Krzemiński T, Kurcok A, Juraszczyk Z, Kozik W, Kapustecki J, Kryj M, Brus R
Department of Pharmacology, Silesian Academy of Medicine, Zabrze, Poland.
Med Biol. 1987;65(5-6):249-53.
The influence of verapamil on cardiovascular effects of prostacyclin (PGI2) in rats was examined. PGI2 administered into the lateral brain ventricle (i.c.v.) or intravenously (i.v.) in a dose of 2.7 x 10(-8)mol evoked hypotension and tachycardia. Pretreatment with verapamil in a dose of 2.0 x 10(-5)mol/kg given intraperitoneally (i.p.) diminished hypotensive effect of PGI2 i.c.v. as well as inhibiting the influence of PGI2 i.c.v. and i.v. upon the heart rate. Bolus injection of PGI2 in a dose of 2.7 x 10(-10), 2.7 x 10(-9) or 2.7 x 10(-8)mol evoked biphasic inotropic and chronotropic effects on isolated rat heart. Short-term increase of the contractile force together with bradycardia and afterwards long-lasting decrease of contractility with sustained, slight tachycardia were observed. Verapamil in a concentration of 1.0 x 10(-6)M blocked biphasic inotropic effect and bradycardia after PGI2 administration. Because some central and peripheral cardiovascular effects of PGI2 were inhibited by verapamil, it is concluded that PGI2 may participate in transmembrane calcium ions movements.
研究了维拉帕米对大鼠前列环素(PGI2)心血管效应的影响。以2.7×10⁻⁸mol的剂量将PGI2注入侧脑室(脑室内)或静脉内,可引起低血压和心动过速。以2.0×10⁻⁵mol/kg的剂量腹膜内给予维拉帕米预处理,可减弱PGI2脑室内给药的降压作用,并抑制PGI2脑室内和静脉内给药对心率的影响。以2.7×10⁻¹⁰、2.7×10⁻⁹或2.7×10⁻⁸mol的剂量快速注射PGI2,可对离体大鼠心脏产生双相变力性和变时性效应。观察到收缩力短期增加并伴有心动过缓,随后收缩力持续长期降低并伴有持续的轻度心动过速。浓度为1.0×10⁻⁶M的维拉帕米可阻断PGI2给药后的双相变力性效应和心动过缓。由于维拉帕米抑制了PGI2的一些中枢和外周心血管效应,因此得出结论,PGI2可能参与跨膜钙离子运动。