Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2010-9-14
pubmed:abstractText
With aging, the skeleton may lose its ability to respond to positive mechanical stimuli. We hypothesized that aged mice are less responsive to loading than young-adult mice. We subjected aged (22 months) and young-adult (7 months) BALB/c male mice to daily bouts of axial tibial compression for 1 week and evaluated cortical and trabecular responses using micro-computed tomography (µCT) and dynamic histomorphometry. The right legs of 95 mice were loaded for 60 rest-inserted cycles per day to 8, 10, or 12?N peak force (generating mid-diaphyseal strains of 900 to 1900 µ? endocortically and 1400 to 3100 µ? periosteally). At the mid-diaphysis, mice from both age groups showed a strong anabolic response on the endocortex (Ec) and periosteum (Ps) [Ec.MS/BS and Ps.MS/BS: loaded (right) versus control (left), p?<?.05]. Generally, bone formation increased with increasing peak force. At the endocortical surface, contrary to our hypothesis, aged mice had a significantly greater response to loading than young-adult mice (Ec.MS/BS and Ec.BFR/BS: 22 months versus 7 months, p?<?.001). Responses at the periosteal surface did not differ between age groups (p?>?.05). The loading-induced increase in bone formation resulted in increased cortical area in both age groups (loaded versus control, p?<?.05). In contrast to the strong cortical response, loading only weakly stimulated trabecular bone formation. Serial (in vivo) µCT examinations at the proximal metaphysis revealed that loading caused a loss of trabecular bone in 7-month-old mice, whereas it appeared to prevent bone loss in 22-month-old mice. In summary, 1 week of daily tibial compression stimulated a robust endocortical and periosteal bone-formation response at the mid-diaphysis in both young-adult and aged male BALB/c mice. We conclude that aging does not limit the short-term anabolic response of cortical bone to mechanical stimulation in our animal model.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-10404017, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-10620076, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-11247935, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-12110765, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-12211431, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-12854840, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-13678781, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-14678854, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-15746986, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-15747345, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-15878316, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-16198164, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-17488199, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-18433300, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-18539556, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-18601464, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-18648530, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-18684086, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-19733269, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-20405109, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-2080717, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-2312452, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-3610670, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-7591386, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-7785469, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-8686511, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-8739896, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-9071468, http://linkedlifedata.com/resource/pubmed/commentcorrection/20499381-9710941
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1523-4681
pubmed:author
pubmed:copyrightInfo
© 2010 American Society for Bone and Mineral Research.
pubmed:issnType
Electronic
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2006-15
pubmed:dateRevised
2011-9-13
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
Aged mice have enhanced endocortical response and normal periosteal response compared with young-adult mice following 1 week of axial tibial compression.
pubmed:affiliation
Department of Orthopaedic Surgery, Washington University, School of Medicine, St Louis, MO 63110, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, N.I.H., Extramural