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鬼针草总黄酮对脂多糖诱导小鼠神经炎症的改善作用及机制
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          唐丰曼 ,庞晓军        1, 2 # ,谢 颜 ,刘春芳(1.广西医科大学药学院,南宁 530021;2.钦州市第二人民医院药学
                                             1
          部,广西 钦州 535000)
          中图分类号  R965      文献标志码  A      文章编号  1001-0408(2023)14-1719-05
          DOI  10.6039/j.issn.1001-0408.2023.14.11

          摘  要  目的  探讨鬼针草总黄酮(TFB)对脂多糖(LPS)诱导小鼠神经炎症的改善作用及机制。方法  将50只C57BL/6小鼠随机
          分为正常对照组、LPS组和TFB低、中、高剂量组,每组10只。TFB低、中、高剂量组小鼠按60、120、240 mg/kg灌胃TFB溶液,正常
          对照组和LPS组小鼠灌胃等体积生理盐水,每日1次,连续给药21 d。从给药第15天起,除正常对照组外,其余组小鼠连续7 d腹
          腔注射LPS(400 μg/kg)建立神经炎症模型。末次给药4 h后麻醉小鼠取脑组织。观察小鼠神经元形态变化,检测小鼠脑组织中一
          氧化氮(NO)和肿瘤坏死因子α(TNF-α)、白细胞介素1β(IL-1β)、IL-6、IL-10的含量,检测小鼠脑组织中炎症通路相关蛋白[诱导
          型NO合酶(iNOS)、环氧合酶2(COX-2)、髓样分化因子88(Myd88)及蛋白激酶C(PKC)]的表达。结果  与正常对照组相比,LPS
          组小鼠脑组织的海马区神经元排列稀疏紊乱,大量神经元固缩,核缩小;脑组织中TNF-α、IL-1β、IL-6、NO含量均显著增加,IL-10
          含量显著降低,iNOS、COX-2、Myd88、PKC蛋白相对表达量均显著升高(P<0.05)。与LPS组相比,TFB低、中、高剂量组小鼠脑组
          织神经元病理变化明显改善,脑组织中上述指标变化均显著逆转(P<0.05)。结论  TFB具有抑制神经炎症的作用,其作用机制可
          能与下调炎症通路相关蛋白iNOS、COX-2、Myd88和PKC表达,减少炎症因子释放有关。
          关键词  鬼针草总黄酮;脂多糖;神经炎症;炎症因子

          Improvement  effects  and  mechanism  of  total  flavonoids  of  Bidens  pilosa  on  lipopolysaccharide-induced

          neuroinflammation in mice
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                        1
                                        1, 2
          TANG Fengman ,PANG Xiaojun ,XIE Yan ,LIU Chunfang (1.  College  of  Pharmacy,  Guangxi  Medical
          University, Nanning 530021, China;2. Dept. of Pharmacy, the Second People’s Hospital of Qinzhou, Guangxi
          Qinzhou 535000, China)
          ABSTRACT   OBJECTIVE  To  investigate  the  effect  and  mechanism  of  total  flavonoids  of  Bidens  pilosa  L. (TFB)  on
          lipopolysaccharide (LPS)-induced neuroinflammation in mice. METHODS Fifty C57BL/6 mice were randomly divided into normal
          control  group,  LPS  group  and  TFB  low-dose,  medium-dose  and  high-dose  groups,  with  10  mice  in  each  group.  TFB  low-dose,
          medium-dose  and  high-dose  groups  were  given  TFB  solution  intragastrically  at  60,  120  and  240  mg/kg,  and  the  normal  control
          group and LPS group were given corresponding volume of normal saline, once a day, for consecutive 21 d. From the 15th day of
          administration, except for the normal control group, other groups were given LPS (400 μg/kg) intraperitoneally for 7 consecutive
          days  to  establish  neuroinflammatory  model.  Brain  tissues  were  taken  under  anesthesia  4  h  after  the  final  administration.  The
          morphological changes of neuronal cells in mice were observed; the contents of nitric oxide (NO), tumor necrosis factor α (TNF-
          α),  interleukin-1β (IL-1β),  IL-6  and  IL-10  were  measured,  and  the  expressions  of  inflammatory  pathway-related  proteins
          [inducible  NO  synthase (iNOS),  cyclooxygenase-2 (COX-2),  myeloid  differentiation  factor  88 (Myd88)  and  protein  kinase  C
         (PKC)] were measured in the brain tissues of mice. RESULTS Compared with the normal control group, the neuronal arrangement
          in the hippocampal region of the brain tissue of mice in the LPS group was sparsely disorganized, with a large number of neuronal
          fixations  and  shrunken  nuclei;  the  contents  of  TNF-α,  IL-1β,  IL-6  and  NO  in  the  brain  tissue  were  significantly  increased,  the
          contents  of  IL-10  were  significantly  decreased,  and  the  relative  expressions  of  iNOS,  COX-2,  Myd88  and  PKC  proteins  were
          significantly  increased (P<0.05).  Compared  with  the  LPS  group,  the  neuronal  pathological  changes  in  the  brain  tissue  of  mice  in
                                                             the  TFB  low-dose,  medium-dose  and  high-dose  groups  were
             Δ  基金项目 钦 州 市 科 学 研 究 与 技 术 开 发 计 划 项 目(No.
          202014810)                                         significantly  improved,  and  the  changes  of  the  above  indices
             *第一作者 硕士研究生。研究方向:药理学。E-mail:tangfman@           in  the  brain  tissue  were  significantly  reversed (P<0.05).
          163.com
                                                             CONCLUSIONS     TFB   has   an   inhibitory   effect   on
             # 通信作者 主任药师,硕士。研究方向:临床药学和中药药理学。
          E-mail:pangxjun@163.com                            neuroinflammation,  and  its  mechanism  of  action  may  be


          中国药房  2023年第34卷第14期                                              China Pharmacy  2023 Vol. 34  No. 14    · 1719 ·
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