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光果甘草提取物、甘草酸、18α-甘草次酸和18β-甘草次酸对鼠伤寒沙门氏菌致突变性的抑制作用

Inhibition of mutagenicity in Salmonella typhimurium by Glycyrrhiza glabra extract, glycyrrhizinic acid, 18 alpha- and 18 beta-glycyrrhetinic acids.

作者信息

Zani F, Cuzzoni M T, Daglia M, Benvenuti S, Vampa G, Mazza P

机构信息

Dipartimento Farmaceutico, Facoltà di Farmacia, Università di Parma, Italy.

出版信息

Planta Med. 1993 Dec;59(6):502-7. doi: 10.1055/s-2006-959748.

Abstract

The effects of Glycyrrhiza glabra L. extract, glycyrrhizinic acid, 18 alpha- and 18 beta-glycyrrhetinic acids on the mutagenicity of the ethyl methanesulfonate, N-methyl-N'-nitro-N-nitrosoguanidine, and ribose-lysine Maillard model systems were investigated by using the Salmonella/microsome reversion assay. The protocol used allowed us to detect desmutagenic and antimutagenic activity and to avoid false positive results due to toxicity. For all the compounds tested, no desmutagenic activity was observed against ethyl methanesulfonate and N-methyl-N'-nitro-N-nitrosoguanidine; only Glycyrrhiza glabra extract showed antimutagenic activity against ethyl methanesulfonate. On using the ribose-lysine mutagenic browning mixture, the desmutagenic activities of the Glycyrrhiza glabra extract, glycyrrhizinic acid, 18 alpha- and 18 beta-glycyrrhetinic acids were observed. 18 beta-Glycyrrhetinic acid was the most active compound. Glycyrrhiza glabra extract also exhibited antimutagenic activity against ribose-lysine.

摘要

采用鼠伤寒沙门氏菌/微粒体回复突变试验,研究了光果甘草提取物、甘草酸、18α-甘草次酸和18β-甘草次酸对甲磺酸乙酯、N-甲基-N'-硝基-N-亚硝基胍以及核糖-赖氨酸美拉德模型体系致突变性的影响。所采用的实验方案使我们能够检测到抗诱变和抗突变活性,并避免因毒性导致的假阳性结果。对于所有测试化合物,未观察到对甲磺酸乙酯和N-甲基-N'-硝基-N-亚硝基胍的抗诱变活性;仅光果甘草提取物对甲磺酸乙酯表现出抗突变活性。在使用核糖-赖氨酸诱变褐变混合物时,观察到光果甘草提取物、甘草酸、18α-甘草次酸和18β-甘草次酸的抗诱变活性。18β-甘草次酸是活性最强的化合物。光果甘草提取物对核糖-赖氨酸也表现出抗突变活性。

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