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Taurine relaxes human radial artery through potassium channel opening action

  • Ulusoy, Kemal Gokhan (Department of Medical Pharmacology, Gulhane Faculty of Medicine, University of Health Sciences) ;
  • Kaya, Erkan (Department of Cardiovascular Surgery, Gaziantep Faculty of Medicine, Gaziantep University) ;
  • Karabacak, Kubilay (Department of Cardiovascular Surgery, Gulhane Faculty of Medicine, University of Health Sciences) ;
  • Seyrek, Melik (Department of Medical Pharmacology, Gulhane Faculty of Medicine, University of Health Sciences) ;
  • Duvan, ibrahim (Department of Cardiovascular Surgery, Guven Hospital) ;
  • Yildirim, Vedat (Department of Anesthesiology, Gulhane Faculty of Medicine, University of Health Sciences) ;
  • Yildiz, Oguzhan (Department of Medical Pharmacology, Gulhane Faculty of Medicine, University of Health Sciences)
  • Received : 2017.04.09
  • Accepted : 2017.06.01
  • Published : 2017.11.01

Abstract

The vascular actions and mechanisms of taurine were investigated in the isolated human radial artery (RA). RA rings were suspended in isolated organ baths and tension was recorded isometrically. First, a precontraction was achieved by adding potassium chloride (KCl, 45 mM) or serotonin (5-hydroxytryptamine, 5-HT, $30{\mu}M$) to organ baths. When the precontractions were stable, taurine (20, 40, 80 mM) was added cumulatively. Antagonistic effect of taurine on calcium chloride ($10{\mu}M$ to 10 mM) -induced contractions was investigated. Taurine-induced relaxations were also tested in the presence of the $K^+$ channel inhibitors tetraethylammonium (1 mM), glibenclamide ($10{\mu}M$) and 4-aminopyridine (1 mM). Taurine did not affect the basal tone but inhibited the contraction induced by 5-HT and KCl. Calcium chloride-induced contractions were significantly inhibited in the presence of taurine (20, 40, 80 mM) (p<0.05). The relaxation to taurine was inhibited by tetraethylammonium (p<0.05). However, glibenclamide and 4-aminopyridine did not affect taurine -induced relaxations. Present experiments show that taurine inhibits 5-HT and KCl -induced contractions in RA, and suggest that large conductance $Ca^{2+}$-activated $K^+$ channels may be involved in taurine -induced relaxation of RA.

