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The Influence of a Cyclooxygenase-1 Inhibitor on Injured and Uninjured Ligaments in the Rat
Background: Results of previous studies have shown that piroxicam, a cyclooxygenase-1-2 inhibitor, improves the strength of healing ligaments, whereas celecoxib, a cyclooxygenase-2 inhibitor, impairs ligament healing. Hypothesis: The selective cyclooxygenase-1 inhibitor, SC-560, will improve the str...
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Published in: | The American journal of sports medicine 2003-07, Vol.31 (4), p.574-576 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Background: Results of previous studies have shown that piroxicam, a cyclooxygenase-1-2 inhibitor, improves the strength of healing ligaments,
whereas celecoxib, a cyclooxygenase-2 inhibitor, impairs ligament healing.
Hypothesis: The selective cyclooxygenase-1 inhibitor, SC-560, will improve the strength of ligament healing in an in vivo rat model.
Study Design: Controlled laboratory study.
Methods: Eighty male Sprague-Dawley rats underwent surgical transection of their medial collateral ligament. Postoperatively, 20 rats
were given SC-560 at a low dose and 20 at a high dose for the first 6 days of recovery; the other 40 received a normal diet.
The animals were sacrificed 14 days later, and both the injured and uninjured ligaments were mechanically tested to failure
in tension.
Results: No significant differences in the strength of injured ligaments were found between drug and placebo treatment. However, the
contralateral uninjured ligaments in the SC-560-treated groups failed at 27% higher energy and 22% higher load.
Conclusions: This cyclooxygenase-1 inhibitor did not improve the strength of ligament healing but did significantly improve the strength
of the contralateral uninjured ligament.
Clinical Relevance: A pure cyclooxygenase-1 inhibitor is probably not indicated as a positive influence on ligament healing but might provide
benefits in ligament injury prevention. |
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ISSN: | 0363-5465 1552-3365 |
DOI: | 10.1177/31.4.574 |