Stojić D, Pesić S, Radenković M, Popović-Roganović J, Pesić Z, Grbović L
Department of Pharmacology, Faculty of Stomatology, University of Belgrade, Dr. Subotića br. 8, 11 000 Belgrade.
J Dent Res. 2007 Jun;86(6):565-70. doi: 10.1177/154405910708600615.
Endothelial vasodilatory substances may play a central role in the local regulation of vascular tone. We hypothesized that these substances can mediate endothelium-dependent vasodilatory responses to acetylcholine (ACh) and vasoactive intestinal peptide (VIP) in the human submandibular artery. We evaluated the contributions of endothelial vasodilatory substances to vessel relaxation in response to ACh and VIP, using different inhibitors of endothelial vasodilation, the nitric oxide synthase inhibitor, the cyclo-oxygenase inhibitor, indomethacin, the potassium channel blocker, and 4-aminopyridine. ACh and VIP caused an endothelium- and concentration-dependent relaxation in this artery. ACh relaxation was completely blocked after the concomitant addition of N(G)-nitro-L-arginine and indomethacin. The vasorelaxant effect of ACh was not influenced by 4-aminopyridine. VIP relaxation was almost completely abolished by 4-aminopyridine, and was partly inhibited by N(G)-nitro-L-arginine, but was not affected by indomethacin. Thus, in the human submandibular artery, ACh and VIP produced endothelium-dependent vasodilation with different underlying mechanisms: release of nitric oxide (NO) and cyclo-oxygenase products for ACh, and release of NO and endothelium-derived hyperpolarizing factor for VIP.
内皮血管舒张物质可能在血管张力的局部调节中起核心作用。我们推测这些物质可介导人下颌下动脉对乙酰胆碱(ACh)和血管活性肠肽(VIP)的内皮依赖性血管舒张反应。我们使用内皮血管舒张的不同抑制剂、一氧化氮合酶抑制剂、环氧化酶抑制剂吲哚美辛、钾通道阻滞剂4-氨基吡啶,评估了内皮血管舒张物质对ACh和VIP引起的血管舒张的作用。ACh和VIP在该动脉中引起内皮和浓度依赖性舒张。同时添加N(G)-硝基-L-精氨酸和吲哚美辛后,ACh诱导的舒张完全被阻断。ACh的血管舒张作用不受4-氨基吡啶影响。4-氨基吡啶几乎完全消除了VIP诱导的舒张,N(G)-硝基-L-精氨酸部分抑制了该舒张,但吲哚美辛对其无影响。因此,在人下颌下动脉中,ACh和VIP通过不同的潜在机制产生内皮依赖性血管舒张:ACh通过释放一氧化氮(NO)和环氧化酶产物,而VIP通过释放NO和内皮源性超极化因子。