Zhang Yan, He Xiao-hong, Chen Xiao-lin, Hu Rui-de, Ma Hong, Wu Gui-fu, He Jian-gui, Zhan Cheng-yang, Jin Ya-fei, Fang Dian-qiu, Zheng Zhen-sheng
Key Laboratory of Assisted Circulation, Cardiovascular Research Institute, First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
Zhonghua Bing Li Xue Za Zhi. 2006 Mar;35(3):159-64.
To study the effects of enhanced external counterpulsation (EECP) on the vascular morphology, and endothelial function using experimentally induced hypercholesterolemic pigs.
Thirty five male pigs were randomly divided into three groups: 7 normal control animals, 11 hypercholesterolemic animals, and 17 hypercholesterolemic animals receiving EECP. Serum cholesterol was measured. The coronary arteries and aortas were sampled for histopathologic and ultrastructural examination. The NF-kappaB protein expression of porcine coronary arteries was investigated by immunofluorescence.
Compared with the normal controls, serum cholesterol levels were significantly higher in the hypercholesterolemic animals with or without EECP. The plaque/intimal area ratio of the aorta decreased significantly in animals receiving EECP [(3.33 +/- 2.40)%, versus (12.03 +/- 7.12)% in those without EECP, P < 0.05]. Lipid deposition, endothelial damage and proliferation of smooth muscle cells were less severe in animals receiving EECP than those not. Moreover, activation and expression of NF-kappaB also decreased significantly (P < 0.05) in animals receiving EECP.
EECP improves the morphology and function of vascular endothelium, and retards the development and progression of atherosclerosis, likely through the inhibition of NF-kappaB signaling pathway.
利用实验性诱导的高胆固醇血症猪,研究增强型体外反搏(EECP)对血管形态及内皮功能的影响。
35只雄性猪随机分为三组:7只正常对照动物、11只高胆固醇血症动物和17只接受EECP的高胆固醇血症动物。检测血清胆固醇。采集冠状动脉和主动脉进行组织病理学和超微结构检查。通过免疫荧光法研究猪冠状动脉中NF-κB蛋白的表达。
与正常对照组相比,接受或未接受EECP的高胆固醇血症动物血清胆固醇水平均显著升高。接受EECP的动物主动脉斑块/内膜面积比显著降低[(3.33±2.40)%,未接受EECP的动物为(12.03±7.12)%,P<0.05]。接受EECP的动物脂质沉积、内皮损伤和平滑肌细胞增殖程度均低于未接受EECP的动物。此外,接受EECP的动物中NF-κB的激活和表达也显著降低(P<0.05)。
EECP可能通过抑制NF-κB信号通路改善血管内皮的形态和功能,延缓动脉粥样硬化的发生和发展。