Amino acid assignment to one of three blood-brain barrier amino acid carriers
Abstract
The percentages of 22 14C-labeled amino acids remaining in rat brain 15 s after carotid injection were measured relative to a simultaneously injected diffusible internal standard, 3HOH. The injected solution also contained a nondiffusible internal standard, [113mIn]EDTA to correct for incomplete brain blood compartment washout. Self-inhibition and cross-inhibition was demonstrated by inclusion of unlabeled amino acids and carboxylic acids. All amino acids tested, excluding proline, alanine, and glycine, could be assigned to one, and only one, blood-brain barrier carrier system. The neutral carrier system transported phenylalanine, leucine, tyrosine, isoleucine, methionine, tryptophane, valine, DOPA, cysteine, histidine, threonine, glutamine, asparagine, and serine. Affinity for a basic amino acid carrier system was demonstrated for arginine, ornithine, and lysine. A third, low-capacity independent carrier system transporting aspartic and glutamic acids was demonstrated.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Transporters of neutral and excitatory amino acids, glycine, taurine, and GABA are enriched abluminally and mediate high-affinity transport from brain to endothelium in a sodium-dependent fashion, after which these amino acids are transported across the luminal membrane into the blood via low-affinity transporters mediating clearance of nitrogen-rich and acidic amino acids into the circulation.
“Transporters of neutral and excitatory AA, glycine, taurine, and GABA are enriched abluminally and with high-affinity transport from brain-to-endothelium in a sodium-dependent fashion, and then, these AA are transported across the luminal membrane of the BBB into the blood via low-affinity transporters mediating AA clearance of nitrogen-rich and acidic AA into the circulation (351, 453).”
From Blood-Brain Barrier: From Physiology to Disease and Back (2019) · cites this paper as [453]
Cited by
Sorted by citations
Blood-Brain Barrier: From Physiology to Disease and Back
Sweeney, M. D., Zhao, Z., Montagne, A., Nelson, A. R., & Zlokovic, B. V. (2019) · Physiological Reviews · doi:10.1152/physrev.00050.2017 · Cited by 2,294 · see citing works
Tryptophan metabolism in the central nervous system: medical implications
Ruddick, J. P., Evans, A. K., Nutt, D. J., Lightman, S. L., Rook, G. A. W., & Lowry, C. A. (2006) · Expert Reviews in Molecular Medicine · doi:10.1017/s1462399406000068 · Cited by 519 · see citing works
Gangwisch, J. E., Hale, L., Garcia, L., Malaspina, D., Opler, M. G., Payne, M. E., Rossom, R. C., & Lane, D. (2015) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.114.103846 · Cited by 278 · see citing works
Neuroplasticity of Dopamine Circuits After Exercise: Implications for Central Fatigue
Foley, T. E., & Fleshner, M. (2008) · NeuroMolecular Medicine · doi:10.1007/s12017-008-8032-3 · Cited by 261 · see citing works
Yokogoshi, H., Kobayashi, M., Mochizuki, M., & Terashima, T. (1998) · Neurochemical Research · doi:10.1023/a:1022490806093 · Cited by 229 · see citing works
Cooper, A., & Jeitner, T. (2016) · Biomolecules · doi:10.3390/biom6020016 · Cited by 223 · see citing works
Brusilow, S. W., Koehler, R. C., Traystman, R. J., & Cooper, A. J. L. (2010) · Neurotherapeutics · doi:10.1016/j.nurt.2010.05.015 · Cited by 209 · see citing works
Glutamine transport by the blood-brain barrier: a possible mechanism for nitrogen removal
Lee, W.-J., Hawkins, R. A., Viña, J. R., & Peterson, D. R. (1998) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1998.274.4.c1101 · Cited by 191 · see citing works
