Thermostabilized chondroitinase ABC Promotes Neuroprotection after Contusion Spinal Cord Injury
سال انتشار: 1399
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 117
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شناسه ملی سند علمی:
JR_JKMU-27-5_001
تاریخ نمایه سازی: 19 دی 1401
چکیده مقاله:
Background: Chondroitinase ABC (cABC), due to its loosening impact on the extracellular matrix scaffold, has been used to enhance regeneration of injured axonal tracts after spinal cord injury (SCI). However, cABC thermal instability at physiological temperature has limited its clinical application. The disaccharide trehalose has been shown to increase the stability of cABC in body temperature. Therefore, the present study was conducted to assess the effect of combined trehalose and cABC on inflammation, lipid peroxidation and histopathological changes following SCI. Methods: Male Wistar rats were randomized into six groups (n=۱۲) including sham, SCI, vehicle, trehalose, cABC and trehalose + cABC. In sham group, only laminectomy was performed. Other groups underwent laminectomy followed by contusion spinal cord injury. Twenty four hours after treatment, the level of IL-۱β, Myeloperoxidase (MPO) and Malondialdehyde (MDA) were measured. Histopathological changes were also scored. Results: Spinal cord injury in rats resulted in severe trauma characterized by increase in inflammation, oxidative stress, neutrophils infiltration, hemorrhage, necrosis and edema. The levels of IL-۱β, MDA and MPO were ۲۶۰.۳±۱۶.۴ nmol/mg protein, ۱.۲±۰.۰۶ mU/mg protein and ۱۸.۹±۰.۷ pg/mg protein, respectively in the vehicle group. However, combined treatment with cABC and trehalose reduced the amount of these factors significantly to ۱۴۲.۴±۱۷ nmol/mg protein, ۰.۵۷±۰.۰۳ mU/mg protein and ۱۳.۸±۰.۴ pg/mg protein, respectively (p <۰.۰۵). In addition, treatment with cABC and trehalose improved histopathological alterations. Conclusions: The present data suggest that coadministration of trehalose and cABC exhibits neuroprotection effect through reducing inflammation and tissue injury events associated with SCI.
کلیدواژه ها:
نویسندگان
Mahboobe Akbari
Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran
Shahriar Dabiri
Professor, Stem Cells Research Center, Kerman University of Medical Sciences, Kerman, Iran
Mohammad Mehdi Moeini-Aghtaei
Assistant Professor, Stem Cells Research Center, Kerman University of Medical Sciences, Kerman, Iran
Mahdieh Nazari-Robati
Assistant Professor, Department of Clinical Biochemistry, Faculty of Medicine, Kerman University of Medical Sciences, Kerman, Iran
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