Relative toxicity of dinophysistoxin-2 (DTX-2) compared with okadaic acid, based on acute intraperitoneal toxicity in mice

被引:83
作者
Aune, Tore
Larsen, Stig
Aasen, John A. B.
Rehmann, Nils
Satake, Masayuki
Hess, Philipp
机构
[1] Norwegian Sch Vet Sci, N-0033 Oslo, Norway
[2] Inst Marine, Oranmore, Co Galway, Ireland
[3] Tohoku Univ, Sendai, Miyagi 980, Japan
关键词
dinophysistoxin-2; DTX-2; OA; toxicity; relative toxicity factor;
D O I
10.1016/j.toxicon.2006.07.033
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
When substituting the Mouse bioassay for lipophilic marine algal toxins in shellfish with analytical methods, science based factors of relative toxicity for all analogues that contribute to health risk to consumers are necessary. The aim of this paper is to establish the relative intraperitoneal toxicity of dinophysistoxin-2 (DTX-2) compared with okadaic acid (OA). The study was performed as an open, randomised parallel group trial with a four level response surface design within each of the two parallels. In accordance with the response surface design model, the LD50 for DTX-2 and OA was 338 and 206 mu g/kg, respectively. By use of common regression analysis, the LD50 of DTX-2 and OA were estimated to 352 mu g/kg and 204 mu g/kg, respectively. The deviations between the LD50 estimates by the two methods was 4% for DTX-2 and less than 1% for OA. Taken together, these results indicate that the relative toxicity of DTX-2 is about 0.6, compared to OA. Results from the PP2A assay correspond very well with the results obtained by the mouse bioassay. The IC50 concentrations for DTX-2 and OA were 5.94 and 2.81 ng/mL, respectively. This indicates that OA is about twice as toxic as DTX-2. Since inhibition of PP2A is acknowledged as the main mechanism of toxicity of the OA group toxins, this supports the establishment of a relative toxicity factor of DTX-2 of 0.6 compared with OA. (c) 2006 Elsevier Ltd. All rights reserved.
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页码:1 / 7
页数:7
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