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Optogenetic self-stimulation in the nucleus accumbens: D1 reward versus D2 ambivalence

https://doi.org/10.1371/journal.pone.0207694
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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/cne.20769openalex-snapshot
A proposed hypothalamic–thalamic–striatal axis for the integration of energy balance, arousal, and food reward
inferredcites →https://doi.org/10.1007/bf00232197openalex-snapshot
Expression of dopamine D2 receptor and choline acetyltransferase mRNA in the dopamine deafferented rat caudate-putamen
inferredcites →https://doi.org/10.1007/s00213-005-0133-1openalex-snapshot
Effects of intranucleus accumbens shell administration of dopamine agonists and antagonists on cocaine-taking and cocaine-seeking behaviors in the rat
inferredcites →https://doi.org/10.1007/s00429-008-0175-3openalex-snapshot
The structural basis for mapping behavior onto the ventral striatum and its subdivisions
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The neural basis of brain-stimulation reward
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From motivation to action: Functional interface between the limbic system and the motor system
inferredcites →https://doi.org/10.1016/0304-3940(90)90671-uopenalex-snapshot
D2 dopamine receptor gene expression by cholinergic neurons in the rat striatum
inferredcites →https://doi.org/10.1016/j.bbr.2004.01.013openalex-snapshot
Dissociation of the role of nucleus accumbens dopamine in responding to reward-predictive cues and waiting for reward
inferredcites →https://doi.org/10.1016/j.bbr.2008.02.003openalex-snapshot
Role of dopamine D1 and D2 receptors in the nucleus accumbens shell on the acquisition and expression of fructose-conditioned flavor–flavor preferences in rats
inferredcites →https://doi.org/10.1016/j.brainresrev.2004.12.033openalex-snapshot
The role of central dopamine D3 receptors in drug addiction: a review of pharmacological evidence
inferredcites →https://doi.org/10.1016/j.conb.2011.02.010openalex-snapshot
Optogenetic manipulation of neural circuitry in vivo
inferredcites →https://doi.org/10.1016/j.cub.2016.02.036openalex-snapshot
Direct and indirect dorsolateral striatum pathways reinforce different action strategies
inferredcites →https://doi.org/10.1016/j.neubiorev.2013.04.002openalex-snapshot
Nucleus accumbens neurotransmission and effort-related choice behavior in food motivation: Effects of drugs acting on dopamine, adenosine, and muscarinic acetylcholine receptors
inferredcites →https://doi.org/10.1016/j.neuroimage.2015.05.006openalex-snapshot
Investigating the dynamics of the brain response to music: A central role of the ventral striatum/nucleus accumbens
inferredcites →https://doi.org/10.1016/j.neuron.2015.09.038openalex-snapshot
Accumbal D1R Neurons Projecting to Lateral Hypothalamus Authorize Feeding
inferredcites →https://doi.org/10.1016/j.neuropharm.2008.06.075openalex-snapshot
Biological substrates of reward and aversion: A nucleus accumbens activity hypothesis
inferredcites →https://doi.org/10.1016/j.neuropharm.2013.04.031openalex-snapshot
Neurocircuitry of drug reward
inferredcites →https://doi.org/10.1016/j.neuropharm.2013.04.042openalex-snapshot
Dopamine D3 receptor deletion or blockade attenuates cocaine-induced conditioned place preference in mice
inferredcites →https://doi.org/10.1016/j.neuroscience.2005.06.048openalex-snapshot
D1-like and D2 dopamine receptor antagonists administered into the shell subregion of the rat nucleus accumbens decrease cocaine, but not food, reinforcement
inferredcites →https://doi.org/10.1016/j.neuroscience.2006.07.035openalex-snapshot
Renewal of an extinguished instrumental response: Neural correlates and the role of D1 dopamine receptors
inferredcites →https://doi.org/10.1016/j.pbb.2008.01.009openalex-snapshot
Development of conditioned place preference induced by intra-accumbens infusion of amphetamine is attenuated by co-infusion of dopamine D1 and D2 receptor antagonists
inferredcites →https://doi.org/10.1016/j.pneurobio.2009.11.003openalex-snapshot
The ventral basal ganglia, a selection mechanism at the crossroads of space, strategy, and reward.
