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  4. Chronic intermittent hypobaric hypoxia ameliorates osteoporosis after spinal cord injury through balancing osteoblast and osteoclast activities in rats

Chronic intermittent hypobaric hypoxia ameliorates osteoporosis after spinal cord injury through balancing osteoblast and osteoclast activities in rats

Frontiers in Endocrinology, 2023 · DOI: 10.3389/fendo.2023.1035186 · Published: May 9, 2023

Spinal Cord InjuryEndocrinologyOrthopedics

Simple Explanation

This study investigates the effects of chronic intermittent hypobaric hypoxia (CIHH) on osteoporosis in rats after spinal cord injury (SCI). CIHH involves exposing the rats to moderate hypoxia, simulating high altitude conditions with interrupted normoxia. The study found that CIHH treatment can reverse the decrease in bone mineral density and improve bone structure in SCI rats. This suggests that CIHH might have a protective effect against osteoporosis caused by SCI. The researchers also looked at the underlying mechanisms and found that CIHH may work by balancing the activity of bone-forming cells (osteoblasts) and bone-resorbing cells (osteoclasts), potentially through the hypoxia-inducible factor-1 alpha (HIF-1a) signaling pathway.

Study Duration
7 weeks
Participants
Wistar rats (male, eight-week-old)
Evidence Level
Not specified

Key Findings

  • 1
    CIHH treatment effectively reversed the SCI-induced reduction of bone mineral density (BMD), bone volume to tissue volume, trabecular thickness and number.
  • 2
    Histomorphometry showed that CIHH treatment increased bone formation of SCI rats, as evidenced by the increased osteoid formation and the decreased number and surface of TRAP-positive osteoclasts.
  • 3
    CIHH treatment improved deviations in osteoblastogenesis and osteoclastogenesis-related biomarkers in SCI rats, suggesting a balance between bone formation and resorption.

Research Summary

This study explores the role of chronic intermittent hypobaric hypoxia (CIHH) in treating osteoporosis following spinal cord injury (SCI) in rats. SCI often leads to osteoporosis, and the study investigates whether CIHH can mitigate this effect. The research demonstrates that CIHH treatment ameliorates osteoporosis in SCI rats by promoting bone formation and preventing the deterioration of trabecular bone. This is achieved by balancing the activities of osteoblasts and osteoclasts. The study concludes that CIHH may offer a potential therapeutic approach for managing SCI-associated osteoporosis by modulating the HIF-1a signaling pathway and balancing bone remodeling processes.

Practical Implications

Potential Therapeutic Intervention

CIHH may represent a novel non-pharmacological intervention for treating osteoporosis in SCI patients.

Underlying Mechanisms

The study highlights the importance of balancing osteoblast and osteoclast activity in SCI-induced bone loss and identifies the HIF-1a pathway as a potential therapeutic target.

Future Research

Further research is needed to explore the optimal CIHH parameters and to validate these findings in human clinical trials.

Study Limitations

  • 1
    Lack of investigation of CIHH on other complications induced by SCI.
  • 2
    Lack of the detection of TRAP levels in serum.
  • 3
    Lack of cell experiment to confirm the in vivo findings.

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