维拉帕米对前列环素循环系统中枢和外周作用的影响。

Medical biology Pub Date : 1987-01-01
T Krzemiński, A Kurcok, Z Juraszczyk, W Kozik, J Kapustecki, M Kryj, R Brus
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引用次数: 0

摘要

观察维拉帕米对大鼠前列环素(PGI2)心血管作用的影响。PGI2以2.7 × 10(-8)mol的剂量注入侧脑室(i.c.v)或静脉注射(i.v)可引起低血压和心动过速。维拉帕米以2.0 × 10(-5)mol/kg的剂量腹腔(i.p)进行预处理,可降低PGI2滴注的降压作用,并抑制PGI2滴注和静脉滴注对心率的影响。PGI2以2.7 × 10(-10)、2.7 × 10(-9)或2.7 × 10(-8)mol的剂量对离体大鼠心脏产生双相性肌力和变时作用。观察到短期收缩力增加并伴有心动过缓,随后长期收缩力下降并伴有持续轻微心动过速。维拉帕米1.0 × 10(-6)M浓度阻断PGI2给药后双相性肌力作用和心动过缓。由于维拉帕米抑制了PGI2的中枢和外周心血管作用,因此PGI2可能参与了钙离子的跨膜运动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of verapamil on central and peripheral effects of prostacyclin on circulatory system in rats.

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.

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