Edwards G, Félétou M, Gardener M J, Glen C D, Richards G R, Vanhoutte P M, Weston A H
School of Biological Sciences, University of Manchester, Manchester M13 9PT, UK.
Br J Pharmacol. 2001 Aug;133(7):1145-53. doi: 10.1038/sj.bjp.0704157.
In porcine coronary arteries, smooth muscle hyperpolarizations produced by the nitric oxide donor, NOR-1, and the prostacyclin analogue, iloprost, were compared with those induced by substance P and bradykinin and attributed to the endothelium-derived hyperpolarizing factor (EDHF). In the presence of 300 microM L-nitroarginine and 10 microM indomethacin, iloprost-induced hyperpolarizations were partially inhibited by 10 microM glibenclamide whereas those to NOR-1, substance P and bradykinin were unaffected. Hyperpolarizations produced by maximally-effective concentrations of NOR-1 and NS1619 were identical (to -65 mV). They were significantly less than those generated by either substance P or bradykinin (to approximately -80 mV) and were abolished by iberiotoxin 100 nM, a concentration which had essentially no effect on responses to substance P or bradykinin. Incubation of segments of intact arteries for 16 - 22 h in bicarbonate-buffered Krebs solution had little effect on EDHF responses to substance P or bradykinin. In contrast, after incubation for this period of time in HEPES-buffered Tyrode solution or Krebs containing 10 mM HEPES the EDHF response to substance P was abolished and that to bradykinin was markedly reduced. The residual bradykinin-induced hyperpolarization following incubation in Tyrode solution was inhibited by iberiotoxin and by 10 microM 17-octadecynoic acid. We conclude that substance P activates only the EDHF pathway in the presence of nitric oxide synthase and cyclo-oxygenase inhibitors. Incubation in HEPES-buffered Tyrode solution abolishes the EDHF responses to substance P and bradykinin to reveal an additional hyperpolarizing mechanism, associated with the opening of K(+) channels, activated only by bradykinin.
在猪冠状动脉中,比较了一氧化氮供体NOR-1和前列环素类似物伊洛前列素引起的平滑肌超极化与P物质和缓激肽诱导的超极化,并将其归因于内皮衍生超极化因子(EDHF)。在存在300μM L-硝基精氨酸和10μM吲哚美辛的情况下,伊洛前列素诱导的超极化被10μM格列本脲部分抑制,而对NOR-1、P物质和缓激肽的超极化则不受影响。最大有效浓度的NOR-1和NS1619产生的超极化相同(至-65mV)。它们明显小于P物质或缓激肽产生的超极化(至约-80mV),并被100nMiberiotoxin消除,该浓度对P物质或缓激肽的反应基本没有影响。完整动脉段在碳酸氢盐缓冲的 Krebs 溶液中孵育16 - 22小时对EDHF对P物质或缓激肽的反应影响很小。相比之下,在此时间段内在HEPES缓冲的Tyrode溶液或含有10mM HEPES的Krebs中孵育后,EDHF对P物质的反应被消除,对缓激肽的反应明显降低。在Tyrode溶液中孵育后残留的缓激肽诱导的超极化被iberiotoxin和10μM 17-十八碳炔酸抑制。我们得出结论,在一氧化氮合酶和环氧化酶抑制剂存在的情况下,P物质仅激活EDHF途径。在HEPES缓冲的Tyrode溶液中孵育可消除EDHF对P物质和缓激肽的反应,从而揭示一种额外的超极化机制,该机制与仅由缓激肽激活的K(+)通道开放有关。