Dynamic network connectivity: a new form of neuroplasticity
Open accessAbstract
Prefrontal cortical (PFC) working memory functions depend on pyramidal cell networks that interconnect on dendritic spines. Recent research has revealed that the strength of PFC network connections can be rapidly and reversibly increased or decreased by molecular signaling events within slender, elongated spines: a process we term Dynamic Network Connectivity (DNC). This newly discovered form of neuroplasticity provides great flexibility in mental state, but also confers vulnerability and limits mental capacity. A remarkable number of genetic and/or environmental insults to DNC signaling cascades are associated with cognitive disorders such as schizophrenia and age-related cognitive decline. These insults can dysregulate network connections and erode higher cognitive abilities, leading to symptoms such as forgetfulness, susceptibility to interference, and disorganized thought and behavior.
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
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 PFC is especially sensitive to its neurochemical environment; relatively small changes in norepinephrine and dopamine levels can produce significant changes in PFC function.
“The PFC is known to be especially sensitive to its neurochemical environment; relatively small changes in the levels of norepinephrine and dopamine can produce significant changes in its function.”
From Catecholamine influences on prefrontal cortical function: Relevance to treatment of attention deficit/hyperactivity disorder and related disorders (2011) · cites this paper as Arnsten et al., 2010
In “Pathways that strengthen network connections” and “Pathways that weaken network connections” (page unavailable), the paper says that norepinephrine and dopamine help determine PFC functional state, with optimal levels strengthening network firing and excessive levels impairing it. It does not establish that relatively small changes in their levels produce significant changes in PFC function. (LLM, conf=0.82)
Experimental — accuracy not yet measuredRecurrent PFC network activity is fragile and extremely sensitive to the neurochemical environment; small changes in arousal systems can markedly alter the connectivity of PFC networks.
“However, recurrent PFC network activity is fragile, and extremely sensitive to the neurochemical environment. Thus, small changes in the arousal systems can markedly alter the connectivity of PFC networks (Arnsten et al., 2010).”
From Catecholamine influences on prefrontal cortical function: Relevance to treatment of attention deficit/hyperactivity disorder and related disorders (2011) · cites this paper as Arnsten et al., 2010
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Stress signalling pathways that impair prefrontal cortex structure and function
Arnsten, A. F. T. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2648 · Cited by 3,299 · see citing works
Self-citationVyas, A., Mitra, R., Shankaranarayana Rao, B. S., & Chattarji, S. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06810.2002 · Cited by 1,662 · see citing works
Regulation of NMDA receptor trafficking by amyloid-β
Snyder, E. M., Nong, Y., Almeida, C. G., Paul, S., Moran, T., Choi, E. Y., Nairn, A. C., Salter, M. W., Lombroso, P. J., Gouras, G. K., et al. (2005) · Nature Neuroscience · doi:10.1038/nn1503 · Cited by 1,561 · cited 1× · see citing works
“2A [63]).”
Inverted-U dopamine D1 receptor actions on prefrontal neurons engaged in working memory
Vijayraghavan, S., Wang, M., Birnbaum, S. G., Williams, G. V., & Arnsten, A. F. T. (2007) · Nature Neuroscience · doi:10.1038/nn1846 · Cited by 1,013 · see citing works
Self-citationThe Neuropsychopharmacology of Fronto-Executive Function: Monoaminergic Modulation
Robbins, T. W., & Arnsten, A. F. T. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135535 · Cited by 957 · see citing works
Self-citationWang, M., Ramos, B. P., Paspalas, C. D., Shu, Y., Simen, A., Duque, A., Vijayraghavan, S., Brennan, A., Dudley, A., Nou, E., et al. (2007) · Cell · doi:10.1016/j.cell.2007.03.015 · Cited by 672 · see citing works
Self-citationDISC1 and PDE4B Are Interacting Genetic Factors in Schizophrenia That Regulate cAMP Signaling
