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Evaluation of an Aβ 1-40-induced cognitive deficit in rat using a reward-directed instrumental learning task

机译:使用奖励指导的仪器学习任务评估Aβ1-40诱导的大鼠认知功能障碍

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Alzheimer's disease (AD) is the most common form of dementia. It is a progressive neurodegenerative disorder that leads to gradual loss of cognitive and functional abilities, and development of behavioral disturbances. Previous studies using Aβ 1-40 microinjection in animal models focused on cognitive deficits in spatial learning and avoidance conditioning. However, no attempt has been made to determine the sensitivity of an Aβ 1-40-manipulated animal model in tasks involving reward-directed instrumental learning (RDIL). Thus, the present study was designed to investigate the effects of intra hippocampal microinjection of Aβ 1-40 on the acquisition and maintenance of a basic instrumental response (lever-pressing), then on the goal directed (higher response ratio) and habit (visual signal discrimination and extinction) learning, as well as on neurotransmitter changes which could potentially alter the regulatory processes involved in instrumental learning. Our present findings demonstrated that the focal hippocampal microinjection of Aβ 1-40 rendered rats unable to process new cue/contextual information in the formation of causal relation, rather than affecting the operant action itself. Although the injected Aβ 1-40 did not directly influence performance, it did prevent the information from being translated into action. Moreover, the neurotransmitter results indicated that multiple neural signaling might be involved in the regulation of RDIL in the Aβ 1-40 injection model. In conclusion, results suggested that our series of instrumental learning tasks may have potential in dementia research as a novel method for testing cognitive behavior.
机译:阿尔茨海默氏病(AD)是痴呆症的最常见形式。它是一种进行性神经退行性疾病,导致逐渐丧失认知和功能能力,并发展为行为障碍。先前在动物模型中使用Aβ1-40显微注射的研究集中在空间学习和回避调节方面的认知缺陷。但是,在涉及奖励导向的工具学习(RDIL)的任务中,尚未尝试确定Aβ1-40操纵的动物模型的敏感性。因此,本研究旨在研究海马显微注射Aβ1-40对获得和维持基本仪器反应(杠杆按压),然后针对目标(更高的反应率)和习惯(视觉)的影响。信号识别和灭绝)学习,以及神经递质的变化,这些变化可能会改变工具学习中涉及的调节过程。我们目前的发现表明,Aβ1-40的局灶性海马显微注射使大鼠无法处理因果关系中的新提示/上下文信息,而不影响操作本身。尽管注入的Aβ1-40不会直接影响性能,但确实可以防止信息转化为作用。此外,神经递质的结果表明在Aβ1-40注射模型中RDIL的调节可能涉及多个神经信号。总之,结果表明我们的一系列仪器学习任务可能作为一种测试认知行为的新方法,在痴呆研究中具有潜力。

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