Long-bone biomechanics in mice selected for body conformation
Two lines of mice divergently selected from the control strain (CBi) against the positive phenotypic correlation between body weight (b.w.) and tail (skeletal) length were obtained ( CBi C : high weight, short tail; CBi L : low weight, long tail). The selected animals showed a different relationship...
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Veröffentlicht in: | Bone (New York, N.Y.) N.Y.), 1997-06, Vol.20 (6), p.539-545 |
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creator | Di Masso, R.J. Font, M.T. Capozza, R.F. Detarsio, G. Sosa, F. Ferretti, J.L. |
description | Two lines of mice divergently selected from the control strain (CBi) against the positive phenotypic correlation between body weight (b.w.) and tail (skeletal) length were obtained (
CBi
C
: high weight, short tail;
CBi
L
: low weight, long tail). The selected animals showed a different relationship between body and skeletal masses. To compare the adequacy between biomass and load-bearing ability of the skeleton, and to describe the eventual role of the bone mechanostat in the production of these changes, cross-sectional and bending properties of both femur diaphyses were determined in CBi,
CBi
L
, and
CBi
L
adult mice of both genders. Cortical bone material quality (elastic modulus) was reduced in the selected lines (
p < 0.001), significantly less in
CBi
C
than in
CBi
L
. In contrast, cross-sectional design (b.w.-adjusted values of moment of inertia, CSMI) was largely improved (
p < 0.001), significantly more in
CBi
C
than in
CBi
L
. These effects determined a greater stiffness and strength in
CBi
C
than in
CBi
L
or CBi weight-paired mice. The elevations of the negative regression lines between elastic modulus and CSMI (“distribution/quality” curves) decreased in the order
CBi
C
>
CBi
L
>
CBi
. Data show that selection improved diaphyseal stiffness and strength in
CBi
C
animals because of an architectural overcompensation for the reduced bone material quality. Therefore, an inadequate control of long-bone architectural design as a function of the mechanical quality of cortical bone and b.w. bearing could have been induced in that line. Assuming bone mechanostatic regulation to be genetically programmed, some of the corresponding biological determinants should be transmitted independently, because and architectural design. The possibility of transmission of an inadequate mechanostatic function (inability to adapt bone modeling to bone material quality as a function of the biomass to be supported) was also shown, as some genotypes could express architectural modifications that largely exceed bone material quality deterioration. |
doi_str_mv | 10.1016/S8756-3282(97)00055-0 |
format | Article |
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CBi
C
: high weight, short tail;
CBi
L
: low weight, long tail). The selected animals showed a different relationship between body and skeletal masses. To compare the adequacy between biomass and load-bearing ability of the skeleton, and to describe the eventual role of the bone mechanostat in the production of these changes, cross-sectional and bending properties of both femur diaphyses were determined in CBi,
CBi
L
, and
CBi
L
adult mice of both genders. Cortical bone material quality (elastic modulus) was reduced in the selected lines (
p < 0.001), significantly less in
CBi
C
than in
CBi
L
. In contrast, cross-sectional design (b.w.-adjusted values of moment of inertia, CSMI) was largely improved (
p < 0.001), significantly more in
CBi
C
than in
CBi
L
. These effects determined a greater stiffness and strength in
CBi
C
than in
CBi
L
or CBi weight-paired mice. The elevations of the negative regression lines between elastic modulus and CSMI (“distribution/quality” curves) decreased in the order
CBi
C
>
CBi
L
>
CBi
. Data show that selection improved diaphyseal stiffness and strength in
CBi
C
animals because of an architectural overcompensation for the reduced bone material quality. Therefore, an inadequate control of long-bone architectural design as a function of the mechanical quality of cortical bone and b.w. bearing could have been induced in that line. Assuming bone mechanostatic regulation to be genetically programmed, some of the corresponding biological determinants should be transmitted independently, because and architectural design. The possibility of transmission of an inadequate mechanostatic function (inability to adapt bone modeling to bone material quality as a function of the biomass to be supported) was also shown, as some genotypes could express architectural modifications that largely exceed bone material quality deterioration.