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多种硝基芳烃及其他硝基化合物在大鼠和小鼠肝细胞DNA修复试验中的遗传毒性。

Genotoxicity of a variety of nitroarenes and other nitro compounds in DNA-repair tests with rat and mouse hepatocytes.

作者信息

Mori H, Sugie S, Yoshimi N, Kinouchi T, Ohnishi Y

出版信息

Mutat Res. 1987 Feb;190(2):159-67. doi: 10.1016/0165-7992(87)90049-2.

DOI:10.1016/0165-7992(87)90049-2
PMID:3821774
Abstract

Genotoxicity of a variety of nitroarenes and other compounds was examined in DNA-repair tests with rat or mouse hepatocytes. Out of 15 nitroarenes tested, 9 compounds, i.e., 1-nitropyrene, 1,3-dinitropyrene, 1,6-dinitropyrene, 1,8-dinitropyrene, 1-nitro-3-acetoxypyrene, 3-nitrofluoranthene, 2-nitrofluorene, 2,7-di-nitrofluorene and 5-nitroacenaphthene elicited positive response of DNA repair in the tests with rat and mouse hepatocytes. Among the positive chemicals, the DNA-repair level of the 3 dinitropyrene isomers was much higher than other nitroarenes. The results indicate that a number of nitroarenes are metabolically activated in the primary culture of rodent hepatocytes, and suggest potential carcinogenicity of 1-nitropyrene and 1-nitro-3-acetoxypyrene the carcinogenicity of which is either not clear or unknown. Of the other nitro compounds, 2-(2-furyl)-3-(5-nitro-2-furyl)acrylamide as well as 4-nitroquinoline 1-oxide were clearly genotoxic in the assays with hepatocytes of both species. However, 5-nitro-2-furaldehyde semicarbazone was negative in both assays with hepatocytes of 2 species.

摘要

在大鼠或小鼠肝细胞的DNA修复试验中检测了多种硝基芳烃和其他化合物的遗传毒性。在测试的15种硝基芳烃中,9种化合物,即1-硝基芘、1,3-二硝基芘、1,6-二硝基芘、1,8-二硝基芘、1-硝基-3-乙酰氧基芘、3-硝基荧蒽、2-硝基芴、2,7-二硝基芴和5-硝基苊在大鼠和小鼠肝细胞试验中引发了DNA修复的阳性反应。在阳性化学物质中,3种二硝基芘异构体的DNA修复水平远高于其他硝基芳烃。结果表明,许多硝基芳烃在啮齿动物肝细胞原代培养中被代谢激活,并提示1-硝基芘和1-硝基-3-乙酰氧基芘具有潜在致癌性,其致癌性尚不明确或未知。在其他硝基化合物中,2-(2-呋喃基)-3-(5-硝基-2-呋喃基)丙烯酰胺以及4-硝基喹啉1-氧化物在两种动物肝细胞试验中均具有明显的遗传毒性。然而,5-硝基-2-糠醛半卡巴腙在两种动物肝细胞试验中均为阴性。

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Genotoxicity of a variety of nitroarenes and other nitro compounds in DNA-repair tests with rat and mouse hepatocytes.多种硝基芳烃及其他硝基化合物在大鼠和小鼠肝细胞DNA修复试验中的遗传毒性。
Mutat Res. 1987 Feb;190(2):159-67. doi: 10.1016/0165-7992(87)90049-2.
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引用本文的文献

1
Simultaneous measurement of unscheduled and replicating DNA synthesis by means of a new cell culture insert DNA retention method: rapid induction of replicating DNA synthesis in response to genotoxic carcinogens.通过一种新的细胞培养插入物DNA保留方法同时测量非预定和复制性DNA合成:对遗传毒性致癌物快速诱导复制性DNA合成。
Jpn J Cancer Res. 1996 Aug;87(8):805-15. doi: 10.1111/j.1349-7006.1996.tb02104.x.
2
Effect of varying the exposure and 3H-thymidine labeling period upon the outcome of the primary hepatocyte DNA repair assay.改变暴露条件和3H-胸腺嘧啶核苷标记时间对原代肝细胞DNA修复试验结果的影响。
Cell Biol Toxicol. 1988 Jun;4(2):199-209. doi: 10.1007/BF00119246.
3
Genotoxicity of a variety of hydrazine derivatives in the hepatocyte primary culture/DNA repair test using rat and mouse hepatocytes.
使用大鼠和小鼠肝细胞的肝细胞原代培养/DNA修复试验中多种肼衍生物的遗传毒性。
Jpn J Cancer Res. 1988 Feb;79(2):204-11. doi: 10.1111/j.1349-7006.1988.tb01578.x.