Literature DB >> 6141036

Active pyrimidine absorption by chicken colon.

E Scharrer, L Stubenhofer, W Tiemeyer, C Bindl.   

Abstract

Pyrimidine absorption by chicken large intestine was investigated employing the everted sac and flux chamber techniques. 3H-labelled uracil was used as substrate. The small intestine and the colon unlike the caecum, transported uracil from the mucosal to the serosal surface against a concentration gradient in the everted sac experiments. Furthermore, there was a net transport of uracil from the mucosal to the serosal side of the colon and jejunum in the flux chamber experiments. Uracil transport by the everted colon sacs against a concentration gradient was inhibited when the purine hypoxanthine was present in the incubation medium. Uracil transport by the everted colon sacs was also inhibited under anaerobic conditions and when 2,4-dinitrophenol was present in the incubation medium. Replacing the Na+ ions of the incubation medium by Li+ ions also caused an inhibition of uracil transport. It is concluded from these results that uracil (and probably other pyrimidines) are absorbed from the chicken colon by a Na+ ion-dependent active transport process having also an affinity for purines.

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Year:  1984        PMID: 6141036     DOI: 10.1016/0300-9629(84)90016-1

Source DB:  PubMed          Journal:  Comp Biochem Physiol A Comp Physiol        ISSN: 0300-9629


  4 in total

1.  Na+ gradient-dependent transport of hypoxanthine by calf intestinal brush border membrane vesicles.

Authors:  A Theisinger; B Grenacher; E Scharrer
Journal:  J Comp Physiol B       Date:  2003-02-11       Impact factor: 2.200

2.  Evidence for incorporation of intact dietary pyrimidine (but not purine) nucleosides into hepatic RNA.

Authors:  H K Berthold; P F Crain; I Gouni; P J Reeds; P D Klein
Journal:  Proc Natl Acad Sci U S A       Date:  1995-10-24       Impact factor: 11.205

Review 3.  Dietary nucleotides and gut mucosal defence.

Authors:  G K Grimble
Journal:  Gut       Date:  1994-01       Impact factor: 23.059

4.  In Vitro Drug Absorption Models. II. Salicylate, Cefoxitin, α-Methyldopa and Theophylline Uptake in Cells and Rings: Correlation with In Vivo Bioavailability.

Authors:  P A Porter; I Osiecka; R T Borchardt; J A Fix; L Frost; C Gardner
Journal:  Pharm Res       Date:  1985-11       Impact factor: 4.200

  4 in total

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