Millar, J. K., Pickard, B. S., Mackie, S., James, R., Christie, S., Buchanan, S. R., Malloy, M. P., Chubb, J. E., Huston, E., Baillie, G. S., et al. (2005) · Science · doi:10.1126/science.1112915 · Cited by 648 · see citing works
Molecular identification of the corticosterone-sensitive extraneuronal catecholamine transporter
Gründemann, D., Schechinger, B., Rappold, G., & Schömig, E. (1998) · Nature Neuroscience · doi:10.1038/1557 · Cited by 374 · see citing works
Protein kinase C overactivity impairs prefrontal cortical regulation of working memory
Birnbaum, S. G., Yuan, P. X., Wang, M., Vijayraghavan, S., Bloom, A. K., Davis, D. J., Gobeske, K. T., Sweatt, J. D., Manji, H. K., & Arnsten, A. F. T. (2004) · Science · doi:10.1126/science.1100021 · Cited by 318 · see citing works
Self-citationPresynaptic regulation of recurrent excitation by D1 receptors in prefrontal circuits
Gao, W.-J., Krimer, L. S., & Goldman-Rakic, P. S. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.1.295 · Cited by 257 · see citing works
Hains, A. B., Vu, M. A. T., Maciejewski, P. K., van Dyck, C. H., Gottron, M., & Arnsten, A. F. T. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908563106 · Cited by 234 · see citing works
Self-citationGill, T. M., Sarter, M., & Givens, B. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-12-04745.2000 · Cited by 228 · see citing works
Wang, H., Stradtman, G. G., Wang, X.-J., & Gao, W.-J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804318105 · Cited by 199 · see citing works
Li, B.-M., & Mei, Z.-T. (1994) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(05)80034-2 · Cited by 186 · see citing works
The beta-1 adrenergic antagonist, betaxolol, improves working memory performance in rats and monkeys
Ramos, B. P., Colgan, L., Nou, E., Ovadia, S., Wilson, S. R., & Arnsten, A. F. T. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.05.022 · Cited by 147 · see citing works
Self-citationTaylor, J. R., Birnbaum, S., Ubriani, R., & Arnsten, A. F. T. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-18-j0001.1999 · Cited by 120 · see citing works
Self-citation
Flagged first, then by citations
Research works printed but not linked: 63
- [2]Moore TL Executive system dysfunction occurs as early as middle-age in the rhesus monkey Neurobiol Aging 2006 27 1484 1493 16183172
- [3]Weinberger DR Physiologic dysfunction of dorsolateral prefrontal cortex in schizophrenia. I. Regional cerebral blood flow evidence Archives General Psychiatry 1986 43 114 124 3947207
- [4]Rubia K Hypofrontality in Attention Deficit Hyperactivity Disorder during higher-order motor control: A study with functional MRI Am J Psychiatry 1999 156 891 896 10360128
- [5]Blumberg HP A functional magnetic resonance imaging study of bipolar disorder: state- and trait-related dysfunction in ventral prefrontal cortices Arch Gen Psychiatry 2003 60 601 609 12796223
- [6]Goldman-Rakic PS Cellular basis of working memory Neuron 1995 14 477 485 7695894
- [10]Hagenston AM mGluR-mediated calcium waves that invade the soma regulate firing in layer V medial prefrontal cortical pyramidal neurons Cerebral Cortex 2008 18 407 423 17573372 PMC3005283
- [11]Bourne J Harris KM Do thin spines learn to be mushroom spines that remember? Curr Opin Neurobiol 2007 17 381 386 17498943
- [12]Friedman HR Goldman-Rakic PS Coactivation of prefrontal cortex and inferior parietal cortex in working memory tasks revealed by 2DG functional mapping in the rhesus monkey J Neurosci 1994 14 2775 2788 8182439 PMC6577453
- [13]Swartz BE Studies of working memory using 18FDG-positron emission tomography in normal controls and subjects with epilepsy Life Sci 1996 58 2057 2064 8637437
- [14]Zola-Morgan S Squire LR Medial temporal lesions in monkeys impair memory on a variety of tasks sensitive to human amnesia Behavioral Neurosci 1985 99 22 34 4041230
- [16]Faber ES Functional interplay between NMDA receptors, SK channels and voltage-gated Ca2+ channels regulates synaptic excitability in the medial prefrontal cortex J Physiol 2010 588 1281 1292 20194128 PMC2872733
- [17]Muly EC Distribution of mGluR1alpha and mGluR5 immunolabeling in primate prefrontal cortex J Comp Neurol 2003 467 521 535 14624486
- [18]Mannaioni G Metabotropic glutamate receptors 1 and 5 differentially regulate CA1 pyramidal cell function J Neurosci 2001 21 5925 5934 11487615 PMC6763150
