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蛋白质合成对于由长期记忆再巩固破坏引发的失忆诱导是必要的。

[Protein synthesis is necessary for induction of amnesia, elicited by disruption of long-term memory reconsolidation].

作者信息

Solntseva S V, Nikitin V P

出版信息

Ross Fiziol Zh Im I M Sechenova. 2010 Mar;96(3):247-58.

Abstract

The NMDA glutamate receptor antagonists (MK-801 or APV) as well as protein synthesis inhibitors (cycloheximide or anisomycine) affect reactivation processes of long-term memory as studied in snail Helix lucorum with food aversion conditioning. It was found that, 24 hours after training, injection of each of the above mentioned substances initiated amnesia with duration more than 3 weeks. Repeated aversion conditioning with the same food (as at initial one) produced no memory restoration. However, amnesia was not observed in snails after simultaneous injection of protein synthesis inhibitor and NMDA glutamate receptor antagonists (MK-801 + cycloheximide or APV + anisomycin) before reminding procedure. In next experiments, cycloheximide was injected 3-9 hours after MK-801/reminding procedure. We have found development of incomplete amnesia in snails with cycloheximide injection 3 or 6 hours after MK-801/reminding procedure and, at repeated aversion conditioning with the same food, memory was quickly restored. Cycloheximide injection 9 hours after MK-801/reminding procedure led to development ofa steady-state amnesia with disruption of aversion conditioning with the same food as at repeated training. We suggest that mechanisms of "MK-801-induced amnesia" (as well as other mechanisms of long-term adaptive processes in the brain) depend on novel protein synthesis and become suppressed after inhibitors of protein synthesis application. "Time window" of amnesia induction process dependence on protein molecules synthesis remains during 6-9 hours after MK-801/reminding procedure.

摘要

在以食物厌恶条件反射对蜗牛Helix lucorum进行的研究中,N-甲基-D-天冬氨酸(NMDA)谷氨酸受体拮抗剂(MK-801或APV)以及蛋白质合成抑制剂(放线菌酮或茴香霉素)会影响长期记忆的重新激活过程。研究发现,在训练24小时后,注射上述任何一种物质都会引发持续超过3周的失忆。用相同食物(如初次训练时)进行重复厌恶条件反射并不能恢复记忆。然而,在提醒程序之前同时注射蛋白质合成抑制剂和NMDA谷氨酸受体拮抗剂(MK-801 + 放线菌酮或APV + 茴香霉素)后,蜗牛并未出现失忆现象。在接下来的实验中,在MK-801/提醒程序后3 - 9小时注射放线菌酮。我们发现,在MK-801/提醒程序后3或6小时注射放线菌酮的蜗牛会出现不完全失忆,并且在使用相同食物进行重复厌恶条件反射时,记忆会迅速恢复。在MK-801/提醒程序后9小时注射放线菌酮会导致出现稳定状态的失忆,且在重复训练时,对相同食物的厌恶条件反射会受到破坏。我们认为,“MK-801诱导的失忆”机制(以及大脑中其他长期适应性过程的机制)依赖于新的蛋白质合成,并且在应用蛋白质合成抑制剂后会受到抑制。在MK-801/提醒程序后6 - 9小时内,失忆诱导过程对蛋白质分子合成的“时间窗口”依然存在。

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