TY - JOUR
T1 - Measurements of the jejunal unstirred layer in normal subjects and patients with celiac disease
AU - Strocchi, Alessandra
AU - Corazza, Ginoroberto
AU - Furne, Julie
AU - Fine, Caryn
AU - Di Sario, Antonio
AU - Gasbarrini, Giovanni
AU - Levitt, Michael D.
PY - 1996/4/15
Y1 - 1996/4/15
N2 - Normal intestinal absorption of nutrients requires efficient luminal mixing to deliver solute to the brush border. Lacking such mixing, the buildup of thick unstirred layers over the mucosa markedly retards absorption of rapidly transported compounds. Using a technique based on the kinetics of maltose hydrolysis, we measured the unstirred layer thickness of the jejunum of normal subjects and patients with celiac disease, as well as that of the normal rat. The jejunum of humans and rats was perfused with varying maltose concentrations, and the apparent Michaelis constant (K(m)) and maximal velocity (V(max)) of maltose hydrolysis were determined from double- reciprocal plots. The true K(m) of intestinal maltase was determined on mucosal biopsies. Unstirred layer thickness was calculated from the in vivo V(max) and apparent Km and the in vitro K(m) of maltase. The average unstirred layer thickness of 11 celiac patients (170 μm) was seven times greater than that of 3 controls (25 μm). The unstirred layer of each celiac exceeded that of the controls. A variety of factors could account for the less efficient luminal stirring observed in celiacs. Although speculative, villous contractility could be an important stirring mechanism that would be absent in celiacs with villous atrophy. This speculation was supported by the finding of a relatively thick unstirred layer (mean: 106 μm) in rats, an animal that lacks villous contractility. Because any increase in unstirred layer slows transport of rapidly absorbed compounds, poor stirring appears to represent a previously unrecognized defect that could contribute to malabsorption in celiac disease and, perhaps, in other intestinal disorders.
AB - Normal intestinal absorption of nutrients requires efficient luminal mixing to deliver solute to the brush border. Lacking such mixing, the buildup of thick unstirred layers over the mucosa markedly retards absorption of rapidly transported compounds. Using a technique based on the kinetics of maltose hydrolysis, we measured the unstirred layer thickness of the jejunum of normal subjects and patients with celiac disease, as well as that of the normal rat. The jejunum of humans and rats was perfused with varying maltose concentrations, and the apparent Michaelis constant (K(m)) and maximal velocity (V(max)) of maltose hydrolysis were determined from double- reciprocal plots. The true K(m) of intestinal maltase was determined on mucosal biopsies. Unstirred layer thickness was calculated from the in vivo V(max) and apparent Km and the in vitro K(m) of maltase. The average unstirred layer thickness of 11 celiac patients (170 μm) was seven times greater than that of 3 controls (25 μm). The unstirred layer of each celiac exceeded that of the controls. A variety of factors could account for the less efficient luminal stirring observed in celiacs. Although speculative, villous contractility could be an important stirring mechanism that would be absent in celiacs with villous atrophy. This speculation was supported by the finding of a relatively thick unstirred layer (mean: 106 μm) in rats, an animal that lacks villous contractility. Because any increase in unstirred layer slows transport of rapidly absorbed compounds, poor stirring appears to represent a previously unrecognized defect that could contribute to malabsorption in celiac disease and, perhaps, in other intestinal disorders.
KW - celiac sprue
KW - intestinal absorption
KW - maltose hydrolysis
UR - http://www.scopus.com/inward/record.url?scp=0029991021&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0029991021&partnerID=8YFLogxK
M3 - Article
C2 - 8638715
AN - SCOPUS:0029991021
SN - 0363-6143
VL - 270
SP - G487-G491
JO - American Journal of Physiology - Cell Physiology
JF - American Journal of Physiology - Cell Physiology
IS - 3 33-3
ER -