Effects of stabilizer magnesium nirate on CMIT/MIT-induced respiratory toxicity.

IF 1.6 4区 医学 Q4 TOXICOLOGY Toxicological Research Pub Date : 2023-03-10 eCollection Date: 2023-07-01 DOI:10.1007/s43188-023-00170-8
Mi-Kyung Song, Yong-Wook Baek, Dong Im Kim, Sung-Hoon Yoon, Kyuhong Lee
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Abstract

Despite a humidifier disinfectant (HD) product containing chloromethylisothiazolinone (CMIT) and methylisothiazolinone (MIT) with approximately 22% magnesium nitrate as a stabilizer, no report on the effects of magnesium nitrate on the respiratory toxicity of CMIT/MIT is available. In this study, Kathon CG and Proclin 200, containing approximately 1.5% CMIT/MIT with different magnesium nitrate concentrations (22.6% and 3%, respectively), were used to compare respiratory effects after intratracheal instillation (ITI) in C57BL/6 mice. C57BL/6 mice were randomized into groups of saline control, magnesium nitrate, Kathon CG, and Proclin 200 with 1.14 mg/kg of CMIT/MIT as the active ingredient, and administration was performed 6 times in a 2-3 day-interval in 2 weeks in all groups. Differential cell count analysis, cytokine analysis, and histological analysis of lung tissue were performed to characterize the injury features. Both Kathon and Proclin 200 induced an increase in inflammatory cell levels in the bronchoalveolar lavage (BAL) fluid, in particular, eosinophils and type 2 T helper cell (Th2)-secreted cytokines. All histopathological changes including granulomatous inflammation, mixed inflammatory cell infiltration, mucous cell hyperplasia, eosinophil infiltration, and pulmonary fibrosis were induced with similar frequency and severity in Kathon CG and Proclin 200 groups. Our results suggested that magnesium nitrate did not affect CMIT/MIT-induced lung injury in the intratracheally instilled model. Further inhalation studies are needed to determine the distribution and toxicity differences of CMIT/MIT in the lungs according to the magnesium nitrate concentration.

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稳定剂nirate镁对CMIT/MIT诱导的呼吸毒性的影响。
尽管加湿器消毒剂(HD)产品含有氯甲基异噻唑啉酮(CMIT)和甲基异噻唑烷酮(MIT),其中约22%的硝酸镁作为稳定剂,但没有关于硝酸镁对CMIT/MIT呼吸毒性影响的报告。在本研究中,Kathon CG和Proclin 200含有约1.5%的CMIT/MIT,具有不同的硝酸镁浓度(分别为22.6%和3%),用于比较C57BL/6小鼠气管内滴注(ITI)后的呼吸效果。C57BL/6小鼠被随机分为生理盐水对照组、硝酸镁组、Kathon CG组和Proclin 200组,其中1.14mg/kg的CMIT/MIT作为活性成分,并且在所有组中在2周内以2-3天的间隔进行6次给药。对肺组织进行差异细胞计数分析、细胞因子分析和组织学分析,以表征损伤特征。Kathon和Proclin 200都诱导支气管肺泡灌洗液(BAL)中炎症细胞水平的增加,特别是嗜酸性粒细胞和2型T辅助细胞(Th2)分泌的细胞因子。Kathon CG和Proclin 200组诱导的所有组织病理学变化,包括肉芽肿性炎症、混合性炎症细胞浸润、粘液细胞增生、嗜酸性粒细胞浸润和肺纤维化,其频率和严重程度相似。我们的结果表明,在气管内滴注模型中,硝酸镁不影响CMIT/MIT诱导的肺损伤。需要进一步的吸入研究来根据硝酸镁浓度确定CMIT/MIT在肺部的分布和毒性差异。
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来源期刊
CiteScore
4.20
自引率
4.30%
发文量
39
期刊介绍: Toxicological Research is the official journal of the Korean Society of Toxicology. The journal covers all areas of Toxicological Research of chemicals, drugs and environmental agents affecting human and animals, which in turn impact public health. The journal’s mission is to disseminate scientific and technical information on diverse areas of toxicological research. Contributions by toxicologists, molecular biologists, geneticists, biochemists, pharmacologists, clinical researchers and epidemiologists with a global view on public health through toxicological research are welcome. Emphasis will be given to articles providing an understanding of the toxicological mechanisms affecting animal, human and public health. In the case of research articles using natural extracts, detailed information with respect to the origin, extraction method, chemical profiles, and characterization of standard compounds to ensure the reproducible pharmacological activity should be provided.
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