Changes in phosphoinositide turnover in isolated guinea pig hearts stimulated with isoproterenol

I. Édes, R. J. Solaro, E. G. Kranias

Research output: Contribution to journalArticle

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Abstract

The incorporation of 32P(i) into phospholamban, troponin I, phosphatidylinositols, and inositol trisphosphates was studied in Langendorff-perfused guinea pig hearts stimulated with isoproterenol. Hearts were perfused with Krebs-Henseleit buffer containing [32P]P(i) and freeze-clamped at different times during the positive inotropic response. Exposure of the hearts to 0.1 μM isoproterenol for up to 1 minute was associated with significant (up to threefold) increases in phospholamban and troponin I phosphorylation, but there was no significant increase in 32P incorporation into phospholipids. However, longer exposure (2 minutes or more) to isoproterenol was associated with increases in the degree of 32P labeling of phosphatidylinositols and phosphatidic acid. Examination of 32P labeling of inositol trisphosphates in the same hearts revealed that the radioactivity associated with these compounds decreased with time. The decreases were significant at times of exposure of 2 minutes or longer to β-adrenergic stimulation. The tissue levels of the inositol 1,4,5-trisphosphate isoform were also measured in hearts perfused with isoproterenol for 3 minutes, and they were found to be significantly lower compared with values obtained in control hearts. The effects of isoproterenol on 32P incorporation into phospholipids and proteins were observed in the presence of prazosin, and they were completely abolished by the β-receptor blocker propranolol. Examination of the phosphoinositide-specific phospholipase C activity in the perfused hearts revealed that isoproterenol stimulation was associated with a decrease in the membrane-associated enzymatic activity at physiological calcium concentrations. These findings indicate that β-adrenergic stimulation of isolated hearts is associated with changes in basal phosphatidylinositol turnover that may be mediated, at least in part, by inhibition of the phospholipase C enzymatic activity specific for phosphatidylinositols.

Original languageEnglish
Pages (from-to)989-996
Number of pages8
JournalCirculation Research
Volume65
Issue number4
Publication statusPublished - 1989

Fingerprint

Phosphatidylinositols
Isoproterenol
Guinea Pigs
Troponin I
Inositol
Adrenergic Agents
Phospholipids
Phosphoinositide Phospholipase C
Phosphatidic Acids
Inositol 1,4,5-Trisphosphate
Prazosin
Type C Phospholipases
Propranolol
Radioactivity
Protein Isoforms
Phosphorylation
Calcium
Membranes

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Changes in phosphoinositide turnover in isolated guinea pig hearts stimulated with isoproterenol. / Édes, I.; Solaro, R. J.; Kranias, E. G.

In: Circulation Research, Vol. 65, No. 4, 1989, p. 989-996.

Research output: Contribution to journalArticle

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