Cited by 1,329Neural and Behavioral Psychology StudiesNeurotransmitter Receptor Influence on BehaviorMemory and Neural Mechanisms

The DOI matches its Crossref record; 144 of the 144 references it cites were found in a registry or an index.

Prefrontal executive and cognitive functions in rodents: neural and neurochemical substrates

Dalley, Jeffrey W., Cardinal, Rudolf N., Robbins, Trevor W.·2004·Neuroscience & Biobehavioral Reviews

DOI 10.1016/j.neubiorev.2004.09.006

Open this paper in CoChat — free account

Abstract

The prefrontal cortex has been implicated in a variety of cognitive and executive processes, including working memory, decision-making, inhibitory response control, attentional set-shifting and the temporal integration of voluntary behaviour. This article reviews current progress in our understanding of the rodent prefrontal cortex, especially evidence for functional divergence of the anatomically distinct sub-regions of the rat prefrontal cortex. Recent findings suggest clear distinctions between the dorsal (precentral and anterior cingulate) and ventral (prelimbic, infralimbic and medial orbital) sub-divisions of the medial prefrontal cortex, and between the orbitofrontal cortex (ventral orbital, ventrolateral orbital, dorsal and ventral agranular cortices) and the adjacent medial wall of the prefrontal cortex. The dorso-medial prefrontal cortex is implicated in memory for motor responses, including response selection, and the temporal processing of information. Ventral regions of the medial prefrontal cortex are implicated in interrelated 'supervisory' attentional functions, including attention to stimulus features and task contingencies (or action-outcome rules), attentional set-shifting, and behavioural flexibility. The orbitofrontal cortex is implicated in lower-order discriminations, including reversal of stimulus-reward associations (reversal learning), and choice involving delayed reinforcement. It is anticipated that a greater understanding of the prefrontal cortex will come from using tasks that load specific cognitive and executive processes, in parallel with discovering new ways of manipulating the different sub-regions and neuromodulatory systems of the prefrontal cortex.

Integrity signals

Registry

Crossref · 10.1016/j.neubiorev.2004.09.006

Cites

144 of 144 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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 Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
The Principles of Psychology
James, W. (1891) · Personality Culture Society · doi:10.1037/11059-000 · Cited by 25,876
Specific impairments of planning
Shallice, T. (1982) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1982.0082 · Cited by 3,741
Psychopharmacology: The Fourth Generation of Progress
Bloom, F. E., & Kupfer, D. J. (1995) · Medical Entomology and Zoology · Cited by 2,985
Specious reward: A behavioral theory of impulsiveness and impulse control.
Ainslie, G. (1975) · Psychological Bulletin · doi:10.1037/h0076860 · Cited by 2,708
The Organization of Networks within the Orbital and Medial Prefrontal Cortex of Rats, Monkeys and Humans
Ongur, D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.206 · Cited by 2,627
Exploring the Central Executive
Baddeley, A. (1996) · The Quarterly Journal of Experimental Psychology Section A · doi:10.1080/713755608 · Cited by 2,390
Emotion and motivation: the role of the amygdala, ventral striatum, and prefrontal cortex
Cardinal, R. N., Parkinson, J. A., Hall, J., & Everitt, B. J. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(02)00007-6 · Cited by 2,129
Self-citation
Varieties of impulsivity
Evenden, J. L. (1999) · Psychopharmacology · doi:10.1007/pl00005481 · Cited by 2,044
The prefontral cortex and cognitive control
Miller, E. K. (2000) · Nature Reviews Neuroscience · doi:10.1038/35036228 · Cited by 2,016

Show all 141 references

Research works printed but not linked: 1

Sagvolden, 1998, Attention deficit/hyperactivity disorder—from brain dysfunctions to behavior, Behav Brain Res, 94, 1

