Osa T, Maruta K
Department of Physiology, Yamaguchi University School of Medicine, Ube, Japan.
Jpn J Physiol. 1987;37(3):515-31. doi: 10.2170/jjphysiol.37.515.
The contractile response of the myometrial longitudinal muscle of pregnant and estrogen-treated rats to adenosine triphosphate (ATP) was investigated. ATP (10(-5)-4 X 10(-3) M) added to Krebs solution caused a generation of spontaneous activity consisting of phasic contractions and an elevation of muscle tone in a dose-dependent manner. Effects of the "test solution" consisting of isotonic K, 4(mM) ATP, 4 Mg, 1-20 EGTA, 20 tris(hydroxymethyl)aminomethan (Tris) maleate (pH 6.8) on the contractile response was then investigated. An initial phasic and a following tonic contraction was evoked by the application of the test solution, when applied after the equilibration of the muscle with Krebs solution. ATP was proved to be an agonist to evoke the Ca-free contraction. The phasic contraction was depressed when the muscle was incubated with Ca-free Krebs solution. The amplitude of the tonic contraction became progressively larger when application of the test solution was repeated. The amplitude was 15-70% as large as the tonic component of the K-contracture induced by 40 mM K. Theophylline (10 mM), 0.1 mM papaverine and 1 microM isoprenaline nearly abolished, and 1 mM cAMP partly depressed the tonic contraction of K-contracture, whereas the tonic contraction induced by the test solution was unaffected. A calmodulin antagonist, W-7 (100 microM) strongly suppressed both the K-contracture and the contraction induced by the test solution, whereas trifluoperazine (10-200 microM) preferentially depressed the K-contracture. The tonic contraction induced by the test solution was strongly depressed when Mg was removed and 20 mM EDTA was applied. From these results, it is discussed that some Ca-independent process is involved in the generation of tonic component of Ca-free contraction developed by the application of the test solution.
研究了怀孕大鼠和经雌激素处理的大鼠子宫肌层纵行肌对三磷酸腺苷(ATP)的收缩反应。向 Krebs 溶液中添加 ATP(10⁻⁵ - 4×10⁻³ M)会引起自发活动,包括相性收缩,并使肌张力呈剂量依赖性升高。然后研究了由等渗钾、4(mM)ATP、4 镁、1 - 20 乙二醇双四乙酸(EGTA)、20 三(羟甲基)氨基甲烷(Tris)马来酸盐(pH 6.8)组成的“测试溶液”对收缩反应的影响。当在肌肉用 Krebs 溶液平衡后应用测试溶液时,会引发初始的相性收缩和随后的强直性收缩。已证明 ATP 是引发无钙收缩的激动剂。当肌肉在无钙的 Krebs 溶液中孵育时,相性收缩受到抑制。当重复应用测试溶液时,强直性收缩的幅度逐渐增大。该幅度为 40 mM 钾诱导的钾挛缩强直性成分的 15 - 70%。茶碱(10 mM)、0.1 mM 罂粟碱和 1 μM 异丙肾上腺素几乎消除了钾挛缩的强直性收缩,1 mM 环磷酸腺苷(cAMP)部分抑制了钾挛缩的强直性收缩,而测试溶液诱导的强直性收缩不受影响。钙调蛋白拮抗剂 W - 7(100 μM)强烈抑制钾挛缩和测试溶液诱导的收缩,而三氟拉嗪(10 - 200 μM)优先抑制钾挛缩。当去除镁并应用 20 mM 乙二胺四乙酸(EDTA)时,测试溶液诱导的强直性收缩受到强烈抑制。从这些结果可以看出,在应用测试溶液产生的无钙收缩的强直性成分的产生过程中涉及一些不依赖钙的过程。