Rubia, K., Lee, F., Cleare, A. J., Tunstall, N., Fu, C. H. Y., Brammer, M., & McGuire, P. (2005) · Psychopharmacology · doi:10.1007/s00213-004-2116-z · Cited by 171 · see citing works
Peters, J. C., & Harper, A. E. (1985) · The Journal of Nutrition · doi:10.1093/jn/115.3.382 · Cited by 163 · see citing works
Pardridge, W. M. (2015) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2015.1042364 · Cited by 159 · see citing works
Acute Tryptophan Depletion. Part I: Rationale and Methodology
Hood, S. D., Bell, C. J., & Nutt, D. J. (2005) · Australian & New Zealand Journal of Psychiatry · doi:10.1080/j.1440-1614.2005.01627.x · Cited by 135 · see citing works
The effects of tyrosine depletion in normal healthy volunteers: implications for unipolar depression
McLean, A., Rubinsztein, J. S., Robbins, T. W., & Sahakian, B. J. (2004) · Psychopharmacology · doi:10.1007/s00213-003-1586-8 · Cited by 125 · see citing works
O'Kane, R. L., & Hawkins, R. A. (2003) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00193.2003 · Cited by 105 · see citing works
Acute serotonin and dopamine depletion improves attentional control: findings from the Stroop task
Scholes, K. E., Harrison, B. J., O'Neill, B. V., Leung, S., Croft, R. J., Pipingas, A., Phan, K. L., & Nathan, P. J. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301262 · Cited by 86 · see citing works
Amino Acids, Peptides, and Proteins
Dietzen, D. J. (2018) · Principles and Applications of Molecular Diagnostics · doi:10.1016/b978-0-12-816061-9.00013-8 · Cited by 82 · see citing works
Longstreth, W. T., Nelson, L. M., Koepsell, T. D., & Van Belle, G. (1991) · Medical Hypotheses · doi:10.1016/0306-9877(91)90183-y · Cited by 51 · see citing works
Munafó, M. R., Mannie, Z. N., Cowen, P. J., Harmer, C. J., & McTavish, S. B. (2007) · Journal of Psychopharmacology · doi:10.1177/0269881107077216 · Cited by 25 · see citing works
Dietary branched-chain amino acids and protein selection by rats
Anderson, S. A., Tews, J. K., & Harper, A. E. (1990) · The Journal of Nutrition · doi:10.1093/jn/120.1.52 · Cited by 22 · see citing works
Zepf, F. D., Landgraf, M., Biskup, C. S., Dahmen, B., Poustka, F., Wöckel, L., & Stadler, C. (2013) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12089 · Cited by 19 · see citing works
Selective effects of simultaneous monoamine depletion on mood and emotional responsiveness
Hughes, J.-M., Matrenza, C., Kemp, A. H., Harrison, B. J., Liley, D., & Nathan, P. J. (2004) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145703003845 · Cited by 16 · see citing works
- Authors
- Oldendorf, W., & Szabo, J.
- Venue
- American Journal of Physiology-Legacy Content
- Publisher
- American Physiological Society
- Published
- 1976-01-01
- Volume
- 230
- Issue
- 1
- Pages
- 94-98
- ISSN
- 0002-9513 (ISSN-L)
- OpenAlex
- W2183452160
- Cited by
- 594
- References
- 0
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 4 · 2023: 2 · 2022: 6 · 2021: 3 · 2020: 10 · 2019: 8 · 2018: 10 · 2017: 6 · 2016: 15 · 2015: 8 · 2014: 8 · 2013: 12 · 2012: 6
- FWCI
- 19.67
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Physiology-Legacy Content (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Keywords
- blood-brain barrier, amino acid transport, carrier systems, amino acid transporters, phenylalanine, leucine, tryptophan, L-arginine, lysine, aspartic acid, glutamate, autoinhibition, cross-inhibition, rat brain
- MeSH terms
- Amides, Amino Acids, Animals, Binding, Competitive, Biological Transport, Active, Blood-Brain Barrier, Carrier Proteins, Female, Fumarates, Lactates, Male, Pyruvates, Stereoisomerism, Succinates, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review