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暴露于1,3 - 丁二烯的大鼠和小鼠中雄性介导效应的比较。

A comparison of male-mediated effects in rats and mice exposed to 1,3-butadiene.

作者信息

Anderson D, Hughes J A, Edwards A J, Brinkworth M H

机构信息

BIBRA International, Carshalton, Surrey, UK.

出版信息

Mutat Res. 1998 Jan 16;397(1):77-84. doi: 10.1016/s0027-5107(97)00197-8.

Abstract

There is current concern that exposure of men to certain agents such as radiation and smoking can adversely affect their offspring in terms of cancer outcome. Studies in laboratory animals after radiation have supported such an association, and other studies after male exposure to radiation and various chemicals have also resulted in congenital malformations. The present study was undertaken to examine congenital malformations in offspring from males exposed to 1,3-butadiene over a lower dose range than that in an earlier mouse study and to determine if there was a species difference in sensitivity between rats and mice. An earlier extended dominant lethal study of male CD-1 mice exposed by inhalation to 12.5 ppm and 1250 ppm of 1,3-butadiene for 6 h/day, 5 days/wk, for 10 weeks produced an increase in F1 abnormalities and late deaths at 12.5 ppm and in early deaths at 1250 ppm. The present study examined the same reproductive effects after exposure of male CD-1 mice for 6 h/day, 5 days/wk, for 4 weeks to 12.5, 65 and 130 ppm of 1,3-butadiene. There was no increase in early deaths at 12.5 ppm as in the earlier study but there were statistically significant increases in early deaths at 65 and 130 ppm study and these were not dose-related. There was a non-significant increase in F1 gross abnormalities at 130 ppm and no increase in late deaths. The present study also examined male Sprague-Dawley rats after exposure to 65,400 and 1250 ppm for 6 h/day, 5 days/wk, for 10 weeks. There were no effects on early deaths, late deaths, or congenital malformations in the rat study. There was a reduction in implants at 65 ppm but this was not considered to be biologically/genetically significant as there was no corresponding increase in early deaths and the response was not dose-related. The differences observed between the rat and mouse studies would confirm the greater sensitivity to 1,3-butadiene of the mouse by comparison with the rat as reported by other workers for other parameters.

摘要

目前人们担心,男性接触某些物质(如辐射和吸烟)会在癌症发生方面对其后代产生不利影响。对实验动物进行辐射后的研究支持了这种关联,而且男性接触辐射和各种化学物质后的其他研究也导致了先天性畸形。本研究旨在检查雄性接触1,3 - 丁二烯的后代中的先天性畸形,接触剂量范围低于早期一项小鼠研究中的剂量,并确定大鼠和小鼠之间在敏感性上是否存在物种差异。早期一项对雄性CD - 1小鼠进行的延长显性致死研究中,小鼠每天吸入12.5 ppm和1250 ppm的1,3 - 丁二烯,每天6小时,每周5天,持续10周,结果在12.5 ppm时F1代异常和晚期死亡增加,在1250 ppm时早期死亡增加。本研究检查了雄性CD - 1小鼠每天接触12.5、65和130 ppm的1,3 - 丁二烯,每天6小时,每周5天,持续4周后的相同生殖效应。与早期研究不同,在12.5 ppm时早期死亡没有增加,但在65和130 ppm的研究中早期死亡有统计学上的显著增加,且这些与剂量无关。在130 ppm时F1代总体异常有不显著的增加,晚期死亡没有增加。本研究还检查了雄性斯普拉格 - 道利大鼠,它们每天接触65、400和1250 ppm的1,3 - 丁二烯,每天6小时,每周5天,持续10周。在大鼠研究中,对早期死亡、晚期死亡或先天性畸形没有影响。在65 ppm时着床数减少,但这不被认为具有生物学/遗传学意义,因为早期死亡没有相应增加且反应与剂量无关。大鼠和小鼠研究之间观察到的差异将证实,与其他研究人员针对其他参数所报告的情况一样,小鼠对1,3 - 丁二烯的敏感性高于大鼠。

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