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地中海贻贝(Mytilus galloprovincialis)对三种常用处方药短期暴露的生化和分子反应。

Biochemical and molecular responses of the Mediterranean mussel (Mytilus galloprovincialis) to short-term exposure to three commonly prescribed drugs.

机构信息

Centro de Ciências do Mar (CCMAR), Universidade do Algarve, Campus de Gambelas, 8005-139, Faro, Portugal.

Aquaculture Research Center, Agro-Technological Institute of Castilla y León (ITACyL), Ctra. Arévalo, s/n. 40196 Zamarramala, Segovia, Spain.

出版信息

Mar Environ Res. 2021 Jun;168:105309. doi: 10.1016/j.marenvres.2021.105309. Epub 2021 Mar 22.

DOI:10.1016/j.marenvres.2021.105309
PMID:33798995
Abstract

Pharmaceuticals represent a group of emerging contaminants. The short-term effect (3 and 7 days) of warfarin (1 and 10 mg L), dexamethasone (0.392 and 3.92 mg L) and imidazole (0.013 and 0.13 mg L) exposure was evaluated on mussels (Mytilus galloprovincialis). Total antioxidant status, glutathione reductase, glutathione peroxidase (GPx) and superoxide dismutase enzyme activities, and the expression of genes involved in the xenobiotic response (ATP binding cassette subfamily B member 1 (abcb1) and several nuclear receptor family J (nr1j) isoforms), were evaluated. All nr1j isoforms are suggested to be the xenobiotic receptor orthologs of the NR1I family. All drugs increased GPx activity and altered the expression of particular nr1j isoforms. Dexamethasone exposure also decreased abcb1 expression. These findings raised some concerns regarding the release of these pharmaceuticals into the aquatic environment. Thus, further studies might be needed to perform an accurate environmental risk assessment of these 3 poorly studied drugs.

摘要

药品是一组新兴的污染物。评估了华法林(1 和 10 mg/L)、地塞米松(0.392 和 3.92 mg/L)和咪达唑仑(0.013 和 0.13 mg/L)暴露对贻贝(Mytilus galloprovincialis)的短期影响(3 天和 7 天)。评估了总抗氧化状态、谷胱甘肽还原酶、谷胱甘肽过氧化物酶(GPx)和超氧化物歧化酶的酶活性,以及参与外源性物质反应的基因的表达(ATP 结合盒亚家族 B 成员 1(abcb1)和几种核受体家族 J(nr1j)同工型)。所有 nr1j 同工型都被认为是 NR1I 家族的外源性物质受体同源物。所有药物均增加了 GPx 活性并改变了特定 nr1j 同工型的表达。地塞米松暴露还降低了 abcb1 的表达。这些发现引起了人们对这些药物释放到水生环境中的一些担忧。因此,可能需要进一步研究来对这 3 种研究甚少的药物进行准确的环境风险评估。

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