inferredcites →https://doi.org/10.1016/s0960-9822(00)00593-5openalex-snapshot
The basal ganglia
inferredcites →https://doi.org/10.1016/s2215-0366(16)00104-8openalex-snapshot
Neurobiology of addiction: a neurocircuitry analysis
inferredcites →https://doi.org/10.1017/s0140525x00020306openalex-snapshot
The anhedonia hypothesis: Mark III
inferredcites →https://doi.org/10.1037/h0058775openalex-snapshot
Positive reinforcement produced by electrical stimulation of septal area and other regions of rat brain.
inferredcites →https://doi.org/10.1038/mp.2013.57openalex-snapshot
Increasing dopamine D2 receptor expression in the adult nucleus accumbens enhances motivation
inferredcites →https://doi.org/10.1038/mp.2015.210openalex-snapshot
Dopamine D2 receptors gate generalization of conditioned threat responses through mTORC1 signaling in the extended amygdala
inferredcites →https://doi.org/10.1038/nature09159openalex-snapshot
Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry
inferredcites →https://doi.org/10.1038/ncomms11829openalex-snapshot
Activation of D2 dopamine receptor-expressing neurons in the nucleus accumbens increases motivation
inferredcites →https://doi.org/10.1038/ncomms13697openalex-snapshot
Ventral tegmental area glutamate neurons co-release GABA and promote positive reinforcement
inferredcites →https://doi.org/10.1038/nn.2219openalex-snapshot
Real-time chemical responses in the nucleus accumbens differentiate rewarding and aversive stimuli
inferredcites →https://doi.org/10.1038/nn.2726openalex-snapshot
Anatomically distinct dopamine release during anticipation and experience of peak emotion to music
inferredcites →https://doi.org/10.1038/nn.3100openalex-snapshot
Distinct roles for direct and indirect pathway striatal neurons in reinforcement
inferredcites →https://doi.org/10.1038/nn.4068openalex-snapshot
Coding the direct/indirect pathways by D1 and D2 receptors is not valid for accumbens projections
inferredcites →https://doi.org/10.1038/npp.2014.118openalex-snapshot
Loss of BDNF Signaling in D1R-Expressing NAc Neurons Enhances Morphine Reward by Reducing GABA Inhibition
inferredcites →https://doi.org/10.1038/npp.2016.10openalex-snapshot
Orexin in Rostral Hotspot of Nucleus Accumbens Enhances Sucrose ‘Liking’ and Intake but Scopolamine in Caudal Shell Shifts ‘Liking’ Toward ‘Disgust’ and ‘Fear’
inferredcites →https://doi.org/10.1038/npp.2016.81openalex-snapshot
Nucleus Accumbens Acetylcholine Receptors Modulate Dopamine and Motivation
inferredcites →https://doi.org/10.1038/s41467-018-03272-2openalex-snapshot
Accumbens dopamine D2 receptors increase motivation by decreasing inhibitory transmission to the ventral pallidum
inferredcites →https://doi.org/10.1056/nejmra1511480openalex-snapshot
Neurobiologic Advances from the Brain Disease Model of Addiction
inferredcites →https://doi.org/10.1101/lm.978708openalex-snapshot
Dopamine D1 and D2 receptors in the nucleus accumbens core and shell mediate Pavlovian-instrumental transfer
inferredcites →https://doi.org/10.1111/ejn.12253openalex-snapshot
Development of behavioral preferences for the optimal choice following unexpected reward omission is mediated by a reduction of D 2‐like receptor tone in the nucleus accumbens
inferredcites →https://doi.org/10.1111/j.1369-1600.2012.00486.xopenalex-snapshot
Blockade of dopamine D3receptors in the nucleus accumbens and central amygdala inhibits incubation of cocaine craving in rats
inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04524.xopenalex-snapshot
Stimulation of D1‐like or D2 dopamine receptors in the shell, but not the core, of the nucleus accumbens reinstates cocaine‐seeking behaviour in the rat
inferredcites →https://doi.org/10.1111/j.1755-5949.2010.00228.xopenalex-snapshot
