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Which mechanisms are involved in taurine-dependent granulocytic immune response or amino- and α-keto acid homeostasis?

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Summary.

We examined the effects of β-alanine (taurine analogue and taurine transport antagonist), taurine (regarding its role in neutrophil (PMN) immunonutrition) and taurine combined either with L-NAME (inhibitor of •NO-synthase), SNAP (•NO donor), DON (glutamine-analogue and inhibitor of glutamine-requiring enzymes), DFMO (inhibitor of ornithine-decarboxylase) and β-alanine on neutrophil amino- and α-keto acid profiles or important PMN immune functions in order to establish whether taurine transport-, nitric oxide-, glutamine- or ornithine-dependent mechanisms are involved in any of the taurine-induced effects. According to the present findings, the taurine-mediated effect appears to be based primarily on a modulation of important transmembraneous transport mechanisms and only secondarily on directly or indirectly induced modifications in intragranulocytic amino- and α-keto acid homoeostasis or metabolism. Although a direct relation to the parallel observed immunological modifications can only be presumed, these results show very clearly that compositional modifications in the free intragranulocytic amino- and α keto-acid pools coinciding with changes in intragranulocytic taurine levels are relevant metabolic determinants that can significantly influence the magnitude and quality of the granulocytic immune response.

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Authors’ address: Prof. Dr. med. habil. Jörg Mühling, MBA, Clinics of Anaesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Giessen and Marburg GmbH, Justus-Liebig-University Giessen, Rudolf-Buchheim-Strasse 7, D-35385 Giessen, Federal Republic of Germany

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Mühling, J., Nickolaus, K., Matejec, R. et al. Which mechanisms are involved in taurine-dependent granulocytic immune response or amino- and α-keto acid homeostasis?. Amino Acids 34, 257–270 (2008). https://doi.org/10.1007/s00726-007-0497-0

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  • DOI: https://doi.org/10.1007/s00726-007-0497-0

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