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• W95726103 abstract "The treatment of burns remains a challenge due to the associated high morbidity and mortality. Besides the administration of physiologic saline, local disinfection, and symptomatic medications, no causal therapy is known to reduce the tissue damage and accelerate wound healing. The aim of the study was to develop a reliable burn model that allows for reproducible quantitative in vivo analysis of the microcirculation, angiogenesis, and leukocyte endothelium interaction after burn injury.Experiments were carried out on male hairless mice (n = 9). Full-thickness burns were inflicted with a hot air jet without any contact to the tissue (117 +/- 2.1 degrees C for 1 second; burn area: 1.3 mm(2)). Intravital fluorescent microscopy, in combination with FITC-dextran as plasma marker, was used to assess microcirculatory standard parameters; leukocytes were stained with rhodamine 6G. Values were obtained before, immediately after, as well as at days 1, 3, 7, and 14 postburn.The nonperfused area decreased during the observed period and perfusion was almost completely due to angiogenesis at day 14. No posttraumatic expansion of the nonperfused area after 24 hours could be observed. Leukocyte endothelium interaction showed its maximum 24 hours postburn. The formation of edema occurred immediately postburn and decreased during the following observation time.The developed burn model allows a reproducible assessment with significant results of the microcirculation, angiogenesis, and leukocyte endothelium interaction without causing mechanical damage to the tissue; therefore, this model qualifies for the further investigations of interventional drugs to decrease the effects of burn injury." @default.
• W95726103 created "2016-06-24" @default.
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• W95726103 date "2009-01-01" @default.
• W95726103 modified "2023-09-23" @default.
• W95726103 title "Burn model for in vivo investigations of microcirculatory changes." @default.
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• W95726103 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2667331" @default.
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