Calcitriol and dihydrotachysterol are both used in clinical practice a
s treatment for several renal and endocrine conditions. However, despi
te their routine use, therapeutic dosages and concomitant adverse effe
cts of these medications have yet to be clarified. In our study, a low
, high and extreme dosage of calcitriol (20, 60, 120 ng/kg/day) or dih
ydrotachysterol (15, 45, 90 mu g/kg/day) was administered to six group
s of male Sprague Dawley rats for four weeks. The seventh group served
as untreated controls. Our results indicated no difference in food in
take, weight gain, or total or ionized plasma calcium among treatment
groups. Rats receiving 90 mu g/kg/day dihydrotachysterol excreted more
calcium than those receiving 120 ng/kg/day calcitriol (p < 0.002). Fe
mur and kidney calcium showed no significant differences for any dosag
es used of either medication. Mean urine calcium was significantly cor
related with ionized plasma calcium (p < 0.006) and kidney calcium (p
< 0.02). Light microscopy revealed evidence of calcification in one ra
t out of six receiving the extreme dose (120 ng/kg/day) of calcitriol
and one rat out of six receiving the extreme dose (90 mu g/kg/day) of
dihydrotachysterol. These results suggest that serum and urine calcium
must be carefully monitored during either form of vitamin D therapy,
but no effect on calcium content or histology of the kidneys was obser
ved in the common therapeutic range.