Abstract
1. Membrane current and mechanical activity were recorded from short segments of frog atrial muscle strips using a double sucrose gap voltage clamp arrangement. Experiments were performed at 4-7° C. Two types of contraction were observed dependent upon the duration of the clamp.
2. Short-lasting depolarizations caused a flow of Ca inward current, ICa, and development of a phasic contraction. Time to peak tension approximated 400 msec. Both ICa and contraction, as functions of membrane potential, had a threshold of about — 40 mV and were maximal at inside positive potentials in normal Ringer fluid. Peak tension decreased at strong depolarizations.
3. The minimum time of depolarization required for initiation of a phasic contraction was 40-70 msec. The time necessary for full activation of contraction was 200-300 msec and comparable to the period of time covered by the flow of ICa.
4. There was no marked change in peak tension upon repetitive depolarization to the same membrane potential.
5. Restoration of (phasic) contractility after a preceding contraction was strongly dependent on the level of membrane potential between conditioning and test pulse. Restoration was half complete at potentials around — 45 mV.
6. Long-lasting depolarizations generated tonic (sustained) contractions superimposed on the phasic (transient) ones. Threshold potential for initiation of tonic contractions was usually positive to the threshold of phasic contractions. The time taken to attain the final level of tension ranged between 0·7 and 3 sec. Plateau tension, as a function of membrane potential, increased with increasing depolarization and reached a flat maximum at about + 50 mV in normal Ringer fluid.
7. At membrane potentials near zero level, plateau tension developed by the tonic mechanism was about twice peak tension due to phasic contraction.
8. Removal of Ca ions from the external medium resulted in an almost complete abolition of phasic contraction within 1-2 min and a gradual decrease of tonic contraction during the first 10 min. Application of a `Ca inhibitor' to normal Ringer fluid caused a strong reduction of both ICa and phasic contraction without affecting tonic contractions.
9. It is concluded that phasic contractions are directly activated by the flow of ICa. Generation of tonic contractions may be attributed to a Ca transfer mechanism different from ICa or a release of Ca from intracellular stores.
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Selected References
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- ANTONI H., DELIUS W. NACHWEIS VON ZWEI KOMPONENTEN IN DER ANSTIEGSPHASE DES AKTIONSPONTENTIALS VON FROSCHMYOKARDFASERN. Pflugers Arch Gesamte Physiol Menschen Tiere. 1965 Apr 6;283:187–202. [PubMed] [Google Scholar]
- Antoni H., Jacob R., Kaufmann R. Mechanische Reaktionen des Frosch- und Säugetiermyokards bei Veränderung der Aktionspotential-Dauer durch konstante Gleichstromimpulse. Pflugers Arch. 1969;306(1):33–57. doi: 10.1007/BF00586610. [DOI] [PubMed] [Google Scholar]
- Beeler G. W., Jr, Reuter H. Membrane calcium current in ventricular myocardial fibres. J Physiol. 1970 Mar;207(1):191–209. doi: 10.1113/jphysiol.1970.sp009056. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Beeler G. W., Jr, Reuter H. The relation between membrane potential, membrane currents and activation of contraction in ventricular myocardial fibres. J Physiol. 1970 Mar;207(1):211–229. doi: 10.1113/jphysiol.1970.sp009057. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Beeler G. W., Jr, Reuter H. Voltage clamp experiments on ventricular myocarial fibres. J Physiol. 1970 Mar;207(1):165–190. doi: 10.1113/jphysiol.1970.sp009055. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brown H. F., Noble S. J. A quantitative analysis of the slow component of delayed rectification in frog atrium. J Physiol. 1969 Oct;204(3):737–747. doi: 10.1113/jphysiol.1969.sp008941. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brown H. F., Noble S. J. Membrane currents underlying delayed rectification and pace-maker activity in frog atrial muscle. J Physiol. 1969 Oct;204(3):717–736. doi: 10.1113/jphysiol.1969.sp008940. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CALDWELL P. C., WALSTER G. STUDIES ON THE MICRO-INJECTION OF VARIOUS SUBSTANCES INTO CRAB MUSCLE FIBRES. J Physiol. 