Lin Yi-Chen, Chen Qin-Ye, Xiao Jie, Shen Li-Chuan, Li Xian-Tao, Yang Yu-Ze, Guo Ping-Fan, Lin Mo-Jun, Lin Da-Cen
Department of Vascular Surgery, First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian Province, People's Republic of China; Key Laboratory of Fujian Province Universities on Ion Channel and Signal Transduction in Cardiovascular Diseases, Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, Fujian Province, People's Republic of China; The First School of Clinical Medicine, Fujian Medical University, Fuzhou, Fujian Province, People's Republic of China.
Key Laboratory of Fujian Province Universities on Ion Channel and Signal Transduction in Cardiovascular Diseases, Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, Fujian Province, People's Republic of China.
Lab Invest. 2023 Mar;103(3):100035. doi: 10.1016/j.labinv.2022.100035. Epub 2023 Jan 10.
For decades, numerous experimental animal models have been developed to examine the pathophysiologic mechanisms and potential treatments for abdominal aortic aneurysms (AAAs) in diverse species with varying chemical or surgical approaches. This study aimed to create an AAA mouse model by the periarterial incubation with papain, which can mimic human AAA with advantages such as simplicity, convenience, and high efficiency. Eighty C57BL/6J male mice were randomly assigned to 1 of the 4 groups: papain (1.0 or 2.0 mg), porcine pancreatic elastase, and phosphate-buffered solution. The aortic segment was wrapped for 20 minutes, and the diameter was measured using ultrasound preoperatively and postoperative days 7 and 14. Then, the mice were killed for histomorphometric and immunohistochemical analyses. According to ultrasound measurements and histomorphometric analyses, on postoperative day 7, 65% of mice in the 1.0-mg papain group and 60% of mice in the 2.0-mg papain group developed AAA. In both papain groups, 100% of mice developed AAA, and 65% of mice in the porcine pancreatic elastase group developed AAA on postoperative day 14. Furthermore, hematoxylin/eosin, elastin van Gieson, and Masson staining of tissues from the papain group revealed thickened media and intimal hyperplasia, collagen sediments, and elastin destruction, indicating that AAA histochemical alteration was similar to that of humans. In addition, the immunohistochemical analysis was conducted to detect infiltrated inflammatory cells, such as macrophages and leukocytes, in the aortic wall and hyperplasic adventitia. The expression of matrix metalloproteinase 2 and 9 was significantly upregulated in papain and human AAA tissues. Periarterial incubation with 1.0 mg of papain for 20 minutes can successfully create an experimental AAA model in mice for 14 days, which can be used to explore the mechanism and treatment of human AAA.
几十年来,人们已经开发了许多实验动物模型,通过不同的化学或手术方法,在不同物种中研究腹主动脉瘤(AAA)的病理生理机制和潜在治疗方法。本研究旨在通过动脉周围注射木瓜蛋白酶创建一种AAA小鼠模型,该模型可以模拟人类AAA,具有简单、方便和高效等优点。80只C57BL/6J雄性小鼠被随机分为4组中的1组:木瓜蛋白酶(1.0或2.0mg)组、猪胰弹性蛋白酶组和磷酸盐缓冲液组。将主动脉段包裹20分钟,并在术前以及术后第7天和第14天使用超声测量直径。然后,处死小鼠进行组织形态计量学和免疫组织化学分析。根据超声测量和组织形态计量学分析,术后第7天,1.0mg木瓜蛋白酶组65%的小鼠和2.0mg木瓜蛋白酶组60%的小鼠发生了AAA。在两个木瓜蛋白酶组中,100%的小鼠发生了AAA,猪胰弹性蛋白酶组65%的小鼠在术后第14天发生了AAA。此外,木瓜蛋白酶组组织的苏木精/伊红、弹性蛋白范吉森和马森染色显示中膜增厚、内膜增生、胶原沉积和弹性蛋白破坏,表明AAA的组织化学改变与人类相似。另外,进行免疫组织化学分析以检测主动脉壁和增生外膜中浸润的炎性细胞,如巨噬细胞和白细胞。基质金属蛋白酶-2和-9在木瓜蛋白酶组和人类AAA组织中的表达显著上调。动脉周围注射1.0mg木瓜蛋白酶20分钟可成功在小鼠中创建为期14天的实验性AAA模型,并可用于探索人类AAA的机制和治疗方法。