Protease-Activated Receptors as Therapeutic Targets in Visceral Pain

被引:34
作者
Cenac, Nicolas [1 ,2 ,3 ]
机构
[1] INSERM, U1043, F-31300 Toulouse, France
[2] CNRS, U5282, F-31300 Toulouse, France
[3] Univ Toulouse, UPS, CPTP, F-31300 Toulouse, France
关键词
Calcium channels; IBD; IBS; neuromediators; Protease; Pain; Inflammation; Protease activated receptor; IRRITABLE-BOWEL-SYNDROME; INFLAMMATORY PAIN; MAST-CELLS; CAPSAICIN RECEPTOR; PROTEASE-ACTIVATED-RECEPTOR-2; SENSITIZES; REFERRED HYPERALGESIA; SERINE PROTEASES; ION-CHANNEL; HYPERSENSITIVITY; NOCICEPTION;
D O I
10.2174/1570159X113119990039
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The protease-activated receptors (PARs) play a pivotal role in inflammatory and nociceptive processes. PARs have raised considerable interest because of their capacity to regulate numerous aspects of viscera physiology and pathophysiology. The present article summarizes research on PARs and proteases as signalling molecules in visceral pain. In particular, experiments in animal models suggest that PAR(2) is important for visceral hypersensitivity. Moreover, endogenous PAR(2) agonists seem to be released by colonic tissue of patients suffering from irritable bowel syndrome, suggesting a role for this receptor in visceral pain perception. Thus, PARs, together with proteases that activate them, represent exciting targets for therapeutic intervention on visceral pain.
引用
收藏
页码:598 / 605
页数:8
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