The dose dependence of
K2CO3 promotion of two-stage urinary bladder
carcinogenesis and the amplifying effects of additional
L-ascorbic acid (AsA) administration were investigated. Male F344 rats were given 0.05%
N-butyl-N-(4-hydroxybutyl)nitrosamine in their
drinking water for 4 weeks and then fed basal diet containing
K2CO3 at levels of 0, 1, 1.5, 2.2, and 3% with or without 5% AsA or 3% NaHCO3 supplementation from weeks 5 to 8 (4 weeks) and weeks 12 to 20 (9 weeks). During weeks 9 to 11 (3 weeks), the rats were fed 3%
uracil in their diet. For controls, rats without
N-butyl-N-(4-hydroxybutyl)nitrosamine treatment were given either 3%
K2CO3, 5% AsA, or both plus the
uracil treatment. The total observation period was 20 weeks.
K2CO3 dose dependently increased the numbers of the putative preneoplastic lesion, papillary or nodular
hyperplasia, and
papillomas in rats initiated with
N-butyl-N-(4-hydroxybutyl)nitrosamine. AsA (5%), while itself exerting no promoting effect, amplified the enhancing influence of
K2CO3 on the induction of papillary or nodular
hyperplasia and
papillomas. The dose-dependent elevation of urinary pH and K+ concentration was associated with
K2CO3 treatment with or without AsA. Thus, increased urinary pH and K+ concentration appear to play important roles in
K2CO3 promotion, and AsA amplifies this promotion.