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环匹阿尼酸对大鼠子宫平滑肌束节律性收缩的影响。

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

作者信息

Kasai Y, Iino M, Tsutsumi O, Taketani Y, Endo M

机构信息

Department of Pharmacology, Faculty of Medicine, University of Tokyo, Japan.

出版信息

Br J Pharmacol. 1994 Aug;112(4):1132-6. doi: 10.1111/j.1476-5381.1994.tb13201.x.

Abstract
  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.
摘要
  1. 我们研究了30℃时环匹阿尼酸(CPA)对大鼠子宫纵肌条节律性收缩及细胞内钙库摄取Ca2+的影响。2. 在无钙溶液中,催产素(1μM)在高钾和含钙溶液中使细胞内钙库加载Ca2+后,可诱导细胞内Ca2+浓度([Ca2+]i)短暂升高并引起收缩。CPA可抑制催产素诱导的Ca2+释放和收缩,CPA的半抑制浓度和完全抑制浓度分别为0.3μM和10μM。相反,在Ca2+加载后加入CPA则无明显抑制作用。3. 在含钙溶液中应用催产素(10 nM)可诱导张力和[Ca2+]i的节律性增加。CPA(10μM)对催产素诱导的节律性收缩无影响。4. 在高浓度(300μM)时,CPA可抑制10 nM催产素诱导的节律性收缩;频率和峰值高度降低,许多肌束的收缩完全被消除。冲洗CPA后,这些抑制作用可逆转。5. CPA(300μM)可抑制含高钾溶液诱导的去极化所导致的[Ca2+]i上升速率。6. 这些结果表明,低浓度的CPA可抑制完整组织条带中Ca2+向细胞内钙库的加载,且钙库不直接参与子宫的节律性收缩。还表明高浓度的CPA可抑制负责产生节律性收缩的机制以及电压依赖性Ca2+通道。

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