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Methothrexate attenuates early neutrophil infiltration and the associated lipid peroxidation in the injured spinal cord but does not induce neurotoxicity in the uninjured spinal cord in rats

Backround The goal of most acute therapies for spinal cord injury (SCI) in humans include attenuation of the early inflammatory response and may limit the extent of tissue injury and the consequent disability. Objective The purpose of this study was to investigate the early effects of methothrexate...

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Bibliographic Details
Published in:Acta neurochirurgica 2012-06, Vol.154 (6), p.1045-1054
Main Authors: Şanlı, Ahmet Metin, Serbes, Gökhan, Sargon, Mustafa F., Çalışkan, Murat, Kılınç, Kamer, Bulut, Hüsamettin, Şekerci, Zeki
Format: Article
Language:English
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Summary:Backround The goal of most acute therapies for spinal cord injury (SCI) in humans include attenuation of the early inflammatory response and may limit the extent of tissue injury and the consequent disability. Objective The purpose of this study was to investigate the early effects of methothrexate (MTX) treatment on myeloperoxidase (MPO) activity, malondialdehyde (MDA) level, and ultrastructural findings in the injured and uninjured spinal cords of rats. The effects of MTX treatment were also compared with methylprednisolone sodium succinate (MPSS) treatment. Methods Winstar rats were divided into seven groups: control; trauma alone (50 g/cm weight drop trauma); SCI + MPSS (30 mg/kg); SCI + low-dose (0.5 mg/kg) MTX (LDMTX); SCI + higher-dose (1 mg/kg) MTX (HDMTX); non-trauma + LDMTX; non-trauma + HDMTX. Results Administration of MTX and MPSS treatments significantly decreased MPO activity ( p  
ISSN:0001-6268
0942-0940
DOI:10.1007/s00701-012-1302-8