Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1989 Apr;96(4):927–939. doi: 10.1111/j.1476-5381.1989.tb11904.x

Mechanisms of positive inotropic effects and delayed relaxation produced by DPI 201-106 in mammalian working myocardium: effects on intracellular calcium handling.

Y Kihara 1, J K Gwathmey 1, W Grossman 1, J P Morgan 1
PMCID: PMC1854417  PMID: 2743084

Abstract

1. We used the bioluminescent protein aequorin, which emits light when it combines with Ca2+, to test the hypothesis that the inotropic and lusitropic actions of DPI 201-106 are due to changes in intracellular Ca2+ handling in papillary muscles from ferrets and guinea-pigs. 2. DPI 201-106 increased peak isometric tension (T) in a dose-dependent manner, with an 83% increase in T as the concentration of DPI 201-106 was increased to 1 x 10(-5) M; however, peak [Ca2+]i did not increase significantly until the concentration of DPI 201-106 reached 3 x 10(-6) M, suggesting a sensitization of the contractile apparatus to Ca2+. 3. Tetrodotoxin (1 x 10(-6) M), which did not reduce the tension response significantly before DPI 201-106, decreased both [Ca2+]i and T in the presence of 1 x 10(-5) M DPI 201-106, suggesting involvement of a sodium channel activation mechanism; however, tetrodotoxin did not completely reverse the calcium sensitization. 4. The shift of the [Ca2+]i versus T relationship was not observed in the presence of another sodium channel agonist, veratridine (3 x 10(-7)-1 x 10(-6) M). 5. In the guinea-pig, DPI 201-106 markedly prolonged relaxation of tension (increase of 60% in the time from peak to 50% tension regression), which was accompanied by the appearance of a second component in the aequorin light signal; effects on relaxation were less prominent in the ferret. 6. Tension prolongation and the second component of the [Ca2+]i transient in the guinea-pig were exacerbated by increased [Ca2+]o and decreased by tetrodotoxin. Ryanodine (3 x 10(-7) M) markedly diminished the calcium transient in controls and the initial component of the calcium transient in the presence of DPI 201-106, but had only a modest effect on the second component. 7. We conclude that although sodium agonism plays a role, sensitization of the contractile apparatus to Ca2+ is an important mechanism in the positive inotropic action of DPI 201-106. 8. The negative lusitropic action of DPI 201-106 varies between ferret and guinea-pig, possibly reflecting differences between these two species in subcellular Ca2+ handling.

