Marine Biotoxins Program, Center for Coastal Environmental Health and Biomolecular Research, NOAA - National Ocean Service, 219 Fort Johnson Road, Charleston, SC 29412, USA.
Toxicon. 2013 Mar 15;64:81-6. doi: 10.1016/j.toxicon.2012.12.026. Epub 2013 Jan 11.
Ciguatoxins are sodium channel activator toxins responsible for ciguatera fish poisoning. In this study, we determined the toxicokinetic parameters of the Pacific ciguatoxin P-CTX-1 in rats after an intravenous (iv) dose of 0.13 ng P-CTX-1 per g of body weight. The ciguatoxin activity was assessed over time in blood using the sensitive functional Neuro2a assay. The data were analyzed with a two-compartmental model. After exposure, the ciguatoxin activity exhibited a rapid (alpha half-life of 6 min) and extensive distribution into tissues (apparent steady state volume of distribution of 7.8 L). Ciguatoxin elimination from blood was slower with a beta half-life estimated at 35.5 h. The toxicokinetic parameters determined from this study were compared to data previously obtained after oral and intraperitoneal exposure of rats to 0.26 ng P-CTX-1 per g of body weight. Maximal bioavailability was determined by the area under the concentration curve, and was used to calculate the absolute P-CTX-1 bioavailabilities for oral and intraperitoneal routes of exposures of 39% and 75%, respectively.
雪卡毒素是一种钠离子通道激活毒素,可导致雪卡鱼中毒。在这项研究中,我们测定了静脉注射(iv)剂量为 0.13ng P-CTX-1/g 体重后,太平洋雪卡毒素 P-CTX-1 在大鼠体内的毒代动力学参数。采用灵敏的功能性 Neuro2a 测定法,随时间测定血液中的雪卡毒素活性。采用双室模型分析数据。暴露后,雪卡毒素活性迅速(α半衰期为 6 分钟)并广泛分布到组织中(表观稳态分布容积为 7.8 L)。雪卡毒素从血液中的消除较慢,β半衰期估计为 35.5 小时。本研究确定的毒代动力学参数与大鼠口服和腹腔内暴露于 0.26ng P-CTX-1/g 体重后获得的数据进行了比较。通过浓度曲线下面积确定最大生物利用度,并用于计算口服和腹腔内暴露途径的绝对 P-CTX-1 生物利用度,分别为 39%和 75%。