首页> 外文期刊>Carcinogenesis >Carcinogenicity and DNA adduct formation of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone and enantiomers of its metabolite 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol in F-344 rats
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Carcinogenicity and DNA adduct formation of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone and enantiomers of its metabolite 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol in F-344 rats

机译:4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁酮及其代谢物4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁醇的致癌性和DNA加合物的形成对F-344大鼠的影响

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摘要

4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) is metabolized to enantiomers of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), found in the urine of virtually all people exposed to tobacco products. We assessed the carcinogenicity in male F-344 rats of (R)-NNAL (5 ppm in drinking water), (S)-NNAL (5 ppm), NNK (5 ppm) and racemic NNAL (10 ppm) and analyzed DNA adduct formation in lung and pancreas of these rats after 10, 30, 50 and 70 weeks of treatment. All test compounds induced a high incidence of lung tumors, both adenomas and carcinomas. NNK and racemic NNAL were most potent; (R)-NNAL and (S)-NNAL had equivalent activity. Metastasis was observed from primary pulmonary carcinomas to the pancreas, particularly in the racemic NNAL group. DNA adducts analyzed were O-2-[4-(3-pyridyl)-4-oxobut-1-yl] thymidine (O-2-POB-dThd), 7-[4-(3-pyridyl)-4-oxobut-1-yl] guanine (7-POB-Gua), O-6-[4-(3-pyridyl)-4-oxobut-1-yl] deoxyguanosine (O-6-POB-dGuo), the 4-(3-pyridyl)-4-hydroxybut-1-yl (PHB) adducts O-2-PHB-dThd and 7-PHB-Gua, O-6-methylguanine (O-6-Me-Gua) and 4-hydroxy1-(3-pyridyl)-1-butanone (HPB)-releasing adducts. Adduct levels significantly decreased with time in the lungs of rats treated with NNK. Pulmonary POB-DNA adducts and O-6-Me-Gua were similar in rats treated with NNK and (S)-NNAL; both were significantly greater than in the (R)-NNAL rats. In contrast, pulmonary PHB-DNA adduct levels were greatest in the rats treated with (R)-NNAL. Total pulmonary DNA adduct levels were similar in (S)NNAL and (R)-NNAL rats. Similar trends were observed for DNA adducts in the pancreas, but adduct levels were significantly lower than in the lung. The results of this study clearly demonstrate the potent pulmonary carcinogenicity of both enantiomers of NNAL in rats and provide important new information regarding DNA damage by these compounds in lung and pancreas.
机译:4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁酮(NNK)代谢为尿液中的4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁醇(NNAL)对映异构体几乎所有接触烟草制品的人。我们评估了雄性F-344大鼠(R)-NNAL(饮用水中5 ppm),(S)-NNAL(5 ppm),NNK(5 ppm)和外消旋NNAL(10 ppm)的致癌性并分析了DNA加合物在治疗10、30、50和70周后,这些大鼠的肺和胰腺中会形成冰。所有测试化合物均引起高发性腺瘤和癌性肺肿瘤。 NNK和外消旋NNAL最有效。 (R)-NNAL和(S)-NNAL具有相同的活性。观察到从原发性肺癌到胰腺的转移,特别是在外消旋的NNAL组。分析的DNA加合物是O-2- [4-(3-吡啶基)-4-氧丁-1-基]胸苷(O-2-POB-dThd),7- [4-(3-吡啶基)-4-氧丁-1-基]鸟嘌呤(7-POB-Gua),O-6- [4-(3-吡啶基)-4-氧代丁-1-基]脱氧鸟苷(O-6-POB-dGuo),4-( 3-吡啶基)-4-羟基丁-1-基(PHB)加成物O-2-PHB-dThd和7-PHB-Gua,O-6-甲基鸟嘌呤(O-6-Me-Gua)和4-羟基1-( 3-吡啶基)-1-丁酮(HPB)释放加合物。在用NNK处理的大鼠的肺中,加合物水平随时间显着降低。在用NNK和(S)-NNAL处理的大鼠中,肺POB-DNA加合物和O-6-Me-Gua相似。两者均显着大于(R)-NNAL大鼠。相反,在用(R)-NNAL处理的大鼠中,肺部PHB-DNA加合物水平最高。 (S)NNAL和(R)-NNAL大鼠的总肺DNA加合物水平相似。胰腺中的DNA加合物观察到类似趋势,但加合物水平显着低于肺中。这项研究的结果清楚地证明了NNAL的两种对映体在大鼠中均具有强大的肺致癌性,并为这些化合物在肺和胰腺中对DNA的损伤提供了重要的新信息。

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