Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1995 Aug 1;486(Pt 3):647–659. doi: 10.1113/jphysiol.1995.sp020841

beta-adrenergic and cholinergic modulation of the inwardly rectifying K+ current in guinea-pig ventricular myocytes.

S Koumi 1, J A Wasserstrom 1, R E Ten Eick 1
PMCID: PMC1156553  PMID: 7473226

Abstract

1. Whole-cell patch-clamp technique was used to study the beta-adrenergic and cholinergic regulation of the inwardly rectifying K+ conductance (gK1) in isolated guinea-pig ventricular myocytes. 2. In Cl(-)-free solutions or in the presence of 9-anthracenecarboxylic acid or Co2+, bath-applied isoprenaline (Iso) partially inhibited the steady-state whole-cell conductance (gss) calculated from the steady-state current (Iss)-voltage (Iss-V) curve at membrane voltages (Vm) negative to the equilibrium potential for potassium (EK). Iss was also inhibited at Vm positive to EK when the extracellular [K+] was 20 mM. The Iso-sensitive component of gss exhibited the characteristics of the inwardly rectifying K+ conductance (gK1). 3. The Iso-induced inhibition of gK1 was reversible, concentration dependent, blocked by propranolol, mimicked by both forskolin and dibutyryl cAMP, and prevented by including a cAMP-dependent protein kinase (PKA) inhibitor in the pipette solution. These findings suggest that PKA mediates the Iso-induced inhibition of gK1. 4. The apparent dissociation constant (KD) for the concentration dependence of Iso-induced inhibition was 0.035 microM and the Hill coefficient was approximately 1.0. A maximal Iso concentration (1 microM) inhibited gK1 by 40 +/- 4.1% (mean +/- S.E.M.; n = 13). 5. Bath application of acetylcholine (ACh, 0.1 microM or more) antagonized the Iso-induced (1 microM) inhibition of gK1; [ACh] > 1.0 microM antagonized 88 +/- 2.1% (n = 10) of the inhibition. ACh increased the KD for Iso to inhibit Iso-sensitive gK1 and also reduced the maximal Iso-induced inhibition. 6. ACh-induced antagonism could be abolished by pre-incubating myocytes with pertussis toxin (PTX), suggesting that a muscarinic receptor-coupled, PTX-sensitive G protein, Gi, is involved. 7. ACh (10 microM) also antagonized approximately 70% of the dibutyryl cyclic AMP (1 mM)-induced inhibition of gK1 (n = 3), suggesting that the ACh-induced antagonism involves more than simply inhibiting the Iso-mediated activation of adenylyl cyclase via the activated Gi. 8. Intracellularly applied okadaic acid (OkA, 1 microM) did not alter gK1 (control = 134 +/- 5.1 nS vs. OkA = 136 +/- 6.1 nS), but the Iso-induced decrease in gK1 was less (P < 0.001) with OkA present (42.1 +/- 2.4 nS, n = 5) than when absent (54.0 +/- 2.2 nS, n = 10). However, ACh (10 microM) failed to antagonize Iso-induced inhibition with OkA present, suggesting involvement of a protein phosphatase.

