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Diabetes, Vol 38, Issue 3 338-342, Copyright © 1989 by American Diabetes Association
Glucagonlike peptide I (7-37) actions on endocrine pancreas
GC Weir, S Mojsov, GK Hendrick and JF Habener
Joslin Diabetes Center, Boston, MA 02215.
Glucagonlike peptide I (7-37) [GLP-I-(7-37)], encoded with glucagon and
glucagonlike peptide II and intervening peptide II in the rat and human
glucagon gene, is processed from proglucagon in both pancreas and intestine
and is a potent stimulator of insulin secretion. Unequivocal insulin
release from the isolated perfused rat pancreas is elicited by a 10(-11) M
concentration of this peptide, and a weak response is found at 10(-12) M.
We found that GLP-I-(7-37) is approximately 100 times more potent than
glucagon in the stimulation of insulin secretion. Insulin release in
response to GLP-I-(7-37) is highly dependent on the ambient glucose
concentration; no response is detectable at a glucose concentration of 2.8
mM, and at 6.6 and 16.7 mM, insulin release is augmented by 4.7 and 22.8
ng/ml, respectively. The pattern of insulin secretion stimulated by
GLP-I-(7-37) is biphasic, with an initial spike followed by a plateau of
sustained release. The effects on insulin release of GLP-I-(7-36) amide, a
GLP-I analogue, and GLP-I-(7-37) at concentrations of 10(-11) M were
indistinguishable. We also found that GLP-I-(7-37) at 10(-9) M does not
influence glucagon secretion and that glucagonlike peptide II and the
intervening peptide II, two other peptides encoded by the glucagon gene,
have no detectable effects on insulin secretion.

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Copyright © 1989 by the American Diabetes Association.
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