Keywords

References

  1. Huxtable RJ. Physiological actions of taurine. Physiol Rev. 1992;72:101-163. https://doi.org/10.1152/physrev.1992.72.1.101
  2. Oja SS, Saransaari P. Pharmacology of taurine. Proc West Pharmacol Soc. 2007;50:8-15.
  3. Militante JD, Lombardini JB. Treatment of hypertension with oral taurine: experimental and clinical studies. Amino Acids. 2002;23:381-393. https://doi.org/10.1007/s00726-002-0212-0
  4. Kohashi N, Katori R. Decrease of urinary taurine in essential hypertension. Jpn Heart J. 1983;24:91-102. https://doi.org/10.1536/ihj.24.91
  5. Abebe W, Mozaffari MS. Role of taurine in the vasculature: an overview of experimental and human studies. Am J Cardiovasc Dis. 2011;1:293-311.
  6. Franconi F, Giotti A, Manzini S, Martini F, Stendardi I, Zilletti L. The effect of taurine on high potassium- and noradrenaline-induced contraction in rabbit ear artery. Br J Pharmacol. 1982;75:605-612. https://doi.org/10.1111/j.1476-5381.1982.tb09180.x
  7. Ristori MT, Verdetti J. Effects of taurine on rat aorta in vitro. Fundam Clin Pharmacol. 1991;5:245-258. https://doi.org/10.1111/j.1472-8206.1991.tb00716.x
  8. Li N, Sawamura M, Nara Y, Ikeda K, Yamori Y. Direct inhibitory effects of taurine on norepinephrine-induced contraction in mesenteric artery of stroke-prone spontaneously hypertensive rats. Adv Exp Med Biol. 1996;403:257-262.
  9. Niu LG, Zhang MS, Liu Y, Xue WX, Liu DB, Zhang J, Liang YQ. Vasorelaxant effect of taurine is diminished by tetraethylammonium in rat isolated arteries. Eur J Pharmacol. 2008;580:169-174. https://doi.org/10.1016/j.ejphar.2007.10.039
  10. Liu Y, Niu L, Zhang W, Cui L, Zhang X, Liang Y, Zhang M. Effects of taurine on contractions of the porcine coronary artery. Pharmacol Rep. 2009;61:681-689. https://doi.org/10.1016/S1734-1140(09)70120-3
  11. Karabacak K, Kaya E, Ulusoy KG, Seyrek M, Kurtoglu M, Doganci S, Yildirim V, Yildiz O, Demirkilic U. Effects of taurine on contractions of human internal mammary artery: a potassium channel opening action. Eur Rev Med Pharmacol Sci. 2015;19:1498-1504.
  12. He GW. Verapamil plus nitroglycerin solution maximally preserves endothelial function of the radial artery: comparison with papaverine solution. J Thorac Cardiovasc Surg. 1998;115:1321-1327. https://doi.org/10.1016/S0022-5223(98)70215-6
  13. Nisanoglu V, Battaloglu B, Ozgur B, Eroglu T, Erdil N. Topical vasodilators for preventing radial artery spasm during harvesting for coronary revascularization: comparison of 4 agents. Heart Surg Forum. 2006;9:E807-812. https://doi.org/10.1532/HSF98.20061070
  14. Yildiz O, Seyrek M, Gul H. Pharmacology of arterial grafts for coronary artery bypass surgery. In: Aronow WS, editor. Artery bypass. Croatia: Intech; 2013. p.251-276.
  15. Mussa S, Choudhary BP, Taggart DP. Radial artery conduits for coronary artery bypass grafting: current perspective. J Thorac Cardiovasc Surg. 2005;129:250-253. https://doi.org/10.1016/j.jtcvs.2004.07.040
  16. Possati G, Gaudino M, Prati F, Alessandrini F, Trani C, Glieca F, Mazzari MA, Luciani N, Schiavoni G. Long-term results of the radial artery used for myocardial revascularization. Circulation. 2003;108:1350-1354. https://doi.org/10.1161/01.CIR.0000087402.13786.D0
  17. Seyrek M, Yildiz O, Ulusoy HB, Yildirim V. Testosterone relaxes isolated human radial artery by potassium channel opening action. J Pharmacol Sci. 2007;103:309-316. https://doi.org/10.1254/jphs.FP0060883
  18. Yildiz O, Seyrek M, Un I, Gul H, Candemir G, Yildirim V. The relationship between risk factors and testosterone-induced relaxations in human internal mammary artery. J Cardiovasc Pharmacol. 2005;45:4-7. https://doi.org/10.1097/00005344-200501000-00002
  19. Guven G, Seyrek M, Vural IM, Cehreli ZC, Yildiz O. Vasodilatory effect of hydroxyethyl methacrylate and triethylene glycol dimethacrylate in rat aorta through calcium antagonistic action. J Endod. 2011;37:353-357. https://doi.org/10.1016/j.joen.2010.11.038
  20. Quayle JM, McCarron JG, Brayden JE, Nelson MT. Inward rectifier $K^{+}$ currents in smooth muscle cells from rat resistance-sized cerebral arteries. Am J Physiol. 1993;265:C1363-1370. https://doi.org/10.1152/ajpcell.1993.265.5.C1363
  21. Xue WX, Zhang MS, Niu LG, Liu Y, Liang YQ. Vasodilation effects and mechanism of taurine on rat thoracic aortas. Chin J Pharmacol Toxicol. 2007;21:23-27.
  22. Tosun M, Paul RJ, Rapoport RM. Intracellular $Ca^{2+}$ elevation and contraction due to prostaglandin F2alpha in rat aorta. Eur J Pharmacol. 1997;340:203-208. https://doi.org/10.1016/S0014-2999(97)01415-5
  23. Xue W, Zhang M, Li J, Wu D, Niu L, Liang Y. Effects of taurine on aortic rings isolated from fructose-fed insulin resistance Sprague-Dawley rat are changed. Cardiovasc Drugs Ther. 2008;22:461-468. https://doi.org/10.1007/s10557-008-6124-9
  24. Briel G, Gylfe E, Hellman B, Neuhoff V. Microdetermination of free amino acids in pancreatic islets isolated from obese-hyperglycemic mice. Acta Physiol Scand. 1972;84:247-253. https://doi.org/10.1111/j.1748-1716.1972.tb05175.x
  25. Moran J, Hernandez-Pech X, Merchant-Larios H, Pasantes-Morales H. Release of taurine in apoptotic cerebellar granule neurons in culture. Pflugers Arch. 2000;439:271-277. https://doi.org/10.1007/s004240050940
  26. Song D, O'Regan MH, Phillis JW. Mechanisms of amino acid release from the isolated anoxic/reperfused rat heart. Eur J Pharmacol. 1998;351:313-322. https://doi.org/10.1016/S0014-2999(98)00318-5
  27. Lambert IH, Kristensen DM, Holm JB, Mortensen OH. Physiological role of taurine-from organism to organelle. Acta Physiol (Oxf). 2015;213:191-212. https://doi.org/10.1111/apha.12365
  28. Schaffer SW, Jong CJ, Ito T, Azuma J. Effect of taurine on ischemiareperfusion injury. Amino Acids. 2014;46:21-30. https://doi.org/10.1007/s00726-012-1378-8

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