Economy of contraction of cardiomyocytes as influenced by different positive inotropic interventions
- PMID: 8760193
- DOI: 10.1152/ajpheart.1996.271.1.H357
Economy of contraction of cardiomyocytes as influenced by different positive inotropic interventions
Abstract
In the present study the effects of the novel cardiotonic agent EMD-57033 on contraction and energetic demand of isolated, electrically stimulated cardiomyocytes were investigated and compared with the effects of enhancement of extracellular calcium and of the beta-mimetic isoproterenol. In a specially designed setup [H. Rose, K.H. Strotmann, S. Pöpping, Y. Fischer, D. Kulsch, and H. Kammermeier. Am. J. Physiol. 261 (Heart Circ. Physiol. 30): H1329-H1334, 1991] parameters of contractile behavior and metabolic demand (O2 consumption) of isolated cardiac myocytes were measured. For a given enhancement of contractile performance (cell shortening) the increase in energetic demand (VO2) after application of EMD-57033 were markedly lower than on treatment with elevated extracellular Ca2+ concentration or with isoproterenol. This economization of positive inotropic effects was proposed to be due to two factors. First, stimulation-related ion cycling was only slightly enhanced with marked increase in contraction amplitude after application of EMD-57033. Second, calcium sensitization reflected in a leftward shift of the calcium concentration needed for half-maximum force development could be interpreted to be mediated by modulation of the cross-bridge dynamics of the myofilaments, where reduction of the switch-off rate of the cross bridges and prolongation of their force-generating states were presumed to be involved. Lowered pH (7.0) decreased economy of contraction. EMD-57033 restored contraction amplitude and economy of contraction at lowered pH.
Similar articles
-
Effects of calcium sensitizers on intracellular calcium handling and myocardial energetics.J Cardiovasc Pharmacol. 1995;26 Suppl 1:S45-51. J Cardiovasc Pharmacol. 1995. PMID: 8907130
-
Functional and energetic effects of the inotropic agents EMD-57033 and BAPTA on the isolated rat heart.Am J Physiol. 1995 Aug;269(2 Pt 1):C472-9. doi: 10.1152/ajpcell.1995.269.2.C472. Am J Physiol. 1995. PMID: 7653529
-
The two mechanisms of action of racemic cardiotonic EMD 53998, calcium sensitization and phosphodiesterase inhibition, reside in different enantiomers.J Cardiovasc Pharmacol. 1993 Jun;21(6):883-92. doi: 10.1097/00005344-199306000-00006. J Cardiovasc Pharmacol. 1993. PMID: 7687712
-
Cardiac Ca2+ signaling and Ca2+ sensitizers.Circ J. 2008 Dec;72(12):1915-25. doi: 10.1253/circj.cj-08-0838. Epub 2008 Nov 4. Circ J. 2008. PMID: 18981594 Review.
-
[New cardiotonic/inodilator agents: energetic aspects].Z Kardiol. 1992;81 Suppl 4:57-63. Z Kardiol. 1992. PMID: 1290307 Review. German.
Cited by
-
High calcium and dobutamine positive inotropy in the perfused mouse heart: myofilament calcium responsiveness, energetic economy, and effects of protein kinase C inhibition.BMC Physiol. 2001;1:12. doi: 10.1186/1472-6793-1-12. Epub 2001 Aug 24. BMC Physiol. 2001. PMID: 11553322 Free PMC article.
-
Kir6.2 is required for adaptation to stress.Proc Natl Acad Sci U S A. 2002 Oct 1;99(20):13278-83. doi: 10.1073/pnas.212315199. Epub 2002 Sep 23. Proc Natl Acad Sci U S A. 2002. PMID: 12271142 Free PMC article.
-
Small molecule drugs to improve sarcomere function in those with acquired and inherited myopathies.Am J Physiol Cell Physiol. 2023 Jul 1;325(1):C60-C68. doi: 10.1152/ajpcell.00047.2023. Epub 2023 May 22. Am J Physiol Cell Physiol. 2023. PMID: 37212548 Free PMC article. Review.
-
SR33805, a Ca2+ antagonist with length-dependent Ca2+ -sensitizing properties in cardiac myocytes.Br J Pharmacol. 2003 May;139(1):99-108. doi: 10.1038/sj.bjp.0705221. Br J Pharmacol. 2003. PMID: 12746228 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous