Postoperative Tendon Loading With Treadmill Running Delays Tendon-to-Bone Healing: Immunohistochemical Evaluation in a Murine Rotator Cuff Repair Model

Susumu Wada, Amir H. Lebaschi, Yusuke Nakagawa, Camila B. Carballo, Tyler J. Uppstrom, Guang Ting Cong, Zoe M. Album, Arielle J. Hall, Liang Ying, Xiang Hua Deng, Scott A. Rodeo

Résultat de rechercheexamen par les pairs

23 Citations (Scopus)

Résumé

Mechanical stress has an important effect on tendon-to-bone healing. The purpose of the present study was to compare tendon-to-bone healing in animals exposed to either tendon unloading (botulinum toxin injection) or excessive loading (treadmill running) in a murine rotator cuff repair model. Forty-eight C57BL/6 mice underwent unilateral supraspinatus tendon detachment and repair. Mice in the unloaded group were injected with botulinum toxin to the supraspinatus muscle. The contralateral shoulder of the unloaded group was used as a control. Mice were euthanized at 1, 2, and 4 weeks after surgery and evaluated with hematoxylin–eosin and immunohistochemical (IHC) staining for Ihh, Gli1, Wnt3a, and β-catenin. The positive staining area on IHC and the Modified Tendon Maturing Score were measured. The score of the unloaded group was significantly higher (better healing) than that of the treadmill group at 4 weeks. Ihh and the glioma-associated oncogene homolog 1 (Gli1) positive area in the unloaded group were significantly higher than those of the control group at 1 week. The peak time-points of the Ihh and Gli1 positive area was 1 week for the unloaded group and 2 weeks for the treadmill group. The Wnt3a positive area in the unloaded group was significantly higher than that of the control group at 2 weeks. The β-catenin positive area in the unloaded group was significantly higher than that of the treadmill group and the control group at 1 week. Our data indicated that the unloaded group has superior tendon maturation compared to the treadmill running group. Excessive tendon loading may delay the tendon healing process by affecting the activity of Ihh and Wnt/β-Catenin pathways.

Langue d'origineEnglish
Pages (de-à)1628-1637
Nombre de pages10
JournalJournal of Orthopaedic Research
Volume37
Numéro de publication7
DOI
Statut de publicationPublished - juill. 2019

Financement

This study was financially supported by funding from the Virginia B. Toulmin Foundation and the Tisch Foundation.

Bailleurs de fondsNuméro du bailleur de fonds
Tisch Foundation
Virginia B. Toulmin Foundation

    ASJC Scopus Subject Areas

    • Orthopedics and Sports Medicine

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