Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2 Pt 2
|
| pubmed:dateCreated |
1996-10-30
|
| pubmed:abstractText |
Perfused rat heart experiments focused on determining the critical O2 level in postischemic myocardium. After a 20-min global ischemia, reperfusion began with O2-saturated saline buffer reflowing at different rates (0.5-12 ml/min). The 1H nuclear magnetic resonance (NMR) signal of the Val E11 myoglobin (Mb) gave an index of the intracellular oxygenation, whereas the 31P-NMR spectra reflected the high-energy phosphate and pH status. At the same time, physiological monitors recorded both contractile function and O2 consumption. Biochemical analysis determined the lactate concentration. Within 6-12 min of reperfusion, the O2 reached a new steady state, which depended directly on the flow rate. Below 12 ml/min reflow, the postischemic O2 level was consistently lower than the corresponding control values. Phosphocreatine, P(i), pH, myocardial O2 consumption, and lactate formation rate exhibited a similar linear relationship with MbO2 saturation in both the control and postischemic myocardium. It appears that neither the cellular energy production nor the steep intracellular O2 gradient has changed substantially in the postischemic myocardium.
|
| pubmed:grant | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cardiotonic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Lactic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Myoglobin,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphates,
http://linkedlifedata.com/resource/pubmed/chemical/anthopleurin-A
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Aug
|
| pubmed:issn |
0002-9513
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
271
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
H687-95
|
| pubmed:dateRevised |
2007-11-14
|
| pubmed:meshHeading |
pubmed-meshheading:8770112-Animals,
pubmed-meshheading:8770112-Cardiotonic Agents,
pubmed-meshheading:8770112-Energy Metabolism,
pubmed-meshheading:8770112-Hydrogen-Ion Concentration,
pubmed-meshheading:8770112-Intracellular Membranes,
pubmed-meshheading:8770112-Lactic Acid,
pubmed-meshheading:8770112-Magnetic Resonance Spectroscopy,
pubmed-meshheading:8770112-Male,
pubmed-meshheading:8770112-Myocardial Contraction,
pubmed-meshheading:8770112-Myocardial Ischemia,
pubmed-meshheading:8770112-Myocardial Reperfusion,
pubmed-meshheading:8770112-Myocardium,
pubmed-meshheading:8770112-Myoglobin,
pubmed-meshheading:8770112-Oxygen Consumption,
pubmed-meshheading:8770112-Peptides,
pubmed-meshheading:8770112-Phosphates,
pubmed-meshheading:8770112-Rats,
pubmed-meshheading:8770112-Rats, Sprague-Dawley
|
| pubmed:year |
1996
|
| pubmed:articleTitle |
Cellular response to reperfused oxygen in the postischemic myocardium.
|
| pubmed:affiliation |
Biological Chemistry Department, University of California, Davis 95616-8635, USA.
|
| pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|