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常用治疗药物对贻贝生理特性的影响,包括扑热息痛和乙酰水杨酸。

Effects of commonly used therapeutic drugs, paracetamol, and acetylsalicylic acid, on key physiological traits of the sea snail Gibbula umbilicalis.

机构信息

Departamento de Biologia, Universidade de Aveiro, Campus de Santiago, 3810-193, Aveiro, Portugal.

Centro de Estudos do Ambiente e do Mar (CESAM), Campus de Santiago, Universidade de Aveiro, 3810-193, Aveiro, Portugal.

出版信息

Environ Sci Pollut Res Int. 2019 Jul;26(21):21858-21870. doi: 10.1007/s11356-019-04653-w. Epub 2019 May 27.

DOI:10.1007/s11356-019-04653-w
PMID:31134547
Abstract

Over time, the consumption of pharmaceutical drugs has highly augmented, directly contributing for an increase of the discharges of these substances into sewage water due to excretion, and their direct release to the environment, with or without adequate treatment. Considering that part of the sewage water is dumped into rivers and seas, this is the major source of contamination of the aquatic environment. Paracetamol and acetylsalicylic acid are among the most worldwide consumed pharmaceutical drugs, frequently found in wastewater discharges and consequently in the aquatic environment in considerable amounts, posing ecotoxicity concerns especially towards aquatic non-target species. Thus, it is important to study the ecotoxicological implications that these drugs might pose to organisms from aquatic environments. The objective of this study was to assess the toxic effects of these two compounds on key biochemical features (antioxidant defenses and damage, metabolism, and cholinergic neurotoxicity) of the marine snail species Gibbula umbilicalis after an acute (96 h) exposure, simulating pulses of contamination. In order to understand the effects that those drugs have on this species, the biochemical biomarkers analyzed were the activities of catalase (CAT), glutathione-S-transferases (GSTs), cholinesterases (ChEs), and the levels of lipid peroxidation (TBARS). After acute exposure to paracetamol, catalase activity decreased significantly in organisms exposed to both highest concentrations; no significant alterations were observed for glutathione-S-transferases activity; TBARS concentration decreased significantly in organisms exposed to the intermediate and both highest concentrations, and cholinesterase activity increased significantly in animals exposed to the lowest concentration. However, after acute exposure to acetylsalicylic acid, catalase activity increased significantly; no significant alterations were observed for glutathione-S-transferases activity, and TBARS concentrations and cholinesterase activity increased. This set of data shows that G. umbilicalis is highly responsive to the presence of the tested drugs, and may thus be a promising species to serve as test organism in future marine ecotoxicological testing. The adoption of this species may broaden the offer of highly ecologically representative test organisms to be included in biomonitoring projects of the coastal and marine environment. Furthermore, it is possible to suggest that both drugs may pose significant deleterious effects of pro-oxidative origin to the physiology of the selected species, with potential adverse ecological consequences, even after short periods of exposure. The absence of neurotoxicity showed that despite being able to trigger antioxidant mechanisms, both drugs did not affect neurotransmission.

摘要

随着时间的推移,药品的消耗量大幅增加,这直接导致这些物质由于排泄和未经适当处理而直接排放到环境中,从而增加了污水排放量。考虑到部分污水被排入河流和海洋,这是水生环境受到污染的主要来源。对乙酰氨基酚和乙酰水杨酸是世界上最常被消耗的药物之一,经常在废水排放中被发现,因此在水生环境中以相当大的数量存在,对水生非目标物种造成生态毒性问题。因此,研究这些药物对水生环境中的生物体可能产生的生态毒理学影响非常重要。本研究的目的是评估这两种化合物对海洋蜗牛物种 G.umbilicalis 的关键生化特征(抗氧化防御和损伤、代谢和胆碱能神经毒性)的急性(96 小时)暴露后的毒性影响,模拟污染脉冲。为了了解这些药物对该物种的影响,分析了生化生物标志物,包括过氧化氢酶(CAT)、谷胱甘肽-S-转移酶(GSTs)、胆碱酯酶(ChEs)和脂质过氧化(TBARS)的水平。在急性暴露于对乙酰氨基酚后,暴露于两种最高浓度的生物体内的过氧化氢酶活性显著降低;谷胱甘肽-S-转移酶活性没有显著变化;暴露于中间浓度和两种最高浓度的生物体内的 TBARS 浓度显著降低,暴露于最低浓度的生物体内的胆碱酯酶活性显著增加。然而,在急性暴露于乙酰水杨酸后,过氧化氢酶活性显著增加;谷胱甘肽-S-转移酶活性没有显著变化,TBARS 浓度和胆碱酯酶活性增加。这组数据表明,G.umbilicalis 对测试药物的存在高度敏感,因此可能是一种有前途的物种,可以作为未来海洋生态毒理学测试的测试生物。采用这种物种可能会扩大包括在沿海和海洋环境生物监测项目中的高度生态代表性测试生物的供应。此外,可以表明这两种药物都可能对所选物种的生理产生显著的氧化性有害影响,即使在短时间暴露后也可能产生潜在的不利生态后果。没有神经毒性表明,尽管这两种药物都能够触发抗氧化机制,但它们都不会影响神经递质的传递。

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