Physical and mechanical characteristics of tibias from transgenic mice expressing mutant bovine growth hormone genes

Citation
Nd. Turner et al., Physical and mechanical characteristics of tibias from transgenic mice expressing mutant bovine growth hormone genes, EXP BIOL ME, 226(2), 2001, pp. 133-139
Citations number
25
Categorie Soggetti
Medical Research General Topics
Journal title
EXPERIMENTAL BIOLOGY AND MEDICINE
ISSN journal
15353702 → ACNP
Volume
226
Issue
2
Year of publication
2001
Pages
133 - 139
Database
ISI
SICI code
1535-3702(200102)226:2<133:PAMCOT>2.0.ZU;2-W
Abstract
Physical and mechanical characteristics of tibia from mice expressing eithe r the M4, Mil, or G119K mutant bovine growth hormone (bGH) gene and display ing large, near-normal, or small-size phenotypes, respectively, were compar ed to those of nontransgenic, control mice (NTC). Three animals of each str ain were euthanized at 28, 38, 48, 58, and 68 days of age. Variables were r egressed against age to establish the pattern of change throughout the expe riment, and the regression results are presented. Tibias from G119K were sh orter (13.1 mm) and lighter (37.3 mg) than those from other strains, and M4 tibias were heavier (87.9 mg) and longer (16.6 mm) at 70 days of age. The ratio of tibia length to body weight suggests longitudinal bone growth was not reduced as much as overall growth in G119K mice. The external and inter nal dimensions of the G119K tibias were smaller than the other strains wher eas the M4 tibias were somewhat larger, Differences in physical dimensions between the NTC and M11 mice did not greatly affect bone mechanical charact eristics. Tibias from M4 mice resisted more load at both flexure and breaki ng compared to the other strains. At 50 days of age, stress at flexure was greater at all ages for G119K mice (12.4 kg/mm(2)) and was decreased in M4 mice (8.5 kg/mm(2)). The bGH mutations produce different effects on bone gr owth and its mechanical characteristics. There also may be differential tis sue responsiveness to the mutant bGH analogs, as longitudinal growth was no t as affected as empty body growth in the G119K mice, These transgenic mous e strains provide valuable models to study bone growth, formation, and refo rmation in response to GH regulation, and more importantly, the M4 and G119 K mice may serve as a model in which the priorities for GH action on bone v s muscle may be determined.