Publications and Research
Document Type
Article
Publication Date
2023
Abstract
Lead (Pb) toxicity is a major health problem and bone is the major reservoir. Lead is detrimental to bone, affects bone remodelingand is associated with elderly fractures. Osteocalcin (OC) affects bone remodeling, improves fracture resistance and decreases with age and in some diseases. The effect of lead in osteocalcin depleted bone is unknown and of interest. We compared bone mineral properties of control and Pb exposed (from 2 to 6 months) femora from female adult C57BL6 OC+/+ and OC−/− mice using Fourier Transform Infrared Imaging (FTIRI), Micro-computed tomography (uCT), bone biomechanical measurements and serum turnover markers (P1NP, CTX). Lead significantly increased turnover in OC+/+ and in OC−/− bones producing increased total volume, area and marrow area/total area with decreased BV/TV compared to controls. The increased turnover decreased mineral/matrix vs. Oc+/+ and increased mineral/matrix and crystallinity vs. OC−/−. PbOC−/− had increased bone formation, cross-sectional area (Imin) and decreased collagen maturity compared OC−/− and PbOC+/+. Imbalanced turnover in PbOC−/− confirmed the role of osteocalcin as a coupler of formation and resorption. Bone strength and stiffness were reduced in OC−/− and PbOC−/− due to reduced material properties vs. OC+/+ and PbOC+/+ respectively. The PbOC−/− bones had increased area to compensate for weaker material properties but were not proportionally stronger for increased size. However, at low lead levels osteocalcin plays the major role in bone strength suggesting increased fracture risk in low Pb2+ exposed elderly could be due to reduced osteocalcin as well. Years of low lead exposure or higher blood lead levels may have an additional effect on bone strength.
Comments
This article was originally published in Bone Reports, available at https://doi.org/10.1016/j.bonr.2023.101672
This work is published under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.