Back to Search Start Over

Growth Hormone As Antiaging Factor in Old Bones

Authors :
Francisco G F Tresguerres
Jesús A.F. Tresguerres
Celia Clemente
Jesús Torres
Isabel F Tresguerres
R. Rodríguez-Torres
Jorge Carballido
Isabel Leco
Source :
Rejuvenation Research. 24:354-365
Publication Year :
2021
Publisher :
Mary Ann Liebert Inc, 2021.

Abstract

Aging induces changes in bone. Growth hormone (GH) is reduced by aging, and age-related changes observed in old bones might be due to a decrease in the GH/insulin-like growth factor-I (IGF-I) axis. GH administration on aged individuals is controversial. This study aimed to assess the effect of systemic GH treatment on bone properties, bone metabolism, and bone mineral density (BMD) in long bone of old rats. Aged Wistar rats were treated with GH at a dose of 2 mg/kg/day during 10 weeks. Plasma osteocalcin, IGF-I, and carboxy-terminal telopeptide of type I collagen levels were measured. Cross-sectional bone areas and BMD were measured by morphometric and densitometric analysis, respectively. Femora were analyzed by three point-bending testing. t-Test was used for statistical evaluation. p < 0.05 was considered to be significant. Significantly enhanced bone area, at the expense of the cortical area, was found in treated rats. The densitometric analysis showed 11% higher BMD in the experimental group. Significantly higher bone flexural modulus, stiffness, and ultimate load were observed in the treated rats. Plasma osteocalcin and IGF-I levels were significantly increased in the treated group, while the resorption marker concentration remained unchanged. Within the limitations of this experimental study, systemic GH administration has shown to enhance biomechanical properties, BMD, cortical mass, and plasma IGF-I and osteocalcin in old treated rats, compared to the control group; consequently, GH could be considered as an alternative therapy against age-related changes in the bone.

Details

ISSN :
15578577 and 15491684
Volume :
24
Database :
OpenAIRE
Journal :
Rejuvenation Research
Accession number :
edsair.doi.dedup.....2e5a448007320285cd0fd048f32cc0cf