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Eur J Cardiothorac Surg 2006;30:329-332
© 2006 Elsevier Science NL

The role of potassium channels in the vasodilatory effect of levosimendan in human internal thoracic arteries

Coskun Ustaa, Bilsen Ekserta, Ilhan Gölbasib, Zekiye Bigatc, Sadi S. Ozdema,*

a Department of Pharmacology, Akdeniz University, Medical Faculty, 07070 Antalya, Turkey
b Department of Cardiovascular Surgery, Akdeniz University, Medical Faculty, Antalya, Turkey
c Department of Anaesthesiology, Akdeniz University, Medical Faculty, Antalya, Turkey

Received 19 January 2006; received in revised form 15 May 2006; accepted 17 May 2006.

* Corresponding author. Tel.: +90 242 227 43 43x44163; fax: +90 242 247 44 82. (Email: sozdem{at}akdeniz.edu.tr).

Objective: We investigated the role of potassium channels in vasodilatory effect of levosimendan in human internal thoracic arteries. Methods: Samples of redundant internal thoracic arteries obtained from patients undergoing a coronary artery bypass graft surgery were cut into 3 mm wide rings and suspended in 20 ml organ baths. Isometric tension was continuously measured with an isometric force transducer connected to a computer-based data acquisition system. Results: Levosimendan (10–8–10–5 M) or cromakalim (10–8–10–5 M) produced concentration-dependent relaxation responses in human internal thoracic arteries precontracted by 10–6 M phenylephrine. The relaxant responses to levosimendan did not differ significantly between endothelium-intact and endothelium-denuded preparations. Incubation of human internal thoracic artery rings with adenosine 3',5'-triphosphate (ATP)-dependent potassium channel blocker glibenclamide (10–6 M) for 30 min significantly inhibited the relaxant responses to both levosimendan and cromakalim. The Ca2+-activated potassium channel blocker iberiotoxin (10–7 M) also caused a significant but smaller inhibition on relaxant responses to levosimendan. Incubation of the rings with the voltage-dependent potassium channel blocker 4-aminopyridine (5 mM) for 10 min did not cause significant alterations in relaxant responses to levosimendan. Conclusions: The findings of this study suggested that levosimendan-induced relaxation responses in human internal thoracic arteries were depended on the activation of ATP-dependent and Ca2+-activated potassium channels.

Key Words: Levosimendan • Potassium channel • Human internal thoracic artery • Vasodilatation




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