Physiological and biochemical adrenergic regulation of the stunned myocardium

  • Dorothy E. Vatner
  • Stephen F. Vatner
Part of the Molecular and Cellular Biochemistry book series (DMCB, volume 28)

Abstract

A dual approach was employed to study ß-adrenergic receptor signal transduction in post ischemic (stunned) myocardium, examining physiological interventions in awake, chronically instrumented pigs and biochemical, cellular mechanisms in sarcolemmal preparations from the stunned hearts using the contralateral non-ischemic zone as a control. Ten min of coronary artery occlusion (CAO) and 30 min coronary artery reperfusion (CAR) resulted in depressed posterior wall-thickening (myocardial stunning). Isoproterenol increased transmural wall thickening more in stunned myocardium than in non-ischemic myocardium. In contrast, the responses of wall thickening to forskolin, actually decreased during stunning compared with control. NKH 477, a water soluble forskolin derivative, that does not activate cardiac nerves, increased wall thickening in non-ischemic tissue similarly to the effects on stunned myocardium. Increasing cardiac neural tone reflexly with inferior venal caval occlusion (IVCO) elicited similar results to forskolin, i.e., stunned myocardium responded with less of an increase in wall thickening as compared with non-ischemic myocardium, ß-adrenergic receptor density, as determined with 125I-cyanopindolol binding, was significantly increased in stunned subendocardium and subepicardium compared with respective values in non-ischemic myocardium. There were no differences in the response of adenylyl cyclase to isoproterenol in stunned and non-ischemic myocardium. The enhanced responsiveness of the ß-adrenergic receptor to isoproterenol stimulation in stunned myocardium corresponded to the increase in ß-adrenergic receptor density. The combination of enhanced responses to isoproterenol, and decreased responses to forskolin and to IVCO and preserved responsiveness to NKH 477, suggest that stunned myocardium is characterized by transient sympathetic neural stunning. The enhanced sensitivity to ß-adrenergic receptor stimulation has important clinical implications, both in terms of therapy of stunned myocardium and detection of stunned and /or hibernating myocardium, i.e., low dose dobutamine echocardiography. (Mol Cell Biochem 186: 131–137, 1998)

