胡杨树脂提取物抗炎活性筛选及化学成分分析
投稿时间:2018-07-02     点此下载全文
引用本文:龚雪,李柱,张娜,王杰,韩奇亨,任凯,张春红,李旻辉.胡杨树脂提取物抗炎活性筛选及化学成分分析[J].中国现代中药,2018,20(12):1494-1498
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作者中文名作者英文名单位中文名单位英文名E-Mail
龚雪 GONG Xue 包头医学院,内蒙古包头014060 Baotou Medical College,Baotou 014060,China  
李柱 LI Zhu 额济纳旗蒙医医院,内蒙古阿拉善盟735400 Ejin Banner Mongolian medicine Hospital,Ejin Banner 735400,China  
张娜 ZHANG Na 包头医学院,内蒙古包头014062 Baotou Medical College,Baotou 014062,China  
王杰 WANG Jie 包头医学院,内蒙古包头014063 Baotou Medical College,Baotou 014063,China  
韩奇亨 HAN Qi-heng 包头医学院,内蒙古包头014064 Baotou Medical College,Baotou 014064,China  
任凯 REN Kai 包头医学院,内蒙古包头014065 Baotou Medical College,Baotou 014065,China  
张春红 ZHANG Chun-hong 包头医学院,内蒙古包头014066 Baotou Medical College,Baotou 014066,China 张春红,教授,研究方向:中药资源保护与质量评价;Tel:(0472)7167795,Email:zchlhh@126.com 
李旻辉 LI Min-hui 包头医学院,内蒙古包头014067 Baotou Medical College,Baotou 014067,China 李旻辉,教授,研究方向:蒙药资源保护与利用;Email:li_minhui@aliyun.com 
基金项目:阿拉善盟2013年应用技术研究与开发资金项目(2013-36);包头医学院博士科研启动基金项目(BSJJ201610)
中文摘要:目的:探讨胡杨树脂提取物对脂多糖(LPS)刺激小鼠单核巨噬白血病细胞RAW 264.7细胞炎症保护作用及利用UPLC-Q-Exactive 四级杆-静电场轨道阱高分辨质谱联用技术,对胡杨树脂化学成分进行识别和鉴定。方法:用不同浓度(12.5、25、50、100、200 μg·mL-1)的胡杨树脂提取物处理RAW 264.7细胞,MTT法检测细胞增殖活性;通过LPS(1 μg·mL-1)诱导RAW 264.7细胞建立炎症模型,用不同浓度胡杨树脂提取物处理炎症模型,MTT法检测胡杨树脂提取物对细胞的保护作用;采用UPLC-Q-Exactive四级杆-静电场轨道阱高分辨质谱仪联用技术,借助数据挖掘方法识别和鉴定胡杨树脂中的化学成分,对其高分辨一级和二级质谱数据进行解析,并与数据库比对,对胡杨树脂化学成分的结构推测和确认。结果:在实验浓度范围内,胡杨树脂提取物对细胞无细胞毒性作用;与LPS模型组比较,浓度为12.5、25、50、100、200 μg·mL-1胡杨树脂提取物均能显著改善LPS诱导小鼠巨噬细胞RAW 264.7的炎症反应,具有较好的浓度依赖性;通过高分辨数据推测鉴定出6个化合物,分别为棕榈油酸、邻苯二甲酸二丁酯、十六酰胺、油酸酰胺、硬脂酰胺、芥酸酰胺。结论:该结果为胡杨树脂的提取分离及抗炎活性作用研究奠定基础,为进一步对胡杨树脂的综合研究提供科学的依据。
中文关键词:胡杨树脂  RAW 264.7细胞  抗炎  UPLC-Q-Exactive 四级杆-静电场轨道阱高分辨质谱
 
Anti-inflammatory Activity and Chemical Composition of Resin Extracts from Populus diversifolia Schrenk.
Abstract:Objective:To investigate the protective effects of resin extracts from Populus diversifolia on the inflammation of mice mononuclear macrophage RAW 264.7 cells induced by lipopolysaccharide(LPS).An ultra-high performance liquid chromatography coupled with hybrid quadrupole-orbitrap mass spectrometry(UPLC-hybrid quadrupole-orbitrap MS)method was developed toanalyze and identify the chemical constituents from resin of P.diversifolia.Methods:The RAW 264.7 cells were treated with different concentrations(12.5,25,50,100,200 μg·mL-1)of resin extracts from P.diversifolia,and cell viability was determined by MTT method.The inflammation model which was established by LPS(1 μg·mL-1)-induced RAW 264.7 cells were used to determine the resin extracts from P.diversifolia.The compounds were found and identified through the serious data mining,structural speculation on basis of the careful analysis of the MS and MS / MS data,and confirmed by comparison with the references and library.Results:The resin extracts from P.diversifolia had no cytotoxicity to RAW 264.7 cells in the experimental concentration range.Compared with model group,the resin extracts from P.diversifolia at the concentrations of 12.5,25,50,100,200 μg·mL-1 could significantly improve the inflammation of RAW 264.7 cells induced by LPS,and showed a well dose-dependent manner.A total of 6 compounds,including palmitoleic acid,dibutyl phthalate,hexadecanamide,oleamide,octadecanamide and erucylamide were identified.Conclusion:The results provide scientific evidence for further studying its chemical composition and pharmacological activity of the P.diversifolia comprehensively and objectively.
keywords:resin from Populus diversifolia Schrenk.  RAW 264.7 cells  anti-inflammatory  UPLC-hybrid quadrupole-orbitrap mass spectrometry
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