Honokiol Metabolites Study in Rat Kidney Employing UHPLC-Q-TOF/MS and 13C Stable Isotope Labeling

被引:1
作者
Wang, Chunyan [1 ,2 ]
Ye, Haoyu [2 ]
Tang, Minghai [2 ]
Wan, Li [1 ]
Qiu, Neng [3 ]
Li, Xiaobin [1 ]
Wang, Hairong [1 ]
Wang, Chunyu [2 ]
Chen, Lijuan [2 ]
机构
[1] Chengdu Univ TCM, Key Lab Standardizat Chinese Herbal Med, State Key Lab Breeding Base Systemat Res Dev & Ut, Sch Pharm,Minist Educ, Chengdu 611137, Peoples R China
[2] Sichuan Univ, State Key Lab Biotherapy, West China Hosp, West China Med Sch, Chengdu 610041, Peoples R China
[3] Sichuan Univ, Sch Chem Engn, Dept Biopharmaceut Engn, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
UHPLC-Q-TOF/MS; Honokiol and C-13 stable isotope; Metabolites; Rat kidney; LIQUID; IDENTIFICATION; DISPOSITION; CONJUGATION; GLUCURONIDE; SULFATE;
D O I
10.1007/s10337-015-2859-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Kidneys are an important organ since they make a significant contribution to the metabolism and excretion of drugs in vivo. The aim of this study was to identity and tentatively elucidate honokiol metabolites in the rat kidney, after healthy rats were exposed to a 1:1 mixture of labeled C-13-honokiol and unlabeled honokiol, by ultra high-performance liquid chromatography coupled with a quadrupole time-of-flight mass spectrometer platform. This platform is well known for its fast acquisition speed, superior sensitivity, high resolution, and excellent mass accuracy. Finally, a total of 19 metabolites belonging to phase II metabolites were identified tentatively by exact mass, and the fragmentation spectra of four metabolites are reported for the first reported time. Our results indicated that honokiol was metabolized via phase II biotransformation including sulfation, acetylation, glucuronidation and amino acid conjugation in rat kidney tissues. This is the first study focused on the honokiol biotransformation in the tissue of kidney, providing important details for a comprehensive standing of the metabolites of honokiol.
引用
收藏
页码:507 / 514
页数:8
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