Suppr超能文献

综述文章:肠易激综合征的医学治疗新受体靶点。

Review article: new receptor targets for medical therapy in irritable bowel syndrome.

机构信息

Clinical Enteric Neuroscience Translational and Epidemiological Research (C.E.N.T.E.R.), College of Medicine, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Aliment Pharmacol Ther. 2010 Jan;31(1):35-46. doi: 10.1111/j.1365-2036.2009.04153.x.

Abstract

BACKGROUND

Despite setbacks to the approval of new medications for the treatment of irritable bowel syndrome, interim guidelines on endpoints for irritable bowel syndrome (IBS) trials have enhanced interest as new targets for medical therapy are proposed based on novel mechanisms or chemical entities.

AIMS

To review the approved lubiprostone, two targets that are not meeting expectations (tachykinins and corticotrophin-releasing hormone), the efficacy and safety of new 5-HT(4) agonists, intestinal secretagogues (chloride channel activators, and guanylate cyclase-C agonists), bile acid modulation, anti-inflammatory agents and visceral analgesics.

METHODS

Review of selected articles based on PubMed search and clinically relevant information on mechanism of action, safety, pharmacodynamics and efficacy.

RESULTS

The spectrum of peripheral targets of medical therapy addresses chiefly the bowel dysfunction of IBS and these effects are associated with pain relief. The pivotal mechanisms responsible for the abdominal pain or visceral sensation in IBS are unknown. The new 5-HT(4) agonists are more specific than older agents and show cardiovascular safety to date. Secretory agents have high specificity, low bioavailability and high efficacy. The potential risks of agents 'borrowed' from other indications (such as hyperlipidaemia, inflammatory bowel disease or somatic pain) deserve further study.

CONCLUSIONS

There is reason for optimism in medical treatment of IBS with a spectrum of agents to treat bowel dysfunction. However, visceral analgesic treatments are still suboptimal.

摘要

背景

尽管有新药物治疗肠易激综合征的批准受挫,但由于基于新机制或化学实体提出了新的医学治疗靶点,因此肠易激综合征(IBS)试验的终点临时指南增强了人们的兴趣。

目的

回顾已批准的利那洛肽,两个未达到预期的靶点(速激肽和促肾上腺皮质激素释放激素),新的 5-HT(4)激动剂、肠分泌剂(氯离子通道激活剂和鸟苷酸环化酶-C 激动剂)、胆汁酸调节、抗炎药和内脏镇痛药的疗效和安全性。

方法

根据 PubMed 搜索和有关作用机制、安全性、药效学和疗效的临床相关信息,对选定的文章进行综述。

结果

医学治疗的外周靶点范围主要针对肠易激综合征的肠道功能障碍,这些作用与缓解疼痛有关。IBS 中导致腹痛或内脏感觉的关键机制尚不清楚。新的 5-HT(4)激动剂比旧的药物更具特异性,迄今为止显示出心血管安全性。分泌剂具有高特异性、低生物利用度和高疗效。从其他适应症(如高脂血症、炎症性肠病或躯体疼痛)“借用”的药物的潜在风险值得进一步研究。

结论

用一系列治疗肠道功能障碍的药物治疗肠易激综合征具有乐观的理由。然而,内脏镇痛药的治疗效果仍然不尽如人意。

相似文献

3
Emerging pharmacologic therapies for irritable bowel syndrome.肠易激综合征的新兴药物疗法
Curr Gastroenterol Rep. 2010 Oct;12(5):408-16. doi: 10.1007/s11894-010-0124-1.
4
New treatment targets for the management of irritable bowel syndrome.治疗肠易激综合征的新靶点。
Curr Opin Endocrinol Diabetes Obes. 2014 Feb;21(1):9-14. doi: 10.1097/MED.0000000000000034.
5
Peripherally acting therapies for the treatment of irritable bowel syndrome.治疗肠易激综合征的外周作用治疗。
Gastroenterol Clin North Am. 2011 Mar;40(1):163-82. doi: 10.1016/j.gtc.2010.12.008.

引用本文的文献

3
Gut-brain Axis and migraine headache: a comprehensive review.肠-脑轴与偏头痛:全面综述。
J Headache Pain. 2020 Feb 13;21(1):15. doi: 10.1186/s10194-020-1078-9.
8
Optimal management of constipation associated with irritable bowel syndrome.肠易激综合征相关性便秘的优化管理
Ther Clin Risk Manag. 2015 May 30;11:691-703. doi: 10.2147/TCRM.S54298. eCollection 2015.
10
Impact of psychological stress on irritable bowel syndrome.心理压力对肠易激综合征的影响。
World J Gastroenterol. 2014 Oct 21;20(39):14126-31. doi: 10.3748/wjg.v20.i39.14126.

本文引用的文献

5
Postinfectious irritable bowel syndrome.感染后肠易激综合征
Gastroenterology. 2009 May;136(6):1979-88. doi: 10.1053/j.gastro.2009.02.074. Epub 2009 May 7.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验