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蛇床子素对糖尿病肾病模型小鼠肾间质纤维化的预防作用
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          黄 倩 ,郑丹丹 ,黄秋虹 ,施子禄 (1.泉州医学高等专科学校基础医学部生理教研室,福建 泉州 362100;
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          2.福建医科大学附属泉州第一医院肾内科,福建 泉州 362000)
          中图分类号  R965      文献标志码  A      文章编号  1001-0408(2022)22-2719-05
          DOI  10.6039/j.issn.1001-0408.2022.22.06

          摘  要  目的  探讨蛇床子素(OST)对糖尿病肾病(DN)模型小鼠肾间质纤维化的影响。方法  采用一次性尾静脉注射链脲佐菌
          素建立糖尿病小鼠模型,成功后继续喂养 12 周建立 DN 模型。将糖尿病模型小鼠分为模型组和 OST 低、中、高剂量(20、40、80
          mg/kg)组,每组10只,糖尿病造模成功后每日灌胃相应药物或溶剂(模型组)1次,持续12周;同时设置正常对照组。末次灌胃后,
          检测各组小鼠空腹血糖、24 h尿蛋白、血肌酐(Scr)、尿素氮水平;Masson染色法观察肾间质区域胶原纤维的沉积情况;免疫组化染
          色法检测肾皮质中E-钙黏蛋白(E-cadherin)和波形蛋白(vimentin)的表达;Western blot法检测肾皮质中卵泡抑素样蛋白1(Fstl1)、
          锌指转录因子1(Snail1)蛋白表达和蛋白激酶B(Akt)磷酸化水平(以p-Akt/Akt比值计)。结果  与正常对照组比较,模型组小鼠空
          腹血糖、24 h 尿蛋白、Scr、尿素氮水平,肾间质胶原纤维沉积占比,肾皮质中 vimentin 表达水平以及 Fstl1、Snail1 蛋白表达水平和
          p-Akt/Akt比值均显著升高(P<0.01),E-cadherin表达水平显著降低(P<0.01)。与模型组比较,OST各剂量组小鼠上述指标变化
          均显著逆转(P<0.05或P<0.01)。结论  OST预防性用药可有效降低DN模型小鼠的空腹血糖,保护其肾功能,抑制肾小管上皮
          细胞间充质转分化,延缓肾间质纤维化进程,其作用机制可能与抑制Fstl1/Akt/Snail1通路有关。
          关键词  蛇床子素;糖尿病肾病;间质纤维化;卵泡抑素样蛋白1;蛋白激酶B;锌指转录因子1;小鼠

          Prevention of renal interstitial fibrosis by osthole in diabetic nephropathy model mice
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          HUANG Qian ,ZHENG Dandan ,HUANG Qiuhong ,SHI Zilu (1.  Teaching  and  Research  Section  of
          Physiology, Basic Medicine Department, Quanzhou Medical College, Fujian Quanzhou 362100, China;2. Dept.
          of  Nephrology,  Quanzhou  First  Hospital  Affiliated  to  Fujian  Medical  University,  Fujian  Quanzhou  362000,
          China)
          ABSTRACT   OBJECTIVE To investigate the effects of osthole (OST) on renal interstitial fibrosis in diabetic nephropathy (DN)
          model  mice.  METHODS  The  diabetic  mice  model  was  established  by  the  tail  vein  injection  of  streptozotocin  once,  and  the  DN
          model  was  established  by  feeding  for  12  weeks  after  successful  modeling  of  diabetes.  Diabetic  model  mice  were  randomly  divided
          into  model  group,  low-dose,  moderate-dose,  high-dose  groups (20,  40,  80  mg/kg)  of  OST,  with  10  mice  in  each  group. After
          successful  modeling  of  diabetes,  the  mice  were  given  corresponding  drugs  or  solvent (model  group)  intragastrically,  once  a  day,
          for  consecutive  12  weeks,  and  the  normal  control  group  was  set  up  at  the  same  time. After  the  last  administration,  the  levels  of
          fasting  blood  glucose,  24  h  urinary  protein,  serum  creatinine (Scr)  and  blood  urea  nitrogen  were  tested  in  each  group.  Masson
          staining  was  used  to  observe  the  deposition  of  collagen  fibers  in  renal  interstitium;  the  expressions  of  E-cadherin  and  vimentin  in
          renal  cortex  were  detected  by  immunohistochemical  staining. The  protein  expressions  of  follistatin-like  protein  1 (Fstl1)  and  Snail
          family  transcriptional  repressor  1 (Snail1),  the  phosphorylation  of  protein  kinase  B (Akt) (calculated  by  p-Akt/Akt)  in  the  renal
          cortex  were  detected  by Western  blot.  RESULTS  Compared  with  normal  control  group,  the  levels  of  fasting  blood  glucose,  24  h
          urinary  protein,  Scr  and  blood  urea  nitrogen,  collagen  fiber  deposition  ratio  of  renal  interstitium,  the  expression  of  vimentin,
          protein expressions of Fstl1 and Snail1, p-Akt/Akt in renal cortex were increased significantly (P<0.01), as well as the expression
          of  E-cadherin   was  decreased  significantly (P<0.01).  Compared  with  model  group,  above  indexes  of  OST  groups  were  reversed
          significantly (P<0.05  or  P<0.01).  CONCLUSIONS  Preventive  use  of  OST  can  effectively  reduce  fasting  blood  glucose  level,
          protect renal function and inhibit epithelial-mesenchymal transition of DN model mice, and delay the progression of renal interstitial
                                                             fibrosis  ,  the  mechanism  of  which  may  be  associated  with  the
             Δ 基金项目 国家自然科学基金资助项目(No.31471100);福建省
                                                             suppression of Fstl1/Akt/Snail1 signaling pathway.
          中青年教师教育科研项目(科技类)(No.JAT201237);泉州市科技计划
          项目(No.2018Z179)                                    KEYWORDS     osthole; diabetic nephropathy; interstitial fibrosis;
             *第一作者 副教授,博士。研究方向:肾脏生理学、糖尿病及其并                  follistatin-like  protein  1;  protein  kinase  B;  Snail  family
          发症的防治。电话:0595-22632100。E-mail:119569406@qq.com     transcriptional repressor 1; mice
             # 通信作者 副主任医师,硕士。研究方向:临床肾脏疾病的诊治。
          电话:0595-22650210。E-mail:cthk2010@zju.edu.cn


          中国药房  2022年第33卷第22期                                              China Pharmacy  2022 Vol. 33  No. 22    · 2719 ·
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