Radiometrical, hormonal and biological correlates of skeletal growth in the female rat from birth to senescence

Del Pozo, Emilio; Janner, Marco; Mackenzie, Andrew R; Arampatzis, Spyridon; Dixon, Arnold K; Perrelet, Romain; Ruch, Walter; Lippuner, Kurt; Zapf, Juergen; Lamberts, Steven W; Mullis, Primus-Eugen (2014). Radiometrical, hormonal and biological correlates of skeletal growth in the female rat from birth to senescence. Growth hormone & IGF research, 24(2-3), pp. 83-88. Elsevier 10.1016/j.ghir.2014.03.003

[img] Text
1-s2.0-S1096637414000227-main.pdf - Published Version
Restricted to registered users only
Available under License Publisher holds Copyright.

Download (1MB)

OBJECTIVE

We investigated the skeletal growth profile of female rats from birth to senescence (100weeks) on the basis of sequential radiometrical, hormonal and biochemical parameters.

DESIGN

Weaning rats entered the study which was divided into two sections: a) sequential measurements of vertebral and tibial growths and bone mineral density (BMD), estimation of mineral content of the entire skeleton (BMC) and chemical analysis of vertebral Ca; and b) determination of basal and pulsatile growth hormone (rGH), insulin-like growth hormone (IGF-I), estradiol (E2), parathyroid hormone (PTH), osteocalcin (OC) and urinary d-pyridinoline (dp) throughout the experimental period.

RESULTS

Vertebral and tibial growths ceased at week 25 whereas BMD and BMC as well as total vertebral Ca exhibited a peak bone mass at week 40. rGH pulsatile profiles were significantly higher in younger animals coinciding with the period of active growth and IGF-I peaked at 7weeks, slowly declining thereafter and stabilizing after week 60. OC and dp closely paralleled IGF-I coinciding with the period of enhanced skeletal growth, remaining thereafter in the low range indicative of reduced bone turnover. E2 increased during reproductive life but the lower values subsequently recorded were still in the physiological range, strongly suggesting a protective role of this steroid on bone remodeling. PTH followed a similar profile to E2, but the significance of this after completion of growth remains unclear.

CONCLUSIONS

Mechanisms governing skeletal growth in the female rat appear similar to those in humans. Bone progression and attainment of peak bone mass are under simultaneous control of rGH, IGF-I and calciotropic hormones and are modulated by E2. This steroid seems to protect the skeleton from resorption before senescence whereas the role of PTH in this context remains uncertain.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Orthopaedic, Plastic and Hand Surgery (DOPH) > Clinic of Osteoporosis
04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Paediatric Medicine
04 Faculty of Medicine > Department of Dermatology, Urology, Rheumatology, Nephrology, Osteoporosis (DURN) > Clinic of Nephrology and Hypertension

UniBE Contributor:

Del Pozo, Emilio, Janner, Marco, Arampatzis, Spyridon, Perrelet, Romain, Lippuner, Kurt, Mullis, Primus-Eugen

Subjects:

600 Technology > 610 Medicine & health

ISSN:

1096-6374

Publisher:

Elsevier

Language:

English

Submitter:

Anette van Dorland

Date Deposited:

18 Mar 2015 12:03

Last Modified:

05 Dec 2022 14:34

Publisher DOI:

10.1016/j.ghir.2014.03.003

PubMed ID:

24735836

Uncontrolled Keywords:

Biological correlates, Hormonal, Radiometrical, Skeletal growth

BORIS DOI:

10.7892/boris.51894

URI:

https://boris.unibe.ch/id/eprint/51894

Actions (login required)

Edit item Edit item
Provide Feedback