Urakami-Harasawa L, Shimokawa H, Nakashima M, Egashira K, Takeshita A
Research Institute of Angiocardiology and Cardiovascular Clinic, Kyushu University School of Medicine, Fukuoka, Japan.
J Clin Invest. 1997 Dec 1;100(11):2793-9. doi: 10.1172/JCI119826.
The endothelium plays an important role in maintaining the vascular homeostasis by releasing vasodilator substances, including prostacyclin (PGI2), nitric oxide (NO), and endothelium-derived hyperpolarizing factor (EDHF). Although the former two substances have been investigated extensively, the importance of EDHF still remains unclear, especially in human arteries. Thus we tested our hypothesis that EDHF plays an important role in human arteries, particularly with reference to the effect of vessel size, its vasodilating mechanism, and the influences of risk factors for atherosclerosis. Isometric tension and membrane potentials were recorded in isolated human gastroepiploic arteries and distal microvessels (100-150 microm in diameter). The contribution of PGI2, NO, and EDHF to endothelium-dependent relaxations was analyzed by inhibitory effects of indomethacin, NG-nitro- L-arginine, and KCl, respectively. The nature of and hyperpolarizing mechanism by EDHF were examined by the inhibitory effects of inhibitors of cytochrome P450 pathway and of various K channels. The effects of atherosclerosis risk factors on EDHF-mediated relaxations were also analyzed. The results showed that (a) the contribution of EDHF to endothelium-dependent relaxations is significantly larger in microvessels than in large arteries; (b) the nature of EDHF may not be a product of cytochrome P450 pathway, while EDHF-induced hyperpolarization is partially mediated by calcium-activated K channels; and (c) aging and hypercholesterolemia significantly impair EDHF-mediated relaxations. These results demonstrate that EDHF also plays an important role in human arteries.
内皮通过释放血管舒张物质,包括前列环素(PGI2)、一氧化氮(NO)和内皮衍生超极化因子(EDHF),在维持血管稳态中发挥重要作用。尽管前两种物质已得到广泛研究,但EDHF的重要性仍不明确,尤其是在人体动脉中。因此,我们验证了我们的假设,即EDHF在人体动脉中起重要作用,特别是涉及血管大小的影响、其血管舒张机制以及动脉粥样硬化危险因素的影响。在离体的人胃网膜动脉和远端微血管(直径100 - 150微米)中记录等长张力和膜电位。分别通过吲哚美辛、NG - 硝基 - L - 精氨酸和氯化钾的抑制作用分析PGI2、NO和EDHF对内皮依赖性舒张的贡献。通过细胞色素P450途径抑制剂和各种钾通道抑制剂的抑制作用研究EDHF的性质和超极化机制。还分析了动脉粥样硬化危险因素对EDHF介导的舒张的影响。结果表明:(a)EDHF对内皮依赖性舒张的贡献在微血管中比在大动脉中显著更大;(b)EDHF的性质可能不是细胞色素P450途径的产物,而EDHF诱导的超极化部分由钙激活钾通道介导;(c)衰老和高胆固醇血症显著损害EDHF介导的舒张。这些结果表明EDHF在人体动脉中也起重要作用。