首页> 外文OA文献 >Vascular risk factors and Alzheimer’s disease. Therapeutic approaches in mouse models
【2h】

Vascular risk factors and Alzheimer’s disease. Therapeutic approaches in mouse models

机译:血管危险因素和阿尔茨海默氏病。小鼠模型中的治疗方法

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

The first aim of this thesis was to elucidate the impact of major vascular risk factors like hypertension, apoE4 and stroke during the very early phase of Alzheimer’s disease (AD) using several mice models. Hypertension has proven to be associated with cerebrovascular impairment already at young age in AD model mice leading to reductions in structural and functional connectivity accompanied by an impaired cognition. Notably, aged AD mice developed an increased systolic blood pressure (SBP) concomitant with several AD-like pathological changes, like impairment in cerebral hemodynamics resulting in an impaired cognition, structural and functional connectivity, increased locomotor activity, and anxiety-related behavior without induced hypertension. Notably, also in aged transgenic apoE4 mice an impaired cerebrovascular circulation, reduced cortical post-synaptic density, lowered white and gray matter integrity in white matter tracts, and a lowered functional connectivity (FC) were detected. In conclusion, the (vascular) risk factors being present or induced in our mouse models have proven to be involved in the very early development of neurodegenerative processes in AD. Another aim of this thesis was to reveal the possible capacity of antihypertensives and specific multi-nutrient diets to serve as preventive or treatment against AD-like symptoms and vascular risk factors for AD. Furthermore, we showed that antihypertensives have beneficial effects on pathological processes of AD like counteracting the impaired cerebral blood flow, and the reduced structural and functional connectivity. Therefore, it is important to improve development of more effective tailor-made blood pressure-lowering treatments for AD patients and to increase awareness for hypertension as a risk factor for AD. Furthermore, we demonstrated the value of a multi-modal approach, including advanced MR neuroimaging tools, for detecting changes in brain structure and function with respect to dietary intervention. The investigated multicomponent diet showed several beneficial effects as preventive but also as therapeutic approach on pathological alterations in mouse models for (vascular) risk factors for AD. Future studies should therefore focus on optimization of multicomponent combinations comprising dietary components of the Mediterranean diet to improve clinical outcome after a stroke to lower the incidence of stroke accompanied by a reduction of the incidence of dementia. Therefore, future research should focus on preventive/ therapeutic approaches using personalized multinutrient dietary approaches targeting pathological processes of dementia. Future studies should evaluate a mixed preventive approach containing cognitive and physical exercise, in combination with a personalized multicomponent diet during the very early phases of AD.
机译:本文的首要目的是使用几种小鼠模型阐明阿尔茨海默氏病(AD)早期的主要血管危险因素(如高血压,apoE4和中风)的影响。高血压已被证明与AD模型小鼠年轻时的脑血管损害有关,导致结构和功能连接性降低,并伴有认知障碍。值得注意的是,老年AD小鼠的收缩压(SBP)升高,伴有多种AD样病理变化,例如脑血流动力学受损,导致认知,结构和功能连接性受损,运动能力增强以及与焦虑相关的行为而未引起高血压。值得注意的是,在衰老的转基因apoE4小鼠中,还检测到脑血管循环受损,皮质突触后密度降低,白质道中白质和灰质完整性降低以及功能连接性(FC)降低。总之,在我们的小鼠模型中存在或诱发的(血管)危险因素已被证明与AD神经退行性过程的早期发展有关。本论文的另一个目的是揭示抗高血压药和特定的多营养饮食可能作为预防或治疗AD样症状和AD血管危险因素的能力。此外,我们表明,降压药对AD的病理过程具有有益的作用,例如可以抵消受损的脑血流量以及减少的结构和功能连接性。因此,重要的是要改进针对AD患者的更有效的量身定制的降压治疗方法的开发,并提高对高血压作为AD危险因素的认识。此外,我们展示了一种包括先进的MR神经影像工具在内的多模式方法的价值,该方法可用于检测饮食干预方面的大脑结构和功能的变化。所研究的多成分饮食在预防(AD)(血管)危险因素的小鼠模型中显示出几种有益的作用,既可作为预防手段,也可作为治疗手段。因此,未来的研究应集中于优化包括地中海饮食中饮食成分的多成分组合,以改善中风后的临床结局,以降低中风的发生率并降低痴呆的发生率。因此,未来的研究应集中在针对痴呆症病理过程的个性化多种营养饮食方法的预防/治疗方法上。未来的研究应评估在AD的早期阶段就结合认知和体育锻炼以及个性化多成分饮食的混合预防方法。

著录项

  • 作者

    Wiesmann M.;

  • 作者单位
  • 年度 2017
  • 总页数
  • 原文格式 PDF
  • 正文语种
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利

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