浙江大学学报(医学版)
浙江大學學報(醫學版)
절강대학학보(의학판)
JOURNAL OF ZHEJIANG UNIVERSITY MEDICAL SCIENCES
2015年
2期
145-153
,共9页
陶珊%梁欣莹%王怡%王毅
陶珊%樑訢瑩%王怡%王毅
도산%량흔형%왕이%왕의
肌细胞,心脏%缺氧%色谱法,高压液相%甘草/药物作用,黄酮类/药理学%甘草酸 /药理学%五味子%麦冬%疾病模型,动物
肌細胞,心髒%缺氧%色譜法,高壓液相%甘草/藥物作用,黃酮類/藥理學%甘草痠 /藥理學%五味子%麥鼕%疾病模型,動物
기세포,심장%결양%색보법,고압액상%감초/약물작용,황동류/약이학%감초산 /약이학%오미자%맥동%질병모형,동물
Myocytes,cardiac%Anoxia%Chromatography,high pressure liquid%Glycyrrhiza uralensis/drug effects%Flavones/pharmacology%Glycyrrhizic acid/pharmacology%Schisandra chinensis%Ophiopogon japonicus%Disease models,animal
目的:基于细胞模型以及高效液相色谱—质谱联用技术对通脉养心丸中心肌保护活性物质进行筛选研究。方法:利用高效液相制备技术对通脉养心丸进行制备分离,然后采用过氧化氢氧化损伤H9 c2大鼠心肌细胞模型对通脉养心丸活性组分进行筛选。利用高效液相色谱—质谱联用技术对活性组分进行分析,通过查阅文献和根据化合物裂解规律,鉴定推断出可能的活性化合物。结果:发现通脉养心丸中10个组分具有明显的心肌保护活性,考察了其中5个组分的半数有效浓度并发现其呈现良好的量效关系。从这5个组分中推断出11个可能的活性化合物,包含甘草酸、甘草香豆素、甘草利酮、Glyasperin A等。结论:筛选出通脉养心丸中心肌保护活性物质,有望为中药复方制剂活性物质筛选研究提供借鉴。
目的:基于細胞模型以及高效液相色譜—質譜聯用技術對通脈養心汍中心肌保護活性物質進行篩選研究。方法:利用高效液相製備技術對通脈養心汍進行製備分離,然後採用過氧化氫氧化損傷H9 c2大鼠心肌細胞模型對通脈養心汍活性組分進行篩選。利用高效液相色譜—質譜聯用技術對活性組分進行分析,通過查閱文獻和根據化閤物裂解規律,鑒定推斷齣可能的活性化閤物。結果:髮現通脈養心汍中10箇組分具有明顯的心肌保護活性,攷察瞭其中5箇組分的半數有效濃度併髮現其呈現良好的量效關繫。從這5箇組分中推斷齣11箇可能的活性化閤物,包含甘草痠、甘草香豆素、甘草利酮、Glyasperin A等。結論:篩選齣通脈養心汍中心肌保護活性物質,有望為中藥複方製劑活性物質篩選研究提供藉鑒。
목적:기우세포모형이급고효액상색보—질보련용기술대통맥양심환중심기보호활성물질진행사선연구。방법:이용고효액상제비기술대통맥양심환진행제비분리,연후채용과양화경양화손상H9 c2대서심기세포모형대통맥양심환활성조분진행사선。이용고효액상색보—질보련용기술대활성조분진행분석,통과사열문헌화근거화합물렬해규률,감정추단출가능적활성화합물。결과:발현통맥양심환중10개조분구유명현적심기보호활성,고찰료기중5개조분적반수유효농도병발현기정현량호적량효관계。종저5개조분중추단출11개가능적활성화합물,포함감초산、감초향두소、감초리동、Glyasperin A등。결론:사선출통맥양심환중심기보호활성물질,유망위중약복방제제활성물질사선연구제공차감。
Objective: Based on cell model and HPLC-MS technology , to screen myocardial protection active compounds from traditional patent medicine Tongmai Yangxin pill ( TMYXP ) . Methods: Fractions of TMYXP were prepared by high performance liquid preparation technology . The cardioprotective effects of prepared fractions were tested on H2O2 oxidation-damaged H9c2 myocardiocytes.The active components were analyzed by high performance liquid chromatography ( HPLC) coupled with high resolution mass spectrometry .The possible active compounds were putatively identified by comparison of their MS ions and molecular weight with literatures . Results:Ten TMYXP components presented significant myocardial protective activities , 5 of which were investigated and presented good dose-effect relationships .Their median effective concentrations ( EC50 ) were respectively 11.66, 17.44, 13.10, 7.332, 15.15 μg/mL.Totally, 11 potential active compounds were analyzed and identified , including Glycyrrhizic acid , Glycycoumarin , Licoisoflavone , Ophiopogonin D′, Licoricon, Gancaonin L, Neoglycyrol, Emodin, Angeloylgomisin H, Angeloylgomisin Q and Glyasperin A .Conclusion:The myocardial protection active compounds of TMYXP were screened successfully .