TY - JOUR
T1 - Bladder freeze ulceration and sodium saccharin feeding in the rat
T2 - Examination for urinary nitrosamines, mutagens and bacteria, and effects on hepatic microsomal enzymes
AU - Hasegawa, R.
AU - John, M. K.St
AU - Cano, M.
AU - Issenberg, P.
AU - Klein, D. A.
AU - Walker, B. A.
AU - Jones, J. W.
AU - Schnell, R. C.
AU - Merrick, B. A.
AU - Davies, M. H.
AU - McMillan, D. T.
AU - Cohen, S. M.
N1 - Funding Information:
Acknowledgements--The authors are grateful to Dr E. Rogan for her advice and comments regarding the mutagenesis assays, J. Baird and P. Yam for technical assistance, and to J. Leemkuil for assistance in the preparation of this manuscript. This work was supported in part by USPHS Grant CA32313 from the National Cancer Institute. The Thermal Energy Analyzer was loaned to us by the National Cancer Institute under contract NO1-CP-33278.
PY - 1984/12
Y1 - 1984/12
N2 - We previously demonstrated that long-term feeding of sodium saccharin, a non-mutagen, induced bladder carcinomas when administered to F344 male rats with regenerative hyperplasia of the urothelium induced by the freeze-ulceration technique, even without prior chemical initiation (Cohen et al. Cancer Res. 1982, 42, 65). In the present study, we examined the urine of rats subjected to freeze ulceration of the bladder and then fed sodium saccharin at 5% in the diet to evaluate the possibility of a mutagen being generated as a result of ulceration and/or saccharin feeding. Urine was collected into a syringe by aspiration from the urinary bladder after ligating the urethra for 2 hr at intervals from day 0 to day 14 after ulceration. After ulceration and/or sodium saccharin feeding, the urine showed no bacterial contamination, no mutagenic activity in the standard Ames assay, no production of nitrosamines, and no nitrosating environment. In addition, no significant changes in activities of liver microsomal enzymes (i.e. cytochrome P-450, NADPH-cytochrome c reductase, aniline hydroxylase, or ethylmorphine N-demethylase) were observed in rats fed sodium saccharin for 1, 5 or 14 days. Thus, freeze ulceration, and the consequent regenerative hyperplasia of the epithelium, compared with sodium saccharin feeding do not involve the administration of an exogenous mutagenic substance or the generation of a detectable mutagen in the urine.
AB - We previously demonstrated that long-term feeding of sodium saccharin, a non-mutagen, induced bladder carcinomas when administered to F344 male rats with regenerative hyperplasia of the urothelium induced by the freeze-ulceration technique, even without prior chemical initiation (Cohen et al. Cancer Res. 1982, 42, 65). In the present study, we examined the urine of rats subjected to freeze ulceration of the bladder and then fed sodium saccharin at 5% in the diet to evaluate the possibility of a mutagen being generated as a result of ulceration and/or saccharin feeding. Urine was collected into a syringe by aspiration from the urinary bladder after ligating the urethra for 2 hr at intervals from day 0 to day 14 after ulceration. After ulceration and/or sodium saccharin feeding, the urine showed no bacterial contamination, no mutagenic activity in the standard Ames assay, no production of nitrosamines, and no nitrosating environment. In addition, no significant changes in activities of liver microsomal enzymes (i.e. cytochrome P-450, NADPH-cytochrome c reductase, aniline hydroxylase, or ethylmorphine N-demethylase) were observed in rats fed sodium saccharin for 1, 5 or 14 days. Thus, freeze ulceration, and the consequent regenerative hyperplasia of the epithelium, compared with sodium saccharin feeding do not involve the administration of an exogenous mutagenic substance or the generation of a detectable mutagen in the urine.
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U2 - 10.1016/0278-6915(84)90142-X
DO - 10.1016/0278-6915(84)90142-X
M3 - Article
C2 - 6439613
AN - SCOPUS:0021673267
SN - 0278-6915
VL - 22
SP - 935
EP - 942
JO - Food and Chemical Toxicology
JF - Food and Chemical Toxicology
IS - 12
ER -