Identification of bioactive ingredients from Babaodan using UPLC-QTOF-MS analysis combined with network pharmacology guided bioassays

被引:6
作者
Sheng, Hongda [1 ]
Li, Yufei [1 ]
Liu, Wei [1 ]
Wang, Yingchao [3 ]
Wang, Shufang [1 ]
Zhan, Zhixue [4 ]
Lai, Zhicheng [4 ]
Guan, Bin [4 ]
Qiang, Shifa [4 ]
Qian, Jing [1 ]
Wang, Yi [1 ,2 ,3 ]
机构
[1] Zhejiang Univ, Pharmaceut Informat Inst, Coll Pharmaceut Sci, Hangzhou 310058, Peoples R China
[2] Tianjin Univ Tradit Chinese Med, State Key Lab Component based Chinese Med, Tianjin 300193, Peoples R China
[3] Zhejiang Univ, Innovat Inst Artificial Intelligence Med, Hangzhou 310018, Peoples R China
[4] Xiamen Tradit Chinese Med Co Ltd, Xiamen 361100, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2022年 / 1206卷
关键词
Babaodan; UPLC-QTOF-MS; Mass spectrometry molecular network; Network pharmacology; Chemical composition and anti-inflammatory; effect; MOLECULAR NETWORKING;
D O I
10.1016/j.jchromb.2022.123356
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Babaodan (BBD) is a traditional Chinese medicine (TCM) prescribed for various inflammatory diseases, including viral hepatitis and acute genitourinary tract infection. Like other TCMs, BBD is a multi-component formula whose chemical composition and mode of action are largely unknown. The current study identified the bioactive ingredients of BBD using ultrahigh-performance liquid chromatography combined with quadrupole time-of-flight mass spectrometry (UPLC-QTOF-MS) followed by mass spectrometry molecular networking analysis. Subsequently, network pharmacology analysis was performed to predict the potential targets and pathways regulated by BBD. Eventually, a panel of compounds was selected and examined for their anti-inflammatory effects using lipopolysaccharide-stimulated RAW264.7 cells. Eighty-six compounds, including saponins, bile acids, and fatty acids, were identified. Tumor necrosis factor-alpha was identified as a key molecule. Pathways in cancer, inflammatory bowel disease, and hepatitis were predicted to be the major regulatory pathways. The results from bioassays validated ginsenoside Rb1, ginsenoside Rd, deoxycholic acid, chenodeoxycholic acid, and taurochenodeoxycholic acid as novel bioactive ingredients in BBD with anti-inflammatory effects. In conclusion, our study explains the anti-inflammatory efficacy of BBD from both chemical and biological aspects, which provides a scientific basis for the clinical application of BBD in inflammation-related diseases.
引用
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页数:11
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