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聚苯乙烯纳米塑料通过激活氧化应激、炎症和细胞凋亡途径加剧庆大霉素诱导的成年大鼠肾毒性。

Polystyrene nanoplastics exacerbate gentamicin-induced nephrotoxicity in adult rat by activating oxidative stress, inflammation and apoptosis pathways.

作者信息

Boukholda Khadija, Elwej Awatef, Slimen Sabrine Ben, Mhadhbi Abir, Marrekchi Rim, Boudawara Ons, Kaya Bülent, Bouchard Michèle, Fetoui Hamadi

机构信息

Laboratory of Toxicology-Microbiology and Environmental Health (17ES06), Faculty of Sciences of Sfax, University of Sfax, BP1171, 3000, Sfax, Tunisia.

Biochemistry Laboratory, Department of Biochemistry, CHU Hedi Chaker, University of Sfax, 3029, Sfax, Tunisia.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2025 Feb 17. doi: 10.1007/s00210-025-03798-5.

Abstract

Nanoplastics (NPs) and pharmaceutical residues are environmental pollutants that can bioaccumulate in the food chain, thus increasing the risk of harmful effects due to concomitant exposure in both humans and animals. However, the impact of such co-exposure on target tissue toxicity and mechanism remains unclear. In this study, we aimed to investigate the effect of combined exposure to widespread polystyrene NP (Ps-NP) contaminant and a widely used antibiotic, gentamicin (GEN) on nephrotoxicity in adult rat. A total of 40 male Wistar rats were assigned into four groups; control group (C), GEN exposed-group (100 mg/kg/day, i.p.), Ps-NPs exposed-group (2.5 mg/kg/day, orally) and co-exposure-group (100 mg Ps-NPs/kg/day orally + 2.6 mg GEN/kg/day i.p.) for 15 consecutive days. Kidneys were excised at sacrifice on day 15 for the examination of: (i) renal function parameters and renal oxidative stress (oxidant and antioxidant markers); (ii) mRNA expression of key regulators of oxidative stress and inflammation response (NF-κB, TNF-α, IL-6 and NRF-2) and mitochondrial apoptosis pathway (Bax, Bcl-2, caspase-9 and caspase-3); (iii) histopathology. Levels of urea and creatinine in serum of NPs or/and GEN-treated rats were significantly increased with marked histopathological changes in the kidney. Additionally, the oxidative stress markers (MDA, PCO and NO) were increased with a decrease of antioxidant enzyme activities. Furthermore, Ps-NPs or/and GEN-treated rats exhibited increased expression of mRNA related to oxidative stress (NRF-2), inflammation (TNF-α, IL-6) and apoptosis (Bax, Bcl-2, caspase-9 and caspase-3). Our results revealed that co-exposure of adult rats to Ps-NPs and GEN had a synergic-adverse effect on the kidney function. This study highlights a new finding regarding the combined toxicity of NPs and pharmaceutical pollutants on kidney function, suggesting potential synergistic interaction between these substances.

摘要

纳米塑料(NPs)和药物残留是环境污染物,可在食物链中生物累积,从而增加人类和动物因同时接触而产生有害影响的风险。然而,这种共同接触对靶组织毒性及其机制的影响仍不清楚。在本研究中,我们旨在探究广泛存在的聚苯乙烯纳米塑料(Ps-NP)污染物与广泛使用的抗生素庆大霉素(GEN)联合暴露对成年大鼠肾毒性的影响。总共40只雄性Wistar大鼠被分为四组:对照组(C)、GEN暴露组(100毫克/千克/天,腹腔注射)、Ps-NPs暴露组(2.5毫克/千克/天,口服)和联合暴露组(100毫克Ps-NPs/千克/天口服 + 2.6毫克GEN/千克/天腹腔注射),连续15天。在第15天处死大鼠时切除肾脏,用于检查:(i)肾功能参数和肾氧化应激(氧化剂和抗氧化剂标志物);(ii)氧化应激和炎症反应关键调节因子(NF-κB、TNF-α、IL-6和NRF-2)以及线粒体凋亡途径(Bax、Bcl-2、caspase-9和caspase-3)的mRNA表达;(iii)组织病理学。NPs或/和GEN处理的大鼠血清中尿素和肌酐水平显著升高,肾脏出现明显的组织病理学变化。此外,氧化应激标志物(MDA、PCO和NO)增加,抗氧化酶活性降低。此外,Ps-NPs或/和GEN处理的大鼠表现出与氧化应激(NRF-2)、炎症(TNF-α、IL-6)和凋亡(Bax、Bcl-2、caspase-9和caspase-3)相关的mRNA表达增加。我们的结果表明,成年大鼠同时暴露于Ps-NPs和GEN对肾功能有协同不良影响。本研究突出了关于NPs和药物污染物对肾功能联合毒性的新发现,表明这些物质之间可能存在协同相互作用。

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