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Diabetes, Vol 24, Issue 6 574-584, Copyright © 1975 by American Diabetes Association
Gluconeogenesis from alanine in normal postabsorptive man. Intrahepatic stimulatory effect of glucagon
JL Chiasson, JE Liljenquist, BC Sinclair-Smith and WW Lacy
Although the stimulatory effect of glucagon on gluconeogenesis has been
well demonstrated in certain systems in vitro, this effect has never been
established in man. The present study was undertaken, therefore, to
determine whether glucagon could stimulate gluconeogenesis from alanine in
normal fasting man. Glucagon might stimulate this process by increasing the
hepatic alanine uptake and/or by shunting the extracted alanine within the
liver into the gluconeogenic pathway. In order to be able to examine these
two aspects of gluconeogenesis, we combined the hepatic vein-brachial
artery catheterization technic with an istopic infusion of alanine-14C.
Alanine-14C specific activity was measured in whole blood and plasma by use
of a rapid chromatographic technic. Since plasma contributed 93 per cent of
the alanine extracted by the splanchnic bed with a specific activity three
times that of the red blood cells, plasma alanine specific activity was
used to study the conversion of alanine to glucose. A constant infusion of
alanine-14C achieved a relatively stable arterial specific activity by
forty minutes. The administration of glucagon by constant infusion (15-50
ng./kg./min.) had no affect on thf splanchnic extraction of alanine. Net
splanchnic glucose-14C production, however, doubled during the glucagon
infusion, and the conversion of alanine to glucose increased from 30 plus
or minus 2 to 58 plus or minus 9 mumol/min. These data (1) demonstrate that
in normal man fasted twelve to fourteen hours, glucagon at supraphysiologic
levels can double the rate of gluconeogenesis from alanine and (2) indicate
that this stimulatory effect of glucagon is exerted within the liver by
shunting the extracted alanine toward new glucose formation rather than by
increasing the hepatic extraction of alanine.

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Copyright © 1975 by the American Diabetes Association.
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