Literature DB >> 8554920

Genetic lineage, bone mass, and physical activity in mice.

M Kaye1, R P Kusy.   

Abstract

Five strains of inbred mice were found to have variations in bone mass although they were similar in body weight. Two of these strains, C57BL/6J and A/J, were studied in greater detail and the former had more bone in both femur and tibia. The increased bone mass was associated with larger quadriceps muscles in the C57BL/6J animals when measured at 18 weeks of age. Activities of animals from these two strains were studied over 24 h periods using a cage with an ultrasonic movement detector and automatic counter. The C57BL/6J animals were more active than the A/J mice. The male C57BL/6J mice tended to have larger testicles and higher testosterone levels than the A/J animals, whereas the female A/J animals had larger ovaries and higher oestradiol levels. As both male and female C57BL/6J animals were more active, it was concluded that the sex hormone differences between the two strains was not responsible for either the changes in bone mass or physical activity. These findings indicate that in the mouse, activity is in part genetically determined. We have hypothesized that this, in turn, could affect muscle mass and secondarily, bone size and strength. If these results can be applied to humans, it would suggest that differences at birth between individuals are important for bone mass in later life and that muscle mass and activity are in part genetically influenced. If this was the case, then muscle mass and strength could be a factor in bone mass and one of the goals in prevention and treatment of osteoporosis should be directed toward preservation and/or augmentation of muscle strength.

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Year:  1995        PMID: 8554920     DOI: 10.1016/s8756-3282(00)00164-2

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  6 in total

1.  Adjusting data to body size: a comparison of methods as applied to quantitative trait loci analysis of musculoskeletal phenotypes.

Authors:  Dean H Lang; Neil A Sharkey; Arimantas Lionikas; Holly A Mack; Lars Larsson; George P Vogler; David J Vandenbergh; David A Blizard; Joseph T Stout; Joseph P Stitt; Gerald E McClearn
Journal:  J Bone Miner Res       Date:  2004-12-20       Impact factor: 6.741

2.  Gene expression analysis of mouse chromosome substitution strains.

Authors:  Keith R Shockley; Gary A Churchill
Journal:  Mamm Genome       Date:  2006-06-12       Impact factor: 2.957

3.  Quantitative trait loci analysis of structural and material skeletal phenotypes in C57BL/6J and DBA/2 second-generation and recombinant inbred mice.

Authors:  Dean H Lang; Neil A Sharkey; Holly A Mack; George P Vogler; David J Vandenbergh; David A Blizard; Joseph T Stout; Gerald E McClearn
Journal:  J Bone Miner Res       Date:  2004-10-11       Impact factor: 6.741

4.  Bone, muscle, and physical activity: structural equation modeling of relationships and genetic influence with age.

Authors:  Dean H Lang; David E Conroy; Arimantas Lionikas; Holly A Mack; Lars Larsson; George P Vogler; David J Vandenbergh; David A Blizard; Gerald E McClearn; Neil A Sharkey
Journal:  J Bone Miner Res       Date:  2009-09       Impact factor: 6.741

5.  Muscle contraction induces osteogenic levels of cortical bone strain despite muscle weakness in a mouse model of Osteogenesis Imperfecta.

Authors:  Alycia G Berman; Jason M Organ; Matthew R Allen; Joseph M Wallace
Journal:  Bone       Date:  2019-12-02       Impact factor: 4.398

6.  Loss of myostatin (GDF8) function increases osteogenic differentiation of bone marrow-derived mesenchymal stem cells but the osteogenic effect is ablated with unloading.

Authors:  M W Hamrick; X Shi; W Zhang; C Pennington; H Thakore; M Haque; B Kang; C M Isales; S Fulzele; K H Wenger
Journal:  Bone       Date:  2007-02-23       Impact factor: 4.398

  6 in total

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