Pakala Rajbabu, Leborgne Laurent, Cheneau Edouard, Chan Rosanna C, Yazdi Hamid, Fournadjiev Jana, Weber Deena, Hellinga David, Kolodgie Frank, Virmani Renu, Waksman Ron
Cardiovascular Research Institute, Washington Hospital Center, 110 Irving Street, NW, Suite 4B-1, Washington, DC 20010, USA.
Cardiovasc Radiat Med. 2003 Jul-Sep;4(3):146-51. doi: 10.1016/S1522-1865(03)00182-3.
Human observations provide rich soil for making hypotheses, but good animal models are essential for understanding the disease and to test treatment modalities. Currently, there is no standard animal model of vulnerable plaque; therefore, the purpose of this study is to develop a pathophysiologically relevant vulnerable plaque model.
New Zealand White rabbits were fed with 1% hypercholesterolemic (HC) diet for 7 days, followed by balloon denudation of both the iliac arteries, and continued on 1% HC diet. Four weeks later, in 12 rabbits one of the iliac arteries was radiated (192-Ir, 15 Gy), and in five rabbits both the iliac arteries were sham treated. Following that, rabbits were fed with 0.15% HC diet. Four weeks later, arteries were processed for histomorphometry or immunohistochemistry.
Serum cholesterol levels were similar in all the groups. In radiated arteries, plaque area was significantly larger (32% larger then in sham). Macrophage-positive area in radiated arteries was 2.4 times greater than the macrophage-positive area in the nonradiated arteries. The area positive for macrophages is also positive for metalloproteinases (MMP)-1. The extent of alpha-actin positive area was significantly less (2.3-fold) in radiated arteries.
The atherosclerotic plaque developed in the current model is predominantly composed of macrophages expressing metalloproteinases with few smooth muscle cells (SMC)--a characteristic of vulnerable plaque. The animal model presented in this study can elucidate at least part of the mechanism of plaque vulnerability and could be used to test treatment modalities to test plaque stability.
人体观察为提出假设提供了丰富的素材,但良好的动物模型对于理解疾病和测试治疗方式至关重要。目前,尚无易损斑块的标准动物模型;因此,本研究的目的是建立一种与病理生理相关的易损斑块模型。
给新西兰白兔喂食1%的高胆固醇(HC)饮食7天,随后对双侧髂动脉进行球囊剥脱术,并继续喂食1%的HC饮食。四周后,对12只兔子的一侧髂动脉进行放射治疗(192铱,15戈瑞),对5只兔子的双侧髂动脉进行假处理。之后,给兔子喂食0.15%的HC饮食。四周后,对动脉进行组织形态计量学或免疫组织化学分析。
所有组的血清胆固醇水平相似。在接受放射治疗的动脉中,斑块面积明显更大(比假处理组大32%)。接受放射治疗的动脉中巨噬细胞阳性面积是非放射治疗动脉中巨噬细胞阳性面积的2.4倍。巨噬细胞阳性区域对金属蛋白酶(MMP)-1也呈阳性。接受放射治疗的动脉中α-肌动蛋白阳性面积的范围明显更小(为假处理组的2.3倍)。
当前模型中形成的动脉粥样硬化斑块主要由表达金属蛋白酶的巨噬细胞组成,平滑肌细胞很少——这是易损斑块的一个特征。本研究中提出的动物模型可以阐明斑块易损性的至少部分机制,并可用于测试治疗方式以检测斑块稳定性。