Abstract

We have developed a method that allows us to measure bone resorption and formation simultaneously in the parietal bones from 22-day fetal rat calvaria. Parietal bones labeled with 45Ca, by injection of the mother, were cultured for 72 h with parathyroid hormone (PTH, bovine 1–34, 1.56 nM) or prostaglandin E 2 (PGE 2, 100 nM), in the presence or absence of indomethacin (Indo, 1 μM) or corticosterone (Cort, 1 μM). Two hours prior to the end of the culture, the bones were pulsed with [ 3H]-proline or [ 3H]-thymidine. Resorption was assessed as the percent of 45Ca released into the medium. Incorporation of [ 3H]-proline into collagenase digestible protein (CDP) and of [ 3H]-thymidine into DNA (TDR) were measured to assess collagen and DNA synthesis, respectively. Basal % 45Ca release was 16 ± 1% and was significantly decreased by Indo and Cort. Cort decreased TDR and CDP while Indo did not. PTH and PGE 2 significantly increased % 45Ca release, and this was not blocked by Indo. However, in the presence of Cort, only PTH increased % 45Ca release while PGE 2 did not. PGE 2 increased TDR under all culture conditions while PTH increased TDR only in the presence of Cort. While PTH and PGE 2 had the same effects on bone resorption, they had different effects on CDP. PGE 2 increased CDP in the presence of Indo or Cort but PTH did not. Thus, this model allows us to study bone resorption, collagen synthesis, and DNA synthesis simultaneously. We have also shown that PTH and PGE 2 differ in their sensitivity to inhibition of resorption by Cort and in their effects on bone formation.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.