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Diabetes, Vol 46, Issue 10 1535-1541, Copyright © 1997 by American Diabetes Association
Role of glutamine as a glucose precursor in fasting humans
RG Hankard, MW Haymond and D Darmaun
Endocrine Research Laboratory, Nemours Children's Clinic, Jacksonville, Florida, USA.
Recently, significant incorporation of labeled carbon into plasma glucose
was documented during infusion of 14C-labeled glutamine in postabsorptive
humans. Such labeling of plasma glucose can occur as a result of two
different processes: either 1) through incorporation of glutamine carbon
into glucose via glutamine entering Krebs cycle at alpha-ketoglutarate or
2) through simple fixation of labeled CO2 resulting from oxidation of
labeled glutamine. Therefore, these studies were designed to determine 1)
whether glutamine contributes carbon to gluconeogenesis other than through
mere CO2 fixation, and, if so, 2) whether the apparent transfer of carbon
from glutamine to glucose increases with fasting. Eight healthy adults were
studied on two consecutive days: once after an overnight (18-h) fast and
again on the second day of fasting (42-h fast). On each study day, subjects
received a simultaneous 5-h infusion of D-[6,6-2H2lglucose,
L-[3,4-13C2lglutamine, and L-[1-14C]leucine. Apparent rates of
incorporation of glutamine carbon into glucose were estimated from the
appearance of 13C into plasma glucose; glucose and glutamine production
rates (appearance rate [Ra]) were determined from plasma [2H2]glucose and
[13C2]glutamine enrichments, respectively. The appearance of 14C into
plasma glucose was used to correct the measured rates of carbon transfer
from glutamine to glucose as a result of CO2 fixation. We observed that of
the apparent contribution of labeled glutamine to gluconeogenesis, only 4%
occurred as a result of fixation of labeled CO2, while 96% seemed to occur
through other routes. We also observed that between 18 and 42 h of fasting,
1) the relative contribution of protein breakdown to glutamine production
was enhanced, while that of de novo synthesis declined; 2) the apparent
contribution of glutamine to glucose production rose from 8 +/- 1 to 16 +/-
3% of overall glucose Ra; and 3) the relative apparent contribution of
glutamine to gluconeogenesis remained constant. From the current data, it
cannot be ascertained to what extent the apparent carbon transfer from
glutamine to glucose represents a true contribution of glutamine to
gluconeogenesis or mere carbon exchange between the trichloroacetic acid
cycle and the gluconeogenic pathway. These findings are nevertheless
compatible with a role of glutamine as a significant precursor of glucose
in fasting humans.

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Copyright © 1997 by the American Diabetes Association.
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