The role of serotonin in intestinal luminal sensing and secretion

被引:102
|
作者
Hansen, M. Berner [1 ,2 ]
Witte, A. -B. [1 ,3 ]
机构
[1] Univ Copenhagen, Bispebjerg Hosp, Dept Gastrointestinal Surg K, DK-2400 Copenhagen NV, Denmark
[2] Astrazeneca Res & Dev, Molndal, Sweden
[3] Karolinska Univ Hosp, Dept Gastroenterol, Stockholm, Sweden
关键词
enteric neurones; enterochromaffin cells; epithelial ion transport; intestinal secretion; serotonin; transient receptor potential vanilloid type 1;
D O I
10.1111/j.1748-1716.2008.01870.x
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
This mini-review addresses the role of the neuroendocrine substance serotonin (5-hydroxytryptamine, 5-HT) in intestinal luminal sensing and secretion. Intestinal sensory neurones are activated by several mechanisms, in particular following stimulation of 'specialized' cells in the mucosa. These specialized cells are the enteroendocrine cells, which contain a wide variety of neuroendocrine transmitters. One of these enteroendocrine cells is the enterochromaffin (EC) cell, which is present throughout the intestines and contains large amounts of serotonin, predominantly in the duodenum in humans. The EC cells act as mucosal sensory transducers and secrete serotonin in response to various physiological and pathological luminal stimuli. Following release, serotonin participates in several mucosal protecting processes, one being secretion. Serotonin stimulates active ion, mucus and fluid secretion. Epithelial 5-HT2 receptors and neuronal 5-HT1P, 5-HT3 and 5-HT4 receptors mediate the secretory effect of serotonin. A transmembrane serotonin transporter terminates epithelial serotonergic signalling. The transient receptor potential ion channel family is important for processing intestinal luminal sensory signalling. Accumulating evidence suggests a significant interaction between serotonin and one of the transient receptor potential ion channels, the capsaicin-sensitive transient receptor potential vanilloid type 1. Accordingly, EC cells, serotonergic receptors and transporter(s), and transient receptor potential vanilloid type-1 ion channels are all explored as pharmacological targets for treatment of some intestinal functional disorders.
引用
收藏
页码:311 / 323
页数:13
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