The DOI matches its Crossref record; 117 of the 117 references it cites were found in a registry or an index.
Neurotransmitter Corelease: Mechanism and Physiological Role
Open accessAbstract
Neurotransmitter identity is a defining feature of all neurons because it constrains the type of information they convey, but many neurons release multiple transmitters. Although the physiological role for corelease has remained poorly understood, the vesicular uptake of one transmitter can regulate filling with the other by influencing expression of the H + electrochemical driving force. In addition, the sorting of vesicular neurotransmitter transporters and other synaptic vesicle proteins into different vesicle pools suggests the potential for distinct modes of release. Corelease thus serves multiple roles in synaptic transmission.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The cited source says what the claim attributes to it.
In the citing paper
“Although many of these neurotransmitter co-release patterns had been documented previously55–57”
From A high-resolution transcriptomic and spatial atlas of cell types in the whole mouse brain (2023) · cites this paper as [56]
In the citing paper
“This creates a pH gradient (DpH) and a vesicular membrane potential (DJ), both of which can power the uptake of neurotransmitters by vesicular transporters (Table 1).16”
From Synaptic and circuit functions of multitransmitter neurons in the mammalian brain (2023) · cites this paper as [16]
In the citing paper
“In multitransmitter neurons, where vesicular packaging of more than one neurotransmitter occurs, it is important to consider how vesicular transporters are differentially sensitive to intravesicular factors such as pH or membrane potential.16”
From Synaptic and circuit functions of multitransmitter neurons in the mammalian brain (2023) · cites this paper as [16]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
A neural substrate of prediction and reward
Schultz, W., Dayan, P., & Montague, P. R. (1997) · Science · doi:10.1126/science.275.5306.1593 · Cited by 9,388 · cited 1×
“Conversely, they slow or pause firing in response to rewards worse than predicted (98).”
Getting formal with dopamine and reward
Schultz, W. (2002) · Neuron · doi:10.1016/s0896-6273(02)00967-4 · Cited by 2,574 · cited 1×
“One possibility is that the glutamate released by dopamine terminals contributes to the prediction-error signal encoded in the firing rates of dopamine neurons (96, 97).”
Vacuolar ATPases: rotary proton pumps in physiology and pathophysiology
Forgac, M. D. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2272 · Cited by 1,626 · cited 2×
“However, rather than using H + flux to produce ATP, the vacuolar H + pump uses ATP hydrolysis to drive H + transport into membranes of the secretory pathway, including endosomes, lysosomes, synaptic vesicles, and LDCVs (16). μ H+ in turn comprises both a chemical gradient (pH) and a membrane potential (ψ), and the tra…”
The Expression of Vesicular Glutamate Transporters Defines Two Classes of Excitatory Synapse
Fremeau, R. T., Troyer, M. D., Pahner, I., Nygaard, G. O., Tran, C. H., Reimer, R. J., Bellocchio, E. E., Fortin, D. L., Storm‐Mathisen, J., & Edwards, R. H. (2001) · Neuron · doi:10.1016/s0896-6273(01)00344-0 · Cited by 1,266 · cited 1×
“The distribution of VGLUT1 and -2 originally suggested a correlation of VGLUT1 with synapses having a low probability of release (such as hippocampal synapses and parallel fiber synapses in the cerebellum) and VGLUT2 with synapses having a high probability of release (114).”
Self-citationDopamine neurons report an error in the temporal prediction of reward during learning
Hollerman, J. R., & Schultz, W. (1998) · Nature Neuroscience · doi:10.1038/1124 · Cited by 1,161 · cited 1×
“One possibility is that the glutamate released by dopamine terminals contributes to the prediction-error signal encoded in the firing rates of dopamine neurons (96, 97).”
Subsecond dopamine release promotes cocaine seeking
Phillips, P. E. M., Stuber, G. D., Heien, M. L. A. V., Wightman, R. M., & Carelli, R. M. (2003) · Nature · doi:10.1038/nature01476 · Cited by 1,113 · cited 1×
“Consistent with these changes in firing, extracellular dopamine measured by fast-scan cyclic voltammetry changes as predicted in rodents performing goal-directed tasks (99).”
Rizzoli, S. O., & Betz, W. J. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1583 · Cited by 975 · cited 1×
“Considerable previous work has shown that only a fraction of the synaptic vesicles in a presynaptic bouton are available for evoked release, even after prolonged stimulation (113).”
