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Uniform Inhibition of Dopamine Neurons in the Ventral Tegmental Area by Aversive Stimuli
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/syn.10177openalex-snapshot
Electrophysiological and pharmacological characteristics of nigral dopaminergic neurons in the conscious, head‐restrained rat
inferredcites →https://doi.org/10.1016/0006-8993(80)90366-2openalex-snapshot
Sensory stimuli alter discharge rate of dopamine (DA) neurons: evidence for two functional types of DA cells in the substantia nigra
inferredcites →https://doi.org/10.1016/0006-8993(87)90988-7openalex-snapshot
Activity of A9 and A10 dopaminergic neurons in unrestrained rats: further characterization and effects of apomorphine and cholecystokinin
inferredcites →https://doi.org/10.1016/0006-8993(89)91263-8openalex-snapshot
Effect of noxious tail pinch on the discharge rate of mesocortical and mesolimbic dopamine neurons: selective activation of the mesocortical system
inferredcites →https://doi.org/10.1016/0006-8993(90)90329-aopenalex-snapshot
Presynaptic regulation of dopamine release in corpus striatum monitored in vitro in real time by fast cyclic voltammetry
inferredcites →https://doi.org/10.1016/0165-0173(93)90013-popenalex-snapshot
The neural basis of drug craving: An incentive-sensitization theory of addiction
inferredcites →https://doi.org/10.1016/0165-0270(95)00144-1openalex-snapshot
A novel single-cell staining procedure performed in vivo under electrophysiological control: morpho-functional features of juxtacellularly labeled thalamic cells and other central neurons with biocytin or Neurobiotin
inferredcites →https://doi.org/10.1016/0166-4328(94)90153-8openalex-snapshot
The involvement of nucleus accumbens dopamine in appetitive and aversive motivation
inferredcites →https://doi.org/10.1016/0306-4522(83)90135-5openalex-snapshot
Intracellular and extracellular electrophysiology of nigral dopaminergic neurons—1. Identification and characterization
inferredcites →https://doi.org/10.1016/0306-4522(88)90307-7openalex-snapshot
Nonlinear relationship between impulse flow and dopamine released by rat midbrain dopaminergic neurons as studied by in vivo electrochemistry
inferredcites →https://doi.org/10.1016/0306-4522(91)90196-uopenalex-snapshot
Phasic versus tonic dopamine release and the modulation of dopamine system responsivity: A hypothesis for the etiology of schizophrenia
inferredcites →https://doi.org/10.1016/0361-9230(82)90021-1openalex-snapshot
Effects of peripheral stimulation on the activity of neurons in the ventral tegmental area, substantia nigra and midbrain reticular formation of rats
inferredcites →https://doi.org/10.1016/s0165-0173(97)00039-8openalex-snapshot
Burst firing in midbrain dopaminergic neurons
inferredcites →https://doi.org/10.1016/s0166-2236(03)00177-2openalex-snapshot
A computational substrate for incentive salience
inferredcites →https://doi.org/10.1016/s0166-4328(98)00102-8openalex-snapshot
An electrophysiological characterization of ventral tegmental area dopaminergic neurons during differential pavlovian fear conditioning in the awake rabbit
inferredcites →https://doi.org/10.1016/s0306-4522(00)00019-1openalex-snapshot
Mesolimbocortical and nigrostriatal dopamine responses to salient non-reward events
inferredcites →https://doi.org/10.1016/s0306-4522(96)00444-7openalex-snapshot
A subset of ventral tegmental area neurons is inhibited by dopamine, 5-hydroxytryptamine and opioids
inferredcites →https://doi.org/10.1016/s0896-6273(02)00967-4openalex-snapshot
Getting Formal with Dopamine and Reward
inferredcites →https://doi.org/10.1038/379449a0openalex-snapshot
Preferential activation of midbrain dopamine neurons by appetitive rather than aversive stimuli
inferredcites →https://doi.org/10.1038/nn1103openalex-snapshot
Afferent modulation of dopamine neuron firing differentially regulates tonic and phasic dopamine transmission
inferredcites →https://doi.org/10.1046/j.1471-4159.1994.63020785.xopenalex-snapshot
Glutamatergic Control of Dopamine Release During Stress in the Rat Prefrontal Cortex
inferredcites →https://doi.org/10.1111/j.1471-4159.1993.tb09837.xopenalex-snapshot
Stress‐Induced Dopamine Release in the Neostriatum: Evaluation of the Role of Action Potentials in Nigrostriatal Dopamine Neurons or Local Initiation by Endogenous Excitatory Amino Acids
inferredcites →https://doi.org/10.1152/jn.1987.57.1.201openalex-snapshot
Responses of nigrostriatal dopamine neurons to high-intensity somatosensory stimulation in the anesthetized monkey
inferredcites →https://doi.org/10.1523/jneurosci.04-11-02877.1984openalex-snapshot
The control of firing pattern in nigral dopamine neurons: burst firing
