Glutamine (Gln) supplementation to enteral and parenteral nutrition has been used as a therapeutic modality to enhance mucosal integrity and function during critical illness, traumatic injury, and sepsis. Gln is a conditionally-essential amino acid that is involved in a variety of biochemical processes in the cell that include nucleic acid synthesis, nitrogen transport and balance, precursor for the tricarboxylic acid (TCA) cycle, glutathione synthesis, and protein synthesis. Gln is known to be the primary energy source for entercytes, but the molecular mechanisms by which Gln exerts its cytoprotective effects have not been determined. Gastrointestinal (GI) homeostasis is achieved through a balance between enterocyte proliferation, differentiation, and programmed cell death (apoptosis). Preliminary studies in our laboratory show that Gln starvation induces apoptosis in rat intestinal epithelial (RIE-1 ) cells. The purpose of this study is to determine the molecular mechanisms by which Gln exerts its anti-apoptotic effect. The role of Gln as a pre cursor for ATP production by the TCA cycle, and a precursor for gluthathione synthesis and their relationship to the protection/induction of apoptosis in RIE -1 cells will be investigated. These studies will provide valuable information on the molecular and biochemical mechanisms by which Gln starvation induces apoptosis in an enterocyte model. Furthermore, the application of this in vitro system to future in vivo models will further define the role of Gln in the maintenance of GI mucosal integrity and function, and may provide new means by which clinicians treat gut pathology found in nutritionally depleted patients during periods of critical illness.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32DK009867-01
Application #
2708499
Study Section
Special Emphasis Panel (ZRG7-SSS-8 (43))
Program Officer
Podskalny, Judith M,
Project Start
1998-07-01
Project End
1999-06-11
Budget Start
1998-07-01
Budget End
1999-06-11
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Texas Medical Br Galveston
Department
Surgery
Type
Schools of Medicine
DUNS #
041367053
City
Galveston
State
TX
Country
United States
Zip Code
77555
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Papaconstantinou, H T; Chung, D H; Zhang, W et al. (2000) Prevention of mucosal atrophy: role of glutamine and caspases in apoptosis in intestinal epithelial cells. J Gastrointest Surg 4:416-23