Effects of vibration training on bone metabolism: Results from a short-term bed rest study
European Journal of Applied Physiology, ISSN: 1439-6319, Vol: 112, Issue: 5, Page: 1741-1750
2012
- 20Citations
- 47Captures
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Metrics Details
- Citations20
- Citation Indexes19
- CrossRef19
- 19
- Policy Citations1
- Policy Citation1
- Captures47
- Readers47
- 47
Article Description
The absence of mechanical loading leads to aprompt increase in bone resorption measured by bone resorption markers. There is high potential that vibration training can positively influence bone metabolism in immobilized subjects, reduce the increase in osteoclastic activity and increase bone formation processes. We investigated whether vibration training at 20 Hz with an amplitude of 2-4 mm influences bone metabolism during immobilization. Eight male subjects (26.4 ± 4.9 years; 78.1 ± 9.5 kg) performed a 14 day bed rest in 6°-head down tilt (HDT). Subjects received vibration training for 2 9 5 min/day or a control intervention without vibration (crossover design). Calcium excretion and bone resorption markers C-telopeptide (CTX) and N-telopeptide (NTX) were analyzed from 24 h urine samples. Bone formation markers, bone alkaline phosphatase (bAP) and procollagen- N propeptide (PINP) were analyzed from fasting blood samples. Our results show an increase in bone resorption very early during HDT bed rest in both interventions (CTX: p<0.01; NTX: p<0.001). Vibration training did not have any different effect on bone resorption markers (CTX: p = 0.10; NTX: p = 0.58), bone formation markers (PINP: p = 0.21; bAP: p = 0.12) and calcium excretion (p<0.64) compared to the control condition. Mere vibration training with 20 Hz for 2 ×5 min/day does not prevent increase in bone resorption as measured with the described methods in our short-term HDT bed rest. © 2011 Springer-Verlag.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84861526722&origin=inward; http://dx.doi.org/10.1007/s00421-011-2137-3; http://www.ncbi.nlm.nih.gov/pubmed/21894450; http://link.springer.com/10.1007/s00421-011-2137-3; http://www.springerlink.com/index/10.1007/s00421-011-2137-3; http://www.springerlink.com/index/pdf/10.1007/s00421-011-2137-3; https://dx.doi.org/10.1007/s00421-011-2137-3; https://link.springer.com/article/10.1007/s00421-011-2137-3
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