Your browser doesn't support javascript.
loading
Sex Is a Determinant for Deoxynivalenol Metabolism and Elimination in the Mouse.
Pestka, James J; Clark, Erica S; Schwartz-Zimmermann, Heidi E; Berthiller, Franz.
Afiliación
  • Pestka JJ; Department of Food Science and Human Nutrition, Michigan State University, East Lansing, MI 48824, USA. Pestka@msu.edu.
  • Clark ES; Center for Integrative Toxicology, Michigan State University, East Lansing, MI 48824, USA. Pestka@msu.edu.
  • Schwartz-Zimmermann HE; Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA. Pestka@msu.edu.
  • Berthiller F; Department of Food Science and Human Nutrition, Michigan State University, East Lansing, MI 48824, USA. clarkerica7@gmail.com.
Toxins (Basel) ; 9(8)2017 08 04.
Article en En | MEDLINE | ID: mdl-28777306
Based on prior observations that deoxynivalenol (DON) toxicity is sex-dependent, we compared metabolism and clearance of this toxin in male and female mice. Following intraperitoneal challenge with 1 mg/kg bw DON, the dose used in the aforementioned toxicity study, ELISA and LC-MS/MS analyses revealed that by 24 h, most DON and DON metabolites were excreted via urine (49-86%) as compared to feces (1.2-8.3%). Females excreted DON and its principal metabolites (DON-3-, DON-8,15 hemiketal-8-, and iso-DON-8-glucuronides) in urine more rapidly than males. Metabolite concentrations were typically 2 to 4 times higher in the livers and kidneys of males than females from 1 to 4 h after dosing. Trace levels of DON-3-sulfate and DON-15-sulfate were found in urine, liver and kidneys from females but not males. Fecal excretion of DON and DON sulfonates was approximately 2-fold greater in males than females. Finally, decreased DON clearance rates in males could not be explained by glucuronidation activities in liver and kidney microsomes. To summarize, increased sensitivity of male mice to DON's toxic effects as compared to females corresponds to decreased ability to clear the toxin via urine but did not appear to result from differences in toxin metabolism.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tricotecenos Límite: Animals / Female / Humans / Male Idioma: En Revista: Toxins (Basel) Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tricotecenos Límite: Animals / Female / Humans / Male Idioma: En Revista: Toxins (Basel) Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza