Comparison of three rat models of coronary microvascular dysfunction induced by sodium laurate
ZHU Jinxian FAN Yawen GONG Shenglan ZHUANG Yuanfei LIU Chungui TANG Xinzheng
Department of Cardiovascular Diseases, the Sixth Clinical Medical College of Guangzhou University of Chinese Medicine Shenzhen Hospital of Guangzhou University of Chinese Medicine (Futian), Guangdong Province, Shenzhen 518034, China
Abstract:Objective To evaluate the optimal scheme of three coronary microcirculation dysfunction models in SD rats induced by sodium laurate. Methods A total of 50 male SD rats aged 6-8 weeks were divided into blank group, sham operation group, and model group 1-3 by random number table method, with ten rats in each group. The blank group did not receive any intervention; in model group 1, the heart was extruded after intercostal expansion and sodium laurate (1 mg/kg) was injected into the apex of the heart once; in model group 2, the heart was extruded after intercostal expansion and sodium laurate (1 mg/kg) was injected into the apex of the heart twice; in model group 3, the heart was extruded after intercostal expansion, the aortic root was clipped and the apex of the heart was injected with sodium laurate (1 mg/kg) once; the sham operation group performed the same operation as model group 2, but the same amount of normal saline was injected. Echocardiogram was used to evaluate cardiac function after 72 h of continuous feeding. The pathological changes of myocardial tissue were observed by HE staining, Heidenhain staining, and Carstairs staining. Results The mortality rate of operational rats was 17.5% (7/40). There was no significant difference in left ventricular ejection fraction (LVEF) between sham operation group and blank group (P > 0.05). Compared with the sham operation group, the LVEF of the model group 1-3 was decreased (P < 0.05); compared with model group 2, LVEF in model group 1 and 3 was increased (P < 0.05). HE staining showed that myocardial cell lysis, rupture, and inflammatory cell infiltration, coronary microvascular thrombosis in different degrees were observed in model group 1-3. Heidenhain staining showed that different degrees of dot, sheet, and mass black staining could be seen in the myocardial fibers of model group 1-3. Carstairs staining showed that purple thrombus which consists of overlapping platelets and fibrin could be seen in the coronary microvascular of model group 1-3. Conclusion Three modeling methods can establish the model of coronary microvascular dysfunction, and the model established by squeezed out the heart after expanding the intercostal space and injecting sodium laurate (1 mg/kg) into the apex twice is more stable and reliable.
朱瑾娴 范雅雯 龚胜兰 庄园妃 刘春贵 唐新征. 月桂酸钠诱导建立三种冠状动脉微循环障碍大鼠模型的比较[J]. 中国医药导报, 2022, 19(25): 19-23.
ZHU Jinxian FAN Yawen GONG Shenglan ZHUANG Yuanfei LIU Chungui TANG Xinzheng. Comparison of three rat models of coronary microvascular dysfunction induced by sodium laurate. 中国医药导报, 2022, 19(25): 19-23.
[1] Kunadian V,Chieffo A,Camici PG,et al. An EAPCI Expert Consensus Document on Ischaemia with Non-Obstructive Coronary Arteries in Collaboration with European Society of Cardiology Working Group on Coronary Pathophysiology & Microcirculation Endorsed by Coronary Vasomotor Disorders International Study Group [J]. Eur Heart J,2020,41(37):3504-3520.
[2] 张运,陈韵岱,傅向华,等.冠状动脉微血管疾病诊断和治疗的中国专家共识[J].中国循环杂志,2017,32(5):421-430.
[3] Rush CJ,Berry C,Oldroyd KG,et al. Prevalence of Coronary Artery Disease and Coronary Microvascular Dysfunction in Patients With Heart Failure With Preserved Ejection Fraction [J]. JAMA Cardiol,2021,6(10):1130-1143.
[4] Dekker N,Veerhoek D,Koning NJ,et al. Postoperative microcirculatory perfusion and endothelial glycocalyx shedding following cardiac surgery with cardiopulmonary bypass [J]. Anaesthesia,2019,74(5):609-618.
[5] Weerts J,Mourmans S,Barandiarán AA,et al. The Role of Systemic Microvascular Dysfunction in Heart Failure with Preserved Ejection Fraction [J]. Biomolecules,2022,12(2):278.
