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LC-MS鉴定肝毒性吡咯里西啶类生物碱千里光碱大鼠体内代谢产物
引用本文:熊爱珍,杨莉,张芳,何芋岐,王长虹,王峥涛. LC-MS鉴定肝毒性吡咯里西啶类生物碱千里光碱大鼠体内代谢产物[J]. 中国药学杂志, 2012, 47(1): 54-60
作者姓名:熊爱珍  杨莉  张芳  何芋岐  王长虹  王峥涛
作者单位:1.上海中医药大学中药研究所,a.中药标准化教育部重点实验室;b.上海市复方中药重点实验室,上海 201203;2.中国药科大学生药学研究室,南京 210038
基金项目:“重大新药创制”科技重大专项(2009ZX09308-003,2009ZX09052-021,2009ZX09052-024);国家自然科学基金(30701104);上海市国际合作基金项目(09540704700)
摘    要:目的 研究肝毒性吡咯里西啶类生物碱千里光碱的大鼠体内代谢。方法 SD大鼠口服千里光碱,收集胆汁、尿液及粪便样本,采用液相色谱-多级质谱联用对代谢产物进行研究,推导其体内代谢模式。结果 正负离子下共检测到38种代谢产物,主要为千里光碱及其代谢物的氮氧化物,羟化产物,水解产物,以及硫酸结合物,葡萄糖醛酸结合物和谷胱甘肽结合物。另外,尿液、胆汁与粪便中检测到的代谢物有一定差异,胆汁和尿液中代谢产物较多。结论 千里光碱在大鼠体内代谢广泛,形成多种代谢产物。

关 键 词:吡咯里西啶类生物碱  千里光碱  多级质谱  体内代谢  

Identification of Metabolites of Senecionine,a Hepatotoxic Pyrrolizidine Alkaloid,by Liquid Chromatography/Tandem Mass Spectrometry
XIONG Ai-zhen,a,YANG Li,a,ZHANG Fang,a,HE Yu-qi,a,WANG Chang-hong,a,WANG Zheng-tao. Identification of Metabolites of Senecionine,a Hepatotoxic Pyrrolizidine Alkaloid,by Liquid Chromatography/Tandem Mass Spectrometry[J]. Chinese Pharmaceutical Journal, 2012, 47(1): 54-60
Authors:XIONG Ai-zhen  a  YANG Li  a  ZHANG Fang  a  HE Yu-qi  a  WANG Chang-hong  a  WANG Zheng-tao
Affiliation:1a,1b,2(1a.The MOE Key Laboratory for Standardization of Chinese Medicines,1b.The Shanghai Key Laboratory for Compound Chinese Medicines,Institute of Chinese Materia Medica,Shanghai University of Traditional Chinese Medicine,Shanghai 201203,China;2.Department of Pharmacognosy,China Pharmaceutical University,Nanjing 210038,China)
Abstract:OBJECTIVE To investigate the metabolic profile of senecionine in rats.METHODS Liquid chromatography-tandem mass spectrometry(LC-MSn) mass spectrometry was used for the analysis of senecionine and its metabolites in rats bile,urine,and feces after a single oral dose of senecionine.RESULTS In total 38 metabolites were identified,including oxidation products,hydroxylation products,hydrolysis products,sulfation products,glucuronidation products,and GSH-conjugations.And metabolites were found to be more abundant in bile and urine than those in feces.CONCLUSION Senecionine undergoes extensive metabolism in rats.
Keywords:hepatotoxic pyrrolizidine alkaloid  senecionine  tandem mass  in vivo metabolism
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