Creatine, central nervous system and creatine deficiency syndromes


Autoria(s): Braissant O.; Uldry J.; Béard E.; Braissant O. (ed.); Wakamatsu H. (ed.); Kuo-Kang I. (ed.); Allegaert K. (ed.); Lenbury Y. (ed.); Wachholtz A. (ed.)
Data(s)

2011

Resumo

It was long thought that most of brain creatine was of peripheral origin. However, recentworks have demonstrated that creatine crosses blood-brain barrier only with poor efficiency, and thatCNS must ensure parts of its creatine needs by its own creatine synthesis pathway, thank to the brainexpression of AGAT and GAMT (creatine synthesis) and SLC6A8 (creatine transporter). This newunderstanding of creatine metabolism and transport in CNS allows a better comprehension of creatinedeficiency syndromes, which are due to deficiencies in AGAT, GAMT and SLC6A8 and mainly affectthe brain of patients who show severe neurodevelopmental delay and present neurological symptomsin early infancy.

Identificador

http://serval.unil.ch/?id=serval:BIB_58F8C05A666F

isbn:978-960-474-278-3

http://my.unil.ch/serval/document/BIB_58F8C05A666F.pdf

http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_58F8C05A666F1

Idioma(s)

en

Publicador

Cambridge: WSEAS Press

Direitos

info:eu-repo/semantics/openAccess

Fonte

Recent Researches in Modern Medicine

Palavras-Chave #Creatine; brain; AGAT; GAMT; SLC6A8; guanidinoacetate; creatine deficiency
Tipo

info:eu-repo/semantics/bookPart

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