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ID:34313360
大小:3.33 MB
页数:50页
时间:2019-03-05
《小半夏汤对水貂呕吐模型作用机制研究》由会员上传分享,免费在线阅读,更多相关内容在学术论文-天天文库。
1、小半夏汤对水貂呕吐模型作用机制研究摘要目的本文对经方《金匮》小半夏汤按原方配伍对半夏、生姜各自的有效成分进行提取,制成质量稳定,方便携带的颗粒制剂,在新型水貂呕吐模型上研究小半夏汤(smallpinelliaedecoction,XBXT)&呕作用及机制。方法用顺铂(7.5mg.kg。1)、阿朴吗啡(1.6mg·kg"1)制备水貂呕吐模型。提取XBXT(半夏:生姜=1:1)有效成分制备成颗粒,给予水貂灌(翊XBXT(相当于给予4.0,1.0g'kg"1生药量)30rnin后,再腹腔注射(功顺铂或阿朴吗啡,研究XBXT对外周和中枢性两种呕吐模型的抑制作用及机制
2、。结果XBXT可抑制顺铂(72h内)引起的急性和延迟性呕吐,减少干呕和呕吐次数并延长呕吐潜伏期(尸3、MechanismofSmallPinelliaeDecocnononMinkVomitModelAbstract0bjective:SmallPinelliaeDecoction(XBXT)isfromtheEasternHanZhangZhongjing’s”GoldenChamber”.XBXTconsistsofPinelliaTuberandGinger.WeextractedtheactiveingredientsfromXBXTtomakethegranulesandusedcisplatinandapomorphinetopreparemin4、kvomitingmodelbygavagetostudytheantiemeticeffectofXBXTanditsmechanism.Methods:TheactiveingredientswereextractedfromXBXT(pinelliatuber:ginger=l:1)tomakethegranules.Cisplatin(7.5mg·kg~,ip)andapomorphine(1.6mg·k91,ip)wereusedtoprepareminkvomitingmodel.After30minofXBXT(equivalentto4.0,5、1.Og·k91crudedrug)ig.adminstration,minkswereadministeredofcisplatinormorphinetostudytheinhibitoryeffectandmechanismofXBXTonthetwomodelsofvomiting.Results:XBXTcouldinhibitacuteanddelayedvomitinginducedbycisplatin(within72h)intheminks,reducethenumberofretchingandvomiting(P6、ngthelatencytovomit(P<0.01),andinhibittheexpressionofNKlreceptorincentral(theareapostrema)andperipheral(ileumtissue)tissues(P7、sion:XBXTCaninhibitvomitinginducedbycisplatinandapomorphine,anditsmechanismisrelatedtotheinhibitionofcentralandperipheralNKlreceptorexpression.Postgraduatestudent:RenXu-ying(Pharmacology)DirectedbyProfessor:YueWangKeywords:smallpinelliaedecoction(XBXT);mink;vomiting;cisplatin;apomo8、rphine目录引言⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯
3、MechanismofSmallPinelliaeDecocnononMinkVomitModelAbstract0bjective:SmallPinelliaeDecoction(XBXT)isfromtheEasternHanZhangZhongjing’s”GoldenChamber”.XBXTconsistsofPinelliaTuberandGinger.WeextractedtheactiveingredientsfromXBXTtomakethegranulesandusedcisplatinandapomorphinetopreparemin
4、kvomitingmodelbygavagetostudytheantiemeticeffectofXBXTanditsmechanism.Methods:TheactiveingredientswereextractedfromXBXT(pinelliatuber:ginger=l:1)tomakethegranules.Cisplatin(7.5mg·kg~,ip)andapomorphine(1.6mg·k91,ip)wereusedtoprepareminkvomitingmodel.After30minofXBXT(equivalentto4.0,
5、1.Og·k91crudedrug)ig.adminstration,minkswereadministeredofcisplatinormorphinetostudytheinhibitoryeffectandmechanismofXBXTonthetwomodelsofvomiting.Results:XBXTcouldinhibitacuteanddelayedvomitinginducedbycisplatin(within72h)intheminks,reducethenumberofretchingandvomiting(P6、ngthelatencytovomit(P<0.01),andinhibittheexpressionofNKlreceptorincentral(theareapostrema)andperipheral(ileumtissue)tissues(P7、sion:XBXTCaninhibitvomitinginducedbycisplatinandapomorphine,anditsmechanismisrelatedtotheinhibitionofcentralandperipheralNKlreceptorexpression.Postgraduatestudent:RenXu-ying(Pharmacology)DirectedbyProfessor:YueWangKeywords:smallpinelliaedecoction(XBXT);mink;vomiting;cisplatin;apomo8、rphine目录引言⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯
6、ngthelatencytovomit(P<0.01),andinhibittheexpressionofNKlreceptorincentral(theareapostrema)andperipheral(ileumtissue)tissues(P7、sion:XBXTCaninhibitvomitinginducedbycisplatinandapomorphine,anditsmechanismisrelatedtotheinhibitionofcentralandperipheralNKlreceptorexpression.Postgraduatestudent:RenXu-ying(Pharmacology)DirectedbyProfessor:YueWangKeywords:smallpinelliaedecoction(XBXT);mink;vomiting;cisplatin;apomo8、rphine目录引言⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯
7、sion:XBXTCaninhibitvomitinginducedbycisplatinandapomorphine,anditsmechanismisrelatedtotheinhibitionofcentralandperipheralNKlreceptorexpression.Postgraduatestudent:RenXu-ying(Pharmacology)DirectedbyProfessor:YueWangKeywords:smallpinelliaedecoction(XBXT);mink;vomiting;cisplatin;apomo
8、rphine目录引言⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯⋯
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