Takamori, S., Rhee, J. S., Rosenmund, C., & Jahn, R. (2000) · Nature · doi:10.1038/35025070 · Cited by 862 · cited 1×
“We do not know the stoichiometry of ionic coupling by the VGLUTs, but the sensitivity to pH (27, 43, 48) supports a H+ exchange mechanism despite the primary dependence of VGLUTs on ψ.”
Uptake of Glutamate into Synaptic Vesicles by an Inorganic Phosphate Transporter
Bellocchio, E. E., Reimer, R. J., Fremeau, R. T., & Edwards, R. H. (2000) · Science · doi:10.1126/science.289.5481.957 · Cited by 795 · cited 3×
“We do not know the stoichiometry of ionic coupling by the VGLUTs, but the sensitivity to pH (27, 43, 48) supports a H+ exchange mechanism despite the primary dependence of VGLUTs on ψ.”
Self-citationCorelease of Two Fast Neurotransmitters at a Central Synapse
Jonas, P., Bischofberger, J., & Sandkühler, J. (1998) · Science · doi:10.1126/science.281.5375.419 · Cited by 784
Research works printed but not linked: 1
- Whittaker VP, 1972, Biochem. Soc. Symp., 1972, 49
Cited by
Sorted by citations
Items 201–283 of 283
Grill, F., Johansson, J. J., Axelsson, J., Brynolfsson, P., Nyberg, L. H., & Rieckmann, A. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.733091 · Cited by 9
“, 2021) or differences of co-release of inhibitory, excitatory, or other modulatory neurotransmitters (Hnasko and Edwards, 2012; Tritsch et al., 2016).”
BackgroundHow much alcohol is in ketamine's antidepressant action?
Bonnet, U. (2016) · Life Sciences · doi:10.1016/j.lfs.2016.11.003 · Cited by 9
Li, T., Chen, X., Cheng, J., Yan, Z., Wu, C., Zhou, D., Fan, G., Li, X., Cong, K., & Xu, L. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.104844 · Cited by 7
Dvořáček, J., Bednářová, A., Krishnan, N., & Kodrík, D. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104570 · Cited by 7
Marcoli, M., Agnati, L. F., Franco, R., Cortelli, P., Anderlini, D., Guidolin, D., Cervetto, C., & Maura, G. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1038874 · Cited by 7
Romei, C., Bonifacino, T., Milanese, M., Usai, C., & Raiteri, L. (2016) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2016.08.013 · Cited by 7
Kim, D., Kang, S. J., Jhang, J., Jo, Y. S., Park, S., Ye, M., Pyeon, G. H., Im, G.-H., Kim, S., & Han, S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.09.622790 · Cited by 8
Is GABA Co-Released with Glutamate from Hippocampal Mossy Fiber Terminals?
Caiati, M. D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5019-12.2013 · Cited by 6
“The coexistence and co-release of different neurotransmitters from the same fiber has been well documented in several brain structures, including the retina, the spinal cord, and the auditory system (Hnasko and Edwards, 2012).”
BackgroundNeurobiological Principles: Neurotransmitters
Hampel, L., & Lau, T. (2020) · Springer eBooks · doi:10.1007/978-3-319-56015-1_365-1 · Cited by 6
Soslau, G. (2019) · Medicine in Drug Discovery · doi:10.1016/j.medidd.2020.100018 · Cited by 6
Mahapatra, C., Gawad, J., Bonde, C. G., & Palkar, M. B. (2025) · Receptors · doi:10.3390/receptors4020009 · Cited by 5
The role of SCAMP5 in central nervous system diseases
Chen, Y., Fan, J., Xiao, D., & Li, X. (2022) · Neurological Research · doi:10.1080/01616412.2022.2107754 · Cited by 5
“gic synapses before synaptic transmission [56].”
Kim, D.-I., Park, S., Ye, M., Chen, J., Jhang, J., Hunker, A. C., Zweifel, L. S., Palmiter, R. D., & Han, S. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.19.524797 · Cited by 6
“properties of neuromodulators suggest that they can function as the main neurotransmitter in neurons, like 33 dopamine and norepinephrine (Eskenazi et al., 2021; Hnasko and Edwards, 2012; Vaaga et al., 2014).”
