Sánchez-Ferrer C F, Marín J, Salaices M, Rico M L, Muñoz-Blanco J L
Gen Pharmacol. 1985;16(5):469-73. doi: 10.1016/0306-3623(85)90006-0.
Thiopental and pentobarbital induced dose-dependent vasodilations in human cerebral arteries previously contracted with noradrenaline (NA), serotonin (5-HT) and KCl. Preincubation with both barbiturates decreased the contractions evoked by the three agents. Pentobarbital and thiopental reduced the Ca2+-induced contractile effects in K+-depolarized arteries and 5-HT-Ca2+ and NA-Ca2+ contractions dose-dependently. The tritium release evoked by K+ from these vessels prelabelled with [3H]NA was significantly reduced by both barbiturates at 10(-3) M and by Ca2+ removal. These results indicate that pentobarbital and thiopental essentially produce a similar interference with Ca2+ influx inhibiting the contractile responses induced by the three vasoactive agents and the exocytotic NA release evoked by K+.
硫喷妥钠和戊巴比妥钠可使预先用去甲肾上腺素(NA)、5-羟色胺(5-HT)和氯化钾收缩的人脑动脉产生剂量依赖性血管舒张。两种巴比妥类药物预孵育可减弱这三种药物引起的收缩。戊巴比妥钠和硫喷妥钠可剂量依赖性地降低钾离子去极化动脉中钙离子诱导的收缩效应以及5-HT-钙离子和NA-钙离子收缩效应。在这些预先用[3H]NA标记的血管中,10(-3)M的两种巴比妥类药物以及去除钙离子均可显著降低钾离子引起的氚释放。这些结果表明,戊巴比妥钠和硫喷妥钠对钙离子内流产生了基本相似的干扰,抑制了三种血管活性药物诱导的收缩反应以及钾离子引起的去甲肾上腺素胞吐释放。