Suppr超能文献

对苯二酚暴露会使类风湿关节炎的症状恶化。

Hydroquinone exposure worsens the symptomatology of rheumatoid arthritis.

机构信息

Department of Clinical and Toxicological Analysis, Faculty of Pharmaceutical Sciences, University of São Paulo, Brazil.

Pharmacology Division, Institute Butantan, São Paulo, Brazil.

出版信息

Chem Biol Interact. 2018 Aug 1;291:120-127. doi: 10.1016/j.cbi.2018.06.016. Epub 2018 Jun 15.

Abstract

The genesis of rheumatoid arthritis (RA) is complex and dependent on genetic background and exposure to environmental xenobiotic. Indeed, smoking is associated to developing and worsening pre-existing RA. Nevertheless, the mechanisms and cigarette compounds involved in the harmful processes have not been elucidated. Here, we investigated if the exposure to hydroquinone (HQ), an abundant pro-oxidative compound of cigarette and benzene metabolite, could worsen the ongoing RA. Hence, collagen-induced arthritis (CIA) was induced in male Wistar rats by s.c. injection of 400 μg (200 μL) of bovine collagen type II emulsified in complete Freund's adjuvant on day 1, and a booster injection was performed on day 7. Exposures to nebulized HQ (25 ppm), saline solution or HQ vehicle solution (5% ethanol in saline) were carried out for 1 h, once a day, on days 21-27 after CIA induction. On day 27, animals were euthanized and samples were collected for further analyses. Exposure to HQ caused loss of weight, intensified paw edema, enhanced levels of tumor necrosis factor-α (TNF-α) and anti-citrullinated protein antibody (ACPA) in the serum; augmented synoviocyte proliferation and influx of aril hydrocarbon receptor (AhR) positive cells into the synovial membrane, altered collagen fibre rearrangement in the synovia, and synoviocytes isolated from HQ exposed rats secreted higher levels of pro-inflammatory cytokines, TNF-α and interleukin-1β. Associated, we point out HQ as an environmental pollutant that aggravates RA, suggesting its participation on worsening RA in smoking patients.

摘要

类风湿关节炎 (RA) 的发病机制复杂,依赖于遗传背景和接触环境异源物。事实上,吸烟与 RA 的发生和恶化有关。然而,参与有害过程的机制和香烟化合物尚未阐明。在这里,我们研究了暴露于对苯二酚 (HQ)(香烟和苯代谢物中的一种丰富的促氧化化合物)是否会加重正在进行的 RA。因此,雄性 Wistar 大鼠通过 sc 注射牛 II 型胶原(溶于完全弗氏佐剂中,每 200 μL 含 400μg)在第 1 天诱导胶原诱导性关节炎 (CIA),并在第 7 天进行加强注射。在 CIA 诱导后第 21-27 天,每天进行一次雾化 HQ(25ppm)、生理盐水或 HQ 载体溶液(5%乙醇在盐水中)暴露 1 小时。在第 27 天,对动物进行安乐死并收集样本进行进一步分析。暴露于 HQ 导致体重减轻、爪肿胀加剧、血清中肿瘤坏死因子-α (TNF-α) 和抗瓜氨酸化蛋白抗体 (ACPA) 水平升高、滑膜细胞增殖增加以及芳香烃受体 (AhR) 阳性细胞流入滑膜、改变滑膜中胶原纤维排列以及从 HQ 暴露的大鼠分离出的滑膜细胞分泌更高水平的促炎细胞因子 TNF-α 和白细胞介素 1β。因此,我们指出 HQ 是一种加重 RA 的环境污染物,表明其参与了吸烟患者 RA 的恶化。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验