Hypothermia improves oral and gastric mucosal microvascular oxygenation during hemorrhagic shock in dogs

Oxid Med Cell Longev. 2013:2013:589606. doi: 10.1155/2013/589606. Epub 2013 Nov 12.

Abstract

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 (μHbO2) 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 (DO2) and oral mucosal (μDO2) oxygen delivery were calculated. Hypothermia increased oral μ HbO2 with no effect on gastric μHbO2. Hemorrhage reduced oral and gastric μHbO2 during normothermia (-36 ± 4% and -27 ± 7%); however, this effect was attenuated during additional hypothermia (-15 ± 5% and -11 ± 5%). The improved μ HbO2 might be based on an attenuated reduction in μ flow during hemorrhage and additional hypothermia (-51 ± 21 aU) compared to hemorrhage and normothermia (-106 ± 19 aU). μDO2 was accordingly attenuated under hypothermia during hemorrhage whereas DO2 did not change. Thus, in this study hypothermia alone improves oral μHbO2 and attenuates the effects of hemorrhage on oral and gastric μ HbO2. This effect seems to be mediated by an increased μDO2 on the basis of increased μ flow.

MeSH terms

  • Animals
  • Dogs
  • Female
  • Gastric Mucosa / blood supply*
  • Gastric Mucosa / drug effects
  • Gastric Mucosa / physiopathology
  • Hemodynamics / drug effects
  • Hypothermia, Induced*
  • Microvessels / drug effects
  • Microvessels / physiopathology*
  • Mouth Mucosa / blood supply*
  • Mouth Mucosa / drug effects
  • Mouth Mucosa / physiopathology
  • Oxygen / pharmacology*
  • Respiration / drug effects
  • Shock, Hemorrhagic / metabolism
  • Shock, Hemorrhagic / physiopathology*
  • Shock, Hemorrhagic / therapy*

Substances

  • Oxygen