Buée L
INSERM U422, Lille, France.
Therapie. 1999 Jan-Feb;54(1):155-65.
Recent data suggest an increase in vascular pathology in ageing including changes in blood-brain barrier permeability and morphological changes in microvasculature. In the present study, cortical brain microvasculature was studied by immunohistochemistry using a monoclonal antibody against a vascular heparan sulfate proteoglycan. Vascular changes were consistently observed in ageing and included decrease in vascular density and presence of atrophic vessels. In Alzheimer's disease (AD), vascular changes were even more severe including presence of coiling vessels and glomerular loop formations. The laminar and regional distribution of these vascular alterations was correlated with the presence of neuropathological lesions (neurofibrillary tangles and amyloid deposits) suggesting a role of vascular changes in AD pathology. The degree of overlap between vascular and neurodegenerative disorders may be more substantial than previously thought. If vasculopathy in Alzheimer's disease is not directly involved in pathogenesis, it may act synergistically with other pathogenetic mechanisms including genetic and environmental factors. This aspect of pathology is particularly interesting in view of its accessibility to therapeutic interventions.
近期数据表明,衰老过程中血管病理学变化有所增加,包括血脑屏障通透性改变和微血管形态变化。在本研究中,采用针对血管硫酸乙酰肝素蛋白聚糖的单克隆抗体,通过免疫组织化学方法研究了大脑皮质微血管。在衰老过程中持续观察到血管变化,包括血管密度降低和萎缩血管的出现。在阿尔茨海默病(AD)中,血管变化更为严重,包括螺旋状血管和肾小球样环形成。这些血管改变的层状和区域分布与神经病理病变(神经原纤维缠结和淀粉样沉积物)的存在相关,提示血管变化在AD病理学中发挥作用。血管疾病和神经退行性疾病之间的重叠程度可能比之前认为的更为显著。如果阿尔茨海默病中的血管病变不直接参与发病机制,它可能与包括遗传和环境因素在内的其他致病机制协同作用。鉴于其对治疗干预的可及性,病理学的这一方面尤其引人关注。