Sexually dimorphic mechanisms of VGLUT-mediated protection from dopaminergic neurodegenerationPreprint
Buck, S. A., Rubin, S. A., Kunkhyen, T., Treiber, C. D., Xue, X., Fenno, L. E., Mabry, S. J., Sundar, V. R., Yang, Z., Shah, D., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.02.560584 · Cited by 5
Self-citationMetabolomics: A Powerful Tool to Understand the Schizophrenia Biology
Zandonadi, F. D. S., dos Santos, E. A. F., Marques, M., & Sussulini, A. (2022) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-97182-3_8 · Cited by 4
Frog retinal ganglion cells projecting to the tectum layer F release acetylcholine as co-mediator
Baginskas, A., Kuraitė, V., & Kuras, A. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.06.028 · Cited by 4
Hirai, H., Konno, K., Yamasaki, M., Watanabe, M., Sakaba, T., & Hashimotodani, Y. (2024) · eLife · doi:10.7554/elife.99711.3 · Cited by 16
Expression of Drosophila melanogaster V-ATPases in Olfactory Sensillum Support Cells
Jain, K., Prelic, S., Hansson, B. S., & Wicher, D. (2024) · Insects · doi:10.3390/insects15121016 · Cited by 3
Neurobiological Principles: Neurotransmitters
Hampel, L., & Lau, T. (2022) · Springer eBooks · doi:10.1007/978-3-030-62059-2_365 · Cited by 3
Mediators of the Nervous System Kinds Characteristic
Bon, E. I. (2023) · Biomedical Journal of Scientific & Technical Research · doi:10.26717/bjstr.2023.48.007692 · Cited by 3
Neurotransmitters of Autonomic Nervous System
Balaban, Z., & Kurt, G. (2023) · Physiology · doi:10.5772/intechopen.112007 · Cited by 3
Optical bionanosensors for neurotransmitter detection
Polo, E. (2018) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7098 · Cited by 3
Prevalent co-release of glutamate and GABA throughout the mouse brainPreprint
Ceballos, C. C., Ma, L., Qin, M., & Zhong, H. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.27.587069 · Cited by 3
Intranasal delivery of therapeutics to degenerating brain regions: From pathways to nanocarriers
Saha, P., Roy, S. J., Bhattacharya, S., & Datta, A. (2025) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2025.107818 · Cited by 4
Chanaday, N. L. (2026) · Advances in neurobiology · doi:10.1007/978-3-032-12594-1_3 · Cited by 2
Morari, M., & Fantin, M. (2015) · The Analyst · doi:10.1039/c4an01918k · Cited by 2
Mondoloni, S., & Mameli, M. (2022) · Neuron · doi:10.1016/j.neuron.2022.03.035 · Cited by 2
Castagnola, T., Castagna, V. C., Cadenas, L. T., Kitcher, S. R., Guilmi, M. N. D., Gómez‐Casati, M. E., Beaulac, H. J., Buonfiglio, P. I., Dalamón, V., Katz, E., et al. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1653-24.2025 · Cited by 3
Key Molecules: Vesicular Neurotransmitter Transporters☆
Reimer, R. J., & Voglmaier, S. M. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.04801-7 · Cited by 2
Reduced signal crosstalk multi neurotransmitter image sensor by microhole array structure
Ogaeri, Y., Lee, Y., Mitsudome, M., Iwata, T., Takahashi, K., & Sawada, K. (2018) · Japanese Journal of Applied Physics · doi:10.7567/jjap.57.06hh01 · Cited by 2
Habenular Synapses and Nicotine
Ables, J. L., Antolin‐Fontes, B., & Ibáñez-Tallon, I. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813035-3.00010-1 · Cited by 2
Neural Information Processing and Computations of Two-Input Synapses
Kim, S. H., Woo, J., Choi, K., Choi, M. Y., & Han, K. (2022) · Neural Computation · doi:10.1162/neco_a_01534 · Cited by 2
“In particular, recent experiments support that neurons can release multiple neurotransmitters (Hnasko & Edwards, 2012; Granger, Wallace, & Sabatini, 2017; Sharif, Ase, Ribeiro-da-Silva, & Séguéla, 2020), in sharp contrast with the conventional wisdom that a neuron releases one type of…”
ResultNonclassic Signaling in the Brain
Deutch, A. Y., Giuffrida, A., & Roberts, J. L. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397179-1.00008-7 · Cited by 2
Farsi, Z. (2016) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5523 · Cited by 1
Antidepressants and Psychological Treatment: Hard Reasons for Synergy
Campagne, D. M. (2021) · Revista de Psicopatología y Psicología Clínica · doi:10.5944/rppc.28235 · Cited by 1
“…Neurotransmitters and other modulators present high levels of co-storage and co-liberation and operate in a coordinated and dependent way (Jing et al., 2001; Blank, Nijholt, Vollstaedt, et al., 2003; Blank, Nijholt, Grammatopoulos, et al., 2003; Hnasko and Edwards, 2012; Merighi, 2018).”
