季铵衍生物作为肠易激综合征的解痉剂

Quaternary ammonium derivatives as spasmolytics for irritable bowel syndrome.

作者信息

Evangelista S

机构信息

Menarini Ricerche SpA, Preclinical Development, Florence, Italy.

出版信息

Curr Pharm Des. 2004;10(28):3561-8. doi: 10.2174/1381612043382972.

Abstract

Quaternary ammonium derivatives such as cimetropium, n-butyl scopolammonium, otilonium and pinaverium bromide have been discovered and developed as potent spasmolytics of the gastrointestinal tract. Their pharmacological activity has been proven in both "in vivo" and "in vitro" studies of hypermotility. "In vitro" experiments showed that they possess antimuscarinic activity at nM level but only pinaverium and otilonium are endowed with calcium channel blocker properties. These latter compounds relaxed the gastrointestinal smooth muscle mainly through a specific inhibition of calcium ion influx through L-type voltage operated calcium channels. Molecular pharmacology trials have indicated that pinaverium and otilonium can bind specific subunits of the calcium channel in the external surface of the plasma membrane and in this way they block the machinery of the contraction. Recent evidence showed that otilonium is able to bind tachykinin NK(2) receptors and not only inhibits one of the major contractile agents but can reduce the activation of afferent nerves devoted to the passage of sensory signals from the periphery to the central nervous system. Thanks to their typical physico-chemical characteristics, they are poorly absorbed by the systemic circulation and generally remain in the gastrointestinal tract where they exert the muscle relaxant activity by a local activity. Some differences exists in the absorption among these compounds: both n-butyl scopolammonium and cimetropium are partially taken up in the bloodstream, pinaverium has a low absorption (8-10 %) but is endowed with an excellent hepato-biliary excretion and otilonium, which has the lowest absorption (3 %), is almost totally excreted by faeces. Quaternary ammonium derivatives are widely used for the treatment of irritable bowel syndrome and recent meta-analyses have supported their efficacy in this disease. Due to its therapeutic index, the use of n-butyl scopolammonium is more indicated to treat acute colics than a chronic disease such as irritable bowel syndrome. Taking into consideration the published trials carried out with validated methodology in irritable bowel syndrome, cimetropium and otilonium are the best demonstrated drugs for the improvement in global assessment, pain and abdominal distension.

摘要

季铵衍生物,如西托溴铵、丁溴东莨菪碱、奥替溴铵和匹维溴铵,已被发现并开发为强效的胃肠道解痉剂。它们的药理活性已在胃肠动力亢进的“体内”和“体外”研究中得到证实。“体外”实验表明,它们在纳摩尔水平具有抗毒蕈碱活性,但只有匹维溴铵和奥替溴铵具有钙通道阻滞剂特性。后两种化合物主要通过特异性抑制L型电压门控钙通道的钙离子内流来松弛胃肠道平滑肌。分子药理学试验表明,匹维溴铵和奥替溴铵可以结合质膜外表面钙通道的特定亚基,从而阻断收缩机制。最近的证据表明,奥替溴铵能够结合速激肽NK(2)受体,不仅能抑制一种主要的收缩剂,还能减少负责将感觉信号从外周传递到中枢神经系统的传入神经的激活。由于其典型的物理化学特性,它们很少被体循环吸收,通常留在胃肠道中,在那里通过局部作用发挥肌肉松弛活性。这些化合物在吸收方面存在一些差异:丁溴东莨菪碱和西托溴铵都有部分被吸收进入血液,匹维溴铵吸收低(8 - 10%),但具有出色的肝胆排泄功能,而奥替溴铵吸收最低(3%),几乎全部通过粪便排泄。季铵衍生物广泛用于治疗肠易激综合征,最近的荟萃分析支持了它们在这种疾病中的疗效。由于其治疗指数,丁溴东莨菪碱更适用于治疗急性绞痛,而不是像肠易激综合征这样的慢性病。考虑到在肠易激综合征中采用经过验证的方法进行的已发表试验,西托溴铵和奥替溴铵是在整体评估改善、疼痛和腹胀方面最有证据支持的药物。

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