Experimental Models of Stress and Pain: Do They Help to Develop New Therapies?

被引:7
作者
Bradesi, Sylvie [1 ]
Mayer, Emeran A.
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Div Digest Dis, Ctr Neurobiol Stress,Dept Med, Los Angeles, CA 90095 USA
关键词
Irritable bowel syndrome; Animal models; Human experimental medicine models; Drug development; Predictive validity; Intermediate phenotypes; IRRITABLE-BOWEL-SYNDROME; FUNCTIONAL GASTROINTESTINAL DISORDERS; BRAIN-GUT AXIS; NOXIOUS COLORECTAL DISTENSION; PSEUDO-AFFECTIVE RESPONSES; 5-HT3 RECEPTOR ANTAGONIST; KAPPA-AGONIST FEDOTOZINE; FACTOR-I RECEPTORS; COLONIC DISTENSION; ANIMAL-MODELS;
D O I
10.1159/000268122
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The majority of functional gastrointestinal disorders are characterised by recurrent abdominal pain, with stress playing an important role in first onset and exacerbation of existing symptoms. These disorders are currently defined by symptom criteria, while their pathophysiology remains controversial and incompletely understood. Modeling these disorders in humans and animals has been difficult. While some of the models have adequate face and construct validity, the predictive validity of most of the models has been disappointing, which has put into question the traditional modeling approach. Similar problems have been encountered in drug development for pain and psychiatric disorders. New approaches have been proposed in the form of reverse translation, which include better characterisation of biological intermediate phenotypes in human disease which can be modeled in humans and in animals. Continuation of the current approach focusing on complex clinical phenotypes is likely to be ineffective for the development of novel and effect treatments. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:55 / 67
页数:13
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