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PMID: 1302274 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Inorganic phosphate decreases the Ca2+ content of the sarcoplasmic reticulum in saponin-treated rat cardiac trabeculae.

The Journal of physiology ·Vol. 458 ·1992-12-00 ·Pages 457-73

Smith GL, Steele DS

Abstract

1. Measurements of [Ca2+] were made in saponin-permeabilized rat ventricular trabeculae using the fluorescent indicator Indo-1. Application of caffeine (20 mM) caused a transient rise in [Ca2+] within the preparation as a result of Ca2+ release from the sarcoplasmic reticulum (SR). The size of the caffeine-induced Ca2+ transient was related to the amount of Ca2+ accumulated by the SR prior to addition of caffeine. Caffeine-induced Ca2+ release was abolished by ryanodine (10 microM), an inhibitor of SR Ca2+ release. 2. At a bathing [Ca2+] of 0.2 microM, the amount of Ca2+ released from the SR on addition of caffeine was sufficient to generate a tension transient. Ca2+ and tension responses were stabilized by application of caffeine at regular intervals (2 min). Addition of 10 mM inorganic phosphate (Pi) induced a transient increase in [Ca2+] within the preparation due to a net release of Ca2+ from the SR. The amplitude of subsequent caffeine-induced Ca2+ transients were reduced to 65 +/- 7.5% (mean +/- S.D., n = 13) of control. In addition, the accompanying tension transient fell to 45 +/- 6.9% of control. Removal of Pi caused a transient decrease in the [Ca2+] within the preparation consistent with a net increase in Ca2+ uptake by the SR. Subsequent caffeine-induced Ca2+ and tension transients returned to control levels. 3. Inclusion of Pi (2-30 mM) in the perfusing solution decreased the size of caffeine-induced Ca2+ and tension transients in a dose-dependent manner. 4. Addition of 10 mM ADP caused a transient increase in [Ca2+] and depressed subsequent caffeine-induced Ca2+ transients to a greater extent than 10 mM Pi. Despite the reduction in Ca2+ release from the SR, tension responses were larger in the presence of 10 mM ADP than under control conditions. This is a consequence of an increase in Ca(2+)-activated force by ADP. 5. A decrease in the amplitude of caffeine-induced Ca2+ transients also occurred on changing from a solution containing 1 mM ADP and 10 mM Pi to a solution with 10 mM ADP and 1 mM Pi. This confirms the previous observation that ADP is more effective than Pi at reducing caffeine-induced Ca2+ released from the SR. 6. Spontaneous oscillations of [Ca2+] and tension occurred in the presence of 0.5 microM Ca2+.(ABSTRACT TRUNCATED AT 400 WORDS)