BackgroundHadjighassem, M. (2024) · International Journal of Clinical Case Reports and Reviews · doi:10.31579/2690-4861/371 · Cited by 1
A computational model for angular velocity integration in a locust heading circuit
Pabst, K., Gkanias, E., Webb, B. H., Homberg, U., & Endres, D. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012155 · Cited by 1
Merighi, A., Sbriz, M., & Lossi, L. (2026) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2026.1839947 · Cited by 1
“This architectural arrangement provides the mechanistic foundation for the temporal stratification and operational models of cotransmission discussed in the following section (Hnasko and Edwards, 2012).”
Reduced Glutamatergic Neurotransmission as Possible Indicator of Unfavorable Prognosis
Alekseeva, E. (2017) · International Journal of Biomedicine · doi:10.21103/article7(1)_ra2 · Cited by 1
“and GABA, excitatory and inhibitory fast neurotransmitters, from a single axon terminal in neurons.[15-17] GNS is involved”
BackgroundReyes‐Pinto, R., Ferrán, J. L., Vega‐Zuniga, T., González‐Cabrera, C., Luksch, H., Mpodozis, J., Puelles, L., & Marin, G. J. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25229 · Cited by 1
“In some of these cases, co- release or co-transmission of glutamate along with another neuro- transmitter has been demonstrated (El Mestikawy et al., 2011; Hnasko & Edwards, 2012; Trudeau & El Mestikawy, 2018; Vaaga et al., 0 4).”
BackgroundDynamical questions in volume transmission
Cruikshank, A., Nijhout, H. F., Best, J. A., & Reed, M. C. (2023) · Journal of Biological Dynamics · doi:10.1080/17513758.2023.2269986 · Cited by 1
“Although we have written as though the HA neurons, DA neurons, GABA neurons and ACh neurons are distinct types of neurons, it is now widely accepted that many neurons corelease multiple neurotransmitters [23, 39].”
BackgroundCerebro y Comportamiento: Una Revisión
Molero‐Chamizo, A., & Urbina, G. N. R. (2012) · Revista Argentina de Ciencias del Comportamiento ( RACC ) · doi:10.32348/1852.4206.v4.n2.5175 · Cited by 1
“Estas sustancias se conocen como neurotransmisores, y son esencialmente moléculas químicas que alteran el estado de reposo de la célula que recibe la señal química (Hnasko & Edwards, 2011).”
BackgroundBalmer, T. S., & Trussell, L. O. (2016) · Neuron · doi:10.1016/j.neuron.2016.05.011 · Cited by 1
“It is possible that VGLUT3 is fine-tuned to operate in an energetic environment that also favors the operation of other transmitter transporters in the same vesicle membrane (Hnasko and Edwards, 2012).”
BackgroundWu, M. V., & Tollkuhn, J. (2017) · bioRxiv · doi:10.1101/114835
“Other neurotransmitters, such as dopamine, can be expressed in Vgat/Vglut2-negative cells, and may contribute important modulatory functions (Hnasko and Edwards, 2012).”
BackgroundSynaptic modifications in hippocampal CA3 pyramidal cells in an Alzheimer's mouse model
Zhang, P. (2018) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6752 · Cited by 1
Co-release of GABA and ACh from medial olivocochlear neurons fine tunes cochlear efferent inhibitionPreprint
Castagnola, T., Castagna, V. C., Kitcher, S. R., Cadenas, L. T., Guilmi, M. N. D., Gómez‐Casati, M. E., Buonfiglio, P. I., Dalamón, V., Katz, E., Elgoyhen, A. B., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.12.607644 · Cited by 1
“Co-release of different neurotransmitters from the same neuron was described many years ago (Hnasko & Edwards, 2012).”
