...
首页> 外文期刊>NMR in biomedicine >Longitudinal assessment of cerebral perfusion and vascular response to hypoventilation in a bigenic mouse model of Alzheimer's disease with amyloid and tau pathology
【24h】

Longitudinal assessment of cerebral perfusion and vascular response to hypoventilation in a bigenic mouse model of Alzheimer's disease with amyloid and tau pathology

机译:含有淀粉样蛋白和TAU病理学的阿尔茨海默病患中血管灌注和血管反应对血管反应的纵向评估

获取原文
获取原文并翻译 | 示例
           

摘要

Alzheimer's disease is the most common neurodegenerative disease, and many patients also present with vascular dysfunction. In this study, we aimed to assess cerebral blood flow (CBF) and cerebrovascular response (CVR) as early, pre-symptomatic (3 months of age), imaging markers in a bigenic model of Alzheimer's disease (APP.V717IxTau.P301L, biAT) and in the monogenic parental strains. We further developed our previously published combination of pulsed arterial spin labeling perfusion MRI and hypo-ventilation paradigm, which allows weaning of the mice from the ventilator. Furthermore, the commonly used isoflurane anesthesia induces vasodilation and is thereby inherently a vascular challenge. We therefore assessed perfusion differences in the mouse models under free-breathing isoflurane conditions. We report (i) that we can determine CBF and hypoventilation-based CVR under ketamine/midazolam anesthesia and wean mice from the ventilator, making it a valuable tool for assessment of CBF and CVR in mice, (ii) that biAT mice exhibit lower cortical CBF than wild-type mice at age 3 months, (iii) that CVR was increased in both biAT and APP.V717I mice but not in Tau.P301L mice, identifying the APP genotype as a strong influencer of brain CVR and (iv) that perfusion differences at baseline are masked by the widely used isoflurane anesthesia.
机译:阿尔茨海默病是最常见的神经退行性疾病,许多患者也存在血管功能障碍。在这项研究中,我们旨在评估脑血流量(CBF)和脑血管反应(CVR),早期症状(年龄3个月),在Alzheimer疾病的增长模型中进行成像标记(App.v717xtau.p301L,Biat )和在单一的亲本菌株中。我们进一步开发了先前公布的脉冲动脉旋转标记灌注MRI和逆向通风范例的组合,这允许从呼吸机断开小鼠。此外,常用的异氟醚麻醉诱导血管沉积,从而固有地是血管攻击。因此,我们在自由呼吸异氟醚条件下评估小鼠模型中的灌注差异。我们报告(i)我们可以从呼吸机中测定基于氯胺酮/咪达唑仑麻醉和干扰小鼠的基于CBF和呼吸悬浮岩的CVR,使其成为评估小鼠中CBF和CVR的有价值的工具,(ii)BIAT小鼠表现出低层皮质CBF比野生型小鼠在3个月,(iii)中,CVR在BIAT和APP.V717I小鼠中增加,但不在TAU.P301L小鼠中增加,鉴定APP基因型作为脑CVR和(iv)的强烈影响者基线的灌注差异被广泛使用的异氟烷麻醉掩盖。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号