TY - JOUR
T1 - Pharmacokinetics of the trichothecene mycotoxin, T-2 toxin, in swine and cattle
AU - Beasley, Val R.
AU - Swanson, Steven P.
AU - Corley, Richard A.
AU - Buck, William B.
AU - Koritz, Gary D.
AU - Burmeister, Harold R.
N1 - Funding Information:
Acknowledgements -- This work was graciously supported in part by the United States Department of Agriculture project no. 901-15-158 and in part by the United States Army Medical Research Institute of Infectious Diseases project no. DAMD 17-82-C2179. Appreciation is also extended to ARTHUR M. SIEGEL, DVM, for assistance in statistical analysis.
PY - 1986
Y1 - 1986
N2 - The pharmacokinetics of the trichothecene mycotoxin, T-2 toxin, were determined in growing gilts and heifers. Following intra-aortal administration in swine and intravenous administration in calves, the disappearance of the parent T-2 toxin followed a 2-compartment open model. Mean elimination phase half-lives were 13.8 and 17.4 min and mean apparent specific volumes of distribution were 0.366 and 0.376 l/kg in swine and calves, respectively. The fraction of T-2 toxin eliminated as parent compound in the urine was negligible. In spite of administration of a lethal oral dose in swine (2.4 mg/kg) and toxic oral doses (up to 3.6 mg/kg) in calves, no parent T-2 toxin was detected in plasma or urine. After intra-aortal administration in swine, tissue concentrations of T-2 toxin were consistently highest in lymphoid organs. Tissue residues of T-2 toxin were rapidly depleted such that, in spite of administration of a potentially lethal intra-aortal dose, no quantifiable T-2 toxin was present in any of the tissues collected at 4 hr after dosing. No T-2 toxin could be detected in liver, even at 1 hr after dosing.
AB - The pharmacokinetics of the trichothecene mycotoxin, T-2 toxin, were determined in growing gilts and heifers. Following intra-aortal administration in swine and intravenous administration in calves, the disappearance of the parent T-2 toxin followed a 2-compartment open model. Mean elimination phase half-lives were 13.8 and 17.4 min and mean apparent specific volumes of distribution were 0.366 and 0.376 l/kg in swine and calves, respectively. The fraction of T-2 toxin eliminated as parent compound in the urine was negligible. In spite of administration of a lethal oral dose in swine (2.4 mg/kg) and toxic oral doses (up to 3.6 mg/kg) in calves, no parent T-2 toxin was detected in plasma or urine. After intra-aortal administration in swine, tissue concentrations of T-2 toxin were consistently highest in lymphoid organs. Tissue residues of T-2 toxin were rapidly depleted such that, in spite of administration of a potentially lethal intra-aortal dose, no quantifiable T-2 toxin was present in any of the tissues collected at 4 hr after dosing. No T-2 toxin could be detected in liver, even at 1 hr after dosing.
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U2 - 10.1016/0041-0101(86)90161-3
DO - 10.1016/0041-0101(86)90161-3
M3 - Article
C2 - 3952762
AN - SCOPUS:0022656629
SN - 0041-0101
VL - 24
SP - 13
EP - 23
JO - Toxicon
JF - Toxicon
IS - 1
ER -