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Nucleus Basalis Stimulation Enhances Working Memory by Stabilizing Attractor Networks in Prefrontal Cortex

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Cognitive Functions in a Patient With Parkinson-Dementia Syndrome Undergoing Deep Brain Stimulation
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Donepezil for dementia due to Alzheimer's disease
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Distribution and intrinsic membrane properties of basal forebrain GABAergic and parvalbumin neurons in the mouse
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Cholinergic innervation of cortex by the basal forebrain: Cytochemistry and cortical connections of the septal area, diagonal band nuclei, nucleus basalis (Substantia innominata), and hypothalamus in the rhesus monkey
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GABAergic neurons in the primate basal forebrain magnocellular complex
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The Input-Output Relationship of the Cholinergic Basal Forebrain
inferredcites →https://doi.org/10.1016/j.cub.2017.07.021openalex-snapshot
Intermittent Stimulation of the Nucleus Basalis of Meynert Improves Working Memory in Adult Monkeys
inferredcites →https://doi.org/10.1016/j.cub.2018.11.012openalex-snapshot
Novelty, Salience, and Surprise Timing Are Signaled by Neurons in the Basal Forebrain
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A software solution for the control of visual behavioral experimentation
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Chronux: A platform for analyzing neural signals
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Gamma and Beta Bursts Underlie Working Memory
inferredcites →https://doi.org/10.1016/j.neuron.2016.09.006openalex-snapshot
Basal Forebrain Cholinergic Circuits and Signaling in Cognition and Cognitive Decline
inferredcites →https://doi.org/10.1016/j.neuron.2018.05.027openalex-snapshot
Muscarinic M1 Receptor Overstimulation Disrupts Working Memory Activity for Rules in Primate Prefrontal Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2019.05.026openalex-snapshot
Prefrontal Cortex Regulates Sensory Filtering through a Basal Ganglia-to-Thalamus Pathway
inferredcites →https://doi.org/10.1016/j.neuron.2019.05.041openalex-snapshot
Neuromodulation of Spike-Timing-Dependent Plasticity: Past, Present, and Future
inferredcites →https://doi.org/10.1016/j.neuropharm.2018.04.026openalex-snapshot
Intermittent stimulation in the nucleus basalis of meynert improves sustained attention in rhesus monkeys
inferredcites →https://doi.org/10.1016/j.nlm.2016.02.008openalex-snapshot
What do phasic cholinergic signals do?
inferredcites →https://doi.org/10.1016/s0896-6273(00)81155-1openalex-snapshot
Stability of the Memory of Eye Position in a Recurrent Network of Conductance-Based Model Neurons
inferredcites →https://doi.org/10.1037//0735-7044.112.3.467openalex-snapshot
Induction of long-term receptive field plasticity in the auditory cortex of the waking guinea pig by stimulation of the nucleus basalis.
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A neuronal population code for sound localization
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Acetylcholine contributes through muscarinic receptors to attentional modulation in V1
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Cholinergic modulation of a specific memory function of prefrontal cortex
inferredcites →https://doi.org/10.1038/nn.3552openalex-snapshot
Fast modulation of visual perception by basal forebrain cholinergic neurons
inferredcites →https://doi.org/10.1038/nn.3645openalex-snapshot
Bump attractor dynamics in prefrontal cortex explains behavioral precision in spatial working memory
inferredcites →https://doi.org/10.1038/nn1790openalex-snapshot
Bayesian inference with probabilistic population codes
inferredcites →https://doi.org/10.1038/nn1846openalex-snapshot
Inverted-U dopamine D1 receptor actions on prefrontal neurons engaged in working memory
inferredcites →https://doi.org/10.1038/nn846openalex-snapshot
Active maintenance in prefrontal area 46 creates distractor-resistant memory
inferredcites →https://doi.org/10.1038/nrn.2016.43openalex-snapshot
The neuroscience of working memory capacity and training
inferredcites →https://doi.org/10.1038/s41586-019-0919-7openalex-snapshot
Discrete attractor dynamics underlies persistent activity in the frontal cortex
inferredcites →https://doi.org/10.1038/s41593-020-0644-4openalex-snapshot
Interplay between persistent activity and activity-silent dynamics in the prefrontal cortex underlies serial biases in working memory
inferredcites →https://doi.org/10.1073/pnas.0901894106openalex-snapshot
Mechanism for top-down control of working memory capacity
inferredcites →https://doi.org/10.1073/pnas.1307849110openalex-snapshot
Nicotinic α7 receptors enhance NMDA cognitive circuits in dorsolateral prefrontal cortex
inferredcites →https://doi.org/10.1073/pnas.1413625112openalex-snapshot
Cortically projecting basal forebrain parvalbumin neurons regulate cortical gamma band oscillations
inferredcites →https://doi.org/10.1073/pnas.1905413116openalex-snapshot
Cell class-specific modulation of attentional signals by acetylcholine in macaque frontal eye field
inferredcites →https://doi.org/10.1073/pnas.93.20.11219openalex-snapshot
Induction of a physiological memory in the cerebral cortex by stimulation of the nucleus basalis.
