Acute Changes in NADPH Oxidase 4 in Early Post‐Traumatic Osteoarthritis. Issue 11 (1st August 2019)

• Record Type: Journal Article
• Authors: Wegner, Adam M.; Campos, Nestor R.; Robbins, Michael A.; Haddad, Andrew F.; Cunningham, Hailey C.; Yik, Jasper H. N.; Christiansen, Blaine A.; Haudenschild, Dominik R.
• Is Part Of: Journal of orthopaedic research. Volume 37:Issue 11(2019)
• Page Start: 2429
• Page End: 2436
• Publication Date: 2019-08-01
• Subjects: post‐traumatic osteoarthritis -- joint injury -- antioxidant -- inflammation -- NADPH oxidase -- Nox4; Orthopedics -- Periodicals; Musculoskeletal system -- Periodicals; 616.7
• DOI: 10.1002/jor.24417
• Languages: English
• ISSNs: 0736-0266

Abstract

ABSTRACT: Knee injuries cause structural damage and acute inflammation that initiates the development of post‐traumatic osteoarthritis (PTOA). NADPH oxidase 4 (Nox4), a member of a family of enzymes that generates reactive oxygen species (ROS), plays a pivotal role in normal development of the musculoskeletal system, but may increase ROS production to harmful levels after joint injury. The role of ROS in both normal joint homeostasis and injury is poorly understood, but inhibition of excessive ROS production by Nox4 after joint injury could be protective to the joint, decreasing oxidative stress, and initiation of PTOA. Knee injuries were simulated using inflammatory cytokines in cultured primary human chondrocytes and a non‐invasive mouse model of PTOA in C57BL/6N and Nox4 knockout mice. There is an acute decrease in Nox4 activity within 24 h after injury in both systems, followed by a subsequent sustained low‐level increase, a novel finding not seen in any other system. Inhibition of Nox4 activity by GKT137831 was protective against early structural changes after non‐invasive knee injury in a mouse model. Nox4 knockout mice had significant differences in structural and mechanical properties of bone, providing further evidence for the role of Nox4 in development of joint tissues and biochemical response after joint injury. Nox4 plays a significant role in the acute phase after joint injury, and targeted inhibition of inflammation caused by Nox4 may be protective against early joint changes in the pathogenesis of PTOA. © 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 37:2429–2436, 2019