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三唑酮对斑马鱼幼鱼期的心血管毒性及其对人类健康的潜在影响。

The cardiovascular toxicity of triadimefon in early life stage of zebrafish and potential implications to human health.

作者信息

Liu Hong-Cui, Chu Tian-Yi, Chen Li-Li, Gui Wen-Jun, Zhu Guo-Nian

机构信息

Institute of Pesticide and Environmental Toxicology, Zhejiang University, Hangzhou 310058, China.

Institute of Pesticide and Environmental Toxicology, Zhejiang University, Hangzhou 310058, China.

出版信息

Environ Pollut. 2017 Dec;231(Pt 1):1093-1103. doi: 10.1016/j.envpol.2017.05.072. Epub 2017 Aug 10.

Abstract

The health risk of triadimefon (TF) to cardiovascular system of human is still unclear, especially to pesticide suicides population, occupational population (farmers, retailers and pharmaceutical workers), and special population (young children and infants, pregnant women, older people, and those with compromised immune systems) who are at a greater risk. Therefore, firstly we explored the toxic effects and possible mechanism of cardiovascular toxicity induced by TF using zebrafish model. Zebrafish at stage of 48 h post fertilization (hpf) exposed to TF for 24 h exhibited morphological malformations which were further confirmed by histopathologic examination, including pericardial edema, circulation abnormalities, serious venous thrombosis and increased distance between the sinus venosus (SV) and bulbus arteriosus (BA) regions of the heart. In addition to morphological changes, TF induced functional deficits in the heart of zebrafish, including bradycardia and a significant reduced cardiac output that became more serious at higher concentrations. To better understand the possible molecular mechanisms underlying cardiovascular toxicity in zebrafish, we investigated the transcriptional level of genes related to calcium signaling pathway and cardiac muscle contraction. Q-PCR (quantitative real-time polymerase chain reaction) results demonstrated that the expression level of genes related to ATPase (atp2a1l, atp1b2b, atp1a3b), calcium channel (cacna1ab, cacna1da) and cardiac troponin C (tnnc1a) were significantly decreased after TF exposure. For the first time, the present study revealed that TF exposure had observable morphological and functional negative impacts on cardiovascular system of zebrafish. Mechanistically, this toxicity might result from the pressure of down-regulation of genes associated with calcium signaling pathway and cardiac muscle contraction following TF exposure. These findings generated here can provide information for better pesticide poisoning treatments, occupational disease prevention, and providing theoretical foundation for risk management measures.

摘要

三唑酮(TF)对人类心血管系统的健康风险仍不明确,尤其是对农药自杀人群、职业人群(农民、零售商和药剂师)以及高风险的特殊人群(幼儿、婴儿、孕妇、老年人和免疫系统受损者)。因此,我们首先利用斑马鱼模型探究了TF诱导心血管毒性的毒性作用及可能机制。受精后48小时(hpf)的斑马鱼暴露于TF 24小时后出现形态畸形,组织病理学检查进一步证实了这一点,包括心包水肿、循环异常、严重的静脉血栓形成以及心脏静脉窦(SV)和动脉球(BA)区域之间的距离增加。除形态变化外,TF还诱导斑马鱼心脏功能缺陷,包括心动过缓和心输出量显著降低,且在较高浓度下更为严重。为了更好地理解斑马鱼心血管毒性潜在的分子机制,我们研究了与钙信号通路和心肌收缩相关基因的转录水平。定量实时聚合酶链反应(Q-PCR)结果表明,暴露于TF后,与ATP酶(atp2a1l、atp1b2b、atp1a3b)、钙通道(cacna1ab、cacna1da)和心肌肌钙蛋白C(tnnc1a)相关的基因表达水平显著降低。本研究首次揭示,暴露于TF对斑马鱼心血管系统有明显的形态和功能负面影响。从机制上讲,这种毒性可能是由于TF暴露后与钙信号通路和心肌收缩相关基因下调的压力所致。这些研究结果可为更好地治疗农药中毒、预防职业病以及为风险管理措施提供理论基础提供信息。

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