Sorted by citations

Items 901–998 of 998

Prelimbic cortex dynorphin/κ opioid receptor system modulates methamphetamine‐induced cognitive impairment
Cheng, Y.-J., Deng, Y.-Z., Deng, D., Wu, M., Chai, J., Wang, Y., Liu, J., & Zhao, M. (2023) · Addiction Biology · doi:10.1111/adb.13323 · Cited by 10
Noradrenaline and acetylcholine responsiveness of glucose-monitoring and glucose-insensitive neurons in the mediodorsal prefrontal cortex
Nagy, B., Szabó, I., Csetényi, B., Hormay, E., Papp, S., Keresztes, D., & Karádi, Z. (2013) · Brain Research · doi:10.1016/j.brainres.2013.11.014 · Cited by 10
Sodium fluoride does not affect the working memory and number of pyramidal cells in rat medial prefrontal cortex
Pulungan, Z. S. A., Sofro, Z. M., & Partadiredja, G. (2016) · Anatomical Science International · doi:10.1007/s12565-016-0384-4 · Cited by 10
Mate assessment behavior is correlated to learning ability in female threespine sticklebacks
Rystrom, T. L., Bakker, T. C. M., & Rick, I. P. (2019) · Current Zoology · doi:10.1093/cz/zoz010 · Cited by 10
Choice-dependent cross-modal interaction in the medial prefrontal cortex of rats
Zheng, M., Xu, J., Keniston, L., Wu, J., Chang, S., & Yu, L. (2021) · Molecular Brain · doi:10.1186/s13041-021-00732-7 · Cited by 12
Personality affects individual variation in olfactory learning and reversal learning in the house cricket, Acheta domesticus
Albers, J., & Reichert, M. S. (2022) · Animal Behaviour · doi:10.1016/j.anbehav.2022.06.013 · Cited by 10
Nerve growth factor-induced plasticity in medial prefrontal cortex interneurons of aged Wistar rats
Pereira, P. A., Millner, T., Vilela, M., Sousa, S. F., Cardoso, A., & Madeira, M. D. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.09.017 · Cited by 11
Requiring collaboration: Hippocampal-prefrontal networks needed in spatial working memory and ageing. A multivariate analysis approach
Zancada-Menéndez, C., Álvarez-Suárez, P., Sampedro‐Piquero, P., Cuesta, M., & Begega, A. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.02.008 · Cited by 11
Activation of type 4 dopaminergic receptors in the prelimbic area of medial prefrontal cortex is necessary for the expression of innate fear behavior
Vergara, M., Keller, V. N., Fuentealba, J. A., & Gysling, K. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.01.050 · Cited by 10
A schizophrenia relevant 5-Choice Serial Reaction Time Task for mice assessing broad monitoring, distractibility and impulsivity
Huang, H., Guadagna, S., Mereu, M., Ciampoli, M., Pruzzo, G., Ballard, T. M., & Papaleo, F. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4611-z · Cited by 11
Nitric oxide in the medial prefrontal cortex contributes to the acquisition of cocaine place preference and synaptic plasticity in the laterodorsal tegmental nucleus
Kamii, H., Taoka, N., Minami, M., & Kaneda, K. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.09.015 · Cited by 11
GABA and Glutamate Synaptic Coadaptations to Chronic Ethanol in the Striatum
Carlson, V. C. C. (2018) · Handbook of experimental pharmacology · doi:10.1007/164_2018_98 · Cited by 10
Representation of actions and outcomes in medial prefrontal cortex during delayed conditional decision-making: Population analyses of single neuron activity
Francoeur, M. J., & Mair, R. G. (2018) · Brain and Neuroscience Advances · doi:10.1177/2398212818773865 · Cited by 10
Corticofugal Modulation and Beyond for Auditory Signal Processing and Plasticity
Suga, N., Ji, W., Ma, X., Tang, J., Xiao, Z., & Yan, J. (2010) · Springer handbook of auditory research · doi:10.1007/978-1-4419-7070-1_11 · Cited by 10
Pde10a
Menniti, F. S., Schmidt, C. J., & Strick, C. A. (2006) · CRC Press eBooks · doi:10.1201/9781420020847.ch12 · Cited by 10
Flexible decision-making is related to strategy learning, vicarious trial and error, and medial prefrontal rhythms during spatial set-shiftingPreprint
Miles, J. T., Mullins, G. L., & Mizumori, S. J. Y. (2024) · Learning & Memory · doi:10.1101/lm.053911.123 · Cited by 11
Multisensory Integration: Is Medial Prefrontal Cortex Signaling Relevant for the Treatment of Higher-Order Visual Dysfunctions?
