Takenaga H, Magaribuchi T, Tamaki H
Jpn J Pharmacol. 1984 Feb;34(2):177-81. doi: 10.1254/jjp.34.177.
Effects of trimebutine maleate (TM-906) on the spontaneous contraction of isolated guinea pig colon were investigated. TM-906 in the concentrations of 10(-6) g/ml and 10(-5) g/ml increased the tone without affecting the amplitude of the spontaneous contraction in the preparations with low tone, whereas it decreased the tone and the amplitude of the spontaneous contraction in the preparations with high tone. At the higher concentration (10(-4) g/ml). TM-906 decreased the tone and finally abolished the spontaneous contraction in any preparation. The increase in tone induced by TM-906 was prevented by diltiazem and exposure to Ca++-free solution, but not by tetrodotoxin, atropine, phentolamine or propranolol, and depended on the extracellular concentration of CaCl2. On the other hand, the decrease in tone and amplitude of the spontaneous contraction produced by TM-906 were not prevented by tetrodotoxin, phentolamine or propranolol. TM-906 further increased the tone increased by 10 mM KCl, while it decreased the tone increased by 30 mM KCl. From results described above, it is suggested that TM-906 possesses both a relaxing effect and an excitatory effect which seem to be due to its direct action on the smooth muscle.
研究了马来酸曲美布汀(TM - 906)对豚鼠离体结肠自发收缩的影响。浓度为10(-6) g/ml和10(-5) g/ml的TM - 906可使低张力标本的张力增加,而不影响自发收缩的幅度,然而,它可使高张力标本的张力和自发收缩幅度降低。在较高浓度(10(-4) g/ml)时,TM - 906可使任何标本的张力降低并最终消除自发收缩。TM - 906诱导的张力增加可被地尔硫䓬和暴露于无钙溶液所阻断,但不能被河豚毒素、阿托品、酚妥拉明或普萘洛尔阻断,且依赖于细胞外氯化钙的浓度。另一方面,TM - 906引起的自发收缩张力和幅度的降低不能被河豚毒素、酚妥拉明或普萘洛尔阻断。TM - 906可进一步增加由10 mM氯化钾引起的张力,而降低由30 mM氯化钾引起的张力。根据上述结果,提示TM - 906具有舒张作用和兴奋作用,这似乎是由于其对平滑肌的直接作用所致。