Tyrosine uptake and regional brain monoamine metabolites in a rat model resembling congenital hyperammonemia
Abstract
Hyperammonemia found in congenital disorders has a toxic effect on the central nervous system. Disturbances of brain neurotransmitter metabolism have been proposed, such as an increased transport of tryptophan into the brain and an increased flux through the serotonin pathway. Results concerning the catecholamine pathway are, however, contradictory. We therefore studied whether hyperammonermia increases brain uptake of the neurotransmitter precursor amino acid tyrosine and whether these changes affect the concentration of neurotransmitters and their metabolites in different brain areas (frontal cortex, caudatus-putamen, thalamus, hypothalamus, hippocampus/substantia nigra, brainstem) of rats made hyperammonemic with urease. The brain uptake of tyrosine was measured in the forebrain, brainstem, and cerebellum. The brain areas were analyzed for dopamine, 3,4-hydroxyphenylacetic acid; homovanillic acid, norepinephrine, and vanillylmandelic acid. The brain uptake index of tyrosine was increased in the forebrain and brainstem of the hyperammonemic rats with concomitantly elevated concentrations in the forebrain of tyrosine, phenylalanine, and tryptophan. The homovanillic acid content was significantly increased in the hypothalamus, hippocampus/substantia nigra and brainstem. The concentrations of norepinephrine, dopamine, and 3, 4-hydroxyphenylacetic acid were not significantly changed. Vanillylmandellic acid was decreased in the caudatus-putamen, thalamus, and hypothalamus. The d…
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Metabolites that were lower in 4s2M (riboflavin, benzaldehyde, 1-aminocyclopropane-1-carboxylic acid) are not primary intermediates of central carbon metabolism and changes in their abundance may reflect shifts in cofactor handling or dietary metabolite uptake rather than broad changes in core metabolic pathways.
“Metabolites that were lower in 4s2M - riboflavin, benzaldehyde, and 1-aminocyclopropane-1-carboxylic acid – are not primary intermediates of central carbon metabolism and changes in their abundance may reflect shifts in cofactor handling or dietary metabolite uptake rather than broad changes in core metabolic pathways”
From Older adult APOE4 mice exhibit modest immunometabolic adaptation following microglial APOE2 replacement (2027) · cites this paper as Colombo et al., 1996
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Nolt, G. L., MacLean, S. M., Golden, L. R., Thorpe, S. P., Stephens, I. O., Funnell, J. L., Brock, C. R., Lucido, C. C., Smith, L., Hernandez, G., et al. (2027) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2026.08.005
- Authors
- Colombo, J.-P., Bachmann, C., Cervantes, H., Kokorovic, M., & Perritaz, R.
- Affiliations
- Centre Hospitalier Universitaire Vaudois (CH)
- University of Bern (CH)
- ORCID
- Bachmann, Claude
- Venue
- Pediatric Research
- Published
- 1996-06
- Volume
- 39
- Issue
- 6
- Pages
- 1036-1040
- ISSN
- 0031-3998 (ISSN-L)
- 1530-0447
- OpenAlex
- W1997127065
- Cited by
- 15
- References
- 0
- Citations by year
- 2026: 1 · 2024: 1 · 2017: 1 · 2013: 4
- FWCI
- 0.42
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Pediatric Research (publishedVersion)
- PubMed (publishedVersion)
- IRIS (submittedVersion)
- SERVAL (Université de Lausanne) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Keywords
- tyrosine uptake, blood-brain barrier, monoamine metabolism, dopaminergic pathways, homovanillic acid, vanillylmandelic acid, norepinephrine, catecholamines, neuropsychiatric disorders
- MeSH terms
- Amino Acids, Ammonia, Animals, Body Weight, Brain, Disease Models, Animal, Dopamine, Eating, Homovanillic Acid, Male, Norepinephrine, Tyrosine, Urease, Vanilmandelic Acid, Rats, Wistar, Rats
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