Key words

myocardial stunning ß-adrenergic receptor adenylyl cyclase coronary artery occlusion coronary artery reperfusion 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    Sato S, Sato N, Kudej RK, Uechi M, Asai K, Shen Y-T, Ishikawa Y, Vatner SF, Vatner DE: ß-Adrenergic receptor signalling in stunned myocardium of conscious pigs. J Mol Cell Cardiol 29: 1387–1400, 1997PubMedCrossRefGoogle Scholar
  2. 2.
    Vatner DE, Sato S, Vatner SF, Stasser RH: Sympathetic signal transduction in myocardial ischemia. In: GR Heyndrickx, SF Vatner, WC Wijns, (eds). Stunning, Hibernation and Preconditioning: Clinical Pathophysiology of Myocardial Ischemia. Lippincott-Raven, Philadelphia, New York, 1997, pp 31–48Google Scholar
  3. 3.
    Iwase M, Ishikawa Y, Shen Y-T, Shannon RP, Sato N, Ganguly PK, Eki T, Vatner DE, Vatner SF: Neurally mediated cardiac effects of forskolin in conscious dogs. Am J Physiol 271(Heart Circ Physiol 40): H1473–H1482, 1996PubMedGoogle Scholar
  4. 4.
    Eckstein RW: Coronary interarterial anastomoses in young pigs, and mongrel dogs. Circ Res 2: 460–465, 1954PubMedCrossRefGoogle Scholar
  5. 5.
    Patterson RE, Kirk ES: Analysis of coronary collateral structure, function, and ischemic border zones in pigs. Am J Physiol 244 (Heart Circ Physiol 13): H23–H31, 1983PubMedGoogle Scholar
  6. 6.
    Shen Y-T, Vatner SF: Differences in myocardial stunning following coronary artery occulsion in conscious dogs, pigs and baboons. Am J Physiol 270: H1312–H1322, 1996PubMedGoogle Scholar
  7. 7.
    Munson RJ, Rodbard D: LIGAND: A versatile computerized approach for characterization of ligand-binding systems. Anal Biochem 107: 220–239, 1980PubMedCrossRefGoogle Scholar
  8. 8.
    Ambrosio G, Jacobus WE, Bergman CA, Weisman HF, Becker LC: Preserved high energy phosphate metabolic reserve in globally’ stunned’ hearts despite reduction of basal ATP content and contractility. J Mol Cell Cardiol 19: 953–964, 1987PubMedCrossRefGoogle Scholar
  9. 9.
    Bolli R, Zhu W-X, Myers MD, Hartley CJ, Roberts R: Beta-adrenergic stimulation reverses postischemic myocardial dysfunction without producing subsequent functional deterioration. Am J Cardiol 56: 964–968, 1985PubMedCrossRefGoogle Scholar
  10. 10.
    Chiu WC, Kedem J, Scholz PM, Weiss HR: Regional asynchrony of segmental contraction may explain the ‘oxygen consumption paradox’ in stunned myocardium. Basic Res Cardiol 89: 149–162, 1994PubMedGoogle Scholar
  11. 11.
    Becker LC, Levine JH, DiPaula AF, Guarnieri T, Aversano T: Reversal of dysfunction in postischemic stunned myocardium by epinephrine and postextrasystolic potentiation. J Am Coll Cardiol 7: 580–589, 1986PubMedCrossRefGoogle Scholar
  12. 12.
    Gorge G, Papageorgiou I, Lerch R: Epinephrine-stimulated contractile and metabolic reserve in postischemic rat myocardium. Basic Res Cardiol 85: 595–605, 1990PubMedCrossRefGoogle Scholar
  13. 13.
    Ciuffo AA, Ouyang P, Becker LC, Levin L, Weisfeldt ML: Reduction of sympathetic inotropic response after ischemia in dogs: Contributor to stunned myocardium. J Clin Invest 75: 1504–1509, 1985PubMedCrossRefGoogle Scholar
  14. 14.
    Fan D, Soei LK, Sassen LMA, Krams R, Verdouw PD: Mechanical efficiency of stunned myocardium is modulated by increased afterload dependency. Cardiovasc Res 29: 428–437, 1995PubMedGoogle Scholar
  15. 15.
    Hashimoto T, Buxton DB, Krivokapick J, Hansen HW, Phelps MD, Schelbert HR: Responses of blood flow, oxygen consumption, and contractile function to inotropic stimulation in stunned canine myocardium. Am Heart J 126: 347–351, 1994Google Scholar
  16. 16.
    Krams R, Soei LK, McFalls EO, Prins EAW, Sassen LMA, Verdouw PD: End-systolic pressure length relations of stunned right and left ventricles after inotropic stimulation. Am J Physiol 265: H2099–H2109, 1993PubMedGoogle Scholar
  17. 17.
    Watanabe S, Buffington CW: Electromechanical association in regionally stunned swine myocardium. Anesthesiology 79: 1266–1277, 1993PubMedCrossRefGoogle Scholar
  18. 18.
    Zhou Z, Laskey RD, Hegge JO, Bunger R, Mentzer RM: Myocardial stunning: A therapeutic conundrum. J Thorac Cardiovas Surg 110: 1391–1401, 1995CrossRefGoogle Scholar
  19. 19.
    Mercier JC, Lando U, Kanmatsuse K, Ninomiya K, Meerbaum S, Fishbein MD, Swan HJC, Ganz W: Divergent effects of inotropic stimulation on the ischemic and severely depressed reperfused myocardium. Circulation 66: 397–400, 1982PubMedCrossRefGoogle Scholar
