Suppr超能文献

外源性腐胺预防α-二氟甲基鸟氨酸对大鼠膀胱癌发生的抑制作用。

Prevention of inhibitory effects of alpha-difluoromethylornithine on rat urinary bladder carcinogenesis by exogenous putrescine.

作者信息

Nowels K, Homma Y, Seidenfeld J, Oyasu R

出版信息

Cancer Biochem Biophys. 1986 Oct;8(4):257-63.

PMID:3802047
Abstract

We previously demonstrated that repeated instillation of alpha-difluoromethylornithine (DFMO), an irreversible inhibitor of ornithine decarboxylase (ODC), inhibits (or retards) urinary bladder carcinogenesis in rats. Since ODC catalyzes the first step in polyamine synthesis, the inhibition of polyamine formation may be responsible for tumor inhibition by DFMO. The present experiment was conducted using male Fischer rats with a heterotopically transplanted urinary bladder (HTB) to determine whether the effects of DFMO are prevented by exogeneous Pu. HTBs were treated with 0.25 mg of N-methyl-N-nitrosourea (MNU) once a week for 3 weeks and the animals were then arbitrarily divided into 6 groups. Beginning one week following the last MNU treatment, all rats received twice a week instillation (0.5 ml each) as follows: Group 1 rats, normal rat urine; Group 2, 2% DFMO in urine; Group 3, 250 microM Pu and 2% DFMO in urine; Group 4, 250 microM Pu in urine; Group 5, urine for 10 weeks followed by 2% DFMO in urine; and Group 6, urine for 10 weeks followed by 250 microM Pu and 2% DFMO in urine. At 10 weeks following the last MNU instillation 5 rats from each of Groups 1 through 4 were killed for determination of urothelial polyamine levels. An additional 4 rats of Group 1 were killed at 10 weeks for histological examination. All remaining rats were killed 20 weeks after the last MNU instillation. Polyamine levels showed no significant difference among the 4 groups. The incidence of carcinoma was significantly lower in the group treated with DFMO (p less than 0.001, Group 1 vs Group 2), confirming our previous observation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们之前证明,反复灌注鸟氨酸脱羧酶(ODC)的不可逆抑制剂α-二氟甲基鸟氨酸(DFMO)可抑制(或延缓)大鼠膀胱癌的发生。由于ODC催化多胺合成的第一步,多胺形成的抑制可能是DFMO抑制肿瘤的原因。本实验使用具有异位移植膀胱(HTB)的雄性Fischer大鼠进行,以确定外源性腐胺(Pu)是否能阻止DFMO的作用。HTB每周用0.25毫克N-甲基-N-亚硝基脲(MNU)处理一次,共3周,然后将动物随机分为6组。在最后一次MNU处理后一周开始,所有大鼠每周接受两次灌注(每次0.5毫升),如下:第1组大鼠,正常大鼠尿液;第2组,尿液中含2% DFMO;第3组,尿液中含250微摩尔Pu和2% DFMO;第4组,尿液中含250微摩尔Pu;第5组,先灌注10周尿液,然后灌注含2% DFMO的尿液;第6组,先灌注10周尿液,然后灌注含250微摩尔Pu和2% DFMO的尿液。在最后一次MNU灌注后10周,处死第1组至第4组每组中的5只大鼠,以测定尿路上皮多胺水平。第1组另外4只大鼠在10周时处死进行组织学检查。所有剩余大鼠在最后一次MNU灌注后20周处死。4组之间的多胺水平无显著差异。DFMO处理组的癌发生率显著较低(p小于0.001,第1组与第2组),证实了我们之前的观察结果。(摘要截断于250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验