Skirzewski, M., Molotchnikoff, S., Hernandez, L. F., & Maya‐Vetencourt, J. F. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.806376 · Cited by 9
CELF4 regulates spine formation and depression-like behaviors of mice
Shen, Y., Zhang, C., Xiao, K., Liu, D., & Xie, G. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.03.067 · Cited by 9
Sunset Yellow induced biochemical and histopathological alterations in rat brain sub-regions
Bhatt, D., Vyas, K., Singh, S. A., John, P. J., & Soni, I. (2024) · Acta Histochemica · doi:10.1016/j.acthis.2024.152155 · Cited by 9
FNDC5/irisin mediates the protective effects of Innovative theta-shaking exercise on mouse memory
Yao, R., Yamada, K., Izawa, S., Kito, T., Sawada, H., Chihara, T., Aizu, N., Iwata, D., & Nishii, K. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e29090 · Cited by 10
Can the role of genetic factors in schizophrenia be enlightened by studies of candidate gene mutant mice behaviour?
Mazzoncini, R., Zoli, M., Tosato, S., Lasalvia, A., & Ruggeri, M. (2009) · The World Journal of Biological Psychiatry · doi:10.1080/15622970902875152 · Cited by 9
Impairment of non-associative learning in a rat experimental model of preclinical stage of Parkinson’s disease
Abdurasulova, I. N., Ekimova, I. V., Matsulevich, A. V., Gazizova, A. R., Клименко, В. М., & Pastukhov, Y. F. (2017) · Doklady Biological Sciences · doi:10.1134/s0012496617050039 · Cited by 9
The synthetic cannabinoid 5F-AMB changes the balance between excitation and inhibition of layer V pyramidal neurons in the mouse medial prefrontal cortex
Domoto, M., Sasase, H., Wada, S., Ito, S., Deyama, S., Hinoi, E., Kaneko, S., & Kaneda, K. (2018) · Psychopharmacology · doi:10.1007/s00213-018-4933-5 · Cited by 9
In a Model of Neuroinflammation Designed to Mimic Delirium, Quetiapine Reduces Cortisol Secretion and Preserves Reversal Learning in the Attentional Set Shifting Task
Carr, Z. J., Miller, L., Ruiz-Velasco, V., Kunselman, A. R., & Karamchandani, K. (2019) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-019-09857-y · Cited by 9
Impact of daytime light intensity on the central orexin (hypocretin) system of a diurnal rodent ( Arvicanthis niloticus )
Lonstein, J. S., Linning‐Duffy, K., Tang, Y., Moody, A., & Yan, L. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15248 · Cited by 9
Rivastigmine improves isolation rearing-induced prepulse inhibition deficits via muscarinic acetylcholine receptors in mice
Higashino, K., Ago, Y., Umeki, T., Hasebe, S., Onaka, Y., Hashimoto, H., Takuma, K., & Matsuda, T. (2015) · Psychopharmacology · doi:10.1007/s00213-015-4123-7 · Cited by 9
Taste reactivity alterations after streptozotocin microinjection into the mediodorsal prefrontal cortex
Nagy, B., Takács, G., Szabó, I., Lénárd, L., & Karádi, Z. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.06.029 · Cited by 9
The role of nicotinic acetylcholine and opioid systems of the ventral orbital cortex in modulation of formalin-induced orofacial pain in rats
Yousofizadeh, S., Tamaddonfard, E., & Farshid, A. A. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.04.002 · Cited by 9
Chronic corticosterone treatment impairs trace conditioning in rats with a neonatal medial prefrontal cortex lesion
Enkel, T., & Koch, M. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.04.033 · Cited by 9
Regulation of 5-HT2A/C receptors and DOI-induced behaviors by protein kinase Cγ
BOWERS, B., Miyamoto-Ditmon, J., & Wehner, J. M. (2006) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2006.09.022 · Cited by 10
Patients with sickle-cell disease exhibit greater functional connectivity and centrality in the locus coeruleus compared to anemic controls
Bhatt, R. R., Zeltzer, L. K., Coloigner, J., Wood, J. C., Coates, T. D., & Labus, J. S. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101686 · Cited by 9
No cognitive processing in the unconscious, anesthetic‐like , state of sleep
Vertes, R. P., & Linley, S. B. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24963 · Cited by 10