[6] Yang JH,Obokata M,Reddy Y,et al. Endothelium-dependent and independent coronary microvascular dysfunction in patients with heart failure with preserved ejection fraction [J]. Eur J Heart Fail,2020,22(3):432-441.
[7] 苏立硕,王贤良,毛静远.冠状动脉微循环障碍动物模型建立的方法及评析[J].中国医学科学院学报,2014,36(5):542-545.
[8] 张振国,李雪峰,朱淑珍,等.介入法建立大鼠冠状动脉微栓塞模型[J].重庆医科大学学报,2018,43(3):338-342.
[9] 綦海,张毛毛,吴健,等.月桂酸钠致心肌微循环栓塞机制的研究[J].中国医学前沿杂志(电子版),2011,3(6):49-53.
[10] Abdu FA,Liu L,Mohammed AQ,et al. Prognostic impact of coronary microvascular dysfunction in patients with myocardial infarction with non-obstructive coronary arteries [J]. Eur J Intern Med,2021,92:79-85.
[11] Taqueti VR,Solomon SD,Shah AM,et al. Coronary microvascular dysfunction and future risk of heart failure with preserved ejection fraction [J]. Eur Heart J,2018, 39(10):840-849.
[12] Wang H,Zhong WJ,Huang MW,et al. Efficacy of dual antiplatelet therapy combined with Naoxintong Capsules [see text] following coronary microembolization induced by homologous microthrombi in rats [J]. Chin J Integr Med,2011,17(12):917-924.
[13] 李磊,孟红旭,辛高杰,等.双参宁心胶囊对冠状动脉微循环障碍大鼠心脏功能及血流动力学的影响[J].中国实验方剂学杂志,2021,27(22):41-50.
[14] Zhang Y,Ma XJ,Guo CY,et al. Pretreatment with a combination of ligustrazine and berberine improves cardiac function in rats with coronary microembolization [J]. Acta Pharmacol Sin,2016,37(4):463-472.
[15] 孙安会,谷捷,吴涛,等.四种常用实验麻醉药物对大鼠心血管系统的影响[J].中国实验动物学报,2016,24(2):120-126.
[16] 李磊,孟红旭,付建华,等.两种造模方法建立大鼠冠脉微循环障碍模型比较研究[J].中国比较医学杂志,2021, 31(12):20-26.
[17] 陈良,蒋锦琪,张道良,等.山莨菪碱治疗冠状动脉微循环障碍的实验观察[J].上海交通大学学报(医学版),2010,30(6):689-692.
[18] Ford TJ,Rocchiccioli P,Good R,et al. Systemic microvascular dysfunction in microvascular and vasospastic angina [J]. Eur Heart J,2018,39(46):4086-4097.
[19] Pries AR,Reglin B. Coronary microcirculatory pathophysiology:can we afford it to remain a black box? [J]. Eur Heart J,2017,38(7):478-488.
[20] Konst RE,Guzik TJ,Kaski JC,et al. The pathogenic role of coronary microvascular dysfunction in the setting of other cardiac or systemic conditions [J]. Cardiovasc Res,2020,116(4):817-828.
[21] Vancheri F,Longo G,Vancheri S,et al. Coronary Microvascular Dysfunction [J]. J Clin Med,2020,9(9):2880.
[22] 沈成兴,梁春,陈良龙,等.经冠状动脉内注射月桂酸钠构建大鼠冠状动脉微栓塞模型[J].中国动脉硬化杂志,2005,13(4):447-450.
[23] 马学宽,古丽葛娜·萨吾尔,张华,等.天香丹对冠脉微循环障碍大鼠Nrf2/ARE信号通路表达的影响[J].中国中西医结合杂志,2020,40(12):1489-1494.
[24] 张雯雯,金颂峰,赵国梁,等.稳斑汤激活Nrf2信号通路减轻氧化应激缓解大鼠冠脉微循环障碍[J].中国老年学杂志,2021,41(23):5271-5275.
[25] 王贤良,苏立硕,毛静远,等.理气化痰活血方药对大鼠冠脉微血管血栓形成及阻塞的影响[J].中国医学科学院学报,2016,38(3):260-264.