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水中镉暴露诱导胭脂鱼肝脏氧化应激、自噬和线粒体功能障碍。

Exposure to waterborne cadmium induce oxidative stress, autophagy and mitochondrial dysfunction in the liver of Procypris merus.

机构信息

Hunan Research Center of Engineering Technology for Utilization of Distinctive Aquatic Resource, Hunan Agricultural University, Changsha, 410128, Hunan, PR China; Collaborative Innovation Center for Efficient and Health Production of Fisheries in Hunan Province, Changde, 415000, PR China.

Department of Bioengineering and Environmental Science, Changsha University, Changsha, 410022, Hunan, PR China.

出版信息

Ecotoxicol Environ Saf. 2020 Nov;204:111051. doi: 10.1016/j.ecoenv.2020.111051. Epub 2020 Aug 4.

Abstract

The present study was performed to determine the effect of waterborne cadmium (Cd) exposure on oxidative stress, autophagy and mitochondrial dysfunction, and to explore the mechanism of Cd-induced liver damage in freshwater teleost Procypris merus. To this end, P. merus were exposed to waterborne 0, 0.25 and 0.5 mg/L Cd for 30 days (equal to 0, 2.22 and 4.45 μmol Cd/l). The waterborne Cd exposure significantly increased hepatic Cd accumulation and impaired histological structure of the liver of P. merus. both low and high-dose waterborne Cd exposure induced oxidative stress in the liver of P. merus, through increases Malondialdehyde (MDA) and reactive oxide species (ROS) accumulation in the liver. The Cd-induced oxidative stress in liver may result from reduction of enzyme activities (superoxide dismutases (SOD), catalases (CAT), GSH-S-transferases (GST)) and transcriptional expression of antioxidant related genes (gpx1, gpx2, cata, gsta1, sod1). Furthermore, the present study showed that waterborne Cd exposure decreased the transcriptional factor (nrf2) expression, which might lead to the down-regulation of antioxidant gene expression. Transmission electron microscopy (TEM) observations demonstrated that waterborne Cd exposure induced autophagy in the liver of P. merus. Gene expression analysis showed that waterborne Cd exposure also induced mRNA expression of a set of genes (beclin1, ulk1, atg5, lc3a, atg4b, atg9a, and p62) involved in the autophagy process, indicating that the influence of Cd on autophagy involved transcription regulation of autophagy gene expression. Waterborne Cd exposure induced a sharp decrease in ATP content in the liver of P. merus. In addition, the expression of mitochondrial function genes (sdha, cox4i1, cox1, atp5f1, and mt-cyb) are significantly decreased in the liver of P. merus in Cd treated groups, manifesting the suppression of Cd on mitochondrial energy metabolism. Taken together, our experiments demonstrate that waterborne Cd exposure induced oxidative stress, autophagy and mitochondrial dysfunction in the liver of P. merus. These results may contribute to the understanding of mechanisms that hepatotoxicity of Cd in teleost.

摘要

本研究旨在确定水相镉(Cd)暴露对淡水硬骨鱼 Procypris merus 氧化应激、自噬和线粒体功能障碍的影响,并探讨 Cd 诱导肝脏损伤的机制。为此,将 P. merus 暴露于水相 0、0.25 和 0.5mg/L Cd 中 30 天(分别相当于 0、2.22 和 4.45μmol Cd/L)。水相 Cd 暴露显著增加了 P. merus 肝脏中的 Cd 积累,并损害了 P. merus 肝脏的组织学结构。低剂量和高剂量水相 Cd 暴露均导致 P. merus 肝脏发生氧化应激,通过增加肝脏丙二醛(MDA)和活性氧(ROS)的积累。肝脏中 Cd 诱导的氧化应激可能是由于酶活性(超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽 S-转移酶(GST))和抗氧化相关基因(gpx1、gpx2、cata、gsta1、sod1)的转录表达减少所致。此外,本研究表明,水相 Cd 暴露降低了转录因子(nrf2)的表达,这可能导致抗氧化基因表达下调。透射电子显微镜(TEM)观察表明,水相 Cd 暴露诱导了 P. merus 肝脏中的自噬。基因表达分析表明,水相 Cd 暴露还诱导了一组参与自噬过程的基因(beclin1、ulk1、atg5、lc3a、atg4b、atg9a 和 p62)的 mRNA 表达,表明 Cd 对自噬的影响涉及自噬基因表达的转录调节。水相 Cd 暴露导致 P. merus 肝脏中 ATP 含量急剧下降。此外,Cd 处理组 P. merus 肝脏中线粒体功能基因(sdha、cox4i1、cox1、atp5f1 和 mt-cyb)的表达显著降低,表明 Cd 抑制了线粒体能量代谢。总之,我们的实验表明,水相 Cd 暴露诱导了 P. merus 肝脏中的氧化应激、自噬和线粒体功能障碍。这些结果可能有助于理解 Cd 在硬骨鱼中肝毒性的机制。

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