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麻黄与杏仁配伍后在支气管哮喘模型大鼠体内的药动学研究
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          陈林林 ,谢金根,樊学程,饶 倩,杨添翼,田佳玉,肖 雄,高文军,李文宏(江西中医药大学药学院,南昌
          330004)

          中图分类号  R969.1      文献标志码  A      文章编号  1001-0408(2024)13-1588-06
          DOI  10.6039/j.issn.1001-0408.2024.13.08

          摘   要  目的  研究麻黄与杏仁配伍后在支气管哮喘模型大鼠血浆和脑脊液中的药动学变化。方法  将SD雄性大鼠随机分为空
          白组、模型组、麻黄组(12 g/kg,以生药量计,下同)、杏仁组(6 g/kg)和麻黄-杏仁药对组(麻黄12 g/kg+杏仁6 g/kg),每组6只。除空
          白组外,其余各组大鼠用2%氯化乙酰胆碱和0.4%磷酸组胺的等体积混合液喷雾诱发支气管哮喘模型,每天1次,连续7 d。每次
          造模前1 h,各组大鼠灌胃相应药物/生理盐水,每天1次,连续7 d。末次给药并激发哮喘后,分别在不同时间点进行采血和脑脊液
          收集。将血浆与脑脊液样品预处理后(以葛根素为内标),采用液相色谱-串联质谱法检测两种样品中麻黄碱/伪麻黄碱、甲基麻黄
          碱和苦杏仁苷的质量浓度。采用DAS 2.0药动学软件通过非房室模型确定主要药动学参数,并比较两药配伍前后药动学参数的
          变化。结果  与麻黄组比较,麻黄-杏仁药对组大鼠血浆和脑脊液中麻黄碱/伪麻黄碱、甲基麻黄碱的cmax、AUC0-21.33 h (或AUC0-10.67 h )均
          显著减少,CLZ/F、VZ/F均显著增加(P<0.05或P<0.01);脑脊液中甲基麻黄碱的tmax显著缩短(P<0.05)。与杏仁组比较,麻黄-杏
          仁药对组大鼠血浆中苦杏仁苷的t1/2显著缩短,CLZ/F显著增加(P<0.01);脑脊液中苦杏仁苷的tmax显著缩短,AUC0-10.67 h、CLZ/F、VZ/F
          均显著增加(P<0.01)。结论  麻黄、杏仁配伍后加快了麻黄生物碱的吸收和消除,从而减少了麻黄生物碱在支气管哮喘模型大鼠
          体内的累积。
          关键词  麻黄;杏仁;配伍;哮喘;药动学

          Pharmacokinetic  study  of  the  complication  of  Ephedra  sinica  and  Prunus  armeniaca  in  bronchial  asthma
          model rats
          CHEN Linlin,XIE Jingen,FAN Xuecheng,RAO Qian,YANG Tianyi,TIAN Jiayu,XIAO Xiong,GAO Wenjun,
          LI Wenhong(School of Pharmacy, Jiangxi University of Chinese Medicine, Nanchang 330004, China)

          ABSTRACT    OBJECTIVE  To  study  the  pharmacokinetic  changes  in  the  plasma  and  cerebrospinal  fluid  of  bronchial  asthma
          model  rats  after  the  complication  of  Ephedra  sinica  and  Prunus  armeniaca.  METHODS  SD  male  rats  were  randomly  divided  into
          blank group, model group, E. sinica group (12 g/kg, calculated by raw drug, similarly hereinafter), P. armeniaca group (6 g/kg)
          and  E.  sinica-P.  armeniaca  drug-pair  group (12  g/kg  of  E.  sinica+6  g/kg  of  P.  armeniaca),  with  6  rats  in  each  group.  Except  for
          the  blank  group,  the  bronchial  asthma  model  was  induced  by  spraying  rats  in  each  group  with  an  equal  volume  mixture  of  2%
          acetylcholine  chloride  and  0.4%  histamine  phosphate,  once  a  day,  for  7  d.  One  hour  before  modeling  every  time,  rats  in  each
          group were gavaged with the corresponding drug/normal saline, once a day, for 7 d. After the final administration and provocation
          of  asthma,  blood  and  cerebrospinal  fluid  collection  were  performed  at  different  time  points.  The  plasma  and  cerebrospinal  fluid
          samples were pre-treated (with geranylgeranyl as the internal standard), and the mass concentrations of ephedrine/pseudoephedrine,
          methyl  ephedrine  and  amygdalin  in  both  samples  were  determined  by  liquid  chromatography-tandem  mass  spectrometry.  DAS  2.0
          pharmacokinetic software was used to determine the main pharmacokinetic parameters through the non-atrial chamber model and to
          compare  the  changes  of  the  pharmacokinetic  parameters  before  and  after  the  combination  of  the  two  drugs.  RESULTS  Compared
          with  E.  sinica  group,  cmax  and  AUC0-21.33 h (or  AUC0-10.67 h )  of  ephedrine/pseudoephedrine  and  methyl  ephedrine  in  the  plasma  and
          cerebrospinal  fluid  of  rats  were  significantly  reduced  in  E.  sinica-P.  armeniaca  drug-pair  group,  while  CLZ/F  and  VZ/F  were
          significantly  increased (P<0.05  or  P<0.01);  tmax  of  methyl  ephedrine  in  the  cerebrospinal  fluid  was  significantly  shortened (P<
          0.05).Compared with P. armeniaca group, the t1/2 of amygdalin in the plasma of rats in E. sinica-P. armeniaca drug-pair group was
          significantly shortened, and CLZ/F was significantly increased (P<0.01); the tmax of bitter amygdalin in the cerebrospinal fluid was
          significantly  shortened,  and  the  AUC0-10.67 h,  CLZ/F,  and  VZ/F  were  significantly  increased (P<0.01).  CONCLUSIONS  The
                                                              combination  of  E.  sinica  and  P.  armeniaca  accelerates  the
              Δ  基金项目 国 家 自 然 科 学 基 金 项 目(No. 82060790,No.
                                                              absorption  and  elimination  of  ephedra  alkaloids,  thus  reducing
          82360856);江西省自然科学基金资助项目(No.20202ACBL206031)
             *第一作者 硕士研究生。研究方向:中药药理学。E-mail:                   the  accumulation  of  ephedra  alkaloids  in  the  bronchial  asthma
          837876682@qq.com                                    model rats.
              # 通信作者 教授,硕士生导师。研究方向:中药药理学。E-mail:              KEYWORDS    Ephedra sinica; Prunus armeniaca; complica-
          liwhong0311@163.com                                 tion; asthma; pharmacokinetics


          · 1588 ·    China Pharmacy  2024 Vol. 35  No. 13                            中国药房  2024年第35卷第13期
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