Premium
Repeated Administration of γ‐VinylGABA Reduces Rat Brain Glutamine Synthetase Activity
Author(s) -
Waniewski Robert A.,
Martin David L.
Publication year - 1995
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.1995.65010355.x
Subject(s) - glutamine synthetase , glutamine , glutamate receptor , medicine , endocrinology , cerebellum , gaba transaminase , biology , in vivo , enzyme , cerebral cortex , cortex (anatomy) , biochemistry , amino acid , chemistry , glutamate decarboxylase , receptor , neuroscience , microbiology and biotechnology
The glutamine cycle has been proposed as a pathway in which glutamine synthesized in glia provides substrate for synthesis of the neurotransmitters glutamate and GABA as they are lost from neurons. To test whether GABA may regulate this pathway, the effect of elevated GABA on the glial enzyme glutamine synthetase was examined in rat brain. Repeated subcutaneous injections of the antiepileptic GABA transaminase inhibitor γ‐vinylGABA at a dose of 150 mg/kg per day for 21 days reduced glutamine synthetase activity by 36% in the cortex and 22% in the cerebellum. At 30 mg/kg per day, glutamine synthetase activity was reduced by 9.5% in the cortex but unchanged in the cerebellum. The reductions were brain specific because the skeletal muscle and liver enzymes were unaffected by γ‐vinylGABA administration. Amino acid analysis of the cortex from γ‐vinylGABA‐treated rats demonstrated a 270% increase in GABA levels after 150 mg/kg but no change after 30 mg/kg. GABA levels and glutamine synthetase activity were inversely correlated. The 150 mg/kg dose significantly lowered cortical glutamine and glutamate levels. The decline in brain glutamine synthetase activity with chronic γ‐vinylGABA administration developed gradually over time and may be due to the slow turnover of this enzyme in vivo.