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J Biol Chem, Vol. 273, Issue 51, 33905-33908, December 18, 1998
Cells but Not in
Cells and Are
Also Observed in Human Islets
,
From the Glucose metabolism by pancreatic
Unit of Endocrinology and Metabolism,
and
cells is essential for stimulation of insulin secretion and
inhibition of glucagon secretion. Studies using rodent islets have
suggested that the ATP/ADP ratio serves as second messenger in
cells. This study compared the effects of glucose on glucose oxidation
([U-14C]glucose) and adenine nucleotides
(luminometric method) in purified rat
and
cells. The rate of
glucose oxidation at 1 mM glucose was higher in
than
cells (4.5-fold, i.e. ~2-fold after normalization for
cell size). It was more strongly stimulated by 10 mM
glucose in
cells (9-fold) than in
cells (5-fold). At 1 mM glucose, ATP levels were similar in both cell types,
which corresponds to an approximately 2-fold higher concentration in
cells (~6.5 mM) than in
cells (~3
mM). In
cells, glucose dose-dependently increased ATP and decreased ADP levels, causing a rise in the ATP/ADP
ratio from 2.4 to 11.6 at 1 and 10 mM, respectively. In
cells, glucose did not affect ATP and ADP levels, and the ATP/ADP ratio
remained stable around 7.5. In human islets, the ATP/ADP ratio
progressively increased between 1 and 10 mM glucose. In duct cells, which often contaminate human islet preparations, an
increase in the ATP/ADP ratio sometimes occurred between 1 and 3 mM glucose. In conclusion, the present observations
establish that the regulation of glucagon secretion by glucose does not involve changes in
cell adenine nucleotides and further support the
role of the ATP/ADP ratio in the control of insulin secretion.
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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