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抗组胺药西替利嗪对菲律宾蛤仔贻贝的生态毒性。

Ecotoxicity of the antihistaminic drug cetirizine to Ruditapes philippinarum clams.

机构信息

Biology Department & CESAM, University of Aveiro, 3810-193 Aveiro, Portugal.

Chemistry Department & CESAM, University of Aveiro, 3810-193 Aveiro, Portugal.

出版信息

Sci Total Environ. 2017 Dec 1;601-602:793-801. doi: 10.1016/j.scitotenv.2017.05.149. Epub 2017 Jun 2.

DOI:10.1016/j.scitotenv.2017.05.149
PMID:28578237
Abstract

Cetirizine (CTZ) is an antihistaminic drug present in the aquatic environment, with limited information on its toxicity to organisms inhabiting this system. This study intended to evaluate the effects of CTZ on oxidative stress and energy metabolism biomarkers in the edible clam Ruditapes philippinarum after a 28days exposure to environmentally relevant CTZ concentrations (0.0, 0.3, 3.0, 6.0 and 12.0μg/L). The results obtained showed that CTZ was accumulated by clams reaching maximum concentrations (up to 22ng/g FW) at the highest CTZ exposure concentrations (6.0 and 12.0μg/L). The bioconcentration factor (average maximum values of ~5) decreased at 12.0μg/L reflecting a reduction in clams uptake or increase of excretion capacity at this condition. The present study revealed that, in general, clams decreased the metabolic potential after exposure to CTZ (decrease in electron transport system activity), a response that led to the maintenance of glycogen content in organisms exposed to CTZ in comparison to control values. Our findings also showed that, CTZ did not exert significant levels of oxidative injury to clams. However, comparing the control with the highest exposure concentrations (6.0 and 12.0μg/L) a significant increase of the antioxidant enzyme superoxide activity (53 and 44%) was observed in clams exposed to CTZ. Moreover, a tendency to increase lipid peroxidation (14 and 9%) and carbonyl groups on proteins (11 and ~3%) was observed in clams exposed to CTZ (6.0 and 12.0μg/L) compared to control condition. Overall the present study suggests that toxic impacts may be induced in R. philippinarum if exposed for longer periods or higher CTZ concentrations.

摘要

西替利嗪(CTZ)是一种存在于水环境中的抗组胺药物,关于其对栖息在该系统中的生物的毒性,信息有限。本研究旨在评估 CTZ 对在环境相关 CTZ 浓度(0.0、0.3、3.0、6.0 和 12.0μg/L)下暴露 28 天后的菲律宾蛤仔(Ruditapes philippinarum)的氧化应激和能量代谢生物标志物的影响。结果表明,蛤仔体内积累了 CTZ,在最高 CTZ 暴露浓度(6.0 和 12.0μg/L)下达到最大浓度(高达22ng/gFW)。生物浓缩因子(平均最大值约为5)在 12.0μg/L 时降低,反映了在此条件下蛤仔摄取减少或排泄能力增加。本研究表明,一般来说,暴露于 CTZ 后蛤仔降低了代谢潜力(电子传递系统活性降低),这种反应导致与对照值相比,暴露于 CTZ 的生物体中的糖原含量得以维持。我们的研究结果还表明,CTZ 对蛤仔没有产生显著的氧化损伤水平。然而,与最高暴露浓度(6.0 和 12.0μg/L)相比,在暴露于 CTZ 的蛤仔中观察到抗氧化酶超氧化物酶活性显著增加(53%和44%)。此外,与对照条件相比,暴露于 CTZ(6.0 和 12.0μg/L)的蛤仔中观察到脂质过氧化(14%和9%)和蛋白质羰基(11%和3%)增加的趋势。总体而言,本研究表明,如果暴露时间更长或 CTZ 浓度更高,菲律宾蛤仔可能会受到毒性影响。

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