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The Journal of Neuroscience, July 15, 1998, 18(14):5225-5233
Preferential Utilization of Acetate by Astrocytes Is Attributable
to Transport
Robert A.
Waniewski and
David L.
Martin
Wadsworth Center, New York State Department of Health, Albany, New
York 12201-0509
Exogenous acetate is preferentially metabolized by astrocytes in
the CNS, but the biochemical basis for this selectivity is unknown. We
observed that rat cortical astrocytes produce
14CO2 from 0.2 mM
[14C]acetate at a rate of 0.43 nmol/min per
milligram of protein, 18 times faster than cortical synaptosomes.
Subsequent studies examined whether this was attributable to cellular
differences in the transport or metabolism of acetate. The activity of
acetyl-CoA synthetase, the first enzymatic step in acetate utilization,
was greater in synaptosomes than in astrocytes (5.0 and 2.9 nmol/min per milligram of protein), indicating that slower metabolism in synaptosomes cannot be attributed to lack of enzymatic activity. [14C]Acetate uptake in astrocytes is rapid and
time-dependent and follows saturation kinetics
(Vmax, 498 nmol/min per milligram of
protein; Km, 9.3 mM).
Uptake is inhibited stereospecifically by L-lactate as well
as by pyruvate, fluoroacetate, propionate, and
-cyano-4-hydroxycinnamate (CHC). Preloading astrocytes with L-lactate or acetate, but not D-lactate,
pyruvate, or glyoxylate, transaccelerates
[14C]acetate uptake. Acetate uptake by astrocytes
appears to be mediated by a carrier with properties similar to that of
monocarboxylate transport. In contrast, studies with synaptosomes
provided no evidence for time-dependent, saturable, transaccelerated,
or CHC-inhibitable uptake of [14C]acetate. The
high rate of transport in astrocytes compared with synaptosomes
explains the rapid incorporation of [14C]acetate
into brain glutamine over glutamate. These findings provide support for
the use of acetate as a marker for glial metabolism and suggest that
extracellular acetate in the brain generated from acetylcholine and
ethanol metabolism is accumulated first by astrocytes.
Key words:
acetate transport; acetate metabolism; monocarboxylate transport; astrocytes; synaptosomes; -cyano-4-hydroxycinnamate
Copyright © 1998 Society for Neuroscience 0270-6474/98/18145225-09$05.00/0
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