Title of article :
Effect of chondroitinase ABC on inflammatory and oxidative response following spinal cord injury
Author/Authors :
Akbari, Mahboobe Department of Clinical Biochemistry - School of Medicine - Kerman University of Medical Sciences , Khaksari, Mohammad Endocrinology and Metabolism Research Center - Institute of Basic and Clinical Physiology Sciences - Kerman University of Medical Sciences , Rezaeezadeh-Roukerd, Maryam Faculty of Veterinary Medicine - Shahid Bahonar University, Kerman , Mirzaee, Moghaddameh Department of Biostatistics and Epidemiology - School of Public Health - Kerman University of Medical Sciences , Nazari-Robati, Mahdieh Neuroscience Research Center - Neuropharmacology Institute - Kerman University of Medical Sciences - Department of Clinical Biochemistry - School of Medicine - Kerman University of Medical Sciences
Abstract :
Objective(s): Chondroitinase ABC (cABC) treatment improves functional recovery following spinal cord injury (SCI) through degrading inhibitory molecules to axon growth. However, cABC involvement in other pathological processes contributing to SCI remains to be investigated. Here, we studied the effect of cABC I on oxidative stress and inflammation developed in a rat model of SCI. Materials and Methods: Male rats (220–250 g) were divided into three groups (n=28) including rats that underwent SCI (SCI group), rats subjected to SCI and received an intrathecal injection of phosphate buffer saline (SCI+PBS group), and rats that underwent SCI and received cABC intrathecally (SCI+E group). Then, the level of TNF-α, Il-1β, malondialdehyde, nitric oxide, and myeloperoxidase in injured tissues, as well as hindlimb motor function, were measured at 4 hr, 1, 3 and 7 days post-SCI. Results: Our data showed that cABC treatment reduced the development of inflammation and oxidative stress associated with SCI at all-time points. In addition, functional recovery was improved in rats that received cABC at 7 days post-SCI. Conclusion: The present findings indicate that cABC treatment can exert its neuroprotective effect through modulation of post-traumatic inflammatory and oxidative response.
Keywords :
Chondroitinase ABC , Functional recovery , Inflammation , Oxidative stress , Spinal cord injury
Journal title :
Astroparticle Physics