rdf:type |
|
lifeskim:mentions |
umls-concept:C0016658,
umls-concept:C0021753,
umls-concept:C0026336,
umls-concept:C0034693,
umls-concept:C0034721,
umls-concept:C0035820,
umls-concept:C0037083,
umls-concept:C0040184,
umls-concept:C0221912,
umls-concept:C0458219,
umls-concept:C1710082,
umls-concept:C2349975
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pubmed:issue |
3
|
pubmed:dateCreated |
2009-7-7
|
pubmed:abstractText |
Tibia fracture in rats initiates a syndrome resembling the complex regional pain syndrome type I. Accumulating evidence indicates that IL-1beta is involved in the modulation of nociceptive information and it acts as an intermediate inflammatory mediator via up-regulation of NGF. We hypothesized that IL-1beta signaling might mediate the development of the CRPS-like changes after tibial fracture, either directly or by stimulating NGF expression. Rats underwent distal tibia fracture and casting for 4 weeks and were chronically treated with an IL-1 receptor antagonist (IL-1ra). Nociceptive testing and assessment of edema and hindpaw warmth were performed at baseline and after cast removal. Bone microarchitecture was evaluated by micro-computed tomography. Confocal immunofluorescence and in situ hybridization techniques were used to evaluate changes in the cutaneous expression of IL-1beta at 4 weeks post-fracture. The nociceptive and vascular effects of intraplantar IL-1beta injections were evaluated in intact rats at different time points after injection. We found that: (1) IL-1ra reduced fracture-induced nociceptive sensitization, but did not decrease hindpaw edema or warmth, (2) fracture chronically up-regulated IL-1beta mRNA and protein expression in hindpaw skin keratinocytes, (3) IL-1beta intraplantar injection induced mechanical allodynia in a dose-dependent manner and stimulated keratinocyte NGF expression in the hindpaw skin, and (4) intraplantar injection of NGF-induced nociceptive sensitization. Collectively, these results indicate that cutaneous IL-1beta signaling can contribute to chronic regional nociceptive sensitization after fracture, possibly by stimulating NGF over-expression in keratinocytes. Our data also highlight the importance of the keratinocyte as the primary source of post-traumatic IL-1beta over-expression.
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pubmed:grant |
|
pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/19473768-10454137,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19473768-10770524,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19473768-10903985,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/19473768-9179382
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
|
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1872-6623
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pubmed:author |
|
pubmed:issnType |
Electronic
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pubmed:volume |
144
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
303-13
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pubmed:dateRevised |
2011-3-29
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pubmed:meshHeading |
pubmed-meshheading:19473768-Animals,
pubmed-meshheading:19473768-Skin,
pubmed-meshheading:19473768-Inflammation,
pubmed-meshheading:19473768-Edema,
pubmed-meshheading:19473768-Rats,
pubmed-meshheading:19473768-Sensory Receptor Cells,
pubmed-meshheading:19473768-Foot,
pubmed-meshheading:19473768-Pain Measurement,
pubmed-meshheading:19473768-Reflex Sympathetic Dystrophy,
pubmed-meshheading:19473768-Male,
pubmed-meshheading:19473768-Hyperemia,
pubmed-meshheading:19473768-Disease Models, Animal,
pubmed-meshheading:19473768-RNA, Messenger,
pubmed-meshheading:19473768-Tibial Fractures,
pubmed-meshheading:19473768-Rats, Sprague-Dawley
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