• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

1-甲基-1-亚硝基脲与1,3-双(2-氯乙基)-1-亚硝基脲联合使用对大鼠的毒性超过相加毒性。

More than additive toxicity of the combination of 1-methyl-1-nitrosourea plus 1,3-bis(2-chloroethyl)-1-nitrosourea in the rat.

作者信息

Zeller W J, Berger M R, Henne T, Weber E

出版信息

Cancer Res. 1986 Apr;46(4 Pt 1):1714-6.

PMID:3948161
Abstract

The combination toxicity index of 1-methyl-1-nitrosourea plus 1,3-bis (2-chloroethyl)-1-nitrosourea determined in the rat was 0.32. This overadditive combination toxicity appears mainly to be due to severe damage of the intestinal mucosa as diagnosed by histological examination and to damage of pluripotent stem cells in the bone marrow as could be assessed by the spleen colony technique. The molar ratio of 1-methyl-1-nitrosourea to 1,3-bis(2-chloroethyl)-1-nitrosourea resulting in maximum mortality was about 6. Concomitantly measured DNA interstrand cross-linking in bone marrow cells revealed a slight increase in DNA interstrand cross-linking following both drugs compared to 1, 3-bis(2-chloroethyl)-1-nitrosourea alone.

摘要

在大鼠中测定的1-甲基-1-亚硝基脲加1,3-双(2-氯乙基)-1-亚硝基脲的联合毒性指数为0.32。这种超相加联合毒性主要似乎是由于组织学检查诊断出的肠黏膜严重损伤以及通过脾集落技术评估的骨髓多能干细胞损伤所致。导致最大死亡率的1-甲基-1-亚硝基脲与1,3-双(2-氯乙基)-1-亚硝基脲的摩尔比约为6。同时测量的骨髓细胞中的DNA链间交联显示,与单独使用1,3-双(2-氯乙基)-1-亚硝基脲相比,两种药物处理后DNA链间交联略有增加。

相似文献

1
More than additive toxicity of the combination of 1-methyl-1-nitrosourea plus 1,3-bis(2-chloroethyl)-1-nitrosourea in the rat.1-甲基-1-亚硝基脲与1,3-双(2-氯乙基)-1-亚硝基脲联合使用对大鼠的毒性超过相加毒性。
Cancer Res. 1986 Apr;46(4 Pt 1):1714-6.
2
Pronounced damage of intestinal tract mucosa by the combination of 1-methyl-1-nitrosourea plus 1,3-bis-(2-chloroethyl)-1-nitrosourea. Effect of drug sequence and time interval of administration.1-甲基-1-亚硝基脲与1,3-双(2-氯乙基)-1-亚硝基脲联合使用对肠道黏膜造成明显损伤。给药顺序和给药时间间隔的影响。
Toxicol Lett. 1986 Jul-Aug;32(1-2):59-64. doi: 10.1016/0378-4274(86)90049-4.
3
Chemical structure of carbamoylating groups and their relationship to bone marrow toxicity and antiglioma activity of bifunctionally alkylating and carbamoylating nitrosoureas.氨甲酰化基团的化学结构及其与双功能烷基化和氨甲酰化亚硝基脲的骨髓毒性和抗胶质瘤活性的关系。
Cancer Res. 1985 Sep;45(9):4185-91.
4
Retrovirus-mediated expression of a DNA repair protein in bone marrow protects hematopoietic cells from nitrosourea-induced toxicity in vitro and in vivo.逆转录病毒介导的骨髓中一种DNA修复蛋白的表达在体外和体内均可保护造血细胞免受亚硝基脲诱导的毒性作用。
Cancer Res. 1995 Jun 15;55(12):2608-14.
5
Increased in vitro toxicity to mouse bone marrow with 1,3-bis(2-chloroethyl)-1-nitrosourea and hyperthermia.1,3-双(2-氯乙基)-1-亚硝基脲与热疗联合应用时,对小鼠骨髓的体外毒性增加。
Cancer Res. 1979 Jul;39(7 Pt 1):2547-9.
6
Myeloprotective effect of diethyldithiocarbamate treatment following 1,3-bis(2-chloroethyl)-1-nitrosourea, adriamycin, or mitomycin C in mice.二乙基二硫代氨基甲酸盐对经1,3-双(2-氯乙基)-1-亚硝基脲、阿霉素或丝裂霉素C处理的小鼠的骨髓保护作用
Cancer Res. 1989 May 15;49(10):2574-7.
7
DNA damage and repair in the bone marrow of rats treated with four chloroethylnitrosoureas.四种氯乙基亚硝脲处理的大鼠骨髓中的DNA损伤与修复
Cancer Res. 1984 Feb;44(2):514-8.
8
Interstrand cross-linking of DNA by 1,3-bis(2-chloroethyl)-1-nitrosourea and other 1-(2-haloethyl)-1-nitrosoureas.1,3-双(2-氯乙基)-1-亚硝基脲及其他1-(2-卤乙基)-1-亚硝基脲对DNA的链间交联作用。
Cancer Res. 1977 May;37(5):1450-4.
9
[Relation between the changes in the structure and synthesis of DNA in the cells of mouse leukemia L1210 induced by 1-methyl-1-nitrosourea and 1,3-bis(2-chloroethyl)-1-nitrosourea].[1-甲基-1-亚硝基脲和1,3-双(2-氯乙基)-1-亚硝基脲诱导的小鼠白血病L1210细胞中DNA结构变化与合成之间的关系]
Biull Eksp Biol Med. 1986 Feb;101(2):192-5.
10
Sensitivity of human and murine hematopoietic precursor cells to 2-[3-(2-chloroethyl)-3-nitrosoureido]-D-glucopyranose and 1,3-bis(2-chloroethyl)-1-nitrosourea.
Cancer Res. 1978 Feb;38(2):257-60.

