Suzuki Y
Department of Obstetrics & Gynecology, Fukushima Medical College, Japan.
Fukushima J Med Sci. 1990 Jun;36(1):29-40.
Endothelin produced concentration-dependent contractions in both non-pregnant and pregnant myometria. These contractions consisted of two components; rhythmic and slowly developing contractions. The rhythmic contractions were abolished by calcium channel antagonists and in calcium-free Krebs-Ringer solution. On the contrary, the slowly developing contraction was little affected by calcium channel antagonists, and considerably reduced in calcium-free Krebs-Ringer solution. These results indicate that the rhythmic contractions are dependent on extracellular calcium and mediated via calcium influx through voltage-dependent calcium channel, and that the slowly developing contraction is dependent on another mechanism than extracellular calcium influx and may be due to the release of calcium from intracellular calcium-stores. Endothelin was more potent in the non-pregnant myometrium than in the pregnant one (-log EC50 (M) values were 9.07 +/- 0.11 in the non-pregnant and 8.41 +/- 0.06 in the pregnant, respectively). In the presence of calcium channel antagonists and in calcium-free Krebs-Ringer solution, endothelin-induced contractions in the non-pregnant myometrium were more markedly depressed than those in the pregnant one. These findings suggest that endothelin receptors exist in rabbit myometrium, and that a functional change at the level of endothelin receptors, the calcium channels to regulate extracellular calcium influx or calcium mobilizing system from intracellular calcium-stores may occur in accordance with being pregnant.
内皮素在未孕和孕子宫肌层均产生浓度依赖性收缩。这些收缩由两个部分组成:节律性收缩和缓慢发展的收缩。节律性收缩可被钙通道拮抗剂以及在无钙的克雷布斯 - 林格溶液中消除。相反,缓慢发展的收缩受钙通道拮抗剂影响较小,而在无钙的克雷布斯 - 林格溶液中显著减弱。这些结果表明,节律性收缩依赖于细胞外钙,并通过电压依赖性钙通道介导的钙内流实现,而缓慢发展的收缩依赖于细胞外钙内流以外的其他机制,可能是由于细胞内钙库释放钙所致。内皮素在未孕子宫肌层比在孕子宫肌层更有效(未孕时-log EC50(M)值为9.07±0.11,孕时为8.41±0.06)。在存在钙通道拮抗剂和无钙的克雷布斯 - 林格溶液时,内皮素诱导的未孕子宫肌层收缩比孕子宫肌层的收缩更明显地受到抑制。这些发现表明兔子宫肌层存在内皮素受体,并且根据妊娠状态,在内皮素受体水平、调节细胞外钙内流的钙通道或细胞内钙库的钙动员系统可能会发生功能变化。