The Man Who Turned Bad
Stein, D. J., & Moeller, F. G. (2005) · CNS Spectrums · doi:10.1017/s1092852900019404 · Cited by 9
Impact of chronic transcranial Random-Noise Stimulation (tRNS) on prefrontal cortex excitation-inhibition balance in juvenile micePreprint
Sánchez-León, C. A., Sánchez‐López, Á., Gómez‐Climent, M. Á., Cordones, I., Kadosh, R. C., & Márquez‐Ruiz, J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.04.282889 · Cited by 9
Correction: Integration of miRNA and Protein Profiling Reveals Coordinated Neuroadaptations in the Alcohol-Dependent Mouse Brain
Gorini, G., Núnez, Y. O., & Mayfield, R. D. (2013) · PLoS ONE · doi:10.1371/annotation/6286be0f-d729-495a-8a72-78995e9ceda7 · Cited by 9
Acetylcholine modulates the precision of prediction error in the auditory cortex
Pérez‐González, D., Lao-Rodríguez, A. B., Aedo, C., & Malmierca, M. S. (2023) · eLife · doi:10.7554/elife.91475 · Cited by 35
Androgen effects on mesoprefrontal dopamine systems in the adult male brain
Kritzer, M. F., Adler, A., & Locklear, M. N. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.07.001 · Cited by 8
Convergent and selective representations of pain, appetitive processes, aversive processes, and cognitive control in the insula
Kwon, M., Bo, K., Botvinik‐Nezer, R., Kragel, P. A., Oudenhove, L. V., Wager, T. D., Ashar, Y. K., Atlas, L. Y., Barrett, L. F., Becker, B., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-71568-9 · Cited by 10
Jujuboside A improves insomnia by maintaining mitochondrial homeostasis in prefrontal neurons
Zhang, Z., Che, X., Feng, T., Zou, J., Chen, G., Guo, W., Ma, C., Yuan, H., Chen, J., & Xu, X. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111372 · Cited by 8
Making and breaking habits: Revisiting the definitions and behavioral factors that influence habits in animals
Handel, S. N., & Smith, R. J. (2023) · Journal of the Experimental Analysis of Behavior · doi:10.1002/jeab.889 · Cited by 10
In relentless pursuit of the white whale: A role for the ventral midline thalamus in behavioral flexibility and adaption?
Panzer, É., Olmo, I. G., de Vasconcelos, A. P., Stéphan, A., & Cassel, J. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105762 · Cited by 9
Cognitive performance change of pediatric patients after conducting frontal transcortical approach to treat lateral ventricular tumor
Zhu, W., He, J., Xiang, L., Wang, L., Lü, Z., Li, C., & Gong, J. (2017) · Child s Nervous System · doi:10.1007/s00381-017-3604-x · Cited by 8
Neural oscillations in the infralimbic cortex after electrical stimulation of the amygdala. Relevance to acute stress processing
Luque‐García, A., Teruel‐Martí, V., Martínez‐Bellver, S., Adell, A., Cervera‐Ferri, A., & Martínez‐Ricós, J. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24416 · Cited by 7
Distinct regulation pattern of Egr-1, BDNF and Arc during morphine-withdrawal conditioned place aversion paradigm: Role of glucocorticoids
García‐Pérez, D., Ferenczi, S., Kovács, K., & Milanés, M. V. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.12.026 · Cited by 9
Problem-solving deficits in methcathinone use disorder
Zhang, H.-B., Zhao, D., Liu, Y., Wang, L., Yang, B., & Yuan, T. (2021) · Psychopharmacology · doi:10.1007/s00213-021-05874-z · Cited by 10
Binge Alcohol Drinking Alters Synaptic Processing of Executive and Emotional Information in Core Nucleus Accumbens Medium Spiny Neurons
Kolpakova, J., van der Vinne, V., Giménez‐Gómez, P., Le, T., You, I., Zhao-Shea, R., Velázquez‐Marrero, C., Tapper, A. R., & Martin, G. E. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.742207 · Cited by 7
Preferential in vivo inhibitory action of serotonin in rat infralimbic versus prelimbic cortex: relevance for antidepressant treatments
López-Terrones, E., Celada, P., Riga, M. S., & Artigas, F. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab396 · Cited by 8
Chronic oral d-galactose intake provokes age-related changes in the rat prefrontal cortex
Martinović, J., Kontić, M. Z., Dragić, M., Todorović, A., Stojanović, I. G., Mitrović, N., Grković, I., & Drakulić, D. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.114072 · Cited by 8