  20. 20.
    La Canna G, Alfieri O, Giubbini R, Gargano M, Ferrari R, Visioli O: Echocardiography during infusion of dobutamine for identification of reversible dysfunction in patients with chronic coronary artery disease. J Am Coll Cardiol 23: 617–626, 1994PubMedCrossRefGoogle Scholar
  21. 21.
    Susanni EE, Manders WT, Knight DR, Vatner DE, Vatner SF, Homcy CJ: One hour of myocardial ischemia decreases the activity of the stimulatory guanine-nucleotide regulatory protein Gs. Circ Res 65(4): 1145–1150, 1989PubMedCrossRefGoogle Scholar
  22. 22.
    Vatner DE, Young MA, Knight DR, Vatner SF: Beta-receptors and adenylate cyclase: Comparison of nonischemic, ischemic, and postmortem tissue. Am J Physiol 258: H140–H144, 1990PubMedGoogle Scholar
  23. 23.
    Vatner DE, Kiuchi K, Manders WT, Vatner SF: Effects of coronary arterial reperfusion on ß-adrenergic receptor-adenylyl cyclase coupling. Am J Physiol 264: H196–H204, 1993PubMedGoogle Scholar
  24. 24.
    Strasser RH, Marquetant R, Kubler W: Adrenergic receptors and sensitization of adenylyl cyclase in acute myocardial ischemia. Circulation 82(Suppl P): 23–29, 1990Google Scholar
  25. 25.
    Strasser RH, Marquetant R: Supersensitivity of the adenylyl cyclase system in acute myocardial ischemia: Evaluation of three independent mechanisms. Basic Res Cardiol 85(Suppl 1): 67–78, 1990PubMedGoogle Scholar
  26. 26.
    Strasser RH, Krimmer J, Braun-Dullaeus R, Marquetant R, Kubier W: Dual sensitization of the adrenergic system in early myocardial ischemia: Independent regulation of the ß-adrenergic receptors and adenylyl cyclase. J Mol Cell Cardiol 22(12): 1405–1423, 1990PubMedCrossRefGoogle Scholar
  27. 27.
    Strasser RH, Marquetant R, Kubler W: Independent sensitization of beta-adrenoceptors and adenylate cyclase in acute myocardial ischaemia. British J Clin Pharmacol 30(Suppl 1): 27S–35S, 1990CrossRefGoogle Scholar
  28. 28.
    Gutterman DD, Morgan DA, Miller FJ: Effect of brief myocardial ischemia on sympathetic coronary vasoconstriction. Circ Res 71(4): 960–969, 1992PubMedCrossRefGoogle Scholar
  29. 29.
    Hageman GR, Gantenberg NS: Attenuation of baroreflex changes in cardiac sympathetic efferent activities during acute myocardial ischemia. Am Heart J 126: 347–351, 1993PubMedCrossRefGoogle Scholar
  30. 30.
    Inoue H, Zipes DP: Time course of denervation of efferent sympathetic and vagal nerves after occlusion of the coronary artery in the canine heart. Circ Res 62(6): 1111–1120, 1988PubMedCrossRefGoogle Scholar
  31. 31.
    Neely BH, Hageman GR: Differential cardiac sympathetic activity during acute myocardial ischemia. Ami Physiol 258: H1534–H1541, 1990Google Scholar
  32. 32.
    Ninomiya I, Matsukawa K, Honda T, Nishiura N, Shirai M: Cardiac sympathetic nerve activity and heart rate during coronary occlusion in awake cats. Am J Physiol 251: H528–H537, 1986PubMedGoogle Scholar
  33. 33.
    Vatner DE: Characterization of the subfractions from a purified sarcolemma preparation of canine left ventricle. J Mol Cell Cardiol 22: 1349–1357, 1990PubMedCrossRefGoogle Scholar
  34. 34.
    Maisel AS, Motulsky HJ, Insel PA: Externalization of ß-adrenergic receptors promoted by myocardial ischemia. Science 230: 183–186, 1985PubMedCrossRefGoogle Scholar
  35. 35.
    Hartzell HC, Mery P-F, Fischmeister R, Szabo G: Sympathetic regulation of cardiac calcium current is due exclusively to cAMP-dependent phosphorylation. Nature 351: 573–576, 1991PubMedCrossRefGoogle Scholar
  36. 36.
    Yatani A, Codina J, Imoto Y, Reeves JP, Birnbaumer L, Brown AM: A G protein directly regulates mammalian cardiac calcium channels. Science 238: 1288–1292, 1987PubMedCrossRefGoogle Scholar
  37. 37.
    Iwase M, Bishop SP, Uechi M, Vatner DE, Shannon RP, Kudej RK, Wight DC, Wagner TE, Ishikawa Y, Homey CJ, Vatner SF: Adverse effects of chronic endogenous sympathetic drive induced by cardiac Gs alpha overexpression. Circ Res 78(4): 517–524, 1996PubMedCrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media Dordrecht 1998

Authors and Affiliations

  • Dorothy E. Vatner
    • 1
  • Stephen F. Vatner
    • 1
  1. 1.Cardiovascular and Pulmonary Research InstituteAllegheny University of the Health SciencesPittsburghUSA

Personalised recommendations