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安帕金CX516对大鼠短期记忆的促进作用:增强延迟非匹配样本任务表现。

Facilitative effects of the ampakine CX516 on short-term memory in rats: enhancement of delayed-nonmatch-to-sample performance.

作者信息

Hampson R E, Rogers G, Lynch G, Deadwyler S A

机构信息

Department of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston Salem, North Carolina 27157, USA.

出版信息

J Neurosci. 1998 Apr 1;18(7):2740-7. doi: 10.1523/JNEUROSCI.18-07-02740.1998.

Abstract

Ampakines are a family of drugs that selectively increase AMPA receptor-gated currents and improve performance on several behavioral tasks. This report describes evidence that ampakines cause a cumulative enhancement of performance in a spatial short-term memory task (Deadwyler et al., 1996). Two groups of rats were trained on a spatial variant of the delayed-nonmatch-to-sample (DNMS) paradigm. One group (n = 12) received the ampakine CX516 (Cortex Pharmaceuticals) alternated with vehicle for 17 consecutive days and then only vehicle for an additional 7 d. The second group (n = 6) received only vehicle injections over the same number of days. CX516 improved performance within sessions, particularly on trials with delays of 6-35 sec. In 9 of 12 rats, the positive effect of the drug was also present on nondrug days between CX516 administration and after cessation of CX516 injections. The animals that received only vehicle injections showed no improvement in DNMS performance over the entire 32 d of testing. Three of the 12 animals given CX516 did not exhibit "carryover" effects of the drug to the intervening (vehicle only) test sessions, but nonetheless exhibited superior performance during the first half of the session on days in which the ampakine was administered. Evaluation of errors suggests that the ampakine eliminated the necessity for a shift in response strategy that produced proactive interference on the following trial. Hippocampal involvement in these ampakine effects is discussed as a prelude to the second article in the series (Hampson et al., 1998).

摘要

安帕金是一类药物,可选择性增加AMPA受体门控电流,并改善多项行为任务的表现。本报告描述了安帕金在空间短期记忆任务中导致表现累积增强的证据(Deadwyler等人,1996年)。两组大鼠在延迟非匹配样本(DNMS)范式的空间变体上接受训练。一组(n = 12)连续17天交替接受安帕金CX516(Cortex制药公司)和赋形剂,然后在接下来的7天仅接受赋形剂。第二组(n = 6)在相同天数内仅接受赋形剂注射。CX516在实验过程中改善了表现,特别是在延迟6 - 35秒的试验中。在12只大鼠中的9只中,药物的积极作用在CX516给药期间和CX516注射停止后的非给药日也存在。仅接受赋形剂注射的动物在整个32天的测试中DNMS表现没有改善。接受CX516的12只动物中有3只在干预(仅赋形剂)测试期间没有表现出药物的“残留”效应,但在给予安帕金的日子里,在上半场仍表现出优异的表现。对错误的评估表明,安帕金消除了在后续试验中产生前摄干扰的反应策略转变的必要性。作为该系列第二篇文章(Hampson等人,1998年)的前奏,讨论了海马体在这些安帕金效应中的作用。

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