Nucleus Reuniens: Circuitry, Function, and Dysfunction
Vertes, R. P., Linley, S. B., & Viena, T. D. (2022) · Neuromethods · doi:10.1007/978-1-0716-2631-3_4 · Cited by 8
From concepts to treatment: a dialog between a preclinical researcher and a clinician in addiction medicine
Vandaele, Y., & Daeppen, J. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02177-5 · Cited by 8
MicroPET/CT assessment of FDG uptake in brain after long-term methylphenidate treatment in nonhuman primates
Zhang, X., Newport, G. D., Callicott, R. J., Liu, S., Thompson, J., Berridge, M. S., Apana, S. M., Slikker, W., Wang, C., & Paule, M. G. (2016) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2016.06.005 · Cited by 8
Do the rat anterior thalamic nuclei contribute to behavioural flexibility?
Kinnavane, L., Amin, E., Aggleton, J. P., & Nelson, A. J. D. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.10.012 · Cited by 8
Age-dependent effects of repeated methamphetamine exposure on locomotor activity and attentional function in rats
Nazari, A., Pérez-Fernández, C., Flores, P., Moreno, M., & Sánchez-Santed, F. (2020) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2020.172879 · Cited by 8
Neuroimaging, Adolescence, and Risky Behavior
Churchwell, J. C., & Yurgelun-Todd, D. A. (2011) · Springer eBooks · doi:10.1007/978-1-4419-1268-8_6 · Cited by 8
Direct and Indirect Mechanisms of Alcohol Teratogenesis: Implications for Understanding Alterations in Brain and Behavior in FASD
Uban, K. A., Bodnar, T. S., Butts, K. A., Sliwowska, J. H., Comeau, W. L., & Weinberg, J. (2010) · Health care and disease management · doi:10.1002/9783527632510.ch5 · Cited by 9
Prefrontal cortical ChAT-VIP interneurons provide local excitation by cholinergic synaptic transmission and control attention
Obermayer, J., Luchicchi, A., de Kloet, S. F., Terra, H., Bruinsma, B., Heistek, T. S., Mnie-Filali, O., Kortleven, C., Kroon, T., Jonker, A. J., et al. (2018) · doi:10.1101/461723 · Cited by 83
Sex-specific alterations in corticotropin-releasing factor regulation of coerulear-cortical network activity
Bates, M. L. S., Arner, J. R., Curtis, A. L., Valentino, R., & Bhatnagar, S. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109317 · Cited by 7
Neuronal activity underlying vocal production in bats
Babl, S. S., Kiai, A., García‐Rosales, F., & Hechavarría, J. C. (2025) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.15410 · Cited by 7
Central Thalamic-Medial Prefrontal Control of Adaptive Responding in the Rat: Many Players in the Chamber
Mair, R. G., Francoeur, M. J., & Gibson, B. M. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.642204 · Cited by 8
Naloxone increases conditioned fear responses during social buffering in male rats
Yamasaki, T., Kiyokawa, Y., Munetomo, A., & Takeuchi, Y. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16343 · Cited by 7
Effects of adolescent alcohol exposure on oligodendrocyte lineage cells and myelination in mice: Age and subregion differences
Huang, D., Li, M., Qiao, Z., Zhou, H., Cai, Y., Li, X., Zhang, Z., & Zhou, J. (2024) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2024.06.006 · Cited by 7
Neural processing of auditory stimuli in rats: Translational aspects using auditory oddball paradigms
Decker, F. M., Jelinek, J., Korb, K., Kamgaing, F. F., Alam, M., Krauss, J. K., Hermann, E. J., & Schwabe, K. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.115428 · Cited by 7
Spatial discrimination reversal and incremental repeated acquisition in adolescent and adult BALB/c mice
Shen, A. N., Pope, D. A., Hutsell, B. A., & Newland, M. C. (2015) · Behavioural Processes · doi:10.1016/j.beproc.2015.06.005 · Cited by 7
Animal Models in Addiction Research
Belin, D., & Dalley, J. W. (2012) · Springer eBooks · doi:10.1007/978-1-4614-3375-0_6 · Cited by 7
Self-citation
Animal Models of Depression – Where Are We Going?
Slattery, D. A., & Cryan, J. F. (2010) · Modern trends in psychiatry · doi:10.1159/000319511 · Cited by 7