Full text

PDF
927

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Allen D. G., Jewell B. R., Wood E. H. Studies of the contractility of mammalian myocardium at low rates of stimulation. J Physiol. 1976 Jan;254(1):1–17. doi: 10.1113/jphysiol.1976.sp011217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Allen D. G., Kurihara S. The effects of muscle length on intracellular calcium transients in mammalian cardiac muscle. J Physiol. 1982 Jun;327:79–94. doi: 10.1113/jphysiol.1982.sp014221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Allen D. G., Orchard C. H. The effects of changes of pH on intracellular calcium transients in mammalian cardiac muscle. J Physiol. 1983 Feb;335:555–567. doi: 10.1113/jphysiol.1983.sp014550. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Alousi A. A., Farah A. E., Lesher G. Y., Opalka C. J., Jr Cardiotonic activity of amrinone--Win 40680 [5-amino-3,4'-bipyridine-6(1H)-one]. Circ Res. 1979 Nov;45(5):666–677. doi: 10.1161/01.res.45.5.666. [DOI] [PubMed] [Google Scholar]
  5. Benotti J. R., Grossman W., Braunwald E., Davolos D. D., Alousi A. A. Hemodynamic assessment of amrinone. A new inotropic agent. N Engl J Med. 1978 Dec 21;299(25):1373–1377. doi: 10.1056/NEJM197812212992501. [DOI] [PubMed] [Google Scholar]
  6. Beress L., Ritter R., Ravens U. The influence of the rate of electrical stimulation on the effects of the Anemonia sulcata Toxin ATX II in guinea pig papillary muscle. Eur J Pharmacol. 1982 Apr 23;79(3-4):265–272. doi: 10.1016/0014-2999(82)90632-x. [DOI] [PubMed] [Google Scholar]
  7. Bers D. M. Ca influx and sarcoplasmic reticulum Ca release in cardiac muscle activation during postrest recovery. Am J Physiol. 1985 Mar;248(3 Pt 2):H366–H381. doi: 10.1152/ajpheart.1985.248.3.H366. [DOI] [PubMed] [Google Scholar]
  8. Bielefeld D. R., Hadley R. W., Vassilev P. M., Hume J. R. Membrane electrical properties of vesicular Na-Ca exchange inhibitors in single atrial myocytes. Circ Res. 1986 Oct;59(4):381–389. doi: 10.1161/01.res.59.4.381. [DOI] [PubMed] [Google Scholar]
  9. Blinks J. R., Wier W. G., Hess P., Prendergast F. G. Measurement of Ca2+ concentrations in living cells. Prog Biophys Mol Biol. 1982;40(1-2):1–114. doi: 10.1016/0079-6107(82)90011-6. [DOI] [PubMed] [Google Scholar]
  10. Bogdanov K. Y., Zakharov S. I., Rosenshtraukh L. V. The origin of two components in contraction of guinea pig papillary muscle in the presence of noradrenaline. Can J Physiol Pharmacol. 1979 Aug;57(8):866–872. doi: 10.1139/y79-132. [DOI] [PubMed] [Google Scholar]
  11. Brill D. M., Wasserstrom J. A. Intracellular sodium and the positive inotropic effect of veratridine and cardiac glycoside in sheep Purkinje fibers. Circ Res. 1986 Jan;58(1):109–119. doi: 10.1161/01.res.58.1.109. [DOI] [PubMed] [Google Scholar]
  12. Buggisch D., Isenberg G., Ravens U., Scholtysik G. The role of sodium channels in the effects of the cardiotonic compound DPI 201-106 on contractility and membrane potentials in isolated mammalian heart preparations. Eur J Pharmacol. 1985 Dec 3;118(3):303–311. doi: 10.1016/0014-2999(85)90141-4. [DOI] [PubMed] [Google Scholar]
  13. Chapman R. A. Control of cardiac contractility at the cellular level. Am J Physiol. 1983 Oct;245(4):H535–H552. doi: 10.1152/ajpheart.1983.245.4.H535. [DOI] [PubMed] [Google Scholar]
  14. Coraboeuf E. Editorial: Membrane electrical activity and double component contraction in cardiac tissue. J Mol Cell Cardiol. 1974 Jun;6(3):215–225. doi: 10.1016/0022-2828(74)90051-0. [DOI] [PubMed] [Google Scholar]
  15. Endoh M., Iijima T., Motomura S. Inhibition by theophylline of the early component of canine ventricular contraction. Am J Physiol. 1982 Mar;242(3):H349–H358. doi: 10.1152/ajpheart.1982.242.3.H349. [DOI] [PubMed] [Google Scholar]
  16. Grossman W., Barry W. H. Diastolic pressure-volume relations in the diseased heart. Fed Proc. 1980 Feb;39(2):148–155. [PubMed] [Google Scholar]
  17. Gwathmey J. K., Morgan J. P. The effects of milrinone and piroximone on intracellular calcium handling in working myocardium from the ferret. Br J Pharmacol. 1985 May;85(1):97–108. doi: 10.1111/j.1476-5381.1985.tb08835.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Hof R. P., Hof A. Mechanism of the vasodilator effects of the cardiotonic agent DPI 201-106. J Cardiovasc Pharmacol. 1985 Nov-Dec;7(6):1188–1192. doi: 10.1097/00005344-198511000-00028. [DOI] [PubMed] [Google Scholar]
  19. Holck M., Osterrieder W. Interaction of the cardiotonic agent DPI 201-106 with cardiac Ca2+ channels. J Cardiovasc Pharmacol. 1988 Apr;11(4):478–482. doi: 10.1097/00005344-198804000-00015. [DOI] [PubMed] [Google Scholar]
  20. Honerjäger P., Reiter M. The relation between the effects of veratridine on action potential and contraction in mammalian ventricular myocardium. Naunyn Schmiedebergs Arch Pharmacol. 1975;289(1):1–28. doi: 10.1007/BF00498026. [DOI] [PubMed] [Google Scholar]
