Hydrogen intervention attenuates chronic hypoxia-induced bone degeneration and multi-organ damage via modulation of the gut microbiota

IF 3.9 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Bone Pub Date : 2026-02-01 Epub Date: 2025-11-11 DOI:10.1016/j.bone.2025.117718
Suying Zhu , Doudou Hao , Yanli Chen , Zhiyou Shi , Yang Zhong , Fengying Zhang , Feng Tang , Suyuan Wang , Yunhong Wu
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Abstract

High-altitude hypoxia disrupts bone metabolic homeostasis and accelerates bone loss. However, effective strategies for preventing and treating hypoxia-induced osteoporosis remain limited. This study aimed to evaluate the protective effects of hydrogen-rich water (HRW) and coral calcium hydride (CCH) against bone degeneration and multi-organ injury in a mouse model of chronic hypoxic exposure. Mice exposed to a hypoxic environment simulating 5500 m altitude for 4 months showed progressive bone deterioration from prolonged hypoxic exposure, which was significantly ameliorated by HRW intervention. Hydrogen intervention also markedly attenuated hypoxia-induced inflammation and damage in multiple organs such as the liver, lungs, kidneys, and colon. Hypoxia exposure led to changes in the diversity of gut microbiota, along with a decrease in the abundance of aerobic bacteria and beneficial bacteria (e.g., Lactobacillus), while hydrogen intervention could partially reverse this dysbiosis. At the molecular level, hypoxia significantly up-regulated the expression of HIF-1α, RANKL, and TRAP in bone tissue, and suppressed Nrf2 protein levels. However, hydrogen intervention did not directly alter the expression of these molecules. Hydrogen intervention may exert a bone-protective effect through the “gut-bone axis” by regulating the homeostasis of gut microbiota and alleviating systemic inflammation and oxidative stress, rather than directly acting on the classical hypoxia signaling pathway. Therefore, hydrogen intervention is a potential strategy to alleviate chronic hypoxia-induced bone loss and multi-organ damage by regulating gut microbiota homeostasis, which provides new insights and directions for the prevention and treatment of high-altitude bone-related diseases.
氢干预通过调节肠道微生物群减轻慢性缺氧诱导的骨变性和多器官损伤。
高原缺氧破坏骨代谢稳态,加速骨质流失。然而,预防和治疗缺氧所致骨质疏松症的有效策略仍然有限。本研究旨在评价富氢水(HRW)和珊瑚氢化钙(CCH)对慢性缺氧小鼠骨变性和多器官损伤的保护作用。小鼠暴露于模拟海拔5500 米的低氧环境4 个月后,由于长时间的低氧暴露,骨骼出现进行性恶化,HRW干预可显著改善这种情况。氢干预也能显著减轻缺氧引起的炎症和多个器官的损伤,如肝、肺、肾和结肠。缺氧暴露导致肠道微生物群多样性的变化,同时好氧细菌和有益细菌(如乳酸杆菌)的丰度减少,而氢干预可以部分逆转这种生态失调。在分子水平上,缺氧显著上调骨组织中HIF-1α、RANKL和TRAP的表达,抑制Nrf2蛋白水平。然而,氢干预并没有直接改变这些分子的表达。氢干预可能通过调节肠道菌群稳态、减轻全身炎症和氧化应激,而不是直接作用于经典的缺氧信号通路,从而通过“肠-骨轴”发挥骨保护作用。因此,氢干预是通过调节肠道菌群稳态来缓解慢性缺氧所致骨质流失和多器官损伤的潜在策略,这为高原骨相关疾病的防治提供了新的见解和方向。
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
Bone
Bone 医学-内分泌学与代谢
CiteScore
8.90
自引率
4.90%
发文量
264
审稿时长
30 days
期刊介绍: BONE is an interdisciplinary forum for the rapid publication of original articles and reviews on basic, translational, and clinical aspects of bone and mineral metabolism. The Journal also encourages submissions related to interactions of bone with other organ systems, including cartilage, endocrine, muscle, fat, neural, vascular, gastrointestinal, hematopoietic, and immune systems. Particular attention is placed on the application of experimental studies to clinical practice.
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