Full text

PDF
658

Selected References

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

  1. Ahmad Z., Green F. J., Subuhi H. S., Watanabe A. M. Autonomic regulation of type 1 protein phosphatase in cardiac muscle. J Biol Chem. 1989 Mar 5;264(7):3859–3863. [PubMed] [Google Scholar]
  2. Bahinski A., Nairn A. C., Greengard P., Gadsby D. C. Chloride conductance regulated by cyclic AMP-dependent protein kinase in cardiac myocytes. Nature. 1989 Aug 31;340(6236):718–721. doi: 10.1038/340718a0. [DOI] [PubMed] [Google Scholar]
  3. Bennett P., McKinney L., Begenisich T., Kass R. S. Adrenergic modulation of the delayed rectifier potassium channel in calf cardiac Purkinje fibers. Biophys J. 1986 Apr;49(4):839–848. doi: 10.1016/S0006-3495(86)83713-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bialojan C., Takai A. Inhibitory effect of a marine-sponge toxin, okadaic acid, on protein phosphatases. Specificity and kinetics. Biochem J. 1988 Nov 15;256(1):283–290. doi: 10.1042/bj2560283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Boyden P. A., Cranefield P. F., Gadsby D. C. Noradrenaline hyperpolarizes cells of the canine coronary sinus by increasing their permeability to potassium ions. J Physiol. 1983 Jun;339:185–206. doi: 10.1113/jphysiol.1983.sp014711. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cheng H. C., Kemp B. E., Pearson R. B., Smith A. J., Misconi L., Van Patten S. M., Walsh D. A. A potent synthetic peptide inhibitor of the cAMP-dependent protein kinase. J Biol Chem. 1986 Jan 25;261(3):989–992. [PubMed] [Google Scholar]
  7. Gadsby D. C. Beta-adrenoceptor agonists increase membrane K+ conductance in cardiac Purkinje fibres. Nature. 1983 Dec 15;306(5944):691–693. doi: 10.1038/306691a0. [DOI] [PubMed] [Google Scholar]
  8. Giles W., Nakajima T., Ono K., Shibata E. F. Modulation of the delayed rectifier K+ current by isoprenaline in bull-frog atrial myocytes. J Physiol. 1989 Aug;415:233–249. doi: 10.1113/jphysiol.1989.sp017720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gilman A. G. G proteins: transducers of receptor-generated signals. Annu Rev Biochem. 1987;56:615–649. doi: 10.1146/annurev.bi.56.070187.003151. [DOI] [PubMed] [Google Scholar]
  10. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  11. Hartzell H. C. Regulation of cardiac ion channels by catecholamines, acetylcholine and second messenger systems. Prog Biophys Mol Biol. 1988;52(3):165–247. doi: 10.1016/0079-6107(88)90014-4. [DOI] [PubMed] [Google Scholar]
  12. Harvey R. D., Hume J. R. Autonomic regulation of a chloride current in heart. Science. 1989 May 26;244(4907):983–985. doi: 10.1126/science.2543073. [DOI] [PubMed] [Google Scholar]
  13. Hescheler J., Mieskes G., Rüegg J. C., Takai A., Trautwein W. Effects of a protein phosphatase inhibitor, okadaic acid, on membrane currents of isolated guinea-pig cardiac myocytes. Pflugers Arch. 1988 Aug;412(3):248–252. doi: 10.1007/BF00582504. [DOI] [PubMed] [Google Scholar]
  14. Isenberg G., Klockner U. Calcium tolerant ventricular myocytes prepared by preincubation in a "KB medium". Pflugers Arch. 1982 Oct;395(1):6–18. doi: 10.1007/BF00584963. [DOI] [PubMed] [Google Scholar]
  15. Kameyama M., Hofmann F., Trautwein W. On the mechanism of beta-adrenergic regulation of the Ca channel in the guinea-pig heart. Pflugers Arch. 1985 Oct;405(3):285–293. doi: 10.1007/BF00582573. [DOI] [PubMed] [Google Scholar]
  16. Katada T., Bokoch G. M., Smigel M. D., Ui M., Gilman A. G. The inhibitory guanine nucleotide-binding regulatory component of adenylate cyclase. Subunit dissociation and the inhibition of adenylate cyclase in S49 lymphoma cyc- and wild type membranes. J Biol Chem. 1984 Mar 25;259(6):3586–3595. [PubMed] [Google Scholar]
