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Hypothermia Improves Oral and Gastric Mucosal Microvascular Oxygenation during Hemorrhagic Shock in Dogs
Hypothermia is known to improve tissue function in different organs during physiological and pathological conditions. The aim of this study was to evaluate the effects of hypothermia on oral and gastric mucosal microvascular oxygenation (μHbO(2)) and perfusion (μflow) under physiological and hemorrh...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845851/ https://www.ncbi.nlm.nih.gov/pubmed/24327826 http://dx.doi.org/10.1155/2013/589606 |
Sumario: | Hypothermia is known to improve tissue function in different organs during physiological and pathological conditions. The aim of this study was to evaluate the effects of hypothermia on oral and gastric mucosal microvascular oxygenation (μHbO(2)) and perfusion (μflow) under physiological and hemorrhagic conditions. Five dogs were repeatedly anesthetized. All animals underwent each experimental protocol (randomized cross-over design): hypothermia (34°C), hypothermia during hemorrhage, normothermia, and normothermia during hemorrhage. Microcirculatory and hemodynamic variables were recorded. Systemic (DO(2)) and oral mucosal (μDO(2)) oxygen delivery were calculated. Hypothermia increased oral μHbO(2) with no effect on gastric μHbO(2). Hemorrhage reduced oral and gastric μHbO(2) during normothermia (−36 ± 4% and −27 ± 7%); however, this effect was attenuated during additional hypothermia (−15 ± 5% and −11 ± 5%). The improved μHbO(2) might be based on an attenuated reduction in μflow during hemorrhage and additional hypothermia (−51 ± 21 aU) compared to hemorrhage and normothermia (−106 ± 19 aU). μDO(2) was accordingly attenuated under hypothermia during hemorrhage whereas DO(2) did not change. Thus, in this study hypothermia alone improves oral μHbO(2) and attenuates the effects of hemorrhage on oral and gastric μHbO(2). This effect seems to be mediated by an increased μDO(2) on the basis of increased μflow. |
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