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基于代谢组学研究蒙药苏格木勒-4对失眠大鼠的改善作用机制                                                                     Δ



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          李艳佳 ,杨 蕊 ,王 昇 ,孙利东 ,白东浩 ,靳尚武 (1.内蒙古医科大学公共卫生学院,呼和浩特 010020;
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          2.呼和浩特市疾病预防控制中心质控科,呼和浩特 010010;3.鄂尔多斯市疾病预防控制中心,内蒙古 鄂尔多斯
          017010;4.鄂尔多斯市第四人民医院,内蒙古 鄂尔多斯 017008)
          中图分类号  R285;R917      文献标志码  A      文章编号  1001-0408(2024)01-0038-06
          DOI  10.6039/j.issn.1001-0408.2024.01.07

          摘   要  目的  研究蒙药苏格木勒-4对失眠大鼠的代谢影响,初步探讨其改善失眠的可能机制。方法  采用夹尾刺激和腹腔注射
          对氯苯丙氨酸溶液复合造模法建立慢性应激失眠大鼠模型。将 24 只雄性大鼠随机分为正常组、模型组、地西泮组(阳性对照,
          0.92 mg/kg)和苏格木勒-4组(5.2 g/kg),每组6只。从夹尾刺激第7天开始,苏格木勒-4组、地西泮组大鼠开始灌胃给药,正常组、
          模型组大鼠灌胃等体积蒸馏水,每天灌胃1次,连续14 d。利用水迷宫实验测试大鼠的学习和记忆能力,利用无创睡眠活动监测
          系统对大鼠24 h睡眠时间进行监测。采用超高效液相色谱串联质谱技术对大鼠血清和海马组织进行代谢组学研究。使用多元统
          计分析方法对各组大鼠血清和海马组织中差异代谢物进行分析,筛选各组间的差异代谢物以及代谢通路。结果  与正常组比较,
          模型组大鼠的逃避潜伏期显著延长、穿越平台次数显著减少、平均24 h睡眠时间百分比显著降低(P<0.05)。与模型组比较,地西
          泮组和苏格木勒-4组大鼠上述指标水平均显著改善(P<0.05)。代谢组学研究发现,大鼠血清和海马组织中共鉴定出5-羟基吲哚
          乙酸、犬尿氨酸、犬尿喹啉酸、5-羟色胺、硫酸苯酚、1-羧基乙基酪氨酸、3-(4-羟基苯基)乳酸、N-乙酰基酪氨酸、酪氨酸共9个差异代
          谢物,主要涉及色氨酸和酪氨酸2条代谢通路。结论  苏格木勒-4可以改善失眠大鼠睡眠时间和行为学表现,其机制可能与调节
          色氨酸、酪氨酸等氨基酸代谢途径有关。
          关键词  蒙药;苏格木勒-4;失眠;代谢组学;氨基酸代谢

          Metabolomics-based study on the improvement mechanism of the Mongolian drug Sugemule-4 on insomnia
          rats
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          LI Yanjia ,YANG Rui ,WANG Sheng ,SUN Lidong ,BAI Donghao ,JIN Shangwu(1. School of Public Health,
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          Inner  Mongolia  Medical  University,  Hohhot  010020,  China;2.  Hohhot  Center  for  Disease  Control  and
          Prevention, Hohhot 010010, China;3. Ordos Center for Disease Control and Prevention, Inner Mongolia Ordos
          017010, China;4. The Fourth People’s Hospital of Ordos, Inner Mongolia Ordos 017008, China)
          ABSTRACT    OBJECTIVE To study the effects of the Mongolian medicine Sugemule-4 on the metabolism of insomnia rats, and
          to preliminarily explore its possible mechanisms for improving insomnia. METHODS The rat model of chronic stress insomnia was
          established  by  tail  clipping  stimulation  and  intraperitoneal  injection  of  p-chlorophenyl  alanine  solution. Twenty-four  male  rats  were
          randomly  divided  into  the  normal  group,  model  group,  diazepam  group (positive  control,  0.92  mg/kg),  and  Sugemule-4  group
         (5.2  g/kg),  with  6  rats  in  each  group.  Since  the  7th  day  of  tail  clipping  stimulation,  the  Sugemule-4  group  and  diazepam  group
          began  to  be  intragastrically  administered  with  relevant  medicine;  the  normal  group  and  model  group  were  intragastrically
          administered  with  an  equal  volume  of  distilled  water,  once  a  day,  for  14  consecutive  days.  The  learning  and  memory  abilities  of
          rats were tested using a water maze experiment, and the non-invasive sleep activity monitoring system was used to monitor the 24-
          hour sleep time of rats. A metabolomics study was conducted on rat serum and hippocampal tissue by using ultra-high-performance
          liquid chromatography-tandem mass spectrometry. The multivariate statistical analysis method was adopted to analyze the differential
          metabolites  in  serum  and  hippocampal  tissue  of  rats,  and  screen  for  differential  metabolites  and  metabolic  pathways  among  those
          groups. RESULTS Compared with the normal group, the escape latency of rats in the model group was significantly increased, the
          times of crossing platforms were significantly reduced, and the percentage of average 24-hour sleep time was significantly reduced
         (P<0.05).  Compared  with  the  model  group,  the  levels  of  the  above  indicators  were  significantly  reversed  in  the  diazepam  group
          and Sugemule-4 group (P<0.05). Metabolomics studies found that a total of 9 differential metabolites were identified in rat serum
          and  hippocampal  tissue,  including  5-hydroxyindoleacetic  acid,  canine  urate,  canine  urinary  quinolinic  acid,  5-hydroxytryptamine,
                                                              phenol  sulfate,  1-carboxyethyltyrosine,  3-(4-hydroxyphenyl)
              Δ 基金项目 内蒙古自治区科技计划项目(No.2019GG120)
             *第一作者 医师,硕士。研究方向:药效物质基础。E-mail:                  lactate,  N-acetyl  tyrosine,  tyrosine  and  phenol  sulfate,  mainly
          15771377839@163.com                                 involving  2  metabolic  pathways  of  tryptophan  and  tyrosine.
              # 通信作者 主任技师,硕士生导师,博士。研究方向:药物药性理                 CONCLUSIONS  Sugemule-4  can  improve  the  sleep  time  and
          论及药效物质基础。E-mail:swjsw1981@163.com                   behavioral  performance  of  insomnia  rats,  and  its  mechanism


          · 38 ·    China Pharmacy  2024 Vol. 35  No. 1                                中国药房  2024年第35卷第1期
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