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Effects of glutamine and ethanol in vitroon lymphocytes from human alcohol abusers and non-abusers.

Authors :
Greig, J. E.
Keast, D.
Palmer, T. N.
Source :
Addiction Biology; Jan2001, Vol. 6 Issue 1, 1 Chart, 2 Graphs
Publication Year :
2001

Abstract

The amino acid L-glutamine is essential for the function of both resting and stimulated lymphocytes, and its uptake is significantly increased after stimulation. The effects of ethanol on the immune system appear to be widespread and significant, and its role as an osmolyte has recently been proposed to be important. The in vitro effect of concurrent glutamine deprivation and ethanol exposure in different osmotic conditions was investigated with respect to the proliferative capability of lymphocytes in vitro from both alcohol abusers and non-abusers, and also the kinetics of glutamine transport across peripheral blood lymphocytes (PBL) membranes from nonabusers. In a physiologically normal situation ethanol increases osmolality, and tonicity remains balanced. However, in situations of electrolyte imbalance ethanol addition may result in osmolality remaining near normal levels, but with hypotonicity. It was found that a lack of glutamine and iso-osmotic hypotonic high ethanol concentrations caused a greater inhibition of mitogen-stimulated lymphocyte proliferation than either factor alone. This was true for PBL from both non-abusers and abusers of alcohol.There was no change in membrane permeability and active transport of glutamine into lymphocytes from non-abusers that were stimulated in vitro in various conditions of ethanol, osmolality and tonicity. While lymphocyte proliferation may be inhibited in certain conditions and this is further affected by a lack of glutamine, the capacity for active glutamine transport was maintained, perhaps due to its essential role in lymphocyte metabolism. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13556215
Volume :
6
Issue :
1
Database :
Complementary Index
Journal :
Addiction Biology
Publication Type :
Academic Journal
Accession number :
3990395
Full Text :
https://doi.org/10.1080/13556210020020139