Thomas T, Sutton E T, Bryant M W, Rhodin J A
Woodlands Medical and Research Center, Oldsmar, Fla. 34677, USA.
J Submicrosc Cytol Pathol. 1997 Jul;29(3):293-304.
beta-amyloid toxicity is central to the pathology of Alzheimer's disease. Recent evidence implicates vascular dysfunction as a contributing factor to the dementia of Alzheimer type. Using intravital microscopy we demonstrate that in vivo administration of beta-amyloid produces extensive vascular disruption including endothelial and smooth muscle damage, adhesion and migration of leukocytes across arteries and venules. Amyloid angiopathy with vascular damage and inflammatory changes are hallmarks in the brains of Alzheimer disease victims. The vascular actions of beta-amyloid are distinct from the neurotoxic properties of the peptide and were prevented by the free radical scavenging enzyme superoxide dismutase. Oxygen radical mediated vascular dysfunction may induce ischemic and inflammatory responses leading to neurodegeneration as seen in Alzheimer's disease.
β-淀粉样蛋白毒性是阿尔茨海默病病理学的核心。最近的证据表明血管功能障碍是阿尔茨海默型痴呆的一个促成因素。通过活体显微镜检查,我们证明在体内给予β-淀粉样蛋白会导致广泛的血管破坏,包括内皮细胞和平滑肌损伤、白细胞在动脉和小静脉中的黏附和迁移。伴有血管损伤和炎症变化的淀粉样血管病是阿尔茨海默病患者大脑的特征。β-淀粉样蛋白的血管作用不同于该肽的神经毒性特性,并且可被自由基清除酶超氧化物歧化酶所阻止。氧自由基介导的血管功能障碍可能会诱发缺血和炎症反应,从而导致如在阿尔茨海默病中所见的神经退行性变。