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Effect of Trimebutine on Contractile Responses in Skinned Ileal Smooth Muscle

机译:曲美布汀对皮肤回肠平滑肌收缩反应的影响

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References(24) Cited-By(3) The effects of trimebutine on Ca2+ release and modulation of Ca2+ sensitivity of contractile elements induced by carbachol (CCh) were investigated using a tension measuring method in β-escin-treated skinned smooth muscle of the longitudinal muscle layer of guinea pig ileum. Trimebutine (10-100 μM) concentration-dependently inhibited tension development brought about by Ca2+ release from intracellular stores induced by CCh (10 μM), but did not affect those induced by inositol 1, 4, 5-trisphosphate (IP3, 25 μM) or caffeine (5 mM). The inhibitory effect was reversible. Trimebutine (100 μM) neither altered the Ca2+ sensitivity of the contractile elements nor affected the effects of GTPγS (50 2+M) and CCh (100 2+M) in potentiating Ca2+ sensitivity of the contractile elements after the Ca2+ storage function had been eliminated by A23187. These results suggest that trimebutine inhibits CCh-induced Ca2+ release by acting at some point during the coupling of muscarinic receptors through a G-protein to phospholipase C and thus reducing the accumulation of IP3.
机译:参考文献(24)引用了(3)使用张力测量法研究了β-七叶红素处理过的皮肤纵向平滑肌中曲美布汀对卡巴胆碱(CCh)诱导的收缩因子Ca2 +释放和Ca2 +敏感性调节的影响。豚鼠回肠的肌肉层。曲美布汀(10-100μM)浓度依赖性地抑制了CCh(10μM)诱导的细胞内存储中Ca2 +释放所引起的张力发展,但并未影响肌醇1,4,4,5-三磷酸(IP3,25μM)诱导的张力发展或咖啡因(5 mM)。抑制作用是可逆的。 Trimebutine(100μM)既不改变收缩因子对Ca2 +的敏感性,也不影响GTPγS(50 2 + M)和CCh(100 2 + M)在消除Ca2 +储存功能后增强收缩因子对Ca2 +敏感性的作用。通过A23187。这些结果表明,曲美布汀通过在毒蕈碱受体通过G蛋白与磷脂酶C偶联的过程中的某个时刻抑制CCh诱导的Ca2 +释放,从而减少IP3的积累。

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