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Effects of cyclopiazonic acid on rhythmic contractions in uterine smooth muscle bundles of the rat.

机译:环吡嗪酸对大鼠子宫平滑肌束节律性收缩的影响。

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摘要

1. We studied the effects of cyclopiazonic acid (CPA) on rhythmic contractions and on Ca2+ uptake by the intracellular stores in longitudinal muscle strips of the rat uterus at 30 degrees C. 2. Oxytocin (1 microM) in Ca(2+)-free solution induced a transient rise in the intracellular Ca2+ concentration ([Ca2+]i) and contraction after Ca2+ loading of the stores in high-K(+)- and Ca(2+)-containing solution. CPA inhibited oxytocin-induced Ca2+ release and contraction, the half and full inhibitory concentrations of CPA being 0.3 and 10 microM, respectively. In contrast, addition of CPA after Ca2+ loading exerted no significant inhibitory effects. 3. Oxytocin (10 nM) applied in Ca(2+)-containing solution induced rhythmic increases in both force and [Ca2+]i. CPA (10 microM) had no effect on oxytocin-induced rhythmic contractions. 4. At a high concentration (300 microM), CPA inhibited the rhythmic contractions induced by 10 nM oxytocin; the frequency and the peak height were decreased, and in many bundles contractions were completely abolished. These inhibitory effects were reversed after CPA washout. 5. CPA (300 microM) inhibited the rate of rise of [Ca2+]i due to depolarization induced by high-K(+)-containing solution. 6. These results suggest that low concentrations of CPA inhibit the loading of Ca2+ into intracellular stores in intact tissue strips, and that the Ca2+ stores are not directly involved in the uterine rhythmic contractions. It is also suggested that a high concentration of CPA inhibits the mechanism that is responsible for the generation of rhythmic contractions as well as voltage-dependent Ca2+ channels.
机译:1.我们研究了环吡嗪酸(CPA)对节律性收缩和30度大鼠子宫纵向肌条中细胞内存储的Ca2 +吸收的影响。2. Ca(2 +)-中的催产素(1 microM)-游离溶液诱导了细胞内Ca2 +浓度([Ca2 +] i)的短暂升高,并且在高K(+)-和Ca(2+)溶液中存储的Ca2 +加载后收缩。 CPA抑制催产素诱导的Ca2 +释放和收缩,CPA的一半和完全抑制浓度分别为0.3和10 microM。相反,添加Ca2 +后加入CPA并没有产生明显的抑制作用。 3.在含Ca(2+)的溶液中应用催产素(10 nM)会引起力和[Ca2 +] i的节律性增加。 CPA(10 microM)对催产素引起的节律性收缩没有影响。 4.在高浓度(300 microM)下,CPA抑制了10 nM催产素引起的节律性收缩。频率和峰高降低,许多束中的收缩被完全消除。 CPA冲洗后,这些抑制作用会逆转。 5. CPA(300 microM)抑制了由高K(+)溶液引起的去极化引起的[Ca2 +] i的上升速率。 6.这些结果表明,低浓度的CPA会抑制Ca2 +进入完整组织条带中的细胞内存储区,并且Ca2 +存储区不直接参与子宫节律性收缩。还表明,高浓度的CPA会抑制引起节律性收缩以及电压依赖性Ca2 +通道生成的机制。

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