天津医药 ›› 2021, Vol. 49 ›› Issue (4): 364-370.doi: 10.11958/20202268

• 实验研究 • 上一篇    下一篇

山莨菪碱对横纹肌溶解致急性肾损伤大鼠保护作用的研究#br#

安丽平1,王伟1,杨洪霞1,安然1,于琨1,吴广礼2,李云峰1△
  

  1. 1河北中医学院基础医学院,河北省心脑血管病中医药防治研究重点实验室(邮编050200);2白求恩和平医院肾内科
  • 收稿日期:2020-08-14 修回日期:2020-12-05 出版日期:2021-04-15 发布日期:2021-04-16
  • 通讯作者: 李云峰 E-mail:fengsong117@126.com
  • 作者简介:安丽平(1979),女,硕士,讲师,主要从事肾病分子生物学研究。E-mail:anliping08@126.com
  • 基金资助:
    国家自然科学基金资助项目(81971434);河北省教育厅青年基金项目(QN2016137);河北省教育厅资助项目(Z2015177);河北省中医药管理局科研计划项目(2016003)

The protective effect of anisodamine on acute renal injury induced by rhabdomyolysis in rats

AN Li-ping1, WANG Wei1, YANG Hong-xia1, AN Ran1, YU Kun1, WU Guang-li2, LI Yun-feng1△   

  1. 1 Basic Medical College, Hebei University of Chinese Medicine, Hebei Key Laboratory of Chinese Medicine Research on Cardio-Cerebrovascular Disease, Hebei 050200, China; 2 Department of Nephrology, Bethune International Peace Hospital of PLA
  • Received:2020-08-14 Revised:2020-12-05 Published:2021-04-15 Online:2021-04-16
  • Contact: LI Yun-feng E-mail:fengsong117@126.com

摘要: 目的 观察山莨菪碱对横纹肌溶解引发急性肾小管上皮细胞溶酶体相关膜蛋白2(LAMP2)和组织蛋白酶B(Cathepsin B)表达的影响并探讨其机制。方法 63只雄性SD大鼠随机均分为对照组、模型组和给药组。模型组和给药组采用甘油肌注法建立横纹肌溶解致急性肾损伤大鼠模型,给药组建模前腹腔注射山莨菪碱(1 mg/kg)。甘油肌注后不同时点,HE染色观察肾组织病理学变化;检测肾功能指标[尿素氮(BUN)、肌酐(Scr)、肌酸激酶(CK)]、血清肌红蛋白(Mb)水平及肾组织中超氧化物歧化酶(SOD)、丙二醛(MDA)含量。甘油肌注诱导急性肾损伤24 h时,采用免疫组化法和Western blot法检测肾组织中LAMP2、Cathepsin B、Megalin蛋白的表达。结果 HE染色示模型组大鼠发生明显肾脏损伤,山莨菪碱给药后肾脏损伤情况明显改善。模型组在甘油肌注24 h和48 h的Scr、12 h和24 h的BUN、6 h的CK、24 h的Mb均高于对照组,而给药组上述各时点的指标水平均低于模型组(P<0.05)。给药组甘油肌注6 h和12 h的MDA含量低于模型组,而SOD活性高于模型组(P<0.05)。甘油肌注24 h时,免疫组化和Western blot结果显示,模型组LAMP2、Cathepsin B、Megalin蛋白表达水平高于对照组,而给药组LAMP2、Cathepsin B、Megalin蛋白表达水平均低于模型组(P<0.05)。结论 山莨菪碱可能通过减少Mb的生成,下调肾组织内LAMP2和Cathepsin B的表达以及抑制氧化应激反应发挥其肾脏保护作用。

关键词: 横纹肌溶解, 急性肾损伤, 溶酶体相关膜蛋白质2, 组织蛋白酶B, 山莨菪碱, 肌红蛋白, 氧化应激

Abstract: Objective To observe the effect of anisodamine on the expressions of lysosome associated membrane protein-2 and cathepsin B in acute renal tubular epithelial cells induced by inrhabdomyolysis in rats and explore the mechanism. Methods Sixty-three male Sprague-Dawley rats were randomly divided into control group, model group and administration group. The rat model of acute kidney injury induced by rhabdomyolysis was established by glycerol intramuscular injection in the model group and the administration group, while the administration group was given anisodamine by intraperitoneal injection (1 mg/kg) before the initial glycerol injection. At different time points after glycerol injection, HE staining was used to observe the pathological changes of kidney tissues. The renal function indicators including serum urea nitrogen (BUN), serum creatinine (Scr), creatine kinase (CK) and serum myoglobin (Mb) were measured. The contents of superoxide dismutase (SOD) and malondialdehyde (MDA) in kidney tissues were detected. After acute kidney injury was induced by intramuscular injection of glycerol for 24 h, the expressions of LAMP2, Cathepsin B and Megalin in kidney tissues were detected by immunohistochemistry and Western blot assay. Results HE staining indicated that the rats in the model group had obvious kidney injury. However, anisodamine significantly ameliorated kidney injury. The serum BUN levels of 12 h and 24 h, Scr of 24 h and 48 h, CK of 6 h, and Mb of 24 h were significantly higher in model group than those of the control group (P<0.05). In contrast, all of these markers at the corresponding time points were significantly ower in anisodamine administration group than those of the model group (P<0.05). In comparison to the model group, the MDA content was significantly decreased at 6 h and 12 h in the administration group (P<0.05), while SOD activity was significantly increased (P<0.05). In addition, the results of immunohistochemistry and Western blot assay showed that the expression levels of LAMP2, Cathepsin B and Megalin at 24 h were significantly higher in the model group than those of the control group and the administration group. However, the expression levels of these proteins in the administration group were significantly lower than those in the model group (P<0.05). Conclusion Anisodamine could perform a protective role to kidney by reducing the production of Mb, down-regulating the expressions of LAMP2 and Cathepsin B in renal tissues and restraining oxidative stress.

Key words: rhabdomyolysis, acute kidney injury, lysosomal-associated membrane protein 2, Cathepsin B, anisodamine, myoglobin, oxidative stress

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