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

Objectives 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. Methods 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 al lyl-isothiocyanate-(AITC)-induced itch mice models. Real-time quantitative PCR, in-vivo study and molecular docking were employed to explore the underlying mechanisms. Key findings 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. Conclusions 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.

Automated summary

This study identified 21 compounds from Sophora flavescens, with 5 potential bioactive compounds discovered. Oxymatrine (OMT) significantly reduced scratching bouts in two histamine-independent itch models and decreased mRNA expression of transient receptor potential ankyrin 1 (TRPA1) channel. OMT also reduced scratching bouts induced by allyl isothiocyanate (AITC).