EFFECT OF 22-OXA-CALCITRIOL ON CALCIUM-METABOLISM IN RATS WITH SEVERESECONDARY HYPERPARATHYROIDISM

The purpose of the present study was to examine the effect of a two da y and a five day administration of 22-oxa-calcitriol (OCT) on calcium metabolism in rats with advanced chronic renal failure and severe seco ndary hyperparathyroidism. A first series of 27 uremic rats received e ither placebo, OCT or calcitriol (0.3 mug i.p./rat) 48 and 24 hours be fore sacrifice. A second series of 18 uremic rats received either plac ebo, OCT (0.3 mug i.p./rat) or calcitriol (0.05 mug i.p./rat) for five days. We found that after 48 hours (series 1) both calcitriol and OCT increased blood ionized calcium (Ca2+) as compared to vehicle (1.23 /- 0.04 and 1.10 +/- 0.02 mm, P < 0.01 and P < 0.05, respectively vs. control, 1.02 +/- 0.03 mm). Duodenal Ca transport (S/M) using the ever ted gut sac technique was not stimulated by OCT, even though it increa sed from 2.8 +/- 0.4 to 7.0 +/- 0.6 (P < 0.01) with calcitriol. In con trast, duodenal calbindin-D9k mRNA expression and protein content incr eased to a similar extent with OCT and calcitriol. Calcitriol was more potent in reducing plasma iPTH1-34 levels than OCT: 344 +/- 75 pg/ml (calcitriol) versus 632 +/- 46 pg/ml (OCT) compared with 897 +/- 74 pg /ml (control), P < 0.01. In the second series of rats, the injection o f OCT (0.3 mug i.p./rat) over five days was less effective than the lo wer dose of calcitriol (0.05 mug i.p./rat) in reducing circulating iPT H: 110 +/- 26 (calcitriol) and 281 +/- 64 (OCT) versus 624 +/-135 pg/m l (control), P < 0.01. The same tendency was observed for both compoun ds regarding the increase in blood Ca2+: 1.36 +/- 0.04 (calcitriol) an d 1.26 +/- 0.04 (OCT) versus 1.05 +/- 0.06 mm (control), P < 0.01. S/M was significantly increased by calcitriol but not by OCT: 4.0 +/- 0.3 (calcitriol) versus 3.0 +/- 0.09 (OCT) versus 2.6 +/- 0.3 (control), P < 0.05. In conclusion, in this model of secondary hyperparathyroidis m, OCT as well as calcitriol treatment increased blood Ca2+ and decrea sed circulating iPTH levels. However, the effects of OCT on both param eters were less marked than those of calcitriol. Both vitamin D deriva tives were equivalent in increasing duodenal calbindin-D9K mRNA and pr otein synthesis, but only calcitriol stimulated intestinal calcium tra nsport.