Ca2+ sensitizing effects of EMD 53998 after troponin replacement in skinned fibres from porcine atria and ventricles

Zacharias Barth, John D. Strauss, Susanne Heyder, Jennifer Van Eyk, Rudolf J. Wiesner, J. Caspar Rüegg

Research output: Contribution to journalArticle

Abstract

Skinned fibres from porcine ventricles exhibited a higher Ca2+ sensitivity (pCa50, i.e. -log10 Ca2+ concentration required for half-maximal activation, for force generation) than atrial fibres. The thiadiazinone derivative EMD 53998 increased Ca2+ sensitivity and Ca2+ efficacy in both preparations. The drug effect depended on the isoform of troponin (Tn). Using the vanadate method TnI and TnC could be partly extracted and replaced by foreign tropin or by the TnI subunit of added foreign troponins. We investigated the relationship between pCa and force development before and after replacement of TnI with foreign troponin (bovine ventricular troponin, cTn, or rabbit skeletal muscle troponin, sTn) in the presence and absence of EMD 53998. Substitution with bovine cTn increased Ca2+ sensitivity to a value characteristic of bovine ventricular skinned fibres (pCa50=5.4) and was further increased by EMD 53998. Substitution with sTn also increased Ca2+ sensitivity, but subsequent addition of EMD 53998 caused little further increase in Ca2+ sensitivity. Following extraction of TnI with vanadate, skinned fibres contracted in a Ca2+-independent manner and failed to relax at a pCa of 8. Relaxation could be induced, however, by bovine ventricular TnI and rabbit skeletal muscle recombinant TnI. This relaxation could be reversed by EMD 53998 (100 μM). The Ca2+-independent force of contracted fibres could also be depressed by a TnI inhibitory peptide, (cTnI 137-148) and, in addition, this effect was antagonized by EMD 53998. These results suggest that EMD 53998 antagonizes the inhibitory action of TnI, possibly by interfering with the interaction of the TnI inhibitory region with actin.

Original languageEnglish (US)
Pages (from-to)220-229
Number of pages10
JournalPflugers Archiv European Journal of Physiology
Volume430
Issue number2
DOIs
StatePublished - Jun 1995
Externally publishedYes

Fingerprint

EMD 53998
Troponin
Swine
Fibers
Vanadates
Muscle
Skeletal Muscle
Substitution reactions
Rabbits
Actins

Keywords

  • Ca sensitivity modulation
  • Ca sensitizer drugs
  • EMD 53998
  • Skinned fibres
  • Troponin substitution

ASJC Scopus subject areas

  • Physiology

Cite this

Ca2+ sensitizing effects of EMD 53998 after troponin replacement in skinned fibres from porcine atria and ventricles. / Barth, Zacharias; Strauss, John D.; Heyder, Susanne; Van Eyk, Jennifer; Wiesner, Rudolf J.; Rüegg, J. Caspar.

In: Pflugers Archiv European Journal of Physiology, Vol. 430, No. 2, 06.1995, p. 220-229.

Research output: Contribution to journalArticle

Barth, Zacharias ; Strauss, John D. ; Heyder, Susanne ; Van Eyk, Jennifer ; Wiesner, Rudolf J. ; Rüegg, J. Caspar. / Ca2+ sensitizing effects of EMD 53998 after troponin replacement in skinned fibres from porcine atria and ventricles. In: Pflugers Archiv European Journal of Physiology. 1995 ; Vol. 430, No. 2. pp. 220-229.
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AU - Barth, Zacharias

AU - Strauss, John D.

AU - Heyder, Susanne

AU - Van Eyk, Jennifer

AU - Wiesner, Rudolf J.

AU - Rüegg, J. Caspar

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N2 - Skinned fibres from porcine ventricles exhibited a higher Ca2+ sensitivity (pCa50, i.e. -log10 Ca2+ concentration required for half-maximal activation, for force generation) than atrial fibres. The thiadiazinone derivative EMD 53998 increased Ca2+ sensitivity and Ca2+ efficacy in both preparations. The drug effect depended on the isoform of troponin (Tn). Using the vanadate method TnI and TnC could be partly extracted and replaced by foreign tropin or by the TnI subunit of added foreign troponins. We investigated the relationship between pCa and force development before and after replacement of TnI with foreign troponin (bovine ventricular troponin, cTn, or rabbit skeletal muscle troponin, sTn) in the presence and absence of EMD 53998. Substitution with bovine cTn increased Ca2+ sensitivity to a value characteristic of bovine ventricular skinned fibres (pCa50=5.4) and was further increased by EMD 53998. Substitution with sTn also increased Ca2+ sensitivity, but subsequent addition of EMD 53998 caused little further increase in Ca2+ sensitivity. Following extraction of TnI with vanadate, skinned fibres contracted in a Ca2+-independent manner and failed to relax at a pCa of 8. Relaxation could be induced, however, by bovine ventricular TnI and rabbit skeletal muscle recombinant TnI. This relaxation could be reversed by EMD 53998 (100 μM). The Ca2+-independent force of contracted fibres could also be depressed by a TnI inhibitory peptide, (cTnI 137-148) and, in addition, this effect was antagonized by EMD 53998. These results suggest that EMD 53998 antagonizes the inhibitory action of TnI, possibly by interfering with the interaction of the TnI inhibitory region with actin.

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