- [19]Paspalas CD Mapping the Regulator of G Protein Signaling 4 (RGS4): Presynaptic and postsynaptic substrates for neuroregulation in prefrontal cortex Cereb Cortex 2009 19 2145 2155 19153107 PMC2722426
- [20]Brennan AR Blockade of IP3-mediated SK channel signaling in the rat medial prefrontal cortex improves spatial working memory Learn Mem 2008 15 93 96 18285467 PMC2275660
- [21]Runyan JD A role for prefrontal calcium-sensitive protein phosphatase and kinase activities in working memory Learn Mem 2005 12 103 110 15805309 PMC1074327
- [23]Ferguson GD Storm DR Why calcium-stimulated adenylyl cyclases? Physiology 2004 19 271 276 15381755
- [24]Delmas P Brown DA Pathways modulating neural KCNQ/M (Kv7) potassium channels Nature Reviews Neuroscience 2005 6 850 862 16261179
- [25]Runyan JD Dash PK Distinct prefrontal molecular mechanisms for information storage lasting seconds versus minutes Learn Mem 2005 12 232 238 15930501 PMC1142450
- [27]Partridge LD Modulation of calcium-activated non-specific cation currents by cyclic AMP-dependent phosphorylation in neurons of Helix J Physiology 1990 429 131 145 PMC1181691 1703569
- [28]Kole MH Inherited cortical HCN1 channel loss amplifies dendritic calcium electrogenesis and burst firing in a rat absence epilepsy model J Physiol 2007 578 Pt2 507 525 17095562 PMC2075144
- [29]Huang Z Loss of dendritic HCN1 subunits enhances cortical excitability and epileptogenesis J Neurosci 2009 29 10979 10988 19726656 PMC2744118
- [30]Poolos NP Pharmacological upregulation of h-channels reduces the excitability of pyramidal neuron dendrites Nature Neuroscience 2002 5 767 774 12118259
- [31]Schroeder BC Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy Nature 1998 396 687 690 9872318
- [33]Roozendaal B The basolateral amygdala interacts with the medial prefrontal cortex in regulating glucocorticoid effects on working memory impairment J Neurosci 2004 24 1385 1392 14960610 PMC6730337
- [35]Radley JJ Repeated stress alters dendritic spine morphology in the rat medial prefrontal cortex J Comp Neurol 2008 507 1141 1150 18157834 PMC2796421
- [38]Liston C Psychosocial stress reversibly disrupts prefrontal processing and attentional control Proc Nat Acad Sci USA 2009 106 912 917 19139412 PMC2621252
- [39]Hao J Estrogen alters spine number and morphology in prefrontal cortex of aged female rhesus monkeys J Neurosci 2006 26 2571 2578 16510735 PMC6793646
- [40]Glantz LA Lewis DA Decreased dendritic spine density on prefrontal cortical pyramidal neurons in schizophrenia Archives General Psychiatry 2000 57 65 73 10632234
- [41]Li BM Alpha-2 adrenergic modulation of prefrontal cortical neuronal activity related to spatial working memory in monkeys Neuropsychopharmacol 1999 21 601 610 10516956
- [43]Ma CL Selective deficit in no-go performance induced by blockade of prefrontal cortical alpha2-adrenoceptors in monkeys Neuroreport 2003 14 1013 1016 12802193
- [44]Biederman J A randomized, double-blind, placebo-controlled study of guanfacine extended release in children and adolescents with attention-deficit/hyperactivity disorder Pediatrics 2008 121 e73 84 18166547
- [45]Arnsten AFT Bjorklund A 2009 Dopamine’s influence on prefrontal cortical cognition: Actions and circuits in behaving primates Dopamine Handbook 230 249 Oxford University Press
- [46]Crofts HS Differential effects of 6-OHDA lesions of the prefrontal cortex and caudate nucleus on the ability to acquire an attentional set Cerebral Cortex 2001 11 1015 1026 11590111
- [48]Paspalas CD Goldman-Rakic PS Presynaptic D1 dopamine receptors in primate prefrontal cortex: target-specific expression in the glutamatergic synapse J Neurosci 2005 25 1260 1267 15689564 PMC6725972
- [50]Kirkpatrick B DISC1 immunoreactivity at the light and ultrastructural level in the human neocortex J Comp Neurol 2006 497 436 450 16736468
- [52]Buccafusco JJ Terry AVJ A reversible model of the cognitive impairment associated with schizophrenia in monkeys: potential therapeutic effects of two nicotinic acetylcholine receptor agonists Biochem Pharmacol 2009 78 852 862 19577545 PMC2728139
- [53]Levin ED Nicotinic receptor subtypes and cognitive function J Neurobiol 2002 53 633 640 12436426
- [54]Duffy AM Spatial and intracellular relationships between the alpha7 nicotinic acetylcholine receptor and the vesicular acetylcholine transporter in the prefrontal cortex of rat and mouse Neuroscience 2009 161 1091 1103 19374941 PMC2720620