</description><identifier>ISSN: 8756-3282</identifier><identifier>EISSN: 1873-2763</identifier><identifier>DOI: 10.1016/S8756-3282(97)00055-0</identifier><identifier>PMID: 9177868</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; Artificial selection ; Biological and medical sciences ; Body conformation ; Body Weight - genetics ; Bone biomechanics ; Bone genetics ; Bone mechanostat ; Elasticity ; Female ; Femur - physiology ; Fundamental and applied biological sciences. Psychology ; Male ; Mice ; Regression Analysis ; Selection, Genetic ; Skeleton and joints ; Space life sciences ; Vertebrates: osteoarticular system, musculoskeletal system ; Weight-Bearing - physiology</subject><ispartof>Bone (New York, N.Y.), 1997-06, Vol.20 (6), p.539-545</ispartof><rights>1997</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-2dd54686bd35e7034f4a2f638072854b7acf3a29dea323130eda23c8c754dd273</citedby><cites>FETCH-LOGICAL-c389t-2dd54686bd35e7034f4a2f638072854b7acf3a29dea323130eda23c8c754dd273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S8756-3282(97)00055-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2745713$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9177868$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Di Masso, R.J.</creatorcontrib><creatorcontrib>Font, M.T.</creatorcontrib><creatorcontrib>Capozza, R.F.</creatorcontrib><creatorcontrib>Detarsio, G.</creatorcontrib><creatorcontrib>Sosa, F.</creatorcontrib><creatorcontrib>Ferretti, J.L.</creatorcontrib><title>Long-bone biomechanics in mice selected for body conformation</title><title>Bone (New York, N.Y.)</title><addtitle>Bone</addtitle><description>Two lines of mice divergently selected from the control strain (CBi) against the positive phenotypic correlation between body weight (b.w.) and tail (skeletal) length were obtained (
CBi
C
: high weight, short tail;
CBi
L
: low weight, long tail). The selected animals showed a different relationship between body and skeletal masses. To compare the adequacy between biomass and load-bearing ability of the skeleton, and to describe the eventual role of the bone mechanostat in the production of these changes, cross-sectional and bending properties of both femur diaphyses were determined in CBi,
CBi
L
, and
CBi
L
adult mice of both genders. Cortical bone material quality (elastic modulus) was reduced in the selected lines (
p < 0.001), significantly less in
CBi
C
than in
CBi
L
. In contrast, cross-sectional design (b.w.-adjusted values of moment of inertia, CSMI) was largely improved (
p < 0.001), significantly more in
CBi
C
than in
CBi
L
. These effects determined a greater stiffness and strength in
CBi
C
than in
CBi
L
or CBi weight-paired mice. The elevations of the negative regression lines between elastic modulus and CSMI (“distribution/quality” curves) decreased in the order
CBi
C
>
CBi
L
>
CBi
. Data show that selection improved diaphyseal stiffness and strength in
CBi
C
animals because of an architectural overcompensation for the reduced bone material quality. Therefore, an inadequate control of long-bone architectural design as a function of the mechanical quality of cortical bone and b.w. bearing could have been induced in that line. Assuming bone mechanostatic regulation to be genetically programmed, some of the corresponding biological determinants should be transmitted independently, because and architectural design. The possibility of transmission of an inadequate mechanostatic function (inability to adapt bone modeling to bone material quality as a function of the biomass to be supported) was also shown, as some genotypes could express architectural modifications that largely exceed bone material quality deterioration.</description><subject>Animals</subject><subject>Artificial selection</subject><subject>Biological and medical sciences</subject><subject>Body conformation</subject><subject>Body Weight - genetics</subject><subject>Bone biomechanics</subject><subject>Bone genetics</subject><subject>Bone mechanostat</subject><subject>Elasticity</subject><subject>Female</subject><subject>Femur - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Male</subject><subject>Mice</subject><subject>Regression Analysis</subject><subject>Selection, Genetic</subject><subject>Skeleton and joints</subject><subject>Space life sciences</subject><subject>Vertebrates: osteoarticular system, musculoskeletal system</subject><subject>Weight-Bearing - physiology</subject><issn>8756-3282</issn><issn>1873-2763</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LxDAQhoMouq7-BKEHET1U89F00oOIiF-w4EE9hzSZaqRNNNkV_Pd23WWvnmZgnndmeAg5YvScUVZfPCuQdSm44qcNnFFKpSzpFpkwBaLkUIttMtkge2Q_548REg2wXbLbMABVqwm5nMXwVrYxYNH6OKB9N8HbXPhQDN5ikbFHO0dXdDEVbXQ_hY1h7Acz9zEckJ3O9BkP13VKXu9uX24eytnT_ePN9ay0QjXzkjsnq1rVrRMSgYqqqwzvaqEocCWrFozthOGNQyO4YIKiM1xYZUFWznEQU3Ky2vuZ4tcC81wPPlvsexMwLrKGhtYSKjqCcgXaFHNO2OnP5AeTfjSjeqlN_2nTSye6Af2nTS9zR-sDi3ZAt0mtPY3z4_XcZGv6Lplgfd5gHCoJTIzY1QrDUca3x6Sz9RgsOp9GjdpF_88jv2aSiHE</recordid><startdate>19970601</startdate><enddate>19970601</enddate><creator>Di Masso, R.J.</creator><creator>Font, M.T.</creator><creator>Capozza, R.F.</creator><creator>Detarsio, G.</creator><creator>Sosa, F.