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PNU-282987对颞叶癫痫模型大鼠认知功能的影响及机制                                                           Δ



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          李永格 ,周 舒 ,刘庆春 ,未小明 ,张 冬 ,马凤巧(1. 南阳医学高等专科学校基础医学部,河南 南阳
                 1*
                           1, 2
          473000;2.昆明医科大学生物医学工程研究中心,昆明 650000)
          中图分类号  R965      文献标志码  A      文章编号  1001-0408(2023)19-2350-06
          DOI  10.6039/j.issn.1001-0408.2023.19.09
          摘   要  目的  研究特异性α7烟碱型乙酰胆碱受体(α7nAChR)激动剂PNU-282987对颞叶癫痫(TLE)模型大鼠认知功能的影响
          及机制。方法  将 60 只大鼠随机分为对照组、模型组、PNU-282987 组(3 mg/kg)和甲基牛扁亭(MLA)+PNU-282987 组(6 mg/kg
          MLA+3 mg/kg PNU-282987),每组15只。除对照组之外,其余各组大鼠均制备TLE模型。造模成功后,各组大鼠腹腔注射相应药
          物或生理盐水,每天1次,连续2周。观察大鼠癫痫发作行为并进行评分,记录发作持续时间;检测大鼠认知功能;观察海马组织
          CA1区神经元病理学形态;检测海马组织中肿瘤坏死因子α(TNF-α)、白细胞介素6(IL-6)和IL-1β水平;检测海马组织中离子钙
          接头蛋白1(IBA-1)阳性表达和α7nAChR、核因子κB(NF-κB)p65、磷酸化NF-κB p65(p-NF-κB p65)蛋白表达水平。结果  与模型
          组比较,PNU-282987 组大鼠癫痫评分和发作持续时间,海马组织中 IBA-1 阳性细胞数量和 TNF-α、IL-6、IL-1β 水平以及 NF-κB
          p65、p-NF-κB p65蛋白表达水平均显著减少/降低(P<0.05);逃避潜伏期时间显著缩短(P<0.05),原平台象限停留时间及穿越平
          台次数均显著增加(P<0.05);海马组织 CA1 区神经元损伤明显减轻;海马组织中 α7nAChR 蛋白表达水平显著升高(P<0.05)。
          与PNU-282987组比较,MLA+PNU-282987组大鼠上述指标均显著逆转(P<0.05)。结论  PNU-282987可改善TLE模型大鼠的认
          知功能障碍,其机制可能是通过激活α7nAChR/NF-κB信号通路,抑制小胶质细胞介导的炎症反应,进而减轻海马神经元损伤。
          关键词  PNU-282987;癫痫;α7nAChR/NF-κB信号通路;小胶质细胞;炎症反应


          Effect and mechanism of PNU-282987 on cognitive function of temporal lobe epilepsy model rats
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          LI Yongge ,ZHOU Shu ,LIU Qingchun ,WEI Xiaoming ,ZHANG Dong ,MA Fengqiao(1.  Dept.  of  Basic
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          Medicine,  Nanyang  Medical  College,  Henan  Nanyang  473000,  China;2.  Biomedical  Engineering  Research
          Center, Kunming Medical University, Kunming 650000, China)
          ABSTRACT    OBJECTIVE  To  investigate  the  effect  and  mechanism  of  α7  nicotinic  acetylcholine  receptor (α7nAChR)  agonists
          PNU-282987 on cognitive function in temporal lobe epilepsy (TLE) model rats. METHODS Sixty rats were randomly divided into
          control group, model group, PNU-282987 group (3 mg/kg) and methyllycaconitine (MLA)+PNU-282987 group (6 mg/kg MLA+3
          mg/kg  PNU-282987),  with  15  rats  in  each  group.  Except  for  control  group,  the  TLE  model  was  established  in  the  other  groups.
          After  the  model  was  successfully  established,  each  group  was  given  relevant  medicine  or  normal  saline  intraperitoneally,  once  a
          day,  for  two  consecutive  weeks. The  epilepsy  attack  of  rats  was  observed  and  scored,  and  the  duration  of  seizures  was  recorded;
          the  cognitive  function  of  rats  was  detected;  pathological  morphology  of  neurons  in  CA1  region  was  observed;  the  levels  of  tumor
          necrosis  factor-α (TNF-α),  interleukin-6 (IL-6)  and  IL-1β  in  the  hippocampus  were  detected;  the  positive  expressions  of  ionized
          calcium-binding adapter molecule-1 (IBA-1), α7nAChR, nuclear factor-κB (NF-κB) p65, p-NF-κB p65 in the hippocampus were
          detected.  RESULTS  Compared  with  model  group,  the  score  and  duration  of  seizures,  the  number  of  IBA-1  positive  cells,  the
          levels  of  TNF- α,  IL-6  and  IL-1β,  the  expressions  of  NF- κB  p65  and  p-NF- κB  p65  protein  decreased  significantly  in  the
          hippocampus (P<0.05);  the  escape  latency  time  was  shortened  significantly (P<0.05),  the  time  spent  in  the  original  platform
          quadrant  and  times  of  crossing  the  platform  increased  significantly (P<0.05);  neuronal  damage  in  the  CA1  region  of  the
          hippocampus  was  significantly  reduced;  the  expression  of  α7nAChR  protein  increased  significantly  in  hippocampus (P<0.05).
          Compared with PNU-282987 group, the above indexes of rats in MLA+PNU-282987 group were reversed significantly (P<0.05).
          CONCLUSIONS PNU-282987 could improve cognitive dysfunction in TLE model rats, and its mechanism may be associated with
          inhibiting  microglia-mediated  inflammatory  response  through  α7nAChR/NF- κB  signaling  pathway,  thus  reducing  hippocampal
          neuronal damage.
          KEYWORDS     PNU-282987; epilepsy; α7nAChR/NF-κB signaling pathway; microglia; inflammatory response


              Δ 基金项目 河南省科技发展计划项目(No.212102310837);河南              癫痫是由脑神经元突发异常放电导致神经系统功
          省高等学校青年骨干教师培养计划项目(No.2018GGJS253);南阳市
                                                              能障碍的常见慢性脑部疾病。癫痫患者中有约 30%~
          科技计划项目(No.JCQY026)
             *第一作者 副教授,硕士。研究方向:癫痫发生机制与治疗。                     40% 会发展成为药物难治性癫痫,临床上以颞叶癫痫
                                                                                                [1]
          E-mail:liyongge19810719@aliyun.com                 (temporal lobe epilepsy,TLE)最为常见 。TLE 易反复

          · 2350 ·    China Pharmacy  2023 Vol. 34  No. 19                            中国药房  2023年第34卷第19期
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