Strontium ranelate reduces cartilage degeneration and subchondral bone remodeling in rat osteoarthritis model.

Acta Pharmacol Sin

Department of Orthopedics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai 200011, China.

Published: March 2013

AI Article Synopsis

  • The study aimed to determine if strontium ranelate (SR) could help reduce cartilage damage and bone changes in osteoarthritis (OA) in rats.
  • The researchers induced OA in rats using a medial meniscal tear operation and administered two dosage levels of SR for either 3 or 6 weeks, assessing cartilage health and bone properties afterward.
  • High-dose SR was found to significantly protect against cartilage degeneration and subchondral bone remodeling, unlike the low-dose SR, indicating its potential as a treatment for OA.

Article Abstract

Aim: To investigate whether strontium ranelate (SR), a new antiosteoporotic agent, could attenuate cartilage degeneration and subchondral bone remodeling in osteoarthritis (OA).

Methods: Medial meniscal tear (MMT) operation was performed in adult SD rats to induce OA. SR (625 or 1800 mg·kg(-1)·d(-1)) was administered via gavage for 3 or 6 weeks. After the animals were sacrificed, articular cartilage degeneration was evaluated using toluidine blue O staining, SOX9 immunohistochemistry and TUNEL assay. The changes in microarchitecture indices and tissue mineral density (TMD), chemical composition (mineral-to-collagen ratio), and intrinsic mechanical properties of the subchondral bones were measured using micro-CT scanning, confocal Raman microspectroscopy and nanoindentation testing, respectively.

Results: The high-dose SR significantly attenuated cartilage matrix and chondrocyte loss at 6 weeks, and decreased chondrocyte apoptosis, improved the expression of SOX9, a critical transcription factor responsible for the expression of anabolic genes type II collagen and aggrecan, at both 3 and 6 weeks. Meanwhile, the high-dose SR also significantly attenuated the subchondral bone remodeling at both 3 and 6 weeks, as shown by the improved microarchitecture indices, TMD, mineral-to-collagen ratio and intrinsic mechanical properties. In contrast, the low-dose SR did not significantly change all the detection indices of cartilage and bone at both 3 and 6 weeks.

Conclusion: The high-dose SR treatment can reduce articular cartilage degeneration and subchondral bone remodeling in the rat MMT model of OA.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4002491PMC
http://dx.doi.org/10.1038/aps.2012.167DOI Listing

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