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甘草提取物和甘草甜素对致突变性的抑制作用。

Inhibition of mutagenicity by glycyrrhiza extract and glycyrrhizin.

作者信息

Tanaka M, Mano N, Akazai E, Narui Y, Kato F, Koyama Y

机构信息

School of Pharmaceutical Science, Toho University, Chiba, Japan.

出版信息

J Pharmacobiodyn. 1987 Dec;10(12):685-8. doi: 10.1248/bpb1978.10.685.

Abstract

The effects of Glycyrrhiza extract and one of its components, glycyrrhizin, on the mutagenicities of several mutagens were investigated by means of a modification of the Ames' test. Both inhibited the mutagenicities of 3-amino-1,4-dimethyl-5 H-pyrido[4,3-b]-indole (Trp-P-1) and 3-amino-1-methyl-5 H-pyrido[4,3-b]indole. Since the Glycyrrhiza extract and glycyrrhizin inhibited the mutagenicity of activated Trp-P-1, it was clear that their inhibitory effects were not due to inhibition of the enzyme activity of the S9 fraction. Both Glycyrrhiza extract and glycyrrhizin also inhibited the mutagenicities of benzo[a]pyrene, 3-methylcholanthrene, 2-naphthylamine, 2-amino-6-methyldipyrido[1,2-a:3',2'-d]-imidazole, dimethylnitrosoamine and dimethylaminoazobenzene. The mutagenicity of 2-(2-furyl)-3-(5-nitro-2-furyl)acrylamide (AF-2) was inhibited by the Glycyrrhiza extract but not by glycyrrhizin. This suggested that a component different from glycyrrhizin, present in the Glycyrrhiza extract, inhibited the mutagenicity of AF-2.

摘要

通过对艾姆斯试验进行改进,研究了甘草提取物及其成分之一甘草酸对几种诱变剂诱变性的影响。二者均抑制了3-氨基-1,4-二甲基-5H-吡啶并[4,3-b]吲哚(Trp-P-1)和3-氨基-1-甲基-5H-吡啶并[4,3-b]吲哚的诱变性。由于甘草提取物和甘草酸抑制了活化型Trp-P-1的诱变性,很明显它们的抑制作用并非源于对S9组分酶活性的抑制。甘草提取物和甘草酸还均抑制了苯并[a]芘、3-甲基胆蒽、2-萘胺、2-氨基-6-甲基二吡啶并[1,2-a:3',2'-d]咪唑、二甲基亚硝胺和二甲基氨基偶氮苯的诱变性。甘草提取物抑制了2-(2-呋喃基)-3-(5-硝基-2-呋喃基)丙烯酰胺(AF-2)的诱变性,但甘草酸未起到抑制作用。这表明甘草提取物中存在的一种不同于甘草酸的成分抑制了AF-2的诱变性。

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