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A radioassay method, i.e. the Receptor Binding Assay, was used for studying the uptake of Paralytic Shellfish Poisoning (PSP) toxins in the green bay mussel Perna viridis highly consumed in the Philippines. This method allowed working at low cell density of Pyrodinium bahamense var compressum (102-103 cells/L) representative of early stages of toxic algal blooms. The results indicated that within 16 hours toxic levels of PSP are reached in the tissues of P. viridis, confirming the suitability of the green mussel as an indicator organism for paralytic shellfish toxicity in bivalves during the early stages of the bloom. Results also demonstrated that the weight-specific toxicity significantly increased with mussel size reduction. This method, based on the competition between the labeled and unlabeled toxin for the sodium channel receptor, offers better sensitivity than the mouse bioassay method. With an increasing amount of toxins in the sample, the amount of radiolabeled toxin binding with the receptor decreases. The amount of radiolabeled toxin (tritiated saxitoxin) is then measured using liquid scintillation counting. Quantification is based on a competition curve established by measuring competitive binding on a rat brain membrane with known concentrations of saxitoxin.
机译:放射测定法,即受体结合测定法,被用于研究在菲律宾大量消费的绿湾贻贝贻贝中的麻痹性贝类中毒(PSP)毒素的摄取。该方法允许在低细胞密度的代表有毒藻华早期阶段的巴氏热霉变种(102-103细胞/ L)下工作。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,证实了青口贻贝作为开花初期的双壳类中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。这种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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