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用于治疗腹泻型肠易激综合征的埃卢多啉

Eluxadoline for the treatment of diarrhoea-predominant irritable bowel syndrome.

作者信息

Scarpellini Emidio, Laterza Lucrezia, Ianiro Gianluca, Tack Jan, Abenavoli Ludovico, Gasbarrini Antonio

机构信息

a Department of Pediatrics , Umberto I University Hospital, 'Sapienza' University of Rome , Rome , Italy.

b Division of Internal Medicine and Gastroenterology , Gemelli University Hospital, Catholic University of Sacred Heart , Rome , Italy.

出版信息

Expert Opin Pharmacother. 2016 Jul;17(10):1395-402. doi: 10.1080/14656566.2016.1182982. Epub 2016 Jun 8.

Abstract

INTRODUCTION

Irritable bowel syndrome (IBS) treatment is challenging physicians because of its multifactorial physiopathology. In particular, abdominal pain and diarrhea management lack one unique effective pharmacological remedy. Opioid receptors, present in the central nervous system (CNS) and the enteric nervous system (ENS), are involved in visceral sensitivity and gastrointestinal motility control. To date only a few opioid receptor modulators are currently in use for the treatment of IBS but with dosage limitations due to the early development of severe constipation.

AREAS COVERED

In this drug evaluation manuscript we review the irritable bowel syndrome therapeutic needs and chemistry, pharmacokinetics and -dynamics, clinical study results with the new opioid receptor ligand eluxadoline for the treatment of diarrhea-predominant irritable bowel syndrome (IBS-D).

EXPERT OPINION

Eluxadoline shows a peculiar pharmacological profile with μ-opioid agonism and δ-opioid antagonism actions. Its efficacy over placebo for the treatment of abdominal pain and diarrhea in IBS-D has been demonstrated in short- and long-term clinical studies in humans. Its safety has been evaluated in the same studies. Interestingly, eluxadoline showed a low rate of constipation development in IBS patients in comparison with known effects of other opioid receptor modulators. Patients with a history of acute pancreatitis should not be treated with eluxadoline.

摘要

引言

肠易激综合征(IBS)的治疗对医生而言颇具挑战,因其病理生理机制具有多因素性。尤其是腹痛和腹泻的管理缺乏一种独特有效的药物治疗方法。存在于中枢神经系统(CNS)和肠神经系统(ENS)中的阿片受体,参与内脏敏感性和胃肠动力控制。迄今为止,仅有少数阿片受体调节剂用于IBS的治疗,但由于严重便秘的早期出现而存在剂量限制。

涵盖领域

在本药物评估手稿中,我们综述了肠易激综合征的治疗需求以及新型阿片受体配体埃卢多啉治疗腹泻型肠易激综合征(IBS-D)的化学、药代动力学和药效学以及临床研究结果。

专家观点

埃卢多啉具有独特的药理学特征,具有μ阿片激动和δ阿片拮抗作用。在人类的短期和长期临床研究中已证明其治疗IBS-D腹痛和腹泻的疗效优于安慰剂。在相同研究中对其安全性进行了评估。有趣的是,与其他阿片受体调节剂的已知作用相比,埃卢多啉在IBS患者中导致便秘的发生率较低。有急性胰腺炎病史的患者不应使用埃卢多啉治疗。

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