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贝类麻痹性神经毒素 Pinnatoxin G 的小鼠急性经口毒性

Acute Oral Toxicity of Pinnatoxin G in Mice.

机构信息

Department of Life Sciences, University of Trieste, Via A. Valerio 6, 34127 Trieste, Italy.

Ifremer, Laboratoire Phycotoxines, Centre Atlantique, 44311 Nantes Cedex, France.

出版信息

Toxins (Basel). 2020 Jan 28;12(2):87. doi: 10.3390/toxins12020087.

Abstract

Pinnatoxin G (PnTx-G) is a marine cyclic imine toxin produced by the dinoflagellate , frequently detected in edible shellfish from Ingril Lagoon (France). As other pinnatoxins, to date, no human poisonings ascribed to consumption of PnTx-G contaminated seafood have been reported, despite its potent antagonism at nicotinic acetylcholine receptors and its high and fast-acting toxicity after intraperitoneal or oral administration in mice. The hazard characterization of PnTx-G by oral exposure is limited to a single acute toxicity study recording lethality and clinical signs in non-fasted mice treated by gavage or through voluntary food ingestion, which showed differences in PnTx-G toxic potency. Thus, an acute toxicity study was carried out using 3 h-fasted CD-1 female mice, administered by gavage with PnTx-G (8-450 µg kg). At the dose of 220 µg kg and above, the toxin induced a rapid onset of clinical signs (piloerection, prostration, hypothermia, abdominal breathing, paralysis of the hind limbs, and cyanosis), leading to the death of mice within 30 min. Except for moderate mucosal degeneration in the small intestine recorded at doses of 300 µg kg, the toxin did not induce significant morphological changes in the other main organs and tissues, or alterations in blood chemistry parameters. This acute oral toxicity study allowed to calculate an oral LD for PnTx-G equal to 208 g kg (95% confidence limits: 155-281 µg kg) and to estimate a provisional NOEL of 120 µg kg.

摘要

Pinnatoxin G (PnTx-G) 是一种由甲藻产生的海洋环亚胺毒素,经常在法国 Ingril 泻湖的食用贝类中检测到。与其他 pinnatoxins 一样,尽管 PnTx-G 对烟碱型乙酰胆碱受体具有强烈的拮抗作用,并且在腹腔内或口服给予小鼠后具有高毒性和快速作用,但迄今为止,尚未有因食用受 PnTx-G 污染的海鲜而中毒的人类病例报告。通过口服暴露对 PnTx-G 的危害特征描述仅限于一项单次急性毒性研究,该研究记录了未禁食的小鼠经灌胃或通过自愿食物摄入接受治疗后的致死率和临床症状,结果显示 PnTx-G 的毒性强度存在差异。因此,使用 3 小时禁食的 CD-1 雌性小鼠进行了一项急性毒性研究,通过灌胃给予 PnTx-G(8-450 µg kg)。在 220 µg kg 及以上剂量下,该毒素会迅速引起临床症状(竖毛、俯卧、体温过低、腹部呼吸、后肢瘫痪和发绀),导致小鼠在 30 分钟内死亡。除了在 300 µg kg 剂量下记录到小肠中度黏膜退行性变外,该毒素不会在其他主要器官和组织中引起明显的形态变化,也不会改变血液化学参数。这项急性口服毒性研究计算出 PnTx-G 的口服 LD 为 208 g kg(95%置信区间:155-281 µg kg),并估计出暂定的 NOEL 为 120 µg kg。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ddf/7076786/fc1b2733f5a9/toxins-12-00087-g001.jpg

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