首页> 外文期刊>Environmental bioindicators >Use of Perna viridis as a Bioindicator of ParalyticShellfish Toxins at Low Pyrodinium bahamense varcompressum Density Using a Radioreceptor Assay
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Use of Perna viridis as a Bioindicator of ParalyticShellfish Toxins at Low Pyrodinium bahamense varcompressum Density Using a Radioreceptor Assay

机译:使用放射受体测定法在低Pyrodinium bahamense varcompressum密度下使用Perna viridis作为麻痹性贝类毒素的生物指标

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A radioassay method, i.e. the Receptor Binding Assay, was used for studying theuptake of Paralytic Shellfish Poisoning (PSP) toxins in the green bay mussel Pernaviridis highly consumed in the Philippines. This method allowed working at low celldensity of Pyrodinium bahamense var compressum (-102-103 cells/L) representativeof early stages of toxic algal blooms. The results indicated that within 16 hours toxiclevels of PSP are reached in the tissues of P. viridis, confirming the suitability of thegreen mussel as an indicator organism for paralytic shellfish toxicity in bivalvesduring the early stages of the bloom. Results also demonstrated that the weight-specific toxicity significantly increased with mussel size reduction. This method, basedon the competition between the labeled and unlabeled toxin for the sodium channelreceptor, offers better sensitivity than the mouse bioassay method. With an increasingamount of toxins in the sample, the amount of radiolabeled toxin binding with thereceptor decreases. The amount of radiolabeled toxin (tritiated saxitoxin) is thenmeasured using liquid scintillation counting. Quantification is based on a competitioncurve established by measuring competitive binding on a rat brain membrane withknown concentrations of saxitoxin.
机译:放射性测定法,即受体结合测定法,用于研究在菲律宾大量消费的绿湾贻贝Pernaviridis中对麻痹性贝类中毒(PSP)毒素的摄取。该方法允许在低细胞密度的Pyrodinium bahamense var compressum(-102-103 cells / L)的低密度下工作,代表了有毒藻华的早期阶段。结果表明,在16小时内,绿脓杆菌的组织中达到了PSP的毒性水平,这证实了绿色贻贝在开花初期对双壳类中作为麻痹性贝类毒性指示生物的适用性。结果还表明,随着贻贝尺寸的减小,体重特异性毒性显着增加。该方法基于标记的和未标记的毒素对钠通道受体之间的竞争,提供了比小鼠生物测定法更好的灵敏度。随着样品中毒素量的增加,与受体结合的放射性标记毒素的量减少。然后使用液体闪烁计数法测量放射性标记毒素(tri化的毒素)的量。定量基于竞争曲线,该竞争曲线是通过测量具有已知浓度的毒素的大鼠脑膜上的竞争结合而建立的。

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