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ID:23166661
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时间:2018-11-04
《透骨消痛颗粒干预oa早期cox-2和inos表达的实验研究》由会员上传分享,免费在线阅读,更多相关内容在工程资料-天天文库。
1、透骨消痛颗粒干预OA早期COX-2和iNOS表达的实验研究高雪伟摘要:目的通过动物试验探讨透骨消痛颗粒对骨性关节炎早期环氧化酶-2(COX-2)和诱导性一氧化氮合酶(iNOS)表达的影响,研究透骨消痛颗粒在膝骨性关节炎治疗中的相关作用机制。方法新西兰大白兔采用改Hulth法造模,造模成功后随机分成3组:模型组、对照组、实验组,和正常组共4组,分别灌胃给药4周后处死动物取材并观测如下指标:关节腔大体观察,滑膜与软骨组织学观察;关节液内NO、NOS、PGE2含量检测,滑膜软骨中iNOS、COX-2含量检测。结果4周
2、后关节液中NO、NOS含量、PGE2浓度,滑膜和软骨中iNOS、COX-2含量,模型组、对照组、实验组均呈高表达,与正常组比较差异有显著性(P〈0.05);对照组、实验组与模型组比较差异有显著性(P〈0.05);对照组与实验组比较差异有显著性(P〈0.05)。结论透骨消痛颗粒可通过抑制COX-2和iNOS在OA早期滑膜和软骨细胞中的表达及其诱导产物PGE2和NO的生成,从而达到控制OA早期炎症、减轻疼痛、缓解症状的作用关键词:透骨消痛颗粒骨性关节炎滑膜软骨COX-2iNOSNOPGE2TheExperiment
3、alResearchaboutgranulaofpenetratingboneremoveingpainintervenetheexpressionofCOX-2andiNOSinearlystageofosteoarthritisXueweiGao,JinshuiZhou,BolingLiuAbstractObjective:Toinvestgatethemechanismofinfluenceaboutgranulaofpenetratingboneremoveingpainintervenetheexpr
4、essionofCOX-2andiNOSinearlystageofosteoarthritisbyanimalsexperiment,toinvestgatemechanismofgranulaofpenetratingboneremoveingpainontreatmentofosteoarthritis.Methods:WedevidedtheNewZealandrabbitsinto3groupsrandomlyafterreplicatedkneeosteoarthritiswithmodifiedH
5、ulthmodelingmcthod:modclgroup.controlgroup,experimentalgroup,withthenormalgroupwere4groupsintotal,wcexecuteallrabbitsaftcrtheywerefedintragasticallyfor4wcckcs.Thenthefollowingdetectionweretakenout:GeneralObservationofarticularcavity;histologicalConversationo
6、fsynoviumandcartilage;contentofNOS,NO,testofiNOSmRNA,concentrationofCOX-2andPGE2withinjoint.ResuIts:Afterfourweekes,therewassignificantcontrast(P<0.05)oftheconcentofNOS,NO,iNOSmRNA,COX-2andPGE2ofmodelgroup,controlgroup,experimentalgroupcomparedwiththenormalg
7、roup;Therewassignificantcontrast(P<0.05)oftheconcentofNOS,NO,iNOSmRNA,COX-2andPGE2ofexperimentalgroupsandcontrolgroupcomparedwiththemodelgroup;Therewassignificantcontrast(P<0.05)oftheconcentofNOS,NO,iNOSmRNA,COX-2andPGE2ofexperimentalgroupcomparedwithcontrol
8、group.ConclusioiuThegranulaofpenetratingboneremoveingpaincancontrolinflammation,relievepainsandalleviatesymptomsinearlystageofosteoarthritisbyinhibitingtheexpressionofCOX-2andiNOSwithincartilage
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