Abstract
Functionally skinned and electrochemically shunted myocytes were prepared by perfusing rat hearts with collagenase in order to obtain a technically improved measurement of sarcomere dynamics and to evaluate the role of sarcoplasmic reticulum in situ with respect to contractile activation. In the presence of micromolar calcium, the myocytes exhibited phasic and propagated contraction waves beginning at one end and proceeding along the myocyte. Beating rates, the propagation velocity of the activation wave, and single sarcomere shortening and relaxation velocities were obtained by manual or automated analysis of 16-mm film recorded at 170 frames/s from a camera attached to a microscope that was equipped with a temperature-controlled stage. In parallel experiments, calcium accumulation by the sarcoplasmic reticulum of the myocytes in situ was measured by direct isotopic tracer methods. The frequency (10-38 min-1) of spontaneous contractions, the velocity (1.9-7.4 microns . s-1) of sarcomere shortening, and the velocity (1.7-6.8 microns . s-1) of sarcomere relaxation displayed identical temperature dependences (Q10 = 2.2), which are similar to that of the calcium pump of sarcoplasmic reticulum and are consistent with a rate limit imposed by enzyme-catalyzed mechanisms on all these parameters. On the other hand, the velocity (77- 159 microns . s-1) of sequential sarcomere activation displayed a lower temperature dependence (Q10 = 1.5), which is consistent with a diffusion-limited and self-propagating release of calcium from one sarcomere to the other. The phasic contractile activity of the dissociated myocytes was inhibited by 10(-8)-10(6) M ryanodine (and not by myolemmal calcium blockers) under conditions in which calcium accumulation by sarcoplasmic reticulum in situ was demonstrated to proceed optimally. The effect of ryanodine is attributed to an interaction of this drug with sarcotubular structures, producing inhibition of calcium release from the sarcoplasmic reticulum. The consequent lack of sarcomere activation underlines the role of sarcoplasmic reticulum uptake and release in the phasic contractile activation of the electrochemically shunted myocytes.
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- Allen D. G., Blinks J. R., Prendergast F. G. Aequorin luminescence: relation of light emission to calcium concentration--a calcium-independent component. Science. 1977 Mar 11;195(4282):996–998. doi: 10.1126/science.841325. [DOI] [PubMed] [Google Scholar]
- Allen R. D., Allen N. S. Video-enhanced microscopy with a computer frame memory. J Microsc. 1983 Jan;129(Pt 1):3–17. doi: 10.1111/j.1365-2818.1983.tb04157.x. [DOI] [PubMed] [Google Scholar]
- Best P. M. Cardiac muscle function: results from skinned fiber preparations. Am J Physiol. 1983 Feb;244(2):H167–H177. doi: 10.1152/ajpheart.1983.244.2.H167. [DOI] [PubMed] [Google Scholar]
- Chiesi M., Ho M. M., Inesi G., Somlyo A. V., Somlyo A. P. Primary role of sarcoplasmic reticulum in phasic contractile activation of cardiac myocytes with shunted myolemma. J Cell Biol. 1981 Dec;91(3 Pt 1):728–742. doi: 10.1083/jcb.91.3.728. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dani A. M., Cittadini A., Inesi G. Calcium transport and contractile activity in dissociated mammalian heart cells. Am J Physiol. 1979 Sep;237(3):C147–C155. doi: 10.1152/ajpcell.1979.237.3.C147. [DOI] [PubMed] [Google Scholar]
- De Clerck N. M., Claes V. A., Brutsaert D. L. Force velocity relations of single cardiac muscle cells: calcium dependency. J Gen Physiol. 1977 Feb;69(2):221–241. doi: 10.1085/jgp.69.2.221. [DOI] [PMC free article] [PubMed] [Google Scholar]
- De Clerck N. M., Claes V. A., Van Ocken E. R., Brutsaert D. L. Sarcomere distribution patterns in single cardiac cells. Biophys J. 1981 Jul;35(1):237–242. doi: 10.1016/S0006-3495(81)84784-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Delay M. J., Ishide N., Jacobson R. C., Pollack G. H., Tirosh R. Stepwise sarcomere shortening: analysis by high-speed cinemicrography. Science. 1981 Sep 25;213(4515):1523–1525. doi: 10.1126/science.7280674. [DOI] [PubMed] [Google Scholar]
