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Colonic smooth muscle cells and colonic motility patterns as a target for irritable bowel syndrome therapy: Mechanisms of action of otilonium bromide

机译:结肠平滑肌细胞和结肠运动模式作为肠易激综合症治疗的靶标:溴化奥替尼的作用机理

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摘要

Otilonium bromide (OB) is a spasmolytic compound of the family of quaternary ammonium derivatives and has been successfully used in the treatment of patients with irritable bowel syndrome (IBS) due to its specific pharmacodynamic effects on motility patterns in the human colon and the contractility of colonic smooth muscle cells. This article examines how. OB inhibits the main patterns of human sigmoid motility in vitro, which are spontaneous rhythmic phasic contractions, smooth muscle tone, contractions induced by stimulation of excitatory motor neurons and contractions induced by direct effect of excitatory neurotransmitters. It does this mainly by blocking calcium influx through L-type calcium channels and interfering with mobilization of cellular calcium required for smooth muscle contraction, thereby limiting excessive intestinal contractility and abdominal cramping. OB also inhibits T-type calcium channels and muscarinic responses. Finally, OB inhibits tachykinin receptors on smooth muscle and primary afferent neurons which may have the joint effect of reducing motility and abdominal pain. All these mechanisms mediate the therapeutic effects of OB in patients with IBS and might be useful in patients with other spastic colonic motility disorders such as diverticular disease.
机译:溴化乙铵(OB)是季铵衍生物家族的解痉化合物,由于其对人肠蠕动模式的特异性药效学作用和对大鼠结肠的收缩作用,已成功用于治疗肠易激综合症(IBS)患者。结肠平滑肌细胞。本文探讨了如何。 OB在体外抑制人的乙状结肠运动的主要模式,即自发性节律性收缩,平滑肌音调,刺激兴奋性运动神经元引起的收缩和兴奋性神经递质的直接作用引起的收缩。它主要是通过阻止钙通过L型钙通道流入并干扰平滑肌收缩所需的细胞钙动员来实现的,从而限制了肠道过度收缩和腹部绞痛。 OB还抑制T型钙通道和毒蕈碱反应。最后,OB抑制平滑肌和初级传入神经元上的速激肽受体,这可能具有减少运动性和腹痛的联合作用。所有这些机制都可介导OB对IBS患者的治疗作用,并且可能对患有其他痉挛性结肠运动障碍(如憩室病)的患者有用。

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