Abstract

Background Coronary artery bypass graft (CABG) surgery is hampered by deleterious vasospasm in the vessel wall, especially in vein grafts. Endothelin (ET) is a strong vasoconstrictor that can be observed in increasing concentrations during CABG surgery. Methods Endothelin-induced vasoconstriction was evaluated in isolated, endothelium-denuded vessel segments of the human saphenous vein (SV), left internal mammary artery (LIMA), and coronary arteries. The ET A and ET B receptor mRNA levels were quantified by real-time polymerase chain reaction (PCR) analysis. Results The ET A and ET B receptor mRNA levels were significantly higher in the SV than in the LIMA and the coronary arteries. ET-1 induced a more efficacious contraction in the SV and LIMA as compared with in the coronary arteries. The ET B receptor agonist, Sarafotoxin 6c (S6c) stimulated constriction of the LIMA and SV, while inactive in the coronary arteries. The concentration-response curve for S6c was biphasic, suggesting activation of ET A receptors at high concentrations as this response could be inhibited by FR139317 (10 μmol/L), and ET B at low concentrations as this response could be inhibited by BQ788 (0.1 μmol/L). Conclusions Endothelin-induced vasoconstriction is mediated by ET A receptors alone in coronary arteries, while a combination of ET A and ET B receptors are of importance in SV and LIMA. Expression of contractile ET B receptors may be a pharmacologic disadvantage that contributes to the vasospasm during CABG surgery. The lower levels of ET A and ET B receptor mRNA in the LIMA and coronary arteries as compared with in the SV may provide one explanation for the better long- and short-term patency of LIMA as compared with SV grafts.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call