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Analgesic and Anti-Inflammatory Activities of Sophocarpine from Sophora viciifolia Hance

Journal 2021 · IF 3.411 · 发表于 2021 年 11 月 8 日
作者: F. L. Wang,H. Wang,J. H. Wang,D. X. Wang,Y. Gao,B. Yang,H. J. Yang,Y. B. Ji,G. S. Xin
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摘要

Sophora viciifolia Hance is an edible plant used in traditional Chinese medicine. Sophocarpine, a tetracyclic quinolizidine alkaloid, is one of the most abundant active ingredients in Sophora viciifolia Hance. Here, we study the analgesic and anti-inflammatory effects, as well as the acute toxicity of sophocarpine from Sophora viciifolia Hance in mice. Sophocarpine (20, 40, and 80 mg/kgbw) significantly prolonged the delay period before a hot plate reaction occurred (all ), and the delay before a tail-flick response was induced by a warm bath (; ). Sophocarpine (40, 80 mg/kg) resulted in dose-dependent inhibition of the writhing reaction induced by acetic acid in mice (; , respectively). Sophocarpine (80 mg/kg) reduced the total duration of a formalin-induced pain response (). Sophocarpine prolonged the foot-licking latency of mice after the hot plate reaction, and this effect was antagonized by calcium chloride and enhanced by verapamil. Sophocarpine (20, 40, and 80 mg/kg) significantly inhibited xylene-induced ear edema (; ; , respectively) and the penetration of acetic acid-induced dye into the peritoneal cavity (; ; , respectively). It also reduced the levels of proinflammatory cytokine interleukin (IL)-1β, IL-6, and prostaglandin E2 (, , ) and those of serum nitric oxide (). The results of this study suggest that sophocarpine possesses certain analgesic and anti-inflammatory activities, which may be related to calcium and inhibition of the secretion of inflammatory factors.