inferredcites →https://doi.org/10.1080/19420889.2017.1389359openalex-snapshot
Potential for intermittent stimulation of nucleus basalis of Meynert to impact treatment of alzheimer's disease
inferredcites →https://doi.org/10.1093/cercor/10.9.910openalex-snapshot
Synaptic Mechanisms and Network Dynamics Underlying Spatial Working Memory in a Cortical Network Model
inferredcites →https://doi.org/10.1093/cercor/bhaa045openalex-snapshot
Role of the Thalamus in Basal Forebrain Regulation of Neural Activity in the Primary Auditory Cortex
inferredcites →https://doi.org/10.1093/cercor/bhr058openalex-snapshot
Changes in Prefrontal Neuronal Activity after Learning to Perform a Spatial Working Memory Task
inferredcites →https://doi.org/10.1124/jpet.102.041616openalex-snapshot
The Cholinergic Hypothesis of Age and Alzheimer’s Disease-Related Cognitive Deficits: Recent Challenges and Their Implications for Novel Drug Development
inferredcites →https://doi.org/10.1126/science.279.5357.1714openalex-snapshot
Cortical Map Reorganization Enabled by Nucleus Basalis Activity
inferredcites →https://doi.org/10.1146/annurev-neuro-071714-034002openalex-snapshot
Plasticity of Cortical Excitatory-Inhibitory Balance
inferredcites →https://doi.org/10.1152/jn.00148.2011openalex-snapshot
Cholinergic modulation of working memory activity in primate prefrontal cortex
inferredcites →https://doi.org/10.1152/jn.2000.83.3.1733openalex-snapshot
Dopamine-Mediated Stabilization of Delay-Period Activity in a Network Model of Prefrontal Cortex
inferredcites →https://doi.org/10.1152/jn.2000.84.1.401openalex-snapshot
Accuracy of Tetrode Spike Separation as Determined by Simultaneous Intracellular and Extracellular Measurements
inferredcites →https://doi.org/10.1152/jn.91092.2008openalex-snapshot
Deep Brain Stimulation of the Globus Pallidus Internus in the Parkinsonian Primate: Local Entrainment and Suppression of Low-Frequency Oscillations
inferredcites →https://doi.org/10.1155/2011/156869openalex-snapshot
FieldTrip: Open Source Software for Advanced Analysis of MEG, EEG, and Invasive Electrophysiological Data
inferredcites →https://doi.org/10.1162/089976699300016809openalex-snapshot
Neuronal Tuning: To Sharpen or Broaden?
inferredcites →https://doi.org/10.1371/journal.pone.0041053openalex-snapshot
Variability of Prefrontal Neuronal Discharges before and after Training in a Working Memory Task
inferredcites →https://doi.org/10.1523/eneuro.0208-18.2018openalex-snapshot
Cell Type- and Layer-Specific Muscarinic Potentiation of Excitatory Synaptic Drive onto Parvalbumin Neurons in Mouse Prefrontal Cortex
inferredcites →https://doi.org/10.1523/jneurosci.0364-17.2017openalex-snapshot
Nicotinic α4β2 Cholinergic Receptor Influences on Dorsolateral Prefrontal Cortical Neuronal Firing during a Working Memory Task
inferredcites →https://doi.org/10.1523/jneurosci.1676-18.2018openalex-snapshot
Specific Basal Forebrain–Cortical Cholinergic Circuits Coordinate Cognitive Operations
inferredcites →https://doi.org/10.1523/jneurosci.2454-15.2015openalex-snapshot
Muscarinic Attenuation of Mnemonic Rule Representation in Macaque Dorsolateral Prefrontal Cortex during a Pro- and Anti-Saccade Task
inferredcites →https://doi.org/10.1523/jneurosci.2485-17.2018openalex-snapshot
Working Memory: Delay Activity, Yes! Persistent Activity? Maybe Not
inferredcites →https://doi.org/10.1523/jneurosci.3198-17.2017openalex-snapshot
Cholinergic Overstimulation Attenuates Rule Selectivity in Macaque Prefrontal Cortex
inferredcites →https://doi.org/10.2139/ssrn.3492110openalex-snapshot
Muscarinic M1 Receptors Modulate Working Memory Performance and Activity Via KCNQ Potassium Channels in Primate Prefrontal Cortex
inferredcites →https://doi.org/10.3389/fncir.2018.00067openalex-snapshot
Evolution in Neuromodulation—The Differential Roles of Acetylcholine in Higher Order Association vs. Primary Visual Cortices
inferredcites →https://doi.org/10.3389/fnsys.2015.00181openalex-snapshot
Role of Prefrontal Persistent Activity in Working Memory

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.tics.2019.12.014openalex-snapshot
Reevaluating the Role of Persistent Neural Activity in Short-Term Memory
inferred← citeshttps://doi.org/10.3389/fncir.2020.00015openalex-snapshot
Plasticity of Persistent Activity and Its Constraints
inferred← citeshttps://doi.org/10.3389/fncir.2021.716965openalex-snapshot
Across-Area Synchronization Supports Feature Integration in a Biophysical Network Model of Working Memory
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