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[用于评估化疗药物的大鼠膀胱肿瘤实验模型]

[Experimental model of urinary bladder tumor in rats for evaluation of chemotherapeutic agents].

作者信息

Hirao Y, Momose H, Samma S, Ozono S, Babaya K, Okajima E

机构信息

Department of Urology, Nara Medical University.

出版信息

Hinyokika Kiyo. 1988 Nov;34(11):1885-93.

PMID:3242363
Abstract

The chemotherapeutic agents were evaluated using the experimental urinary bladder tumor rat model induced by N-butyl-N-(4-hydroxybutyl) nitrosamine (BBN). Nine hundred and fourteen male rats received 0.05% BBN in drinking water for 8 weeks, and were divided into 35 groups to follow the regimens of chemotherapeutic agents. Thirty one groups received the agents after BBN treatment, and 4 groups were given the oral agents starting simultaneously with BBN treatment. All rats were killed at 20 weeks and incidence of the urinary bladder was examined histopathologically. The following 13 agents were evaluated; adriamycin (ADM), mitomycin-C (MMC), cyclophosphamide (CPM), 5-fluoro-uracil (5-Fu), N-(2-tetrahydrofuryl)-5-fluorouracil (FT-207), neocarcinostatine (NCS), carbazil quinone (CQ), bleomycin (BLM), vincristine (VCR) and cis-diammine-dichloroplatinum (CDDP) were dosed intraperitoneally, and N-(2-tetrahydrofuryl)-5-fluorouracil (FT-207), 1: 4 mixture of FT-207 and uracil (UFT) and 1-Hexylcarbamoyl-5-fluorouracil (HCFU) were dosed orally. Among these agents, 5-Fu, FT-207, CQ, VCR, CDDP, UFT and HCFU were effective in inhibiting the incidence of urinary bladder tumor induced by BBN. In conclusion, the experimental bladder tumor rat model induced by BBN seems to be useful in evaluating the effective chemotherapeutic agents for a superficial bladder cancer. The importance of the experimental animal model for the evaluation of chemotherapeutic agents is discussed.

摘要

使用由N-丁基-N-(4-羟丁基)亚硝胺(BBN)诱导的实验性大鼠膀胱肿瘤模型对化疗药物进行评估。914只雄性大鼠饮用含0.05%BBN的水8周,然后分为35组,按照化疗药物方案进行治疗。31组在BBN治疗后接受药物治疗,4组在BBN治疗开始时同时给予口服药物。所有大鼠在20周时处死,对膀胱发病率进行组织病理学检查。评估了以下13种药物;阿霉素(ADM)、丝裂霉素-C(MMC)、环磷酰胺(CPM)、5-氟尿嘧啶(5-Fu)、N-(2-四氢呋喃基)-5-氟尿嘧啶(FT-207)、新制癌菌素(NCS)、卡巴醌(CQ)、博来霉素(BLM)、长春新碱(VCR)和顺二氨二氯铂(CDDP)通过腹腔注射给药,N-(2-四氢呋喃基)-5-氟尿嘧啶(FT-207)、FT-207与尿嘧啶(UFT)的1:4混合物以及1-己基氨基甲酰基-5-氟尿嘧啶(HCFU)通过口服给药。在这些药物中,5-Fu、FT-207、CQ、VCR、CDDP、UFT和HCFU可有效抑制BBN诱导的膀胱肿瘤发病率。总之,BBN诱导的实验性大鼠膀胱肿瘤模型似乎可用于评估浅表性膀胱癌的有效化疗药物。讨论了实验动物模型在评估化疗药物中的重要性。

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