MECHANICAL-PROPERTIES, BONE-MINERAL CONTENT, AND BONE-COMPOSITION (COLLAGEN, OSTEOCALCIN, IGF-I) OF THE RAT FEMUR - INFLUENCE OF OVARIECTOMY AND NANDROLONE DECANOATE (ANABOLIC-STEROID) TREATMENT
J. Aerssens et al., MECHANICAL-PROPERTIES, BONE-MINERAL CONTENT, AND BONE-COMPOSITION (COLLAGEN, OSTEOCALCIN, IGF-I) OF THE RAT FEMUR - INFLUENCE OF OVARIECTOMY AND NANDROLONE DECANOATE (ANABOLIC-STEROID) TREATMENT, Calcified tissue international, 53(4), 1993, pp. 269-277
Nandrolone decanoate (ND) is an anabolic steroid with a positive effec
t on bone mass in osteoporotic patients. The mechanism of action, (i.e
., reduction of bone resorption and/or stimulation of bone formation),
the ultimate effect on mechanical properties, and the most effective
dosage are not yet clear. To address these issues, dose-related effect
s of the long-term effect of ND on serum and bone biochemistry, bone m
ineral content, and bone mechanical properties in ovariectomized (OVX)
rats (12 weeks old at the start of the experiment) were studied for 6
months. The results were compared with those obtained in age-matched,
intact, and OVX rats. OVX caused in the femur a significant increase
in net periosteal bone formation and net endosteal bone resorption of
bone collagen content and torsional strength, and of serum alkaline ph
osphatase, osteocalcin, and insulin-like growth factor-I (IGF-I) level
s, whereas cortical bone density and calcium/creatinine and phosphorus
/creatinine in 24-hour urine were significantly reduced. Treatment of
OVX rats with 1 mg ND/14 days resulted in a significant increase in pe
riosteal bone formation, femur length, cortical and trabecular bone mi
neral content and density, torsion stiffness and strength, and bone IG
F-I content, and a decrease in serum osteocalcin, urinary calcium/crea
tinine levels, and bone collagen content compared with OVX controls. T
he higher ND dosage of 2.5 mg/14 days did not improve the results. ND
treatment did not reverse all changes induced by OVX to the level of t
he intact controls. These results indicate that ND acts as an antireso
rptive drug and as a bone formation stimulating drug. Furthermore, the
increased bone mass and bone mineral density is associated with impro
ved bone strength and stiffness and the presence of an increased amoun
t of IGF-I. IGF-I is a growth factor considered to play a role in the
maintenance of normal skeletal balance by a paracrine or autocrine mec
hanism.