ABSTRACT
Toxicokinetics and the toxicological effects of culture material containing fumonisin B(1) (FB(1)) were studied in male weaned piglets by clinical, pathological, biochemical and sphingolipid analyses. The animals received a single oral dose of 5 mg FB(1)/kg of body weight, obtained from Fusarium verticillioides culture material. FB(1) was detected by HPLC in plasma collected at 1-h intervals up to 6h and at 12-h intervals up to 96 h. FB(1) eliminated in feces and urine was quantified over a 96-h period and in liver samples collected 96 h post-intoxication. Blood samples were obtained at the beginning and end of the experiment to determine serum enzyme activity, total bilirubin, cholesterol, sphinganine (Sa), sphingosine (So) and the Sa/So ratio. FB(1) was detected in plasma between 30 min and 36 h after administration. The highest concentration of FB(1) was observed after 2 h, with a mean concentration of 282 microg/ml. Only 0.93% of the total FB(1) was detected in urine between 75 min and 41 h after administration, the highest mean concentration (561 microg/ml) was observed during the interval after 8 at 24 h. Approximately 76.5% of FB(1) was detected in feces eliminated between 8 and 84 h after administration, with the highest levels observed between 8 and 24 h. Considering the biochemical parameters, a significant increase only occurred in cholesterol, alkaline phosphatase and aspartate aminotransferase activities. In plasma and urine, the highest Sa and Sa/So ratios were obtained at 12 and 48 h, respectively.
Subject(s)
Carcinogens, Environmental/administration & dosage , Carcinogens, Environmental/toxicity , Fumonisins/administration & dosage , Fumonisins/toxicity , Fusarium/chemistry , Administration, Oral , Alkaline Phosphatase/blood , Animal Feed , Animals , Aspartate Aminotransferases/blood , Carcinogens, Environmental/pharmacokinetics , Cholesterol/blood , Dose-Response Relationship, Drug , Feces/chemistry , Fumonisins/pharmacokinetics , Male , Orchiectomy , Sphingosine/analogs & derivatives , Sphingosine/blood , Sphingosine/urine , Swine/blood , Swine/urineABSTRACT
The optimization of the thin layer chromatography (TLC) method to determine aflatoxins in feedstuffs and the evaluation of their occurrence in feedstuffs for milk-yielding does in the state of Bahia were studied. Eighty feedstuff samples were collected from five farms, located in the Recôncavo Baiano, from November 2000 to August 2002. The samples were analyzed using TLC modified method. In this study, the detection and quantification limits were 5 and 8m g/kg, respectively. The percentage of average recoveries obtained for AFB1, AFB2, AFG1, and AFG2 were 81.0; 97.2; 89.3; and 90.3 percent, respectively; and the coefficient of variation ranged from 0.83 to 4.1 percent. The results revealed that the optimization of TLC methodology is efficient to analyze aflatoxins in feedstuffs. The presence of these aflatoxins was not detected in any of the analyzed samples, demonstrating good quality of those products, regarding the contamination by these toxins.
Subject(s)
Animals , Animal Feed , Aflatoxins/analysis , Goats , MethodsABSTRACT
The optimization of the thin layer chromatography (TLC) method to determine aflatoxins in feedstuffs and the evaluation of their occurrence in feedstuffs for milk-yielding does in the state of Bahia were studied. Eighty feedstuff samples were collected from five farms, located in the Recôncavo Baiano, from November 2000 to August 2002. The samples were analyzed using TLC modified method. In this study, the detection and quantification limits were 5 and 8m g/kg, respectively. The percentage of average recoveries obtained for AFB1, AFB2, AFG1, and AFG2 were 81.0; 97.2; 89.3; and 90.3 percent, respectively; and the coefficient of variation ranged from 0.83 to 4.1 percent. The results revealed that the optimization of TLC methodology is efficient to analyze aflatoxins in feedstuffs. The presence of these aflatoxins was not detected in any of the analyzed samples, demonstrating good quality of those products, regarding the contamination by these toxins.(AU)