MedStar Authors catalog › Details for: Examination of local and systemic in vivo responses to electrical injury using an electrical burn delivery system.
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Examination of local and systemic in vivo responses to electrical injury using an electrical burn delivery system.

by Shupp, Jeffrey W; Moffatt, Lauren T; Leto, Ellen J; Jo, Daniel Y; Randad, Pranay R; Jeng, James C; Jordan, Marion H.
Citation: Journal of Burn Care & Research. 33(1):118-29, 2012 Jan-Feb..Journal: Journal of burn care & research : official publication of the American Burn Association.ISSN: 1559-047X.Full author list: Shupp JW; Moffatt LT; Nguyen T; Ramella-Roman JC; Hammamieh R; Miller SA; Leto EJ; Jo DY; Randad PR; Jett M; Jeng JC; Jordan MH.UI/PMID: 22079918.Subject(s): Animals | Biological Markers/me [Metabolism] | Blood Chemical Analysis | *Burns, Electric/ge [Genetics] | *Burns, Electric/me [Metabolism] | Burns, Electric/pa [Pathology] | Cytokines/an [Analysis] | *Cytokines/me [Metabolism] | Disease Models, Animal | Down-Regulation | Gene Expression Regulation | Immunohistochemistry | Injury Severity Score | Laser-Doppler Flowmetry | Male | Physical Examination | Polymerase Chain Reaction/mt [Methods] | *RNA, Messenger/an [Analysis] | Random Allocation | Rats | Rats, Sprague-Dawley | Risk Factors | Wound Healing/ph [Physiology]Institution(s): MedStar Washington Hospital CenterDepartment(s): Surgery/Burn ServicesActivity type: Journal Article.Medline article type(s): Comparative Study | Journal Article | Research Support, Non-U.S. Gov'tOnline resources: Click here to access online Digital Object Identifier: http://dx.doi.org/10.1097/BCR.0b013e3182373a50 (Click here) Abbreviated citation: J Burn Care Res. 33(1):118-29, 2012 Jan-Feb.Local Holdings: Available online through MWHC library: 2006 - present, Available in print through MWHC library: 2006 - present.Abstract: Electrical injuries are devastating and are difficult to manage due to the complexity of the tissue damage and physiological impacts. A paucity of literature exists which describes models for electrical injury. To date, those models have been used primarily to demonstrate thermal and morphological effects at the points of contact. Creating a more representative model for human injury and further elucidating the physics and pathophysiology of this unique form of tissue injury could be helpful in designing stage-appropriate therapy and improving limb salvage. An electrical burn delivery system was developed to accurately and reliably deliver electrical current at varying exposure times. A series of Sprague-Dawley rats were anesthetized and subjected to injury with 1000 V of direct current at incremental exposure times (2-20 seconds). Whole blood and plasma were obtained immediately before shock, immediately postinjury, and then hourly for 3 hours. Laser Doppler images of tissue adjacent to the entrance and exit wounds were obtained at the outlined time points to provide information on tissue perfusion. The electrical exposure was nonlethal in all animals. The size and the depth of contact injury increased in proportion to the exposure times and were reproducible. Skin adjacent to injury (both entrance and exit sites) exhibited marked edema within 30 minutes. In adjacent skin of upper extremity wounds, mean perfusion units increased immediately postinjury and then gradually decreased in proportion to the severity of the injuries. In the lower extremity, this phenomenon was only observed for short contact times, while longer contact times had marked malperfusion throughout. In the plasma, interleukin-10 and vascular endothelial growth factor levels were found to be augmented by injury. Systemic transcriptome analysis revealed promising information about signal networks involved in dermatological, connective tissue, and neurological pathophysiological processes. A reliable and reproducible in vivo model has been developed for characterizing the pathophysiology of high-tension electrical injury. 130912s in perfusion were observed near and between entrance and exit wounds that appear consistent with injury severity. Further studies are underway to correlate differential mRNA expression with injury severity.

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