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Subchronic Feeding Study of the Mycotoxin Fumonisin B1 in B6C3F1 Mice and Fischer 344 Rats

Subchronic Feeding Study of the Mycotoxin Fumonisin B1 in B6C3F1 Mice and Fischer 344 Rats. Voss, K. A., Chamberlain, W. J., Bacon, C. W., Herbert, R. A., Walters, D. B., and Norred, W. P. (1995). Fundam. Appl. Toxicol.24, 102-110. Fumonisin B1 (FB1) is a mycotoxin produced by Fusarium moniliforme,...

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Published in:Fundamental and applied toxicology 1995-01, Vol.24 (1), p.102-110
Main Authors: Voss, Kenneth A., Chamberlain, William J., Bacon, Charles W., Herbert, Ronald A., Walters, Douglas B., Norred, William P.
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container_title Fundamental and applied toxicology
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Chamberlain, William J.
Bacon, Charles W.
Herbert, Ronald A.
Walters, Douglas B.
Norred, William P.
description Subchronic Feeding Study of the Mycotoxin Fumonisin B1 in B6C3F1 Mice and Fischer 344 Rats. Voss, K. A., Chamberlain, W. J., Bacon, C. W., Herbert, R. A., Walters, D. B., and Norred, W. P. (1995). Fundam. Appl. Toxicol.24, 102-110. Fumonisin B1 (FB1) is a mycotoxin produced by Fusarium moniliforme, a common fungus which occurs naturally on corn, and other Fusarium species. FB1 and other fumonisins are now recognized as having potentially important animal and human health implications. However, few toxicological data are currently available. Male and female B6C3F1 mice and Fischer 344 rats were fed diets containing 0, 1, 3, 9, 27, or 81 ppm FB1 (⩾98% purity) for 13 weeks. No differences in behavior or appearance, body weight or food consumption between control and FB1-fed groups were found. In mice, hepatopathy and altered serum chemical profiles indicative of hepatotoxicity were found in females fed the 81 ppm diet. No adverse effects were found in female mice fed ⩽27 ppm FB1 or in male mice at any dietary level studied. In rats, nephrosis involving the outer medulla was found in males fed ⩾9 ppm and, to a lesser degree, in females fed 81 ppm FB1, while decreased kidney weight was found in both sexes at dietary levels ⩾9 ppm FB1. Although the liver is a target organ of FB1 in rats, hepatotoxicity was not found in rats fed diets containing up to 81 ppm FB1 for 90 days. Thus, FB1 was toxic to both species following subchronic oral exposure, although significant interspecies differences in the no observed effect levels and organ-specific responses were found.
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Voss, K. A., Chamberlain, W. J., Bacon, C. W., Herbert, R. A., Walters, D. B., and Norred, W. P. (1995). Fundam. Appl. Toxicol.24, 102-110. Fumonisin B1 (FB1) is a mycotoxin produced by Fusarium moniliforme, a common fungus which occurs naturally on corn, and other Fusarium species. FB1 and other fumonisins are now recognized as having potentially important animal and human health implications. However, few toxicological data are currently available. Male and female B6C3F1 mice and Fischer 344 rats were fed diets containing 0, 1, 3, 9, 27, or 81 ppm FB1 (⩾98% purity) for 13 weeks. No differences in behavior or appearance, body weight or food consumption between control and FB1-fed groups were found. In mice, hepatopathy and altered serum chemical profiles indicative of hepatotoxicity were found in females fed the 81 ppm diet. No adverse effects were found in female mice fed ⩽27 ppm FB1 or in male mice at any dietary level studied. In rats, nephrosis involving the outer medulla was found in males fed ⩾9 ppm and, to a lesser degree, in females fed 81 ppm FB1, while decreased kidney weight was found in both sexes at dietary levels ⩾9 ppm FB1. Although the liver is a target organ of FB1 in rats, hepatotoxicity was not found in rats fed diets containing up to 81 ppm FB1 for 90 days. 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Voss, K. A., Chamberlain, W. J., Bacon, C. W., Herbert, R. A., Walters, D. B., and Norred, W. P. (1995). Fundam. Appl. Toxicol.24, 102-110. Fumonisin B1 (FB1) is a mycotoxin produced by Fusarium moniliforme, a common fungus which occurs naturally on corn, and other Fusarium species. FB1 and other fumonisins are now recognized as having potentially important animal and human health implications. However, few toxicological data are currently available. Male and female B6C3F1 mice and Fischer 344 rats were fed diets containing 0, 1, 3, 9, 27, or 81 ppm FB1 (⩾98% purity) for 13 weeks. No differences in behavior or appearance, body weight or food consumption between control and FB1-fed groups were found. In mice, hepatopathy and altered serum chemical profiles indicative of hepatotoxicity were found in females fed the 81 ppm diet. No adverse effects were found in female mice fed ⩽27 ppm FB1 or in male mice at any dietary level studied. In rats, nephrosis involving the outer medulla was found in males fed ⩾9 ppm and, to a lesser degree, in females fed 81 ppm FB1, while decreased kidney weight was found in both sexes at dietary levels ⩾9 ppm FB1. Although the liver is a target organ of FB1 in rats, hepatotoxicity was not found in rats fed diets containing up to 81 ppm FB1 for 90 days. 