In order to assess the respective contribution of the exocrine and endocrin
e moieties of the pancreas to the overall net uptake of selected monosaccha
rides by the pancreatic gland, the apparent distribution space of L-[1-C-14
]glucose, 3-O-[C-14-methyl]-D-glucose, D-[U-C-14]glucose, D-[U-C-14]mannose
and D-[U-C-14]fructose was measured in pieces of pancreas obtained from ei
ther control rats or animals injected with streptozotocin. Although the tim
e course for the uptake of 3-O-[C-14-methyl]-D-glucose, D-[U-C-14]glucose,
D-[U-C-14]mannose and D-[U-C-14]fructose was much slower in the pieces of p
ancreas than that previously documented in isolated pancreatic islets, no s
ignificant difference could, as a rule, be detected between the results obt
ained in pancreatic pieces of control and streptozotocin rats. A comparable
situation prevailed in the pancreas of animals examined 3 min after the in
travenous injection of 3-O-[C-14-methyl]-D-glucose. D-Glucose inhibited the
uptake of 3-O-[C-14-methyl]-D-glucose and that of D-[U-C-14]fructose. Like
wise, 3-O-methyl-D-glucose inhibited the uptake of D-[U-C-14]glucose. Cytoc
halasin B (20 muM) also inhibited the uptake of 3-O-[C-14-methyl]-D-glucose
and D-[U-C-14]glucose, but not that of D-[U-C-14]fructose. D-Mannoheptulos
e hexaacetate, but not the unesterified heptose, inhibited the metabolism o
f tritiated and C-14-labelled D-glucose, as well as the net uptake of D-[U-
C-14]glucose and D-[U-C-14]mannose and, to a lesser extent, that of D-[U-C-
14]fructose. These findings indicate that despite marked differences betwee
n endocrine and exocrine pancreatic cells in terms of both the time course
for the uptake of several hexoses and the inhibition of their phosphorylati
on by D-mannoheptulose, little or no preferential labelling of the endocrin
e moiety of the pancreas by the C-14-labelled hexoses is observed, at least
when judged from their distribution space in pancreatic pieces or the whol
e pancreatic gland. Nevertheless, the findings made with D-mannoheptulose a
nd its hexaacetate eater raise the view that this heptose could conceivably
be used to achieve a sizeable preferential labelling of the endocrine panc
reas under the present experimental conditions. Copyright (C) 2000 John Wil
ey & Sons, Ltd.