antagonists, cycloleucine and 7-chlorokynurenic acid, on the induction of long-term potentiation (LTP) in CA1 of rat hippocampal slices were examined. A 5 min administration of cycloleucine (20-100 microM) or 7-chlorokynurenic acid (1-5 microM) during the delivery of high-frequency stimulation blocked the induction of LTP without affecting baseline synaptic transmission. Coapplication of 100 microM glycine with cycloleucine or 7-chlorokynurenic acid masked the inhibitory effect on the induction of LTP, supporting the hypothesis that these compounds act as glycine antagonists. These results indicate that glycine is a necessary factor for the induction of LTP in CA1 of the rat hippocampus.

摘要

研究了士的宁不敏感的甘氨酸受体拮抗剂环亮氨酸和7-氯犬尿氨酸对大鼠海马切片CA1区长期增强(LTP)诱导的影响。在高频刺激传递期间给予5分钟的环亮氨酸(20 - 100微摩尔)或7-氯犬尿氨酸(1 - 5微摩尔)可阻断LTP的诱导,而不影响基线突触传递。将100微摩尔甘氨酸与环亮氨酸或7-氯犬尿氨酸共同应用可掩盖对LTP诱导的抑制作用,支持这些化合物作为甘氨酸拮抗剂起作用的假说。这些结果表明甘氨酸是大鼠海马CA1区LTP诱导的必要因素。

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