Literature DB >> 2842121

Discrepancy between effects of cholera toxin on net fluid movement and cAMP levels in rat jejunum, ileum, and colon.

U M Farack1, R Gerzer, T M Keravis, K Loeschke.   

Abstract

Regional differences in the response to cholera toxin were evaluated in rat jejunum, ileum, and colon in vivo. Ligated intestinal loops were exposed to a supramaximal concentration of cholera toxin for 5 hr, and net fluid transport, adenosine 3',5'-monophosphate (cAMP) concentrations, and adenylate cyclase and phosphodiesterase activities of mucosal homogenates were determined. The fluid transport response and the specific activities of adenylate cyclase (with and without cholera toxin) and phosphodiesterase declined progressively from the jejunum to the colon. In contrast, cAMP concentrations (with and without cholera toxin) were lowest in the jejunum and highest in the colon. These results demonstrate that cAMP concentrations of the total mucosal homogenate do not parallel cholera toxin-induced fluid secretion in the three intestinal segments. Rather, the activities of adenylate cyclase and phosphodiesterase suggest a relation between fluid secretion and the turnover of cAMP.

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Year:  1988        PMID: 2842121     DOI: 10.1007/BF01535793

Source DB:  PubMed          Journal:  Dig Dis Sci        ISSN: 0163-2116            Impact factor:   3.199


  27 in total

1.  Failure to reverse cholera toxin induced intestinal secretion by agents which decrease mucosal cAMP.

Authors:  G W Forsyth; D L Hamilton; A Scoot; K E Goertz; R A Kapitany
Journal:  Can J Physiol Pharmacol       Date:  1979-09       Impact factor: 2.273

2.  Cholera toxin-induced glycoprotein secretion in rabbit small intestine.

Authors:  H P Sherr; R B Mertens
Journal:  Gastroenterology       Date:  1979-07       Impact factor: 22.682

3.  An improved protein binding assay for cyclic AMP.

Authors:  C O Brostrom; C Kon
Journal:  Anal Biochem       Date:  1974-04       Impact factor: 3.365

Review 4.  Vibrio cholerae enterotoxin and its mode of action.

Authors:  N F Pierce; W B Greenough; C C Carpenter
Journal:  Bacteriol Rev       Date:  1971-03

Review 5.  The chemistry and biology of cholera toxin.

Authors:  C Y Lai
Journal:  CRC Crit Rev Biochem       Date:  1980

6.  Cyclic nucleotide phosphodiesterase activities from pig coronary arteries. Lack of interconvertibility of major forms.

Authors:  T M Keravis; J N Wells; J G Hardman
Journal:  Biochim Biophys Acta       Date:  1980

7.  Stimulation of intestinal mucosal adenyl cyclase by cholera enterotoxin and prostaglandins.

Authors:  D V Kimberg; M Field; J Johnson; A Henderson; E Gershon
Journal:  J Clin Invest       Date:  1971-06       Impact factor: 14.808

8.  Effect of indomethacin on cholera-induced fluid movement, unidirectional sodium fluxes, and intestinal cAMP.

Authors:  A Wald; G S Gotterer; G R Rajendra; N A Turjman; T R Hendrix
Journal:  Gastroenterology       Date:  1977-01       Impact factor: 22.682

9.  Effect of propranolol on bile acid- and cholera enterotoxin-stimulated cAMP and secretion in rabbit intestine.

Authors:  M Taub; G Bonorris; A Chung; M J Coyne; L J Schoenfield
Journal:  Gastroenterology       Date:  1977-01       Impact factor: 22.682

10.  Comparative study of the effect of cholera toxin and sodium deoxycholate on the paracellular permeability and on net fluid and electrolyte transfer in the rat colon.

Authors:  K J Goerg; M Gross; G Nell; W Rummel; L Schulz
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1980-05       Impact factor: 3.000

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  3 in total

1.  Colon water transport in transgenic mice lacking aquaporin-4 water channels.

Authors:  K S Wang; T Ma; F Filiz; A S Verkman; J A Bastidas
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2000-08       Impact factor: 4.052

2.  Effect of cholera toxin on intestinal elimination of ciprofloxacin in rabbits.

Authors:  A Musafija; A Barzilai; J Ramon; E Rubinstein
Journal:  Antimicrob Agents Chemother       Date:  1998-02       Impact factor: 5.191

3.  Chloride secretion induced by phorbol dibutyrate and forskolin in the human colonic carcinoma cell line HT-29Cl.19A is regulated by different mechanisms.

Authors:  R B Bajnath; K Dekker; H R De Jonge; J A Groot
Journal:  Pflugers Arch       Date:  1995-09       Impact factor: 3.657

  3 in total

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