Oxidative stress as a critical factor might involve in intervertebral disc degeneration via regulating NOXs/FOXOs

• Published in: Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association Vol. 28; no. 1; pp. 105 - 111
• Main Authors: Liu, Qi, Tan, Zhangbin, Xie, Chuhai, Ling, Long, Hu, Hailan
• Format: Journal Article
• Language: English
• Published: Japan Elsevier B.V 01.01.2023
• Subjects: Aggrecans - metabolism; Aggrecans - pharmacology; Animals; Antioxidants - pharmacology; Apoptosis; Catalase - metabolism; Catalase - pharmacology; Forkhead Transcription Factors; Intervertebral Disc - pathology; Intervertebral Disc Degeneration - pathology; Matrix Metalloproteinase 13 - metabolism; Matrix Metalloproteinase 13 - pharmacology; NADPH Oxidases; Oxidative Stress; Rats
• ISSN: 0949-2658; 1436-2023
• DOI: 10.1016/j.jos.2021.09.010

Oxidative stress is involved in many musculoskeletal diseases, such as osteoarthritis. However, the effect of oxidative stress on intervertebral disc degeneration (IDD) is still unclear. This study was aimed to provide an evidence of oxidative stress involved in IDD, and propose a new insight into pathogenesis of IDD. Sixteen rats were randomly divided into sham and cervical muscle section (CMS) groups. The intervertebral disc degeneration scores (DDS) were assessed by histological staining at 8 weeks. Intracellular reactive oxygen species mainly comes from nicotinamide adenine dinucleotide phosphate oxidases (NOXs), while its clearance relies on antioxidant enzymes which regulated by forkhead transcription factor O (FOXOs). Thus, the oxidative stress was evaluated by the expression of NOXs and FOXOs. Meanwhile, the protein expression of Aggrecan, matrix metalloproteinase-13 (MMP-13), NOXs, FOXOs and antioxidant proteins (Manganese superoxide dismutase: MnSOD and Catalase) were tested in nucleus pulposus cells (NPCs) under tert-butyl hydroperoxide (TBHP) intervention. CMS induced IDD by enhancing DDS in 8 weeks, and the expression of NOX2 and NOX4 were significantly increased and the expression of FOXO3 and FOXO4 were remarkably decreased in the CMS rats. With the stimulation of TBHP, the contents of NOX2 and NOX4 in NPCs increased significantly, and the antioxidant proteins of FOXO1, FOXO3, FOXO4, MnSOD and Catalase and the matrix proteins of Aggrecan decreased remarkably, while MMP-13 significantly increased after TBHP intervention. The present study proposed that regulation of NOXs and FOXOs alters oxidative stress in intervertebral disc, which indicates that the intervention of oxidative stress would provide a new strategy to the treatment of IDD.