Importance of glutamine for gamma-aminobutyric acid synthesis in rat neostriatum in vivo

J Neurochem. 1988 Oct;51(4):1294-9. doi: 10.1111/j.1471-4159.1988.tb03099.x.


This work was carried out to evaluate the importance of glial cells in providing precursors for the in vivo synthesis of gamma-aminobutyric acid (GABA). Fluorocitrate, which selectively inhibits the tricarboxylic acid cycle in glial cells, was administered locally in rat neostriatum. Inhibition of the glial cell tricarboxylic acid cycle led to a decrease both in glutamine level and in gamma-vinyl GABA (GVG)-induced GABA accumulation, an observation indicating reduced GABA synthesis. The role of glutamine, which is synthesized in glial cells as a precursor for GABA, was further investigated by inhibition of glutamine synthetase with intrastriatally administered methionine sulfoximine. In this case, the glutamine level was reduced to near zero values, and the GVG-induced GABA accumulation was only half that of normal. The results show that glutamine is an important precursor for GABA synthesis, but it cannot be the sole precursor because it was not possible to depress the GVG-induced GABA accumulation completely.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminocaproates / pharmacology
  • Animals
  • Citrates / pharmacology
  • Citric Acid Cycle / drug effects
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism*
  • Glutamate-Ammonia Ligase / antagonists & inhibitors
  • Glutamine / metabolism*
  • Male
  • Methionine Sulfoximine / pharmacology
  • Neuroglia / drug effects
  • Neuroglia / metabolism
  • Rats
  • Rats, Inbred Strains
  • Vigabatrin
  • gamma-Aminobutyric Acid / biosynthesis*


  • Aminocaproates
  • Citrates
  • Glutamine
  • Methionine Sulfoximine
  • fluorocitrate
  • gamma-Aminobutyric Acid
  • Glutamate-Ammonia Ligase
  • Vigabatrin