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Creatine and guanidinoacetate transport at bloodâbrain and bloodâcerebrospinal fluid barriers
- Source :
- Journal of inherited metabolic disease
- Publication Year :
- 2012
- Publisher :
- Wiley, 2012.
-
Abstract
- While it was thought that most of cerebral creatine is of peripheral origin, AGAT and GAMT are well expressed in CNS where brain cells synthesize creatine. While the creatine transporter SLC6A8 is expressed by microcapillary endothelial cells (MCEC) at blood-brain barrier (BBB), it is absent from their surrounding astrocytes. This raised the concept that BBB has a limited permeability for peripheral creatine, and that the brain supplies a part of its creatine by endogenous synthesis. This review brings together the latest data on creatine and guanidinoacetate transport through BBB and blood-CSF barrier (BCSFB) with the clinical evidence of AGAT-, GAMT- and SLC6A8-deficient patients, in order to delineate a clearer view on the roles of BBB and BCSFB in the transport of creatine and guanidinoacetate between periphery and CNS, and on brain synthesis and transport of creatine. It shows that in physiological conditions, creatine is taken up by CNS from periphery through SLC6A8 at BBB, but in limited amounts, and that CNS also needs its own creatine synthesis. No uptake of guanidinoacetate from periphery occurs at BBB except under GAMT deficiency, but a net exit of guanidinoacetate seems to occur from CSF to blood at BCSFB, predominantly through the taurine transporter TauT.
- Subjects :
- medicine.medical_specialty
Glycine
Endogeny
Biology
Creatine
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Cerebrospinal fluid
Taurine transporter
Internal medicine
Genetics
medicine
Animals
Humans
Creatine transporter
Genetics (clinical)
Cerebrospinal Fluid
030304 developmental biology
0303 health sciences
Biological Transport
Guanidinoacetate N-methyltransferase
Creatine synthesis
Endocrinology
chemistry
Biochemistry
Blood-Brain Barrier
Clinical evidence
030217 neurology & neurosurgery
Subjects
Details
- ISSN :
- 15732665 and 01418955
- Volume :
- 35
- Database :
- OpenAIRE
- Journal :
- Journal of Inherited Metabolic Disease
- Accession number :
- edsair.doi.dedup.....d0b4c1171af946e91c44e7dcdc71c927
- Full Text :
- https://doi.org/10.1007/s10545-011-9433-2