后藤- kakizaki大鼠模式分离改变

Chelsey C. Damphousse, Jaclyn K. Medeiros, Nicole E. Micks, Diano F. Marrone
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引用次数: 0

摘要

在过去的50年里,2型糖尿病的患病率稳步上升。与这种疾病相关的健康风险包括认知能力下降和患痴呆症的风险增加。为了进一步研究糖尿病和认知之间的联系,我们在Goto-Kakizaki (GK)大鼠(一种强大的糖尿病模型)中测试了记忆表现和海马功能。相对于年龄匹配的Wistar大鼠,GK大鼠在一项联合记忆任务中表现出损伤,该任务不仅需要根据物体的物理特征来区分物体,还需要根据最后一次见到物体的地点和时间来区分物体。伴随这些缺陷的是齿状回颗粒细胞中Egr1(一种对记忆至关重要的即时早期基因)表达模式的改变,这与导致海马表征不稳定的齿状回活性降低相一致。这些数据支持了糖尿病导致海马加速衰老的假说,并有助于将这种疾病与海马回路的变化联系起来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Altered pattern separation in Goto-Kakizaki rats

Altered pattern separation in Goto-Kakizaki rats

Type 2 diabetes mellitus has steadily increased in prevalence over the past five decades. Among the health risks associated with this disorder are cognitive decline and are increased risk of developing dementia. To further investigate the link between diabetes and cognition, here we test memory performance and hippocampal function in the Goto-Kakizaki (GK) rat, a robust model of diabetes. Relative to age-matched Wistar rats, GK rats show impairments in a conjunctive memory task that requires discriminating objects not only on the basis of their physical characteristics, but also on the basis of where and when they were last seen. Concomitant to these deficits are changes in the pattern of expression of Egr1 (an immediate-early gene critical for memory) in dentate gyrus granule cells, consistent with dentate hypoactivity leading to unstable hippocampal representations. These data support the hypothesis that diabetes confers a phenotype of accelerated senescence on the hippocampus, and help to link this disorder with changes in hippocampal circuits.

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