Sg. Corradini et al., HUMAN GALLBLADDER MUCOSAL FUNCTION - EFFECTS ON INTRALUMINAL FLUID AND LIPID-COMPOSITION IN HEALTH AND DISEASE, Digestive diseases and sciences, 43(2), 1998, pp. 335-343
Gallbladder mucosal absorption of fluid during fasting is a well-known
process. Indirect in vivo and recent in vitro evidence for physiologi
cally relevant gallbladder absorption of cholesterol and phospholipids
from bile has been observed in humans. The present study explored and
compared by indirect means the relative efficiences of human gallblad
der mucosal absorption of fluid and lipids in health and disease. Bili
ary lipids and pigment content were measured in fasting gallbladder bi
le samples obtained from gallstone-free controls and from four study g
roups: multiple and solitary cholesterol gallstone patients, and morbi
dly obese subjects with and without gallstones. Bile salts and pigment
content were significantly greater in gallstone-free controls than in
all other disease study groups, This was interpreted as evidence of m
ore effective gallbladder mucosal fluid absorption in nonobese gallsto
ne-free controls compared to that in all other groups, Correlation plo
t analyses of biliary lipids showed lower concentrations of phospholip
ids than expected from the index bile salt concentrations, The same wa
s found for cholesterol concentrations but only in supersaturated samp
les, These findings were much more pronounced in gallstone free-contro
ls and were accordingly interpreted as evidence of more efficient gall
bladder absorption of both phospholipids and cholesterol in controls c
ompared with that found in each of the disease study groups, Moreover,
impaired gallbladder mucosal function, while invariably associated wi
th cholesterol gallstone disease, was not found to be a necessary cons
equence of the physical presence of stones. It is concluded that effic
ient gallbladder mucosal absorption of both fluid and apolar lipids fr
om bile is a normal physiological process that is often seriously impa
ired in the presence of either cholesterol gallstone disease or at lea
st one of its precursor forms.