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有机氯化合物对白鲸皮肤成纤维细胞体外微核的诱导作用。

Induction of micronuclei in vitro by organochlorine compounds in beluga whale skin fibroblasts.

作者信息

Gauthier J M, Dubeau H, Rassart E

机构信息

Département des Sciences Biologiques, Université du Québec à Montréal, C.P. 8888, Succursale Centre-Ville, Montréal, Québec,

出版信息

Mutat Res. 1999 Feb 2;439(1):87-95. doi: 10.1016/s1383-5718(98)00178-8.

Abstract

Beluga whales (Delphinapterus leucas) inhabiting the St. Lawrence estuary are highly contaminated with environmental pollutants and have a high incidence of cancer. Environmental contaminants may be partly responsible for the high cancer incidence observed in this population. DNA damage plays an important role in the development of cancer. The micronuclei (MN) assay was used to test the genotoxic potential of organochlorine (OC) pesticides with and without external metabolic factor in skin fibroblasts of an Arctic beluga whale. Toxaphene, chlordane and p,p'-DDT induced significant (p<0. 05) concentration-response increases of micronucleated cells (MNCs). Statistically significant increases in MNCs, ranging from 1.7- to 5-folds when compared to control cultures, were observed for 0.05, 0. 5, 5 and 10 microg/ml toxaphene, 2, 5 and 10 microg/ml chlordane and 10 and 15 microg/ml p,p'-DDT. Presence of exogeneous metabolic factor (S9) completely abolished the MN induction potency of chlordane and p,p'-DDT, and toxaphene induced MN formation at higher concentrations (0.5 microg/ml) than without S9 mix. The ecotoxicological significance of MN induction by low concentrations of toxaphene is unknown and do not imply that toxaphene is involved in the etiology of cancer in St. Lawrence beluga whales. However, because of the known genotoxicity of toxaphene and the long lifespan of beluga whales, it cannot be excluded that toxaphene may pose a long-term genetic hazard to the more contaminated whales of this population.

摘要

栖息在圣劳伦斯河口的白鲸(白鲸属)受到环境污染物的高度污染,且癌症发病率很高。环境污染物可能是导致该种群中观察到的高癌症发病率的部分原因。DNA损伤在癌症发展中起重要作用。微核(MN)试验用于测试北极白鲸皮肤成纤维细胞中有机氯(OC)农药在有无外部代谢因子情况下的遗传毒性潜力。毒杀芬、氯丹和p,p'-滴滴涕诱导微核化细胞(MNCs)的浓度-反应显著增加(p<0.05)。与对照培养物相比,观察到0.05、0.5、5和10微克/毫升毒杀芬、2、5和10微克/毫升氯丹以及10和15微克/毫升p,p'-滴滴涕导致MNCs有统计学显著增加,增幅为1.7至5倍。外源性代谢因子(S9)的存在完全消除了氯丹和p,p'-滴滴涕的微核诱导能力,且毒杀芬在有S9混合物时比没有时在更高浓度(0.5微克/毫升)下诱导微核形成。低浓度毒杀芬诱导微核的生态毒理学意义尚不清楚,也不意味着毒杀芬参与圣劳伦斯白鲸的癌症病因。然而,由于毒杀芬已知的遗传毒性以及白鲸的长寿,不能排除毒杀芬可能对该种群中污染更严重的鲸鱼构成长期遗传危害。

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