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SJLB 小鼠发生 tauopathy 诱导的帕金森病。

SJLB mice develop tauopathy-induced parkinsonism.

机构信息

Department of Pharmaceutical Health Care, Faculty of Pharmaceutical Sciences, Himeji Dokkyo University, 7-2-1 Kamiohno, Himeji, Hyogo 670-8524, Japan.

出版信息

Neurosci Lett. 2010 Apr 12;473(3):182-5. doi: 10.1016/j.neulet.2010.02.032. Epub 2010 Feb 21.

Abstract

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) is an inherited dementia caused by tauopathy. Recently, we established the N279K mutant human tau transgenic mice SJLB. Although SJLB mice show cognitive dysfunction with insoluble tau in the brain, it has remained unclear whether they show signs of parkinsonism. To clarify this issue, we studied whether SJLB mice in fact develop parkinsonism. Behavioral analysis showed shorter stride length than that of non-transgenic control mice in the footprint test and movement disorder in the pole test, thus mimicking some features of human parkinsonism. We also found that these symptoms were not affected by dopamine treatment. These results indicate that SJLB mice show signs of parkinsonism and they could be of usefulness not only for studies of dementing disease but also of parkinsonism induced by tauopathy.

摘要

与染色体 17 相关的额颞叶痴呆和帕金森病(FTDP-17)是一种由 tau 病引起的遗传性痴呆症。最近,我们建立了 N279K 突变人类 tau 转基因小鼠 SJLB。尽管 SJLB 小鼠在大脑中显示出不溶性 tau 引起的认知功能障碍,但仍不清楚它们是否表现出帕金森病的迹象。为了阐明这一问题,我们研究了 SJLB 小鼠是否实际上患有帕金森病。行为分析显示,足迹测试中的步幅长度短于非转基因对照小鼠,杆测试中的运动障碍,从而模拟了一些人类帕金森病的特征。我们还发现,这些症状不受多巴胺治疗的影响。这些结果表明 SJLB 小鼠表现出帕金森病的迹象,它们不仅对痴呆症的研究有用,而且对 tau 病引起的帕金森病也有用。

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