Journal article
Hepatocyte transplantation (HTx) corrects selected neurometabolic abnormalities in murine intermediate maple syrup urine disease (iMSUD)
Biochimica et biophysica acta. Molecular basis of disease, Vol.1792(10), pp.1004-1010
2009
Handle:
https://hdl.handle.net/2376/112724
PMCID: PMC2753721
PMID: 19699299
Abstract
Skvorak et al.
[1] demonstrated the therapeutic efficacy of HTx in a murine model of iMSUD, confirming significant metabolic improvement and survival. To determine the effect of HTx on extrahepatic organs, we examined the metabolic effects of HTx in brain from iMSUD animals. Amino acid analysis revealed that HTx corrected increased ornithine, partially corrected depleted glutamine, and revealed a trend toward alloisoleucine correction. For amino acid and monoamine neurotransmitters, decreased GABA was partially corrected with HTx, while the
l-histidine dipeptide of GABA, homocarnosine, was decreased in iMSUD mice and hypercorrected following HTx. Elevated branched-chain amino acids (BCAA; leucine, isoleucine, and valine) in MSUD can deplete brain tyrosine and tryptophan (the precursors of monoamine neurotransmitters, dopamine (DA) and serotonin (5-hydroxytryptamine; 5-HT)) through competition via the large neutral amino acid transporter. HTx corrected decreased DA levels and the DA metabolite, 3-methoxytyramine, and partially corrected the DA intermediate 3,4-dihydroxyphenylacetate (DOPAC) and 5-HT levels, despite normal tyrosine and tryptophan levels in iMSUD mouse brain. We further observed enhanced intracellular turnover of both DA and 5-HT in iMSUD mouse brain, both of which partially corrected with HTx. Our results suggest new pathomechanisms of neurotransmitter metabolism in this disorder and support the therapeutic relevance of HTx in iMSUD mice, while providing proof-of-principle that HTx has corrective potential in extrahepatic organs.
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Details
- Title
- Hepatocyte transplantation (HTx) corrects selected neurometabolic abnormalities in murine intermediate maple syrup urine disease (iMSUD)
- Creators
- Kristen J Skvorak - Department of Pediatrics, University of Pittsburgh School of Medicine, USAElizabeth J Hager - Department of Pediatrics, University of Pittsburgh School of Medicine, USAErland Arning - Institute of Metabolic Disease, Baylor University Medical Center, Dallas, TX, USATeodoro Bottiglieri - Institute of Metabolic Disease, Baylor University Medical Center, Dallas, TX, USAHarbhajan S Paul - Biomed Research & Technologies, Inc., Wexford, Pennsylvania, USAStephen C Strom - Department of Pathology, University of Pittsburgh School of Medicine, USAGregg E Homanics - Department of Anesthesiology, University of Pittsburgh School of Medicine, USAQin Sun - Biochemical Genetics Laboratory, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USAErwin E.W Jansen - VU Medical Center, Metabolic Laboratory, Free University, Amsterdam, The NetherlandsCornelis Jakobs - VU Medical Center, Metabolic Laboratory, Free University, Amsterdam, The NetherlandsWilliam J Zinnanti - Penn State College of Medicine, Hershey, PA, USAK. Michael Gibson - Department of Pediatrics, University of Pittsburgh School of Medicine, USA
- Publication Details
- Biochimica et biophysica acta. Molecular basis of disease, Vol.1792(10), pp.1004-1010
- Academic Unit
- Pharmacotherapy, Department of
- Publisher
- Elsevier B.V
- Identifiers
- 99900547558901842
- Language
- English
- Resource Type
- Journal article