The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
Active transport of gamma-aminobutyric acid and glycine into synaptic vesicles
Open accessAbstract
Although gamma-aminobutyric acid (GABA) and glycine are recognized as major amino acid inhibitory neurotransmitters in the central nervous system, their storage is poorly understood. In this study we have characterized vesicular GABA and glycine uptakes in the cerebrum and spinal cord, respectively. We present evidence that GABA and glycine are each taken up into isolated synaptic vesicles in an ATP-dependent manner and that the uptake is driven by an electrochemical proton gradient. Uptake for both amino acids exhibited kinetics with low affinity (Km in the millimolar range) similar to vesicular glutamate uptake. The ATP-dependent GABA uptake was not inhibited by the putative amino acid neurotransmitters glycine, taurine, glutamate, or aspartate or by GABA analogs, agonists, and antagonists. Similarly, ATP-dependent glycine uptake was hardly affected by GABA, taurine, glutamate, or aspartate or by glycine analogs or antagonists. The GABA uptake was not affected by chloride, which is in contrast to the uptake of the excitatory neurotransmitter glutamate, whereas the glycine uptake was slightly stimulated by low concentrations of chloride. Tissue distribution studies indicate that the vesicular uptake systems for GABA, glycine, and glutamate are distributed in different proportions in the cerebrum and spinal cord. These results suggest that the vesicular uptake systems for GABA, glycine, and glutamate are distinct from each other.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The text we found for this paper looks like another document, so the self-check wasn’t run.
Citations
Cites
PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 316,394
AN ELECTRON-TRANSPORT SYSTEM ASSOCIATED WITH THE OUTER MEMBRANE OF LIVER MITOCHONDRIA
Sottocasa, G. L., Kuylenstierna, B., Ernster, L., & Bergstrand, A. (1967) · The Journal of Cell Biology · doi:10.1083/jcb.32.2.415 · Cited by 2,316
First visualization of glutamate and GABA in neurones by immunocytochemistry
Storm‐Mathisen, J., Leknes, A. K., Bore, A. T., Vaaland, J. L., Edminson, P. D., Haug, F. Š., & Ottersen, O. P. (1983) · Nature · doi:10.1038/301517a0 · Cited by 869
Omura, T., & Takesuè, S. (1970) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a129248 · Cited by 633
Gamma-Aminobutyric Acid Binding to Receptor Sites in the Rat Central Nervous System
Zukin, S. R., Young, A. B., & Snyder, S. H. (1974) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.71.12.4802 · Cited by 588
Logan, W. J., & Snyder, S. H. (1972) · Brain Research · doi:10.1016/0006-8993(72)90540-9 · Cited by 478
Characterization of Glutamate Uptake into Synaptic Vesicles
Naito, S., & Ueda, T. (1985) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1985.tb07118.x · Cited by 446
Self-citationStrychnine Binding Associated with Glycine Receptors of the Central Nervous System
Young, A. B., & Snyder, S. H. (1973) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.70.10.2832 · Cited by 389
Active transport of γ-aminobutyric acid by membrane vesicles isolated from rat brain
Kanner, B. I. (1978) · Biochemistry · doi:10.1021/bi00600a011 · Cited by 253
Adenosine triphosphate-dependent uptake of glutamate into protein I-associated synaptic vesicles.
