实验动物与比较医学 ›› 2020, Vol. 40 ›› Issue (4): 314-.DOI: 10.3969/j.issn.1674-5817.2020.04.007

• 论著 • 上一篇    下一篇

盐敏感性高血压小鼠模型的建立

姚玎1,周晶1,严国锋1,王会阳1,汪雅荻2,马政文1   

  1. 1. 上海交通大学医学院实验动物科学部,上海 200025; 2. 上海市格致中学,上海 200001
  • 收稿日期:2019-07-17 出版日期:2020-08-25 发布日期:2020-11-23
  • 作者简介:姚玎(1985—), 男, 实验师, 研究方向: 实验动物与比较医学。E-mail: yaod@shsmu.edu.cn
  • 基金资助:
    上海市自然科学基金(18ZR1437800)

Establishment of Salt-sensitive Hypertension Model in C57BL/6J Mice

YAO Ding1, ZHOU Jing1, YAN Guofeng1, WANG Huiyang1, WANG Yadi2, MA Zhengwen1   

  1. 1. Department of Laboratory Animal Science, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China;  2. Gezhi High School of Shanghai, Shanghai 200001, China
  • Received:2019-07-17 Online:2020-08-25 Published:2020-11-23

摘要: 目的    建立盐敏感性高血压小鼠模型,用降压药硝苯地平验证模型的有效性。方法     采用C57BL/6J小鼠为研究对象,分别设定常规饲料饲喂的正常组、高盐饲料饲喂的高盐组和高盐饲料饲喂后给予硝苯地平的干预组。采用无创血压测量系统测量各组小鼠的血压变化情况;采用血液生化分析仪测定小鼠血清的肝功能、肾功能、血脂、血糖和离子等生化指标;通过苏木精-伊红染色观察小鼠肝、肾和颈动脉的组织学变化。结果    与正常组小鼠血压相比,高盐组小鼠的收缩压和舒张压均显著升高(均P<0.01),而干预组小鼠血压显著下降(均P<0.01)。与正常组相比,高盐组小鼠的肝功能指标天冬氨酸转氨酶、碱性磷酸酶、白蛋白、血清总蛋白和直接胆红素水平,以及血脂指标胆固醇、肾功能指标尿酸、钙离子和镁离子水平都有显著变化(均P<0.05),而干预组则逐步恢复。组织病理学显示,高盐组小鼠的肝和肾都有不同程度的损伤。结论   高盐饮食可成功建立盐敏感性高血压小鼠模型,硝苯地平可有效降低模型小鼠的血压。

关键词: 盐敏感性高血压, 硝苯地平, 降压药, 小鼠模型

Abstract: Objective     To establish a mouse model of salt-sensitive hypertension, and to verify the effectiveness of the model using by nifedipine, an antihypertensive drug. Methods    C57BL/6J mice were divided into the normal control group, high-salt diet group and high-salt diet with nifedipine group. The blood pressure change of mice was measured by non-invasive blood pressure system (CODA system). The biochemical indexes of liver function, renal function, blood lipid, blood sugar and ions were measured by the blood biochemical analyzer, and the histological changes of the liver, kidney and carotid artery were observed after hematoxylin-eosin staining. Results    Compared with the normal mice, the systolic and diastolic blood pressure in the high-salt diet group increased significantly (both P<0.01), and those in the high-salt diet with nifedipine group decreased significantly (both P<0.01), and there were statistically significant differences. The liver function indexes (aspartate transaminase, alkaline phosphatase, albumin, total serum protein, and direct bilirubin), blood lipid index (cholesterol), renal function index (uric acid) and ionic levels (Ca, Mg) in high-salt diet group were significantly different from the control group, and those in the high-salt diet with nifedipine group were gradually recovered after nifedipine intervention. The pathological histology showed that the liver and kidney of the high-salt diet group had different degrees of injury. Conclusion    High-salt diet can successfully establish a mice model of salt-sensitive hypertension, and nifedipine can effectively lower the blood pressure of the model mice.

Key words: Salt-sensitive hypertension, Nifedipine, Hypotensor, Mouse model

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