e-Article
The effects of prophylactic zinc and melatonin application on experimental spinal cord ischemia–reperfusion injury in rabbits: experimental study.
Document Type
Article
Author
Source
Subject
*MEDICAL research
*ZINC
*MELATONIN
*SPINAL cord abnormalities
*ISCHEMIA
*RABBITS
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Language
ISSN
1362-4393
Abstract
Study design:Experimental study.Objectives: To determine the neuroprotective effects of zinc and melatonin on spinal cord ischemia–reperfusion (I/R) injuries of rabbits.Setting: The Experimental Research Centre of Selçuk University, Konya, Turkey.Methods:Twenty-four male rabbits underwent spinal cord ischemia by clamping the thoraco-abdominal aorta for 20 min. Twenty minutes before the aortic clamping, animals received zinc, melatonin or a combination of both. Neurological examination of the animals was performed three times during reperfusion period. The animals were killed 24 h after reperfusion. Spinal cord samples were taken for biochemical and histopathological evaluation.Results:Pre-treated animals with zinc, melatonin or combination displayed better neurological outcomes than the I/R group (P<0.05). Zinc, melatonin and combined treatment prevented spinal cord injury by reducing apoptosis rate (P<0.05) and preserving intact ganglion cell numbers (P<0.05). Zinc pre-treatment protected spinal cord by preventing malondialdehyde (MDA) formation (P=0.002), increasing glutathione peroxidase (GPx) activity (P=0.002) and decreasing xanthine oxidase enzyme activity (P=0.026) at molecular level. Melatonin treatment also resulted with MDA formation (P=0.002), increased GPx activity (P=0.002) and decreased xanthine oxidase activity (P=0.026).Conclusion:The results of the study showed that prophylactic zinc and melatonin use in spinal cord I/R not only suppressed lipid peroxidation by activating antioxidant systems but also had significant neuroprotective effects by specifically improving the neurological and histopathological situation.Spinal Cord (2007) 45, 722–730; doi:10.1038/sj.sc.3102035; published online 13 February 2007 [ABSTRACT FROM AUTHOR]