Literature DB >> 28867511

Glutamine and citrulline concentrations reflect nitric oxide synthesis in the human nervous system.

I Pérez-Neri1, J Ramírez-Bermúdez2, C Ojeda-López2, S Montes1, J L Soto-Hernández3, C Ríos4.   

Abstract

INTRODUCTION: Although citrulline is produced by nitric oxide (NO) synthase upon activation of the NMDA glutamate receptor, nitrite and nitrate (NOx) concentration is considered the best marker of NO synthesis, as citrulline is also metabolised by other enzymes. This study analyses the correlation between human cerebrospinal fluid NOx and citrulline concentrations in order to determine the extent to which citrulline reflects NO synthesis and glutamatergic neurotransmission.
METHODS: Participants were patients with acute neurological diseases undergoing lumbar puncture (n=240). NOx and amino acid concentrations were determined by HPLC.
RESULTS: NOx concentrations did not vary significantly where infection (p=0,110) or inflammation (p=0,349) were present. Multiple regression analysis showed that NOx concentration was correlated with glutamine (r=-0,319, p<0,001) and citrulline concentrations (r=0,293, p=0,005) but not with the citrulline/arginine ratio (r=-0,160, p=0,173). ANCOVA confirmed that NOx concentration was correlated with citrulline concentration (F=7,6, p=0,007) but not with the citrulline/arginine ratio (F=2,2, p=0,136), or presence of infection (F=1,8, p=0,173) or inflammation (F=1,4, p=0,227). No association was found between NOx and arginine or glutamate concentrations.
CONCLUSION: The results suggest that CSF citrulline concentration reflects NOx synthesis to some extent, despite the contribution of other metabolic pathways. In addition, this study shows that glutamine is an important modulator of NO synthase activity, and that arginine and glutamate are not correlated with NOx.
Copyright © 2017 Sociedad Española de Neurología. Publicado por Elsevier España, S.L.U. All rights reserved.

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Keywords:  Amino acid; Aminoácido; Brain; Cerebro; Inhibidor; Inhibitor; Isoform; Isoforma; Metabolism; Metabolismo; Neurological diseases; Trastorno neurológico

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Year:  2017        PMID: 28867511     DOI: 10.1016/j.nrl.2017.07.013

Source DB:  PubMed          Journal:  Neurologia (Engl Ed)        ISSN: 2173-5808


  2 in total

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  2 in total

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