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Glutamine
and the immune response
Wernerman, Jan
Department
of Anaesthesia and Intensive Care, Huddinge
University Hospital,
S-141 86 Huddinge, Stockholm Sweden.
In hospital nutrition
the focus upon glutamine as a conditionally
essential nutrient has evoked a lot of interest
recently. The background is an understanding
of glutamine"s role for rapidly diveiding
cells such as immunocompetent cells and enterocytes.
These cells utilise glutamine as an oxidative
substrate and they prefer glutamine over glucose
when both are available, In a situation of stress
this preference for glutamine becomes even more
evident. The background for this is suggested
to be an effective metabolic regulation allowing
the production of mucleotides to increase hundred
or even thousand fold very rapidly by diverting
a small fraction of this flux through the oxidative
system. On whole body basis the efflux of glutamine
from skeletal muscle, which is the major producer
of glutamine, is always evident. Also in the
fed state, when muscle is taking up most of
amino acids there is a constant production of
glutamine. Skeletal muscle produce glutamine
by transamination reactions from other amino
acids and by synthesising a ketoglutarate in
the TCA-cycle. In metabolic stress the production
of glutamine in muscle is enhanced. Muscle is
rapidly depleted by this production which for
long-stayers in the ICU and during the rehabilitation
phase leaves the patient depleted. Although
the need for glutamine in the acute situation
may be life-saving for the patient, the depletion
of muscle proteins may be a serious problem
and increase mortality later during the course
of disease.
Nutritional supplementation
with glutamine may therefore have a rational
in the acute situation by improving immunologic
competence and gastrointestinal function for
the patient 1,2,3 Later on, in the course of
disease, glutamine supplementation may save
muscle proteins which is shown to be beneficent
for the patient during the rehabilitation phase4
. So far the instrument to diagnose glutamine
depletion in individual patients is not at hand.
Clinical studies performed are therefore including
patients who are glutamine depleted and those
who are not glutamine depleted. It is therefore
not surprising that results sometimes are difficult
to interpret. In general terms there are a large
number of studies showing a positive nitrogen
balance in response to glutamine treatment.
Furthermore, in bone marrow transplant patients
there is decrease in infectious complications
5,6 , immune cell activation in vitro is enhanced1
and infectious complications following trauma
are also attenuated 7,8 . The latter has been
shown also after enteral administration of glutamine.
As indicated above, a six-month survival in
ICU-patients is also improved by glutamine,
an effect that should primarily be attributed
to the lower lever of depletion seen in patients
after glutamine supplementation of nutrition4.
The acute effect on the immune response may
be more of a pharmacological effect of glutamine.
There are convincing experimental evidence on
this point, but clinical studies, beside those
in bone marrow transplant patients, are presently
not at hand.
REFERENCES:
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O'Riordan MG, FearonKC,
Ross JA, Rogers P, Falconer JS, Bartolo DCC,
Garden OJ, Cater DC. (1994) Glutamine supplemented
total parenteral nutrition enhances T-lymphocyte
response in surgical patients undergoing colorectal
resection. Ann Surg 220-212-221.
-
Hulst RRWJ van der,
Kreel BK van, Meyenfeldt MF van, Brummer R-Jm,
Arends J-W, Deutz NEP, Soeters PB (1993) The
role of parenteral glutamine administration
in preserving gut integity, Lancet 334-1363-1365.
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Tremel H, Kienle B,
Weilemann LS, Stehle P, Furst P (1994) Glutamine
dipeptide-supplemented parenteral nutrition
maintains intesinal function in the critically
ill. Gastroenterology 107:1595-1601.
-
Griffiths RD, Jones
C, Palmer TEA (1997) A six-month outcome of
critically ill patients given glutamine supplemented
parenteral nutrition. Nutrition 13:293-302.
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Ziegler TR, Young
LS, Benefell K, Scheltinga M, Hortos K, Bye
R, Morrow FD, Jacobs DO, Smith RJ, Antin JH,
Wilmore DW (1992) Clinical and metabolic efficacy
of glutamine-supplemented parenteral nutrition
after bone marrow transplantation. Ann Intern
Med 116:821-828.
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Schloerb PR, Amare
M (1993) Total parenteral nutrition with glutamine
in bone marrow transplantation and other clinical
applications (a randomizd double-blind study).
J Parent Enter Nutr 17:407-413.
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Houdijk APJ, Rijnsburger
ER, Jansen J, Wesdorp RIC, Weis JK, McCamish
MA, Teerlink T, Meuwissen SGM, Haarman HJTM,
Thijs LG, Leeuwen PAM van (1998) Glutamin
enriched enteral nutrition reduces infectious
morbidity in multi-trauma patients: a double-blind,
prospective, randomized trial, Lancet 352:772-776.
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Moore FA, Moore EE,
Kudsk KA, Brown RO, Bower RH, Koruda MJ, Baker
CC, Barbul A (1994) Clinical Benefits of an
immune-enhancing diet for early postinjury
enteral feeding J Trauma 37:607-6
From "The
5th Congress of the PENSA" Kuala Lumpur, October
28-30, 1999 Page : 27 |
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