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Mechanism of hyperthyroidism-induced modulation of the L-type Ca2+ current in guinea pig ventricular myocytes

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Abstract

The positive inotropic effects of thyroid hormone in the heart, increased force and velocity of contraction have been mostly attributed to modulation of myosin ATPase isoenzymes (V1, V2 and V3), and sarcoplasmic reticulum Ca2+ pumping activity. In addition, we have suggested that the effects on ventricular contraction result from a thyroid hormone-induced increase in L-type Ca2+ current (I Ca, L). Due to the central role of I Ca, L in excitation-contraction coupling, we studied mechanisms whereby thyroid hormone augments this current. Since thyroid hormone modulates adenylate cyclase activity in various tissues, we tested the hypothesis that the hormone activates adenylate cyclase, leading to increased cyclic adenosine monophosphate (cAMP) levels, protein kinase A activation, Ca2+ channel phosphorylation and increased I Ca, L. We therefore stimulated or inhibited different sites along the “adenylate cyclase cascade”, and measured I Ca, L and isometric twitch in ventricular myocytes and papillary muscles from euthyroid and hyperthyroid guinea pigs. Our major findings were as follows. In euthyroid myocytes, 0.1 μM isoproterenol (Iso) increased I Ca, L (at V M=0 mV) from −7.04±0.72 to −22.26±1.88 pA/pF, P<0.05, while in hyperthyroid myocytes (I Ca, L=-21.48±2.94 pA/pF), Iso was ineffective. In euthyroid myocytes, intracellular application of cAMP (50 μM) was as potent as Iso, but ineffective in hyperthyroid myocytes. In hyperthyroid myocytes, a protein kinase A inhibitor (2 μM) lowered I Ca, L from −26.82±1.54 to -10.17±1.70 pApF (P<0.05), but had no effect in euthyroid myocytes. In hyperthyroid myocytes, acetylcholine (ACh) (1 μM) decreased I Ca, L from −26.86±1.49 to −18.33±1.25 pA/pF (P<0.05), while in euthyroid myocytes ACh decreased ICa, L from −6.80±0.61 to −6.00±0.39 pA/pF (NS). Accordingly, in hyperthyroid papillary muscles, ACh decreased twitch tension by 36.4±2.8%, but in euthyroid preparations only by 9.4±5.1% (P<0.05). These findings suggest that thyroid-hormone-induced increase in I Ca, L contributing to positive inotropy, is mediated by activation of the adenylate cyclase cascade.

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References

  1. Alpert NR, Mulieri LA, Litten RZ (1979) Functional significance of altered myosin adenosine triphosphatase activity in enlarged hearts. Am J Cardiol 44:947–953

    Google Scholar 

  2. Arai M, Otsu K, MacLennan DH, Alpert NR, Perasamy M (1991) Effect of thyroid hormone on the expression of mRNA encoding sarcoplasmic reticulum proteins. Circ Res 69:266–276

    Google Scholar 

  3. Beekman RE, Van Hardeveld C, Simonides WS (1988) Effect of thyroid state on cytosolic free calcium in resting and electrically stimulated cardiac myocytes. Biochim Biophys Acta 969:18–27

    Google Scholar 

  4. Bilezikian JP, Loeb JN (1983) The influence of hyperthyroidism and hypothyroidism on alpha- and beta-adrenergic receptors systems and adrenergic responsiveness. Endocr Rev 4:378–388

    Google Scholar 

  5. Binah O, Rubinstein I, Gilat E (1987) Effects of thyroid hormone on the action potential and membrane currents of guinea pig ventricular myocytes. Pflügers Arch 409:214–216

    Google Scholar 

  6. Felzen B, Rubinstein I, Lotan R, Binah O (1991) Developmental changes in ventricular action potential properties in guinea-pigs are modulated by age-related changes in the thyroid state. J Mol Cell Cardiol 23:787–794

    Google Scholar 

  7. Fischmeister R, Shrier A (1989) Interactive effects of isoprenaline, forskoline and acetylcholine on Ca2+ current in frog ventricular myocytes. J Physiol (Lond) 417:213–239

    Google Scholar 

  8. Flink IL, Reder JH, Morkin E (1979) Thyroid hormone stimulates synthesis of cardiac myosin isoenzyme. Comparison of the two dimensional patterns of cyanogen bromide peptides of cardiac myosin heavy chains from euthyroid and thyrotoxic rabbits. J Biol Chem 254:3105–3110

    Google Scholar 

  9. Guarnieri T, Filburn CR, Beard ES, Lakatta EG (1980) Enhanced contractile response and protein kinase activation of threshold levels of beta-adrenergic stimulation in hyperthyroid rat heart. J Clin Invest 65:861–868

    Google Scholar 

  10. Hamill OP, Marty A, Neher E, Sakmann B, Sigworth H (1981) Improved patch clamp techniques for high-resolution current recording from cell-free membrane patches. Pflügers Arch 391:85–100

