Document Detail


Mechanisms involved in the gastro-protective effect of STW 5 (Iberogast) and its components against ulcers and rebound acidity.
MedLine Citation:
PMID:  16963243     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The protective effect of a commercial preparation (STW 5, Iberogast), containing the extracts of bitter candy tuft, lemon balm leaf, chamomile flower, caraway fruit, peppermint leaf, liquorice root, Angelica root, milk thistle fruit and greater celandine herb, against the development of gastric ulcers was previously reported in an earlier publication (Khayyal et al., 2001). All extracts produced a dose dependent anti-ulcerogenic effect associated with a reduced acid output, an increased mucin secretion, an increase in prostaglandin E(2) release and a decrease in leukotrienes. The effect on pepsin content was not uniform and did not seem to bear a relationship with the anti-ulcerogenic activity. The best effects were observed with the combined formulation, STW 5. Furthermore, the effect of the latter in protecting against the development of rebound gastric acidity was examined experimentally in rats and compared with the effect of some commercial antacid preparations (Rennie, Talcid and Maaloxan). A model of testing rebound acidity was developed by inducing a marginal increase in gastric acidity through the administration of indomethacin, in such a way that it could be easily neutralized, allowing any eventual secondary increase in acidity to be measured within a few hours of administration. In addition, the serum gastrin level was measured after drug treatment to establish any correlation between it and any rebound acidity. The results obtained demonstrated that STW 5 did not only lower the gastric acidity as effectively as the commercial antacid, but it was more effective in inhibiting the secondary hyperacidity. Moreover, STW 5 was capable of inhibiting the serum gastrin level in rats, an effect which ran parallel to its lowering effect on gastric acid production.
Authors:
M T Khayyal; M Seif-El-Nasr; M A El-Ghazaly; S N Okpanyi; O Kelber; D Weiser
Related Documents :
9017763 - Proton pump inhibitors and acid-related diseases.
18561923 - Chromoendoscopy with indigo carmine dye added to acetic acid in the diagnosis of gastri...
18964803 - Non-aqueous titration of quinine and quinidine sulphates by use of barium perchlorate.
Publication Detail:
Type:  Journal Article     Date:  2006-09-11
Journal Detail:
Title:  Phytomedicine : international journal of phytotherapy and phytopharmacology     Volume:  13 Suppl 5     ISSN:  0944-7113     ISO Abbreviation:  Phytomedicine     Publication Date:  2006  
Date Detail:
Created Date:  2006-12-01     Completed Date:  2007-04-11     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9438794     Medline TA:  Phytomedicine     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  56-66     Citation Subset:  IM    
Affiliation:
Department of Pharmacology, Faculty of Pharmacy, Cairo University, Egypt.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Gastric Acidity Determination
Gastric Juice / drug effects*
Gastrins / blood,  drug effects*
Indomethacin
Male
Phytotherapy
Plant Extracts / pharmacology*,  therapeutic use
Rats
Rats, Wistar
Stomach Ulcer / drug therapy*
Chemical
Reg. No./Substance:
0/Gastrins; 0/Plant Extracts; 0/iberogast; 53-86-1/Indomethacin

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Application of sucrose fatty acid esters in transdermal therapeutic systems.
Next Document:  Omega-3 fatty acids and monoamine neurotransmission.