NAA and NAAG variation in neuronal activation during visual stimulation

N-acetyl-aspartyl-glutamate (NAAG) and its hydrolysis product N-acetyl-L-aspartate (NAA) are among the most important brain metabolites. NAA is a marker of neuron integrity and viability, while NAAG modulates glutamate release and may have a role in neuroprotection and synaptic plasticity. Investiga...

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Main Authors: G. Castellano, C.S.B. Dias, B. Foerster, L.M. Li, R.J.M. Covolan
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2012-11-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012001100006
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spelling doaj-99985f1bf9ad42238a5631ca450296b72020-11-24T23:09:17ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X1414-431X2012-11-01451110311036NAA and NAAG variation in neuronal activation during visual stimulationG. CastellanoC.S.B. DiasB. FoersterL.M. LiR.J.M. CovolanN-acetyl-aspartyl-glutamate (NAAG) and its hydrolysis product N-acetyl-L-aspartate (NAA) are among the most important brain metabolites. NAA is a marker of neuron integrity and viability, while NAAG modulates glutamate release and may have a role in neuroprotection and synaptic plasticity. Investigating on a quantitative basis the role of these metabolites in brain metabolism in vivo by magnetic resonance spectroscopy (MRS) is a major challenge since the main signals of NAA and NAAG largely overlap. This is a preliminary study in which we evaluated NAA and NAAG changes during a visual stimulation experiment using functional MRS. The paradigm used consisted of a rest period (5 min and 20 s), followed by a stimulation period (10 min and 40 s) and another rest period (10 min and 40 s). MRS from 17 healthy subjects were acquired at 3T with TR/TE = 2000/288 ms. Spectra were averaged over subjects and quantified with LCModel. The main outcomes were that NAA concentration decreased by about 20% with the stimulus, while the concentration of NAAG concomitantly increased by about 200%. Such variations fall into models for the energy metabolism underlying neuronal activation that point to NAAG as being responsible for the hyperemic vascular response that causes the BOLD signal. They also agree with the fact that NAAG and NAA are present in the brain at a ratio of about 1:10, and with the fact that the only known metabolic pathway for NAAG synthesis is from NAA and glutamate.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012001100006Proton magnetic resonance spectroscopyFunctional experimentsBrain activationBrain energy metabolismN-acetyl-L-aspartateN-acetyl-aspartyl-glutamate
collection DOAJ
language English
format Article
sources DOAJ
author G. Castellano
C.S.B. Dias
B. Foerster
L.M. Li
R.J.M. Covolan
spellingShingle G. Castellano
C.S.B. Dias
B. Foerster
L.M. Li
R.J.M. Covolan
NAA and NAAG variation in neuronal activation during visual stimulation
Brazilian Journal of Medical and Biological Research
Proton magnetic resonance spectroscopy
Functional experiments
Brain activation
Brain energy metabolism
N-acetyl-L-aspartate
N-acetyl-aspartyl-glutamate
author_facet G. Castellano
C.S.B. Dias
B. Foerster
L.M. Li
R.J.M. Covolan
author_sort G. Castellano
title NAA and NAAG variation in neuronal activation during visual stimulation
title_short NAA and NAAG variation in neuronal activation during visual stimulation
title_full NAA and NAAG variation in neuronal activation during visual stimulation
title_fullStr NAA and NAAG variation in neuronal activation during visual stimulation
title_full_unstemmed NAA and NAAG variation in neuronal activation during visual stimulation
title_sort naa and naag variation in neuronal activation during visual stimulation
publisher Associação Brasileira de Divulgação Científica
series Brazilian Journal of Medical and Biological Research
issn 0100-879X
1414-431X
publishDate 2012-11-01
description N-acetyl-aspartyl-glutamate (NAAG) and its hydrolysis product N-acetyl-L-aspartate (NAA) are among the most important brain metabolites. NAA is a marker of neuron integrity and viability, while NAAG modulates glutamate release and may have a role in neuroprotection and synaptic plasticity. Investigating on a quantitative basis the role of these metabolites in brain metabolism in vivo by magnetic resonance spectroscopy (MRS) is a major challenge since the main signals of NAA and NAAG largely overlap. This is a preliminary study in which we evaluated NAA and NAAG changes during a visual stimulation experiment using functional MRS. The paradigm used consisted of a rest period (5 min and 20 s), followed by a stimulation period (10 min and 40 s) and another rest period (10 min and 40 s). MRS from 17 healthy subjects were acquired at 3T with TR/TE = 2000/288 ms. Spectra were averaged over subjects and quantified with LCModel. The main outcomes were that NAA concentration decreased by about 20% with the stimulus, while the concentration of NAAG concomitantly increased by about 200%. Such variations fall into models for the energy metabolism underlying neuronal activation that point to NAAG as being responsible for the hyperemic vascular response that causes the BOLD signal. They also agree with the fact that NAAG and NAA are present in the brain at a ratio of about 1:10, and with the fact that the only known metabolic pathway for NAAG synthesis is from NAA and glutamate.
topic Proton magnetic resonance spectroscopy
Functional experiments
Brain activation
Brain energy metabolism
N-acetyl-L-aspartate
N-acetyl-aspartyl-glutamate
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012001100006
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