Physiology Department, Biosciences Institute, São Paulo State University-UNESP, Botucatu, São Paulo.
J Med Food. 2009 Dec;12(6):1411-5. doi: 10.1089/jmf.2008.0269.
The present study reveals the pharmacological action of Serjania erecta Radlk. (Family Sapindaceae), an important medicinal plant species used in the Brazilian Pantanal against gastric pain. The methanolic (Me) and chloroformic (Se) extracts obtained from leaves of S. erecta were challenged by a very strong necrotizing agent in rodents, absolute ethanol. Se was also confronted with a nitric oxide synthase inhibitor (N(G)-nitro-L-arginine methyl ester), a capsaicin cation channel transient receptor potential vanilloid type 1 antagonist (ruthenium red), or a sulfhydryl-blocker (N-ethylmaleimide) to evaluate the participation of these cytoprotective factors in gastroprotection. In an in vivo experimental model, Me and Se presented several degrees of gastroprotective action without signs of acute toxicity. The best gastroprotective effect was restricted to all doses of Se. The mechanisms involving the gastroprotective action of Se are related to an augmented defense mechanism of the gastrointestinal mucosa consisting of sensory neurons, nitric oxide, and sulfhydryl groups that prevent and attenuate the ulcer process. The presence of polyisoprenoids in the Se explains the potent gastroprotective action of this medicinal species. Effective gastroprotective action and the absence of acute toxicity indicate this species may be a promising herbal drug against gastric disease.
本研究揭示了 Serjania erecta Radlk.(芸香科)的药理学作用,这种药用植物是巴西潘塔纳尔地区用于治疗胃痛的重要物种。从 S. erecta 的叶子中获得的甲醇(Me)和氯仿(Se)提取物在啮齿动物中受到了很强的坏死剂(绝对乙醇)的挑战。Se 还与一氧化氮合酶抑制剂(N(G)-硝基-L-精氨酸甲酯)、辣椒素阳离子通道瞬时受体电位香草素 1 拮抗剂(钌红)或巯基阻滞剂(N-乙基马来酰亚胺)进行了对抗,以评估这些细胞保护因子在胃保护中的参与情况。在体内实验模型中,Me 和 Se 表现出不同程度的胃保护作用,没有急性毒性的迹象。Se 的最佳胃保护作用仅限于所有剂量。Se 的胃保护作用机制与胃肠道黏膜的增强防御机制有关,该机制包括感觉神经元、一氧化氮和巯基,可预防和减轻溃疡过程。Se 中存在多异戊二烯解释了这种药用植物具有强大的胃保护作用。有效的胃保护作用和没有急性毒性表明,该物种可能是一种有前途的治疗胃病的草药药物。