This study determined the effects of nicotine on serum concentrations of se
veral calciotropic hormones, and bone formation and resorption end-points i
n 7 month old, adult female rats. Animals were administered either saline (
n= 9/group), low dose nicotine at 3.0 mg/kg/day (n=10/group) or high dose n
icotine at 4.5 mg/kg/day (n=11/group) by subcutaneous osmotic minipumps. Ar
the end of a three months treatment period, serum concentrations of calciu
m, phosphorus, parathyroid hormone, calcitonin, 25-hydroxyvitamin D and 1,2
5-dihydroxyvitamin D were determined. Femora, tibiae, and lumbar vertebrae
(3-5) were collected and bone parameters evaluated included mineral density
and content (femora and vertebrae), strength (femora and vertebrae) and hi
stomorphometry (tibiae). Animals given nicotine had significantly lower lev
els of 25-hydroxyvitamin D than controls [20.8 +/- 1.4 ng/ml for the low do
se group and 20.7 +/- 1.0 ng/ml for the high dose group versus 27.6 +/- 1.3
ng/ml for the control group (mean +/- S.E.M.), P<0.01]. The high dose nico
tine group had smaller vertebral areas (5.4 +/- 0.2 mm(2) versus 6.2 +/- 0.
2 mm(2), P<0.05) and a lower bone mineral content than the controls (0.024
+/- 0.001 g versus 0.030 +/- 0.001 g, P<0.05). Tibial endocortical mineral
apposition rate was also significantly lower in the high dose nicotine grou
p than in the control group (1.06 +/- 0.13 mu m/day versus 1.42 +/- 0.08 mu
m/day, P<0.05). No significant treatment differences were detected in bone
density, cancellous bone histomorphometry, or bone strength. Results from
the present study suggest that nicotine administration may adversely affect
bone formation and decrease body storage of vitamin D.