Dopamine Receptor Homooligomers and Heterooligomers in Schizophrenia
inferredcites →https://doi.org/10.1111/nyas.12677openalex-snapshot
Musical pleasure and reward: mechanisms and dysfunction
inferredcites →https://doi.org/10.1126/science.1188472openalex-snapshot
Cell Type–Specific Loss of BDNF Signaling Mimics Optogenetic Control of Cocaine Reward
inferredcites →https://doi.org/10.1126/science.1193771openalex-snapshot
Cholinergic Interneurons Control Local Circuit Activity and Cocaine Conditioning
inferredcites →https://doi.org/10.1179/030801810x12723585301192openalex-snapshot
The Pleasure of Making Sense of Music
inferredcites →https://doi.org/10.1371/journal.pone.0011223openalex-snapshot
Desire and Dread from the Nucleus Accumbens: Cortical Glutamate and Subcortical GABA Differentially Generate Motivation and Hedonic Impact in the Rat
inferredcites →https://doi.org/10.1371/journal.pone.0094771openalex-snapshot
Positive Reinforcement Mediated by Midbrain Dopamine Neurons Requires D1 and D2 Receptor Activation in the Nucleus Accumbens
inferredcites →https://doi.org/10.1523/jneurosci.0444-16.2016openalex-snapshot
Decreasing Striatopallidal Pathway Function Enhances Motivation by Energizing the Initiation of Goal-Directed Action
inferredcites →https://doi.org/10.1523/jneurosci.0450-13.2013openalex-snapshot
Cue-Evoked Cocaine "Craving": Role of Dopamine in the Accumbens Core
inferredcites →https://doi.org/10.1523/jneurosci.1039-08.2008openalex-snapshot
Opposing Patterns of Signaling Activation in Dopamine D1and D2Receptor-Expressing Striatal Neurons in Response to Cocaine and Haloperidol
inferredcites →https://doi.org/10.1523/jneurosci.1051-12.2012openalex-snapshot
Role of Dopamine Tone in the Pursuit of Brain Stimulation Reward
inferredcites →https://doi.org/10.1523/jneurosci.1339-11.2011openalex-snapshot
Nucleus Accumbens Dopamine/Glutamate Interaction Switches Modes to Generate Desire versus Dread: D1Alone for Appetitive Eating But D1and D2Together for Fear
inferredcites →https://doi.org/10.1523/jneurosci.1524-14.2015openalex-snapshot
Optogenetic Stimulation of Accumbens Shell or Shell Projections to Lateral Hypothalamus Produce Differential Effects on the Motivation for Cocaine
inferredcites →https://doi.org/10.1523/jneurosci.3141-16.2017openalex-snapshot
Optogenetic Central Amygdala Stimulation Intensifies and Narrows Motivation for Cocaine
inferredcites →https://doi.org/10.1523/jneurosci.3377-16.2017openalex-snapshot
Ventrolateral Striatal Medium Spiny Neurons Positively Regulate Food-Incentive, Goal-Directed Behavior Independently of D1 and D2 Selectivity
inferredcites →https://doi.org/10.1523/jneurosci.4458-13.2014openalex-snapshot
Opioid Hedonic Hotspot in Nucleus Accumbens Shell: Mu, Delta, and Kappa Maps for Enhancement of Sweetness “Liking” and “Wanting”
inferredcites →https://doi.org/10.2165/00023210-200923020-00005openalex-snapshot
Dopamine Dysregulation Syndrome
inferredcites →https://doi.org/10.3389/fnana.2011.00031openalex-snapshot
The Dopamine D1–D2 Receptor Heteromer in Striatal Medium Spiny Neurons: Evidence for a Third Distinct Neuronal Pathway in Basal Ganglia

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Optical Control of Drd2 Reveals a New Role of Drd2 for Motor Function in the Lgp Excitatory Neurons
inferred← citeshttps://doi.org/10.1002/bies.202400016openalex-snapshot
A unified theoretical framework underlying the regulation of motivated behavior
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Developmental Trajectories of Anhedonia in Preclinical Models
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Dissecting Mechanisms of Motivation within the Nucleus Accumbens Using Optogenetics
