Alanine metabolism, transport, and cycling in the brain

Date

2007

Authors

Broer, Stefan
Broer, Angelika
Hansen, Jonas T.
Bubb, William A
Balcar, Vladimir J
Nasrallah, Fatima A.
Garner, Brett
Rae, Caroline

Journal Title

Journal ISSN

Volume Title

Publisher

Blackwell Publishing Ltd

Abstract

Brain glutamate/glutamine cycling is incomplete without return of ammonia to glial cells. Previous studies suggest that alanine is an important carrier for ammonia transfer. In this study, we investigated alanine transport and metabolism in Guinea pig brain cortical tissue slices and prisms, in primary cultures of neurons and astrocytes, and in synaptosomes. Alanine uptake into astrocytes was largely mediated by system L isoform LAT2, whereas alanine uptake into neurons was mediated by Na+-dependent transporters with properties similar to system B0 isoform B0AT2. To investigate the role of alanine transport in metabolism, its uptake was inhibited in cortical tissue slices under depolarizing conditions using the system L transport inhibitors 2-aminobicyclo[2.2.1]heptane-2-carboxylic acid and cycloleucine (1-aminocyclopentanecarboxylic acid; cLeu). The results indicated that alanine cycling occurs subsequent to glutamate/glutamine cycling and that a significant proportion of cycling occurs via amino acid transport system L. Our results show that system L isoform LAT2 is critical for alanine uptake into astrocytes. However, alanine does not provide any significant carbon for energy or neurotransmitter metabolism under the conditions studied.

Description

Keywords

Keywords: 2 aminobicyclo[2.2.1]heptane 2 carboxylic acid; alanine; amino acid transporter; cycloleucine; animal cell; animal experiment; animal tissue; article; astrocyte; brain cortex; brain slice; controlled study; depolarization; guinea pig; nerve cell; neurotra 13C NMR spectroscopy; Glutamine transport; LAT2; Nitrogen metabolism

Citation

Source

Journal of Neurochemistry

Type

Journal article

Book Title

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2037-12-31