Abstract
The neutral amino acid transporters SNAT1-3 and ASCT1 play critical roles in the recycling of glutamine, and subsequently glutamate, via the glutamine-glutamate cycle. Hypoxia-ischemia was induced in rat pups using the Rice-Vannucci model. Brains were harvested at 1 h, 24 h and 7 days after ischemia. The expression of NAATs was evaluated using immunoblotting, real-time PCR, and immunohistochemistry. Results were compared with age-matched controls and shams. SNAT1 mRNA decreased at 1 h after injury in both hemispheres when compared with the control animals and correlated with a decrease in protein expression at 24 h in the hippocampus and cortex. SNAT1 protein expression increased globally at 7 days after injury and specifically in the hippocampus. Finally, SNAT2 and 3 demonstrated subtle changes in various brain regions after injury. These data suggest that neutral amino acid transporters remain largely intact after hypoxia-ischemia.
Copyright (c) 2006 S. Karger AG, Basel.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Transport System A / genetics
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Amino Acid Transport System A / metabolism*
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Amino Acid Transport System ASC / genetics
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Amino Acid Transport System ASC / metabolism
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Amino Acid Transport Systems / genetics
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Amino Acid Transport Systems / metabolism
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Amino Acid Transport Systems, Neutral / genetics
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Amino Acid Transport Systems, Neutral / metabolism
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Amino Acids, Neutral / metabolism
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Animals
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Brain / growth & development*
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Brain / physiology*
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Gene Expression Regulation, Developmental
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Hypoxia-Ischemia, Brain / metabolism*
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Hypoxia-Ischemia, Brain / physiopathology*
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Immunoblotting
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Immunohistochemistry
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Rats
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Rats, Sprague-Dawley
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Reverse Transcriptase Polymerase Chain Reaction
Substances
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Amino Acid Transport System A
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Amino Acid Transport System ASC
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Amino Acid Transport Systems
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Amino Acid Transport Systems, Neutral
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Amino Acids, Neutral
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Slc1a4 protein, rat
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Slc38a1 protein, rat
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Slc38a2 protein, rat
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system N protein 1