Aging and the neurovascular unit

被引:25
作者
del Zoppo, Gregory J. [1 ]
机构
[1] Univ Washington, Sch Med, Harborview Med Ctr, Dept Neurol,Dept Med,Div Hematol, Seattle, WA 98104 USA
来源
THROMBOLYSIS AND ACUTE STROKE TREATMENT: PREPARING FOR THE NEXT DECADE | 2012年 / 1268卷
关键词
aging; amyloid deposition; ischemic stroke; microvessels; permeability barriers; neurovascular unit; FOCAL CEREBRAL-ISCHEMIA; PROTEIN; 18; KDA; HEMORRHAGIC TRANSFORMATION; MATRIX METALLOPROTEINASES; INTRACEREBRAL HEMORRHAGE; EXTRACELLULAR-MATRIX; AMYLOID ANGIOPATHY; ALZHEIMERS-DISEASE; ENDOTHELIAL-CELL; BRAIN ISCHEMIA;
D O I
10.1111/j.1749-6632.2012.06686.x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
With the demonstration that acute recanalization of obstructed symptomatic cerebral arteries during ischemic stroke can result in substantial improvement in clinical outcome, the variability in clinical responses, and in hemorrhagic transformation, requires attention. This short review addresses the effect of aging and amyloid deposition disease on microvessel integrity, interactions within the neurovascular unit, cerebral tissue susceptibility to ischemic injury, and postischemic inflammation, and ultimately on the outcomes and safety of acute recanalization during ischemic stroke. Microvessels and neighboring neurons respond simultaneously to focal ischemia. The cellular components and matrix barriers of the neurovascular unit all respond to ischemia; however, their coordinate interactions are not understood. Furthermore, there is little known about the cell-cell and cell-matrix interactions within the unit, or about the effect of beta-amyloid on microvessel responses during ischemia. These considerations indicate the need for a coordinated research effort to understand the origins of the variability in recanalization outcome.
引用
收藏
页码:127 / 133
页数:7
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