[替罗普胺、曲美布汀和溴化辛溴铵在易激结肠中的多重结肠测压的临床和仪器评价:1 .单次静脉给药]。

Pharmatherapeutica Pub Date : 1986-01-01
M Galeone, F Stock, G Moise, D Cacioli, E Benazzi, A Riva
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引用次数: 0

摘要

60例急性或亚急性结肠易激门诊患者随机分配接受单次静脉注射剂量50mg替罗普胺、50mg马来酸曲美布汀或10mg溴化奥替溴铵。注射前后行多次结肠测压,监测张力、正弦收缩波强度、频率、瞬缩、振动及自主收缩能力。任何药物均未观察到张力的显著变化,但是,虽然替罗普胺未改变自愿收缩能力,但曲美布汀和奥替隆对张力有明显的抑制作用。替罗普胺对自发结肠收缩的总强度没有显著影响,而曲美布汀和奥替溴铵则有一定程度的降低。此外,使用替罗普胺和曲美布汀(在较小程度上),肌肉力量的重新分配显著增加了相推进波,减少了无效的短暂性和振动性收缩,而使用奥替溴铵只记录了减少的波幅,而没有改变短暂性痉挛的频率。基于这些观察结果,替罗普胺被评估为至少与奥替溴胺一样有效的抗痉挛药,至少与曲美布汀一样有效的同步剂,同时将自己与两种参考药物分开,因为它是唯一一种同时作为抗痉挛药和同步剂的药物。
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[Clinical and instrumental evaluation by multiple colonic manometry of tiropramide, trimebutine and octylonium bromide in the irritable colon: I. Administration by single i.v].

Sixty out-patients with acute or sub-acute irritable colon were randomly allocated to receive a single intravenous dose of 50 mg tiropramide, 50 mg trimebutine maleate or 10 mg octilonium bromide. Before and after injection, multiple colonic manometry was performed, monitoring tonus, intensity and frequency of sinusoid contraction waves, transitories and vibrations, as well as the voluntary contraction capacity. Significant variations in tonus were not observed with any drug, but, while tiropramide left unmodified the voluntary contractile ability, a significant inhibition was observed with trimebutine and octilonium. The overall power of spontaneous colonic contractions did not vary significantly with tiropramide, whereas some decrease was observed with trimebutine, and a substantial one with octilonium. Moreover, while with tiropramide and, to a lesser extent, with trimebutine there was a significant redistribution of muscular power so as to increase phasic propulsion waves and to decrease the ineffective transitory and vibrational contractions, with octilonium only a decreased wave amplitude was recorded without alteration of the frequency of transient spasms. Based on these observations, tiropramide was evaluated as being at least as effective an antispasmodic as octilonium and at least as effective a synchronizer as trimebutine, while setting itself aside from both reference drugs as it was the only one to act contemporarily as both an antispasmodic and a synchronizer.

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