Organizing activity of Fgf8 on the anterior telencephalon
Sato, T., Kikkawa, T., Saito, T., Itoi, K., & Osumi, N. (2017) · Development Growth & Differentiation · doi:10.1111/dgd.12411 · Cited by 7
Neurobiological and Ecological Correlates of Avian Innovation
Audet, J. (2020) · Integrative and Comparative Biology · doi:10.1093/icb/icaa107 · Cited by 7
[Effect of spinal manipulation on brain functional activity in patients with lumbar disc herniation].
Yuan, W.-A., Shen, Z., Xue, L., Tan, W., Cheng, Y.-W., Zhan, S., & Zhan, H. (2015) · PubMed Central · doi:10.3785/j.issn.1008-9292.2015.03.002 · Cited by 7
Fos immunolabelling evidence for brain regions involved in the Pavlovian degraded contingency effect and in its disruption by atropine.
Carnicella, S., de Vasconcelos, A. P., Pain, L., Majchrzak, M., & Oberling, P. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.03.005 · Cited by 4
A stable, distributed code for cue value in mouse cortex during reward learningPreprint
Ottenheimer, D. J., Hjort, M. M., Bowen, A. J., Steinmetz, N. A., & Stuber, G. D. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.13.499930 · Cited by 7
Beta and High Gamma Oscillations in the Cortico-striatal Network Reflect Reward Certainty on a Probabilistic Reversal Learning Task
Koloski, M. F., Salimi, M., Hulyalkar, S., Tang, T., Barnes, S. A., Mishra, J., & Ramanathan, D. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0858-25.2025 · Cited by 7
Disrupted synapses: prefrontal cortex-reward circuit dysfunction in stress-induced depression-like behaviors
Mahmud, A., & Karaman, M. A. (2026) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2026.1843871 · Cited by 7
Modulation of prefrontal couplings by prior belief-related responses in ventromedial prefrontal cortex
Wang, B., Drammis, S. M., Hummos, A., Halassa, M. M., & Pleger, B. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1278096 · Cited by 7
A Prefrontal→Periaqueductal Gray Pathway Differentially Engages Autonomic, Hormonal, and Behavioral Features of the Stress-Coping Response
Skog, T. D., Johnson, S. B., Hinz, D. C., Lingg, R. T., Schulz, E. N., Luna, J. T., Beltz, T. G., Romig‐Martin, S. A., Gantz, S. C., Xue, B., et al. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0844-24.2024 · Cited by 6
Prelimbic cortex is involved in the regulation of morphine-induced conditioned place preference in both resistant and sensitive mice
Zheng, R., Chen, Y., Zhang, J., Liu, Q., Zheng, Y., & Wang, Z. (2025) · Scientific Reports · doi:10.1038/s41598-025-87084-7 · Cited by 6
Morphine-induced place preference affects mRNA expression of G protein α subunits in rat brain
Zelek-Molik, A., Bielawski, A., Kreiner, G., Popik, P., Vetulani, J., & Nalepa, I. (2012) · Pharmacological Reports · doi:10.1016/s1734-1140(12)70850-2 · Cited by 6
Discretion for behavioral selection affects development of habit formation after extended training in rats
Soma, S., Suematsu, N., Yoshida, J., Ríos, A., & Shimegi, S. (2018) · Behavioural Processes · doi:10.1016/j.beproc.2018.10.014 · Cited by 6
Methamphetamine and Modulation Functionality of the Prelimbic Cortex for Developing a Possible Treatment of Alzheimer’s Disease in an Animal Model
Shyu, B., Gao, Z.-Y., Wu, J. J.-S., He, A. B. H., Cheng, C.-N., & Huang, A. C. W. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.751913 · Cited by 6
Long-term efavirenz exposure induced neuroinflammation and cognitive deficits in C57BL/6 mice
Zhang, R., Bao, J., Qiao, J., Li, W., Qian, F., Hu, K., & Sun, B. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2021.11.015 · Cited by 6
Adolescent neurostimulation of dopamine circuit reverses genetic deficits in frontal cortex function
Mastwal, S. S., Li, X., Stowell, R. D., Manion, M. T. C., Zhang, W., Kim, N., Yoon, K., Song, H., Ming, G., & Wang, K. H. (2023) · eLife · doi:10.7554/elife.87414 · Cited by 14
Methylmercury and Fish Nutrients in Experimental Models
Newland, M. C. (2012) · Springer eBooks · doi:10.1007/978-1-4614-2383-6_4 · Cited by 6
