Impaired intestinal sugar transport in cirrhotic rats: correction by low doses of insulin-like growth factor I

Gastroenterology. 1997 Oct;113(4):1180-7. doi: 10.1053/gast.1997.v113.pm9322513.

Abstract

Background & aims: Malnutrition is a complication of liver cirrhosis accompanied by reduced insulin-like growth factor I (IGF-I) availability. The aim of this study was to analyze the effect of IGF-I on intestinal D-galactose absorption in cirrhotic rats.

Methods: IGF-I (2 micrograms.100 g body wt-1.day-1) or saline were given for 14 days to rats in whom cirrhosis was induced with CCl4. Galactose transport and sodium-glucose/galactose-ligand transporter 1 (SGLT-1) expression were assessed in jejunal rings and in brush border membrane vesicles (BBMVs).

Results: Compared with that in controls, galactose transport in everted jejunal rings was significantly reduced in cirrhotic rats but showed normal values after IGF-I treatment. The kinetic study of D-galactose uptake by BBMVs showed decreased maximal velocity (Vmax) and diminished transporter affinity in cirrhotic rats. These kinetic parameters reverted to normal after IGF-I treatment. Microvilli were significantly elongated in cirrhotic rats but of normal size in the IGF-I-treated group. The expression of SGLT-1 on BBMVs (Western blot) and on the luminal membrane of enterocytes (immunohistochemistry) was not reduced in cirrhotic animals compared with controls or IGF-treated cirrhotic rats.

Conclusions: Intestinal sugar transport is disturbed in experimental cirrhosis, and this alteration is corrected by IGF-I.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • Bilirubin / blood
  • Blood Glucose / metabolism
  • Blood Proteins / metabolism
  • Carbon Tetrachloride
  • Cholesterol / blood
  • Galactose / metabolism*
  • In Vitro Techniques
  • Insulin-Like Growth Factor I / pharmacology*
  • Intestinal Absorption / drug effects
  • Intestinal Absorption / physiology*
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / metabolism*
  • Intestinal Mucosa / pathology
  • Jejunum
  • Kinetics
  • Liver Cirrhosis, Experimental / chemically induced
  • Liver Cirrhosis, Experimental / pathology
  • Liver Cirrhosis, Experimental / physiopathology*
  • Male
  • Microvilli / drug effects
  • Microvilli / metabolism*
  • Microvilli / ultrastructure
  • Rats
  • Rats, Wistar
  • Reference Values

Substances

  • Blood Glucose
  • Blood Proteins
  • Insulin-Like Growth Factor I
  • Cholesterol
  • Carbon Tetrachloride
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Bilirubin
  • Galactose