GABA-glutamate corelease is a mechanism for state-dependent neurotransmissionPreprint
Warlow, S. M., Dowlat, D. S., Hollon, N. G., Faget, L. C., Oriol, L., Zell, V., Zweifel, L. S., & Hnasko, T. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.19.689286 · Cited by 1
“Cotransmission of GABA and glutamate throughout the brain may serve a variety of functions such as promoting neural development, or as a compensatory response to prevent seizures 2,23,30 .”
Self-citationNeural mechanisms of memory reconsolidation
Exton-McGuinness, M. T. J. (2014) · University of Birmingham Institutional Research Archive (University of Birmingham) · Cited by 1
Transport Mechanisms of the Vesicular Glutamate Transporter 1
Preobraschenski, J. (2013) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3832 · Cited by 1
Receptor A2a de adenosina: estudo da modulação da liberação de neurotransmissores em modelo in vitro
Matsumoto, J. P. D. P. (2012) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.41.2012.tde-03042013-115748
Structure-function analysis of the Vesicular glutamate transporter 1 (VGLUT1) C-terminus
Jordan, J.-C. (2015) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-8460
SYNAPTIC ARCHITECTURE OF THE ACOUSTIC STARTLE RESPONSE PATHWAY (Thesis format: Monograph)
Smoka, M. (2014) · Scholarship@Western (Western University)
Juvenile mossy fibres: two pipers in the same pub?
Tóth, K. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.239699
Understanding Mood Disorders Using Electrophysiology and Circuit Breaking
Liu, H., & Chaudhury, D. (2017) · Springer eBooks · doi:10.1007/978-3-319-57363-2_14
McKenzie, C. (2018) · Institute of Science and Technology Austria · doi:10.15479/at:ista:7132
Maternal Ube3a is Required for Neurotypical Motivational Drive and GABA co-release
Wallace, J. B. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/m272-rx76
Molecular mechanisms of synaptic vesicle recycling with a focus on Endophilin A and Rabconnectin-3a
Gowrisankaran, S. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7717
Expansionsmikroskopie des Rattenhirns zur subzellulären Lokalisation synaptischer Proteine
Kemna, N. A. (2022) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9052
Panina, Y. A., Uspenskaya, Y. A., Lopatina, O. L., & Salmina, A. B. (2022) · Annals of Clinical and Experimental Neurology · doi:10.54101/acen.2022.1.4
Investigating the role of neutral sphingomyelinases in membrane vesicle trafficking
Choezom, D. (2022) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9238
Canavero, S. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-817000-7.00002-8
Dopamine enhances multisensory responses in the dorsomedial striatumPreprint
Sáez, M., Alegre-Cortés, J., Morgenstern, N. A., Garcı́a-Frigola, C., de la Torre‐Martínez, R., & Reig, R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.25.559270
“Finally, several ex vivo studies described how dopaminergic neurons can co-release GABA 58,59 or glutamate 60–64 .”
BackgroundHirai, H., Konno, K., Yamasaki, M., Watanabe, M., Sakaba, T., & Hashimotodani, Y. (2024) · eLife · doi:10.7554/elife.99711.1
Hirai, H., Konno, K., Yamasaki, M., Watanabe, M., Sakaba, T., & Hashimotodani, Y. (2024) · eLife · doi:10.7554/elife.99711.2 · Cited by 1
Varga, A. G., Reid, B. T., Maletz, S. N., Dossat, A. M., & Levitt, E. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.21.639476
“…exerted by glutamate that may activate single action potentials and convey temporally precise commands, while dopamine influences a delayed, but long-lasting state of increased excitability, allowing other excitatory synapses to induce postsynaptic firing and potentially prompting plasticity 8 .”