Distinct Changes in CREB Phosphorylation in Frontal Cortex and Striatum During Contingent and Non-Contingent Performance of a Visual Attention Task
Pozzi, L., Sacchetti, G., Agnoli, L., Mainolfi, P., Invernizzi, R. W., & Carli, M. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00065 · Cited by 6
Neurological approaches for investigating West Nile virus disease and its treatment in rodents
Morrey, J. D., Siddharthan, V., & Wang, H. (2013) · Antiviral Research · doi:10.1016/j.antiviral.2013.09.010 · Cited by 6
Perspectives Emerging From Neuroscience on How People Become Addicted and What to Do About It
Littrell, J. L. (2010) · Journal of Social Work Practice in the Addictions · doi:10.1080/1533256x.2010.498741 · Cited by 6
Neonatal Medial Frontal Cortex Lesions Disrupt Circadian Activity Patterns
Phillips, C. I., Smith, V. M., Antle, M. C., & Dyck, R. H. (2009) · Developmental Neuroscience · doi:10.1159/000232559 · Cited by 6
Quinolinic acid-immunoreactivity in the naïve mouse brain
Lopez, Y. P., Kenis, G., Rutten, B. P. F., Myint, A.-M., Steinbusch, H. W. M., & van den Hove, D. (2015) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2015.10.010 · Cited by 6
Knockout and Mutant Rats
Müller, M., Olivier, J., & Homberg, J. R. (2009) · Neuromethods · doi:10.1007/978-1-60761-474-6_2 · Cited by 4
Reward Mechanisms Across Aggressive and Addictive Forms of Externalizing Psychopathology
Venables, N. C. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.06.028 · Cited by 6
Adversity in early adolescence promotes an enduring anxious phenotype and increases serotonergic innervation of the infralimbic medial prefrontal cortex
Tao, C. S., Dhamija, P., Booij, L., & Menard, J. L. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.09.004 · Cited by 7
Phencyclidine-induced cognitive impairments in repeated touchscreen visual reversal learning tests in rats
Savolainen, K., Ihalainen, J. A., Hämäläinen, E., Tanila, H., & Forsberg, M. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.113057 · Cited by 6
Frontal-Sensory Cortical Projections Become Dispensable for Attentional Performance Upon a Reduction of Task Demand in Mice
Norman, K. J., Bateh, J., Maccario, P., Cho, C., Caro, K., Nishioka, T., Koike, H., & Morishita, H. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.775256 · Cited by 6
Mutations of tyrosine 467 in the human norepinephrine transporter attenuate HIV-1 Tat-induced inhibition of dopamine transport while retaining physiological function
Strauss, M. J., Porter, K. D., Quizon, P. M., Davis, S. E., Lin, S., Yuan, Y., Martínez-Muñiz, G. A., Sun, W., Zhan, C., & Zhu, J. (2022) · PLoS ONE · doi:10.1371/journal.pone.0275182 · Cited by 6
Effects of Intermittent Hypoxia on Neurological Function
Gozal, D. (2009) · Contemporary clinical neuroscience · doi:10.1007/978-1-60327-579-8_9 · Cited by 6
Using Preclinical Models to Understand the Neural Basis of Negative Urgency
Bardo, M. T., Weiss, V. G., & Rebec, G. V. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813693-5.00001-0 · Cited by 6
Incoordination between spikes and LFPs in Aβ1−42-mediated memory deficits in rats
Bai, W., Hu, Y., Liu, T., Wei, J., & Tian, X. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00411 · Cited by 6
Cortical asymmetry: catching an object in free fall
Velasques, B., Machado, S. E. D. C., Portella, C. E., Silva, J. G., Terra, P., Ferreira, C., Basile, L., Cagy, M., Piedade, R. A. M., & Ribeiro, P. F. M. (2007) · Arquivos de Neuro-Psiquiatria · doi:10.1590/s0004-282x2007000400015 · Cited by 6
Effects of perinatal undernutrition on the basilar dendritic arbor of the anterior cingulate pyramidal neurons in lactating dams
Salas, M., Torrero, C., Regalado, M., & Rubio, L. (2015) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2015-2042 · Cited by 6
Repeated diazepam administration reversed working memory impairments and glucocorticoid alterations in the prefrontal cortex after short but not long alcohol-withdrawal periods
Dominguez, G., Henkous, N., Piérard, C., Belzung, C., Mons, N. E., & Béracochéa, D. (2018) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-018-0595-3 · Cited by 6

