Zhang H, Bolton T B, Piekarska A E, McPherson G A
Department of Pharmacology and Clinical Pharmacology, St. George's Hospital Medical School, University of London, UK.
Eur J Pharmacol. 1998 Apr 17;347(1):119-23. doi: 10.1016/s0014-2999(98)00082-x.
The effect of the lipophilic quaternary ion, tetraphenylphosphonium, on membrane potential of segments of rat small mesenteric artery and on the current in single voltage-clamped smooth muscle cells from rabbit portal vein was studied. In rat small mesenteric artery, tetraphenylphosphonium (1-30 microM) caused membrane depolarization of approximately 23 mV and decreased or abolished the hyperpolarization induced by the KATP channel opener, levcromakalim (0.1-3 microM). In rabbit portal vein K+ currents induced by levcromakalim (10 microM) or pinacidil (10 microM) were completely inhibited by tetraphenylphosphonium (IC50 0.5 microM). The results show that tetraphenylphosphonium antagonizes the KATP current induced by K+ channel openers in vascular smooth muscle possibly by acting on the KATP channel itself.
研究了亲脂性季铵离子四苯基鏻对大鼠小肠系膜动脉节段膜电位以及对兔门静脉单电压钳制平滑肌细胞电流的影响。在大鼠小肠系膜动脉中,四苯基鏻(1 - 30微摩尔)引起约23毫伏的膜去极化,并降低或消除了由KATP通道开放剂左卡尼汀(0.1 - 3微摩尔)诱导的超极化。在兔门静脉中,四苯基鏻(IC50为0.5微摩尔)完全抑制了由左卡尼汀(10微摩尔)或吡那地尔(10微摩尔)诱导的K +电流。结果表明,四苯基鏻可能通过作用于KATP通道本身来拮抗血管平滑肌中由K +通道开放剂诱导的KATP电流。