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pubmed-article:1903482pubmed:abstractTextThe effects of different ventilation methods on cardiac output measured by the indicator-dilution method, liver blood flow measured by a deuterium washout technique using 2H nuclear magnetic resonance (NMR) and liver concentrations of ATP and intracellular pH determined with 31P NMR were compared in anesthetized rats. No differences in mean arterial blood pressure were demonstrable with the different modes of ventilation. However, significant drops in cardiac output were observed between freely breathing and animals ventilated with positive pressure but not the high frequency oscillatory method (407 +/- 46 and 520 +/- 88 vs. 633 +/- 86 ml/min/kg, p less than 0.05 and p = NS, respectively). Moreover, liver blood flow was significantly reduced during positive pressure but not high frequency oscillatory ventilation compared with free breathing rats (32 +/- 4 and 43 +/- 10 vs. 46 +/- 8 ml/100 g, p less than 0.05 and p = NS, respectively). 31P NMR spectroscopy revealed no effects of either ventilation method on tissue ATP or intracellular pH as estimated by the chemical shift of inorganic phosphate. These data suggest that controlled ventilation in normal rats accomplished with standard positive pressure methods is associated with major decreases in cardiac output and liver blood flow despite maintenance of normal blood pressure. High frequency oscillatory ventilation appears to effect less compromise of cardiac output and hepatic perfusion than positive pressure ventilation and may, therefore, be preferable for some biological studies.lld:pubmed
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pubmed-article:1903482pubmed:authorpubmed-author:ShapiroJ IJIlld:pubmed
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pubmed-article:1903482pubmed:pagination229-34lld:pubmed
pubmed-article:1903482pubmed:dateRevised2007-11-15lld:pubmed
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pubmed-article:1903482pubmed:year1991lld:pubmed
pubmed-article:1903482pubmed:articleTitleControlled ventilation during NMR spectroscopic studies: hemodynamic and biochemical consequences.lld:pubmed
pubmed-article:1903482pubmed:affiliationGiles F. Filley Laboratory, Webb Waring Lung Institute, University of Colorado School of Medicine, Denver 80262.lld:pubmed
pubmed-article:1903482pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1903482pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed