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N-Acetylaspartyl-Glutamate Metabolism in the Cingulated Cortices as a Biomarker of the Etiology in ASD: A 1H-MRS Model.
Jiménez-Espinoza, Carmen; Marcano Serrano, Francisco; González-Mora, José Luis.
Afiliación
  • Jiménez-Espinoza C; Laboratory Neurochemistry & Neuroimages, Department of Basic Medical Sciences, Faculty of Health Sciences, Physiology Section, University of La Laguna, 38200 Tenerife, Spain.
  • Marcano Serrano F; Laboratory Neurochemistry & Neuroimages, Department of Basic Medical Sciences, Faculty of Health Sciences, Physiology Section, University of La Laguna, 38200 Tenerife, Spain.
  • González-Mora JL; Magnetic Resonance Service for Biomedical Research (SRMIB), IMETISA, Canary University Hospital, 38320 Tenerife, Spain.
Molecules ; 26(3)2021 Jan 28.
Article en En | MEDLINE | ID: mdl-33525414
As brain functional resonance magnetic studies show an aberrant trajectory of neurodevelopment, it is reasonable to predict that the degree of neurochemical abnormalities indexed by magnetic resonance spectroscopy (1H-MRS) might also change according to the developmental stages and brain regions in autism spectrum disorders (ASDs). Since specific N-Acetyl-aspartate (NAA) changes in children's metabolism have been found in the anterior cingulate cortex (ACC) but not in the posterior cingulate cortex (PCC), we analyzed whether the metabolites of ASD youths change between the cingulate cortices using 1H-MRS. l-glutamate (Glu) and l-Acetyl-aspartate (NAA) are products from the N-Acetyl-aspartyl-glutamate (NAAG) metabolism in a reaction that requires the participation of neurons, oligodendrocytes, and astrocytes. This altered tri-cellular metabolism has been described in several neurological diseases, but not in ASD. Compared to the typical development (TD) group, the ASD group had an abnormal pattern of metabolites in the ACC, with a significant increase of glutamate (12.10 ± 3.92 mM; p = 0.02); additionally, N-Acetyl-aspartyl-glutamate significantly decreased (0.41 ± 0.27 mM; p = 0.02) within ASD metabolism abnormalities in the ACC, which may allow the development of new therapeutic possibilities.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biomarcadores / Corteza Cerebral / Dipéptidos / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: España Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biomarcadores / Corteza Cerebral / Dipéptidos / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: España Pais de publicación: Suiza