Center for Health and the Environment, School of Veterinary Medicine, University of California-Davis, Davis, CA 95616-8732, USA.
Dept of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, AZ 85721-0207.
Toxicol Lett. 2024 Jun;397:89-102. doi: 10.1016/j.toxlet.2024.05.014. Epub 2024 May 18.
Aging increases susceptibility to lung disease, but the topic is understudied, especially in relation to environmental exposures with the bulk of rodent studies using young adults. This study aims to define the pulmonary toxicity of naphthalene (NA) and the impacts of a dietary antioxidant, ergothioneine (ET), in the liver and lungs of middle-aged mice. NA causes a well-characterized pattern of conducting airway epithelial injury in the lung in young adult mice, but NA's toxicity has not been characterized in middle-aged mice, aged 1-1.5 years. ET is a dietary antioxidant that is synthesized by bacteria and fungi. The ET transporter (ETT), SLC22A4, is upregulated in tissues that experience high levels of oxidative stress. In this study, middle-aged male and female C57BL/6 J mice, maintained on an ET-free synthetic diet from conception, were gavaged with 70 mg/kg of ET for five consecutive days. On day 8, the mice were exposed to a single intraperitoneal NA dose of 50, 100, 150, or 200 mg/kg. At 24 hours post NA injection samples were collected and analyzed for ET concentration and reduced (GSH) and oxidized glutathione (GSSG) concentrations. Histopathology, morphometry, and gene expression were examined. Histopathology of mice exposed to 100 mg/kg of NA suggests reduction in toxicity in the terminal airways of both male (p ≤ 0.001) and female (p ≤ 0.05) middle-aged mice by the ET pretreatment. Our findings in this study are the first to document the toxicity of NA in middle-aged mice and show some efficacy of ET in reducing NA toxicity.
衰老会增加患肺病的易感性,但这个话题的研究还不够充分,尤其是在与大量啮齿动物研究使用年轻成年人相关的环境暴露方面。本研究旨在确定萘(NA)的肺部毒性,以及膳食抗氧化剂麦硫因(ET)对中年小鼠肝脏和肺部的影响。NA 会导致年轻成年小鼠肺部的传导气道上皮损伤呈现出一种特征性模式,但尚未在中年小鼠(1-1.5 岁)中对其毒性进行特征描述。ET 是一种由细菌和真菌合成的膳食抗氧化剂。ET 转运蛋白(ETT)SLC22A4 在经历高水平氧化应激的组织中上调。在这项研究中,从中年雄性和雌性 C57BL/6J 小鼠受孕开始,用不含 ET 的合成饮食喂养,连续 5 天每天灌胃 70mg/kg 的 ET。第 8 天,用 50、100、150 或 200mg/kg 的单次腹腔内 NA 剂量对小鼠进行暴露。在 NA 注射后 24 小时收集样本并分析 ET 浓度、还原型(GSH)和氧化型谷胱甘肽(GSSG)浓度。进行组织病理学、形态计量学和基因表达分析。暴露于 100mg/kg NA 的小鼠的组织病理学表明,ET 预处理可减少雄性(p≤0.001)和雌性(p≤0.05)中年小鼠终末气道的毒性。本研究中的发现首次记录了中年小鼠中 NA 的毒性,并表明 ET 在降低 NA 毒性方面具有一定的效果。