Hermsmeyer K
Cardiovascular Research Laboratory, Chiles Research Institute, Providence Medical Center, Portland, Oregon.
Drugs. 1988;36 Suppl 7:29-32. doi: 10.2165/00003495-198800367-00005.
Cellular investigation of the vasodilator, pinacidil, was carried out to determine the membrane mechanisms leading to vascular muscle relaxation. Patch clamp recording of whole cell currents from isolated vascular muscle cells of rat azygos vein demonstrated a significant increase in K+ currents when 1 to 50 mumol/L pinacidil was added. The increases of K+ current by pinacidil were small (number of openings increased by 2%) when the recording pipette (and intracellular solution) contained 10 mmol/L EGTA, but were relatively large (50-300% increase in number of openings) when calcium in the intracellular solution was greater than 300 mumol/L. These observations suggest that pinacidil causes vasodilatation by increasing potassium conductance, primarily or completely via the large (200pS), calcium-dependent K+ channel.
对血管扩张剂吡那地尔进行细胞研究,以确定导致血管平滑肌舒张的膜机制。对大鼠奇静脉分离的血管平滑肌细胞进行全细胞膜片钳记录,结果显示,加入1至50 μmol/L吡那地尔后,钾电流显著增加。当记录电极内液(pipette)含有10 mmol/L乙二醇双四乙酸(EGTA)时,吡那地尔引起的钾电流增加较小(开放次数增加2%),但当细胞内液中钙浓度大于300 μmol/L时,增加幅度相对较大(开放次数增加50%-300%)。这些观察结果表明,吡那地尔主要或完全通过大电导(200 pS)、钙依赖性钾通道增加钾电导,从而引起血管舒张。