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Chamberlain, William J. ; Bacon, Charles W. ; Herbert, Ronald A. ; Walters, Douglas B. ; Norred, William P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c484t-5806b4b227595e4933415cdc67ce508d0d33971704cfce0837119f11a2ad46d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adrenal Glands - drug effects</topic><topic>Adrenal Glands - pathology</topic><topic>ANATOMIA ANIMAL</topic><topic>ANATOMIE ANIMALE</topic><topic>Animals</topic><topic>Behavior, Animal - drug effects</topic><topic>Biological and medical sciences</topic><topic>Body Weight - drug effects</topic><topic>Carcinogens, Environmental - toxicity</topic><topic>Chemical and Drug Induced Liver Injury</topic><topic>Cholesterol - blood</topic><topic>COMPORTAMIENTO</topic><topic>COMPORTEMENT</topic><topic>COMPOSICION DE LA SANGRE</topic><topic>COMPOSITION DU SANG</topic><topic>Creatinine - blood</topic><topic>DIFERENCIAS BIOLOGICAS</topic><topic>DIFFERENCE BIOLOGIQUE</topic><topic>Dose-Response Relationship, Drug</topic><topic>Eating - drug effects</topic><topic>EFECTOS SECUNDARIOS</topic><topic>EFFET SECONDAIRE</topic><topic>ENFERMEDADES HEPATICAS</topic><topic>ENFERMEDADES RENALES</topic><topic>ENZIMAS</topic><topic>ENZYME</topic><topic>Female</topic><topic>Fumonisins</topic><topic>GIBBERELLA FUJIKUROI</topic><topic>HISTOPATHOLOGIE</topic><topic>HISTOPATOLOGIA</topic><topic>INGESTION DE PIENSOS</topic><topic>Kidney - anatomy &amp; 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Voss, K. A., Chamberlain, W. J., Bacon, C. W., Herbert, R. A., Walters, D. B., and Norred, W. P. (1995). Fundam. Appl. Toxicol.24, 102-110. Fumonisin B1 (FB1) is a mycotoxin produced by Fusarium moniliforme, a common fungus which occurs naturally on corn, and other Fusarium species. FB1 and other fumonisins are now recognized as having potentially important animal and human health implications. However, few toxicological data are currently available. Male and female B6C3F1 mice and Fischer 344 rats were fed diets containing 0, 1, 3, 9, 27, or 81 ppm FB1 (⩾98% purity) for 13 weeks. No differences in behavior or appearance, body weight or food consumption between control and FB1-fed groups were found. In mice, hepatopathy and altered serum chemical profiles indicative of hepatotoxicity were found in females fed the 81 ppm diet. No adverse effects were found in female mice fed ⩽27 ppm FB1 or in male mice at any dietary level studied. In rats, nephrosis involving the outer medulla was found in males fed ⩾9 ppm and, to a lesser degree, in females fed 81 ppm FB1, while decreased kidney weight was found in both sexes at dietary levels ⩾9 ppm FB1. Although the liver is a target organ of FB1 in rats, hepatotoxicity was not found in rats fed diets containing up to 81 ppm FB1 for 90 days. Thus, FB1 was toxic to both species following subchronic oral exposure, although significant interspecies differences in the no observed effect levels and organ-specific responses were found.</abstract><cop>Boston, MA</cop><cop>San Diego, CA</cop><cop>New York, NY</cop><pub>Elsevier Science (USA)</pub><pmid>7713333</pmid><doi>10.1006/faat.1995.1012</doi><tpages>9</tpages></addata></record>
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identifier ISSN: 0272-0590
ispartof Fundamental and applied toxicology, 1995-01, Vol.24 (1), p.102-110
issn 0272-0590
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subjects Adrenal Glands - drug effects
Adrenal Glands - pathology
ANATOMIA ANIMAL
ANATOMIE ANIMALE
Animals
Behavior, Animal - drug effects
Biological and medical sciences
Body Weight - drug effects
Carcinogens, Environmental - toxicity
Chemical and Drug Induced Liver Injury
Cholesterol - blood
COMPORTAMIENTO
COMPORTEMENT
COMPOSICION DE LA SANGRE
COMPOSITION DU SANG
Creatinine - blood
DIFERENCIAS BIOLOGICAS
DIFFERENCE BIOLOGIQUE
Dose-Response Relationship, Drug
Eating - drug effects
EFECTOS SECUNDARIOS
EFFET SECONDAIRE
ENFERMEDADES HEPATICAS
ENFERMEDADES RENALES
ENZIMAS
ENZYME
Female
Fumonisins
GIBBERELLA FUJIKUROI
HISTOPATHOLOGIE
HISTOPATOLOGIA
INGESTION DE PIENSOS
Kidney - anatomy & histology
Kidney - drug effects
Kidney - pathology
Liver - drug effects
Liver - pathology
Liver Diseases - blood
MALADIE DU FOIE
Male
Medical sciences
METHODE D'APPLICATION
METODOS DE APLICACION
Mice
Mice, Inbred Strains
MICOTOXINAS
MYCOTOXINE
Mycotoxins - toxicity
NEPHROPATHIE
Organ Size - drug effects
PESO
Plant poisons toxicology
POIDS
PRISE ALIMENTAIRE (ANIMAUX)
RAT
RATA
RATON
Rats
Rats, Inbred F344
REIN
RINONES
SOURIS
Species Specificity
TOXICIDAD POR INGESTION
TOXICITE PAR INGESTION
TOXICOLOGIA
TOXICOLOGIE
Toxicology
title Subchronic Feeding Study of the Mycotoxin Fumonisin B1 in B6C3F1 Mice and Fischer 344 Rats
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