Kalaria R N
Department of Neurology, Case Western Reserve University School of Medicine (BRB5), Cleveland, OH 44106, USA.
Pharmacol Ther. 1996;72(3):193-214. doi: 10.1016/s0163-7258(96)00116-7.
The integrity of the cerebral vasculature is crucial to the maintenance of cognitive functions during ageing. Prevailing evidence suggests that cerebrovascular functions decline during normal ageing, with pronounced effects in Alzheimer's disease (AD). The causes of these changes largely remain unknown. While previous studies recorded ageing-related impairments, such as atherosclerosis and loss of innervation in basal surface arteries of the brain, it only recently has been realized that a number of subtle alterations in both the intracranial resistance vessels and the smaller capillaries is apparent in both ageing animals and humans. The dominant changes include alterations in composition of connective tissues and smooth muscle of large vessel walls, thickening of the vascular basement membrane, thinning of the endothelium in some species, loss of endothelial mitochondria and increased pericytes. Some of these attributes appear more affected in AD. Other abnormalities entail profound irregularities in the course of microvessels, unexplained inclusions in the basement membrane and changes in unique proteins and membrane lipids associated with the blood-brain barrier. Brain imaging and permeability studies show no clear functional evidence to support the structural and biochemical anomalies, but it is plausible that focal and transient breach of the blood-brain barrier in ageing, and more notably in AD, occurs. Thus, circumscribed neuronal populations in certain brain regions could become vulnerable. Furthermore, the characteristic deposition of amyloid in vessels in AD may exacerbate the decline in vascular function and promote chronic hypoperfusion. Although not explicit from current studies, it is likely that the brain vasculature is continually modified by growth and repair mechanisms in attempts to maintain perfusion during ageing and disease.
脑血管系统的完整性对于衰老过程中认知功能的维持至关重要。现有证据表明,在正常衰老过程中脑血管功能会下降,在阿尔茨海默病(AD)中影响更为显著。这些变化的原因很大程度上仍然未知。虽然先前的研究记录了与衰老相关的损伤,如动脉粥样硬化和脑基底表面动脉神经支配的丧失,但直到最近才意识到,在衰老动物和人类中,颅内阻力血管和较小的毛细血管都出现了一些细微的变化。主要变化包括大血管壁结缔组织和平滑肌成分的改变、血管基底膜增厚、某些物种内皮变薄、内皮线粒体丢失以及周细胞增加。其中一些特征在AD中似乎受影响更大。其他异常包括微血管走行的严重不规则、基底膜中无法解释的内含物以及与血脑屏障相关的独特蛋白质和膜脂的变化。脑成像和通透性研究没有明确的功能证据支持这些结构和生化异常,但在衰老过程中,尤其是在AD中,血脑屏障发生局灶性和短暂性破坏是合理的。因此,某些脑区的特定神经元群体可能变得脆弱。此外,AD中血管内淀粉样蛋白的特征性沉积可能会加剧血管功能下降并促进慢性灌注不足。虽然目前的研究没有明确表明,但在衰老和疾病过程中,脑血管系统可能会通过生长和修复机制不断进行调整,以维持灌注。