Authors: Dalley, J. W., Cardinal, R. N., & Robbins, T. W.
Affiliations: University of Cambridge (GB)
Corresponding author: Dalley, Jeffrey W.
ORCID: Dalley, Jeffrey W.
Cardinal, Rudolf N.
Robbins, Trevor W.
Venue: Neuroscience & Biobehavioral Reviews
Publisher: Elsevier BV
Published: 2004-01
Volume: 28
Issue: 7
Pages: 771-784
ISSN: 0149-7634 (ISSN-L)
DOI: 10.1016/j.neubiorev.2004.09.006
OpenAlex: W2140549509
Cited by: 1,329
References: 141
Citations by year: 2026: 30 · 2025: 36 · 2024: 39 · 2023: 49 · 2022: 42 · 2021: 59 · 2020: 57 · 2019: 53 · 2018: 80 · 2017: 78 · 2016: 61 · 2015: 79 · 2014: 63 · 2013: 83 · 2012: 79
FWCI: 4.27
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Neuroscience & Biobehavioral Reviews (publishedVersion)
PubMed (publishedVersion)
Funders: Wellcome Trust
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Keywords: prefrontal cortex, executive function, cognitive function, dorsomedial prefrontal cortex, ventromedial prefrontal cortex, orbitofrontal cortex, anterior cingulate cortex, prelimbic cortex, infralimbic cortex, working memory, decision-making, set-shifting, behavioral flexibility, reversal learning, neuromodulatory systems
MeSH terms: Acetylcholine, Animals, Brain Chemistry, Cognition, Decision Making, Memory, Short-Term, Motor Activity, Norepinephrine, Problem Solving, Reaction Time, Prefrontal Cortex

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

Prefrontal executive and cognitive functions in rodents: neural and neurochemical substrates

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks