Melatonin alleviates sodium sulfite-induced osteoporosis in mice via suppression of the ferroptosis pathway

IF 8.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Qiuping He, Lei Xie, Haining Peng, Xiao Xiao, Tengbo Yu
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Abstract

Sodium sulfite (SS) is a common food additive that is widely absorbed and distributed throughout the body, but its excessive intake has been linked to adverse health effects. Here, we investigate the impact of chronic SS exposure on bone tissue and the underlying mechanisms. Using a mouse model, we demonstrate that prolonged SS exposure induces significant bone loss, which correlates with alterations in ferroptosis-related markers. In vitro, SS exposure activates ferroptosis, which is characterized by elevated reactive oxygen species levels and impaired osteogenic differentiation in MC3T3 cells. Notably, melatonin, a potent endogenous antioxidant, mitigates SS-induced oxidative stress, inhibits ferroptosis, restores osteoblast function, and alleviates bone loss in mice. These findings highlight ferroptosis as a critical contributor to SS-induced osteoporosis and identify melatonin as a promising therapeutic agent for its prevention and treatment.

褪黑素通过抑制铁下垂途径减轻亚硫酸钠诱导的小鼠骨质疏松症。
亚硫酸钠(SS)是一种常见的食品添加剂,被人体广泛吸收和分布,但过量摄入会对健康产生不利影响。在这里,我们研究慢性SS暴露对骨组织的影响及其潜在机制。通过小鼠模型,我们证明了长时间的SS暴露会导致显著的骨质流失,这与铁中毒相关标记物的改变有关。在体外,SS暴露会激活铁下沉,其特征是活性氧水平升高和MC3T3细胞成骨分化受损。值得注意的是,褪黑素是一种有效的内源性抗氧化剂,可以减轻ss诱导的氧化应激,抑制铁下沉,恢复成骨细胞功能,减轻小鼠骨质流失。这些发现强调了铁下垂是ss诱导骨质疏松症的关键因素,并确定褪黑素是一种有前途的治疗药物,可以预防和治疗铁下垂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Apoptosis
Apoptosis 生物-生化与分子生物学
CiteScore
9.10
自引率
4.20%
发文量
85
审稿时长
1 months
期刊介绍: Apoptosis, a monthly international peer-reviewed journal, focuses on the rapid publication of innovative investigations into programmed cell death. The journal aims to stimulate research on the mechanisms and role of apoptosis in various human diseases, such as cancer, autoimmune disease, viral infection, AIDS, cardiovascular disease, neurodegenerative disorders, osteoporosis, and aging. The Editor-In-Chief acknowledges the importance of advancing clinical therapies for apoptosis-related diseases. Apoptosis considers Original Articles, Reviews, Short Communications, Letters to the Editor, and Book Reviews for publication.
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