23Na and 31P nuclear magnetic resonance studies of ischemia-induced ventricular fibrillation. Alterations of intracellular Na+ and cellular energy

Circ Res. 1995 Aug;77(2):394-406. doi: 10.1161/01.res.77.2.394.

Abstract

To clarify the role of Na+i, pHi, and high-energy phosphate (HEP) levels in the initiation and maintenance of ischemia-induced ventricular fibrillation (VF), interleaved 23Na and 31P nuclear magnetic resonance spectra were collected on perfused rat hearts during low-flow ischemia (51 minutes, 1.2 mL/g wet wt). When untreated, 50% of the hearts from normal (sham) rats and 89% of the hypertrophied hearts from aorticbanded (band) rats (P < .01 versus sham) exhibited VF. Phosphocreatine content was significantly higher in sham than band hearts during control perfusion (53.3 +/- 1.6 versus 39.8 +/- 2.0 mumol/g dry wt). Before VF at 20 minutes of ischemia, Na+i accumulation was greater in hearts that eventually developed VF than in hearts that did not develop VF for both band and sham groups (144% versus 128% of control in sham; P < .005) and was the strongest metabolic predictor of VF; ATP depletion was also greater for VF hearts in the sham group. Infusion of the Na(+)-H+ exchange inhibitor 5-(N,N-hexamethylene)-amiloride prevented VF in sham and band hearts; reduced Na+i accumulation but similar HEP depletion were observed compared with VF hearts before the onset of VF. Rapid changes in Na+i, pHi, and HEP began with VF, resulting in intracellular Na+i overload (approximately 300% of control) and increased HEP depletion. A delayed postischemic functional recovery occurred in VF hearts, which correlated temporally with the recovery of Na+i. In conclusion, alterations in Na+i were associated with spontaneous VF transitions, consistent with involvement of excess Na+i accumulation in VF initiation and maintenance and with previously reported alterations in Ca2+i with VF.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Analysis of Variance
  • Animals
  • Cardiomegaly / metabolism
  • Energy Metabolism*
  • In Vitro Techniques
  • Lactates / metabolism
  • Magnetic Resonance Spectroscopy*
  • Male
  • Myocardial Ischemia / complications*
  • Myocardial Ischemia / metabolism
  • Perfusion
  • Phosphocreatine / metabolism
  • Phosphorus Isotopes
  • Rats
  • Rats, Sprague-Dawley
  • Sodium / metabolism*
  • Sodium Isotopes
  • Time Factors
  • Ventricular Fibrillation / etiology
  • Ventricular Fibrillation / metabolism*

Substances

  • Lactates
  • Phosphorus Isotopes
  • Sodium Isotopes
  • Phosphocreatine
  • Adenosine Triphosphate
  • Sodium