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短期暴露于聚甲基丙烯酸甲酯纳米塑料会改变真鲷肌肉的抗氧化反应、发育和生长。

Short-term exposure to polymethylmethacrylate nanoplastics alters muscle antioxidant response, development and growth in Sparus aurata.

机构信息

Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, 08193 Barcelona, Spain.

Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, 08193 Barcelona, Spain; Institute of Biotechnology and Biomedicine, Universitat Autònoma de Barcelona, 08193 Barcelona, Spain.

出版信息

Mar Pollut Bull. 2021 Nov;172:112918. doi: 10.1016/j.marpolbul.2021.112918. Epub 2021 Sep 8.

Abstract

Polymethylmethacrylate (PMMA) plastic fragments have been found abundant in the environment, but the knowledge regarding its effects on the physiology of aquatic animals is still poorly studied. Here the short-term (96 h) effects of waterborne exposure to PMMA nanoplastics (PMMA-NPs) on the muscle of gilthead sea bream (Sparus aurata) fingerlings was evaluated at a concentration range that includes 0.001 up to 10 mg/L. The expression of key transcripts related to cell stress, tissue repair, immune response, antioxidant status and muscle development, together with several biochemical endpoints and metabolic parameters. Results indicate that exposure to PMMA-NPs elicit mildly antioxidant responses, enhanced the acetylcholinesterase (AChE) activity, and inhibited key regulators of muscle development (growth hormone receptors ghr-1/ghr-2 and myostatin, mstn-1 transcripts). However, no effects on pro-inflammatory cytokines (interleukin 1β, il1β and tumor necrosis factor α, tnfα) expression nor on the levels of energetic substrates (glucose, triglycerides and cholesterol) were found.

摘要

聚甲基丙烯酸甲酯(PMMA)塑料碎片在环境中大量存在,但有关其对水生动物生理影响的知识仍研究甚少。本研究在浓度范围为 0.001 至 10mg/L 的条件下,评估了水相暴露于 PMMA 纳米塑料(PMMA-NPs)对金头鲷(Sparus aurata)鱼苗肌肉的短期(96h)影响。研究了与细胞应激、组织修复、免疫反应、抗氧化状态和肌肉发育相关的关键转录本的表达,以及几种生化终点和代谢参数。结果表明,暴露于 PMMA-NPs 会引发轻度的抗氧化反应,提高乙酰胆碱酯酶(AChE)活性,并抑制肌肉发育的关键调节因子(生长激素受体 ghr-1/ghr-2 和肌肉生长抑制素,mstn-1 转录本)。然而,未发现对促炎细胞因子(白细胞介素 1β,il1β 和肿瘤坏死因子α,tnfα)表达或能量底物(葡萄糖、甘油三酯和胆固醇)水平有影响。

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