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粒径依赖性聚苯乙烯珠和汞之间的毒相互作用对卤淡水溞(Daphnia celebensis)汞积累和多药耐药(MXR)的影响。

Size-dependent toxic interaction between polystyrene beads and mercury on the mercury accumulation and multixenobiotic resistance (MXR) of brackish water flea Diaphanosoma celebensis.

机构信息

Department of Biotechnology, College of Convergence Engineering, Sangmyung University, Seoul 03016, Republic of Korea.

School of Earth Sciences and Environmental Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea.

出版信息

Ecotoxicol Environ Saf. 2024 Nov 1;286:117131. doi: 10.1016/j.ecoenv.2024.117131. Epub 2024 Oct 15.

Abstract

Due to their worldwide distribution and persistence, mercury (Hg), and nano- and microplastics (NMPs) pose major threats to global ocean ecosystems. Hg and NMPs co-exist in the ocean and can interact with each other. However, information on the toxicity of this interaction to marine biota remains limited. Thus, we investigated the toxicological interaction between HgCl (Hg) and NMPs by studying the influence of different sizes of polystyrene beads (0.05-, 0.5-, and 6-μm) on Hg accumulation in the brackish water flea Diaphanosoma celebensis. The Hg adsorption capacity of NPs (0.05-μm) was higher than that of MPs (0.5- and 6-μm). Only the group co-exposed to both Hg and NPs showed increased Hg content in D. celebensis. Multixenobiotic resistance (MXR) activity and transcriptional modulation of transporter genes (ABCBs and ABCCs) were decreased by NMP exposure, particularly by NPs, suggesting MXR disruption by NPs. However, only the activity of multidrug resistance-associated proteins (MRPs; ABCCs) increased with Hg exposure and decreased upon NP+Hg co-exposure, indicating an important role of ABCC in Hg efflux. Furthermore, in vivo toxicity tests showed a synergistic toxic interaction between Hg and NPs on the reproduction of D. celebensis. Our findings suggest that NPs have the potential to enhance the toxicity of Hg, increasing Hg accumulation not only by serving Hg as a carrier but also by disrupting MXR.

摘要

由于汞(Hg)、纳米塑料和微塑料(NMPs)在全球范围内分布广泛且具有持久性,它们对全球海洋生态系统构成了重大威胁。Hg 和 NMPs 共存于海洋中并相互作用。然而,关于这种相互作用对海洋生物群毒性的信息仍然有限。因此,我们通过研究不同粒径聚苯乙烯珠(0.05μm、0.5μm 和 6μm)对卤淡水溞(Diaphanosoma celebensis)中 Hg 积累的影响,研究了 HgCl(Hg)和 NMPs 的毒理学相互作用。纳米塑料(0.05μm)的 Hg 吸附能力高于微塑料(0.5μm 和 6μm)。只有同时暴露于 Hg 和 NPs 的组中,D. celebensis 中的 Hg 含量增加。多药耐药相关蛋白(MRPs;ABCCs)的活性和转运蛋白基因(ABCBs 和 ABCCs)的转录调控因 NMP 暴露而降低,尤其是 NPs,表明 NPs 破坏了 MXR。然而,只有 Hg 暴露会增加多药耐药相关蛋白(MRPs;ABCCs)的活性,而在 NP+Hg 共暴露时则会降低,表明 ABCC 在 Hg 外排中起重要作用。此外,体内毒性试验表明 Hg 和 NPs 对 D. celebensis 繁殖具有协同毒性作用。我们的研究结果表明,NPs 有可能增强 Hg 的毒性,不仅通过充当 Hg 的载体增加 Hg 积累,还通过破坏 MXR 来增加 Hg 积累。

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