Stimulation of phosphatidylinositol metabolism in the isolated, perfused rat heart

E. A. Woodcock, L. B. Schmauk White, A. I. Smith, J. K. McLeod

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Abstract

Receptor-stimulated phosphatidylinositol turnover has been studied in isolated, perfused, [3H]inositol-labelled rat hearts by measuring accumulation of inositol phosphates in the presence of lithium chloride. Inositol phosphate accumulation was stimulated by norepinephrine (3 x 10-5 M) and carbachol (10-3 M), the increases averaging from 931 ± 59 (n = 6, mean ± SEM, cpm/g heart) to 4,165 ± 609 (n = 6, p < 0.01) for norepinephrine and to 1,853 ± 354 (n = 6, p < 0.05) for carbachol. The norepinephrine stimulation was antagonized by prazosin (10-7 M) but not by propranolol (10-7 M), indicating mediation via α1-adrenoceptors. The carbachol stimulation was antagonized by atropine (10-7 M). The stimulation by norepinephrine was significantly higher in right atria (837 ± 151 to 6,614 ± 1,210, n = 6, cpm/g tissue) than in other regions of the heart. Both norepinephrine and carbachol stimulated the formation of inositol monophosphate, inositol bisphosphate, and inositol trisphosphate with norepinephrine stimulation being detected as early as 15 seconds. Furthermore, the inositol trisphosphate was identified as the -1,4,5 isomer by anion exchange high-performance liquid chromatography. These data are consistent with the hydrolysis of phosphatidylinositol-(4,5)-bisphosphate yielding inositol-(1,4,5)-trisphosphate. Inositol-(1,3,4)-trisphosphate was not detected in heart preparations, suggesting unusual metabolism of inositol-(1,4,5)-trisphosphate in heart tissue.

Original languageEnglish
Pages (from-to)625-631
Number of pages7
JournalCirculation Research
Volume61
Issue number5
DOIs
Publication statusPublished - 1 Jan 1987

Cite this

Woodcock, E. A. ; Schmauk White, L. B. ; Smith, A. I. ; McLeod, J. K. / Stimulation of phosphatidylinositol metabolism in the isolated, perfused rat heart. In: Circulation Research. 1987 ; Vol. 61, No. 5. pp. 625-631.
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Stimulation of phosphatidylinositol metabolism in the isolated, perfused rat heart. / Woodcock, E. A.; Schmauk White, L. B.; Smith, A. I.; McLeod, J. K.

In: Circulation Research, Vol. 61, No. 5, 01.01.1987, p. 625-631.

Research output: Contribution to journalArticleResearchpeer-review

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T1 - Stimulation of phosphatidylinositol metabolism in the isolated, perfused rat heart

AU - Woodcock, E. A.

AU - Schmauk White, L. B.

AU - Smith, A. I.

AU - McLeod, J. K.

PY - 1987/1/1

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N2 - Receptor-stimulated phosphatidylinositol turnover has been studied in isolated, perfused, [3H]inositol-labelled rat hearts by measuring accumulation of inositol phosphates in the presence of lithium chloride. Inositol phosphate accumulation was stimulated by norepinephrine (3 x 10-5 M) and carbachol (10-3 M), the increases averaging from 931 ± 59 (n = 6, mean ± SEM, cpm/g heart) to 4,165 ± 609 (n = 6, p < 0.01) for norepinephrine and to 1,853 ± 354 (n = 6, p < 0.05) for carbachol. The norepinephrine stimulation was antagonized by prazosin (10-7 M) but not by propranolol (10-7 M), indicating mediation via α1-adrenoceptors. The carbachol stimulation was antagonized by atropine (10-7 M). The stimulation by norepinephrine was significantly higher in right atria (837 ± 151 to 6,614 ± 1,210, n = 6, cpm/g tissue) than in other regions of the heart. Both norepinephrine and carbachol stimulated the formation of inositol monophosphate, inositol bisphosphate, and inositol trisphosphate with norepinephrine stimulation being detected as early as 15 seconds. Furthermore, the inositol trisphosphate was identified as the -1,4,5 isomer by anion exchange high-performance liquid chromatography. These data are consistent with the hydrolysis of phosphatidylinositol-(4,5)-bisphosphate yielding inositol-(1,4,5)-trisphosphate. Inositol-(1,3,4)-trisphosphate was not detected in heart preparations, suggesting unusual metabolism of inositol-(1,4,5)-trisphosphate in heart tissue.

AB - Receptor-stimulated phosphatidylinositol turnover has been studied in isolated, perfused, [3H]inositol-labelled rat hearts by measuring accumulation of inositol phosphates in the presence of lithium chloride. Inositol phosphate accumulation was stimulated by norepinephrine (3 x 10-5 M) and carbachol (10-3 M), the increases averaging from 931 ± 59 (n = 6, mean ± SEM, cpm/g heart) to 4,165 ± 609 (n = 6, p < 0.01) for norepinephrine and to 1,853 ± 354 (n = 6, p < 0.05) for carbachol. The norepinephrine stimulation was antagonized by prazosin (10-7 M) but not by propranolol (10-7 M), indicating mediation via α1-adrenoceptors. The carbachol stimulation was antagonized by atropine (10-7 M). The stimulation by norepinephrine was significantly higher in right atria (837 ± 151 to 6,614 ± 1,210, n = 6, cpm/g tissue) than in other regions of the heart. Both norepinephrine and carbachol stimulated the formation of inositol monophosphate, inositol bisphosphate, and inositol trisphosphate with norepinephrine stimulation being detected as early as 15 seconds. Furthermore, the inositol trisphosphate was identified as the -1,4,5 isomer by anion exchange high-performance liquid chromatography. These data are consistent with the hydrolysis of phosphatidylinositol-(4,5)-bisphosphate yielding inositol-(1,4,5)-trisphosphate. Inositol-(1,3,4)-trisphosphate was not detected in heart preparations, suggesting unusual metabolism of inositol-(1,4,5)-trisphosphate in heart tissue.

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