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   <subfield code="a">Pathways involved in alanyl-glutamine-induced changes in neutrophil amino- and α-keto acid homeostasis or immunocompetence</subfield>
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   <subfield code="c">[J. Mühling, D. Burchert, T. W. Langefeld, R. Matejec, H. Harbach, J. Engel, M. Wolff, I. D. Welters, M. Fuchs, T. Menges, M. Krüll, G. Hempelmann]</subfield>
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   <subfield code="a">Summary.: We examined the effects of DON [glutamine-analogue and inhibitor of glutamine-requiring enzymes], alanyl-glutamine (regarding its role in neutrophil immunonutrition) and alanyl-glutamine combined with L-NAME, SNAP, DON, β-alanine and DFMO on neutrophil amino and α-keto acid concentrations or important neutrophil immune functions in order to establish whether an inhibitor of •NO-synthase [L-NAME], an •NO donor [SNAP], an analogue of taurine and a taurine transport antagonist [β-alanine], an inhibitor of ornithine-decarboxylase [DFMO] as well as DON could influence any of the alanyl-glutamine-induced effects. In summary, irrespective of which pharmacological, metabolism-inhibiting or receptor-mediated mechanisms were involved, our results showed that impairment of granulocytic glutamine uptake, modulation of intracellular glutamine metabolisation and/or de novo synthesis as well as a blockade of important glutamine-dependent metabolic processes may led to significant modifications of physiological and immunological functions of the affected cells.</subfield>
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   <subfield code="a">Keywords: Alanyl-glutamine - DON - L-NAME - SNAP - β-Alanine - DFMO neutrophil - Amino acids - α-Keto acids - Immune function</subfield>
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   <subfield code="D">J.</subfield>
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