    Google Scholar 

  11. Hammond HK, White RC, Buxton ILO, Saltzstein P, Brunton LL, Longhurst JC (1987) Increased myocardial beta-receptors and adrenergic responses in hyperthyroid pigs. Am J Physiol 252:H283-H290

    Google Scholar 

  12. Hashimoto H, Nakanishi M (1978) Influence of thyroid hormone on the positive inotropic effects mediated by alpha-and beta-adrenergic adrenoreceptors in isolated guinea pig atria and rabbit papillary muscle. Eur J Pharmacol 50:337–347

    Google Scholar 

  13. Hescheler J, Kameyama M, Trautwein W (1986) On the mechanism of muscarinic inhibition of the cardiac Ca current. Pflügers Arch 407:182–189

    Google Scholar 

  14. Hohl CM, Wetzel S, Fertel RH, Wimsatt DK, Brierley GP, Altschuld RA (1989) Hyperthyroid adult rat cardiomyocytes. I. Nucleotide content, beta-and alpha-adrenoreceptors, and cAMP production. Am J Physiol 257:C948-C956

    Google Scholar 

  15. Isenberg G, Klockner U (1982) Calcium tolerant ventricular myocytes prepared by preincubation in a “KB medium”. Pflügers Arch 395:6–18

    Google Scholar 

  16. Kameyama M, Hofmann F, Trautwein W (1985) On the mechanism of beta-adrenergic regulation of the Ca channel in the guinea-pig heart. Pflügers Arch 405:285–293

    Google Scholar 

  17. Kameyama M, Hescheler J, Hofmann F, Trautwein W (1986) Modulation of Ca current during the phosphorylation cycle in guinea pig heart. Pflügers Arch 407:123–128

    Google Scholar 

  18. Kim D, Smith TW (1985) Effects of thyroid hormone on calcium handling in cultured chick ventricular cells. J Physiol (Lond) 364:131–149

    Google Scholar 

  19. Morkin E, Flink IL, Goldman S (1983) Biochemical and physiologic effects of thyroid hormones on cardiac performance. Prog Cardiovasc Dis 25:436–464

    Google Scholar 

  20. Osaka T, Joyner RW (1992) Developmental changes in the beta-adrenergic modulation of calcium currents in rabbit ventricular cells. Circ Res 70:104–115

    Google Scholar 

  21. Palti Y, Adelman WJ (1969) Measurements of axonal membrane conductances and capacity by means of a varying potential control voltage clamp. J Membr Biol 1:431–458

    Google Scholar 

  22. Rapiejko PJ, Malbon CC (1987) Short-term hyperthyroidism modulates adenosine receptors and catalytic activity of adenylate cyclase in adipocytes. Biochem J 241:765–771

    Google Scholar 

  23. Rohrer D, Dillman WH (1988) Thyroid hormone markedly increases the mRNA coding for sarcoplasmic reticulum Ca2+-ATPase in the rat heart. J Biol Chem 263:6941–6944

    Google Scholar 

  24. Rubinstein I, Binah O (1989) Thyroid hormone modulates membrane currents in guinea pig ventricular myocytes. Naunyn Schmiedebergs Arch Pharmacol 340:705–711

    Google Scholar 

  25. Segal J, Buckley C, Ingbar S (1985) Stimulation of adenylate cyclase activity in rat thymocytes in vitro by 3,5,3′-triiodothyronine. Endocrinology 116:2036–2043

    Google Scholar 

  26. Stiles GL, Caron MG, Lefkowitz RJ (1984) Beta adrenergic receptors: biochemical mechanisms of physiological regulation. Physiol Rev 64:661–739

    Google Scholar 

  27. Suko J (1973) The calcium pump of cardiac sarcoplasmic recitulum: functional alterations at different levels of thyroid state in rabbits. J Physiol (Lond) 228:563–582

    Google Scholar 

  28. Sundaresan PR, Banerjee SP (1978) Differential regulation of beta adrenergic receptor coupled adenylate cyclase by thyroid hormones in rat liver and heart: possible role of corticosteroids. Horm Res 27:109–118

    Google Scholar 

  29. Wei JY, Spurgeon HA, Lakatta EG (1982) Electromechanical responsiveness of hyperthyroid cardiac muscle to beta-adrenergic stimulation. Am J Physiol 243:E114-E122

    Google Scholar 

  30. Winegrad S, Weisberg A, Lin EL, McClellan G (1986) Adrenergic regulation of myosin adenosine triphosphatase activity. Circ Res 58:83–95

    Google Scholar 

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Mager, S., Palti, Y. & Binah, O. Mechanism of hyperthyroidism-induced modulation of the L-type Ca2+ current in guinea pig ventricular myocytes. Pflügers Arch 421, 425–430 (1992). https://doi.org/10.1007/BF00370252

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  • DOI: https://doi.org/10.1007/BF00370252

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