inferredcites →https://doi.org/10.1523/jneurosci.18-19-08003.1998openalex-snapshot
Electrophysiological Characterization of GABAergic Neurons in the Ventral Tegmental Area
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Abnormal response of dopaminergic neurons to nicotine without perturbation of nicotinic receptors in αCGRP knock-out mice
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Dopamine-induced changes in neural network patterns supporting aversive conditioning
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Optogenetic dissection of neural circuits underlying emotional valence and motivated behaviors
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Dopamine signals related to appetitive and aversive events in paradigms that manipulate reward and avoidability
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Pavlovian-instrumental interactions in active avoidance: The bark of neutral trials
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Dopamine tunes prefrontal outputs to orchestrate aversive processing
inferred← citeshttps://doi.org/10.1016/j.brainres.2022.147887openalex-snapshot
Nucleus accumbens dopamine receptors mediate the stress-induced analgesia in an animal model of acute pain
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2012.04.001openalex-snapshot
Temporal changes in c-Fos activation patterns induced by conditioned fear
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2024.111168openalex-snapshot
NaHS alleviates neuropathic pain in mice by inhibiting IL-17-mediated dopamine (DA) neuron necroptosis in the VTA
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2007.10.007openalex-snapshot
What is reinforced by phasic dopamine signals?
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2008.07.001openalex-snapshot
Mental fatigue: Costs and benefits
inferred← citeshttps://doi.org/10.1016/j.cbpa.2008.06.035openalex-snapshot
Microelectrodes for studying neurobiology
inferred← citeshttps://doi.org/10.1016/j.cell.2007.09.018openalex-snapshot
Molecular Adaptations Underlying Susceptibility and Resistance to Social Defeat in Brain Reward Regions
inferred← citeshttps://doi.org/10.1016/j.cell.2015.07.014openalex-snapshot
Intact-Brain Analyses Reveal Distinct Information Carried by SNc Dopamine Subcircuits
inferred← citeshttps://doi.org/10.1016/j.cell.2015.07.015openalex-snapshot
Circuit Architecture of VTA Dopamine Neurons Revealed by Systematic Input-Output Mapping
inferred← citeshttps://doi.org/10.1016/j.cell.2018.06.042openalex-snapshot
A Genetically Encoded Fluorescent Sensor Enables Rapid and Specific Detection of Dopamine in Flies, Fish, and Mice
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.04.068openalex-snapshot
Synergistic Nigral Output Pathways Shape Movement
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108156openalex-snapshot
Functional Dissection of Basal Ganglia Inhibitory Inputs onto Substantia Nigra Dopaminergic Neurons
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.108867openalex-snapshot
Lateral ventral tegmental area GABAergic and glutamatergic modulation of conditioned learning
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113589openalex-snapshot
Distinct spatiotemporal brainstem pathways of outcome valence during reward- and punishment-based learning
inferred← citeshttps://doi.org/10.1016/j.coemr.2022.100388openalex-snapshot
Stressed and wired: The effects of stress on the VTA circuits underlying motivated behavior
inferred← citeshttps://doi.org/10.1016/j.conb.2005.10.006openalex-snapshot
The basal ganglia: learning new tricks and loving it
inferred← citeshttps://doi.org/10.1016/j.conb.2006.03.006openalex-snapshot
The computational neurobiology of learning and reward
inferred← citeshttps://doi.org/10.1016/j.conb.2008.08.003openalex-snapshot
Reinforcement learning: The Good, The Bad and The Ugly
inferred← citeshttps://doi.org/10.1016/j.conb.2009.10.001openalex-snapshot
The dynamics of dopamine in control of motor behavior
inferred← citeshttps://doi.org/10.1016/j.conb.2012.11.012openalex-snapshot
Updating dopamine reward signals
inferred← citeshttps://doi.org/10.1016/j.conb.2013.01.005openalex-snapshot
Reinforcement signalling in Drosophila; dopamine does it all after all
inferred← citeshttps://doi.org/10.1016/j.conb.2017.08.015openalex-snapshot
The many worlds hypothesis of dopamine prediction error: implications of a parallel circuit architecture in the basal ganglia
inferred← citeshttps://doi.org/10.1016/j.conb.2020.02.002openalex-snapshot
Aversion hot spots in the dopamine system
inferred← citeshttps://doi.org/10.1016/j.cub.2012.05.053openalex-snapshot