MeSH Terms
Animals Caffeine/pharmacology Calcium/metabolism Dose-Response Relationship, Drug Heart/drug effects In Vitro Techniques Myocardial Contraction/drug effects Myocardium/metabolism Phosphates/pharmacology Rats Rats, Sprague-Dawley Sarcoplasmic Reticulum/metabolism Spectrometry, Fluorescence
Chemicals
Phosphates Caffeine Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Smith G L
Institute of Physiology, University of Glasgow.
Steele D S
References (26)
26 references, click to expand
  1. The role of [Ca2+]i and [Ca2+] sensitization in the caffeine contracture of rat myocytes: measurement of [Ca2+]i and [caffeine]i.
    J Physiol. 1990 Jun;425:55-70 PMID: 2213589
  2. Activity of phosphorylase in total global ischaemia in the rat heart. A phosphorus-31 nuclear-magnetic-resonance study.
    Biochem J. 1981 Apr 15;196(1):171-8 PMID: 7306067
  3. Effect of ischemia on calcium-dependent fluorescence transients in rabbit hearts containing indo 1. Correlation with monophasic action potentials and contraction.
    Circulation. 1988 Oct;78(4):1047-59 PMID: 2844438
  4. Stimulation of Ca2+ efflux from sarcoplasmic reticulum by preincubation with ATP and inorganic phosphate.
    Biochem J. 1987 Nov 1;247(3):497-504 PMID: 2962569
  5. Effects of metabolic blockade on intracellular calcium concentration in isolated ferret ventricular muscle.
    Circ Res. 1988 Jun;62(6):1223-36 PMID: 3383366
  6. Synchronous occurrence of spontaneous localized calcium release from the sarcoplasmic reticulum generates action potentials in rat cardiac ventricular myocytes at normal resting membrane potential.
    Circ Res. 1987 Oct;61(4):498-503 PMID: 3652397
  7. The reversal of the calcium pump of cardiac sarcoplasmic reticulum.
    Basic Res Cardiol. 1977 Mar-Jun;72(2-3):147-52 PMID: 140656
  8. Calculator programs for computing the composition of the solutions containing multiple metals and ligands used for experiments in skinned muscle cells.
    J Physiol (Paris). 1979;75(5):463-505 PMID: 533865
  9. Contractions induced by a calcium-triggered release of calcium from the sarcoplasmic reticulum of single skinned cardiac cells.
    J Physiol. 1975 Aug;249(3):469-95 PMID: 809571
  10. Reperfusion injury and its pharmacologic modification.
    Circulation. 1989 Oct;80(4):1049-62 PMID: 2571429
  11. The effects of metabolic inhibition on intracellular calcium and pH in isolated rat ventricular cells.
    J Physiol. 1989 Apr;411:393-418 PMID: 2614727
  12. The consequences of simulated ischaemia on intracellular Ca2+ and tension in isolated ferret ventricular muscle.
    J Physiol. 1989 Mar;410:297-323 PMID: 2795481
  13. Subcellular origin of the oxalate- or inorganic phosphate-stimulated Ca2+ transport by smooth muscle microsomes: revisitation of the old problem by a new approach using saponin.
    Biochim Biophys Acta. 1985 Sep 25;819(1):148-52 PMID: 2931116
  14. The effects of repeated exposure to anoxia on intracellular calcium, glycogen and lactate in isolated ferret heart muscle.
    Pflugers Arch. 1988 Nov;413(1):83-9 PMID: 3217230
  15. Myocardial contractile function during ischemia and hypoxia.
    Circ Res. 1987 Feb;60(2):153-68 PMID: 3552284
  16. Differential effects of reoxygenation on intracellular calcium and isometric tension.
    Pflugers Arch. 1987 Aug;409(4-5):448-53 PMID: 3627961
  17. Effect of rigor and cycling cross-bridges on the structure of troponin C and on the Ca2+ affinity of the Ca2+-specific regulatory sites in skinned rabbit psoas fibers.
    J Biol Chem. 1987 Oct 5;262(28):13627-35 PMID: 3654633
  18. The effects of inorganic phosphate and creatine phosphate on force production in skinned muscles from rat ventricle.
    J Physiol. 1986 Jan;370:585-604 PMID: 3958986
  19. A nuclear magnetic resonance study of metabolism in the ferret heart during hypoxia and inhibition of glycolysis.
    J Physiol. 1985 Apr;361:185-204 PMID: 3989725
  20. Mechanism of Ca2+ transport by Ca2+-Mg2+-ATPase pump: analysis of major states and pathways.
    Am J Physiol. 1983 Jan;244(1):G3-12 PMID: 6129804
  21. Calcium release and ionic changes in the sarcoplasmic reticulum of tetanized muscle: an electron-probe study.
    J Cell Biol. 1981 Sep;90(3):577-94 PMID: 6974735
  22. The effect of calcium and phosphate on the biphasic calcium uptake by the sarcoplasmic reticulum.
    Z Naturforsch C. 1975 Nov-Dec;30(6):777-80 PMID: 130009
  23. Calcium oxalate and calcium phosphate capacities of cardiac sarcoplasmic reticulum.
    Biochim Biophys Acta. 1985 Sep 10;818(3):373-85 PMID: 3876113
  24. Ionic mobility in muscle cells.
    Science. 1969 Dec 5;166(3910):1297-8 PMID: 5350329
  25. Adenine nucleotide stimulation of Ca2+-induced Ca2+ release in sarcoplasmic reticulum.
    J Biol Chem. 1984 Feb 25;259(4):2365-74 PMID: 6698971
  26. Changes of intracellular milieu with fatigue or hypoxia depress contraction of skinned rabbit skeletal and cardiac muscle.
    J Physiol. 1989 May;412:155-80 PMID: 2600830
Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1992-12-00
Pages
457-73
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1175165
Subset
IM
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