Department of Biological and Environmental Sciences, University of Messina, 98166 Messina, Italy.
Department of Biology and CESAM, University of Aveiro, 3810-193 Aveiro, Portugal.
Sci Total Environ. 2016 Apr 1;548-549:13-24. doi: 10.1016/j.scitotenv.2016.01.008. Epub 2016 Jan 19.
Oxidative stress has been described as a key pathway to initiate mercury (Hg) toxicity in fish. However, the mechanisms underlying Hg-induced oxidative stress in fish still need to be clarified. To this aim, environmental metabolomics in combination with a battery of conventional oxidative stress biomarkers were applied to the gills of golden grey mullet (Liza aurata) collected from Largo do Laranjo (LAR), a confined Hg contaminated area, and São Jacinto (SJ), selected as reference site (Aveiro Lagoon, Portugal). Higher accumulation of inorganic Hg and methylmercury was found in gills of fish from LAR relative to SJ. Nuclear magnetic resonance (NMR)-based metabolomics revealed changes in metabolites related to antioxidant protection, namely depletion of reduced glutathione (GSH) and its constituent amino acids, glutamate and glycine. The interference of Hg with the antioxidant protection of gills was corroborated through oxidative stress endpoints, namely the depletion of glutathione peroxidase and superoxide dismutase activities at LAR. The increase of total glutathione content (reduced glutathione+oxidized glutathione) at LAR, in parallel with GSH depletion aforementioned, indicates the occurrence of massive GSH oxidation under Hg stress, and an inability to carry out its regeneration (glutathione reductase activity was unaltered) or de novo synthesis. Nevertheless, the results suggest the occurrence of alternative mechanisms for preventing lipid peroxidative damage, which may be associated with the enhancement of membrane stabilization/repair processes resulting from depletion in the precursors of phosphatidylcholine (phosphocholine and glycerophosphocholine), as highlighted by NMR spectroscopy. However, the observed decrease in taurine may be attributable to alterations in the structure of cell membranes or interference in osmoregulatory processes. Overall, the novel concurrent use of metabolomics and conventional oxidative stress endpoints demonstrated to be sensitive and effective towards a mechanistically based assessment of Hg toxicity in gills of wild fish, providing new insights into the toxicological pathways underlying the oxidative stress.
氧化应激已被描述为引发鱼类汞(Hg)毒性的关键途径。然而,Hg 诱导鱼类氧化应激的机制仍需阐明。为此,本研究采用环境代谢组学结合一系列传统的氧化应激生物标志物,研究了取自拉戈多拉兰霍(LAR)(一个受 Hg 污染的封闭区域)和圣哈辛托(SJ)(葡萄牙阿威罗泻湖的参考点)的金色灰鲻(Liza aurata)鳃中的氧化应激。结果表明,与 SJ 相比,LAR 鱼鳃中的无机 Hg 和甲基汞积累更高。基于核磁共振(NMR)的代谢组学揭示了与抗氧化保护相关的代谢物发生变化,即还原型谷胱甘肽(GSH)及其组成氨基酸谷氨酸和甘氨酸耗竭。氧化应激终点证实了 Hg 对鳃抗氧化保护的干扰,即在 LAR 处谷胱甘肽过氧化物酶和超氧化物歧化酶活性耗竭。GSH 耗竭表明 GSH 大量氧化,而 GSH 还原酶活性未改变,无法进行其再生或从头合成,这与 LAR 总谷胱甘肽含量(还原型谷胱甘肽+氧化型谷胱甘肽)增加相吻合。然而,结果表明存在替代机制来防止脂质过氧化损伤,这可能与磷脂酰胆碱(磷酸胆碱和甘油磷酸胆碱)前体耗竭导致的膜稳定/修复过程增强有关,这一点通过 NMR 光谱得到了强调。然而,观察到牛磺酸的减少可能归因于细胞膜结构的改变或对渗透调节过程的干扰。总之,代谢组学和传统氧化应激终点的新的同时应用被证明对评估野生鱼类鳃中 Hg 毒性具有敏感性和有效性,为氧化应激的毒理学途径提供了新的见解。