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1.
Food Chem Toxicol ; 22(3): 227-32, 1984 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-6538540

RESUMEN

The metabolism and distribution of [2-14C]- and 35S-labelled 3,4-epithiobutanenitrile (4ETN), a thiirane occurring naturally in cruciferous vegetables, was studied in the rat. A dose of c. 11 mg 4ETN/kg body weight was rapidly transformed into water-soluble compounds and was mainly excreted in the urine, irrespective of the route of administration (oral or ip). The main metabolite in the urine was identified by gas chromatography-mass spectrometry as a mercapturic acid derivative. Low residual radioactivity demonstrated in organs 72 hr after administration was consistent with an earlier report that the thiirane may function as a weak biological alkylating agent.


Asunto(s)
Nitrilos/metabolismo , Animales , Radioisótopos de Carbono , Heces/análisis , Femenino , Cromatografía de Gases y Espectrometría de Masas , Masculino , Nitrilos/orina , Ratas , Ratas Endogámicas , Distribución Tisular
2.
Toxicol Lett ; 6(4-5): 221-4, 1980 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-7423549

RESUMEN

14C-activity in the urine of female rats appeared to be independent of dose when single oral doses of [14C]maneb, a fungicide, manganese ethylene-bis(dithiocarbamate), were given. This was found with [14C]maneb synthesized from [U-14C]ethylenediamine. In the dose range, 23 microgram/kg to 1.4 g/kg of maneb, the excreted activity in urine of 39 female rats was 48.8 +/- 12.6% (n=39).


Asunto(s)
Maneb/orina , Tiocarbamatos/orina , Absorción , Animales , Relación Dosis-Respuesta a Droga , Heces/análisis , Femenino , Ratas
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