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In vivo studies of cellular energy state, pH, and sodium in rat liver after thermal injury.

Identifieur interne : 000C22 ( Ncbi/Curation ); précédent : 000C21; suivant : 000C23

In vivo studies of cellular energy state, pH, and sodium in rat liver after thermal injury.

Auteurs : Z F Xia [États-Unis] ; J W Horton ; P Y Zhao ; N. Bansal ; E E Babcock ; A D Sherry ; C R Malloy

Source :

RBID : pubmed:8045826

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English descriptors

Abstract

In vivo 31P- and 23Na-magnetic resonance spectroscopy was used to measure phosphorus metabolites, intracellular pH, cytosolic free Mg2+, and intracellular Na+ in the liver of rats 24 h after 40% total body surface area full-thickness burn injury. Studies were performed during infusion of thulium (III) 1,4,7,10-tetraazacyclododecane N,N',N",N"'-tetra(methylenephosphonate), which served as the Na+ shift agent. Compared with the sham-burn group, there was a significant increase in hepatic intracellular Na+ along with a decrease in intracellular pH and free Mg2+. The ratio of intra- to extra-cellular Na+ increased, indicating a decreased Na+ gradient that may determine the hepatic transmembrane potential difference. Hepatic beta-ATP/P(i) also significantly decreased, which suggests that either ATP utilization is significantly accelerated or ATP synthesis is inhibited after the thermal injury. Of the cations measured (Na+, Mg2+, H+), the change in intracellular Na+ was most dramatic. This study demonstrates that major burn injury may cause profound changes in hepatic bioenergetics and ionic metabolism 24 h after injury and that intracellular Na+ may be a sensitive indicator of hepatic dysfunction 24 h after injury. Because these animals tolerated the shift reagent, thulium (III) 1,4,7,10-tetraazacyclododecane N,N',N",N"'-tetra(methylenephosphonate), nuclear magnetic resonance spectroscopy may prove valuable in monitoring intracellular cations in the liver after major injury.

PubMed: 8045826

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pubmed:8045826

Le document en format XML

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<name sortKey="Xia, Z F" sort="Xia, Z F" uniqKey="Xia Z" first="Z F" last="Xia">Z F Xia</name>
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<nlm:affiliation>Department of Surgery, Mary Nell and Ralph B. Rogers Magnetic Resonance Center, Dallas, Texas.</nlm:affiliation>
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<name sortKey="Zhao, P Y" sort="Zhao, P Y" uniqKey="Zhao P" first="P Y" last="Zhao">P Y Zhao</name>
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<name sortKey="Bansal, N" sort="Bansal, N" uniqKey="Bansal N" first="N" last="Bansal">N. Bansal</name>
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<name sortKey="Babcock, E E" sort="Babcock, E E" uniqKey="Babcock E" first="E E" last="Babcock">E E Babcock</name>
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<title level="j">Journal of applied physiology (Bethesda, Md. : 1985)</title>
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<term>Animals</term>
<term>Blood Pressure (drug effects)</term>
<term>Body Water (metabolism)</term>
<term>Burns (metabolism)</term>
<term>Burns (pathology)</term>
<term>Energy Metabolism (physiology)</term>
<term>Hydrogen-Ion Concentration</term>
<term>Liver (injuries)</term>
<term>Liver (metabolism)</term>
<term>Liver (pathology)</term>
<term>Magnesium (metabolism)</term>
<term>Magnetic Resonance Spectroscopy</term>
<term>Male</term>
<term>Membrane Potentials (physiology)</term>
<term>Organometallic Compounds</term>
<term>Organophosphorus Compounds</term>
<term>Phosphorus Isotopes</term>
<term>Rats</term>
<term>Rats, Sprague-Dawley</term>
<term>Sodium (blood)</term>
<term>Sodium (metabolism)</term>
<term>Sodium Isotopes</term>
<term>Thulium</term>
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<term>Animaux</term>
<term>Brûlures (anatomopathologie)</term>
<term>Brûlures (métabolisme)</term>
<term>Composés organiques du phosphore</term>
<term>Composés organométalliques</term>
<term>Concentration en ions d'hydrogène</term>
<term>Eau corporelle (métabolisme)</term>
<term>Foie (anatomopathologie)</term>
<term>Foie (métabolisme)</term>
<term>Foie (traumatismes)</term>
<term>Isotopes du phosphore</term>
<term>Isotopes du sodium</term>
<term>Magnésium (métabolisme)</term>
<term>Mâle</term>
<term>Métabolisme énergétique (physiologie)</term>
<term>Potentiels de membrane (physiologie)</term>
<term>Pression sanguine ()</term>
<term>Rat Sprague-Dawley</term>
<term>Rats</term>
<term>Sodium (métabolisme)</term>
<term>Sodium (sang)</term>
<term>Spectroscopie par résonance magnétique</term>
<term>Thulium</term>
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<term>Sodium</term>
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<term>Magnesium</term>
<term>Sodium</term>
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<term>Brûlures</term>
<term>Foie</term>
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<term>Blood Pressure</term>
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<term>Liver</term>
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<term>Body Water</term>
<term>Burns</term>
<term>Liver</term>
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<term>Eau corporelle</term>
<term>Foie</term>
<term>Magnésium</term>
<term>Sodium</term>
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<term>Burns</term>
<term>Liver</term>
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<term>Métabolisme énergétique</term>
<term>Potentiels de membrane</term>
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<term>Energy Metabolism</term>
<term>Membrane Potentials</term>
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<term>Sodium</term>
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<term>Hydrogen-Ion Concentration</term>
<term>Magnetic Resonance Spectroscopy</term>
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<term>Phosphorus Isotopes</term>
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<term>Rats, Sprague-Dawley</term>
<term>Sodium Isotopes</term>
<term>Thulium</term>
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<term>Composés organiques du phosphore</term>
<term>Composés organométalliques</term>
<term>Concentration en ions d'hydrogène</term>
<term>Isotopes du phosphore</term>
<term>Isotopes du sodium</term>
<term>Mâle</term>
<term>Pression sanguine</term>
<term>Rat Sprague-Dawley</term>
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<term>Spectroscopie par résonance magnétique</term>
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<front>
<div type="abstract" xml:lang="en">In vivo 31P- and 23Na-magnetic resonance spectroscopy was used to measure phosphorus metabolites, intracellular pH, cytosolic free Mg2+, and intracellular Na+ in the liver of rats 24 h after 40% total body surface area full-thickness burn injury. Studies were performed during infusion of thulium (III) 1,4,7,10-tetraazacyclododecane N,N',N",N"'-tetra(methylenephosphonate), which served as the Na+ shift agent. Compared with the sham-burn group, there was a significant increase in hepatic intracellular Na+ along with a decrease in intracellular pH and free Mg2+. The ratio of intra- to extra-cellular Na+ increased, indicating a decreased Na+ gradient that may determine the hepatic transmembrane potential difference. Hepatic beta-ATP/P(i) also significantly decreased, which suggests that either ATP utilization is significantly accelerated or ATP synthesis is inhibited after the thermal injury. Of the cations measured (Na+, Mg2+, H+), the change in intracellular Na+ was most dramatic. This study demonstrates that major burn injury may cause profound changes in hepatic bioenergetics and ionic metabolism 24 h after injury and that intracellular Na+ may be a sensitive indicator of hepatic dysfunction 24 h after injury. Because these animals tolerated the shift reagent, thulium (III) 1,4,7,10-tetraazacyclododecane N,N',N",N"'-tetra(methylenephosphonate), nuclear magnetic resonance spectroscopy may prove valuable in monitoring intracellular cations in the liver after major injury.</div>
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