Skip to main content
Log in

Effects of glyburide (glibenclamide) on myocardial function in Langendorff perfused rabbit heart and on myocardial contractility and slow calcium current in guinea-pig single myocytes

  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Abstract

Glyburide, also known as glibenclamide, was shown to have positive inotropic effect in human and animal hearts. The objectives of the present study was to investigate the effects of glyburide on developed left ventricular pressure (DLVP), coronary flow (CF), and heart rate (HR), in isolated rabbit heart as well as its effects on myocardial contractility and L-type calcium current, iCa, in guinea pig myocytes. Rabbit hearts were mounted on Langendorff apparatus and perfused with an oxygenated Krebs for 30 min until reaching steady state to be followed by 20 min of experimental perfusion divided into 5 min of control perfusion and 15 min of perfusion with Glyburide (10 μM). Ventricular myocytes were isolated by enzymatic dispersion technique and superfused in an oxygenated Tyrode solution. Cells were voltage-clamped at holding potential −40 mV to inactivate Na+ current and a step depolarizations, 200 msec duration, to 0 mV was applied to elicit iCa. The contractions of the myocytes were measured by optical methods. Glyburide significantly increased DLVP by 30% and CF by 36% but had no effect on HR. Glyburide increased cell contractility by 7 ± 6, 18 ± 7, 28 ± 9 and 54 ± 15% for 0.1, 1, 10 and 100 μM respectively, p < 0.001. Meanwhile it depressed iCa by 9 ± 6 and 19 ± 8% for 1 and 10 μM respectively. In conclusion, glyburide increased contractility of guinea pig single myocytes and of isolated rabbit heart, as indicated by increased developed left ventricular pressure while it depressed iCa. It is hypothesized that an elevation in intracellular calcium, which caused increased myocardial contractility, could be attributed to an increase in intracellular Na+ that could increase intracellular calcium via Na+/Ca2+ exchange.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Smallwood JK, Ertel JP, Steinberg MI: Modification by glibenclamide of the electrophysiological consequences of myocardial ischemia in dog and rabbit. Arch Pharmacol 342: 214-220, 1990

    Google Scholar 

  2. Linden J, Brooker G: The positive inotropic action of sulfonylureas. Diabetes 27: 694-698, 1978

    Google Scholar 

  3. Pogatsa G, Dubeez E: The direct effect of hypoglycemic sulfonylureas on myocardial contractile force and arterial blood pressure. Diabetologia 13: 515-519, 1977

    Google Scholar 

  4. Schaffer SW, Poole WG, Lampson WG, Kramer JH: Effect of Tolbutamide on the mechanical function of the isolated rat heart subjected to global ischemia. J Mol Cell Cardiol 13: 341-345, 1981

    Google Scholar 

  5. Rothschid MA, Rothschild AH, Pfeifer MA: The inotropic action of Tolbutamide and Glyburide. Clin Pharmacol Ther 45: 642-649, 1989

    Google Scholar 

  6. Khatib SY, Al-Hader AA: Effect of glyburide on ATP, creatine phosphate and LVP in isolated rabbit heart. J Moll Cell Cardiol 24(suppl 1): O-07, 1993

    Google Scholar 

  7. Decking UK, Reffelman T, Schrader J, Kammermeier H: Hypoxia-induced activation of KATP channels limit energy depletion in the guinea-pig heart. Am J Physiol 269: H734-H742, 1995

    Google Scholar 

  8. Docherty JC, Gunter HT, Kuzio B, Shoemaker L, Yang L, Deslauriers R: Effects of Cromakalim and Glibenclamide on myocardial high-energy phosphates and intracellular pH during ischemia-reperfusion. J Mol Cell Cardiol 29: 1665-1673, 1997

    Google Scholar 

  9. Mitani A, Kinoshita K, Fukamachi K, Sakamoto M, Kurisu K, Tsuruhara Y, Fukamura F, Nakashima A, Tokunaga K: Effects of Glibenclamide and Nicorandil on cardiac function during ischemia and reperfusion in isolated perfused rat heart. Am J Physiol 261: H1864-H1871, 1991

    Google Scholar 

  10. Kim SH, Cho KW, Chang SH, Kim SZ, Chae SW: Glibenclamide suppresses stretch-activated ANP secretion: Involvement of K+ATP channel and L-type Ca2+ channel modulation. Pflügers Arch 434: 362-372, 1997

