Weingärtner Oliver, Kasper Michael, Reynen Klaus, Bramke Silvia, Marquetant Rainer, Sedding Daniel G, Braun-Dullaeus Rüdiger, Strasser Ruth H
Department of Internal Medicine II/Cardiology, University of Technology, Dresden Heart Center, Dresden, Germany.
Coron Artery Dis. 2005 Sep;16(6):391-400. doi: 10.1097/00019501-200509000-00009.
Animal models of restenosis have been a cornerstone of testing potential therapies and have improved the understanding of the underlying mechanisms. The aim of this study was to provide an in-depth comparison of the progression of restenotic lesion formation after arterial injury in apolipoprotein E -/- and C57BL/6 control mice.
In this study, we investigated the difference in lesion formation of apolipoprotein E -/- and C57BL/6 controls on a high-cholesterol, high-fat diet after arterial injury. One week prior to arterial injury of the left femoral artery, mice were started on a high-cholesterol, high-fat diet. Diets were continued after arterial injury until euthanization. At five consecutive time points (2, 5, 10, 15, and 21 days), the intimal hyperplasia in the injured arteries was analyzed.
In the C57BL/6 control mice, a continuously increasing lesion formation, consisting primarily of alpha-smooth muscle actin-positive cells, was observed. Lesion formation in apolipoprotein E -/- mice was significantly more pronounced, resulting in complete occlusion of the arteries in four out of five vessels after 21 days. Lesions in apolipoprotein E -/- mice consisted predominantly of lipid-loaded foam cells and alpha-smooth muscle actin-positive cells. Further histological evaluation demonstrated cholesterol crystals in the lesions and neovascularizsation in cases of occlusion.
Thus, apoE -/- mice on a high-cholesterol, high-fat diet provide a more valid model for the characterization of the development of restenotic lesions after mechanical irritation such as angioplasty than C57BL/6 mice.
再狭窄动物模型一直是测试潜在治疗方法的基石,并增进了对潜在机制的理解。本研究的目的是深入比较载脂蛋白E基因敲除小鼠和C57BL/6对照小鼠动脉损伤后再狭窄病变形成的进展情况。
在本研究中,我们调查了载脂蛋白E基因敲除小鼠和C57BL/6对照小鼠在高脂高胆固醇饮食条件下动脉损伤后病变形成的差异。在左股动脉损伤前一周,小鼠开始高脂高胆固醇饮食。动脉损伤后继续喂食直至安乐死。在连续五个时间点(2、5、10、15和21天),分析损伤动脉的内膜增生情况。
在C57BL/6对照小鼠中,观察到病变形成持续增加,主要由α-平滑肌肌动蛋白阳性细胞组成。载脂蛋白E基因敲除小鼠的病变形成明显更显著,21天后五分之四的血管出现动脉完全闭塞。载脂蛋白E基因敲除小鼠的病变主要由富含脂质的泡沫细胞和α-平滑肌肌动蛋白阳性细胞组成。进一步的组织学评估显示病变中有胆固醇结晶,闭塞病例中有新生血管形成。
因此,高脂高胆固醇饮食的载脂蛋白E基因敲除小鼠比C57BL/6小鼠更适合作为机械刺激(如血管成形术)后再狭窄病变发展特征研究的有效模型。