1963 Nov;169:353–372. doi: 10.1113/jphysiol.1963.sp007261. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chapman R. A., Niedergerke R. Effects of calcium on the contraction of the hypodynamic frog heart. J Physiol. 1970 Dec;211(2):389–421. doi: 10.1113/jphysiol.1970.sp009284. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chapman R. A., Niedergerke R. Interaction between heart rate and calcium concentration in the control of contractile strength of the frog heart. J Physiol. 1970 Dec;211(2):423–443. doi: 10.1113/jphysiol.1970.sp009285. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chapman R. A., Tunstall J. The dependence of the contractile force generated by frog auricular trabeculae upon the external calcium concentration. J Physiol. 1971 May;215(1):139–162. doi: 10.1113/jphysiol.1971.sp009462. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Clark A. J. The action of ions and lipoids upon the frog's heart. J Physiol. 1913 Oct 17;47(1-2):66–107. doi: 10.1113/jphysiol.1913.sp001614. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ebashi S., Endo M., Otsuki I. Control of muscle contraction. Q Rev Biophys. 1969 Nov;2(4):351–384. doi: 10.1017/s0033583500001190. [DOI] [PubMed] [Google Scholar]
- Fozzard H. A., Hellman D. C. Relationship between membrane voltage and tension in voltage-clamped cardiac purkinje fibres. Nature. 1968 May 11;218(5141):588–589. doi: 10.1038/218588a0. [DOI] [PubMed] [Google Scholar]
- Fuchs F., Briggs F. N. The site of calcium binding in relation to the activation of myofibrillar contraction. J Gen Physiol. 1968 May;51(5):655–676. doi: 10.1085/jgp.51.5.655. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons W. R., Fozzard H. A. Voltage dependence and time dependence of contraction in sheep cardiac Purkinje fibers. Circ Res. 1971 Apr;28(4):446–460. doi: 10.1161/01.res.28.4.446. [DOI] [PubMed] [Google Scholar]
- Goto M., Kimoto Y., Kato Y. A study on the excitation-contraction coupling of the bullfrog ventricle with voltage clamp technique. Jpn J Physiol. 1971 Apr;21(2):159–173. doi: 10.2170/jjphysiol.21.159. [DOI] [PubMed] [Google Scholar]
- HODGKIN A. L., HOROWICZ P. Potassium contractures in single muscle fibres. J Physiol. 1960 Sep;153:386–403. doi: 10.1113/jphysiol.1960.sp006541. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Haas H. G., Kern R., Einwächter H. M., Tarr M. Kinetics of Na inactivation in frog atria. Pflugers Arch. 1971;323(2):141–157. doi: 10.1007/BF00586445. [DOI] [PubMed] [Google Scholar]
- Hagiwara S., Nakajima S. Differences in Na and Ca spikes as examined by application of tetrodotoxin, procaine, and manganese ions. J Gen Physiol. 1966 Mar;49(4):793–806. doi: 10.1085/jgp.49.4.793. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KAVALER F. Membrane depolarization as a cause of tension development in mammalian ventricular muscle. Am J Physiol. 1959 Nov;197:968–970. doi: 10.1152/ajplegacy.1959.197.5.968. [DOI] [PubMed] [Google Scholar]
- Katz A. M. Contractile proteins of the heart. Physiol Rev. 1970 Jan;50(1):63–158. doi: 10.1152/physrev.1970.50.1.63. [DOI] [PubMed] [Google Scholar]
- LUTTGAU H. C., NIEDERGERKE R. The antagonism between Ca and Na ions on the frog's heart. J Physiol. 1958 Oct 31;143(3):486–505. doi: 10.1113/jphysiol.1958.sp006073. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Léoty C., Raymond G., Gargouïl Y. M. Tension phasique et tonique de la fibre myocardique de grenouille et les courants ioniques transmembranaires; étude en voltage imposé et par microphotométrie. C R Acad Sci Hebd Seances Acad Sci D. 1970 Oct 28;271(17):1545–1548. [PubMed] [Google Scholar]
- Morad M., Orkand R. K. Excitation-concentration coupling in frog ventricle: evidence from voltage clamp studies. J Physiol. 1971 Dec;219(1):167–189. doi: 10.1113/jphysiol.1971.sp009656. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morad M., Trautwein W. The effect of the duration of the action potential on contraction in the mammalian heart muscle. Pflugers Arch Gesamte Physiol Menschen Tiere. 1968;299(1):66–82. doi: 10.1007/BF00362542. [DOI] [PubMed] [Google Scholar]
- NIEDERGERKE R. MOVEMENTS OF CA IN FROG HEART VENTRICLES AT REST AND DURING CONTRACTURES. J Physiol. 1963 Jul;167:515–550. doi: 10.1113/jphysiol.1963.sp007166. [DOI] [PMC free article] [PubMed] [Google Scholar]
