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记忆与失忆的行为模型。

Behavioral models of memory and amnesia.

作者信息

Slangen J L, Earley B, Jaffard R, Richelle M, Olton D S

机构信息

Psychofysiologie, CA Utrecht, The Netherlands.

出版信息

Pharmacopsychiatry. 1990 Feb;23 Suppl 2:81-3; discussion 84. doi: 10.1055/s-2007-1014539.

Abstract

In modelling memory and amnesia, the different forms of cognition must be distinguished. For memory, distinctions between acquisition, storage, and retrieval must be made and the different kinds of memory (e.g., immediate, working, reference) identified. Other notions, such as attention, orientation, and vigilance also belong under the heading "cognition". Thus the term "cognition enhancer" is imprecise because it does not indicate which kind of cognition is to be enhanced. Animal models should be developed for each type of cognition, be based on information from the clinic, and attempt to be specific. Examples of models more specific than the passive avoidance test were discussed and included the radial maze, in which different kinds of memory could be analyzed and correlated with, for example, changes in central cholinergic activity. From the point of view of drug development an important distinction was made between "empirical" and "simulation" models. In other areas of psychopharmacology "empirical" models have been widely used because they show predictable responses to known reference compounds. In the field of cognition there are no generally recognized reference compounds and therefore no "empirical" models. There is therefore a need for "simulation" models which imitate the various aspects of cognition and its pathology. The major criterion for validating this kind of model is that it should show changes similar to those observed in humans either resulting from a particular pathology or from a particular drug treatment.

摘要

在对记忆和失忆进行建模时,必须区分不同形式的认知。对于记忆,必须区分获取、存储和检索,并识别不同类型的记忆(例如,即时记忆、工作记忆、参考记忆)。其他概念,如注意力、定向和警觉性也属于“认知”范畴。因此,“认知增强剂”这个术语不准确,因为它没有表明要增强哪种认知。应该为每种认知类型开发动物模型,以临床信息为基础,并力求具有特异性。文中讨论了比被动回避试验更具特异性的模型实例,包括放射状迷宫,在该模型中可以分析不同类型的记忆,并将其与例如中枢胆碱能活性的变化相关联。从药物开发的角度来看,“经验性”模型和“模拟性”模型之间存在重要区别。在精神药理学的其他领域,“经验性”模型已被广泛使用,因为它们对已知参考化合物显示出可预测的反应。在认知领域,没有普遍认可的参考化合物,因此也没有“经验性”模型。因此,需要“模拟性”模型来模仿认知及其病理学的各个方面。验证这类模型的主要标准是,它应该显示出与人类因特定病理学或特定药物治疗而观察到的变化相似的变化。

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