药学实践杂志
藥學實踐雜誌
약학실천잡지
THE JOURNAL OF PHARMACEUTICAL PRACTICE
2014年
3期
209-211,219
,共4页
韩琳%吕超%李敏%黄慧梅%畅婉琳%彭成成%柳润辉
韓琳%呂超%李敏%黃慧梅%暢婉琳%彭成成%柳潤輝
한림%려초%리민%황혜매%창완림%팽성성%류윤휘
麝香保心丸%心肌细胞%缺氧-复氧模型%活性成分筛选
麝香保心汍%心肌細胞%缺氧-複氧模型%活性成分篩選
사향보심환%심기세포%결양-복양모형%활성성분사선
Shexiang Baoxin Pill ( SBP)%cardiomyocyte%hypoxia/reoxygenation model%screening of active components
目的:建立原代心肌细胞缺氧-复氧模型,并对麝香保心丸及其20种血中活性成分进行抗缺氧-复氧损伤的活性筛选。方法取新生(1~3 d)SD乳鼠的心脏,建立原代心肌细胞的缺氧-复氧损伤模型,并采用四甲基偶氮唑盐(MTT)比色法进行麝香保心丸及其入血成分的活性筛选。结果麝香保心丸在50μg/ml浓度下具有较好的保护原代心肌细胞缺氧-复氧损伤的作用;人参皂苷Rb1、人参皂苷Rb2、蟾毒灵和麝香酮具有较好的保护原代心肌细胞缺氧-复氧损伤的作用。结论麝香保心丸具有抗心肌细胞缺氧-复氧损伤的作用,人参皂苷Rb1、人参皂苷Rb2、蟾毒灵和麝香酮是其主要的有效成分。该研究为麝香保心丸深入的药效和机制研究奠定了基础。
目的:建立原代心肌細胞缺氧-複氧模型,併對麝香保心汍及其20種血中活性成分進行抗缺氧-複氧損傷的活性篩選。方法取新生(1~3 d)SD乳鼠的心髒,建立原代心肌細胞的缺氧-複氧損傷模型,併採用四甲基偶氮唑鹽(MTT)比色法進行麝香保心汍及其入血成分的活性篩選。結果麝香保心汍在50μg/ml濃度下具有較好的保護原代心肌細胞缺氧-複氧損傷的作用;人參皂苷Rb1、人參皂苷Rb2、蟾毒靈和麝香酮具有較好的保護原代心肌細胞缺氧-複氧損傷的作用。結論麝香保心汍具有抗心肌細胞缺氧-複氧損傷的作用,人參皂苷Rb1、人參皂苷Rb2、蟾毒靈和麝香酮是其主要的有效成分。該研究為麝香保心汍深入的藥效和機製研究奠定瞭基礎。
목적:건립원대심기세포결양-복양모형,병대사향보심환급기20충혈중활성성분진행항결양-복양손상적활성사선。방법취신생(1~3 d)SD유서적심장,건립원대심기세포적결양-복양손상모형,병채용사갑기우담서염(MTT)비색법진행사향보심환급기입혈성분적활성사선。결과사향보심환재50μg/ml농도하구유교호적보호원대심기세포결양-복양손상적작용;인삼조감Rb1、인삼조감Rb2、섬독령화사향동구유교호적보호원대심기세포결양-복양손상적작용。결론사향보심환구유항심기세포결양-복양손상적작용,인삼조감Rb1、인삼조감Rb2、섬독령화사향동시기주요적유효성분。해연구위사향보심환심입적약효화궤제연구전정료기출。
Objective To build hypoxia/reoxygenation injury model in cultured neonatal rat cardiomyocyte and screen active components from Shexiang Baoxin Pill ( SBP) absorbed in blood against hypoxia/reoxygenation injury .Methods Cardiomyocytes were isolated and purified from hearts of neonatal Sprague Dawley rats (1~3 days old) and were used to build hypoxia/reoxygenation injury model.The components of SBP absorbed in blood were screened by methyl thiazolil tetracolium (MTT) colorimetic method.Results SBP showed significant protective effect against cardiomyocytes hypoxia /reoxygenation injury atthe concentration of 50 μg/ml.Ginsen-oside Rb1, Rb2, bufalin and muscone of twenty components from SBP absorbed in blood also possessed significant protective effect a -gainst cardiomyocytes hypoxia/reoxygenation injury .Conclusion SBP have the protective activity against cardiomyocytes hypoxia /reoxygenation injury , and ginsenoside Rb1, Rb2, bufalin, muscone are the main active components of SBP .This experiment offered basis for further pharmacodynamics and mechanism study of SBP .