High Systolic Blood Pressure Induces Cerebral Microvascular Endothelial Dysfunction, Neurovascular Unit Damage, and Cognitive Decline in Mice

Author:

de Montgolfier Olivia12,Pinçon Anthony12,Pouliot Philippe3,Gillis Marc-Antoine2,Bishop Jonathan4,Sled John G.45,Villeneuve Louis2,Ferland Guylaine62,Lévy Bernard I.7,Lesage Frédéric23,Thorin-Trescases Nathalie2,Thorin Éric82

Affiliation:

1. From the Department of Pharmacology and Physiology (O.d.M., A.P.), Université de Montréal, Quebec, Canada

2. Montreal Heart Institute, Research Center, Quebec, Canada (O.d.M., A.P., M.-A.G., L.V., G.F., F.L., N.T.-T., E.T.)

3. Ecole Polytechnique de Montréal, Quebec, Canada (P.P., F.L.)

4. Mouse Imaging Centre, The Hospital for Sick Children, Toronto, Ontario, Canada (J.B., J.G.S.)

5. Department of Medical Biophysics, University of Toronto, Ontario, Canada (J.G.S.)

6. Department of Nutrition (G.F.), Université de Montréal, Quebec, Canada

7. Institut des Vaisseaux et du Sang, Hôpital Lariboisière, Paris, France (B.I.L.).

8. Department of Surgery (E.T.), Université de Montréal, Quebec, Canada

Abstract

A chronic and gradual increase in pulse pressure (PP) is associated with cognitive decline and dementia in older individuals, but the mechanisms remain ill-defined. We hypothesized that a chronic elevation of PP would cause brain microvascular endothelial mechanical stress, damage the neurovascular unit, and ultimately induce cognitive impairment in mice, potentially contributing to the progression of vascular dementia and Alzheimer disease. To test our hypothesis, male control wild-type mice and Alzheimer disease model APP/PS1 (amyloid precursor protein/presenilin 1) mice were exposed to a transverse aortic constriction for 6 weeks, creating a PP overload in the right carotid (ipsilateral). We show that the transverse aortic constriction procedure associated with high PP induces a cascade of vascular damages in the ipsilateral parenchymal microcirculation: in wild-type mice, it impairs endothelial dilatory and blood brain barrier functions and causes microbleeds, a reduction in microvascular density, microvascular cell death by apoptosis, leading to severe hypoperfusion and parenchymal cell senescence. These damages were associated with brain inflammation and a significant reduction in learning and spatial memories. In APP/PS1 mice, that endogenously display severe cerebral vascular dysfunctions, microbleeds, parenchymal inflammation and cognitive dysfunction, transverse aortic constriction–induced high PP further aggravates cerebrovascular damage, Aβ (beta-amyloid) accumulation, and prevents learning. Our study, therefore, demonstrates that brain microvessels are vulnerable to a high PP and mechanical stress associated with transverse aortic constriction, promoting severe vascular dysfunction, disruption of the neurovascular unit, and cognitive decline. Hence, chronic elevated amplitude of the PP could contribute to the development and progression of vascular dementia including Alzheimer disease.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3