Abstract
Botulinum toxin is an extraordinarily potent molecule that has an unusually long duration of action. Despite this, there is little information available on natural mechanisms for metabolism or elimination and virtually no information on pharmacologically induced mechanisms for metabolism and elimination. Therefore, a number of experiments were performed on laboratory animals that addressed two major issues: 1) the effect of blood on the structure, function, and biologic half-life of the toxin, and 2) the effect of neutralizing antibodies on half-life and elimination of circulating toxin. In the first series of studies, the metabolic transformation of toxin was assessed by incubating it in blood for varying lengths of time. At each time point, aliquots were examined to determine the amount of toxin, the structure of toxin, the catalytic activity of toxin, and the neuromuscular blocking activity of toxin. This work demonstrated that blood did not alter any characteristic of the toxin molecule. Experiments were also done in which toxin was administered to mice and rats at doses that produced clinical poisoning. The results demonstrated that the elimination half-life for native (nonmetabolized) toxin in blood and serum was 230 to 260 min. During the second series of studies, the rate of elimination of circulating toxin was studied in the presence of antibodies directed against the carboxyl-terminal half of the toxin molecule. This work demonstrated that neutralizing antibodies 1) enhanced clearance of toxin from the circulation and 2) enhanced tissue accumulation of toxin, particularly in liver and spleen.
Footnotes
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doi:10.1124/jpet.106.104661.
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This work was supported in part by National Institutes of Health Contract N01-AI30028, National Institutes of Health Grants NS22153 and GM57342, and by a Sponsored Research Agreement from DOR Biopharma (Miami, FL).
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ABBREVIATIONS: BoNT, botulinum neurotoxin; BoNT/A, BoNT type A; PAGE, polyacrylamide gel electrophoresis.
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↵1 These authors contributed equally to this work.
- Received March 22, 2006.
- Accepted June 14, 2006.
- The American Society for Pharmacology and Experimental Therapeutics
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