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Memory Effects of Benzodiazepines: Memory Stages and Types Versus Binding-Site Subtypes

机译:苯并二氮卓的记忆效应:记忆阶段和类型与绑定站点亚型

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Benzodiazepines are well established as inhibitory modulators of memory processing. This effect is especially prominent when applied before the acquisition phase of a memory task. This minireview concentrates on the putative subtype selectivity of the acquisition-impairing action of benzodiazepines. Namely, recent genetic studies and standard behavioral tests employing subtype-selective ligands pointed to the predominant involvement of two subtypes of benzodiazepine binding sites in memory modulation. Explicit memory learning seems to be affected through theGABAAreceptors containing theα1andα5subunits, whereas the effects on procedural memory can be mainly mediated by theα1subunit. The pervading involvement of theα1subunit in memory modulation is not at all unexpected because this subunit is the major subtype, present in 60% of allGABAAreceptors. On the other hand, the role ofα5subunits, mainly expressed in the hippocampus, in modulating distinct forms of memory gives promise of selective pharmacological coping with certain memory deficit states.
机译:苯并二氮卓在内存加工的抑制调节剂中得到了很好的建立。在存储器任务的采集阶段应用时,这种效果特别突出。该MILEVIEW精力集中在苯并二氮杂卓的采集损伤作用的推定亚型选择性。即,最近的遗传研究和使用亚型选择性配体的标准行为试验指向苯二氮卓在记忆调节中的两种亚颗粒的主要涉及。显式记忆学习似乎通过含有α1Andα5subunits的神悟遗传器来影响,而对程序记忆的影响可以主要由α1subunit介导。 α1subunit在记忆调节中的遗传涉及并不意外,因为这个亚基是主要的亚型,目前在60%的Allgabaereceptors。另一方面,α5subunits的作用主要在海马中调节不同形式的记忆形式,使得具有某些记忆缺陷状态的选择性药理学应对。

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