The consequences of simulated ischaemia on intracellular Ca2+ and tension in isolated ferret ventricular muscle - PubMed (original) (raw)
The consequences of simulated ischaemia on intracellular Ca2+ and tension in isolated ferret ventricular muscle
D G Allen et al. J Physiol. 1989 Mar.
Abstract
1. In order to study cellular events occurring in ischaemia, we have developed a method for simulating ischaemia in an isolated papillary muscle. Muscles were suspended in a chamber and changed from conventional superfusion with Tyrode solution to gas perfusion with 95% N2/5% CO2 (N2 gas perfusion), thus simultaneously stopping oxygenation and flow. Surface cells of the preparation were injected with the photoprotein aequorin in order to monitor intracellular free calcium concentration [( Ca2+]i). 2. Gas perfusion with 95% O2/5% CO2 (O2 gas perfusion) had little effect on the tension or Ca2+ transients. Superfusion with Tyrode solution equilibrated with 95% N2/5% CO2 (N2 Tyrode) caused tension to decline to 30-40% of control, but had little effect on the amplitude of the Ca2+ transients. N2 gas perfusion caused tension to fall more rapidly and to a lower level than superfusion with N2 Tyrode. Ca2+ transients showed a small initial decline followed by a slowly developing increase in magnitude and duration. 3. Long exposures to N2 gas perfusion caused tension to decline to very low levels and Ca2+ transients to increase to a maximum. After a variable length of time, resting tension began to increase. At approximately the same time, Ca2+ transients began to decrease and eventually disappeared. Resting Ca2+ increased during N2 gas perfusion and remained elevated when the Ca2+ transients had declined. These changes could be reversed by restarting superfusion with standard Tyrode or by perfusion with O2 gas. 4. N2 gas perfusion caused a depolarization of the resting potential and an abbreviation of the action potential. In a long exposure the action potential eventually failed. These changes could be reversed by restarting superfusion with standard Tyrode or by perfusion with O2 gas. 5. Many of the effects of N2 gas perfusion could be mimicked by the addition of 20 mM-lactic acid to the superfusing solution, which caused a profound reduction of tension and also an increase in the amplitude and duration of the Ca2+ transients. Calculation of the changes in intracellular pH caused by the addition of lactic acid suggest that the fall in intracellular pH produced by lactic acid was similar to that occurring in ischaemia. 6. Repeated exposures to N2 gas perfusion caused tension to fall more rapidly and an increased resting tension to develop more rapidly. The slowly developing rise in Ca2+ transients was abolished and a rise in resting Ca2+ occurred more quickly. 7. When muscles were quiescent, exposure to N2 gas perfusion caused an increase in resting light.(ABSTRACT TRUNCATED AT 400 WORDS)
Similar articles
- The role of the sarcoplasmic reticulum in the response of ferret and rat heart muscle to acidosis.
Orchard CH. Orchard CH. J Physiol. 1987 Mar;384:431-49. doi: 10.1113/jphysiol.1987.sp016462. J Physiol. 1987. PMID: 3656151 Free PMC article. - The effects of changes of pH on intracellular calcium transients in mammalian cardiac muscle.
Allen DG, Orchard CH. Allen DG, et al. J Physiol. 1983 Feb;335:555-67. doi: 10.1113/jphysiol.1983.sp014550. J Physiol. 1983. PMID: 6410050 Free PMC article. - Measurements of intracellular calcium concentration in heart muscle: the effects of inotropic interventions and hypoxia.
Allen DG, Orchard CH. Allen DG, et al. J Mol Cell Cardiol. 1984 Feb;16(2):117-28. doi: 10.1016/s0022-2828(84)80700-2. J Mol Cell Cardiol. 1984. PMID: 6371253 Review. - Kinetic investigations in single muscle fibres using luminescent and fluorescent Ca2+ probes.
Ashley CC, Potter JD, Strang P, Godber J, Walton A, Griffiths PJ. Ashley CC, et al. Cell Calcium. 1985 Apr;6(1-2):159-81. doi: 10.1016/0143-4160(85)90042-9. Cell Calcium. 1985. PMID: 3893726 Review.
Cited by
- Changes in myoplasmic pH and calcium concentration during exposure to lactate in isolated rat ventricular myocytes.
Cairns SP, Westerblad H, Allen DG. Cairns SP, et al. J Physiol. 1993 May;464:561-74. doi: 10.1113/jphysiol.1993.sp019651. J Physiol. 1993. PMID: 8229818 Free PMC article. - Effects of lactate on the relative contribution of Ca2+ extrusion mechanisms to relaxation in guinea-pig ventricular myocytes.
Terracciano CM, MacLeod KT. Terracciano CM, et al. J Physiol. 1997 May 1;500 ( Pt 3)(Pt 3):557-70. doi: 10.1113/jphysiol.1997.sp022042. J Physiol. 1997. PMID: 9161975 Free PMC article. - Abnormalities in intracellular calcium regulation and contractile function in myocardium from dogs with pacing-induced heart failure.
Perreault CL, Shannon RP, Komamura K, Vatner SF, Morgan JP. Perreault CL, et al. J Clin Invest. 1992 Mar;89(3):932-8. doi: 10.1172/JCI115674. J Clin Invest. 1992. PMID: 1311723 Free PMC article. - Hypoxia-activated apoptosis of cardiac myocytes requires reoxygenation or a pH shift and is independent of p53.
Webster KA, Discher DJ, Kaiser S, Hernandez O, Sato B, Bishopric NH. Webster KA, et al. J Clin Invest. 1999 Aug;104(3):239-52. doi: 10.1172/JCI5871. J Clin Invest. 1999. PMID: 10430605 Free PMC article. - R 56865 exerts cardioprotective properties independent of the intracellular Na(+)-overload in the guinea pig heart.
Hartmann M, Decking UK. Hartmann M, et al. Naunyn Schmiedebergs Arch Pharmacol. 2003 Sep;368(3):160-5. doi: 10.1007/s00210-003-0791-7. Epub 2003 Sep 2. Naunyn Schmiedebergs Arch Pharmacol. 2003. PMID: 14513202
References
- J Pharmacol Exp Ther. 1966 Feb;151(2):221-35 - PubMed
- J Physiol. 1983 Feb;335:555-67 - PubMed
- Am J Pathol. 1972 Jun;67(3):417-40 - PubMed
- J Physiol. 1974 Aug;240(3):703-24 - PubMed
- J Physiol. 1975 Sep;250(2):231-45 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous