Cerebral Small Vessel Disease: Targeting Oxidative Stress as a Novel Therapeutic Strategy?

被引:72
作者
De Silva, T. Michael [1 ]
Miller, Alyson A. [2 ]
机构
[1] Monash Univ, Biomed Discovery Inst, Dept Pharmacol, Melbourne, Vic 3004, Australia
[2] RMIT Univ, Sch Hlth & Biomed Sci, Cerebrovasc & Stroke Lab, Melbourne, Vic, Australia
来源
FRONTIERS IN PHARMACOLOGY | 2016年 / 7卷
基金
英国医学研究理事会;
关键词
cerebral small vessel disease; oxidative stress and redox regulation; NADPH oxidases (Noxs); brain injury; cognitive impairment; pharmacological strategies; BLOOD-BRAIN-BARRIER; NADPH-OXIDASE ACTIVITY; WHITE-MATTER LESIONS; OXYGEN SPECIES MEDIATE; IMPROVES CEREBROVASCULAR FUNCTION; ENDOTHELIUM-DEPENDENT RESPONSES; ENLARGED PERIVASCULAR SPACES; SMOOTH-MUSCLE-CELLS; ANGIOTENSIN-II; AMYLOID-ANGIOPATHY;
D O I
10.3389/fphar.2016.00061
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cerebral small vessel disease (SVD) is a major contributor to stroke, and a leading cause of cognitive impairment and dementia. Despite the devastating effects of cerebral SVD, the pathogenesis of cerebral SVD is still not completely understood. Moreover, there are no specific pharmacological strategies for its prevention or treatment. Cerebral SVD is characterized by marked functional and structural abnormalities of the cerebral microcirculation. The clinical manifestations of these pathological changes include lacunar infarcts, white matter hyperintensities, and cerebral microbleeds. The main purpose of this review is to discuss evidence implicating oxidative stress in the arteriopathy of both non-amyloid and amyloid (cerebral amyloid angiopathy) forms of cerebral SVD and its most important risk factors (hypertension and aging), as well as its contribution to cerebral SVD-related brain injury and cognitive impairment. We also highlight current evidence of the involvement of the NADPH oxidases in the development of oxidative stress, enzymes that are a major source of reactive oxygen species in the cerebral vasculature. Lastly, we discuss potential pharmacological strategies for oxidative stress in cerebral SVD, including some of the historical and emerging NADPH oxidase inhibitors.
引用
收藏
页数:18
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