  17. Koumi S., Wasserstrom J. A., Ten Eick R. E. Beta-adrenergic and cholinergic modulation of inward rectifier K+ channel function and phosphorylation in guinea-pig ventricle. J Physiol. 1995 Aug 1;486(Pt 3):661–678. doi: 10.1113/jphysiol.1995.sp020842. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Matsuda J. J., Lee H., Shibata E. F. Enhancement of rabbit cardiac sodium channels by beta-adrenergic stimulation. Circ Res. 1992 Jan;70(1):199–207. doi: 10.1161/01.res.70.1.199. [DOI] [PubMed] [Google Scholar]
  19. Mitra R., Morad M. A uniform enzymatic method for dissociation of myocytes from hearts and stomachs of vertebrates. Am J Physiol. 1985 Nov;249(5 Pt 2):H1056–H1060. doi: 10.1152/ajpheart.1985.249.5.H1056. [DOI] [PubMed] [Google Scholar]
  20. Mogul D. J., Rasmussen H. H., Singer D. H., Ten Eick R. E. Inhibition of Na-K pump current in guinea pig ventricular myocytes by dihydroouabain occurs at high- and low-affinity sites. Circ Res. 1989 Jun;64(6):1063–1069. doi: 10.1161/01.res.64.6.1063. [DOI] [PubMed] [Google Scholar]
  21. Narahashi T., Tsunoo A., Yoshii M. Characterization of two types of calcium channels in mouse neuroblastoma cells. J Physiol. 1987 Feb;383:231–249. doi: 10.1113/jphysiol.1987.sp016406. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Neumann J., Gupta R. C., Schmitz W., Scholz H., Nairn A. C., Watanabe A. M. Evidence for isoproterenol-induced phosphorylation of phosphatase inhibitor-1 in the intact heart. Circ Res. 1991 Dec;69(6):1450–1457. doi: 10.1161/01.res.69.6.1450. [DOI] [PubMed] [Google Scholar]
  23. Nishiwaki S., Fujiki H., Suganuma M., Furuya-Suguri H., Matsushima R., Iida Y., Ojika M., Yamada K., Uemura D., Yasumoto T. Structure-activity relationship within a series of okadaic acid derivatives. Carcinogenesis. 1990 Oct;11(10):1837–1841. doi: 10.1093/carcin/11.10.1837. [DOI] [PubMed] [Google Scholar]
  24. Powell T., Twist V. W. Isoprenaline stimulation of cyclic AMP production by isolated cells from adult rat myocardium. Biochem Biophys Res Commun. 1976 Oct 4;72(3):1218–1225. doi: 10.1016/s0006-291x(76)80260-4. [DOI] [PubMed] [Google Scholar]
  25. Reuter H., Scholz H. The regulation of the calcium conductance of cardiac muscle by adrenaline. J Physiol. 1977 Jan;264(1):49–62. doi: 10.1113/jphysiol.1977.sp011657. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Tareen F. M., Ono K., Noma A., Ehara T. Beta-adrenergic and muscarinic regulation of the chloride current in guinea-pig ventricular cells. J Physiol. 1991;440:225–241. doi: 10.1113/jphysiol.1991.sp018705. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Tromba C., Cohen I. S. A novel action of isoproterenol to inactivate a cardiac K+ current is not blocked by beta and alpha adrenergic blockers. Biophys J. 1990 Sep;58(3):791–795. doi: 10.1016/S0006-3495(90)82422-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Tytgat J., Vereecke J., Carmeliet E. A combined study of sodium current and T-type calcium current in isolated cardiac cells. Pflugers Arch. 1990 Oct;417(2):142–148. doi: 10.1007/BF00370691. [DOI] [PubMed] [Google Scholar]
  29. Watanabe A. M., Besch H. R., Jr Interaction between cyclic adenosine monophosphate and cyclic gunaosine monophosphate in guinea pig ventricular myocardium. Circ Res. 1975 Sep;37(3):309–317. doi: 10.1161/01.res.37.3.309. [DOI] [PubMed] [Google Scholar]
  30. Yazawa K., Kameyama M. Mechanism of receptor-mediated modulation of the delayed outward potassium current in guinea-pig ventricular myocytes. J Physiol. 1990 Feb;421:135–150. doi: 10.1113/jphysiol.1990.sp017937. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES