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Selected Publication:

Beubler, E; Schuligoi, R.
Mechanisms of cholera toxin-induced diarrhea.
Ann N Y Acad Sci. 2000; 915(3):339-346 Doi: 10.1111/j.1749-6632.2000.tb05262.x
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Leading authors Med Uni Graz
Beubler Eckhard
Co-authors Med Uni Graz
Schuligoi Rufina
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Abstract:
In the pathogenesis of cholera, cyclic adenosine monophosphate, 5-hydroxytryptamine, prostaglandins, and the function of neuronal structures have been implicated. To elucidate the role of different isoforms of cyclooxygenase (COX)-1 and COX-2, selective COX-2 inhibitors were used. The selective COX-2 inhibitors NS-398 and DFU completely suppressed cholera toxin-induced prostaglandin E2 biosynthesis and caused a dose-dependent inhibition of cholera toxin-induced fluid secretion in the rat jejunum in vivo. Constitutive expression of COX-1 but also of COX-2 mRNA was found in mucosal scrapings of the rat jejunum. Cholera toxin had no effect on COX-1 as well as COX-2 mRNA expression. Treatment of rats with dexamethasone did not effect cholera toxin-induced prostaglandin E2 biosynthesis and did not influence the expression of COX-2 mRNA, further substantiating that cholera toxin does not cause an induction of COX-2 mRNA. Treatment of rats with E. coli lipopolysaccharide caused a marked increase in COX-2 mRNA expression that was inhibited by dexamethasone. In conclusion, the results provide evidence that cholera toxin, in addition to other mediators, uses prostaglandin E2 to exert its secretory effect and that in the case of cholera toxin prostaglandins are metabolized via COX-2.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Cholera Toxin - toxicity
Cyclooxygenase 1 - toxicity
Cyclooxygenase 2 - toxicity
Cyclooxygenase 2 Inhibitors - toxicity
Cyclooxygenase Inhibitors - pharmacology
Dexamethasone - pharmacology
Diarrhea - chemically induced
Dinoprostone - metabolism
Dose-Response Relationship, Drug - metabolism
Furans - pharmacology
Gene Expression Regulation, Enzymologic - pharmacology
Glucocorticoids - pharmacology
Intestinal Mucosa - drug effects
Isoenzymes - metabolism
Jejunum - metabolism
Lipopolysaccharides - pharmacology
Membrane Proteins - pharmacology
Nitrobenzenes - pharmacology
Prostaglandin-Endoperoxide Synthases - metabolism
RNA, Messenger - analysis
Rats - analysis
Sulfonamides - pharmacology

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