- [55]Brennan AR Arnsten AF Neuronal mechanisms underlying attention deficit hyperactivity disorder: the influence of arousal on prefrontal cortical function Ann N Y Acad Sci 2008 1129 236 245 18591484 PMC2863119
- [56]Peters A Neurobiological bases of age-related cognitive decline in the rhesus monkey J Neuropathol Exp Neurol 1996 55 861 874 8759775
- [57]Ramos B Dysregulation of protein kinase A signaling in the aged prefrontal cortex: New strategy for treating age-related cognitive decline Neuron 2003 40 835 845 14622586
- [58]Moore TL Cognitive impairment in aged rhesus monkeys associated with monoamine receptors in the prefrontal cortex Behav Brain Res 2005 160 208 221 15863218
- [59]Ramos B Alpha-2A-adrenoceptor stimulation improves prefrontal cortical regulation of behavior through inhibition of cAMP signaling in aging animals Learning and Memory 2006 13 770 776 17101879 PMC1783631
- [60]Wenk GL Age-related changes in multiple neurotransmitter systems in the monkey brain Neurobio Aging 1989 10 11 19 2569169
- [61]Siddiqi Z Age-related neuronal loss from the substantia nigra-pars compacta and ventral tegmental area of the rhesus monkey Journal of Neuropathology & Experimental Neurology 1999 58 959 971 10499438
- [62]Cai JX Arnsten AFT Dose-dependent effects of the dopamine D1 receptor agonists A77636 or SKF81297 on spatial working memory in aged monkeys J Pharmacol Exp Ther 1997 283 183 189 9336323
- [64]Blanchard BJ Mechanism of membrane depolarization caused by the Alzheimer Abeta1–42 peptide Biochem Biophys Res Commun 2002 293 1197 1203 12054502
- [65]Barch DM The cognitive neuroscience of schizophrenia Annu Rev Clin Psychol 2005 1 321 353 17716091
- [66]Ford JM Reduced communication between frontal and temporal lobes during talking in schizophrenia Biol Psychiatry 2002 51 485 492 11922884
- [67]Corlett PR Disrupted prediction-error signal in psychosis: evidence for an associative account of delusions Brain 2007 130 Pt 9 2387 2400 17690132 PMC3838942
- [68]Perlstein WM Relation of prefrontal cortex dysfunction to working memory and symptoms in schizophrenia Am J Psychiatry 2001 158 1105 1113 11431233
- [69]Vidal CN Dynamically spreading frontal and cingulate deficits mapped in adolescents with schizophrenia Arch Gen Psychiatry 2006 63 25 34 16389194
- [70]Ross CA Neurobiology of schizophrenia Neuron 2006 52 139 153 17015232
- [71]Krystal JH NMDA receptor antagonist effects, cortical glutamatergic function, and schizophrenia: toward a paradigm shift in medication development Psychopharmacology 2003 169 215 233 12955285
- [72]Martin LF Freedman R Schizophrenia and the alpha7 nicotinic acetylcholine receptor Int Rev Neurobiol 2007 78 225 246 17349863
- [73]Ishizuka K A review of Disrupted-In-Schizophrenia-1 (DISC1): neurodevelopment, cognition, and mental conditions Biol Psychiatry 2006 59 1189 1197 16797264
- [74]Liu J Combining fMRI and SNP data to investigate connections between brain function and genetics using parallel ICA Hum Brain Mapp 2009 30 241 255 18072279 PMC2668960
- [75]Blackwood DH Muir WJ Clinical phenotypes associated with DISC1, a candidate gene for schizophrenia Neurotox Res 2004 6 35 41 15184103
- [76]Mirnics K Disease-specific changes in regulator of G-protein signaling 4 (RGS4) expression in schizophrenia Mol Psychiatry 2001 6 293 301 11326297
- [77]Erdely HA Regional alterations in RGS4 protein in schizophrenia Synapse 2006 59 472 479 16565965
- [78]Lewis DA Gonzalez-Burgos GR Pathophysiologically based treatment interventions in schizophrenia Nature Medicine 2006 12 1016 1022 16960576
- [79]Hahn CG Altered neuregulin 1-erbB4 signaling contributes to NMDA receptor hypofunction in schizophrenia Nat Med 2006 12 824 828 16767099
Cited by
Sorted by citations
The Brain on Stress: Vulnerability and Plasticity of the Prefrontal Cortex over the Life Course
McEwen, B. S., & Morrison, J. H. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.028 · Cited by 1,079 · see citing works
The ageing cortical synapse: hallmarks and implications for cognitive decline
Morrison, J. H., & Baxter, M. G. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3200 · Cited by 965 · see citing works
Dendritic spine pathology in schizophrenia
Glausier, J. R., & Lewis, D. A. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2012.04.044 · Cited by 581 · see citing works