Naito, S., & Ueda, T. (1983) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)33100-4 · Cited by 209
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–120 of 120
Lane, J. D. (1992) · Neurochemical Research · doi:10.1007/bf00969898 · Cited by 4
The glutamatergic nerve terminal
Nicholls, D. G. (1994) · Springer eBooks · doi:10.1007/978-3-642-78757-7_6 · Cited by 4
Hu, J. H., Leitzell, K., Wang, D., & Quick, M. W. (2006) · Wiley eBooks · doi:10.1002/9780470101001.hcn016 · Cited by 4
GABA and its role in the regulation of the airway tone
Григорьевна, Ш. Е., & Naumov, D. E. (2020) · Bulletin physiology and pathology of respiration · doi:10.36604/1998-5029-2020-76-97-106 · Cited by 3
Amino acid uptake systems in lizard and chick brain cells
Sayegh, J. F., & Lajtha, Á. (1991) · Neurochemical Research · doi:10.1007/bf00965681 · Cited by 3
Sun, L., Zampese, E., Pancani, T., Wokosin, D. L., Tkatch, T., & Surmeier, D. J. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.1452-25.2026 · Cited by 2
Overview: Presynaptic Terminal Proteins Orchestrate Stepwise Synaptic Vesicle Phases
Mochida, S. (2014) · Springer eBooks · doi:10.1007/978-4-431-55166-9_1 · Cited by 2
Host Defensive and Pharmacological Study of Chlorella Vulgaris Strain CK
Hasegawa, T., Kumamoto, S., Nomoto, K., & Yoshikai, Y. (2005) · Studies in natural products chemistry · doi:10.1016/s1572-5995(05)80046-8 · Cited by 2
Neurotransmitters and Pharmacology
Browning, R. A. (2016) · CRC Press eBooks · doi:10.1201/9781439849828-8 · Cited by 1
Whole Endosome Recording of Vesicular Neurotransmitter Transporter Currents
Chang, R., & Edwards, R. H. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-1916-2_3 · Cited by 1
Extrasynaptic GABA Type A Receptors in the Mechanism of Action of Ethanol
Chandra, D. (2008) · D-Scholarship@Pitt (University of Pittsburgh)
IMAGING AND PROPERTIES OF EXTRASYNAPTIC GABA A RECEPTORS IN THE BRAIN
Sinkkonen, S. T. (2004)
Padilla-martin, K., n, J. B. B.-R., Blancas, R. B. P., Uribe-Escamilla, R., & Alfaro-RodrÃguez, A. (2008)
Transport of Amino Acid Neurotransmitters into Synaptic Vesicles
Takamori, S. (2014) · Springer eBooks · doi:10.1007/978-4-431-55166-9_12
Yamashita, M., & Hori, T. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-1916-2_9
Neurotransmitters and Pharmacology
Browning, R. A. (2010) · CRC Press eBooks · doi:10.1201/9781439849828-c4
Dopamine–Glutamate and Dopamine–GABA Co-release
Scimemi, A. (2025) · Advances in neurobiology · doi:10.1007/978-3-031-96364-3_8
Vglut3 : un rôle essentiel dans la cochlée et implication dans la surdité DFNA25.
Bersot, T. (2011) · theses.fr (ABES) · doi:10.70675/0723bdc3z5c56z42cdz8c1dz029a1cc1f7a1
付茹婷, Liu, J., Fang, L., & Guo, J. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-06141-y
Huang, P., Huang, X., Guo, K., Yu, F., Shen, X., Lu, F., Xie, Y., Xie, B., Davis, W. M., Fan, X., et al. (2026) · doi:10.65215/ltspreprints.2026.11.02.000378
Metadata
- Authors
- Kish, P. E., Fischer-Bovenkerk, C., & Ueda, T.
- Affiliations
- University of Michigan (US)
- Mental Health Research Institute, University of Michigan, Ann Arbor 48109.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1989-05
- Volume
- 86
- Issue
- 10
- Pages
- 3877-3881
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC287244
- OpenAlex
- W2088408205
- Cited by
- 119
- References
- 35
- Citations by year
- 2026: 2 · 2025: 1 · 2023: 1 · 2022: 3 · 2020: 1 · 2018: 2 · 2017: 1 · 2016: 4 · 2014: 3 · 2013: 1 · 2012: 1
- FWCI
- 4.94
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (5T32MHT5794-07)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- GABA, glycine, synaptic vesicles, vesicular uptake, inhibitory neurotransmitter, ATP-dependent uptake, proton gradient, cerebrum, spinal cord, chloride, amino acid transporters, neurotransmitter storage
- MeSH terms
- Adenosine Triphosphatases, Animals, Biological Transport, Active, Brain, Chlorides, gamma-Aminobutyric Acid, Glutamates, Glycine, Hydrogen-Ion Concentration, Ionophores, Kinetics, Membrane Potentials, Spinal Cord, Structure-Activity Relationship, Synaptic Vesicles, Tissue Distribution, Neurotransmitter Agents, Rats, In Vitro Techniques
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