Suying Zhu , Doudou Hao , Yanli Chen , Zhiyou Shi , Yang Zhong , Fengying Zhang , Feng Tang , Suyuan Wang , Yunhong Wu
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引用次数: 0
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.
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.