Department of Molecular & Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, LA 71130-3932, USA.
Microcirculation. 2010 Apr;17(3):192-205. doi: 10.1111/j.1549-8719.2009.00015.x.
Hypertension, hypercholesterolemia, diabetes, and obesity are among a growing list of conditions that have been designated as major risk factors for cardiovascular disease (CVD). While CVD risk factors are well known to enhance the development of atherosclerotic lesions in large arteries, there is also evidence that the structure and function of microscopic blood vessels can be profoundly altered by these conditions. The diverse responses of the microvasculature to CVD risk factors include oxidative stress, enhanced leukocyte- and platelet-endothelial cell adhesion, impaired endothelial barrier function, altered capillary proliferation, enhanced thrombosis, and vasomotor dysfunction. Emerging evidence indicates that a low-grade systemic inflammatory response that results from risk factor-induced cell activation and cell-cell interactions may underlie the phenotypic changes induced by risk factor exposure. A consequence of the altered microvascular phenotype and systemic inflammatory response is an enhanced vulnerability of tissues to the deleterious effects of secondary oxidative and inflammatory stresses, such as ischemia and reperfusion. Future efforts to develop therapies that prevent the harmful effects of risk factor-induced inflammation should focus on the microcirculation.
高血压、高胆固醇血症、糖尿病和肥胖症等越来越多的疾病已被确定为心血管疾病 (CVD) 的主要危险因素。虽然众所周知,CVD 危险因素会增强大动脉粥样硬化病变的发展,但也有证据表明,这些条件会严重改变微血管的结构和功能。微血管对 CVD 危险因素的反应多种多样,包括氧化应激、白细胞和血小板内皮细胞黏附增强、内皮屏障功能受损、毛细血管增殖改变、血栓形成增强和血管舒缩功能障碍。新出现的证据表明,危险因素引起的细胞激活和细胞间相互作用导致的低度全身性炎症反应可能是危险因素暴露引起的表型变化的基础。微血管表型和全身性炎症反应的改变的后果是组织对继发性氧化和炎症应激(如缺血再灌注)的有害影响的易感性增强。未来开发预防危险因素引起的炎症有害影响的治疗方法的努力应集中在微循环上。