Inhibitory effects of female sex hormones on urinary stone formation in rats

Citation
M. Iguchi et al., Inhibitory effects of female sex hormones on urinary stone formation in rats, KIDNEY INT, 56(2), 1999, pp. 479-485
Citations number
22
Categorie Soggetti
Urology & Nephrology","da verificare
Journal title
KIDNEY INTERNATIONAL
ISSN journal
00852538 → ACNP
Volume
56
Issue
2
Year of publication
1999
Pages
479 - 485
Database
ISI
SICI code
0085-2538(199908)56:2<479:IEOFSH>2.0.ZU;2-V
Abstract
Background. The effects of female sex hormones on urinary stone formation a re not known. This study was conducted to investigate the effects of these hormones on stone formation by using an ethylene glycol (EG) and vitamin D- induced rat urolithiasis model. Methods. Adult female Wistar rats were fed the same diet for four weeks and were then divided into four groups (N = 10 each). One group was administer ed 0.5 mi of olive oil three times per week for four weeks as a control. Th e other three groups were administered 0.5 mu g of vitamin D-3 and 0.5 mi o f 5% EG three times per week for four weeks. The rats in two of these three groups were oophorectomized, and the rats of the remaining group underwent a sham operation on the day before the start of the four-week treatment pe riod. One of the two oophorectomized groups was then administered a supplem entation of female sex hormones (0.1 mg of estrogen and 2.5 mg of progester one 3 times per week for 4 weeks). On the first day of the fifth week of th e experimental period, the degree of crystal deposition was determined hist ologically, and the calcium content in renal tissue was measured. We also i nvestigated the level of osteopontin (OPN) mRNA in renal tissues by Norther n blot analysis. OPN is a matrix protein thought to be a promoter of stone formation. Results. The urinary oxalate excretion, crystal deposition and calcium cont ent in renal tissue and the expression of OPN-mRNA were greater in the ooph orectomized rats compared with the controls, and the same parameters were i nhibited by the female sex hormone supplementation. Conclusions. These results suggest that female sex hormones can inhibit ren al crystal deposition in EG-treated rats by suppressing the urinary oxalate excretion and the expression of OPN.