» Articles » PMID: 26895739

Substrain-specific Differences in Bone Parameters, Alpha-2-macroglobulin Circulating Levels, and Osteonecrosis Incidence in a Rat Model

Overview
Journal J Orthop Res
Publisher Wiley
Specialty Orthopedics
Date 2016 Feb 21
PMID 26895739
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Osteonecrosis of the femoral head (ONFH) is a potentially devastating complication that occurs in up to 40% of young adults receiving chronic glucocorticoid (GC) therapy. Through a validated GC therapy rat model, we have previously shown that Wistar Kyoto (WK) rats exhibit a genetic susceptibility to GC-induced ONFH compared to Sasco Fischer (F344) rats. We have undertaken this study in order to investigate differences between these two strains for their bone parameters, alpha-2-macroglobulin (A2M) circulating levels and incidence of GC-induced osteonecrosis of the femoral head. WK and F344 rats were treated either with 1.5 mg/kg/day of prednisone or placebo for 6 months. Blood was taken every month. The femoral heads were harvested for histological examination to detect ONFH and analyzed with micro-computed tomography. After 3 months of GC-therapy, plasma A2M was elevated in treated rats only. GC-treated WK rats exhibited histological evidence of early ONFH through higher rates of cellular apoptosis and empty osteocyte lacunae in the subchondral bone compared to placebos and to F344 rats. Furthermore, micro-CT analysis exhibited femoral head collapse only in GC-treated WK rats. Interestingly, GC-treated F344 rats exhibited significant micro-CT changes, but such changes were less concentrated in the articular region and were accompanied histologically with increased marrow fat. These µCT and histological findings suggest that elevated A2M serum level is not predictive and suitable as an indicative biomarker for early GC-induced ONFH in rodents. Elevated A2M levels observed during GC treatment suggests that it plays role in the host reparative response to GC-associated effects. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 35:1183-1194, 2017.

Citing Articles

Pathological mechanisms and related markers of steroid-induced osteonecrosis of the femoral head.

Li L, Zhao S, Leng Z, Chen S, Shi Y, Shi L Ann Med. 2024; 56(1):2416070.

PMID: 39529511 PMC: 11559024. DOI: 10.1080/07853890.2024.2416070.


[α2-macroglobulin alleviates glucocorticoid-induced avascular necrosis of the femoral head in mice by promoting proliferation, migration and angiogenesis of vascular endothelial cells].

Zhu Q, Lu Y, Peng Y, He J, Wei Z, Li Z Nan Fang Yi Ke Da Xue Xue Bao. 2024; 44(4):712-719.

PMID: 38708505 PMC: 11073947. DOI: 10.12122/j.issn.1673-4254.2024.04.13.


Long Noncoding RNA Zinc Finger Antisense 1 Affects Glucocorticoid-Induced Osteonecrosis of the Femoral Head by Performing as a ceRNA for MicroRNA-124-3p and Accelerating Transforming Growth Factor Type III Receptor.

Lan X, Xiong Y, Ma H, Zou L, Yuan Z, Xiao Y Comput Math Methods Med. 2022; 2022:4487864.

PMID: 35898479 PMC: 9313949. DOI: 10.1155/2022/4487864.


hsa_circ_0058122 knockdown prevents steroid-induced osteonecrosis of the femoral head by inhibiting human umbilical vein endothelial cells apoptosis via the miR-7974/IGFBP5 axis.

Yao T, Wang L, Ding Z, Yin Z J Clin Lab Anal. 2022; 36(4):e24134.

PMID: 35274778 PMC: 8993663. DOI: 10.1002/jcla.24134.


Relationship of α2-Macroglobulin with Steroid-Induced Femoral Head Necrosis: A Chinese Population-Based Association Study in Southeast China.

Fang S, Li Y, Jiang J, Chen P Orthop Surg. 2019; 11(3):481-486.

PMID: 31243924 PMC: 6595108. DOI: 10.1111/os.12492.