inferred← citeshttps://doi.org/10.1007/978-1-0716-0830-2_20openalex-snapshot
Optogenetic Stimulation of the Central Amygdala Using Channelrhodopsin
inferred← citeshttps://doi.org/10.1007/s00213-019-05409-7openalex-snapshot
Dose-dependent effects of estrogen on prediction error related neural activity in the nucleus accumbens of healthy young women
inferred← citeshttps://doi.org/10.1007/s00213-023-06370-2openalex-snapshot
Opioid withdrawal: role in addiction and neural mechanisms
inferred← citeshttps://doi.org/10.1007/s12264-021-00632-9openalex-snapshot
Projections from D2 Neurons in Different Subregions of Nucleus Accumbens Shell to Ventral Pallidum Play Distinct Roles in Reward and Aversion
inferred← citeshttps://doi.org/10.1016/j.addicn.2024.100179openalex-snapshot
Targeting the ventral pallidum in obesity
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Brain regulation of hunger and motivation: The case for integrating homeostatic and hedonic concepts and its implications for obesity and addiction
inferred← citeshttps://doi.org/10.1016/j.bbr.2019.111976openalex-snapshot
Effects of haloperidol on cognitive function and behavioural flexibility in the IntelliCage social home cage environment
inferred← citeshttps://doi.org/10.1016/j.biopsych.2019.10.027openalex-snapshot
A Critical Role of Basolateral Amygdala–to–Nucleus Accumbens Projection in Sleep Regulation of Reward Seeking
inferred← citeshttps://doi.org/10.1016/j.biopsych.2019.11.001openalex-snapshot
From Signaling Molecules to Circuits and Behaviors: Cell-Type–Specific Adaptations to Psychostimulant Exposure in the Striatum
inferred← citeshttps://doi.org/10.1016/j.biopsych.2021.06.017openalex-snapshot
Gene-Targeted, CREB-Mediated Induction of ΔFosB Controls Distinct Downstream Transcriptional Patterns Within D1 and D2 Medium Spiny Neurons
inferred← citeshttps://doi.org/10.1016/j.biopsych.2022.07.022openalex-snapshot
CREB Binding at the Zfp189 Promoter Within Medium Spiny Neuron Subtypes Differentially Regulates Behavioral and Physiological Adaptations Over the Course of Cocaine Use
inferred← citeshttps://doi.org/10.1016/j.biopsych.2023.05.008openalex-snapshot
Balance Between Projecting Neuronal Populations of the Nucleus Accumbens Controls Social Behavior in Mice
inferred← citeshttps://doi.org/10.1016/j.biopsych.2024.05.020openalex-snapshot
Presynaptic and Postsynaptic Mesolimbic Dopamine D3 Receptors Play Distinct Roles in Cocaine Versus Opioid Reward in Mice
inferred← citeshttps://doi.org/10.1016/j.bosn.2025.11.001openalex-snapshot
Understanding the contribution of nucleus accumbens D1- and D2-neurons for rewarding and aversive behaviors
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.02.095openalex-snapshot
Nucleus Accumbens Cell Type- and Input-Specific Suppression of Unproductive Reward Seeking
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110380openalex-snapshot
Distinct role of nucleus accumbens D2-MSN projections to ventral pallidum in different phases of motivated behavior
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110874openalex-snapshot
Cholinergic interneurons mediate cocaine extinction in male mice through plasticity across medium spiny neuron subtypes
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112190openalex-snapshot
D1 and D2 neurons in the nucleus accumbens enable positive and negative control over sugar intake in mice
inferred← citeshttps://doi.org/10.1016/j.cobeha.2021.02.013openalex-snapshot
Positive affect: nature and brain bases of liking and wanting
inferred← citeshttps://doi.org/10.1016/j.cobeha.2024.101462openalex-snapshot
Dopamine in the nucleus accumbens in valence-based learning: is it really important?
