Screening Bioactive Compounds of Siraitia grosvenorii by Immobilized β 2 -Adrenergic Receptor Chromatography and Druggability Evaluation

• Published in: Frontiers in pharmacology Vol. 10; p. 915
• Main Authors: Jia, Xiaoni, Liu, Jiajun, Shi, Baimei, Liang, Qi, Gao, Juan, Feng, Gangjun, Chang, Zhongman, Li, Qian, Zhang, Xiaohong, Chen, Jianbo, Zhao, Xinfeng
• Format: Journal Article
• Language: English
• Published: Switzerland 2019
• Subjects: receptor chromatography; β2-adrenergic receptor; high-throughput screening; pharmacokinetics; Siraitia grosvenorii
• ISSN: 1663-9812; 1663-9812

As the first and key step of traditional Chinese medicine (TCM)-guided drug development, lead discovery necessitates continuous exploration of new methodology for screening bioactive compounds from TCM. This work intends to establish a strategy for rapidly recognizing β -adrenergic receptor (β -AR) target compounds from the fruit of (LHG). The method involved immobilization of β -AR onto amino-microsphere to synthesize the receptor column, the combination of the column to high-performance liquid chromatography (HPLC) to screen bioactive compounds of LHG, the identification of the compounds by HPLC coupled with mass spectrometry (MS), and the evaluation of druggability through pharmacokinetic examination by HPLC-MS/MS. Mogroside V was screened and identified as the β -AR-targeted bioactive compounds in LHG. This compound exhibited desired pharmacokinetic behavior including the time to reach peak plasma concentrations of 45 min, the relatively low elimination of 138.5 min, and the high bioavailability. These parameters indicated that mogroside V has a good druggability for the development of new drugs fighting β -AR-mediated respiratory ailments like asthma. The combination of the methods in this work is probably becoming a powerful strategy for screening and early evaluating the bioactive compounds specifically binding to G-protein-coupled receptor target from complex matrices including TCM.