How Dopamine Enhances an Optimism Bias in Humans
inferred← citeshttps://doi.org/10.1016/j.cub.2019.08.041openalex-snapshot
Goal-Oriented Behaviour: The Ventral Tegmental Area in Motivated Movements
inferred← citeshttps://doi.org/10.1016/j.cub.2021.08.052openalex-snapshot
Dopamine release in the nucleus accumbens core signals perceived saliency
inferred← citeshttps://doi.org/10.1016/j.cub.2025.07.021openalex-snapshot
Flexible updating of reward and punishment contingencies by VTA GABA neurons
inferred← citeshttps://doi.org/10.1016/j.ejphar.2006.06.081openalex-snapshot
Biphasic effect of apomorphine on rat nociception and effect of dopamine D2 receptor antagonists
inferred← citeshttps://doi.org/10.1016/j.euroneuro.2012.04.006openalex-snapshot
Lu AA21004, a novel multimodal antidepressant, produces regionally selective increases of multiple neurotransmitters—A rat microdialysis and electrophysiology study
inferred← citeshttps://doi.org/10.1016/j.expneurol.2010.03.020openalex-snapshot
The endocannabinoid system and nondrug rewarding behaviours
inferred← citeshttps://doi.org/10.1016/j.ijdevneu.2010.08.002openalex-snapshot
Developmental pathology, dopamine, stress and schizophrenia
inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2018.02.012openalex-snapshot
Rewarding images do not invoke the reward positivity: They inflate it
inferred← citeshttps://doi.org/10.1016/j.isci.2018.03.008openalex-snapshot
Aversion or Salience Signaling by Ventral Tegmental Area Glutamate Neurons
inferred← citeshttps://doi.org/10.1016/j.jbvi.2022.e00340openalex-snapshot
Baby, I'm addicted! The pleasure-pain pathway that shifts entrepreneurial passion to entrepreneurial addiction: Pivotal role of dopamine
inferred← citeshttps://doi.org/10.1016/j.jchemneu.2015.12.016openalex-snapshot
Multiplexed neurochemical signaling by neurons of the ventral tegmental area
inferred← citeshttps://doi.org/10.1016/j.jmp.2008.12.005openalex-snapshot
Reinforcement learning in the brain
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2015.08.017openalex-snapshot
Real time adenosine fluctuations detected with fast-scan cyclic voltammetry in the rat striatum and motor cortex
inferred← citeshttps://doi.org/10.1016/j.molmet.2020.101076openalex-snapshot
Infusion of donor feces affects the gut–brain axis in humans with metabolic syndrome
inferred← citeshttps://doi.org/10.1016/j.nbd.2006.04.010openalex-snapshot
Protective activation of the endocannabinoid system during ischemia in dopamine neurons
inferred← citeshttps://doi.org/10.1016/j.nbd.2018.09.008openalex-snapshot
Dichotomy between motor and cognitive functions of midbrain cholinergic neurons
inferred← citeshttps://doi.org/10.1016/j.nbd.2025.106831openalex-snapshot
Binding of HCN channels to GABAB receptors in dopamine neurons of the VTA limits synaptic inhibition and prevents the development of anxiety
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2009.11.019openalex-snapshot
Neural mechanisms of acquired phasic dopamine responses in learning
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2009.11.021openalex-snapshot
Identifying the neurobiology of altered reinforcement sensitivity in ADHD: A review and research agenda
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2010.02.001openalex-snapshot
Brain reward circuitry beyond the mesolimbic dopamine system: A neurobiological theory
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2010.04.006openalex-snapshot
Effects of stress and aversion on dopamine neurons: Implications for addiction
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2011.04.012openalex-snapshot
The mesoaccumbens dopamine in coping with stress
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2016.06.004openalex-snapshot
The fate of memory: Reconsolidation and the case of Prediction Error
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2017.10.024openalex-snapshot
Influences of social reward experience on behavioral responses to drugs of abuse: Review of shared and divergent neural plasticity mechanisms for sexual reward and drugs of abuse
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2018.03.012openalex-snapshot
Pleasure: The missing link in the regulation of sleep
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2018.04.014openalex-snapshot
The neuroanatomic complexity of the CRF and DA systems and their interface: What we still don’t know
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2019.10.015openalex-snapshot
Stress-induced plasticity and functioning of ventral tegmental dopamine neurons
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2021.10.011openalex-snapshot
Bidirectional role of dopamine in learning and memory-active forgetting