inferred← citeshttps://doi.org/10.1016/j.cub.2024.02.041openalex-snapshot
Basolateral amygdala parvalbumin interneurons coordinate oscillations to drive reward behaviors
inferred← citeshttps://doi.org/10.1016/j.cub.2025.02.007openalex-snapshot
Reward expectation and receipt differentially modulate the spiking of accumbens D1+ and D2+ neurons
inferred← citeshttps://doi.org/10.1016/j.isci.2025.112456openalex-snapshot
Melanocortin 4 receptor-expressing neurons in the lateral stripe of the striatum regulate affect and motor control
inferred← citeshttps://doi.org/10.1016/j.jgr.2021.05.007openalex-snapshot
Korean Red Ginseng inhibits methamphetamine addictive behaviors by regulating dopaminergic and NMDAergic system in rodents
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2020.10.010openalex-snapshot
Spaceflight and brain plasticity: Spaceflight effects on regional expression of neurotransmitter systems and neurotrophic factors encoding genes
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2025.106125openalex-snapshot
From valence encoding to motivated behavior: A focus on the nucleus accumbens circuitry
inferred← citeshttps://doi.org/10.1016/j.neures.2025.104957openalex-snapshot
Neurotransmitter receptor gene expression patterns associated with reward-related neural representations
inferred← citeshttps://doi.org/10.1016/j.neuron.2019.05.031openalex-snapshot
High-Frequency Activation of Nucleus Accumbens D1-MSNs Drives Excitatory Potentiation on D2-MSNs
inferred← citeshttps://doi.org/10.1016/j.neuron.2020.06.011openalex-snapshot
VTA Glutamate Neuron Activity Drives Positive Reinforcement Absent Dopamine Co-release
inferred← citeshttps://doi.org/10.1016/j.neuron.2023.11.023openalex-snapshot
D1 and D2 medium spiny neurons in the nucleus accumbens core have distinct and valence-independent roles in learning
inferred← citeshttps://doi.org/10.1016/j.neuron.2026.03.023openalex-snapshot
Dual-engram architecture within a single striatal cell type distinctly controls alcohol relapse and extinction
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2020.108307openalex-snapshot
Loss of mu and delta opioid receptors on neurons expressing dopamine receptor D1 has no effect on reward sensitivity
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2021.108725openalex-snapshot
Illuminating subcortical GABAergic and glutamatergic circuits for reward and aversion
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2022.05.025openalex-snapshot
Anterior Insular-nucleus Accumbens Pathway Controls Refeeding-induced Analgesia under Chronic Inflammatory Pain Condition
inferred← citeshttps://doi.org/10.1016/j.physbeh.2020.113152openalex-snapshot
‘Liking’ and ‘wanting’ in eating and food reward: Brain mechanisms and clinical implications
inferred← citeshttps://doi.org/10.1016/j.physbeh.2025.115216openalex-snapshot
Increased responsivity to pharmacological manipulations of dopamine D1 receptors in binge eating prone rats
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2020.110094openalex-snapshot
Optogenetics: A revolutionary approach for the study of depression
inferred← citeshttps://doi.org/10.1038/s41380-021-01163-5openalex-snapshot
Key transcription factors mediating cocaine-induced plasticity in the nucleus accumbens
inferred← citeshttps://doi.org/10.1038/s41380-023-02131-xopenalex-snapshot
Disentangling the role of NAc D1 and D2 cells in hedonic eating
inferred← citeshttps://doi.org/10.1038/s41386-019-0479-4openalex-snapshot
Role of nucleus accumbens core but not shell in incubation of methamphetamine craving after voluntary abstinence
inferred← citeshttps://doi.org/10.1038/s41386-023-01634-zopenalex-snapshot
Calcitonin receptor signaling in nucleus accumbens D1R- and D2R-expressing medium spiny neurons bidirectionally alters opioid taking in male rats
inferred← citeshttps://doi.org/10.1038/s41386-026-02460-9openalex-snapshot
Nucleus accumbens medial shell D1 and D2 medium spiny neurons signal the valence of conditioned stimuli in a sex-dependent manner
inferred← citeshttps://doi.org/10.1038/s41467-022-35384-1openalex-snapshot
Cell-type specific profiling of histone post-translational modifications in the adult mouse striatum
inferred← citeshttps://doi.org/10.1038/s41467-023-38025-3openalex-snapshot
Error-related signaling in nucleus accumbens D2 receptor-expressing neurons guides inhibition-based choice behavior in mice
inferred← citeshttps://doi.org/10.1038/s41467-024-50099-1openalex-snapshot
NPAS4 supports cocaine-conditioned cues in rodents by controlling the cell type-specific activation balance in the nucleus accumbens
inferred← citeshttps://doi.org/10.1038/s41467-024-53690-8openalex-snapshot
Temporal dynamics of nucleus accumbens neurons in male mice during reward seeking
inferred← citeshttps://doi.org/10.1038/s41467-024-55269-9openalex-snapshot
Dynamic representation of appetitive and aversive stimuli in nucleus accumbens shell D1- and D2-medium spiny neurons
inferred← citeshttps://doi.org/10.1038/s41467-026-70634-6openalex-snapshot
Role of the primate ventral striatum as a neural hub bridging option valuation and action selection
inferred← citeshttps://doi.org/10.1038/s41583-019-0122-8openalex-snapshot
Affective valence in the brain: modules or modes?
