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槲皮素对鼠伤寒沙门氏菌菌株中2-乙酰氨基芴和苯并[a]芘诱变性的影响。

The effect of quercetin on the mutagenicity of 2-acetylaminofluorene and benzo[alpha]pyrene in Salmonella typhimurium strains.

作者信息

Ogawa S, Hirayama T, Nohara M, Tokuda M, Hirai K, Fukui S

出版信息

Mutat Res. 1985 Mar;142(3):103-7. doi: 10.1016/0165-7992(85)90048-x.

Abstract

The comutagenic and desmutagenic effect of quercetin on the mutagenicity of typical mutagens e.g. 2-acetylaminofluorene (AAF), 4-nitroquinoline-1-oxide (4NQO) and benzo[alpha]pyrene (B[a]P), in Salmonella typhimurium TA98, TA100 and TA98/1,8 DNP6 were examined. In the mixed application of AAF with quercetin in the presence of mammalian metabolic activation system (S9 mix), the numbers of revertants in TA98 increased by as much 2.2-5.0-fold compared with the sum of those in the separate applications of AAF and quercetin. A 1.4-2.7-fold increase was observed in TA100. Quercetin did not affect the mutagenicity of 4NQO, and depressed that of B[a]P. Dose-response curves for mutagenicity of quercetin with or without AAF (5 micrograms/plate) were examined. The results suggest that quercetin, present in a molarity of up to 1.5 times that of AAF, is apparently effective in enhancing the mutagenicity of AAF, because a linear dose-response curve was observed in the range of 0-5 micrograms/plate quercetin with AAF although quercetin alone was not mutagenic in the same range. Dose-response curves for mutagenicity of quercetin with or without 5 micrograms/plate B[a]P did not increase compared with that for quercetin alone. The mutagenicity of the mixed application of B[a]P with quercetin was reduced to about 60% of the sum of separate application at doses ranging from 25 to 100 micrograms/plate of quercetin. Since enhancement and depression of mutagenicity by quercetin were observed for indirect mutagens, AAF and B[a]P, respectively, in the presence of S9 mix, quercetin may affect the metabolic pathway of these mutagens.

摘要

检测了槲皮素对典型诱变剂如2-乙酰氨基芴(AAF)、4-硝基喹啉-1-氧化物(4NQO)和苯并[a]芘(B[a]P)在鼠伤寒沙门氏菌TA98、TA100和TA98/1,8 DNP6中的致突变性的协同诱变和抗诱变作用。在哺乳动物代谢激活系统(S9混合物)存在的情况下,将AAF与槲皮素混合应用时,与单独应用AAF和槲皮素相比,TA98中的回复突变菌落数增加了2.2至5.0倍之多。在TA100中观察到增加了1.4至2.7倍。槲皮素不影响4NQO的致突变性,并降低了B[a]P的致突变性。检测了有或没有AAF(5微克/平板)时槲皮素致突变性的剂量反应曲线。结果表明,当槲皮素的摩尔浓度高达AAF的1.5倍时,它显然能有效增强AAF的致突变性,因为在含有AAF的情况下,在0至5微克/平板槲皮素范围内观察到了线性剂量反应曲线,尽管单独的槲皮素在相同范围内没有致突变性。有或没有每平板5微克B[a]P时槲皮素致突变性的剂量反应曲线与单独槲皮素的相比没有增加。在每平板25至100微克槲皮素的剂量范围内,B[a]P与槲皮素混合应用的致突变性降低到单独应用之和的约60%。由于在S9混合物存在的情况下,分别观察到槲皮素对间接诱变剂AAF和B[a]P的致突变性有增强和抑制作用,槲皮素可能会影响这些诱变剂的代谢途径。

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