Literature DB >> 8837040

Gamma-glutamyl peptides and related amino acids in rat hippocampus in vitro: effect of depolarization and gamma-glutamyl transpeptidase inhibition.

X Li1, O Orwar, C Revesjö, M Sandberg.   

Abstract

The concentrations of gamma-glutamylglutamate, gamma-glutamylglutamine, gamma-glutamylcysteine, glutamate, aspartate, glutamine, cyst(e)ine and glutathione (including disulfides) were determined by HPLC analysis of both the tissue and the surrounding medium of incubated rat hippocampal slices. High potassium concentrations (50 mM; 2 x 4 min) increased the medium concentration of gamma-glutamylglutamate (maximal net efflux 0.07 +/- 0.06 pmol/mg protein/min; n = 8 +/- SD) with a relative time delay compared to the increase in glutamate (maximal net efflux 264 +/- 88 pmol/mg protein/min). Release of gamma-glutamylcysteine, the glutathione precursor, demonstrated an immediate response and gradually approached prestimulus levels (maximal net efflux 0.36 +/- 0.13 pmol/mg protein/min). Addition of acivicin (0.2 mM), a gamma-glutamyl transpeptidase (EC 2.3.2.2.) blocker, during preincubation for 45 min reduced the tissue concentrations (pmol/mg protein) of gamma-glutamylglutamate (19.4 +/- 8.2 (control) vs. 5.8 +/- 3.6 (+ acivicin)), gamma-glutamylglutamine (40.3 +/- 6.7 vs. 25.7 +/- 4.2 pmol/mg protein), glutamine (9.9 +/- 2.0 vs. 4.6 +/- 1.2 nmol/mg protein) and cysteine (1.0 +/- 0.2 vs. 0.56 +/- 0.18 nmol/mg protein). Incubation with acivicin (0.2 mM) reduced the net efflux of gamma-glutamylglutamine (0.79 +/- 0.19 vs. 0.21 +/- 0.07 pmol/mg protein/min) whereas that of the glutathione was increased (4.7 +/- 1.0 vs. 20 +/- 3 pmol/mg protein/min). The medium concentrations of glutamate in both low and high potassium were unaffected by acivicin, while the high potassium induced increase in gamma-glutamylglutamate was blocked. The results demonstrate differential efflux patterns of gamma-glutamyl dipeptides from brain slices and show that in vitro the activity of gamma-glutamyl transpeptidase regulates extracellular concentrations of glutathione, gamma-glutamylglutamine and gamma-glutamylglutamate.

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Year:  1996        PMID: 8837040     DOI: 10.1016/0197-0186(95)00148-4

Source DB:  PubMed          Journal:  Neurochem Int        ISSN: 0197-0186            Impact factor:   3.921


  3 in total

1.  The gamma-glutamyl transpeptidase inhibitor acivicin preserves glutathione released by astroglial cells in culture.

Authors:  R Dringen; O Kranich; B Hamprecht
Journal:  Neurochem Res       Date:  1997-06       Impact factor: 3.996

2.  Searching for mechanisms of N-methyl-D-aspartate-induced glutathione efflux in organotypic hippocampal cultures.

Authors:  Camilla Wallin; Abdul-Karim Abbas; Mattias Tranberg; Stephen G Weber; Holger Wigström; Mats Sandberg
Journal:  Neurochem Res       Date:  2003-02       Impact factor: 3.996

3.  The Glutathione Metabolite γ-Glutamyl-Glutamate Partially Activates Glutamate NMDA Receptors in Central Neurons With Higher Efficacy for GluN2B-Containing Receptors.

Authors:  Fatiha Sebih; Nawfel Mokrane; Pierre Fontanel; Mete Kayatekin; Mahira Kaabeche; Janique Guiramand; Catherine Cohen-Solal; Thierry Cens; Matthieu Rousset; Pierre Charnet; Marie-Céleste De Jésus Ferreira; Jean-Baptiste Thibaud; Claudine Ménard; Sonia Cantel; Valérie Rolland; Michel Vignes; Julien Roussel
Journal:  Front Pharmacol       Date:  2022-01-03       Impact factor: 5.810

  3 in total

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