Mc. Mckenna et al., EXOGENOUS GLUTAMATE CONCENTRATION REGULATES THE METABOLIC-FATE OF GLUTAMATE IN ASTROCYTES, Journal of neurochemistry, 66(1), 1996, pp. 386-393
The metabolic fate of glutamate in astrocytes has been controversial s
ince several studies reported >80% of glutamate was metabolized to glu
tamine; however, other studies have shown that half of the glutamate w
as metabolized via the tricarboxylic acid (TCA) cycle and half convert
ed to glutamine. Studies were initiated to determine the metabolic fat
e of increasing concentrations of [U-C-13]glutamate in primary culture
s of cerebral cortical astrocytes from rat brain, When astrocytes from
rat brain were incubated with 0.1 mM [U-C-13]glutamate 85% of the C-1
3 metabolized was converted to glutamine. The formation of [1,2,3-C-13
(3)]glutamate demonstrated metabolism of the labeled glutamate via the
TCA cycle. When astrocytes were incubated with 0.2-0.5 mM glutamate,
C-13 from glutamate was also incorporated into intracellular aspartate
and into lactate that was released into the media. The amount of [C-1
3] lactate was essentially unchanged within the range of 0.2-0.5 mM gl
utamate, whereas the amount of [C-13]aspartate continued to increase i
n parallel with the increase in glutamate concentration, The amount of
glutamate metabolized via the TCA cycle progressively increased from
15.3 to 42.7% as the extracellular glutamate concentration increased f
rom 0.1 to 0.5 mM, suggesting that the concentration of glutamate is a
major factor determining the metabolic fate of glutamate in astrocyte
s. Previous studies using glutamate concentrations from 0.01 to 0.5 mM
and astrocytes from both rat and mouse brain are consistent with thes
e findings.