Dopamine–Glutamate and Dopamine–GABA Co-release
Scimemi, A. (2025) · Advances in neurobiology · doi:10.1007/978-3-031-96364-3_8
VGLUT2 in Parkinson’s disease: an emerging therapeutic target
Freyberg, Z., Torregrossa, M. M., & Rocha, E. M. (2026) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2026.2619754
Gao, H., Desmoulins, L. D., Molinas, A., Dugas, C. M., Zsombok, A., & Derbenev, A. V. (2026) · The Journal of Physiology · doi:10.1113/jp288116
“In addition to postsynaptic receptor activation, these neurotransmitters can retrogradely act on pre-synaptic receptors and affect vesicular packaging of neurotransmitters (Hnasko & Edwards, 2012).”
Saidi, L., Rioux, V., Wallman, M., Rajan, S. S., Metzakopian, E., Lévesque, M., Proulx, C. D., & Parent, M. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.23.707446
Presynaptic mechanisms of short-term plasticity at hippocampal mossy fibersynapses
Llinares, B. G. I. (2014) · theses.fr (ABES) · doi:10.70675/260d23d6z0385z420bz9500z71856e7257bd
Mansouri-Guilani, N. (2017) · theses.fr (ABES) · doi:10.70675/99ced3b5zeac6z4eb2z8e6cz01bcad7cf2d9
Synaptic modifications in hippocampal CA3 pyramidal cells in an Alzheimer's mouse model
Zhang, P. (2017) · theses.fr (ABES) · doi:10.70675/74cb83e0z6db8z4bb5z838dz6e1bb1c6275f
Use of Sf9 cells identifies V-ATPase as a target of pyridalyl
Sugioka, D., Nakamori, M., Ozoe, F., Utsumi, T., & Ozoe, Y. (2026) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2026.107109
Varga, A. G., Reid, B. T., Maletz, S. N., Dossat, A. M., & Levitt, E. S. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.2199-25.2026 · Cited by 1
Acid-sensing ion channels as sensors of brain metabolic state
Du, J., Ge, Q., & Park, K. A. (2026) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-026-03202-y
An optogenetic actuator for reversible alkalization of acidic presynaptic compartments
Bagaeva, D. F., Yaskovets, A. A., Nosov, G. A., Bondarev, N. A., Ilyinsky, N. S., Bregestovski, P. D., & Gordeliy, V. (2026) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2026.154572
Multi-plasticity synergy with adaptive mechanism assignment for training spiking neural networks
Li, Z., Wang, H., Liu, Y., Ma, C., Gordleeva, S., & Yu, Q. (2026) · Frontiers in Neuroscience · doi:10.3389/fnins.2026.1939650
Circuit-specific remodeling of synaptic co-transmission in stress-responsive networks
Park, H., Kim, H., Sim, M., Ham, D., & Chung, C. (2026) · Animal Cells and Systems · doi:10.1080/19768354.2026.2730204
“Co-transmission has emerged as a physiologically relevant mode of synaptic communication in which a single neuron can signal through more than one neurotransmitter (Trudeau 2004; Hnasko and Edwards 2012; Nusbaum et al. 2017; Svensson et al. 2019; Ceballos et al. 2024).”
Metadata
- Authors
- Hnasko, T. S., & Edwards, R. H.
- Affiliations
- University of California, San Francisco (US)
- Venue
- Annual Review of Physiology
- Publisher
- Annual Reviews
- Published
- 2012-03-17
- Volume
- 74
- Issue
- 1
- Pages
- 225-243
- ISSN
- 0066-4278 (ISSN-L)
- 1545-1585
- PMC
- PMC4090038
- OpenAlex
- W2136916973
- Cited by
- 284
- References
- 117
- Citations by year
- 2026: 11 · 2025: 7 · 2024: 27 · 2023: 15 · 2022: 22 · 2021: 19 · 2020: 20 · 2019: 18 · 2018: 22 · 2017: 24 · 2016: 26 · 2015: 24 · 2014: 27 · 2013: 14 · 2012: 8
- FWCI
- 1.49
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Annual Review of Physiology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (R01MH050712)
- National Institute on Drug Abuse (K01DA026504)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Keywords
- synaptic vesicles, vesicular uptake, vesicle sorting, synaptic transmission, neurotransmitter identity
- MeSH terms
- Acetylcholine, Animals, Anions, Cations, Chlorides, gamma-Aminobutyric Acid, Humans, Hydrogen-Ion Concentration, Synaptic Transmission, Protons, Synaptic Vesicles, Biogenic Monoamines, Neurotransmitter Agents, Glutamic Acid, Vesicular Neurotransmitter Transport Proteins
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