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移植大鼠气管对7,12-二甲基苯并(a)蒽的定量暴露。

Quantitative exposure of grafted rat tracheas to 7, 12-dimethylbenz(a)anthracene.

作者信息

Griesemer R A, Nettesheim P, Martin D H, Caton J E

出版信息

Cancer Res. 1977 May;37(5):1266-71.

PMID:404031
Abstract

A method was developed for continuously exposing tracheal epithelium to measured amounts of carcinogen. Beeswax was the vehicle for sustained release of carcinogen, and tracheas transplanted to s.c. sites were target tissues. In the experiment reported here, transplanted rat tracheas were exposed to a potent carcinogen, 7,12-di-methyl benz(a)anthracene (DMBA). The rate of release of DMBA from the beeswax carrier within the tracheal lumen approached first order when the initial concentration of carcinogen was high (3200 to 325 microng in a 24.45-mg pellet). With lower concentrations, where the carcinogen was dissolved in the beeswax, initial release was rapid, and most of the carcinogen was delivered within 4 weeks. At high DMBA dose levels, the entire tracheal epithelium was uniformly replaced by keratinizing squamous metaplasia after 1 week of exposure, and after 2 months, when from 280 to 910 microng DMBA had been delivered, all transplants had developed invasive squamous carcinomas. Sarcomas also developed in 19% of the transplants. At lower dose levels the epithelial reactions were more varied, and tumor development was more protracted. The lowest DMBA dose presently known to diduce carcinomas in this experimental model is 40 microng, which is in the dose range used for tumor initiation in skin carcinogenesis studies in mice.

摘要

已开发出一种将气管上皮持续暴露于定量致癌物的方法。蜂蜡作为致癌物的缓释载体,移植到皮下部位的气管为靶组织。在本文报道的实验中,移植的大鼠气管暴露于一种强效致癌物7,12 - 二甲基苯并(a)蒽(DMBA)。当气管腔内蜂蜡载体中致癌物的初始浓度较高(在一个24.45毫克的药片中为3200至325微克)时,DMBA从蜂蜡载体中的释放速率接近一级反应。在较低浓度下,致癌物溶解于蜂蜡中,初始释放迅速,且大部分致癌物在4周内释放完毕。在高DMBA剂量水平下,暴露1周后整个气管上皮被角化鳞状化生均匀取代,2个月后,当已递送280至910微克DMBA时,所有移植组织均发展为浸润性鳞状癌。19%的移植组织还发生了肉瘤。在较低剂量水平下,上皮反应更为多样,肿瘤发生过程更为漫长。在该实验模型中目前已知能诱发癌症的最低DMBA剂量为40微克,这处于小鼠皮肤致癌研究中用于肿瘤起始的剂量范围内。

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