Vitamin D (vit D) deficiency is common in the elderly. and the aim of this
study was to investigate whether vit D deprivation in ovariectomized (ovx)
and normal rats would reduce fracture strength. Forty mature female Wistar
rats were randomized into four groups: two were ovariectomized (ovx) and tw
o were sham-operated (sham). One ovx and one sham group were fed a vit D-de
ficient diet (Ovx-D and Sham-D), and the control groups were fed normal rat
chow (Ovx and Sham) for 12 weeks. Vit D deficiency was substantiated after
12 weeks by undetectable serum concentrations of 25OHD in the Sham-D and O
vx-D groups. Sr-85 activity was lower in Sham-D than in the other groups (P
< 0.005). Tibial and femoral weights and lengths showed no differences. Di
stal tibial trabecular bone volume was reduced in both ovx groups compare w
ith sham (P < 0.005). Bone mineral density (BMD) was higher in sham than in
Sham-D and both ovx groups (P < 0.005). Femoral area moment of inertia inc
reased and ultimate stress decreased in Ovx-D compared with ovx (P < 0.05).
Other biomechanical properties of the femoral shafts did not differ signif
icantly. The femoral neck was significantly weaker in Ovx-D than in the oth
er groups. In conclusion, ovx de creased tibial trabecular bone volume and
both ovx and vit D depletion reduced femoral BMD in rats. Vit D depletion r
educed the ultimate stress in the femoral shaft, and the combined depletion
of estrogen and vit D significantly reduced the fracture strength in the f
emoral neck. This fits well with clinical evidence of how postmenopausal st
atus combined with vit D deficiency lead to an increased risk of hip fractu
res, making this animal model a possible tool for investigating measures to
prevent such fractures.