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Determination of cerebrospinal fluid concentrations of arginine and dimethylarginines in patients with subarachnoid haemorrhage
Institute of Clinical Pharmacology, Otto-von-Guericke University Magdeburg, Magdeburg, Germany.
Department of Health Promotion and Family Care, Faculty of Health Sciences, University, Pécs, Hungary.
Department of Neurosurgery, Faculty of Medicine, University, Pécs, Hungary.
Department of Neurosurgery, Faculty of Medicine, University, Pécs, Hungary.ORCID iD: 0000-0002-2190-9278
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2007 (English)In: Journal of Neuroscience Methods, ISSN 0165-0270, E-ISSN 1872-678X, Vol. 164, no 1, p. 155-160Article in journal (Refereed) Published
Abstract [en]

Elevated cerebrospinal fluid (CSF) concentrations of asymmetric dimethylarginine (ADMA), an endogenous inhibitor of nitric oxide synthase (NOS), are assumed to be related to delayed vasospasm after subarachnoid haemorrhage (SAH). However, data on CSF concentrations of L-arginine, ADMA and its structural isomer symmetric dimethylarginine (SDMA) are very sparse in humans. We here present a new hydrophilic interaction chromatography-tandem mass spectrometry (HILIC-MS-MS) method for the precise determination of these substances in CSF. The method requires only minimal sample preparation and features isotope labeled internal standards. First data of patients with SAH showed that on the day of admission CSF concentration values of L-arginine and ADMA were not significantly different from controls, but increased markedly during the course of the hospital stay. The decrease of the L-arginine to ADMA ratio points to a progressive impairment of the NO production rate in the brain after SAH which is confirmed by a simultaneous decrease in nitrate and nitrite concentrations in CSF. 

Place, publisher, year, edition, pages
Elsevier, 2007. Vol. 164, no 1, p. 155-160
Keywords [en]
CSF, traumatic brain injury, subarachnoid haemorrhage, l-arginine, ADMA, SDMA
National Category
Neurology
Identifiers
URN: urn:nbn:se:oru:diva-113419DOI: 10.1016/j.jneumeth.2007.04.005ISI: 000248170300017PubMedID: 17512604Scopus ID: 2-s2.0-34250672761OAI: oai:DiVA.org:oru-113419DiVA, id: diva2:1854985
Available from: 2024-04-29 Created: 2024-04-29 Last updated: 2024-04-29Bibliographically approved

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