引用本文的文献

1
Effect of temozolomide and dacarbazine on O6-alkylguanine-DNA alkyltransferase activity and sensitivity of human tumor cells and xenografts to 1,3-bis(2-chloroethyl)-1-nitrosourea.替莫唑胺和达卡巴嗪对O6-烷基鸟嘌呤-DNA烷基转移酶活性以及人肿瘤细胞和异种移植瘤对1,3-双(2-氯乙基)-1-亚硝基脲敏感性的影响
Cancer Chemother Pharmacol. 1993;32(1):59-63. doi: 10.1007/BF00685877.
2
Sequential therapy with dacarbazine and carmustine: a phase I study.达卡巴嗪与卡莫司汀序贯治疗:一项I期研究。
Cancer Chemother Pharmacol. 1994;34(6):509-14. doi: 10.1007/BF00685663.
3
Inhibition of O6-alkylguanine-DNA alkyltransferase in animal and human ovarian tumor cell lines by O6-benzylguanine and sensitization to BCNU.
O6-苄基鸟嘌呤对动物和人类卵巢肿瘤细胞系中O6-烷基鸟嘌呤-DNA烷基转移酶的抑制作用及对卡莫司汀的增敏作用。
Cancer Chemother Pharmacol. 1995;35(3):262-6. doi: 10.1007/BF00686559.
4
Sensitization of human colon tumour cell lines to carmustine by depletion of O6-alkylguanine-DNA alkyltransferase.通过消耗O6-烷基鸟嘌呤-DNA烷基转移酶使人类结肠肿瘤细胞系对卡莫司汀敏感化。
J Cancer Res Clin Oncol. 1995;121(4):225-9. doi: 10.1007/BF01366966.
5
Increased cytotoxicity of 1-(2-chloroethyl)-1-nitroso-3(4-methyl)-cyclohexylurea by pretreatment with O6-methylguanine in resistant but not in sensitive human melanoma cells.在耐药而非敏感的人黑色素瘤细胞中,通过用O6-甲基鸟嘌呤预处理,1-(2-氯乙基)-1-亚硝基-3(4-甲基)-环己基脲的细胞毒性增加。
J Cancer Res Clin Oncol. 1987;113(4):387-91. doi: 10.1007/BF00397725.