inferred← citeshttps://doi.org/10.1038/s41583-019-0189-2openalex-snapshot
Striatal circuits for reward learning and decision-making
inferred← citeshttps://doi.org/10.1038/s41593-022-01021-9openalex-snapshot
Opponent control of behavior by dorsomedial striatal pathways depends on task demands and internal state
inferred← citeshttps://doi.org/10.1038/s41593-023-01518-xopenalex-snapshot
Updating the striatal–pallidal wiring diagram
inferred← citeshttps://doi.org/10.1038/s42003-026-10047-9openalex-snapshot
Prefrontal modulation of striatal engagement: a hierarchical framework for goal-directed behavior
inferred← citeshttps://doi.org/10.1038/s44323-025-00059-9openalex-snapshot
Motivation meets sleep: tuning arousal via nucleus accumbens and Basal Ganglia circuits
inferred← citeshttps://doi.org/10.1073/pnas.2210953120openalex-snapshot
Epigenetic function during heroin self-administration controls future relapse-associated behavior in a cell type-specific manner
inferred← citeshttps://doi.org/10.1073/pnas.2211688119openalex-snapshot
Dynamic processing of hunger and thirst by common mesolimbic neural ensembles
inferred← citeshttps://doi.org/10.1093/med/9780197688908.003.0007openalex-snapshot
Brain Mechanisms of Food “Liking” and “Wanting”
inferred← citeshttps://doi.org/10.1101/2021.05.27.446063openalex-snapshot
Distinct threat and valence signals in rat nucleus accumbens core
inferred← citeshttps://doi.org/10.1101/2021.08.29.458113openalex-snapshot
Cholinergic interneurons mediate cocaine extinction through similar plasticity across medium spiny neuron subtypes
inferred← citeshttps://doi.org/10.1101/2022.08.11.503670openalex-snapshot
The cognitive basis of intracranial self-stimulation of midbrain dopamine neurons
inferred← citeshttps://doi.org/10.1101/2022.09.04.506434openalex-snapshot
NPAS4 supports drug-cue associations and relapse-like behavior through regulation of the cell type-specific activation balance in the nucleus accumbens
inferred← citeshttps://doi.org/10.1101/2022.11.28.518147openalex-snapshot
Balance between direct and indirect pathways of the nucleus accumbens controls social behavior in mice
inferred← citeshttps://doi.org/10.1101/2023.03.25.534237openalex-snapshot
Dual roles for nucleus accumbens core dopamine D1-expressing neurons projecting to the substantia nigra pars reticulata in limbic and motor control
inferred← citeshttps://doi.org/10.1101/2023.04.21.537763openalex-snapshot
Nucleus accumbens neurons dynamically encode positive and aversive associative learning
inferred← citeshttps://doi.org/10.1101/2023.09.02.556060openalex-snapshot
Reward expectation selectively boosts the firing of accumbens D1+ neurons during motivated approach
inferred← citeshttps://doi.org/10.1101/2024.01.08.574751openalex-snapshot
The ventral hippocampus and nucleus accumbens underlie long-term social memory about female conspecifics in male mice
inferred← citeshttps://doi.org/10.1101/2024.02.22.581563openalex-snapshot
Dynamic representation of appetitive and aversive stimuli in nucleus accumbens shell D1- and D2-medium spiny neurons
inferred← citeshttps://doi.org/10.1101/2024.05.31.596779openalex-snapshot
Melanocortin 4 receptor-expressing neurons in the lateral stripe of the striatum are involved in affect regulation and motor control
inferred← citeshttps://doi.org/10.1101/2024.09.27.615291openalex-snapshot
Temporal Dynamics of Nucleus Accumbens Neurons in Male Mice During Reward Seeking
inferred← citeshttps://doi.org/10.1101/2025.03.17.643720openalex-snapshot
PACAP Signaling Network in the Nucleus Accumbens Core Regulates Reinstatement Behavior in Rat
inferred← citeshttps://doi.org/10.1111/adb.70090openalex-snapshot
PACAP Signalling Network in the Nucleus Accumbens Core Regulates Reinstatement Behaviour in Rat
inferred← citeshttps://doi.org/10.1111/jnc.16063openalex-snapshot
Nucleus accumbens neurons dynamically respond to appetitive and aversive associative learning
