Article Text

Download PDFPDF
New insights into intestinal secretion
  1. Jörg D Schulzke1,
  2. Britta Siegmund1,
  3. Dorothee Günzel2
  1. 1 Department of Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité Berlin, Berlin, Germany
  2. 2 Institute of Clinical Physiology, Campus Benjamin Franklin, Charité Berlin, Berlin, Germany
  1. Correspondence to Professor Jörg D Schulzke, Department of Gastroenterology, Infectious Diseases and Rheumatology, Campus Benjamin Franklin, Charité Berlin, Berlin, Germany; joerg.schulzke{at}charite.de

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Apart from malabsorption and intestinal barrier dysfunction (via a ‘leak-flux’ mechanism), diarrhoea may reflect active ion secretion in the small intestine and/or colon. In recent years, our understanding about intestinal secretory mechanisms has increased enormously. Important new findings are (1) chloride, bicarbonate and potassium may be secreted simultaneously, but via independent transport processes and (2) movement of a specific ion across cell membranes may occur via several types of channels selective for that ion, but differing in their molecular structure and intrinsic biophysical properties. Additionally, Linley and coworkers now present evidence that (3) specific types of chloride and potassium channels involved in chloride and potassium secretion are differentially expressed in the apical membrane of enterocytes and goblet cells along the surface cell-crypt cell axis. Thus, we are now in a position to reconsider the ancient concept of exclusively secretory crypt cells and absorptive surface cells.1

In general, underlying active intestinal ion secretion is Na+/K+-ATPase-dependent primary transport, which results in low intracellular sodium and high intracellular potassium concentrations. The sodium gradient across the basolateral membrane facilitates basolateral chloride or bicarbonate uptake via sodium-coupled cotransport (secondary active transport), as a result of which these anions accumulate intracellularly above their electrochemical equilibrium. As a result of this gradient across the apical membrane, they are subsequently secreted into …

View Full Text

Footnotes

  • Correction notice Reference list has been updated since published Online First.

  • Contributors All three authors contributed to the writing of parts of the commentary article.

  • Competing interests None.

  • Provenance and peer review Commissioned; internally peer reviewed.

Linked Articles