Arterial spin labeling demonstrates preserved regional cerebral blood flow in the P301L mouse model of tauopathy.

Diana Kindler, Cinzia Maschio, Ruiqing Ni, Valerio Zerbi, Daniel Razansky, Jan Klohs
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引用次数: 6

Abstract

There is growing evidence for the vascular contribution to cognitive impairment and dementia in Alzheimer's disease (AD) and other neurodegenerative diseases. While perfusion deficits have been observed in patients with Alzheimer's disease and tauopaties, little is known about the role of tau in vascular dysfunction. In the present study, regional cerebral blood (rCBF) was characterized in P301L mice with arterial spin labeling. No differences in rCBF in P301L mice compared to their age-matched non-transgenic littermates at mid (10-12 months of age) and advanced (19-21 months of age) disease stages. This was concomitant with preservation of cortical brain structure as assessed with structural T2-weighted magnetic resonance imaging. These results show that hypoperfusion and neurodegeneration are not a phenotype of P301L mice. More studies are thus needed to understand the relationship of tau, neurodegeneration and vascular dysfunction and its modulators in AD and primary tauopathies.

Abstract Image

Abstract Image

Abstract Image

动脉自旋标记显示P301L小鼠脑病模型中保留了局部脑血流。
越来越多的证据表明,在阿尔茨海默病(AD)和其他神经退行性疾病中,血管会导致认知障碍和痴呆。虽然在阿尔茨海默病和牛头手术患者中观察到灌注缺陷,但对tau蛋白在血管功能障碍中的作用知之甚少。在本研究中,用动脉自旋标记法对P301L小鼠的区域脑血(rCBF)进行了表征。在疾病中期(10-12月龄)和晚期(19-21月龄),P301L小鼠的rCBF与年龄匹配的非转基因幼崽相比没有差异。通过结构t2加权磁共振成像评估,这与大脑皮层结构的保存同时存在。这些结果表明,灌注不足和神经退行性变不是P301L小鼠的表型。因此,需要更多的研究来了解AD和原发性tau病变中tau、神经变性和血管功能障碍及其调节剂的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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