Literature DB >> 32424601

L-Aspartate, L-Ornithine and L-Ornithine-L-Aspartate (LOLA) and Their Impact on Brain Energy Metabolism.

Abhijit Das1,2, Dominik Fröhlich3, Lavanya B Achanta1,3, Benjamin D Rowlands1,3, Gary D Housley3, Matthias Klugmann3, Caroline D Rae4,5.   

Abstract

L-Ornithine-L-aspartate (LOLA), a crystalline salt, is used primarily in the management of hepatic encephalopathy. The degree to which it might penetrate the brain, and the effects it might have on metabolism in brain are poorly understood. Here, to investigate the effects of LOLA on brain energy metabolism we incubated brain cortical tissue slices from guinea pig (Cavea porcellus) with the constituent amino acids of LOLA, L-ornithine or L-aspartate, as well as LOLA, in the presence of [1-13C]D-glucose and [1,2-13C]acetate; these labelled substrates are useful indicators of brain metabolic activity. L-Ornithine produced significant "sedative" effects on brain slice metabolism, most likely via conversion of ornithine to GABA via the ornithine aminotransferase pathway, while L-aspartate showed concentration-dependent excitatory effects. The metabolic effects of LOLA reflected a mix of these two different processes and were concentration-dependent. We also investigated the effect of an intraperitoneal bolus injection of L-ornithine, L-aspartate or LOLA on levels of metabolites in kidney, liver and brain cortex and brain stem in mice (C57Bl6J) 1 h later. No significant changes in metabolite levels were seen following the bolus injection of L-aspartate, most likely due to rapid metabolism of aspartate before reaching the target tissue. Brain cortex glutamate was decreased by L-ornithine but no other brain effects were observed with any other compound. Kidney levels of aspartate were increased after injection of L-ornithine and LOLA which may be due to interference by ornithine with the kidney urea cycle. It is likely that without optimising chronic intravenous infusion, LOLA has minimal impact on healthy brain energy metabolism due to systemic clearance and the blood - brain barrier.

Entities:  

Keywords:  13C NMR spectroscopy; Amino acid metabolism; Aspartate; Brain energy metabolism; LOLA; Ornithine

Mesh:

Substances:

Year:  2020        PMID: 32424601     DOI: 10.1007/s11064-020-03044-9

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  3 in total

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Journal:  Front Cell Infect Microbiol       Date:  2022-05-20       Impact factor: 6.073

2.  Developmental delay and late onset HBSL pathology in hypomorphic Dars1M256L mice.

Authors:  Matthias Klugmann; Elizabeth Kalotay; Fabien Delerue; Lars M Ittner; Andre Bongers; Josephine Yu; Margaret J Morris; Gary D Housley; Dominik Fröhlich
Journal:  Neurochem Res       Date:  2022-03-31       Impact factor: 4.414

3.  A Hypomorphic Dars1 D367Y Model Recapitulates Key Aspects of the Leukodystrophy HBSL.

Authors:  Dominik Fröhlich; Marisa I Mendes; Andrew J Kueh; Andre Bongers; Marco J Herold; Gajja S Salomons; Gary D Housley; Matthias Klugmann
Journal:  Front Cell Neurosci       Date:  2021-01-20       Impact factor: 5.505

  3 in total

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