- NIEDERGERKE R. Movements of Ca in beating ventricles of the frog heart. J Physiol. 1963 Jul;167:551–580. doi: 10.1113/jphysiol.1963.sp007167. [DOI] [PMC free article] [PubMed] [Google Scholar]
- NIEDERGERKE R. The staircase phenomenon and the action of calcium on the heart. J Physiol. 1956 Dec 28;134(3):569–583. doi: 10.1113/jphysiol.1956.sp005666. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Niedergerke R., Orkand R. K. The dual effect of calcium on the action potential of the frog's heart. J Physiol. 1966 May;184(2):291–311. doi: 10.1113/jphysiol.1966.sp007916. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Noble D., Tsien R. W. Outward membrane currents activated in the plateau range of potentials in cardiac Purkinje fibres. J Physiol. 1969 Jan;200(1):205–231. doi: 10.1113/jphysiol.1969.sp008689. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Noble D., Tsien R. W. Reconstruction of the repolarization process in cardiac Purkinje fibres based on voltage clamp measurements of membrane current. J Physiol. 1969 Jan;200(1):233–254. doi: 10.1113/jphysiol.1969.sp008690. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Noble D., Tsien R. W. The kinetics and rectifier properties of the slow potassium current in cardiac Purkinje fibres. J Physiol. 1968 Mar;195(1):185–214. doi: 10.1113/jphysiol.1968.sp008454. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Orkand R. K. Facilitation of heart muscle contraction and its dependence on external calcium and sodium. J Physiol. 1968 May;196(2):311–325. doi: 10.1113/jphysiol.1968.sp008509. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PORTZEHL H., CALDWELL P. C., RUEEGG J. C. THE DEPENDENCE OF CONTRACTION AND RELAXATION OF MUSCLE FIBRES FROM THE CRAB MAIA SQUINADO ON THE INTERNAL CONCENTRATION OF FREE CALCIUM IONS. Biochim Biophys Acta. 1964 May 25;79:581–591. doi: 10.1016/0926-6577(64)90224-4. [DOI] [PubMed] [Google Scholar]
- Rougier O., Vassort G., Garnier D., Gargouil Y. M., Coraboeuf E. Existence and role of a slow inward current during the frog atrial action potential. Pflugers Arch. 1969;308(2):91–110. doi: 10.1007/BF00587018. [DOI] [PubMed] [Google Scholar]
- Sands S. D., Winegrad S. Treppe and total calcium content of the frog ventricle. Am J Physiol. 1970 Mar;218(3):908–910. doi: 10.1152/ajplegacy.1970.218.3.908. [DOI] [PubMed] [Google Scholar]
- Sommer J. R., Johnson E. A. Cardiac muscle. A comparative ultrastructural study with special reference to frog and chicken hearts. Z Zellforsch Mikrosk Anat. 1969;98(3):437–468. [PubMed] [Google Scholar]
- Staley N. A., Benson E. S. The ultrastructure of frog ventricular cardiac muscle and its relationship to mechanism of excitation-contraction coupling. J Cell Biol. 1968 Jul;38(1):99–114. doi: 10.1083/jcb.38.1.99. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tarr M., Trank J. Equivalent circuit of frog atrial tissue as determined by voltage clamp-unclamp experiments. J Gen Physiol. 1971 Nov;58(5):511–522. doi: 10.1085/jgp.58.5.511. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tarr M. Two inward currents in frog atrial muscle. J Gen Physiol. 1971 Nov;58(5):523–543. doi: 10.1085/jgp.58.5.523. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vassort G., Rougier O., Favelier J. Influence du potentiel de membrane et des courants transmembranaires sur l'activité contractile des faisceaux sino-auriculaires de la grenouille. Arch Int Physiol Biochim. 1971 Apr;79(2):401–406. doi: 10.3109/13813457109085323. [DOI] [PubMed] [Google Scholar]
- Vassort G., Rougier O. Membrane potential and slow inward current dependence of frog cardiac mechanical activity. Pflugers Arch. 1972;331(3):191–203. doi: 10.1007/BF00589126. [DOI] [PubMed] [Google Scholar]
- Winegrad S. Studies of cardiac muscle with a high permeability to calcium produced by treatment with ethylenediaminetetraacetic acid. J Gen Physiol. 1971 Jul;58(1):71–93. doi: 10.1085/jgp.58.1.71. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wood E. H., Heppner R. L., Weidmann S. Inotropic effects of electric currents. I. Positive and negative effects of constant electric currents or current pulses applied during cardiac action potentials. II. Hypotheses: calcium movements, excitation-contraction coupling and inotropic effects. Circ Res. 1969 Mar;24(3):409–445. doi: 10.1161/01.res.24.3.409. [DOI] [PubMed] [Google Scholar]
