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亨廷顿病转基因大鼠模型的记忆缺陷。

Memory deficits in the transgenic rat model of Huntington's disease.

机构信息

Department of Neuroscience, Maastricht University, Maastricht, The Netherlands.

出版信息

Behav Brain Res. 2012 Feb 1;227(1):194-8. doi: 10.1016/j.bbr.2011.11.009. Epub 2011 Nov 15.

Abstract

Memory deficits are common in patients with Huntington's disease (HD) and have a substantial impact on the quality of life of patients and their relatives. A good model resembling the human memory deficits is needed for research purposes. In this study we investigated the memory function of the transgenic rat model of Huntington's disease (tgHD) in the object location (OLT) and the object recognition task (ORT). Several studies have shown that the recent developed tgHD rat model resembles the human phenotype of HD. Impairments of spatial and object recognition memory in the OLT and ORT, however, have to our knowledge not yet been reported in this transgenic model. Our findings show that in both early and late stages of the disease the tgHD rats have clear deficits for both visuospatial and visual object memory. Since HD patients are known to be impaired in both types of memory, these results confirm the validity of this tgHD rat as a model for the human HD phenotype.

摘要

记忆缺陷在亨廷顿病(HD)患者中很常见,对患者及其亲属的生活质量有重大影响。因此需要一种良好的模型来模拟人类的记忆缺陷。在这项研究中,我们在物体定位(OLT)和物体识别任务(ORT)中研究了亨廷顿病转基因大鼠模型(tgHD)的记忆功能。多项研究表明,最近开发的 tgHD 大鼠模型类似于人类 HD 的表型。然而,据我们所知,在这种转基因模型中尚未报道 OLT 和 ORT 的空间和物体识别记忆受损。我们的研究结果表明,在疾病的早期和晚期阶段,tgHD 大鼠在视空间和视觉物体记忆方面都存在明显缺陷。由于众所周知 HD 患者在这两种类型的记忆中都受到损害,因此这些结果证实了这种 tgHD 大鼠作为人类 HD 表型模型的有效性。

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