Department of Cardiovascular Surgery, Cumhuriyet University School of Medicine, Sivas 58140, Turkey.
Can J Physiol Pharmacol. 2009 Aug;87(8):595-601. doi: 10.1139/y09-043.
Radial artery (RA) vasospasm remains a potential cause of early graft failure after coronary artery bypass graft surgery, despite pretreatment with alpha-adrenergic or calcium channel blockers. Our aim was to investigate the mechanism of the vasorelaxant effects of Rho-kinase inhibitors (Y-27632 and fasudil) on the human RA. Segments were obtained from 30 patients undergoing coronary artery bypass graft and were divided into 3-4 mm vascular rings. The rings were stimulated with 10(-5) mol/L phenylephrine (PE) by using the isolated tissue bath technique and were relaxed with 10(-6) mol/L acetylcholine. Relaxation responses were recorded for Y-27632 (10(-9)-10(-4) mol/L), fasudil (10(-9)-10(-4) mol/L), and sodium nitroprusside (SNP) (10(-9)-10(-5) mol/L). Y-27632 and fasudil relaxation responses were repeated in either N(G)-nitro-L-arginine (L-NNA), which is a specific endothelial nitric oxide synthase inhibitor, or 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ), which is a guanylate cyclase inhibitor. SNP relaxation responses were repeated in 10(-8) mol/L Y-27632 and 10(-8) mol/L fasudil. Y-27632 and fasudil caused concentration-dependent vasorelaxation in RA rings precontracted with PE, and maximal relaxation (100%) was recorded at the highest concentration used (10(-4) mol/L). The vasorelaxant effects of Y-27632 and fasudil were significantly reduced in the presence of L-NNA and ODQ, and the pD2 values of Y-27632 and fasudil were not changed. The vasorelaxant effects of SNP were significantly increased in the presence of Y-27632 and fasudil, and the pD(2) values of SNP were not changed. These findings indicate that Y-27632 and fasudil caused concentration-dependent vasorelaxation in the RA rings. Because this effect was decreased in a dose-dependent manner by L-NNA and ODQ, the relaxant effects of Y-27632 and fasudil could be due to stimulation by nitric oxide that is being released. Rho-kinase inhibitors may have an important role in preventing vasospasm in arterial grafts used for coronary artery surgery.
桡动脉(RA)痉挛仍然是冠状动脉旁路移植术后早期移植物失败的潜在原因,尽管在术前使用了α-肾上腺素能或钙通道阻滞剂。我们的目的是研究 Rho-激酶抑制剂(Y-27632 和法舒地尔)对人 RA 的血管舒张作用的机制。从 30 名接受冠状动脉旁路移植术的患者中获得节段,并将其分为 3-4mm 血管环。使用离体组织浴技术,用 10(-5)mol/L 苯肾上腺素(PE)刺激环,并使用 10(-6)mol/L 乙酰胆碱使其松弛。记录 Y-27632(10(-9)-10(-4)mol/L)、法舒地尔(10(-9)-10(-4)mol/L)和硝普钠(SNP)(10(-9)-10(-5)mol/L)的松弛反应。Y-27632 和法舒地尔的松弛反应在 N(G)-硝基-L-精氨酸(L-NNA)(一种特异性内皮型一氧化氮合酶抑制剂)或 1H-[1,2,4]恶二唑[4,3-a]喹喔啉-1-酮(ODQ)(一种鸟苷酸环化酶抑制剂)中重复。SNP 松弛反应在 10(-8)mol/L Y-27632 和 10(-8)mol/L 法舒地尔中重复。Y-27632 和法舒地尔引起 PE 预收缩的 RA 环的浓度依赖性血管舒张,最高浓度(10(-4)mol/L)时记录最大舒张(100%)。Y-27632 和 ODQ 存在时,Y-27632 和 fasudil 的血管舒张作用明显降低,Y-27632 和 fasudil 的 pD2 值不变。SNP 的血管舒张作用在 Y-27632 和 fasudil 存在时显著增加,SNP 的 pD2 值不变。这些发现表明,Y-27632 和 fasudil 引起 RA 环的浓度依赖性血管舒张。由于 L-NNA 和 ODQ 以剂量依赖性方式降低这种作用,因此 Y-27632 和 fasudil 的舒张作用可能是由于释放的一氧化氮的刺激所致。Rho-激酶抑制剂在预防用于冠状动脉手术的动脉移植物血管痉挛方面可能具有重要作用。