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N-亚硝基双(2-羟丙基)胺及其相关化合物在大鼠肺和肝S9存在下的致突变性。

Mutagenicity of N-nitrosobis(2-hydroxypropyl)amine and its related compounds in the presence of rat lung and liver S9.

作者信息

Mori Y, Niwa T, Takahashi H, Toyoshi K, Denda A, Takahashi S, Konishi Y

出版信息

Cancer Lett. 1983 Apr;18(3):271-5. doi: 10.1016/0304-3835(83)90235-5.

DOI:10.1016/0304-3835(83)90235-5
PMID:6406040
Abstract

The mutagenic activities of N-nitrosobis(2-hydroxypropyl)amine (BHP) and its related compounds were studied in Salmonella typhimurium TA100 and TA98 strains by Ames's liquid incubation assay in the presence or absence of lung and liver S9 of rats treated with polychlorinated biphenyl (PCB). BHP and its related compounds, N-nitroso-(2-hydroxypropyl)(2-oxopropyl)amine (HPOP), N-nitrosobis(2-oxopropyl)amine (BOP), N-nitrosobis(2-acetoxypropyl)amine (BAP), and N-nitroso-2,6-dimethylmorpholine (NDMM) showed negative mutagenicity in the absence of lung and liver S9 in TA100 and TA98 strains while those compounds showed positive in the presence of liver S9 in TA100 strain. HPOP and BOP showed positive mutagenic activity in the presence of lung S9 in TA100 strain. HPOP showed the strongest mutagenic activity in the presence of lung and liver S9.

摘要

采用艾姆斯液体培养试验,在存在或不存在经多氯联苯(PCB)处理的大鼠肺和肝S9的情况下,研究了N-亚硝基双(2-羟丙基)胺(BHP)及其相关化合物在鼠伤寒沙门氏菌TA100和TA98菌株中的致突变活性。BHP及其相关化合物,N-亚硝基-(2-羟丙基)(2-氧代丙基)胺(HPOP)、N-亚硝基双(2-氧代丙基)胺(BOP)、N-亚硝基双(2-乙酰氧基丙基)胺(BAP)和N-亚硝基-2,6-二甲基吗啉(NDMM),在TA100和TA98菌株中不存在肺和肝S9时显示出阴性致突变性,而这些化合物在TA100菌株中存在肝S9时显示出阳性。HPOP和BOP在TA100菌株中存在肺S9时显示出阳性致突变活性。HPOP在存在肺和肝S9时显示出最强的致突变活性。

相似文献

1
Mutagenicity of N-nitrosobis(2-hydroxypropyl)amine and its related compounds in the presence of rat lung and liver S9.N-亚硝基双(2-羟丙基)胺及其相关化合物在大鼠肺和肝S9存在下的致突变性。
Cancer Lett. 1983 Apr;18(3):271-5. doi: 10.1016/0304-3835(83)90235-5.
2
Mutagenic activation of carcinogenic N-nitrosopropylamines by rat liver: evidence for a cytochrome P-450 dependent reaction.大鼠肝脏对致癌性N-亚硝基丙胺的诱变激活作用:细胞色素P-450依赖性反应的证据。
Carcinogenesis. 1985 Mar;6(3):415-20. doi: 10.1093/carcin/6.3.415.
3
Activation of carcinogenic N-nitrosopropylamines to mutagens by lung and pancreas S9 fractions from various animal species and man.来自不同动物物种和人类的肺及胰腺S9组分将致癌性N-亚硝基丙胺激活为诱变剂。
Mutat Res. 1986 May;160(3):159-69. doi: 10.1016/0027-5107(86)90125-9.
4
A comparative study of the mutagenic activation of N-nitrosopropylamines by various animal species and man: evidence for a cytochrome P-450 dependent reaction.不同动物物种和人类对N-亚硝基丙胺诱变激活的比较研究:细胞色素P-450依赖性反应的证据。
Jpn J Cancer Res. 1986 Feb;77(2):107-17.
5
Mutagenic activation of carcinogenic N-nitrosopropylamines by liver S9 fractions from mice, rats and hamsters: evidence for a cytochrome P-450-dependent reaction.小鼠、大鼠和仓鼠肝脏S9组分对致癌性N-亚硝基丙胺的诱变激活:细胞色素P-450依赖性反应的证据。
Carcinogenesis. 1986 Mar;7(3):375-9. doi: 10.1093/carcin/7.3.375.
6
A comparative study of the mutagenic activation of carcinogenic N-nitrosopropylamines by various animal species and man.
IARC Sci Publ. 1987(84):141-3.
7
Mutagenicity of several pancreatic carcinogenic derivatives of N-nitrosodipropylamine in the Ames assay.N-亚硝基二丙胺的几种胰腺癌致癌衍生物在艾姆斯试验中的致突变性。
Mutat Res. 1980 Mar;77(3):215-9. doi: 10.1016/0165-1218(80)90053-1.
8
Participation of phenobarbital-inducible cytochrome P450 in the mutagenic activation of N-nitrosopropylamines by liver and lung 9000 g fractions from five animal species and man.苯巴比妥诱导的细胞色素P450在来自五种动物物种和人类的肝脏及肺9000g组分对N-亚硝基丙胺的诱变活化中的作用。
IARC Sci Publ. 1991(105):398-403.
9
Carcinogenic potency of N-nitrosomethyl(2-hydroxypropyl)amine and other metabolic relatives of N-nitrosobis(2-hydroxypropyl)amine by single intraperitoneal injection on the lung of rats.N-亚硝基甲基(2-羟丙基)胺及N-亚硝基双(2-羟丙基)胺的其他代谢相关物经单次腹腔注射对大鼠肺部的致癌潜能
Jpn J Cancer Res. 1988 Jun;79(6):698-704. doi: 10.1111/j.1349-7006.1988.tb02225.x.
10
Species specificity in the metabolism of N-nitrosobis(2-oxopropyl)amine and N-nitroso(2-hydroxypropyl)(2-oxopropyl)amine to mutagens by isolated rat and hamster hepatocytes.大鼠和仓鼠离体肝细胞将N-亚硝基双(2-氧代丙基)胺和N-亚硝基(2-羟丙基)(2-氧代丙基)胺代谢为诱变剂的物种特异性。
Cancer Res. 1987 Sep 15;47(18):4776-81.

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