- Fabiato A. Effects of ryanodine in skinned cardiac cells. Fed Proc. 1985 Dec;44(15):2970–2976. [PubMed] [Google Scholar]
- Fabiato A., Fabiato F. Calculator programs for computing the composition of the solutions containing multiple metals and ligands used for experiments in skinned muscle cells. J Physiol (Paris) 1979;75(5):463–505. [PubMed] [Google Scholar]
- Fabiato A. Myoplasmic free calcium concentration reached during the twitch of an intact isolated cardiac cell and during calcium-induced release of calcium from the sarcoplasmic reticulum of a skinned cardiac cell from the adult rat or rabbit ventricle. J Gen Physiol. 1981 Nov;78(5):457–497. doi: 10.1085/jgp.78.5.457. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fabiato A. Rapid ionic modifications during the aequorin-detected calcium transient in a skinned canine cardiac Purkinje cell. J Gen Physiol. 1985 Feb;85(2):189–246. doi: 10.1085/jgp.85.2.189. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fabiato A. Time and calcium dependence of activation and inactivation of calcium-induced release of calcium from the sarcoplasmic reticulum of a skinned canine cardiac Purkinje cell. J Gen Physiol. 1985 Feb;85(2):247–289. doi: 10.1085/jgp.85.2.247. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ford L. E., Podolsky R. J. Regenerative calcium release within muscle cells. Science. 1970 Jan 2;167(3914):58–59. doi: 10.1126/science.167.3914.58. [DOI] [PubMed] [Google Scholar]
- Frank M., Sleator W. W. Effect of ryanodine on myocardial calcium. Naunyn Schmiedebergs Arch Pharmacol. 1975;290(1):35–47. doi: 10.1007/BF00499988. [DOI] [PubMed] [Google Scholar]
- Fry D. M., Scales D., Inesi G. The ultrastructure of membrane alterations of enzymatically dissociated cardiac myocytes. J Mol Cell Cardiol. 1979 Nov;11(11):1151–1163. doi: 10.1016/s0022-2828(79)80002-4. [DOI] [PubMed] [Google Scholar]
- GROSSMAN A., FURCHGOTT R. F. THE EFFECTS OF VARIOUS DRUGS ON CALCIUM EXCHANGE IN THE ISOLATED GUINEA-PIG LEFT AURICLE. J Pharmacol Exp Ther. 1964 Aug;145:162–172. [PubMed] [Google Scholar]
- González-Serratos H. Inward spread of activation in vertebrate muscle fibres. J Physiol. 1971 Feb;212(3):777–799. doi: 10.1113/jphysiol.1971.sp009356. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HILLYARD I. W., PROCITA L. The effect of ryanodine on the contractile strength of mammalian cardiac (atrial) muscle. J Pharmacol Exp Ther. 1959 Sep;127:22–28. [PubMed] [Google Scholar]
- Hilgemann D. W., Delay M. J., Langer G. A. Activation-dependent cumulative depletions of extracellular free calcium in guinea pig atrium measured with antipyrylazo III and tetramethylmurexide. Circ Res. 1983 Dec;53(6):779–793. doi: 10.1161/01.res.53.6.779. [DOI] [PubMed] [Google Scholar]
- Hunter D. R., Haworth R. A., Berkoff H. A. Modulation of cellular calcium stores in the perfused rat heart by isoproterenol and ryanodine. Circ Res. 1983 Nov;53(5):703–712. doi: 10.1161/01.res.53.5.703. [DOI] [PubMed] [Google Scholar]
- Inesi G., Millman M., Eletr S. Temperature-induced transitions of function and structure in sarcoplasmic reticulum membranes. J Mol Biol. 1973 Dec 25;81(4):483–504. doi: 10.1016/0022-2836(73)90518-4. [DOI] [PubMed] [Google Scholar]
- Inoué S. Video image processing greatly enhances contrast, quality, and speed in polarization-based microscopy. J Cell Biol. 1981 May;89(2):346–356. doi: 10.1083/jcb.89.2.346. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jones L. R., Besch H. R., Jr, Sutko J. L., Willerson J. T. Ryanodine-induced stimulation of net Ca++ uptake by cardiac sarcoplasmic reticulum vesicles. J Pharmacol Exp Ther. 1979 Apr;209(1):48–55. [PubMed] [Google Scholar]
- Kort A. A., Capogrossi M. C., Lakatta E. G. Frequency, amplitude, and propagation velocity of spontaneous Ca++-dependent contractile waves in intact adult rat cardiac muscle and isolated myocytes. Circ Res. 1985 Dec;57(6):844–855. doi: 10.1161/01.res.57.6.844. [DOI] [PubMed] [Google Scholar]
- Kushmerick M. J., Podolsky R. J. Ionic mobility in muscle cells. Science. 1969 Dec 5;166(3910):1297–1298. doi: 10.1126/science.166.3910.1297. [DOI] [PubMed] [Google Scholar]
