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萝卜硫素(西兰花的一种成分)对食物来源的杂环胺诱变性的抑制作用

Inhibition of mutagenicity of food-derived heterocyclic amines by sulforaphane--a constituent of broccoli.

作者信息

Kaur I P

机构信息

University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh, 160014, India.

出版信息

Indian J Exp Biol. 2003 Mar;41(3):216-9.

Abstract

Sulforaphane, a constituent of broccoli was investigated for its antimutagenic potential against different classes of cooked food mutagens (heterocyclic amines). These include imidazoazaarenes such as 2-amino-3-methylimidazo[4,5-f]quinoline (IQ), 2-amino-3,4-dimethylimidazo[4,5-f]quinoline (MeIQ), 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx) and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP); pyridoindole derivatives such as 3-amino-1,4-dimethyl-5H-pyrido[4,3-b]indole (Trp-P-1) and 3-amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2); and, dipyridoimidazole derivative such as 2-amino-6-methyldipyrido[1,2-a:3',2'-d]imidazole (Glu-P-1). Tests were carried out by Ames Salmonella/reversion assay using Salmonella typhimurium TA98 (frame shift mutation sensitive) and TA100 (base pair mutation sensitive) bacterial strains in the presence of Aroclor 1254-induced rat liver S9. Results of these in vitro antimutagenicity studies strongly suggest that sulforaphane is a potent inhibitor of the mutagenicity induced by imidazoazaarenes such as IQ, MeIQ and MeIQx (approximately 60% inhibition) and moderately active against pyridoindole derivatives such as Trp-P-1 and Trp-P-2 (32-48% inhibition), but ineffective against dipyridoimidazole derivative (Glu-P-1) in TA 100.

摘要

对西兰花的一种成分萝卜硫素针对不同种类的烹饪食物诱变剂(杂环胺)的抗诱变潜力进行了研究。这些诱变剂包括咪唑并氮杂芳烃,如2-氨基-3-甲基咪唑并[4,5-f]喹啉(IQ)、2-氨基-3,4-二甲基咪唑并[4,5-f]喹啉(MeIQ)、2-氨基-3,8-二甲基咪唑并[4,5-f]喹喔啉(MeIQx)和2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP);吡啶并吲哚衍生物,如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(Trp-P-2);以及二吡啶并咪唑衍生物,如2-氨基-6-甲基二吡啶并[1,2-a:3',2'-d]咪唑(Glu-P-1)。使用鼠伤寒沙门氏菌TA98(对移码突变敏感)和TA100(对碱基对突变敏感)菌株,在艾氏剂1254诱导的大鼠肝脏S9存在的情况下,通过Ames沙门氏菌回复突变试验进行测试。这些体外抗诱变性研究的结果有力地表明,萝卜硫素是IQ、MeIQ和MeIQx等咪唑并氮杂芳烃诱导的诱变性的有效抑制剂(约60%抑制),对Trp-P-1和Trp-P-2等吡啶并吲哚衍生物有中等活性(32-48%抑制),但对TA 100中的二吡啶并咪唑衍生物(Glu-P-1)无效。

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