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PMID: 16573641 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Intracerebral accumulation of glutaric and 3-hydroxyglutaric acids secondary to limited flux across the blood-brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl-CoA dehydrogenase deficiency.

Journal of neurochemistry ·Vol. 97 ·No. 3 ·2006-05-00 ·Pages 899-910

Sauer SW, Okun JG, Fricker G, Mahringer A, Müller I, Crnic LR, Mühlhausen C, Hoffmann GF, Hörster F, Goodman SI, Harding CO, Koeller DM, Kölker S

Abstract

Glutaric acid (GA) and 3-hydroxyglutaric acids (3-OH-GA) are key metabolites in glutaryl co-enzyme A dehydrogenase (GCDH) deficiency and are both considered to be potential neurotoxins. As cerebral concentrations of GA and 3-OH-GA have not yet been studied systematically, we investigated the tissue-specific distribution of these organic acids and glutarylcarnitine in brain, liver, skeletal and heart muscle of Gcdh-deficient mice as well as in hepatic Gcdh-/- mice and in C57Bl/6 mice following intraperitoneal loading. Furthermore, we determined the flux of GA and 3-OH-GA across the blood-brain barrier (BBB) using porcine brain microvessel endothelial cells. Concentrations of GA, 3-OH-GA and glutarylcarnitine were significantly elevated in all tissues of Gcdh-/- mice. Strikingly, cerebral concentrations of GA and 3-OH-GA were unexpectedly high, reaching similar concentrations as those found in liver. In contrast, cerebral concentrations of these organic acids remained low in hepatic Gcdh-/- mice and after intraperitoneal injection of GA and 3-OH-GA. These results suggest limited flux of GA and 3-OH-GA across the BBB, which was supported in cultured porcine brain capillary endothelial cells. In conclusion, we propose that an intracerebral de novo synthesis and subsequent trapping of GA and 3-OH-GA should be considered as a biochemical risk factor for neurodegeneration in GCDH deficiency.

MeSH Terms
Amino Acids/metabolism Animals Biological Transport/physiology Blood-Brain Barrier/physiopathology Blotting, Western/methods Brain/cytology,metabolism Carnitine/analogs & derivatives,metabolism Cells, Cultured Dicarboxylic Acids/metabolism Disease Models, Animal Endothelial Cells/metabolism Glucose/metabolism Glutarates/metabolism Glutaryl-CoA Dehydrogenase/deficiency Heart/physiology Liver/metabolism Mice Mice, Inbred C57BL Mice, Knockout Models, Biological Muscles/metabolism Neurodegenerative Diseases/genetics,physiopathology Risk Factors Statistics, Nonparametric Swine Time Factors Tissue Distribution/physiology
Chemicals
3-hydroxyglutaric acid Amino Acids Dicarboxylic Acids Glutarates acylcarnitine Glutaryl-CoA Dehydrogenase glutaric acid Glucose Carnitine
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Sauer Sven W
Department of General Pediatrics, Division of Inborn Metabolic Diseases, University Children's Hospital Heidelberg, Heidelberg, Germany.
Okun Jürgen G
Fricker Gert
Mahringer Anne
Müller Ines
Crnic Linda R
Mühlhausen Chris
Hoffmann Georg F
Hörster Friederike
Goodman Stephen I
Harding Cary O
Koeller David M
Kölker Stefan
Article Info
Journal
Journal of neurochemistry
Abbr.
J Neurochem
ISSN
0022-3042
Published
2006-05-00
Epub
2006-00-29
Pages
899-910
Language
English
Region
England
NLM ID
2985190R
Subset
IM
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