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食用受氮杂螺旋酸污染的贝类导致人类患病原因的新见解。

New insights into the causes of human illness due to consumption of azaspiracid contaminated shellfish.

作者信息

Chevallier O P, Graham S F, Alonso E, Duffy C, Silke J, Campbell K, Botana L M, Elliott C T

机构信息

Advanced Asset Technology Centre, Institute for Global Food Security, Queen's University Belfast, Stranmillis Road, Belfast, BT9 5AG, UK.

Beaumont Research Institute, 3811 W Thirteen Mile Road, Royal Oak, MI, 48073.

出版信息

Sci Rep. 2015 Apr 30;5:9818. doi: 10.1038/srep09818.

DOI:10.1038/srep09818
PMID:25928256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4415421/
Abstract

Azaspiracid (AZA) poisoning was unknown until 1995 when shellfish harvested in Ireland caused illness manifesting by vomiting and diarrhoea. Further in vivo/vitro studies showed neurotoxicity linked with AZA exposure. However, the biological target of the toxin which will help explain such potent neurological activity is still unknown. A region of Irish coastline was selected and shellfish were sampled and tested for AZA using mass spectrometry. An outbreak was identified in 2010 and samples collected before and after the contamination episode were compared for their metabolite profile using high resolution mass spectrometry. Twenty eight ions were identified at higher concentration in the contaminated samples. Stringent bioinformatic analysis revealed putative identifications for seven compounds including, glutarylcarnitine, a glutaric acid metabolite. Glutaric acid, the parent compound linked with human neurological manifestations was subjected to toxicological investigations but was found to have no specific effect on the sodium channel (as was the case with AZA). However in combination, glutaric acid (1 mM) and azaspiracid (50 nM) inhibited the activity of the sodium channel by over 50%. Glutaric acid was subsequently detected in all shellfish employed in the study. For the first time a viable mechanism for how AZA manifests itself as a toxin is presented.

摘要

直到1995年,人们才知道azaspiracid(AZA)中毒事件,当时在爱尔兰捕捞的贝类导致了以呕吐和腹泻为症状的疾病。进一步的体内/体外研究表明,AZA暴露与神经毒性有关。然而,这种毒素的生物学靶点仍不清楚,而该靶点有助于解释其如此强大的神经学活性。研究人员选择了爱尔兰海岸线的一个区域,采集贝类样本并使用质谱法检测其中的AZA。2010年确认了一次疫情爆发,并使用高分辨率质谱法比较了污染事件前后采集的样本的代谢物谱。在受污染的样本中,有28种离子的浓度较高。严格的生物信息学分析揭示了包括戊二酰肉碱(一种戊二酸代谢物)在内的7种化合物的推定鉴定结果。与人类神经学表现相关的母体化合物戊二酸接受了毒理学研究,但发现它对钠通道没有特定影响(AZA的情况则不同)。然而,戊二酸(1 mM)和azaspiracid(50 nM)联合使用时,会使钠通道的活性抑制超过50%。随后在该研究使用的所有贝类中都检测到了戊二酸。首次提出了AZA作为毒素发挥作用的可行机制。

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