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玉屏风加味鼻喷剂对 AR 模型大鼠鼻黏膜损伤的保护作用及机

          制研究
                     Δ


                *
          习 媛 ,贺心宁,刘玉崟,张 娜,刘 婷,梁方琪,田 理(成都中医药大学附属医院耳鼻喉科,成都
                                                                  #
          610032)

          中图分类号  R965;R276.1      文献标志码  A      文章编号  1001-0408(2023)10-1204-07
          DOI  10.6039/j.issn.1001-0408.2023.10.10

          摘   要  目的  研究玉屏风加味鼻喷剂(YPF+)对变应性鼻炎(AR)模型大鼠鼻黏膜损伤的保护作用及潜在机制。方法  以卵清蛋
          白(OVA)诱导建立大鼠AR模型。将造模成功的大鼠随机分为模型组、YPF+组(每侧50 μg,每天2次)和阳性对照组(糠酸莫米松
          鼻喷雾剂,每侧50 μg,每天1次),并设空白组,每组10只。各药物组大鼠给予相应药物,空白组和模型组大鼠给予等量生理盐水,
          连续 4 周。末次给药结束 30 min 后,记录各组大鼠的行为评分,观察其鼻黏膜组织的病理改变;检测其鼻黏膜组织中活性氧
         (ROS)水平,核苷酸结合寡聚化结构域样受体蛋白3(NLRP3)、胱天蛋白酶1(caspase-1)、gasdermin D(GSDMD)蛋白及mRNA的
          表达水平,以及血清中白细胞介素1β(IL-1β)、IL-18含量。结果  与空白组比较,模型组大鼠鼻黏膜组织结构紊乱,炎症细胞浸润
          严重,并可见固有层血管扩张;其行为学评分和病理评分,鼻黏膜组织中ROS水平,NLRP3、caspase-1、GSDMD蛋白及其mRNA的
          表达水平,以及血清IL-1β、IL-18含量均显著升高(P<0.05)。与模型组比较,各药物组大鼠鼻黏膜损伤症状均有不同程度改善,
          上述指标均显著降低(P<0.05)。结论  YPF+可改善大鼠鼻黏膜损伤,减轻其喷嚏、鼻痒、鼻涕等AR症状,这种作用可能与其减少
          鼻黏膜ROS产生、下调NLRP3/caspase-1/GSDMD通路有关。
          关键词  玉屏风加味鼻喷剂;变应性鼻炎;NLRP3/caspase-1/GSDMD通路;活性氧


          Study  on  protective  effect  and  mechanism  of  Modified Yupingfeng  nasal  spray  on  nasal  mucosal  injury  in
          AR model rats
          XI Yuan,HE Xinning,LIU Yuyin,ZHANG Na,LIU Ting,LIANG Fangqi,TIAN Li (Dept.  of
          Otorhinolaryngology,  the Affiliated  Hospital  of  Chengdu  University  of  Traditional  Chinese  Medicine,  Chengdu
          610032, China)

          ABSTRACT    OBJECTIVE  To  study  protective  effect  and  potential  mechanism  of  Modified  yupingfeng  nasal  spray (YPF+)  on
          nasal mucosal injury in allergic rhinitis (AR) model rats. METHODS AR model was induced by ovalbumin (OVA) and randomly
          divided into model group, YPF+group (50 µg/side,twice a day), positive control group (Mometasone furoate aqueous nasal spray,
          50  µg/side,once  a  day);  the  blank  group  was  set  up,  with  10  rats  in  each  group.  Administration  groups  were  given  relevant
          medicine, and blank group and model group were given equivalent normal saline for consecutive 4 weeks. Thirty minutes after last
          medication,  the  behavioral  scores  of  rats  were  recorded,  and  the  pathological  changes  of  their  nasal  mucosa  tissue  were  observed.
          The level of reactive oxygen species (ROS) in nasal mucosa tissue was detected. The protein and mRNA expressions of nucleotide-
          binding oligomerization domain-like receptor protein 3 (NLRP3),caspase-1,gasdermin D (GSDMD) were detected; the contents of
          interleukin-1β (IL-1β)  and  IL-18  in  serum  were  also  determined.  RESULTS  Compared  with  blank  group,  in  model  group,  the
          nasal  mucosa  tissue  structure  was  disordered,  inflammatory  cells  infiltrated  seriously,  and  lamina  propria  vascular  dilation  was
          visible;  its  behavioral  score  and  pathological  score,  the  level  of  ROS,  protein  and  mRNA  expressions  of  NLRP3,  caspase-1  and
          GSDMD, serum contents of IL-1β and IL-18 in nasal mucosa tissue were increased significantly (P<0.05). Compared with model
          group,  the  symptoms  of  nasal  mucosal  injury  in  rats  of  each  drug  group  were  improved  to  varying  degrees,  and  the  above
          indicators  were  significantly  reduced (P<0.05).  CONCLUSIONS  YPF+  may  improve  nasal  mucosal  injury  of  rats,  relieve  AR
          symptoms  such  as  sneezing,  itchy  nose,  runny  nose,  the  mechanism  of  which  may  be  associated  with  reducing  the  production  of
                                                              ROS  in  nasal  mucosa  and  downregulating  NLRP3/caspase-1/
              Δ 基金项目 四川省科技计划项目(No.2021YFS0036);四川省中
                                                              GSDMD pathway.
          医药院士后备人才培养项目(No.2100601)                            KEYWORDS    Modified  yupingfeng  nasal  spray;  allergic
             *第一作者 医师,硕士研究生。研究方向:中医药防治变态反应
          性耳鼻咽喉疾病的基础。E-mail:2418079767@qq.com                 rhinitis;  NLRP3/caspase-1/GSDMD  pathway;  reactive  oxygen
                                                              species
              # 通信作者 主任医师,教授,博士生导师。研究方向:中医药防治
          变态反应性耳鼻咽喉疾病。E-mail:ctcmdan@stu.cdutcm.edu.cn


          · 1204 ·    China Pharmacy  2023 Vol. 34  No. 10                            中国药房  2023年第34卷第10期
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