The effect of estrogen deficiency on calcium balance in mature rats

Citation
Cr. Draper et al., The effect of estrogen deficiency on calcium balance in mature rats, CALCIF TIS, 64(4), 1999, pp. 325-328
Citations number
19
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
CALCIFIED TISSUE INTERNATIONAL
ISSN journal
0171967X → ACNP
Volume
64
Issue
4
Year of publication
1999
Pages
325 - 328
Database
ISI
SICI code
0171-967X(199904)64:4<325:TEOEDO>2.0.ZU;2-Y
Abstract
The role of estrogen in the regulation of calcium balance is still poorly u nderstood. A calcium balance study was performed to examine the effects of estrogen status in relation to fecal calcium loss as a component of bone lo ss after oophorectomy (OOX) in the mature rat. The components of the classi c calcium balance were compared with calcium balance estimates obtained fro m whole body bone density. Six month or older Sprague Dawley rats were allo cated to either a sham-operated or OOX group and fed a 0.1% calcium diet. T he bone mineral density (BMD) and bone mineral content (BMC) were measured at baseline, 6 weeks, and 9 weeks. A calcium balance was done for 6 days be fore and 6 weeks post OOX. The fall in BMD from baseline to 9 weeks in the OOX group was significantly greater than in the sham-operated group. The ca lcium balance was more negative at baseline than at 6 weeks in both groups of animals because they had not adapted to the low calcium diet. However, t he increase in calcium balance was significantly less in the OOX animals th an in the sham-operated animals. The greater the rise in calcium balance fr om the baseline to the 6 weeks balance the less the fall in the calcium con tent of the whole body (Spearman correlation: r = 0.604 P = 0.008). The fal l in fecal calcium, but not urine calcium or calcium consumed, was negative ly correlated with the change in whole body BMC (Spearman correlation: feca l calcium r = -0.763 P = 0.001). Thus, the primary effect of estrogen defic iency on calcium balance in the mature rat appears to be calcium flux in th e bowel, rather than renal calcium handling.