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Decreased plasma neuroactive amino acids and increased nitric oxide levels in melancholic major depressive disorder

BACKGROUND: Amino acid neurotransmitters and nitric oxide (NO) are involved in the pathogenesis of major depressive disorder (MDD). Here we want to establish whether changes in their plasma levels may serve as biomarker for the melancholic subtype of this disorder. METHODS: Plasma levels of glutamic...

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Autores principales: Lu, Yun-Rong, Fu, Xin-Yan, Shi, Li-Gen, Jiang, Yan, Wu, Juan-Li, Weng, Xiao-Juan, Wang, Zhao-Pin, Wu, Xue-Yan, Lin, Zheng, Liu, Wei-Bo, Li, Hui-Chun, Luo, Jian-Hong, Bao, Ai-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036745/
https://www.ncbi.nlm.nih.gov/pubmed/24767108
http://dx.doi.org/10.1186/1471-244X-14-123
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author Lu, Yun-Rong
Fu, Xin-Yan
Shi, Li-Gen
Jiang, Yan
Wu, Juan-Li
Weng, Xiao-Juan
Wang, Zhao-Pin
Wu, Xue-Yan
Lin, Zheng
Liu, Wei-Bo
Li, Hui-Chun
Luo, Jian-Hong
Bao, Ai-Min
author_facet Lu, Yun-Rong
Fu, Xin-Yan
Shi, Li-Gen
Jiang, Yan
Wu, Juan-Li
Weng, Xiao-Juan
Wang, Zhao-Pin
Wu, Xue-Yan
Lin, Zheng
Liu, Wei-Bo
Li, Hui-Chun
Luo, Jian-Hong
Bao, Ai-Min
author_sort Lu, Yun-Rong
collection PubMed
description BACKGROUND: Amino acid neurotransmitters and nitric oxide (NO) are involved in the pathogenesis of major depressive disorder (MDD). Here we want to establish whether changes in their plasma levels may serve as biomarker for the melancholic subtype of this disorder. METHODS: Plasma levels of glutamic acid (Glu), aspartic acid (Asp), glycine (Gly), gamma-aminobutyric acid (GABA), and NO were determined in 27 medicine-naïve melancholic MDD patients and 30 matched controls. Seven of the MDD patients participated also in a follow-up study after 2 months’ antidepressant treatment. The relationship between plasma and cerebral-spinal fluid (CSF) levels of these compounds was analyzed in an additional group of 10 non-depressed subjects. RESULTS: The plasma levels of Asp, Gly and GABA were significantly lower whereas the NO levels were significantly higher in melancholic MDD patients, also after 2 months of fluoxetine treatment. In the additional 10 non-depressed subjects, no significant correlation was observed between plasma and CSF levels of these compounds. CONCLUSION: These data give the first indication that decreased plasma levels of Asp, Gly and GABA and increased NO levels may serve as a clinical trait-marker for melancholic MDD. The specificity and selectivity of this putative trait-marker has to be investigated in follow-up studies.
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spelling pubmed-40367452014-05-29 Decreased plasma neuroactive amino acids and increased nitric oxide levels in melancholic major depressive disorder Lu, Yun-Rong Fu, Xin-Yan Shi, Li-Gen Jiang, Yan Wu, Juan-Li Weng, Xiao-Juan Wang, Zhao-Pin Wu, Xue-Yan Lin, Zheng Liu, Wei-Bo Li, Hui-Chun Luo, Jian-Hong Bao, Ai-Min BMC Psychiatry Research Article BACKGROUND: Amino acid neurotransmitters and nitric oxide (NO) are involved in the pathogenesis of major depressive disorder (MDD). Here we want to establish whether changes in their plasma levels may serve as biomarker for the melancholic subtype of this disorder. METHODS: Plasma levels of glutamic acid (Glu), aspartic acid (Asp), glycine (Gly), gamma-aminobutyric acid (GABA), and NO were determined in 27 medicine-naïve melancholic MDD patients and 30 matched controls. Seven of the MDD patients participated also in a follow-up study after 2 months’ antidepressant treatment. The relationship between plasma and cerebral-spinal fluid (CSF) levels of these compounds was analyzed in an additional group of 10 non-depressed subjects. RESULTS: The plasma levels of Asp, Gly and GABA were significantly lower whereas the NO levels were significantly higher in melancholic MDD patients, also after 2 months of fluoxetine treatment. In the additional 10 non-depressed subjects, no significant correlation was observed between plasma and CSF levels of these compounds. CONCLUSION: These data give the first indication that decreased plasma levels of Asp, Gly and GABA and increased NO levels may serve as a clinical trait-marker for melancholic MDD. The specificity and selectivity of this putative trait-marker has to be investigated in follow-up studies. BioMed Central 2014-04-27 /pmc/articles/PMC4036745/ /pubmed/24767108 http://dx.doi.org/10.1186/1471-244X-14-123 Text en Copyright © 2014 Lu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Lu, Yun-Rong
Fu, Xin-Yan
Shi, Li-Gen
Jiang, Yan
Wu, Juan-Li
Weng, Xiao-Juan
Wang, Zhao-Pin
Wu, Xue-Yan
Lin, Zheng
Liu, Wei-Bo
Li, Hui-Chun
Luo, Jian-Hong
Bao, Ai-Min
Decreased plasma neuroactive amino acids and increased nitric oxide levels in melancholic major depressive disorder
title Decreased plasma neuroactive amino acids and increased nitric oxide levels in melancholic major depressive disorder
title_full Decreased plasma neuroactive amino acids and increased nitric oxide levels in melancholic major depressive disorder
title_fullStr Decreased plasma neuroactive amino acids and increased nitric oxide levels in melancholic major depressive disorder
title_full_unstemmed Decreased plasma neuroactive amino acids and increased nitric oxide levels in melancholic major depressive disorder
title_short Decreased plasma neuroactive amino acids and increased nitric oxide levels in melancholic major depressive disorder
title_sort decreased plasma neuroactive amino acids and increased nitric oxide levels in melancholic major depressive disorder
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036745/
https://www.ncbi.nlm.nih.gov/pubmed/24767108
http://dx.doi.org/10.1186/1471-244X-14-123
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