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Departments of 1 Human Physiology and 3 Internal Medicine, Liver Unit, School of Medicine, University of Navarra, 31080 Pamplona, Spain; and 2 Department of Internal Medicine, Biomedical Campus, Libero Istituto Universitario, 00155 Rome, Italy
Insulin-like growth factor I (IGF-I)
bioavailability is reduced in liver cirrhosis, a condition frequently
associated with malnutrition. We have analyzed in vivo absorption of
D-galactose by jejunal loops in
rats with CCl4-induced liver
cirrhosis and the influence of IGF-I on intestinal sugar transport in
this disease. Two different study protocols were followed. In
protocol
1, healthy control rats or cirrhotic
rats received saline or IGF-I (2 µg · 100 g body
wt
1 · day
1)
for 2 wk. In protocol
2, control and cirrhotic rats received saline or IGF-I as a bolus injection of 1 µg/100 g body wt followed by continuous infusion of the same dose for 100 min. In vivo
D-galactose absorption was
reduced in cirrhotic rats compared with healthy controls. IGF-I, as
both a chronic (protocol
1) and acute treatment (protocol
2), was able to improve sugar
transport in cirrhotic rats but had no effect on sugar absorption in
healthy rats. A significant elongation of enterocyte microvilli was
observed in cirrhotic animals; this alteration was totally or partially
corrected by chronic or acute IGF-I administration. Our results show
that in vivo jejunal sugar transport and microvilli structure are
altered in liver cirrhosis and that IGF-I, among other effects, may
correct these changes by modulating cytoskeletal organization in enterocytes.
liver cirrhosis; malnutrition; malabsorption; glucose and galactose transport; microvilli
This article has been cited by other articles:
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M. Pascual, I. Castilla-Cortazar, E. Urdaneta, J. Quiroga, M. Garcia, A. Picardi, and J. Prieto Altered intestinal transport of amino acids in cirrhotic rats: the effect of insulin-like growth factor-I Am J Physiol Gastrointest Liver Physiol, August 1, 2000; 279(2): G319 - G324. [Abstract] [Full Text] [PDF] |
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