- Lakatta E. G., Capogrossi M. C., Kort A. A., Stern M. D. Spontaneous myocardial calcium oscillations: overview with emphasis on ryanodine and caffeine. Fed Proc. 1985 Dec;44(15):2977–2983. [PubMed] [Google Scholar]
- Lakshminarayanaiah N., Bianchi C. P. Pharmacology of excitation-contraction coupling in skeletal muscle. Rev Pure Appl Pharmacol Sci. 1983 Jan-Mar;4(1):27–54. [PubMed] [Google Scholar]
- Marban E., Wier W. G. Ryanodine as a tool to determine the contributions of calcium entry and calcium release to the calcium transient and contraction of cardiac Purkinje fibers. Circ Res. 1985 Jan;56(1):133–138. doi: 10.1161/01.res.56.1.133. [DOI] [PubMed] [Google Scholar]
- Meissner G. Adenine nucleotide stimulation of Ca2+-induced Ca2+ release in sarcoplasmic reticulum. J Biol Chem. 1984 Feb 25;259(4):2365–2374. [PubMed] [Google Scholar]
- NAYLER W. G. Effect of ryanodine on cardiac muscle. Am J Physiol. 1963 Jun;204:975–978. doi: 10.1152/ajplegacy.1963.204.6.975. [DOI] [PubMed] [Google Scholar]
- Nayler W. G., Daile P., Chipperfield D., Gan K. Effect of ryanodine on calcium in cardiac muscle. Am J Physiol. 1970 Dec;219(6):1620–1626. doi: 10.1152/ajplegacy.1970.219.6.1620. [DOI] [PubMed] [Google Scholar]
- Penefsky Z. J., Kahn M. Mechanical and electrical effects of ryanodine on mammalian heart muscle. Am J Physiol. 1970 Jun;218(6):1682–1686. doi: 10.1152/ajplegacy.1970.218.6.1682. [DOI] [PubMed] [Google Scholar]
- Penefsky Z. J. Ultrastructural studies of the site of action of ryanodine on heart muscle. Pflugers Arch. 1974 Mar 11;347(3):185–198. doi: 10.1007/BF00592596. [DOI] [PubMed] [Google Scholar]
- Pessah I. N., Waterhouse A. L., Casida J. E. The calcium-ryanodine receptor complex of skeletal and cardiac muscle. Biochem Biophys Res Commun. 1985 Apr 16;128(1):449–456. doi: 10.1016/0006-291x(85)91699-7. [DOI] [PubMed] [Google Scholar]
- Pollack G. H., Iwazumi T., ter Keurs H. E., Shibata E. F. Sarcomere shortening in striated muscle occurs in stepwise fashion. Nature. 1977 Aug 25;268(5622):757–759. doi: 10.1038/268757a0. [DOI] [PubMed] [Google Scholar]
- Pollack G. H., Krueger J. W. Sarcomere dynamics in intact cardiac muscle. Eur J Cardiol. 1976 May;4 (Suppl):53–65. [PubMed] [Google Scholar]
- Rieser G., Sabbadini R., Paolini P., Fry M., Inesi G. Sarcomere motion in isolated cardiac cells. Am J Physiol. 1979 Jan;236(1):C70–C77. doi: 10.1152/ajpcell.1979.236.1.C70. [DOI] [PubMed] [Google Scholar]
- Roos K. P., Brady A. J. Individual sarcomere length determination from isolated cardiac cells using high-resolution optical microscopy and digital image processing. Biophys J. 1982 Dec;40(3):233–244. doi: 10.1016/S0006-3495(82)84478-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SLEATOR W., Jr, FURCHGOTT R. F., DE GUBAREFF T., KRESPI V. ACTION POTENTIALS OF GUINEA PIG ATRIA UNDER CONDITIONS WHICH ALTER CONTRACTION. Am J Physiol. 1964 Feb;206:270–282. doi: 10.1152/ajplegacy.1964.206.2.270. [DOI] [PubMed] [Google Scholar]
- Sutko J. L., Ito K., Kenyon J. L. Ryanodine: a modifier of sarcoplasmic reticulum calcium release in striated muscle. Fed Proc. 1985 Dec;44(15):2984–2988. [PubMed] [Google Scholar]
- 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]
- 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]
- Sutko J. L., Willerson J. T., Templeton G. H., Jones L. R., Besch H. R., Jr Ryanodine: its alterations of cat papillary muscle contractile state and responsiveness to inotropic interventions and a suggested mechanism of action. J Pharmacol Exp Ther. 1979 Apr;209(1):37–47. [PubMed] [Google Scholar]
- Tarr M., Trank J. W., Leiffer P., Shepherd N. Sarcomere length-resting tension relation in single frog atrial cardiac cells. Circ Res. 1979 Oct;45(4):554–559. doi: 10.1161/01.res.45.4.554. [DOI] [PubMed] [Google Scholar]
- Walter R. J., Berns M. W. Computer-enhanced video microscopy: digitally processed microscope images can be produced in real time. Proc Natl Acad Sci U S A. 1981 Nov;78(11):6927–6931. doi: 10.1073/pnas.78.11.6927. [DOI] [PMC free article] [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]
