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2337872 
Journal Article 
Orally administered nicotine induces urothelial hyperplasia in rats and mice 
Dodmane, PR; Arnold, LL; Pennington, KL; Cohen, SM 
2014 
Toxicology
ISSN: 0300-483X
EISSN: 1879-3185 
315 
49-54 
English 
Tobacco smoking is a major risk factor for multiple human cancers including urinary bladder carcinoma. Tobacco smoke is a complex mixture containing chemicals that are known carcinogens in humans and/or animals. Aromatic amines a major class of DNA-reactive carcinogens in cigarette smoke, are not present at sufficiently high levels to fully explain the incidence of bladder cancer in cigarette smokers. Other agents in tobacco smoke could be excreted in urine and enhance the carcinogenic process by increasing urothelial cell proliferation. Nicotine is one such major component, as it has been shown to induce cell proliferation in multiple cell types in vitro. However, in vivo evidence specifically for the urothelium is lacking. We previously showed that cigarette smoke induces increased urothelial cell proliferation in mice. In the present study, urothelial proliferative and cytotoxic effects were examined after nicotine treatment in mice and rats. Nicotine hydrogen tartrate was administered in drinking water to rats (52 ppm nicotine) and mice (514 ppm nicotine) for 4 weeks and urothelial changes were evaluated. Histopathologically, 7/10 rats and 4/10 mice showed simple hyperplasia following nicotine treatment compared to none in the controls. Rats had an increased mean BrdU labeling index compared to controls, although it was not statistically significantly elevated in either species. Scanning electron microscopic visualization of the urothelium did not reveal significant cytotoxicity. These findings suggest that oral nicotine administration induced urothelial hyperplasia (increased cell proliferation), possibly due to a mitogenic effect of nicotine and/or its metabolites. 
IRIS
• Arsenic Hazard ID
          iAs MOA Literature Categorization
               Oxidative Stress
• Arsenic (Inorganic)
     4. Adverse Outcome Pathways/Networks Screening
          Excluded/Not relevant
               Electronic discard
• Arsenic MOA
     2. Electronic Discard
     1. MOA Literature Screening
          MOA Cluster