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石油精炼厂废水的慢性及启动/促进皮肤生物测定。

Chronic and initiation/promotion skin bioassays of petroleum refinery streams.

作者信息

Skisak C M, Furedi-Machacek E M, Schmitt S S, Swanson M S, Vernot E H

机构信息

Pennzoil Company, Houston, TX 77252, USA.

出版信息

Environ Health Perspect. 1994 Jan;102(1):82-7. doi: 10.1289/ehp.9410282.

Abstract

Nine refinery streams were tested in both chronic and initiation/promotion (I/P) skin bioassays. In the chronic bioassay, groups of 50 C3H/HeJ mice received twice weekly applications of 50 microl of test article for at least 2 years. In the initiation phase of the I/P bioassay, groups of CD-1 mice received an initiating dose of 50 microl of test article for 5 consecutive days, followed by promotion with 50 microl of phorbol-12-myristate-13-acetate (0.01% w/v in acetone) for 25 weeks. In the promotion phase of the I/P bioassay, CD-1 mice were initiated with 50 microl of 7,12-dimethylbenzanthracene (0.1% w/v in acetone) or acetone, followed by promotion with 50 microl of test article twice weekly for 25 weeks. The most volatile of the streams, sweetened naphtha, and the least volatile, vacuum residuum, were noncarcinogenic in both assays. Middle distillates, with a boiling range of 150 degrees-370 degrees C, demonstrated carcinogenic activity in the chronic bioassay and acted as promoters but not initiators in the I/P bioassay. Untreated mineral oil streams displayed initiating activity and were carcinogenic in the chronic bioassay, presumably due to the presence of polycyclic aromatic hydrocarbons of requisite size and structure. A highly solvent-refined mineral oil stream lacked initiating activity. These results indicate that the I/P bioassay, which takes 6 months to complete, may be a good qualitative predictor of the results of a chronic bioassay, at least for petroleum streams. Furthermore, the I/P bioassay can provide insight into possible mechanisms of tumor development.

摘要

在慢性和启动/促癌(I/P)皮肤生物测定中对九条炼油厂物流进行了测试。在慢性生物测定中,每组50只C3H/HeJ小鼠每周接受两次50微升受试物涂抹,持续至少2年。在I/P生物测定的启动阶段,每组CD-1小鼠连续5天接受50微升受试物的启动剂量,随后用50微升佛波醇-12-肉豆蔻酸酯-13-乙酸酯(在丙酮中0.01% w/v)进行促癌处理,持续25周。在I/P生物测定的促癌阶段,CD-1小鼠用50微升7,12-二甲基苯并蒽(在丙酮中0.1% w/v)或丙酮启动,随后每周两次用50微升受试物进行促癌处理,持续25周。挥发性最强的物流甜化石脑油和挥发性最弱的减压渣油在两种测定中均无致癌性。沸程为150℃至370℃的中间馏分在慢性生物测定中表现出致癌活性,在I/P生物测定中起促癌剂作用但不起启动剂作用。未经处理的矿物油物流表现出启动活性,在慢性生物测定中具有致癌性,可能是由于存在具有所需大小和结构的多环芳烃。一种高度溶剂精制的矿物油物流缺乏启动活性。这些结果表明,耗时6个月完成的I/P生物测定可能是慢性生物测定结果的良好定性预测指标,至少对于石油物流是如此。此外,I/P生物测定可以深入了解肿瘤发生的可能机制。

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