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通过动员内源性靶向骨重塑实现对骨应力损伤的早期保护。

Early protection against bone stress injuries by mobilization of endogenous targeted bone remodeling.

作者信息

Ding Yuanjun, Yang Yongqing, Xu Fei, Tan Zhifen, Liu Xiyu, Shao Xi, Kang Fei, Yan Zedong, Luo Erping, Wang Jing, Luo Zhuojing, Cai Jing, Jing Da

机构信息

Department of Biomedical Engineering, Fourth Military Medical University, Xi'an, China.

Department of Radiation Oncology, Peking University Third Hospital, Beijing, China.

出版信息

iScience. 2023 Aug 11;26(9):107605. doi: 10.1016/j.isci.2023.107605. eCollection 2023 Sep 15.

Abstract

Bone stress injuries are common overuse injuries, especially in soldiers, athletes, and performers. In contrast to various post-injury treatments, early protection against bone stress injuries can provide greater benefit. This study explored the early protection strategies against bone stress injuries by mobilization of endogenous targeted bone remodeling. The effects of various pharmaceutical/biophysical approaches, individual or combinational, were investigated by giving intervention before fatigue loading. We optimized the dosage and administration parameters and found that early intervention with pulsed electromagnetic field and parathyroid hormone (i.e., PEMF+PTH) resulted in the most pronounced protective effects among all the approaches against the bone stress injuries. In addition, the mechanisms by which the strategy mobilizes targeted bone remodeling and enhances the self-repair capacity of bone were systematically investigated. This study proposes strategies to reduce the incidence of bone stress injuries in high-risk populations (e.g., soldiers and athletes), particularly for those before sudden increased physical training.

摘要

骨应力损伤是常见的过度使用损伤,在士兵、运动员和表演者中尤为常见。与各种损伤后治疗方法不同,早期预防骨应力损伤能带来更大益处。本研究通过动员内源性靶向骨重塑探索了预防骨应力损伤的早期保护策略。通过在疲劳负荷前进行干预,研究了各种药物/生物物理方法单独或联合使用的效果。我们优化了剂量和给药参数,发现脉冲电磁场和甲状旁腺激素的早期干预(即PEMF+PTH)在所有预防骨应力损伤的方法中产生了最显著的保护作用。此外,还系统地研究了该策略动员靶向骨重塑并增强骨自我修复能力的机制。本研究提出了降低高危人群(如士兵和运动员)骨应力损伤发生率的策略,特别是针对那些突然增加体育训练量之前的人群。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346c/10470328/33edc5abf20e/fx1.jpg

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