N-nitrosodiethylamine initiation of carcinogenesis in Japanese medaka (Oryzias latipes): Hepatocellular proliferation, toxicity, and neoplastic lesions resulting from short term, low level exposure
Nj. Brown-peterson et al., N-nitrosodiethylamine initiation of carcinogenesis in Japanese medaka (Oryzias latipes): Hepatocellular proliferation, toxicity, and neoplastic lesions resulting from short term, low level exposure, TOXICOL SCI, 50(2), 1999, pp. 186-194
To investigate relationships among carcinogen exposure, cell proliferation,
and carcinogenesis, 14-day post-hatch Japanese medaka (Oryzias latipes) we
re exposed to 0, 10, 25, 50, or 100 ppm N-nitrosodiethylamine (DEN) for 48
h under static renewal conditions. They were then held in clean water until
sampling at 3 and 6 months. The frequencies of hepatic lesions and neoplas
ms were determined from hematoxylin/eosin-stained paraffin sections. A sign
ificant (p < 0.0001) concentration-related increase in hepatic vacuolated f
oci occurred in 3- and 6-month samples, with males having a significantly (
p = 0.02) higher incidence than females. Concentration-related increases in
degenerative lesions were documented for spongiosis hepatis at 3 months (p
= 0.053) and hepatic vacuoles at 6 months (p = 0.005). There was a signifi
cant (p = 0.0001) concentration-related increase in macrophage aggregates a
t 6 months. Basophilic foci were significantly related (p < 0.0001) to DEN
concentration at 3 months post-exposure and were unaffected by gender or ag
e. At both 3 and 6 months, there were significant concentration-related inc
reases in hepatocellular carcinoma (p less than or equal to 0.02), Hepatocy
te proliferation in 3-month whole specimens was quantified using an immunoh
istochemical assay for proliferating-cell nuclear antigen. Trend tests and
a probit dose-response model showed a significantly positive correlation (p
= 0.015) between proliferating hepatocytes and DEN concentrations. These r
esults confirm that short-term exposure to low and moderate levels of DEN i
nitiates concentration-dependent carcinogenic effects in medaka that are ap
parent at 3 months post exposure. DEN could be an effective initiator in an
initiation/promotion assay for medaka using a 48-h exposure period, DEN co
ncentrations less than or equal to 10 ppm, and a 6-month sampling period.