  21. January C. T., Fozzard H. A. The effects of membrane potential, extracellular potassium, and tetrodotoxin on the intracellular sodium ion activity of sheep cardiac muscle. Circ Res. 1984 Jun;54(6):652–665. doi: 10.1161/01.res.54.6.652. [DOI] [PubMed] [Google Scholar]
  22. King B. W., Bose D. Mechanism of biphasic contractions in strontium-treated ventricular muscle. Circ Res. 1983 Jan;52(1):65–75. doi: 10.1161/01.res.52.1.65. [DOI] [PubMed] [Google Scholar]
  23. Kohlhardt M., Fröbe U., Herzig J. W. Modification of single cardiac Na+ channels by DPI 201-106. J Membr Biol. 1986;89(2):163–172. doi: 10.1007/BF01869712. [DOI] [PubMed] [Google Scholar]
  24. Lado M. G., Sheu S. S., Fozzard H. A. Changes in intracellular Ca2+ activity with stimulation in sheep cardiac Purkinje strands. Am J Physiol. 1982 Jul;243(1):H133–H137. doi: 10.1152/ajpheart.1982.243.1.H133. [DOI] [PubMed] [Google Scholar]
  25. Malecot C. O., Bers D. M., Katzung B. G. Biphasic contractions induced by milrinone at low temperature in ferret ventricular muscle: role of the sarcoplasmic reticulum and transmembrane calcium influx. Circ Res. 1986 Aug;59(2):151–162. doi: 10.1161/01.res.59.2.151. [DOI] [PubMed] [Google Scholar]
  26. Morgan J. P., Blinks J. R. Intracellular Ca2+ transients in the cat papillary muscle. Can J Physiol Pharmacol. 1982 Apr;60(4):524–528. doi: 10.1139/y82-072. [DOI] [PubMed] [Google Scholar]
  27. Morgan J. P., DeFeo T. T., Morgan K. G. A chemical procedure for loading the calcium indicator acquorin into mammalian working myocardium. Pflugers Arch. 1984 Mar;400(3):338–340. doi: 10.1007/BF00581571. [DOI] [PubMed] [Google Scholar]
  28. Morgan J. P., Morgan K. G. Calcium and cardiovascular function. Intracellular calcium levels during contraction and relaxation of mammalian cardiac and vascular smooth muscle as detected with aequorin. Am J Med. 1984 Nov 5;77(5A):33–46. doi: 10.1016/s0002-9343(84)80006-6. [DOI] [PubMed] [Google Scholar]
  29. Morgan J. P., Morgan K. G. Stimulus-specific patterns of intracellular calcium levels in smooth muscle of ferret portal vein. J Physiol. 1984 Jun;351:155–167. doi: 10.1113/jphysiol.1984.sp015239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Morgan J. P. The effects of digitalis on intracellular calcium transients in mammalian working myocardium as detected with aequorin. J Mol Cell Cardiol. 1985 Nov;17(11):1065–1075. doi: 10.1016/s0022-2828(85)80122-x. [DOI] [PubMed] [Google Scholar]
  31. Mullins L. J. The generation of electric currents in cardiac fibers by Na/Ca exchange. Am J Physiol. 1979 Mar;236(3):C103–C110. doi: 10.1152/ajpcell.1979.236.3.C103. [DOI] [PubMed] [Google Scholar]
  32. Narahashi T. Chemicals as tools in the study of excitable membranes. Physiol Rev. 1974 Oct;54(4):813–889. doi: 10.1152/physrev.1974.54.4.813. [DOI] [PubMed] [Google Scholar]
  33. Page E., Surdyk-Droske M. Distribution, surface density, and membrane area of diadic junctional contacts between plasma membrane and terminal cisterns in mammalian ventricle. Circ Res. 1979 Aug;45(2):260–267. doi: 10.1161/01.res.45.2.260. [DOI] [PubMed] [Google Scholar]
  34. Reiter M., Stickel F. J. Der Einfluss der Kontraktionsfrequenz auf das Aktionspotential des Meerschweinchem-Papillarmuskels. Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1968;260(4):342–365. [PubMed] [Google Scholar]
  35. Salzmann R., Scholtysik G., Clark B., Berthold R. Cardiovascular actions of DPI 201-106, a novel cardiotonic agent. J Cardiovasc Pharmacol. 1986 Sep-Oct;8(5):1035–1043. doi: 10.1097/00005344-198609000-00023. [DOI] [PubMed] [Google Scholar]
  36. Scholtysik G., Salzmann R., Berthold R., Herzig J. W., Quast U., Markstein R. DPI 201-106, a novel cardioactive agent. Combination of cAMP-independent positive inotropic, negative chronotropic, action potential prolonging and coronary dilatory properties. Naunyn Schmiedebergs Arch Pharmacol. 1985 May;329(3):316–325. doi: 10.1007/BF00501887. [DOI] [PubMed] [Google Scholar]
  37. Sutko J. L., Kenyon J. L. Ryanodine modification of cardiac muscle responses to potassium-free solutions. Evidence for inhibition of sarcoplasmic reticulum calcium release. J Gen Physiol. 1983 Sep;82(3):385–404. doi: 10.1085/jgp.82.3.385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Sutko J. L., Willerson J. T. Ryanodine alteration of the contractile state of rat ventricular myocardium. Comparison with dog, cat, and rabbit ventricular tissues. Circ Res. 1980 Mar;46(3):332–343. doi: 10.1161/01.res.46.3.332. [DOI] [PubMed] [Google Scholar]
  39. Wier W. G., Kort A. A., Stern M. D., Lakatta E. G., Marban E. Cellular calcium fluctuations in mammalian heart: direct evidence from noise analysis of aequorin signals in Purkinje fibers. Proc Natl Acad Sci U S A. 1983 Dec;80(23):7367–7371. doi: 10.1073/pnas.80.23.7367. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES