BLÁHOVÁ, Lucie, Jiří KOHOUTEK, E. KADLECOVA, L. KOZAKOVA and Luděk BLÁHA. Assessment of non-derivatized beta-N-methylamino-L-alanine (BMAA) neurotoxin in free form in urine of patients with nonspecific neurological symptoms. Toxicon. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD, 2017, vol. 133, July, p. 48-57. ISSN 0041-0101. Available from: https://dx.doi.org/10.1016/j.toxicon.2017.04.011.
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Basic information
Original name Assessment of non-derivatized beta-N-methylamino-L-alanine (BMAA) neurotoxin in free form in urine of patients with nonspecific neurological symptoms
Authors BLÁHOVÁ, Lucie (203 Czech Republic, belonging to the institution), Jiří KOHOUTEK (203 Czech Republic, belonging to the institution), E. KADLECOVA (203 Czech Republic), L. KOZAKOVA (203 Czech Republic) and Luděk BLÁHA (203 Czech Republic, guarantor, belonging to the institution).
Edition Toxicon, OXFORD, PERGAMON-ELSEVIER SCIENCE LTD, 2017, 0041-0101.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30104 Pharmacology and pharmacy
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 2.352
RIV identification code RIV/00216224:14310/17:00100223
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1016/j.toxicon.2017.04.011
UT WoS 000403864000006
Keywords in English Liquid chromatography-tandem mass spectrometry (LC-MS/MS); Hydrophilic interaction liquid chromatography (HILIC); Beta-N-methylamino-L-alanine (BMAA); Human urine
Tags NZ, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Michaela Hylsová, Ph.D., učo 211937. Changed: 6/3/2018 13:31.
Abstract
The beta-N-methylamino-L-alanine (BMAA) is a non-proteinogenic amino acid discussed to be produced by cyanobacteria forming harmful blooms. Since BMAA is suspected etiological agent in neurodegenerative diseases, there is a need to study and validate whether and in what concentrations can BMAA be present in human tissues. The aim of the present study was to validate analytical and extraction procedures for quantification of non-derivatized BMAA in the urine using liquid chromatography and commercial ELISA Kit. The study was focused on BMAA in different forms - dissolved, protein associated and total. The validated protocol included SPE followed by HILIC MS/MS for analyses of non-derivatized free form of BMAA with a limit of quantification 20 ng/mL. The methods for other BMAA forms (i.e.protein-associated and total) were also assessed but high matrix interferences did not allow their implementation. The method was used for analyses of free BMAA in 23 urine samples from healthy volunteers and psychiatric patients suffering from nonspecific neurological symptoms. Traces of BMAA were suspectedly detected in a single urine sample but they were not unequivocally proved according to all conservative analytical criteria. BMAA was also not confirmed in a repeatedly collected sample from the same person. The evaluated commercial BMAA ELISA Kit (Abraxis) was not suitable for determination of BMAA in extracted urine samples because of systematically highly false positive results. In agreement with recent findings, analyses of BMAA appear to methodologically challenging, and further research on BMAA in human tissues (or its precursors with potency to form BMAA under natural conditions or eventually - during sample processing) is needed to clarify its potential ethiological role in neurodegenerative diseases.
Links
LM2015051, research and development projectName: Centrum pro výzkum toxických látek v prostředí (Acronym: RECETOX RI)
Investor: Ministry of Education, Youth and Sports of the CR
LO1214, research and development projectName: Centrum pro výzkum toxických látek v prostředí (Acronym: RECETOX)
Investor: Ministry of Education, Youth and Sports of the CR
PrintDisplayed: 12/5/2024 13:04