Response of myocardial metabolites to graded regional ischemia: 31P NMR spectroscopy of porcine myocardium in vivo

Saul Schaefer, S. A. Camacho, J. Gober, R. G. Obregon, M. A. DeGroot, E. H. Botvinick, B. Massie, M. W. Weiner

Research output: Contribution to journalArticle

45 Scopus citations

Abstract

The changes in myocardial high energy phosphates and pH during regional ischemia, and their potential role in mediating functional abnormalities, is unclear. To determine the degree of regional blood flow reduction required to induce changes in high energy phosphates and pH, and to correlate these metabolic changes with alterations in blood flow, 31P nuclear magnetic resonance spectroscopy was employed in an in vivo porcine model of graded coronary stenosis. Simultaneous measurements of regional blood flow and phosphate compounds were made during various steady-state degrees of regional ischemia in which subendocardial blood was reduced by as much as 80%. ATP did not fall over the total range of graded ischemia, while phosphocreatine (PCr), inorganic phosphate (P(i)), and pH all changed progressively after blood flow was reduced below 50% of normal. The ratio of PCr/P(i) (a measure of the energy reserve of the myocardium) was strongly correlated to subendocardial blood flow (r = 0.94) and declined by 25% when blood flow was reduced by only 21% below normal. These findings indicate that PCr/P(i) is a sensitive marker of ischemia and support the hypothesis that the in vivo energy status of the myocardium is closely coupled to myocardial blood flow.

Original languageEnglish (US)
Pages (from-to)968-976
Number of pages9
JournalCirculation Research
Volume64
Issue number5
StatePublished - 1989
Externally publishedYes

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

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    Schaefer, S., Camacho, S. A., Gober, J., Obregon, R. G., DeGroot, M. A., Botvinick, E. H., Massie, B., & Weiner, M. W. (1989). Response of myocardial metabolites to graded regional ischemia: 31P NMR spectroscopy of porcine myocardium in vivo. Circulation Research, 64(5), 968-976.