inferred← citeshttps://doi.org/10.1166/mex.2023.2375openalex-snapshot
Study on inhibitory effect of GC-miR-143 inhibitor nanoparticles on D2 receptor-mediated neurological behavioral damage in lacunar infarction
inferred← citeshttps://doi.org/10.1177/1073858420974336openalex-snapshot
Monoamines: Dopamine, Norepinephrine, and Serotonin, Beyond Modulation, “Switches” That Alter the State of Target Networks
inferred← citeshttps://doi.org/10.13005/10.13005/bpj/3264openalex-snapshot
Acute Fluoxetine Induces Rapid Reorganization of Limbic Oscillatory Dynamics: Gamma Oscillations and Cross-Frequency Coupling as Correlates of Antidepressant-Like Behavior
inferred← citeshttps://doi.org/10.1371/journal.pbio.3001338openalex-snapshot
Context coding in the mouse nucleus accumbens modulates motivationally relevant information
inferred← citeshttps://doi.org/10.1371/journal.pone.0317605openalex-snapshot
Nucleus accumbens D2-expressing neurons: Balancing reward and licking disruption through rhythmic optogenetic stimulation
inferred← citeshttps://doi.org/10.1523/eneuro.0082-23.2023openalex-snapshot
Dual Roles for Nucleus Accumbens Core Dopamine D1-Expressing Neurons Projecting to the Substantia Nigra Pars Reticulata in Limbic and Motor Control in Male Mice
inferred← citeshttps://doi.org/10.1523/eneuro.0146-20.2020openalex-snapshot
μ-Opioid Receptors on Distinct Neuronal Populations Mediate Different Aspects of Opioid Reward-Related Behaviors
inferred← citeshttps://doi.org/10.1523/eneuro.0157-25.2025openalex-snapshot
Dopamine Receptor 1 Specific CRISPRa Mice Exhibit Disrupted Behaviors and Striatal Baseline Cellular Activity
inferred← citeshttps://doi.org/10.1523/jneurosci.0299-20.2020openalex-snapshot
The Nucleus Accumbens Core is Necessary to Scale Fear to Degree of Threat
inferred← citeshttps://doi.org/10.1523/jneurosci.0595-22.2022openalex-snapshot
Differential Patterns of Synaptic Plasticity in the Nucleus Accumbens Caused by Continuous and Interrupted Morphine Exposure
inferred← citeshttps://doi.org/10.1523/jneurosci.0865-25.2026openalex-snapshot
Optogenetic Hedonic Hotspots in the Orbitofrontal Cortex and Insula: Causing Enhancement of Sweetness “Liking”
inferred← citeshttps://doi.org/10.1523/jneurosci.1107-21.2021openalex-snapshot
Threat and Bidirectional Valence Signaling in the Nucleus Accumbens Core
inferred← citeshttps://doi.org/10.1523/jneurosci.1327-23.2024openalex-snapshot
Circuit-Wide Gene Network Analysis Reveals Sex-Specific Roles for Phosphodiesterase 1b in Cocaine Addiction
inferred← citeshttps://doi.org/10.1523/jneurosci.1451-21.2021openalex-snapshot
A Conditioned Place Preference for Heroin Is Signaled by Increased Dopamine and Direct Pathway Activity and Decreased Indirect Pathway Activity in the Nucleus Accumbens
inferred← citeshttps://doi.org/10.1523/jneurosci.1473-24.2024openalex-snapshot
Optogenetic Control of Dopamine Receptor 2 Reveals a Novel Aspect of Dopaminergic Neurotransmission in Motor Function
inferred← citeshttps://doi.org/10.1523/jneurosci.1749-24.2025openalex-snapshot
A2A-Positive Neurons in the Nucleus Accumbens Core Regulate Effort Exertion
inferred← citeshttps://doi.org/10.1523/jneurosci.1907-22.2022openalex-snapshot
Ventral Subiculum Inputs to Nucleus Accumbens Medial Shell Preferentially Innervate D2R Medium Spiny Neurons and Contain Calcium Permeable AMPARs
inferred← citeshttps://doi.org/10.1523/jneurosci.2902-19.2020openalex-snapshot
Desire or Dread from Nucleus Accumbens Inhibitions: Reversed by Same-Site Optogenetic Excitations
inferred← citeshttps://doi.org/10.2174/1381612826666200204141057openalex-snapshot
Modulatory Effects of Food Restriction on Brain and Behavioral Effects of Abused Drugs
inferred← citeshttps://doi.org/10.3389/fnbeh.2024.1420028openalex-snapshot
The nucleus accumbens in reward and aversion processing: insights and implications
inferred← citeshttps://doi.org/10.3389/fncir.2020.577880openalex-snapshot
