Oxymatrine screened from Sophora flavescens by cell membrane immobilized chromatography relieves histamine-independent itch

This study aimed to discover the active compounds of Sophora flavescens Ait. (SF), the anti-itch effects and underlying mechanisms of oxymatrine (OMT), one of the bioactive compounds from SF. Dorsal root ganglion cell membrane immobilized chromatography was used to screen potential anti-pruritic act...

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Veröffentlicht in:Journal of pharmacy and pharmacology 2021-12, Vol.73 (12), p.1617-1629
Hauptverfasser: Zhang, Zhe, Pan, Jianhao, Zhu, Tao, Malewicz, Nathalie, Ye, Kaihe, Rong, Jianhui, Luo, Yong, Situ, Yongli, Verkhratsky, Alexei, Wang, Yong, Zhao, Jianhao, Tang, Dan, Nie, Hong
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Sprache:eng
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Zusammenfassung:This study aimed to discover the active compounds of Sophora flavescens Ait. (SF), the anti-itch effects and underlying mechanisms of oxymatrine (OMT), one of the bioactive compounds from SF. Dorsal root ganglion cell membrane immobilized chromatography was used to screen potential anti-pruritic active compounds from SF. The scratching behaviour was analysed to systematically study the anti-pruritic effects of OMT in chloroquine- (CQ), peptide Ser-Leu-Ile-Gly-Arg-Leu- (SLIGRL), histamine- (HIS) and allyl-isothiocyanate-(AITC)-induced itch mice models. Real-time quantitative PCR, in-vivo study and molecular docking were employed to explore the underlying mechanisms. All in all, 21 compounds of SF were identified and 5 potential bioactive compounds were discovered. OMT significantly reduced scratching bouts in two HIS-independent itch models induced by CQ and SLIGRL but was not effective in the HIS-induced itch model. OMT reduced scratching bouts in a dose-dependent manner and decreased the messenger RNA (mRNA) expression of transient receptor potential ankyrin 1 (TRPA1) channel in two HIS-independent itch models; in addition, OMT reduced the wipes and scratching bouts induced by AITC. This study discovered five potential anti-pruritic compounds including OMT in the SF extract, and OMT has strong anti-pruritic effects in HIS-independent itch via TRPA1 channel.
ISSN:0022-3573
2042-7158
DOI:10.1093/jpp/rgab145