Source:http://linkedlifedata.com/resource/pubmed/id/17308846
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2007-3-27
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pubmed:abstractText |
A full-thickness burn wound model was used to evaluate the effects of a topically applied gel-based nitric oxide donor on wound healing in rats. The histological study demonstrated that the nitric oxide (NO) application significantly promoted re-epithelization that resulted in a fast recovery of burn wound. The histological sections further revealed that inflammatory cell infiltration in the NO-treated group was significantly increased in comparison to the control group. The enhanced accumulation of inflammatory cells resulted in a higher expression of myeloperoxidase (MPO) that was detected with imunoblotting. An immunohistochemistry study with CD31, a specific marker for endothelial cells, indicated that NO treatment markedly stimulated angiogenesis. Evaluation of collagen synthesis by immunohistochemistry with procollagen antibody demonstrated a significantly increased collagen synthesis in NO-treated wound bed. We concluded that NO treatment promoted re-epithelialization and wound closure by means of enhanced inflammatory cell infiltration, and that it promoted angiogenesis and facilitated collagen synthesis in the wound bed.
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pubmed:grant | |
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 |
Apr
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pubmed:issn |
0364-2313
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
624-31
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pubmed:dateRevised |
2007-12-3
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pubmed:meshHeading |
pubmed-meshheading:17308846-Administration, Topical,
pubmed-meshheading:17308846-Animals,
pubmed-meshheading:17308846-Blotting, Western,
pubmed-meshheading:17308846-Burns,
pubmed-meshheading:17308846-Disease Models, Animal,
pubmed-meshheading:17308846-Gels,
pubmed-meshheading:17308846-Immunoenzyme Techniques,
pubmed-meshheading:17308846-Male,
pubmed-meshheading:17308846-Neovascularization, Physiologic,
pubmed-meshheading:17308846-Nitric Oxide,
pubmed-meshheading:17308846-Peroxidase,
pubmed-meshheading:17308846-Rats,
pubmed-meshheading:17308846-Rats, Sprague-Dawley,
pubmed-meshheading:17308846-Sodium Nitrite,
pubmed-meshheading:17308846-Wound Healing
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pubmed:year |
2007
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pubmed:articleTitle |
Nitric oxide accelerates the recovery from burn wounds.
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pubmed:affiliation |
Department of Integrative Biology and Pharmacology, Institute of Molecular Medicine, The University of Texas-Health Science Center at Houston, 6431 Fannin St, Houston, Texas 77030, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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