氨氮胁迫对四指线鱼幼鱼鳃组织生理、生化和代谢水平的影响

IF 4.1 2区 环境科学与生态学 Q1 MARINE & FRESHWATER BIOLOGY Aquatic Toxicology Pub Date : 2024-08-11 DOI:10.1016/j.aquatox.2024.107049
Jing-hui Jin , Eric Amenyogbe , Ye Yang , Zhong-liang Wang , Yi Lu , Rui-tao Xie , Eric Kwabena Droepenu , Jian-sheng Huang
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引用次数: 0

摘要

本研究考察了氨氮胁迫对池塘养殖的四指线鱼幼鱼的影响。采用生态毒理学方法评估了体重为 7.4 ± 0.6 克的幼鱼的 96 小时中位致死浓度(LC50-96h)和氨氮安全浓度。研究设计包括暴露于 LC50-96h 氨氮水平的应激组和未暴露于氨氮的对照组。为了研究氨氮对鳃组织的生理、生化和代谢影响,在胁迫12、24、48和96小时后采集鳃组织样本,48小时后恢复处理。与对照组相比,氨氮对四指线鲷幼鱼有不利影响,LC50-96小时和安全浓度值分别为20.70 mg/L和2.07 mg/L。接触氨氮会对鳃造成严重破坏,包括鳃片融合、上皮细胞脱落和分泌氯的细胞增殖。即使经过 48 小时的恢复期,这种组织损伤仍然存在。氨氮胁迫引发了鳃中抗氧化酶活性(超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶)和丙二醛含量的增加,表明从 12 小时开始就出现了氧化应激。虽然酶活性随着时间的推移而降低,但氧化应激即使在恢复后也持续存在,这表明需要持续进行抗氧化防御。代谢组学分析表明,在氨氮胁迫下,423 种代谢物发生了显著变化。L-精氨酸、牛磺酸、20-羟基花生四烯酸、11,12-二羟基-5Z、8Z 和 14Z 二十碳三烯酸等关键代谢物呈上升趋势;尿苷、腺苷、L-谷胱甘肽和胸腺嘧啶 5′-三磷酸呈下降趋势。这些变化反映了新陈代谢对压力的适应。在富集代谢途径中,主要的差异途径是膜运输、脂质代谢和氨基酸代谢。48 小时后,观察到 396 种代谢物与对照组相比存在明显差异。值得注意的是,L-精氨酸、胆碱和 L-组氨酸增加,而亚油酸、腺苷和谷胱甘肽减少。氨基酸和脂质代谢途径是受影响的主要途径。在氨氮胁迫下,四指丝鱼幼体增加了不饱和脂肪酸和饱和脂肪酸的合成,以应对低温,并通过消耗亚精胺来增强免疫功能。这种适应性有助于清除脂肪酸合成过程中产生的过氧化物,从而保护细胞免受氧化损伤。这项研究为池塘养殖和培育耐氨氮鱼类品系提供了启示。
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Effects of ammonia nitrogen stress on the physiological, biochemical, and metabolic levels of the gill tissue of juvenile four-finger threadfin (Eleutheronema tetradactylum)

In this study, the impact of ammonia nitrogen stress on juvenile four-finger threadfin in pond culture was examined. The 96-hour median lethal concentration (LC50-96h) and safe concentration of ammonia nitrogen were assessed in juveniles with a body weight of 7.4 ± 0.6 g using ecotoxicological methods. The study design included a stress group exposed to LC50-96h levels of ammonia nitrogen and a control group without ammonia nitrogen exposure. To examine the physiological, biochemical, and metabolic effects of ammonia nitrogen on gill tissue, gill tissue samples were collected after 12, 24, 48, and 96 h of stress, with a resumption of treatment after 48 h. Compared to the control group, ammonia nitrogen adversely affected juvenile four-finger threadfin, with LC50-96h and safe concentration values of 20.70 mg/L and 2.07 mg/L, respectively. Exposure to ammonia nitrogen resulted in substantial gill damage, including fusion of lamellae, epithelial cell loss, and proliferation of chlorine-secreting cells. This tissue damage persisted even after a 48-h recovery period. Ammonia nitrogen stress triggered an increase in antioxidant enzyme activity (superoxide dismutase, catalase, and glutathione peroxidase) and malondialdehyde levels in gills, indicating oxidative stress from 12 h onwards. Although enzyme activity decreased over time, oxidative stress persisted even after recovery, suggesting an ongoing need for antioxidant defense. Metabolomics analysis showed significant alterations in 423 metabolites under ammonia nitrogen stress. Key metabolites such as L-arginine, taurine, 20-hydroxyarachidonic acid, 11,12-dihydroxy-5Z, 8Z, and 14Z eicosotrienic acid followed an increasing trend; uridine, adenosine, L-glutathione, and thymidine 5′-triphosphate followed a decreasing trend. These changes reflect metabolic adaptations to stress. In enriched metabolic pathways, the main differential pathways are membrane transport, lipid metabolism, and amino acid metabolism. After 48 h, significant differences were observed in 396 metabolites compared to the control group. Notably, L-arginine, choline, and L-histidine increased, while linoleic acid, adenosine, and glutathione decreased. Amino acid and lipid metabolism pathways were key affected pathways. Under ammonia nitrogen stress, juvenile four-finger threadfin increased the synthesis of unsaturated and saturated fatty acids to cope with low temperatures and bolster immune function by consuming spermidine. This adaptation helps to clear peroxides generated during fatty acid synthesis, thereby protecting cells from oxidative damage. This study provides insights for pond aquaculture and breeding of ammonia nitrogen-tolerant fish strains.

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来源期刊
Aquatic Toxicology
Aquatic Toxicology 环境科学-毒理学
CiteScore
7.10
自引率
4.40%
发文量
250
审稿时长
56 days
期刊介绍: Aquatic Toxicology publishes significant contributions that increase the understanding of the impact of harmful substances (including natural and synthetic chemicals) on aquatic organisms and ecosystems. Aquatic Toxicology considers both laboratory and field studies with a focus on marine/ freshwater environments. We strive to attract high quality original scientific papers, critical reviews and expert opinion papers in the following areas: Effects of harmful substances on molecular, cellular, sub-organismal, organismal, population, community, and ecosystem level; Toxic Mechanisms; Genetic disturbances, transgenerational effects, behavioral and adaptive responses; Impacts of harmful substances on structure, function of and services provided by aquatic ecosystems; Mixture toxicity assessment; Statistical approaches to predict exposure to and hazards of contaminants The journal also considers manuscripts in other areas, such as the development of innovative concepts, approaches, and methodologies, which promote the wider application of toxicological datasets to the protection of aquatic environments and inform ecological risk assessments and decision making by relevant authorities.
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