N-acetylcysteine treatment following spinal cord trauma reduces neural tissue damage and improves locomotor function in mice
Author(s) -
Jian Guo,
Yiqiao Li,
Zhong Chen,
Zhennian He,
Bin Zhang,
Yonghuan Li,
Jianghua Hu,
Mingyuan Han,
Yuanlin Xu,
Yongfu Li
Publication year - 2015
Publication title -
molecular medicine reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.727
H-Index - 56
eISSN - 1791-3004
pISSN - 1791-2997
DOI - 10.3892/mmr.2015.3390
Subject(s) - oxidative stress , spinal cord , spinal cord injury , acetylcysteine , medicine , mitochondrion , bioenergetics , traumatic brain injury , apoptosis , neuroinflammation , traumatic injury , neuroscience , biology , inflammation , anesthesia , immunology , surgery , microbiology and biotechnology , antioxidant , biochemistry , psychiatry
Following spinal cord trauma, mitochondrial dysfunction associated with increased oxidative stress is a critical event leading to leukocyte inflammatory responses, neuronal cell death and demyelination, contributing to permanent locomotor and neurological disability. The present study demonstrated that the mitochondrial enhancer N-acetylcysteine (NAC) may restore redox balance via enhancement of mitochondrial respiratory activity following traumatic spinal cord injury (SCI). In addition, NAC ameliorates oxidative stress-induced neuronal loss, demyelination, leukocyte infiltration and inflammatory mediator expression and improves long-term locomotor function. Furthermore, neuronal survival and neurological recovery are significantly correlated with increased mitochondrial bioenergetics in SCI following treatment with NAC. Therefore, NAC may represent a potential therapeutic agent for preserving mitochondrial dynamics and integrity following traumatic SCI.
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