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特发性便秘:大便过少,了解过少。

Idiopathic constipation: too few stools and too little knowledge.

作者信息

Briejer M R, Schuurkes J A, Sarna S K

机构信息

Department of Gastrointestinal Pharmacology, Janssen Research Foundation, Beerse, Belgium.

出版信息

Trends Pharmacol Sci. 1999 Jan;20(1):1-3. doi: 10.1016/s0165-6147(98)01278-4.

DOI:10.1016/s0165-6147(98)01278-4
PMID:10101952
Abstract

The precise abnormalities of colonic motility patterns in idiopathic constipation, and the alterations at the cellular, neural, myogenic and biochemical levels that underlie these patterns, are not yet understood. One promising approach in the treatment of constipation seems to be to design drugs that can stimulate GMCs to produce mass movements and consequently defaecation. This could possibly be achieved with the selective 5-HT4 receptor agonists prucalopride and SDZ HTF-919, which are currently in advanced clinical trials. Other mechanisms that provide a means to induce GMCs, such as NK1 receptor agonism, deserve further exploration.

摘要

特发性便秘中结肠动力模式的确切异常情况,以及构成这些模式基础的细胞、神经、肌源性和生化水平的改变,目前尚不清楚。治疗便秘的一种有前景的方法似乎是设计能刺激集团蠕动收缩(GMCs)以产生推进性蠕动并进而促进排便的药物。这可能通过选择性5-羟色胺4(5-HT4)受体激动剂普芦卡必利和SDZ HTF-919来实现,这两种药物目前正处于高级临床试验阶段。其他诱导集团蠕动收缩的机制,如NK1受体激动作用,值得进一步探索。

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Idiopathic constipation: too few stools and too little knowledge.特发性便秘:大便过少,了解过少。
Trends Pharmacol Sci. 1999 Jan;20(1):1-3. doi: 10.1016/s0165-6147(98)01278-4.
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Effect of enterokinetic prucalopride on intestinal motility in fast rats.
促肠动力药普芦卡必利对禁食大鼠肠道蠕动的影响。
World J Gastroenterol. 2003 Sep;9(9):2065-7. doi: 10.3748/wjg.v9.i9.2065.
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An improved in vitro bioassay for the study of 5-HT(4) receptors in the human isolated large intestinal circular muscle.一种用于研究人离体大肠环形肌中5-羟色胺(4)受体的改良体外生物测定法。
Br J Pharmacol. 2000 Apr;129(8):1601-8. doi: 10.1038/sj.bjp.0703254.