Jang J J, Takahashi M, Furukawa F, Toyoda K, Hasegawa R, Sato H, Hayashi Y
Jpn J Cancer Res. 1986 Nov;77(11):1091-4.
The effects of a single intragastric application of dibutyltin dichloride (DT), at a dose of 30 mg/kg body weight, on N-nitrosobis(2-oxopropyl)amine (BOP)-induced pancreatic carcinogenesis were studied in female Syrian golden hamsters. DT, which has been shown to selectively induce bile duct injury, was administered either 1 week before or after BOP initiation. BOP was injected subcutaneously once a week for 5 weeks at a dose of 10 mg/kg body weight. Controls were injected with BOP alone or given DT without carcinogen. Animals sacrificed at the end of the 25-week experimental period showed a significant inhibitory effect of DT on pancreatic carcinoma induction when DT was given before BOP treatment, although no such influence was evident with DT treatment following BOP exposure. These results indicate that the bile duct and more especially common bile-duct injury induced by DT may be relevant to the inhibition of the initiation stage of BOP-induced pancreatic carcinoma development in Syrian hamsters.
在雌性叙利亚金黄地鼠中,研究了单剂量胃内给予二氯化二丁基锡(DT)(剂量为30毫克/千克体重)对N-亚硝基双(2-氧代丙基)胺(BOP)诱导的胰腺癌发生的影响。已证明DT能选择性诱导胆管损伤,在BOP启动前1周或启动后给予DT。BOP以10毫克/千克体重的剂量每周皮下注射1次,共注射5周。对照组单独注射BOP或给予DT但不给予致癌物。在25周实验期结束时处死的动物显示,当在BOP治疗前给予DT时,DT对胰腺癌诱导有显著抑制作用,尽管在BOP暴露后给予DT治疗没有明显影响。这些结果表明,DT诱导的胆管尤其是胆总管损伤可能与抑制叙利亚仓鼠中BOP诱导的胰腺癌发生起始阶段有关。