Prokineticin 1 inhibits spontaneous giant contractions in the murine proximal colon through nitric oxide release

被引:24
|
作者
Hoogerwerf, W. A. [1 ]
机构
[1] Univ Texas, Med Branch, Div Gastroenterol & Hepatol, Galveston, TX 77555 USA
来源
NEUROGASTROENTEROLOGY AND MOTILITY | 2006年 / 18卷 / 06期
关键词
enteric nervous system; G-protein coupled receptors; gastrointestinal motility; myenteric plexus; prokineticin;
D O I
10.1111/j.1365-2982.2006.00776.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Prokineticins are novel peptides with reported effects on gastrointestinal contractility. Prokineticin actions are mediated by distinct prokineticin receptors (PKR1 and PKR2). This study investigated the role of prokineticin 1 in colonic contractility as well as sites of expression of its receptor in the mouse proximal colon by immunohistochemistry and confocal microscopy. Prokineticin 1 suppressed giant contractions in circular muscle. The inhibitory effect of prokineticin 1 on giant contractions was blocked by the nitric oxide synthase (NOS) inhibitor N(omega)-nitro-L-arginine methyl ester (L-NAME). In vitro, prokineticin 1 stimulated nitric oxide release from longitudinal muscle-myenteric plexus cultures. This effect was blocked by L-NAME. PKR1 is expressed on myenteric plexus neurons and colocalizes with a small subset of nNOS expressing neurons. This study suggests that PKR1 mediates an inhibitory effect in vitro, most likely through direct or indirect stimulation of nitric oxide release. PKR1 and its natural ligand, prokineticin 1 may be important for modulation of colonic motility.
引用
收藏
页码:455 / 463
页数:9
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