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七叶皂苷钠调控 SIRT1/NF-κB 信号通路对帕金森病大鼠的神经

          保护作用
                        Δ


                                               #
                *
          周慧敏 ,陈 静,欧诒丹,王御林,钟纯正(儋州市人民医院神经内科,海南 儋州 571700)
          中图分类号  R965      文献标志码  A      文章编号  1001-0408(2024)06-0689-06
          DOI  10.6039/j.issn.1001-0408.2024.06.09

          摘  要  目的  探究七叶皂苷钠通过调控沉默信息调节因子1(SIRT1)/核因子κB(NF-κB)信号通路发挥对帕金森病大鼠的神经
          保护作用。方法  采用6-羟基多巴胺注射法构建帕金森病大鼠模型,将建模成功的48只大鼠随机分为模型组、七叶皂苷钠低剂量
          组(1.8 mg/kg)、七叶皂苷钠高剂量组(3.6 mg/kg)、七叶皂苷钠+EX527 组(七叶皂苷钠 3.6 mg/kg+SIRT1 抑制剂 EX527 5 mg/kg),
          每组12只;另取12只健康大鼠作为假手术组。各药物组大鼠腹腔注射相应药液,每天1次,持续21 d。末次给药结束24 h后,检
          测大鼠运动及认知功能,观察其黑质区和海马组织CA1区神经元形态,检测其黑质纹状体中多巴胺(DA)含量和黑质区酪氨酸羟
          化酶(TH)、α突触核蛋白(α-Syn)表达水平,检测其血清中促炎因子[白细胞介素6(IL-6)、IL-18]、抗炎因子(IL-10)水平及黑质纹
          状体中SIRT1、磷酸化NF-κB p65(p-NF-κB p65)、NF-κB p65蛋白表达水平。结果  与假手术组比较,模型组大鼠黑质区和海马组
          织CA1区神经元损伤严重;其旋转圈数、逃避潜伏期、黑质区α-Syn蛋白表达水平、血清中促炎因子水平、黑质纹状体中p-NF-κB
          p65与NF-κB p65蛋白的相对表达量之比均显著升高或延长(P<0.05),目标象限停留时间、黑质纹状体中DA含量及黑质区TH蛋
          白表达水平、血清中抗炎因子水平、黑质纹状体中SIRT1蛋白表达水平均显著缩短或降低(P<0.05)。与模型组比较,七叶皂苷钠
          各剂量组大鼠神经元损伤程度减轻,各定量指标均显著改善,且高剂量组的改善更为明显(P<0.05),而EX527可逆转高剂量七叶
          皂苷钠的改善作用(P<0.05)。结论  七叶皂苷钠可通过上调SIRT1蛋白表达来抑制NF-κB信号激活,从而抑制帕金森病大鼠的
          神经炎症,改善其运动及认知功能障碍,最终起到神经保护作用。
          关键词  七叶皂苷钠;帕金森病;沉默信息调节因子1/核因子κB信号通路;运动功能;认知功能;炎症反应;神经保护

          Neuroprotective  effect  of  sodium  aescinate  on  rats  with  Parkinson’s  disease  by  regulating  SIRT1/NF-κB
          signaling pathway
          ZHOU Huimin,CHEN Jing,OU Yidan,WANG Yulin,ZHONG Chunzheng(Dept.  of  Neurology,  Danzhou
          People’s Hospital, Hainan Danzhou 571700, China)


          ABSTRACT   OBJECTIVE  To  explore  the  neuroprotective  effect  of  sodium  aescinate  on  rats  with  Parkinson’s  disease  by
          regulating  the  silent  information  regulator  1 (SIRT1)/nuclear  factor-κB (NF-κB)  signaling  pathway.  METHODS  The  Parkinson’s
          disease  rat  model  was  constructed  by  using  6-hydroxydopamine  injection  method.  Forty-eight  rats  successfully  modeled  were
          randomly  divided  into  model  group,  sodium  aescinate  low-dose  group (1.8  mg/kg),  sodium  aescinate  high-dose  group (3.6  mg/kg),
          sodium  aescinate+EX527 (sodium  aescinate  3.6  mg/kg+SIRT1  inhibitor  EX527  5  mg/kg)  group,  with  12  rats  in  each  group.
          Another  12  healthy  rats  were  selected  as  the  sham  operation  group.  Each  group  was  injected  with  the  corresponding  drug  solution
          intraperitoneally,  once  a  day,  for  21  consecutive  days.  Twenty-four  hours  after  the  end  of  the  last  administration,  the  motor  and
          cognitive  functions  of  rats  were  detected,  and  the  morphology  of  neurons  in  the  substantia  nigra  and  CA1  region  of  hippocampal
          tissue  were  observed.  The  content  of  dopamine (DA)  in  the  nigrostriatal  and  the  expression  levels  of  tyrosine  hydroxylase (TH)
          and α-synuclein (α-Syn) in the substantia nigra were detected. The serum levels of pro-inflammatory factor [interleukin-6 (IL-6),
          IL-18], anti-inflammatory factor (IL-10), and the expression levels of SIRT1, phosphorylated NF-κB p65 (p-NF-κB p65) and NF-
          κB p65 protein in nigrostriatal were detected. RESULTS Compared with sham operation group, the neurons in the substantia nigra
          and  CA1  region  of  hippocampal  tissue  were  seriously  damaged  in  model  group;  the  number  of  rotations,  escape  latency,  the
          expression levels of α-Syn in substantia nigra, the levels of serum pro-inflammatory factors, the relative expression ratio of p-NF-
          κB  p65  and  NF-κB  p65  protein  in  nigrostriatal  were  increased  or  prolonged  significantly (P<0.05);  the  target  quadrant  residence
          time,  the  content  of  DA  in  nigrostriatal,  the  expression  level  of  TH  in  substantia  nigra,  the  serum  level  of  anti-inflammatory
                                                             factor,  and  the  expression  level  of  SIRT1  protein  in  substantia
             Δ 基金项目 海南省卫生健康行业科研项目(No.21A200535)
                                                             nigra  striatum  were  significantly  decreased  or  shortened (P<
             *第一作者 主治医师,硕士。研究方向:中西医结合治疗神经疾
                                                             0.05).  Compared  with  model  group,  the  damage  degrees  of
          病。E-mail:zhouhuimin563@163.com
             # 通信作者 主任医师,硕士。研究方向:中西医结合治疗神经疾                  neuron  in  sodium  aescinate  groups  were  alleviated,  and  the
          病。E-mail:zcz196565@163.com                         quantitative  indicators  were  significantly  improved,  which


          中国药房  2024年第35卷第6期                                                 China Pharmacy  2024 Vol. 35  No. 6    · 689 ·
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