Nakanishi K, Fukushima S, Hagiwara A, Tamano S, Ito N
J Natl Cancer Inst. 1982 Mar;68(3):497-500.
Studied were conducted to determine whether initial treatment with N-2-fluorenylacetamide (2-FAA) or N-butyl-N-(4-hydroxybutyl)nitrosamine (BBN) followed by treatment with either phenobarbital sodium (PB) or sodium saccharin (SS) induced or enhanced liver and/or bladder tumorigenesis. Male inbred F344 rats were given 0.05% PB and 5.0% SS in the diet for 32 weeks after 4-week administration of 0.02% 2-FAA treatment and induced hyperplastic liver nodules after BBN treatment. The SS significantly enhanced induction of bladder hyperplasias, but not papilloma after BBN treatment, and induced bladder hyperplasias after 2-FAA treatment. However, PB had no effect on the bladder and SS had no effect on the liver after either 2-FAA or BBN treatment. The data indicate that although 2-FAA and BBN have tumor-initiating effects in the liver and urinary bladder, the tumor-promoting effects of PB and SS are organ-specific. The tumor-promoting effect of PB for the liver is relatively greater than that of SS for the urinary bladder.
开展研究以确定先用N - 2 - 芴基乙酰胺(2 - FAA)或N - 丁基 - N -(4 - 羟基丁基)亚硝胺(BBN)处理,随后用苯巴比妥钠(PB)或糖精钠(SS)处理是否会诱导或增强肝脏和/或膀胱肿瘤发生。雄性近交F344大鼠在给予0.02% 2 - FAA处理4周后,或在给予BBN处理后,在饮食中给予0.05% PB和5.0% SS,持续32周。BBN处理后,SS显著增强了膀胱增生的诱导,但未增强乳头状瘤的诱导,且在2 - FAA处理后诱导了膀胱增生。然而,2 - FAA或BBN处理后,PB对膀胱无影响,SS对肝脏无影响。数据表明,虽然2 - FAA和BBN在肝脏和膀胱中有肿瘤启动作用,但PB和SS的肿瘤促进作用具有器官特异性。PB对肝脏的肿瘤促进作用相对大于SS对膀胱的肿瘤促进作用。