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Nuclear factor‐κB decoy amelioration of spinal cord injury‐induced inflammation and behavior outcomes
Author(s) -
Rafati Danny Salah,
Geissler Katja,
Johnson Kathia,
Unabia Geda,
Hulsebosch Claire,
NesicTaylor Olivera,
PerezPolo J. Regino
Publication year - 2007
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.21508
Subject(s) - relb , decoy , hmgb1 , p50 , spinal cord injury , hyperalgesia , inflammation , chemistry , spinal cord , neuroprotection , nitric oxide synthase , protein subunit , gabaergic , pharmacology , nitric oxide , nociception , transcription factor , medicine , neuroscience , biology , biochemistry , receptor , gene
Spinal cord injury (SCI) results in a pathophysiology characterized by multiple locomotor and sensory deficits, resulting in altered nociception and hyperalgesia. SCI triggers an early and prolonged inflammatory response, with increased interleukin‐1β levels. Transient changes are observed in subunit populations of the transcription factor nuclear factor‐κB (NF‐κB). There were decreases in neuronal c‐Rel levels and inverse increases in p65 and p50 levels. There were no changes in neuronal p52 or RelB subunits after SCI at any time point tested. Similarly, SCI had no effect on oligodendroglial levels of any NF‐κB subunit. There were significant early increases in COX‐2 and inducible nitric oxide synthase mRNA and protein levels after SCI. We used synthetic double‐stranded “decoy” deoxyoligonucleotides containing selective NF‐κB protein dimer binding consensus sequences. Decoys targeting the p65/p50 binding site on the COX‐2 promoter decreased SCI‐induced cell losses, NF‐κB p65/p50 DNA‐binding activity, and COX‐2 and iNOS protein levels. NF‐κB p65/p50 targeted decoys improved early locomotor recovery after moderate but not severe SCI, yet ameliorated SCI‐induced hypersensitization after both moderate and severe SCI. To determine whether changes in GABA activity played a role in decreased hypersensitivity after SCI and p65/p50 targeted decoy, we counted γ‐aminobutyric acid (GABA)‐containing neurons in laminae 1–3. There were significantly more GABAergic neurons in the p65/p50 targeted decoy‐treated group at the level of injury. © 2007 Wiley‐Liss, Inc.