pubmed-article:18255189 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18255189 | lifeskim:mentions | umls-concept:C0043250 | lld:lifeskim |
pubmed-article:18255189 | lifeskim:mentions | umls-concept:C0026336 | lld:lifeskim |
pubmed-article:18255189 | lifeskim:mentions | umls-concept:C0043240 | lld:lifeskim |
pubmed-article:18255189 | lifeskim:mentions | umls-concept:C0441655 | lld:lifeskim |
pubmed-article:18255189 | lifeskim:mentions | umls-concept:C0000894 | lld:lifeskim |
pubmed-article:18255189 | lifeskim:mentions | umls-concept:C1704419 | lld:lifeskim |
pubmed-article:18255189 | lifeskim:mentions | umls-concept:C0536060 | lld:lifeskim |
pubmed-article:18255189 | lifeskim:mentions | umls-concept:C0591833 | lld:lifeskim |
pubmed-article:18255189 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:18255189 | pubmed:dateCreated | 2008-3-11 | lld:pubmed |
pubmed-article:18255189 | pubmed:abstractText | We investigated the effect of topical temporin A in the management of methicillin-resistant strain of Staphylococcus aureus (MRSA)-infected experimental surgical wounds in mice. The wound, cut through the panniculus carnosus of BALB/c mice, was inoculated with 5x10(7) colony-forming units of MRSA. Mice were treated with Allevyn, temporin A-soaked Allevyn, Allevyn and daily intraperitoneal teicoplanin (7mg/kg), temporin A-soaked Allevyn and daily intraperitoneal teicoplanin. Main outcome measurements were: quantitative bacterial culture, histological examination with assessment of micro-vessel density and of vascular endothelial growth factor (VEGF) expression in tissue sections, and VEGF plasma levels alike. Treatment with temporin-A associated with teicoplanin injection significantly reduced bacterial load to 0.85 x 10(1)+/-0.1 x 10(1)CFU/ml. Histological examination showed that infected mice receiving temporin A-soaked Allevyn (with or without teicoplanin) had a higher degree of granulation tissue formation and collagen deposition compared to the other treated groups. A significant increase in serum VEGF expression was observed in mice receiving temporin A topically and temporin A topically associated with intraperitoneal teicoplanin. In conclusion our results demonstrated that temporin A is effective in the management of infected wounds, by a significant bacterial growth inhibition and acceleration of wound repair process. | lld:pubmed |
pubmed-article:18255189 | pubmed:language | eng | lld:pubmed |
pubmed-article:18255189 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18255189 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18255189 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18255189 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18255189 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18255189 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18255189 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18255189 | pubmed:month | Apr | lld:pubmed |
pubmed-article:18255189 | pubmed:issn | 0196-9781 | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:CirioniOscarO | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:GiacomettiAnd... | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:GhiselliRober... | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:OrlandoFioren... | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:SabaVittorioV | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:ScaliseGiorgi... | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:KamyszWojciec... | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:GoteriGaiaG | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:OffidaniAnnam... | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:SimonettiOria... | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:ScaliseAlessa... | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:SilvestriCarm... | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:KamyszElzbiet... | lld:pubmed |
pubmed-article:18255189 | pubmed:author | pubmed-author:BaruccaClaudi... | lld:pubmed |
pubmed-article:18255189 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18255189 | pubmed:volume | 29 | lld:pubmed |
pubmed-article:18255189 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18255189 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18255189 | pubmed:pagination | 520-8 | lld:pubmed |
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pubmed-article:18255189 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18255189 | pubmed:articleTitle | Temporin A is effective in MRSA-infected wounds through bactericidal activity and acceleration of wound repair in a murine model. | lld:pubmed |
pubmed-article:18255189 | pubmed:affiliation | Dermatological Clinic, Università Politecnica delle Marche, Ancona, Italy. o.simonetti@univpm.it | lld:pubmed |
pubmed-article:18255189 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18255189 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18255189 | lld:pubmed |