    Google Scholar 

  11. Dubach V, Burelschardt D, Raeder E, Forgo I et al.: Effect of intravenous Tolbutamide and Glibenclamide on myocardial contractility. Cardiology 64: 208-294, 1979

    Google Scholar 

  12. Boyett MR, Honjo H, Harrison S, Zang W, Kirby M: Ultra slow voltage-dependent inactivation of the calcium current in guineas-pig and ferret ventricular myocytes. Pflügers Arch 428: 39-50, 1994

    Google Scholar 

  13. Boyett MR, Moore M, Jewell BR, Montgomery RAP, Kirby MS, Orchard CH: An improved apparatus for the optical recording of contraction of single heart cells. Pflügers Arch 413: 197-205, 1988

    Google Scholar 

  14. Schaffer SW, Boen HT, Mahmood SM: Effect of Glyburide on myocardial metabolism and function. Am J Med 79(suppl 3B): 48-52, 1985

    Google Scholar 

  15. Wikstrom BG, Ronquist G, Waldenstrom A: Glyburide enhancement of lactate production in ischemic heart is modified by preconditioning: An in vivo experimental study in pigs by microdialysis technique. J Cardiovasc Pharmacol 27: 622-628, 1996

    Google Scholar 

  16. Ganong WF: Review of Medical Physiology. Appelton & Lange, Connecticut, 1991, pp 530, 574

    Google Scholar 

  17. Lodge NJ, Colatsky TJ, Cullinan CA, Follmer CH: Electromechanical effects of the putative potassium channel activator Celikalim on feline atrial and ventricular muscle. J Pharmacol Exp Ther 261: 1153-1159, 1992

    Google Scholar 

  18. Olbrich H, Muller M, Lindner S, Henke B et al.: Glimepiride inhibits the Relmakalim induced decrease in intracellular free calcium and contraction of isolated heart muscle cells from guinea pig to a lesser extent than Glibencalimde. Int J Cardiol 72: 53-63, 1999

    Google Scholar 

  19. Lopez JR, Jahangir R, Jahangir A, Shen WK, Terzie A: Potassium channel openers prevent potassium-induced calcium loading of cardiac cells: Possible implication in cardioplegia. J Thorac Cardiovasc Surg 112: 820-831, 1996

    Google Scholar 

  20. Frampton JE, Orchard CH, Boyett MR: Diastolic, systolic and sarcoplasmic [Ca2+] during inotropic interventions in isolated rat myocytes. J Physiol 437: 351-375, 1991

    Google Scholar 

  21. Harrison S, Frampton J, McCall E, Boyett MR, Orchard CH: Contraction and intracellular Ca2+, Na+, and H+ during acidosis in rat ventricular myocytes. Am J Physiol 262: C348-C357, 1992

    Google Scholar 

  22. Maxwell K, Scott J, Omelchenko A, Lukas A, Liyan L, Hnatowich M et al.: Functional role of regulation of Na+/Ca2+ exchange assessed in transgenic mouse hearts. AJP-Heart Circ Physiol 277: H2212-H2221, 1999

    Google Scholar 

  23. Harrison SM, McCall E, Boyett MR: The relationship between contraction and intracellular sodium in rat and guinea pig ventricular myocytes. J Physiol 449: 517-550, 1992

    Google Scholar 

  24. Ribalet B, Mirrell CJ, Johnson DG, Levin SR: Sulfonylurea binding to a low-affinity site inhibits the Na/K-ATPase and the KATP channel in insulin-secreting cells. J Gen Physiol 107: 231-241, 1996

    Google Scholar 

  25. Billman GE, Avendano C, Halliwill JR, Burroughs JM: The effects of the ATP-dependent potassium channel antagonist, Glyburide, on coronary blood and susceptibility to ventricular fibrillation in unanesthetized dogs. J Cardiovasc Pharmacol 21: 197-204, 1993

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Khatib, S.Y., Boyett, M.R. Effects of glyburide (glibenclamide) on myocardial function in Langendorff perfused rabbit heart and on myocardial contractility and slow calcium current in guinea-pig single myocytes. Mol Cell Biochem 242, 81–87 (2003). https://doi.org/10.1023/A:1021137712039

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1021137712039

Navigation