Evaluation of triple quantum-filtered 23Na NMR spectroscopy in the in situ rat liver.
Identifieur interne : 002B23 ( Main/Merge ); précédent : 002B22; suivant : 002B24Evaluation of triple quantum-filtered 23Na NMR spectroscopy in the in situ rat liver.
Auteurs : V. Seshan [États-Unis] ; A D Sherry ; N. BansalSource :
- Magnetic resonance in medicine [ 0740-3194 ] ; 1997.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Sodium.
- chemical : Organometallic Compounds, Organophosphorus Compounds, Thulium.
- metabolism : Liver.
- methods : Magnetic Resonance Spectroscopy.
- Animals, Male, Rats, Rats, Sprague-Dawley.
Abstract
Triple quantum (TQ)-filtered 23Na NMR spectroscopy and the shift reagent, TmDOTP5-, have been used to evaluate the contributions of intra- (Na+i) and extracellular (Na+e) sodium to the TQ-filtered signal in the rat liver, in situ. Na+e contributed significantly to the total TQ-filtered signal in live animals, and the intensity of this signal did not change postmortem. The TQ-filtered Na+i signal increased by approximately 380% over a period of 1 h postmortem, whereas the single quantum (SQ) Na+i increased by 90%. The constancy of the TQ-filtered Na+i signal indicates that changes in total TQ-filtered 23Na signal intensity in liver (without a shift reagent) may accurately reflect changes in TQ-filtered Na+i signal intensity. The large percent increase in the TQ-filtered Na+i signal as compared to the SQ signal suggests that the fraction of Na+i interacting with macromolecules increases after death.
PubMed: 9358457
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<affiliation wicri:level="1"><nlm:affiliation>Mary Nell and Ralph B. Rogers Magnetic Resonance Center, Department of Radiology, University of Texas Southwestern Medical Center, Dallas 75235-9085, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Mary Nell and Ralph B. Rogers Magnetic Resonance Center, Department of Radiology, University of Texas Southwestern Medical Center, Dallas 75235-9085</wicri:regionArea>
<wicri:noRegion>Dallas 75235-9085</wicri:noRegion>
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<author><name sortKey="Sherry, A D" sort="Sherry, A D" uniqKey="Sherry A" first="A D" last="Sherry">A D Sherry</name>
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<author><name sortKey="Sherry, A D" sort="Sherry, A D" uniqKey="Sherry A" first="A D" last="Sherry">A D Sherry</name>
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<series><title level="j">Magnetic resonance in medicine</title>
<idno type="ISSN">0740-3194</idno>
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<term>Liver (metabolism)</term>
<term>Magnetic Resonance Spectroscopy (methods)</term>
<term>Male</term>
<term>Organometallic Compounds</term>
<term>Organophosphorus Compounds</term>
<term>Rats</term>
<term>Rats, Sprague-Dawley</term>
<term>Sodium (metabolism)</term>
<term>Thulium</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term>
<term>Composés organiques du phosphore</term>
<term>Composés organométalliques</term>
<term>Foie (métabolisme)</term>
<term>Mâle</term>
<term>Rat Sprague-Dawley</term>
<term>Rats</term>
<term>Sodium (métabolisme)</term>
<term>Spectroscopie par résonance magnétique ()</term>
<term>Thulium</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Sodium</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Organometallic Compounds</term>
<term>Organophosphorus Compounds</term>
<term>Thulium</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Liver</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Magnetic Resonance Spectroscopy</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Foie</term>
<term>Sodium</term>
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<term>Male</term>
<term>Rats</term>
<term>Rats, Sprague-Dawley</term>
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<term>Composés organométalliques</term>
<term>Mâle</term>
<term>Rat Sprague-Dawley</term>
<term>Rats</term>
<term>Spectroscopie par résonance magnétique</term>
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<front><div type="abstract" xml:lang="en">Triple quantum (TQ)-filtered 23Na NMR spectroscopy and the shift reagent, TmDOTP5-, have been used to evaluate the contributions of intra- (Na+i) and extracellular (Na+e) sodium to the TQ-filtered signal in the rat liver, in situ. Na+e contributed significantly to the total TQ-filtered signal in live animals, and the intensity of this signal did not change postmortem. The TQ-filtered Na+i signal increased by approximately 380% over a period of 1 h postmortem, whereas the single quantum (SQ) Na+i increased by 90%. The constancy of the TQ-filtered Na+i signal indicates that changes in total TQ-filtered 23Na signal intensity in liver (without a shift reagent) may accurately reflect changes in TQ-filtered Na+i signal intensity. The large percent increase in the TQ-filtered Na+i signal as compared to the SQ signal suggests that the fraction of Na+i interacting with macromolecules increases after death.</div>
</front>
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