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IQ和MeIQ向细菌诱变剂的代谢转化。

Metabolic conversion of IQ and MeIQ to bacterial mutagens.

作者信息

Alldrick A J, Lake B G, Flynn J, Rowland I R

出版信息

Mutat Res. 1986 Nov;163(2):109-14. doi: 10.1016/0027-5107(86)90041-2.

Abstract

The metabolic conversion of 2-amino-3-methyl- and 2-amino-3,4-dimethyl-imidazo[4,5-f]quinoline (IQ and MeIQ respectively) to bacterial mutagens was studied using a bacterial mutation assay. Studies were performed using S9 fractions derived from either corn oil (uninduced) or Aroclor-1254-treated Sprague-Dawley rats. Aroclor 1254 treatment lowered the S9 protein concentration required for optimum levels of mutagenesis, enhanced the numbers of mutants observed and altered the effects of metabolic inhibitors and cofactors added to the assay. Studies with uninduced preparations revealed that IQ and MeIQ exhibited similar responses to the effects of metabolic inhibitors and cofactors involved in detoxication reactions. Both IQ and MeIQ activation appeared to be inhibited by the biogenic amines tryptamine and tyramine and inactivated by conjugation with either acetyl coenzyme A or glutathione.

摘要

使用细菌突变试验研究了2-氨基-3-甲基咪唑并[4,5-f]喹啉(IQ)和2-氨基-3,4-二甲基咪唑并[4,5-f]喹啉(MeIQ)向细菌诱变剂的代谢转化。研究使用了来自玉米油(未诱导)或经多氯联苯混合物1254处理的斯普拉格-道利大鼠的S9组分进行。多氯联苯混合物1254处理降低了诱变作用达到最佳水平所需的S9蛋白浓度,增加了观察到的突变体数量,并改变了添加到试验中的代谢抑制剂和辅因子的作用。对未诱导制剂的研究表明,IQ和MeIQ对解毒反应中涉及的代谢抑制剂和辅因子的作用表现出相似的反应。IQ和MeIQ的激活似乎都受到生物胺色胺和酪胺的抑制,并通过与乙酰辅酶A或谷胱甘肽结合而失活。

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