Hyperostosis of the Marrow Cavity Caused by Misoprostol in CD-1 Strain Mice
Open Access
- 1 November 1987
- journal article
- research article
- Published by SAGE Publications in Veterinary Pathology
- Vol. 24 (6) , 545-548
- https://doi.org/10.1177/030098588702400612
Abstract
Misoprostol, a synthetic prostaglandin E1, was administered to CD-1 mice daily by gavage for 21 months in a safety study. Hyperostosis of the marrow cavity in the sternum and femur was found predominantly in female mice of the medium (1,600 mcg/kg/day) and high dosage (16,000 mcg/kg/day) groups. Many of the mice with hyperostosis also had cystic ovaries and cystic endometrial hyperplasia indicative of hyperestrinism. It is postulated that the hyperostosis was the result not only of the effects of misoprostol but also of endogenous estrogen. Since misoprostol did not cause hyperostosis in either rats or dogs, it is probable that this effect in mice is unique.Keywords
This publication has 8 references indexed in Scilit:
- Twentyone-Month Evaluation of Misoprostol for Carcinogenicity in CD-1 MiceToxicologic Pathology, 1987
- Two-Year Evaluation of Misoprostol for Carcinogenicity in CD Sprague-Dawley RatsToxicologic Pathology, 1987
- The effects of prostaglandin E2 in growing rats: Increased metaphyseal hard tissue and cortico-endosteal bone formationCalcified Tissue International, 1985
- Regulation of Bone FormationNew England Journal of Medicine, 1983
- Cortical hyperostosis following long-term administration of prostaglandin E1 in infants with cyanotic congenital heart diseaseThe Journal of Pediatrics, 1980
- The Reproductive TractPublished by Springer Nature ,1978
- Formalin Fixation for Electron Microscopy: A Re-evaluationAmerican Journal of Clinical Pathology, 1973
- Collagen Formation and Endochondral Ossification in Estrogen Treated Mice.Experimental Biology and Medicine, 1966