Thromboxane receptor stimulation suppresses guanylate cyclase-mediated relaxation of radial arteries

Background. The internal mammary artery (IMA) and the radial artery (RA) are routinely used in coronary artery bypass grafting. However, RA grafts have a higher incidence of postoperative vasospasm and comparatively poor patency rates. The present study was undertaken to investigate the signaling pathways mediating contraction and relaxation in the IMA and RA with the aim of better understanding the mechanism underlying the propensity of RA grafts to spasm. Methods. We examined the contractile responses of the IMA and RA to KC1 (a depolarizing agent), phenylephrine (an alpha-adrenergic agonist), and U46619 (a thromboxane analogue). Results. Contractions induced by KC1 or U46619 did not significantly differ in IMA and RA. By contrast, phenylephrine evoked significantly greater contraction of the IMA than the RA. Contractions induced by both phenylephrine and U46619 were dose-dependently inhibited by nifedipine ( an L-type calcium channel blocker). Estimation of thromboxane A(2) (TxA(2)) and prostacyclin (PGI(2)) synthesis revealed that the TxA(2) to PGI(2) ratio in the RA was twice that in the IMA. Moreover, acetylcholine-induced and nitroglycerin-induced relaxation of RA precontracted with U46619 was significantly impaired, as compared with RA precontracted with phenylephrine. These data suggest that inhibition of nitroglycerin-induced soluble guanylate cyclase activity by U46619 was at least partially responsible for the diminished vasodilatory response of RA to nitric oxide. Conclusions. Our findings suggest that by reducing nitric oxide-stimulated soluble guanylate cyclase activity, the higher TxA(2) to PGI(2) ratios in RA, and the elevated serum TxA(2) levels seen during coronary artery bypass grafting operations, may underlie the vasospasm and poor patency rates seen with the RA.