Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Interpretation of Hexose-dependent Electrical Potential Differences in Small Intestine

Abstract

ACTIVELY transported sugars added to the solution bathing the mucosal surface of the small intestine produce an increase in the electrical potential difference (p.d.) and short-circuit current (Isc) across the tissue1–4. Schultz and Zalusky1 have shown that the increase in the IscIsc) across rabbit ileum is a function of both sugar and sodium concentrations in the bathing solution. When sodium was replaced with potassium, the maximum ΔIsc caused by addition of sugars was a linear function of sodium concentration. Recently, Barry et al.5 reported that the increase in the p.d. (Δp.d.) following addition of galactose to the mucosal bathing solution of everted sacs of rat mid-intestine is independent of sodium concentration when mannitol is used to replace sodium chloride, but is approximately a linear function of sodium concentration when potassium is used to replace sodium. They have concluded that the “galactose dependent potential is unaffected by sodium concentration but is reduced by increasing potassium concentration”. Lyon and Crane6 have reported that, in rat jejunum, the maximum Δp.d. resulting from addition of actively transported sugars is independent of sodium concentration when tris [2-amino-2(hydroxymethyl)-1,3-propanediol] is used to replace sodium, but decreases when potassium is used as replacement ion.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Schultz, S. G., and Zalusky, R., J. Gen. Physiol., 47, 1043 (1964).

    Article  CAS  Google Scholar 

  2. Barry, R. J. C., Dikstein, S., Matthews, J., Smyth, D. H., and Wright, E. M., J. Physiol., 171, 316 (1964).

    Article  CAS  Google Scholar 

  3. Barry, R. J. C., Smyth, D. H., and Wright, E. M., J. Physiol., 181, 410 (1965).

    Article  CAS  Google Scholar 

  4. Asano, T., Proc. Soc. Exp. Biol. and Med., 119, 189 (1965).

    Article  CAS  Google Scholar 

  5. Barry, R. J. C., Eggenton, J., Smyth, D. H., and Wright, E. M., J. Physiol., 182, 40 P (1966).

    Article  Google Scholar 

  6. Lyon, I., and Crane, R. K., Biochim. Biophys. Acta, 112, 278 (1966).

    Article  CAS  Google Scholar 

  7. Schultz, S. G., and Zalusky, R., J. Gen. Physiol., 47, 567 (1964).

    Article  CAS  Google Scholar 

  8. Asano, T., Amer. J. Physiol., 207, 415 (1964).

    Article  CAS  Google Scholar 

  9. Schultz, S. G., Zalusky, R., and Gass, jun., A. E., J. Gen. Physiol., 48, 375 (1964).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

SCHULTZ, S., CURRAN, P. & WRIGHT, E. Interpretation of Hexose-dependent Electrical Potential Differences in Small Intestine. Nature 214, 509–510 (1967). https://doi.org/10.1038/214509a0

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/214509a0

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing