夏源, 王春瑜, 李姿毅, 周芹, 朱嘉伟, 孟晓静, 黄伟婵, 王军义, 陈青松. 铅锰联合暴露致斑马鱼发育神经毒性及JNK表达变化[J]. 环境与职业医学, 2023, 40(5): 583-588. DOI: 10.11836/JEOM22224
引用本文: 夏源, 王春瑜, 李姿毅, 周芹, 朱嘉伟, 孟晓静, 黄伟婵, 王军义, 陈青松. 铅锰联合暴露致斑马鱼发育神经毒性及JNK表达变化[J]. 环境与职业医学, 2023, 40(5): 583-588. DOI: 10.11836/JEOM22224
XIA Yuan, WANG Chunyu, LI Ziyi, ZHOU Qin, ZHU Jiawei, MENG Xiaojing, HUANG Weichan, WANG Junyi, CHEN Qingsong. Effects of lead and manganese combined exposure on neurodevelopmental toxicity and JNK expression in zebrafish[J]. Journal of Environmental and Occupational Medicine, 2023, 40(5): 583-588. DOI: 10.11836/JEOM22224
Citation: XIA Yuan, WANG Chunyu, LI Ziyi, ZHOU Qin, ZHU Jiawei, MENG Xiaojing, HUANG Weichan, WANG Junyi, CHEN Qingsong. Effects of lead and manganese combined exposure on neurodevelopmental toxicity and JNK expression in zebrafish[J]. Journal of Environmental and Occupational Medicine, 2023, 40(5): 583-588. DOI: 10.11836/JEOM22224

铅锰联合暴露致斑马鱼发育神经毒性及JNK表达变化

Effects of lead and manganese combined exposure on neurodevelopmental toxicity and JNK expression in zebrafish

  • 摘要: 背景

    铅和锰是环境中广泛存在的重金属污染物,可通过食物链在人体内蓄积,产生神经毒性,并促进神经退行性疾病的发生。特别是在儿童早期,发育中的血脑屏障和神经系统对环境污染物高度敏感。以往的研究大多集中于铅和锰等重金属的单一毒性效应,而联合毒性效应的研究仍然匮乏,涉及的机制也尚未明确。c-Jun氨基末端激酶(JNK)与神经元的发育和再生有关,一些研究发现JNK参与铅和锰所致的神经毒性,但其在铅锰联合毒性中的作用未知。

    目的

    初步探讨环境低剂量重金属铅锰联合暴露所致斑马鱼神经发育毒性的机制和JNK的表达变化。

    方法

    将受精后(hour post fertilization, hpf)2 h斑马鱼胚胎分为对照组、铅暴露组(0.1 mg·L−1 醋酸铅)、锰暴露组(0.3 mg·L−1 氯化锰)、铅锰联合暴露组(0.1 mg·L−1 醋酸铅+0.3 mg·L−1 氯化锰),暴露7 d。观察斑马鱼自主抽动、死亡率和运动行为,检测斑马鱼体内JNK mRNA表达变化。

    结果

    实验结果显示环境剂量重金属铅锰单独及联合暴露后斑马鱼死亡率和自主抽动没有显著变化(P>0.05)。运动分析结果显示,与对照组比较,锰暴露组斑马鱼运动次数和运动距离轻微升高,差异有统计学意义(P<0.01);铅暴露组斑马鱼运动次数和运动距离降低50%,铅锰联合暴露组斑马鱼运动次数和运动距离降低80%,差异有统计学意义(P<0.01);与铅暴露组比较,铅锰联合暴露组斑马鱼运动次数和运动距离下降60%,差异有统计学意义(P<0.05)。实时荧光定量法检测结果显示,与对照组比较,铅锰联合暴露组斑马鱼体内JNK mRNA表达水平升高,差异有统计学意义(P<0.01)。

    结论

    环境低剂量铅锰联合暴露对斑马鱼的发育神经毒性具有协同作用,JNK可能参与铅锰联合暴露致斑马鱼神经发育毒性。

     

    Abstract: Background

    Lead and manganese are heavy metal pollutants widely existing in the environment, which can accumulate in the human body through the food chain, exert neurotoxicity, and cause neurodegenerative disorders. Especially in early childhood, the developing blood-brain barrier and nervous system are highly susceptible to environmental chemical pollutants. Most of the previous studies focused on the toxic effects of single heavy metal such as lead or manganese, while the studies on combined toxic effect are still scarce, and involved mechanisms are still unclear. c-Jun N-terminal kinase (JNK) is involved in neuronal development and regeneration, and some studies have found that JNK is involved in lead or manganese induced neurotoxicity. Its role in the toxicity of combined lead and manganese is unknown.

    Objective

    To understand the neurodevelopmental toxicity mechanism and to observe changes of JNK expression in zebrafish induced by combined lead and manganese exposure at environmentlly low concentrations.

    Methods

    Zebrafish embryos within 2 h post fertilization (hpf) were divided into four groups: control group, lead exposure group (0.1 mg·L−1 lead acetate), manganese exposure group (0.3 mg·L−1 manganous chloride), and lead-manganese combined exposure group (0.1 mg·L−1 lead acetate +0.3 mg·L−1 manganous chloride) and exposed to lead or/and manganese at designed levels for 7 d. Spontaneous movements and motor locomotion were observed, and mortality rate were calculated. The changes of JNK mRNA expression in zebrafish were evaluated.

    Results

    The experimental results showed that no significant effect of lead or/and manganese on spontaneous movements and mortality rate was found in zebrafish compared with the control group (P>0.05). The results of locomotion analysis showed that compared with the control group, the activity counts and activity distance of zebrafish in the manganese exposure group were slightly increased (P<0.01); the activity counts and activity distance of zebrafish in the lead exposure group were reduced by 50% and those in the lead-manganese exposure group were reduced by 80% (P<0.01). Compared with the lead exposure group, the activity counts and activity distance of zebrafish in the lead-manganese combined exposure group decreased significantly by 60% (P<0.05). The real-time quantitative PCR results showed that the JNK mRNA expression level was significantly increased in the lead-manganese combined exposure group compared with the control group(P<0.01).

    Conclusion

    Lead exposure combined with manganese exposure at environmentlly low concentration can induce neurodevelopmental toxicity to zebrafish. JNK may be involved in neurodevelopmental toxicity induced by the combined exposure to lead and manganese.

     

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