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首页> 外文期刊>Behavioural Brain Research: An International Journal >Episodic-like memory is sensitive to both Alzheimer's-like pathological accumulation and normal ageing processes in mice
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Episodic-like memory is sensitive to both Alzheimer's-like pathological accumulation and normal ageing processes in mice

机译:情景记忆对小鼠的阿尔茨海默氏样病理积累和正常衰老过程均敏感

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Episodic memory depends on the hippocampus and is sensitive to both Alzheimer's disease (AD) pathology and normal ageing. We showed previously that 3xTgAD mice express a specific, episodic-memory deficit at 6 months of age in the What-Where-Which occasion (WWWhich) task (Davis, Easton, Eacott and Gigg, 2013). This task requires the integration of object-location and contextual cues to form an episodic-like memory. Here, we explore the cumulative effect of AD pathology on WWWhich memory by testing very young and middle-aged mice (3 and 12 months old, respectively). For comparison, we included an alternative episodic-like task (What-Where-When; WWWhen) and an object temporal order (Recency) task to explore claims that WWWhen types of memory are open to non-episodic solutions.We found that in contrast to their performance at 6 months, 3-month-old 3xTgAD mice formed WWWhich episodic-like memories; however, their performance at this age was poorer than in matched controls. In contrast, 3xTgAD and control animals aged 12 months were both impaired on the WWWhich task. Finally, 3xTgAD mice with a WWWhich deficit were unimpaired in both Recency and WWWhen tasks.These results support conclusions that: (1) young 3xTgAD mice express episodic-like memory, albeit depressed relative to controls; (2) age-related changes result in a deficit on the hippocampal-dependent WWWhich episodic memory task; and (3) control and 3xTgAD mice can use recency (trace strength) rather than episodic-like memory for tasks that contain a temporal 'When' component. These results, in combination with our previous findings, support an age-related decline in WWWhich episodic-like memory in mice. Furthermore, this decline is accelerated in the 3xTgAD model.
机译:发作性记忆取决于海马,并且对阿尔茨海默氏病(AD)病理和正常衰老均敏感。先前我们已经证明3xTgAD小鼠在“在哪里”(WWWhich)场合(WWWhich)任务中,在6个月大时会表达一种特定的,发作性的记忆缺陷(Davis,Easton,Eacott和Gigg,2013)。此任务需要将对象位置和上下文提示进行整合以形成类似情节的记忆。在这里,我们通过测试非常年轻和中年的小鼠(分别为3个月和12个月大)来探索AD病理学对WWW记忆的累积作用。为了进行比较,我们包括了另一种类似情景的任务(What-Where-When; WWWhen)和一个对象时间顺序(Recency)任务,以探索有关WWWhen的内存类型对非周期性解决方案开放的主张。 3个月大的3xTgAD小鼠在6个月时的表现形成了WWW丰富的情节式记忆。但是,他们在这个年龄段的表现要比配对对照组差。相反,在WWWhich任务中,年龄为12个月的3xTgAD和对照动物均受损。最后,具有WWW高缺陷的3xTgAD小鼠在Recency和WWWhen任务中均未受损。这些结果支持以下结论:(1)年轻的3xTgAD小鼠表达发作性记忆,尽管相对于对照组而言情绪低落; (2)与年龄相关的变化导致依赖海马的WWW情景记忆任务缺乏; (3)对照组和3xTgAD小鼠可以使用新近度(痕迹强度)而不是像情节般的记忆来处理包含时间“时间”成分的任务。这些结果与我们先前的发现相结合,支持了小鼠中WWW发作性记忆的年龄相关性下降。此外,在3xTgAD模型中,这种下降加速了。

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