Okajima E, Hiramatsu T, Kihoin K, Ijuin M, Hirao Y, Ohara S, Babaya K, Tanaka M, Maruyama Y
Gan To Kagaku Ryoho. 1982 Mar;9(3):473-9.
The effect of Tegafur (FT-207) by oral administration on the development of urinary bladder tumors in Wistar strain male rats induced by N-butyl-N-(4-hydroxybutyl) nitrosamine (BBN) was studied. Urinary bladder tumors were induced in 18 of 20 rats (90.0%) when rats were given 0.05% BBN in the drinking water for 8 weeks and then given water without BBN for 12 weeks. When FT-207 100mg/kg B. W./day was given in their diet after treatment with 0.05% BBN for 8 weeks, tumors developed in the urinary bladder with low incidence (9 of 16 rats: 56.3%). Hematotoxicity was not observed in all animals treated with FT-207. These results shows that FT-207 also inhibited the development of urinary bladder tumors treated with BBN in rats by oral administration, which were similar those our previous results showed by intraperitoneal administration of FT-207.
研究了口服替加氟(FT - 207)对N - 丁基 - N -(4 - 羟丁基)亚硝胺(BBN)诱导的Wistar品系雄性大鼠膀胱肿瘤发生的影响。当大鼠饮用含0.05%BBN的水8周,然后饮用不含BBN的水12周时,20只大鼠中有18只(90.0%)诱发了膀胱肿瘤。在用0.05%BBN处理8周后,在其饮食中给予100mg/kg体重/天的FT - 207,膀胱肿瘤的发生率较低(16只大鼠中有9只:56.3%)。在用FT - 207处理的所有动物中均未观察到血液毒性。这些结果表明,口服FT - 207也能抑制BBN诱发的大鼠膀胱肿瘤的发生,这与我们之前腹腔注射FT - 207的结果相似。