Hypothetical Roles of the Olfactory Tubercle in Odor-Guided Eating Behavior
inferred← citeshttps://doi.org/10.3389/fncir.2021.762441openalex-snapshot
Circuit Investigation of Social Interaction and Substance Use Disorder Using Miniscopes
inferred← citeshttps://doi.org/10.3389/fncir.2023.1086053openalex-snapshot
Ventral pallidal regulation of motivated behaviors and reinforcement
inferred← citeshttps://doi.org/10.3389/fnins.2026.1881674openalex-snapshot
Nucleus accumbens DRD2 receptor agonism attenuates escape behavior
inferred← citeshttps://doi.org/10.3389/fnsyn.2021.734975openalex-snapshot
Endocannabinoid Modulation of Nucleus Accumbens Microcircuitry and Terminal Dopamine Release
inferred← citeshttps://doi.org/10.3389/fnsyn.2021.799274openalex-snapshot
Cell-Type-Specific Adaptions in Striatal Medium-Sized Spiny Neurons and Their Roles in Behavioral Responses to Drugs of Abuse
inferred← citeshttps://doi.org/10.3389/fnsys.2020.581830openalex-snapshot
The Lateral Preoptic Area and Its Projection to the VTA Regulate VTA Activity and Drive Complex Reward Behaviors
inferred← citeshttps://doi.org/10.3389/fpsyt.2021.559401openalex-snapshot
Reward Processing and Circuit Dysregulation in Posttraumatic Stress Disorder
inferred← citeshttps://doi.org/10.3390/ijms25063455openalex-snapshot
Optical Intracranial Self-Stimulation (oICSS): A New Behavioral Model for Studying Drug Reward and Aversion in Rodents
inferred← citeshttps://doi.org/10.3410/f.735001483.793560814openalex-snapshot
Faculty Opinions recommendation of Affective valence in the brain: modules or modes?
inferred← citeshttps://doi.org/10.4196/kjpp.2022.26.5.307openalex-snapshot
Distinct cell populations of ventral tegmental area process motivated behavior
inferred← citeshttps://doi.org/10.64898/2026.01.13.699373openalex-snapshot
Striatal Acetylcholine Dip-Rebound Is Induced by Direct-Pathway Neurons and Encode Action-Outcome Contingency
inferred← citeshttps://doi.org/10.64898/2026.01.24.701496openalex-snapshot
Dissociable neuronal substrates for positive and negative valence stimuli in the nucleus accumbens
inferred← citeshttps://doi.org/10.70675/1eda447azd2ecz4675zbc7azd4baf9a480dbopenalex-snapshot
Rôle des hétéromères formés par les récepteurs de la dopamine et du glutamate dans les adaptations à long terme induites par la cocaïne
inferred← citeshttps://doi.org/10.70675/4121b221z3107z40a2za0dfz06b8fde8c4b0openalex-snapshot
Le rôle respectif des différents populations de neurones épineux moyens du noyau accumbens dans la motivation et la prise alimentaire
inferred← citeshttps://doi.org/10.70675/4ae5cdecz30c8z4ef1z8279zbbc222444aadopenalex-snapshot
Marqueurs moléculaires de l'escalade de consommation d'héroïne et de la rechute sous un traitement de substitution, la méthadone
inferred← citeshttps://doi.org/10.70675/b11d29f4z1bf3z4003z81f9z8c69988b277bopenalex-snapshot
Rang social, système dopaminergique et réponse au stress
inferred← citeshttps://doi.org/10.70675/b8ead46dzaf07z4156zb06bzc3755176fcfcopenalex-snapshot
Rôle des afférences thalamiques au noyau accumbens dans les comportements motivés chez le rat
inferred← citeshttps://doi.org/10.70675/c632ab07z5b2ez4f68zaa26z9533043f65abopenalex-snapshot
Contribution d'une activité neuronale pacemaker dans l'expression et l'adaptation d'un comportement motivé chez l'aplysie
inferred← citeshttps://doi.org/10.70675/deeb43a5z6accz4998z8619z6a33d6f4be8eopenalex-snapshot
Neuronal basis of decision-making under opposed valence affective states
inferred← citeshttps://doi.org/10.70675/e45d048ez2538z4905zba74z1de16201406aopenalex-snapshot
Socio-communicative and nucleus accumbens core dysfunctions in fragile X syndrome
inferred← citeshttps://doi.org/10.7554/elife.50519openalex-snapshot
The orphan receptor GPR88 blunts the signaling of opioid receptors and multiple striatal GPCRs
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