The multi-herbal drug STW 5 (Iberogast®) has prosecretory action in the human intestine

被引:33
|
作者
Krueger, D. [1 ]
Gruber, L. [1 ]
Buhner, S. [1 ]
Zeller, F. [2 ]
Langer, R. [3 ]
Seidl, S. [3 ]
Michel, K. [1 ]
Schemann, M. [1 ]
机构
[1] Tech Univ Munich, Dept Human Biol, D-85350 Freising Weihenstephan, Germany
[2] Clin Ctr Freising, Dept Surg, Freising Weihenstephan, Germany
[3] Tech Univ Munich, Dept Pathol, D-85350 Freising Weihenstephan, Germany
来源
NEUROGASTROENTEROLOGY AND MOTILITY | 2009年 / 21卷 / 11期
关键词
chloride secretion; cystic fibrosis transmembrane conductance regulator; enteric nervous system; human intestine; Iberogast; IRRITABLE-BOWEL-SYNDROME; FUNCTIONAL DYSPEPSIA; DOUBLE-BLIND; COMPONENTS; LUBIPROSTONE; LINACLOTIDE; MULTICENTER; SECRETION;
D O I
10.1111/j.1365-2982.2008.01242.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
P>There is growing evidence that STW 5 (Iberogast (R), fixed combination of hydroethanolic herbal extracts), besides being effective in functional dyspepsia, also improves symptoms in irritable bowel syndrome (IBS). Clinical data indicate that modulation of mucosal secretion is a promising approach to treat intestinal disorders associated with IBS. We therefore explored the effect of STW 5 on secretion in the human intestine and the mechanisms by which it acts. The Ussing chamber technique was used to measure mucosal secretion in human intestinal mucosa/submucosa preparations and in human epithelial cell line T84. In addition, we recorded STW 5 effects on human enteric neurons with voltage sensitive dye imaging. In human tissue and T84 cells STW 5 induced a dose-dependent increase in ion secretion that was significantly reduced by the Na-K-Cl cotransporter blocker bumetanide, the adenylate cyclase inhibitor MDL-12 330, the non-specific and selective cystic fibrosis transmembrane conductance regulator (CFTR) inhibitors glibenclamide and CFTRinh-172, respectively, and the blocker of calcium dependent Cl- channels (ClCa) SITS (4-acetamido-4-isothiocyanatostilbene-2,2-disulphonic acid). It was unaffected by amiloride, a blocker of epithelial Na+ channels. In human tissue, the nerve blocker tetrodotoxin significantly suppressed the STW 5 response. STW 5 evoked an increased spike discharge in 51% of human submucous neurons. Results suggest that STW 5 is a secretogogue in the human intestine by direct epithelial actions and through activation of enteric neurons. The prosecretory effect is due to increased epithelial Cl- fluxes via CFTR and Ca-dependent ClCa channels. STW 5 may be a novel option to treat secretory disorders associated with IBS and constipation.
引用
收藏
页码:1203 / +
页数:8
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