Ion transport in the experimental short bowel syndrome of the rat

Gastroenterology. 1992 Feb;102(2):497-504. doi: 10.1016/0016-5085(92)90096-h.


The adaptational changes of epithelial ion transport in the short bowel syndrome were studied. Ileal remnants of rats were investigated 8 weeks after 70% proximal small intestinal resection. Pure epithelial resistance measured by impedance analysis decreased from 27 +/- 1 to 21 +/- 1 omega.cm2, and polyethylene glycol 4000 fluxes increased from 2.5 +/- 0.3 to 3.6 +/- 0.3, indicating increased permeability of the short bowel. Unidirectional flux measurements in control ileum showed absorptive net fluxes of Na+ and Cl- that were assigned to electroneutral NaCl absorption and a short-circuit current that was accounted for by the residual flux (HCO3- secretion). Neither NaCl absorption nor HCO3- secretion were altered in the short bowel. Also, electrogenic Cl- secretion, defined after maximal stimulation by theophylline and prostaglandin E1 was not changed in the short bowel. In contrast, electrogenic Na+/glucose cotransport increased in Vmax from 2.0 +/- 0.3 in controls to 5.0 +/- 1.0 in the short bowel. Tight junction structure was studied by freeze-fracture electron microscopy. The number of horizontal strands was unchanged, whereas tight junction depth was slightly increased in the short bowel. Microvillus area of short bowels was increased by 20% in villus regions. Under the light microscope, villus height was increased by 30%. In conclusion, the short bowel mucosa undergoes adaptive responses to reduced overall absorptive area by increasing glucose-dependent electrogenic Na+ absorption to 250%, which is partly caused by increased villus and microvillus surface area. Electrogenic Cl- and HCO3- secretion and electroneutral NaCl absorption remained unchanged. The decreased epithelial resistance is caused by mucosal surface amplification.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adaptation, Physiological
  • Animals
  • Biological Transport, Active
  • Chlorides / metabolism
  • Electrolytes / metabolism*
  • Female
  • Freeze Fracturing
  • Glucose / metabolism
  • Glucose / physiology
  • In Vitro Techniques
  • Intestinal Absorption*
  • Microvilli / pathology
  • Microvilli / physiology
  • Rats
  • Rats, Inbred Strains
  • Short Bowel Syndrome / metabolism*
  • Short Bowel Syndrome / pathology
  • Short Bowel Syndrome / physiopathology
  • Sodium / metabolism
  • Time Factors


  • Chlorides
  • Electrolytes
  • Sodium
  • Glucose