Format

Send to

Choose Destination
J Orthop Res. 2019 May 1. doi: 10.1002/jor.24319. [Epub ahead of print]

Efficacy of Combining PRP and MMP Inhibitors in Treating Moderately Damaged Tendons Ex Vivo.

Author information

1
Department of Mechanical Engineering, Université de Sherbrooke, Sherbrooke, Québec J1K 2R1, Canada.
2
Department of Chemical and Biotechnological Engineering, Université de Sherbrooke, Sherbrooke, Québec J1K 2R1, Canada.
3
Department of Pharmacology-Physiology, Université de Sherbrooke, Sherbrooke, Québec J1H 5N4, Canada.

Abstract

Platelet-rich plasma (PRP) and broad-spectrum matrix metalloproteinase inhibitors (MMPIs) have been used as therapeutic options for tendinopathy. However, mixed results have been reported regarding their efficacy. We posited that the combination of these two treatment strategies would be more beneficial for healing tendons than each treatment alone. Rat tail tendons were harvested and cultured without mechanical stress for 0, 4, or 10 days. Single and combination treatment with PRP and MMPIs with either broad- or narrow-spectrum (MMP-13 selective), was administered to 4-day stress-deprived (SD) tendons, an ex vivo model for moderate tendinopathy. This treatment was applied to the damaged tendons over 6 days. At the end of their culture time, the tendons were subjected to traction testing and pathohistology, immunohistochemistry, and viability assays. The results showed better histological features for the PRP + narrow-spectrum MMPI group compared with all individual treatment modalities. Moreover, higher fiber density, more elongated nucleus shape, smaller space between fibers, and a trend toward higher mechanical strength were noted for PRP + narrow-spectrum MMPI group compared with 10-day SD tendons. This study shows that the combination of PRP + narrow-spectrum MMPI is a potentially effective treatment approach for tendinopathy.

KEYWORDS:

MMP-13; biomechanical properties; histopathology; rat; tendinopathy

PMID:
31042324
DOI:
10.1002/jor.24319

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center