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Creatine deficiency syndromes and the importance of creatine synthesis in the brain

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Abstract

Creatine deficiency syndromes, due to deficiencies in AGAT, GAMT (creatine synthesis pathway) or SLC6A8 (creatine transporter), lead to complete absence or very strong decrease of creatine in CNS as measured by magnetic resonance spectroscopy. Brain is the main organ affected in creatine-deficient patients, who show severe neurodevelopmental delay and present neurological symptoms in early infancy. AGAT- and GAMT-deficient patients can be treated by oral creatine supplementation which improves their neurological status, while this treatment is inefficient on SLC6A8-deficient patients. While it has long been thought that most, if not all, of brain creatine was of peripheral origin, the past years have brought evidence that creatine can cross blood–brain barrier, however, only with poor efficiency, and that CNS must ensure parts of its creatine needs by its own endogenous synthesis. Moreover, we showed very recently that in many brain structures, including cortex and basal ganglia, AGAT and GAMT, while found in every brain cell types, are not co-expressed but are rather expressed in a dissociated way. This suggests that to allow creatine synthesis in these structures, guanidinoacetate must be transported from AGAT- to GAMT-expressing cells, most probably through SLC6A8. This new understanding of creatine metabolism and transport in CNS will not only allow a better comprehension of brain consequences of creatine deficiency syndromes, but will also contribute to better decipher creatine roles in CNS, not only in energy as ATP regeneration and buffering, but also in its recently suggested functions as neurotransmitter or osmolyte.

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Acknowledgments

This work was supported by the Swiss National Science Foundation, grants 3100A0-116859 and 31003A-130278.

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  1. Inborn Errors of Metabolism, Clinical Chemistry Laboratory, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Avenue Pierre-Decker 2, CI 02/33, 1011, Lausanne, Switzerland

    Olivier Braissant, Hugues Henry, Elidie Béard & Joséphine Uldry

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  1. Olivier Braissant
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Correspondence to Olivier Braissant.

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Braissant, O., Henry, H., Béard, E. et al. Creatine deficiency syndromes and the importance of creatine synthesis in the brain. Amino Acids 40, 1315–1324 (2011). https://doi.org/10.1007/s00726-011-0852-z

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