Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, 98166 Messina, Italy.
Department of Veterinary Science, University of Messina, 98168 Messina, Italy.
Biomolecules. 2022 Apr 10;12(4):564. doi: 10.3390/biom12040564.
Endocrine disruptors (EDs) are chemical substances capable of affecting endocrine system functioning and interfering with organ morphogenesis and physiological functions. The development and regeneration of bone tissues have a complex hormonal regulation, and therefore, bone tissue cells can be considered potential targets for endocrine disruptors. In that regard, the aim of this research was to investigate the impact of ED exposure on the inflammatory response and oxidative stress in an experimental model of collagen-induced arthritis (CIA). Arthritis was induced by an emulsion of type II collagen (CII) and complete Freund's adjuvant, which was administered intradermally on days 0 and 21. Mice from day 21 to day 35 received the following EDs by oral gavage: cypermethrin (CP), diethyl phthalate (DEP), vinclozolin (VCZ), 17α-ethinylestradiol (EE), perfluorooctanesulfonic acid (PFOS) and atrazine (ATR). ED exposure caused worsening of clinical signs (erythema and edema in the hind paws), histological and radiographic changes, as well as behavioral deficits, induced by CII injections. Furthermore, ED exposure significantly increased the degree of inflammation and oxidative damage induced by arthritis; this upregulation was more evident after exposure to ATR than to other EDs. The results from our study suggest that exposure to EDs may play a deleterious role in the progression of RA; therefore, exposure to EDs should be limited.
内分泌干扰物 (EDs) 是能够影响内分泌系统功能并干扰器官形态发生和生理功能的化学物质。骨骼组织的发育和再生具有复杂的激素调节,因此,骨骼组织细胞可以被认为是内分泌干扰物的潜在靶标。在这方面,本研究的目的是研究 ED 暴露对胶原诱导性关节炎 (CIA) 实验模型中炎症反应和氧化应激的影响。关节炎通过 II 型胶原蛋白 (CII) 和完全弗氏佐剂的乳液诱导,于第 0 天和第 21 天皮内注射。从第 21 天到第 35 天,通过口服灌胃给予以下 EDs:氯菊酯 (CP)、邻苯二甲酸二乙酯 (DEP)、氯唑灵 (VCZ)、17α-乙炔雌二醇 (EE)、全氟辛烷磺酸 (PFOS) 和莠去津 (ATR)。ED 暴露导致 CII 注射引起的临床症状(后爪红斑和水肿)、组织学和放射照相变化以及行为缺陷恶化。此外,ED 暴露显著增加了关节炎引起的炎症和氧化损伤程度;与其他 EDs 相比,ATR 暴露后的上调更为明显。我们的研究结果表明,ED 暴露可能在 RA 的进展中起有害作用;因此,应限制 ED 暴露。