Arnsten, A. F. T., Wang, M. J., & Paspalas, C. D. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.038 · Cited by 538 · see citing works
Self-citationCatecholamine Influences on Dorsolateral Prefrontal Cortical Networks
Arnsten, A. F. T. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.01.027 · Cited by 493 · see citing works
Self-citationNeuronal basis of age-related working memory decline
Wang, M., Gamo, N. J., Yang, Y., Jin, L. E., Wang, X.-J., Laubach, M., Mazer, J. A., Lee, D., & Arnsten, A. F. T. (2011) · Nature · doi:10.1038/nature10243 · Cited by 485 · see citing works
Self-citationCognitive Network Neuroscience
Medaglia, J. D., Lynall, M.-E., & Bassett, D. S. (2015) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00810 · Cited by 419 · see citing works
Arnsten, A. F. T., & Pliszka, S. R. (2011) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.01.020 · Cited by 383 · see citing works
Self-citationDendritic spine changes associated with normal aging
Dickstein, D. L., Weaver, C. M., Luebke, J. I., & Hof, P. R. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2012.09.077 · Cited by 289 · see citing works
Gamo, N. J., Wang, M., & Arnsten, A. F. T. (2010) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2010.06.015 · Cited by 232 · see citing works
Self-citationPsychostimulants and motivated behavior: Arousal and cognition
Berridge, C. W., & Arnsten, A. F. T. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.11.005 · Cited by 104 · see citing works
Self-citationGamo, N. J., Lur, G., Higley, M. J., Wang, M., Paspalas, C. D., Vijayraghavan, S., Yang, Y., Ramos, B. P., Peng, K., Kata, A., et al. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.01.009 · Cited by 97 · see citing works
Self-citationMolecular Profiles of Pyramidal Neurons in the Superior Temporal Cortex in Schizophrenia
Pietersen, C. Y., Mauney, S. A., Kim, S. S., Lim, M. P., Rooney, R. J., Goldstein, J. M., Petryshen, T. L., Seidman, L. J., Shenton, M. E., McCarley, R. W., et al. (2014) · Journal of Neurogenetics · doi:10.3109/01677063.2014.882918 · Cited by 87 · see citing works
Arnsten, A. F. T., & Wang, M. (2016) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010715-103617 · Cited by 50 · see citing works
Self-citationRole of disrupted in schizophrenia 1 (DISC1) in stress-induced prefrontal cognitive dysfunction
Gamo, N. J., Duque, A., Paspalas, C. D., Kata, A., Fine, R., Boven, L., Bryan, C., Lo, T., Anighoro, K., Bermudez, L., et al. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.104 · Cited by 37 · see citing works
Self-citationSakamoto, K., Katori, Y., Saito, N., Yoshida, S., Aihara, K., & Mushiake, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080906 · Cited by 13 · see citing works
Enhancement of Function of the Prefrontal Cortex to Improve Symptoms of Schizophrenia
Sarma Bardoloi, P. (2020) · Acta Scientific Neurology · doi:10.31080/asne.2020.03.0183 · Cited by 4 · see citing works
- Authors
- Arnsten, A. F. T., Paspalas, C. D., Gamo, N. J., Yang, Y., & Wang, M.
- Affiliations
- Yale University (US)
- Corresponding author
- Arnsten, Amy F.T.
- Venue
- Trends in Cognitive Sciences
- Publisher
- Elsevier BV
- Published
- 2010-08
- Volume
- 14
- Issue
- 8
- Pages
- 365-375
- ISSN
- 1364-6613 (ISSN-L)
- PMC
- PMC2914830
- OpenAlex
- W2034673701
- Cited by
- 160
- References
- 16
- Citations by year
- 2026: 2 · 2024: 5 · 2023: 6 · 2022: 7 · 2021: 13 · 2020: 8 · 2019: 9 · 2018: 11 · 2017: 13 · 2016: 8 · 2015: 16 · 2014: 16 · 2013: 15 · 2012: 22
- FWCI
- 1.33
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Trends in Cognitive Sciences (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Alliance for Research on Schizophrenia and Depression
- National Institute on Alcohol Abuse and Alcoholism (RL1AA017536)
- National Institute on Aging (R37AG006036, P01AG030004, R01AG006036, AG06036)
- National Center for Research Resources (U54RR024350)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- neuroplasticity, prefrontal cortex, working memory, dendritic spines, synaptic plasticity, schizophrenia, age-related cognitive decline, cognitive disorders, molecular signaling
- MeSH terms
- Aging, Animals, Cognition Disorders, Dopamine, Humans, Models, Neurological, Neural Pathways, Neuronal Plasticity, Neurons, Schizophrenia, Neural Networks, Computer, Prefrontal Cortex, Nonlinear Dynamics
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