Literature DB >> 23886855

The cyanobacterial amino acid β-N-methylamino-l-alanine perturbs the intermediary metabolism in neonatal rats.

Mikael K R Engskog1, Oskar Karlsson, Jakob Haglöf, Albert Elmsjö, Eva Brittebo, Torbjörn Arvidsson, Curt Pettersson.   

Abstract

The neurotoxic amino acid β-N-methylamino-l-alanine (BMAA) is produced by most cyanobacteria. BMAA is considered as a potential health threat because of its putative role in neurodegenerative diseases. We have previously observed cognitive disturbances and morphological brain changes in adult rodents exposed to BMAA during the development. The aim of this study was to characterize changes of major intermediary metabolites in serum following neonatal exposure to BMAA using a non-targeted metabolomic approach. NMR spectroscopy was used to obtain serum metabolic profiles from neonatal rats exposed to BMAA (40, 150, 460mg/kg) or vehicle on postnatal days 9-10. Multivariate data analysis of binned NMR data indicated metabolic pattern differences between the different treatment groups. In particular five metabolites, d-glucose, lactate, 3-hydroxybutyrate, creatine and acetate, were changed in serum of BMAA-treated neonatal rats. These metabolites are associated with changes in energy metabolism and amino acid metabolism. Further statistical analysis disclosed that all the identified serum metabolites in the lowest dose group were significantly (p<0.05) decreased. The neonatal rat model used in this study is so far the only animal model that displays significant biochemical and behavioral effects after a low short-term dose of BMAA. The demonstrated perturbation of intermediary metabolism may contribute to BMAA-induced developmental changes that result in long-term effects on adult brain function.
Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  ALS/PDC; Amyotrophic lateral sclerosis/Parkinsonism-dementia complex; BMAA; Cyanobacteria; Energy metabolism; HSQC; Metabolomics; NMR; Neurotoxin; OPLS-DA; PCA; PND; orthogonal projections to latent structures discriminant analysis; postnatal day; principal component analysis; two-dimensional heteronuclear single quantum coherence spectroscopy; β-N-methylamino-l-alanine

Mesh:

Substances:

Year:  2013        PMID: 23886855     DOI: 10.1016/j.tox.2013.07.010

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  12 in total

Review 1.  The Potential Role of BMAA in Neurodegeneration.

Authors:  Tracie Caller; Patricia Henegan; Elijah Stommel
Journal:  Neurotox Res       Date:  2017-06-13       Impact factor: 3.911

2.  Intravenous injection of l-BMAA induces a rat model with comprehensive characteristics of amyotrophic lateral sclerosis/Parkinson-dementia complex.

Authors:  Ke-Wei Tian; Hong Jiang; Bei-Bei Wang; Fan Zhang; Shu Han
Journal:  Toxicol Res (Camb)       Date:  2015-11-10       Impact factor: 3.524

3.  MALDI imaging delineates hippocampal glycosphingolipid changes associated with neurotoxin induced proteopathy following neonatal BMAA exposure.

Authors:  Oskar Karlsson; Wojciech Michno; Yusuf Ransome; Jörg Hanrieder
Journal:  Biochim Biophys Acta Proteins Proteom       Date:  2016-12-09       Impact factor: 3.036

4.  Searching for a link between the L-BMAA neurotoxin and amyotrophic lateral sclerosis: a study protocol of the French BMAALS programme.

Authors:  Aurélie Delzor; Philippe Couratier; Farid Boumédiène; Marie Nicol; Michel Druet-Cabanac; François Paraf; Annick Méjean; Olivier Ploux; Jean-Philippe Leleu; Luc Brient; Marion Lengronne; Valérie Pichon; Audrey Combès; Saïda El Abdellaoui; Vincent Bonneterre; Emmeline Lagrange; Gérard Besson; Dominique J Bicout; Jean Boutonnat; William Camu; Nicolas Pageot; Raul Juntas-Morales; Valérie Rigau; Estelle Masseret; Eric Abadie; Pierre-Marie Preux; Benoît Marin
Journal:  BMJ Open       Date:  2014-09-01       Impact factor: 2.692

5.  Intracellular fibril formation, calcification, and enrichment of chaperones, cytoskeletal, and intermediate filament proteins in the adult hippocampus CA1 following neonatal exposure to the nonprotein amino acid BMAA.

Authors:  Oskar Karlsson; Anna-Lena Berg; Jörg Hanrieder; Gunnel Arnerup; Anna-Karin Lindström; Eva B Brittebo
Journal:  Arch Toxicol       Date:  2014-05-06       Impact factor: 5.153

6.  β-N-Methylamino-L-alanine (BMAA) perturbs alanine, aspartate and glutamate metabolism pathways in human neuroblastoma cells as determined by metabolic profiling.

Authors:  Mikael K R Engskog; Lisa Ersson; Jakob Haglöf; Torbjörn Arvidsson; Curt Pettersson; Eva Brittebo
Journal:  Amino Acids       Date:  2017-02-04       Impact factor: 3.520

Review 7.  NMR Techniques in Metabolomic Studies: A Quick Overview on Examples of Utilization.

Authors:  Joanna Kruk; Marek Doskocz; Elżbieta Jodłowska; Anna Zacharzewska; Joanna Łakomiec; Kornelia Czaja; Jacek Kujawski
Journal:  Appl Magn Reson       Date:  2016-11-02       Impact factor: 0.831

8.  Environmental neurotoxin interaction with proteins: Dose-dependent increase of free and protein-associated BMAA (β-N-methylamino-L-alanine) in neonatal rat brain.

Authors:  Oskar Karlsson; Liying Jiang; Lisa Ersson; Tim Malmström; Leopold L Ilag; Eva B Brittebo
Journal:  Sci Rep       Date:  2015-10-26       Impact factor: 4.379

9.  The effects of the toxic cyanobacterium Limnothrix (strain AC0243) on Bufo marinus larvae.

Authors:  Olivia Daniels; Larelle Fabbro; Sandrine Makiela
Journal:  Toxins (Basel)       Date:  2014-03-06       Impact factor: 4.546

10.  Maternal transfer of the cyanobacterial neurotoxin β-N-methylamino-L-alanine (BMAA) via milk to suckling offspring.

Authors:  Marie Andersson; Oskar Karlsson; Ulrika Bergström; Eva B Brittebo; Ingvar Brandt
Journal:  PLoS One       Date:  2013-10-23       Impact factor: 3.240

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