</creator><creator>Ferretti, J.L.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19970601</creationdate><title>Long-bone biomechanics in mice selected for body conformation</title><author>Di Masso, R.J. ; Font, M.T. ; Capozza, R.F. ; Detarsio, G. ; Sosa, F. ; Ferretti, J.L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-2dd54686bd35e7034f4a2f638072854b7acf3a29dea323130eda23c8c754dd273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Artificial selection</topic><topic>Biological and medical sciences</topic><topic>Body conformation</topic><topic>Body Weight - genetics</topic><topic>Bone biomechanics</topic><topic>Bone genetics</topic><topic>Bone mechanostat</topic><topic>Elasticity</topic><topic>Female</topic><topic>Femur - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Male</topic><topic>Mice</topic><topic>Regression Analysis</topic><topic>Selection, Genetic</topic><topic>Skeleton and joints</topic><topic>Space life sciences</topic><topic>Vertebrates: osteoarticular system, musculoskeletal system</topic><topic>Weight-Bearing - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Di Masso, R.J.</creatorcontrib><creatorcontrib>Font, M.T.</creatorcontrib><creatorcontrib>Capozza, R.F.</creatorcontrib><creatorcontrib>Detarsio, G.</creatorcontrib><creatorcontrib>Sosa, F.</creatorcontrib><creatorcontrib>Ferretti, J.L.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bone (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Di Masso, R.J.</au><au>Font, M.T.</au><au>Capozza, R.F.</au><au>Detarsio, G.</au><au>Sosa, F.</au><au>Ferretti, J.L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-bone biomechanics in mice selected for body conformation</atitle><jtitle>Bone (New York, N.Y.)</jtitle><addtitle>Bone</addtitle><date>1997-06-01</date><risdate>1997</risdate><volume>20</volume><issue>6</issue><spage>539</spage><epage>545</epage><pages>539-545</pages><issn>8756-3282</issn><eissn>1873-2763</eissn><abstract>Two lines of mice divergently selected from the control strain (CBi) against the positive phenotypic correlation between body weight (b.w.) and tail (skeletal) length were obtained (
CBi
C
: high weight, short tail;
CBi
L
: low weight, long tail). The selected animals showed a different relationship between body and skeletal masses. To compare the adequacy between biomass and load-bearing ability of the skeleton, and to describe the eventual role of the bone mechanostat in the production of these changes, cross-sectional and bending properties of both femur diaphyses were determined in CBi,
CBi
L
, and
CBi
L
adult mice of both genders. Cortical bone material quality (elastic modulus) was reduced in the selected lines (
p < 0.001), significantly less in
CBi
C
than in
CBi
L
. In contrast, cross-sectional design (b.w.-adjusted values of moment of inertia, CSMI) was largely improved (
p < 0.001), significantly more in
CBi
C
than in
CBi
L
. These effects determined a greater stiffness and strength in
CBi
C
than in
CBi
L
or CBi weight-paired mice. The elevations of the negative regression lines between elastic modulus and CSMI (“distribution/quality” curves) decreased in the order
CBi
C
>
CBi
L
>
CBi
. Data show that selection improved diaphyseal stiffness and strength in
CBi
C
animals because of an architectural overcompensation for the reduced bone material quality. Therefore, an inadequate control of long-bone architectural design as a function of the mechanical quality of cortical bone and b.w. bearing could have been induced in that line. Assuming bone mechanostatic regulation to be genetically programmed, some of the corresponding biological determinants should be transmitted independently, because and architectural design. The possibility of transmission of an inadequate mechanostatic function (inability to adapt bone modeling to bone material quality as a function of the biomass to be supported) was also shown, as some genotypes could express architectural modifications that largely exceed bone material quality deterioration.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>9177868</pmid><doi>10.1016/S8756-3282(97)00055-0</doi><tpages>7</tpages></addata></record> |
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ispartof | Bone (New York, N.Y.), 1997-06, Vol.20 (6), p.539-545 |
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source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Animals Artificial selection Biological and medical sciences Body conformation Body Weight - genetics Bone biomechanics Bone genetics Bone mechanostat Elasticity Female Femur - physiology Fundamental and applied biological sciences. Psychology Male Mice Regression Analysis Selection, Genetic Skeleton and joints Space life sciences Vertebrates: osteoarticular system, musculoskeletal system Weight-Bearing - physiology |
title | Long-bone biomechanics in mice selected for body conformation |
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