The Disposition and Metabolism of N‐Nitrosodiethylamine in Adult, Infant and Foetal Tissues of the Syrian Golden Hamster
- 1 February 1984
- journal article
- research article
- Published by Wiley in Acta Pharmacologica et Toxicologica
- Vol. 54 (2) , 104-114
- https://doi.org/10.1111/j.1600-0773.1984.tb01902.x
Abstract
Low‐temperature whole‐body autoradiography in Syrian golden hamsters, 11 and 15 days pregnant, given N‐14C‐nitrosodiethylamine, indicated an ability of the non‐metabolized substance to freely pass the cellular membranes of the maternal, placental and foetal tissues. Experiments in vitro with tissues of adult hamsters showed a capacity of the nasal olfactory and respiratory mucosa, the trachea, the lung, the lateral nasal gland, the liver and the kidney to degrade the N‐nitrosodiethylamine. Autoradiography showed a localization of non‐volatile N‐14C‐nitrosodiethylamine metabolites in these tissues in vivo. Since the mentioned tissues are the targets for the N‐nitrosodiethylamine‐induced neoplastic or preneoplastic lesions in the hamster, our results indicate that the ability of the sensitive tissues to perform the degradation of the substance is correlated to the tumour organotrophy. The main targets for the N‐nitrosodiethylamine carcinogenicity ‐ the nasal olfactory and respiratory mucosa and the trachea ‐ were found to be very active in degrading the substance, and it was shown that cytochrome P450 is present in these tissues. Microautoradiography of the nasal mucosa showed the highest labelling over the subepithelial glands (Bowman's glands) in the olfactory region, but other areas were also labelled. In the 15 day pregnant hamster, autoradiography showed a marked in vivo localization of non‐volatile metabolites in the foetal nasal and tracheo‐bronchial mucosa and liver, which was not observed in the 11 day pregnant hamster. The in vivo data were shown to correlate to an in vitro capacity by the nasal mucosa, the lung and the liver of the 15 day old foetus to metabolize the substance. N‐nitrosodiethylamine is a transplacental carcinogen only when administered on one of the last four days of pregnancy (day 12–15), and our results are in accord with the assumption that only at this late stage of pregnancy has the differentiation of the sensitive tissues reached a stage at which the substance can be metabolized to its ultimate carcinogen. In vitro experiments in 4, 10, and 20 day old infant hamsters showed a high capacity of the nasal mucosa, the lung and the liver to metabolize the N‐nitrosodiethylamine at these early stages of life.Keywords
This publication has 32 references indexed in Scilit:
- Foetal Distribution and Metabolism of N-Nitrosodiethylamine in MiceActa Pharmacologica et Toxicologica, 2009
- Extrahepatic sites of metabolism of carbon tetrachloride in ratsChemico-Biological Interactions, 1983
- Labeling in cells of the nasal cavity of hamsters treated with tritiated N-nitrosodiethylamineCancer Letters, 1982
- Sites of metabolism of N-nitrosodiethylamine in miceChemico-Biological Interactions, 1981
- Immunofluorescence of NADPH-Cytochrome c (P450) Reductase in Rat and Minipig Tissues Injected with PhenobarbitalScience, 1980
- Pathogenesis of Diethylnitrosamine-Induced Tumors in the Trachea of the Syrian Golden HamsterPathology - Research and Practice, 1980
- Binding of nitrosamines to cytochrome P-450 of liver microsomesChemico-Biological Interactions, 1979
- Studies on the Distribution and Metabolism of 14C‐dimethylnitrosamine in Foetal and Young MiceActa Pharmacologica et Toxicologica, 1979
- Ultrastructure of N‐diethylnitrosamine induced tumours in the nasal olfactory region of the Syrian golden hamsterThe Journal of Pathology, 1978
- Evidence for the Clara cell as a site of cytochrome P450-dependent mixed-function oxidase activity in lungNature, 1977