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2023.105307openalex-snapshot
Stress to inflammation and anhedonia: Mechanistic insights from preclinical and clinical models
inferred← citeshttps://doi.org/10.1016/j.neuint.2013.10.016openalex-snapshot
Good riddance to dopamine: Roles for the dopamine transporter in synaptic function and dopamine-associated brain disorders
inferred← citeshttps://doi.org/10.1016/j.neuint.2019.104494openalex-snapshot
Mechanical allodynia induced by optogenetic sensory nerve excitation activates dopamine signaling and metabolism in medial nucleus accumbens
inferred← citeshttps://doi.org/10.1016/j.neuint.2020.104935openalex-snapshot
Accumbal D2R-medium spiny neurons regulate aversive behaviors through PKA-Rap1 pathway
inferred← citeshttps://doi.org/10.1016/j.neulet.2009.05.035openalex-snapshot
Bifeprunox and aripiprazole suppress in vivo VTA dopaminergic neuronal activity via D2 and not D3 dopamine autoreceptor activation
inferred← citeshttps://doi.org/10.1016/j.neunet.2009.06.008openalex-snapshot
Computational perspectives on forebrain microcircuits implicated in reinforcement learning, action selection, and cognitive control
inferred← citeshttps://doi.org/10.1016/j.neunet.2023.09.032openalex-snapshot
Reward prediction-errors weighted by cue salience produces addictive behaviours in simulations, with asymmetrical learning and steeper delay discounting
inferred← citeshttps://doi.org/10.1016/j.neures.2011.12.004openalex-snapshot
The influence of passband limitation on the waveform of extracellular action potential
inferred← citeshttps://doi.org/10.1016/j.neures.2016.01.004openalex-snapshot
Neural mechanisms of the nucleus accumbens circuit in reward and aversive learning
inferred← citeshttps://doi.org/10.1016/j.neures.2017.04.009openalex-snapshot
Promising techniques to illuminate neuromodulatory control of the cerebral cortex in sleeping and waking states
inferred← citeshttps://doi.org/10.1016/j.neures.2019.10.009openalex-snapshot
Reverse-filtering on extracellular action potential for waveform analysis
inferred← citeshttps://doi.org/10.1016/j.neures.2024.07.003openalex-snapshot
Bidirectional valence coding in amygdala intercalated clusters: A neural substrate for the opponent-process theory of motivation
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2008.09.039openalex-snapshot
The bivalent side of the nucleus accumbens
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2011.04.038openalex-snapshot
Continuous theta-burst stimulation (cTBS) over the lateral prefrontal cortex alters reinforcement learning bias
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2019.116457openalex-snapshot
Reproducibility assessment of neuromelanin-sensitive magnetic resonance imaging protocols for region-of-interest and voxelwise analyses
inferred← citeshttps://doi.org/10.1016/j.neuron.2006.05.007openalex-snapshot
Hierarchical Control of Dopamine Neuron-Firing Patterns by Nicotinic Receptors
inferred← citeshttps://doi.org/10.1016/j.neuron.2006.07.026openalex-snapshot
Dopamine Scales Performance in the Absence of New Learning
inferred← citeshttps://doi.org/10.1016/j.neuron.2006.08.023openalex-snapshot
Leptin Receptor Signaling in Midbrain Dopamine Neurons Regulates Feeding
inferred← citeshttps://doi.org/10.1016/j.neuron.2008.01.022openalex-snapshot
Unique Properties of Mesoprefrontal Neurons within a Dual Mesocorticolimbic Dopamine System
inferred← citeshttps://doi.org/10.1016/j.neuron.2009.02.001openalex-snapshot
The Rostromedial Tegmental Nucleus (RMTg), a GABAergic Afferent to Midbrain Dopamine Neurons, Encodes Aversive Stimuli and Inhibits Motor Responses
inferred← citeshttps://doi.org/10.1016/j.neuron.2009.07.025openalex-snapshot
Dopamine Enables In Vivo Synaptic Plasticity Associated with the Addictive Drug Nicotine
inferred← citeshttps://doi.org/10.1016/j.neuron.2010.02.012openalex-snapshot
Vesicular Glutamate Transport Promotes Dopamine Storage and Glutamate Corelease In Vivo
inferred← citeshttps://doi.org/10.1016/j.neuron.2010.03.002openalex-snapshot
Predicting Value of Pain and Analgesia: Nucleus Accumbens Response to Noxious Stimuli Changes in the Presence of Chronic Pain
inferred← citeshttps://doi.org/10.1016/j.neuron.2010.05.011openalex-snapshot
Distinct Roles of Synaptic Transmission in Direct and Indirect Striatal Pathways to Reward and Aversive Behavior
inferred← citeshttps://doi.org/10.1016/j.neuron.2011.12.006openalex-snapshot
A Role for Phasic Dopamine Neuron Firing in Habit Learning
inferred← citeshttps://doi.org/10.1016/j.neuron.2012.02.015openalex-snapshot
GABA Neurons of the VTA Drive Conditioned Place Aversion
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