• Benyam Yosef, Yu Zhou, Kathryn Mouschouris, James Poteracki, Shay Soker, and Tracy Criswell.
• Department of Cardiac Surgery, Brigham and Young Women's Hospital, 75 Francis St., Boston, MA 02115.
• Mil Med. 2020 Jan 7; 185 (Suppl 1): 25-34.

IntroductionUpon injury, skeletal muscle undergoes a multiphase process beginning with degeneration of the damaged tissue, which is accompanied by inflammation and finally regeneration. One consequence of an injured microenvironment is excessive production of reactive oxygen species, which results in attenuated regeneration and recovery of function ultimately leading to fibrosis and disability. The objective of this research was to test the potential of the antioxidant, N-Acetyl-L-Cysteine (NAC), as a mediator of reactive oxygen species damage that results from traumatic muscle injury in order to support repair and regeneration of wounded muscle tissue and improve function recovery.Materials And MethodsAdult female Lewis rats were subjected to compartment syndrome injury as previously published by our group. Rats received intramuscular injections of NAC or vehicle at 24, 48, and 72 hours postinjury. Muscle function, tissue fibrosis, and the expression of myogenic and angiogenic markers were measured.ResultsMuscle function was significantly improved, and tissue fibrosis was significantly decreased in NAC-treated muscles.ConclusionsThese results suggest that NAC treatment of skeletal muscle after injury may be a viable option for the prevention of long-term fibrosis and scar formation, facilitating recovery of muscle function.© Association of Military Surgeons of the United States 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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