Bioassay of 4'-(chloroacetyl)-acetanilide for possible carcinogenicity.

{"title":"Bioassay of 4'-(chloroacetyl)-acetanilide for possible carcinogenicity.","authors":"","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>A bioassay for the possible carcinogenicity of 4'-(chloroacetyl)-acetanilide was conducted using Fischer 344 rats and B6C3F1 mice. 4'-(Chloroacetyl)-acetanilide was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species. Twenty animals of each sex and species were placed on test as controls. The high and low dietary concentrations of 4'-(chloroacetyl)-acetanilide were, respectively, 2,000 and 1,000 ppm for rats and 10,000 and 5,000 ppm for mice. The compound was administered for 87 weeks of a 102-week period in rats and for 90 weeks of a 105-week period in mice. Mice were killed at the end of the last week of compound administration, while rats were observed for 1 week after compound administration ceased. There were no significant positive associations between the concentration of 4'-(chloroacetyl)-acetanilide administered and mortality in rats or mice of either sex. Adequate numbers of animals in all groups survived sufficiently long to be at risk from late-developing tumors. Dose-related mean body weight depression was observed for males and females of both species, indicating that the concentrations of 4'-(chloroacetyl)-acetanilide administered to the animals in this bioassay may have approximated the maximum tolerated concentrations. None of the statistical tests for any site in rats of either sex or in male mice indicated a significant positive association between compound administration and tumor incidence. Although there was a significant positive association between the concentration of the compound administered and the incidences of hepatocellular adenomas in female mice, the Fischer exact comparisons were not significant. Under the conditions of this bioassay, 4'-(chloroacetyl)-acetanilide was not carcinogenic when administered in the diet to Fischer 344 rats or B6C3F1 mice of either sex.</p>","PeriodicalId":18935,"journal":{"name":"National Cancer Institute carcinogenesis technical report series","volume":"177 ","pages":"1-103"},"PeriodicalIF":0.0000,"publicationDate":"1979-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"National Cancer Institute carcinogenesis technical report series","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

A bioassay for the possible carcinogenicity of 4'-(chloroacetyl)-acetanilide was conducted using Fischer 344 rats and B6C3F1 mice. 4'-(Chloroacetyl)-acetanilide was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species. Twenty animals of each sex and species were placed on test as controls. The high and low dietary concentrations of 4'-(chloroacetyl)-acetanilide were, respectively, 2,000 and 1,000 ppm for rats and 10,000 and 5,000 ppm for mice. The compound was administered for 87 weeks of a 102-week period in rats and for 90 weeks of a 105-week period in mice. Mice were killed at the end of the last week of compound administration, while rats were observed for 1 week after compound administration ceased. There were no significant positive associations between the concentration of 4'-(chloroacetyl)-acetanilide administered and mortality in rats or mice of either sex. Adequate numbers of animals in all groups survived sufficiently long to be at risk from late-developing tumors. Dose-related mean body weight depression was observed for males and females of both species, indicating that the concentrations of 4'-(chloroacetyl)-acetanilide administered to the animals in this bioassay may have approximated the maximum tolerated concentrations. None of the statistical tests for any site in rats of either sex or in male mice indicated a significant positive association between compound administration and tumor incidence. Although there was a significant positive association between the concentration of the compound administered and the incidences of hepatocellular adenomas in female mice, the Fischer exact comparisons were not significant. Under the conditions of this bioassay, 4'-(chloroacetyl)-acetanilide was not carcinogenic when administered in the diet to Fischer 344 rats or B6C3F1 mice of either sex.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
4'-(氯乙酰基)-乙酰苯胺可能致癌性的生物测定。
用Fischer 344大鼠和B6C3F1小鼠进行了4′-(氯乙酰)-乙酰苯胺可能致癌性的生物测定。4'-(氯乙酰基)-乙酰苯胺以两种浓度中的任意一种加入饲料中,每组50只雄性和50只雌性动物。各性别、各物种各20只作为对照进行试验。4′-(氯乙酰)-乙酰苯胺的高、低膳食浓度分别为大鼠为2000 ppm和1000 ppm,小鼠为10000 ppm和5000 ppm。大鼠102周中的87周,小鼠105周中的90周。复方给药最后一周处死小鼠,停药后观察大鼠1周。给药4′-(氯乙酰)乙酰苯胺的浓度与大鼠或小鼠的死亡率之间没有显著的正相关。所有组中都有足够数量的动物存活了足够长的时间,从而有患晚期肿瘤的风险。两种动物的雄性和雌性均观察到与剂量相关的平均体重下降,表明在本生物试验中给予动物的4'-(氯乙酰基)-乙酰苯胺浓度可能接近最大耐受浓度。在任何部位的统计测试中,无论是大鼠还是雄性小鼠,都没有显示复方给药与肿瘤发病率之间有显著的正相关。虽然在雌性小鼠中,化合物的浓度与肝细胞腺瘤的发生率之间存在显著的正相关,但Fischer精确比较并不显著。在这种生物试验条件下,4'-(氯乙酰)-乙酰苯胺在饲喂Fischer 344大鼠或B6C3F1小鼠时均无致癌性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Bioassay of sulfisoxazole for possible carcinogenicity. Bioassay of diazinon for possible carcinogenicity. Bioassay of aldicarb for possible carcinogenicity. Bioassay of malaoxon for possible carcinogenicity. Bioassay of C.I. vat yellow 4 for possible carcinogenicity.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1