Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1966 Feb;182(3):559–573. doi: 10.1113/jphysiol.1966.sp007837

Sodium-glucose interactions in the goldfish intestine

M W Smith
PMCID: PMC1357487  PMID: 16992220

Abstract

1. Everted sacs of goldfish intestine transfer glucose and water to their serosal surfaces and the total transfer is greater in the anterior intestine than in the intestinal bulb or rectum.

2. Transmural potentials, with the serosa positive to the mucosa, were recorded from all parts of the goldfish intestine but were highest in the anterior intestine and the rectum. In both these areas the total potential was dependent partly upon the presence of glucose.

3. Reducing the concentration of sodium bathing the mucosa of the anterior intestine reduced the glucose-evoked potential in a non-linear way. The steady-state potentials, with or without glucose, first increased and later decreased as the sodium concentration was further reduced.

4. Reducing the concentration of glucose bathing the mucosa from 27 to 5 mM slightly increased the glucose-evoked potential. Further reduction of the glucose concentration caused the glucose-evoked potential to fall.

5. Phlorrhizin inhibited the glucose-evoked potential. The degree of inhibition was proportional to the log concentration of phlorrhizin over the range 2 × 10-7-6 × 10-5M. The steady-state potential with glucose present was lower than when glucose was absent at phlorrhizin concentrations, 6 × 10-6-6 × 10-5M.

6. The glucose-evoked potential increased rapidly over the temperature range 5-15° C and more slowly from 15 to 30° C. The steady-state potentials also increased with temperature, the rate of increase being greater when glucose was present. Below 15° C the glucose-independent potential was higher and above 15° C lower than the steady-state potential recorded with glucose present.

7. These findings are discussed in terms of sodium—glucose interaction taking place at the luminal side of the mucosal cell, on the outside of the mucosal cell membrane.

Full text

PDF
559

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BARRY R. J., DIKSTEIN S., MATTHEWS J., SMYTH D. H., WRIGHT E. M. ELECTRICAL POTENTIALS ASSOCIATED WITH INTESTINAL SUGAR TRANSFER. J Physiol. 1964 Jun;171:316–338. doi: 10.1113/jphysiol.1964.sp007379. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BIHLER I., CRANE R. K. Studies on the mechanism of intestinal absorption of sugars. V. The influence of several cations and anions on the active transport of sugars, in vitro, by various preparations of hamster small intestine. Biochim Biophys Acta. 1962 May 7;59:78–93. doi: 10.1016/0006-3002(62)90699-6. [DOI] [PubMed] [Google Scholar]
  3. CEREIJIDO M., HERRERA F. C., FLANIGAN W. J., CURRAN P. F. THE INFLUENCE OF NA CONCENTRATION ON NA TRANSPORT ACROSS FROG SKIN. J Gen Physiol. 1964 May;47:879–893. doi: 10.1085/jgp.47.5.879. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. CLARKSON T. W., CROSS A. C., TOOLE S. R. Electrical potentials across isolated small intestine of the rat. Am J Physiol. 1961 Jun;200:1233–1235. doi: 10.1152/ajplegacy.1961.200.6.1233. [DOI] [PubMed] [Google Scholar]
  5. COOPERSTEIN I. L., HOGBEN C. A. Ionic transfer across the isolated frog large intestine. J Gen Physiol. 1959 Jan 20;42(3):461–473. doi: 10.1085/jgp.42.3.461. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. CORDIER D., MAURICE A., CHANEL J. Influence de la température sur l'absorption intestinale des oses chez la tanche (Tinca vulgaris). C R Seances Soc Biol Fil. 1954 Aug-Sep;148(15-18):1417–1418. [PubMed] [Google Scholar]
  7. CRANE R. K. Hypothesis for mechanism of intestinal active transport of sugars. Fed Proc. 1962 Nov-Dec;21:891–895. [PubMed] [Google Scholar]
  8. CSAKY T. Z. Significance of sodium ions in active intestinal transport of nonelectrolytes. Am J Physiol. 1961 Dec;201:999–1001. doi: 10.1152/ajplegacy.1961.201.6.999. [DOI] [PubMed] [Google Scholar]
  9. CSAKY T. Z., THALE M. Effect of ionic environment on intestinal sugar transport. J Physiol. 1960 Apr;151:59–65. [PMC free article] [PubMed] [Google Scholar]
  10. FRAZIER H. S., DEMPSEY E. F., LEAF A. Movement of sodium across the mucosal surface of the isolated toad bladder and its modification by vasopressin. J Gen Physiol. 1962 Jan;45:529–543. doi: 10.1085/jgp.45.3.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. HANSEN O. Specificity of the glucose oxidase reaction and interference with the quantitative glucose oxidase-peroxidase-O-dianisidine method. Scand J Clin Lab Invest. 1962;14:651–655. doi: 10.1080/00365516209051298. [DOI] [PubMed] [Google Scholar]
  12. HOLLANDS B. C., SMITH M. W. PHOSPHATASES OF THE GOLDFISH INTESTINE. J Physiol. 1964 Dec;175:31–37. doi: 10.1113/jphysiol.1964.sp007501. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. NEWEY H., SANFORD P. A., SMYTH D. H. URANYL IONS AND INTESTINAL HEXOSE TRANSFER. Nature. 1965 Jan 23;205:389–390. doi: 10.1038/205389a0. [DOI] [PubMed] [Google Scholar]
  14. RIKLIS E., QUASTEL J. H. Effects of cations on sugar absorption by isolated surviving guinea pig intestine. Can J Biochem Physiol. 1958 Mar;36(3):347–362. [PubMed] [Google Scholar]
  15. SCHULTZ S. G., ZALUSKY R. ION TRANSPORT IN ISOLATED RABBIT ILEUM. I. SHORT-CIRCUIT CURRENT AND NA FLUXES. J Gen Physiol. 1964 Jan;47:567–584. doi: 10.1085/jgp.47.3.567. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. SCHULTZ S. G., ZALUSKY R. ION TRANSPORT IN ISOLATED RABBIT ILEUM. II. THE INTERACTION BETWEEN ACTIVE SODIUM AND ACTIVE SUGAR TRANSPORT. J Gen Physiol. 1964 Jul;47:1043–1059. doi: 10.1085/jgp.47.6.1043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. SMITH M. W. THE IN VITRO ABSORPTION OF WATER AND SOLUTES FROM THE INTESTINE OF GOLDFISH, CARASSIUS AURATUS. J Physiol. 1964 Dec;175:38–49. doi: 10.1113/jphysiol.1964.sp007502. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. STOKES R. M., FROMM P. O. GLUCOSE ABSORPTION AND METABOLISM BY THE GUT OF RAINBOW TROUT. Comp Biochem Physiol. 1964 Sep;13:53–69. doi: 10.1016/0010-406x(64)90084-2. [DOI] [PubMed] [Google Scholar]
  19. Smith M. W. Electrical properties and glucose transfer in the goldfish intestine. Experientia. 1964 Nov 15;20(11):613–614. doi: 10.1007/BF02144815. [DOI] [PubMed] [Google Scholar]
  20. Smith M. W. Influence of temperature acclimatization on sodium--glucose interactions in the goldfish intestine. J Physiol. 1966 Feb;182(3):574–590. doi: 10.1113/jphysiol.1966.sp007838. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. WILSON T. H., WISEMAN G. The use of sacs of everted small intestine for the study of the transference of substances from the mucosal to the serosal surface. J Physiol. 1954 Jan;123(1):116–125. doi: 10.1113/jphysiol.1954.sp005036. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES