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Prefrontal executive and cognitive functions in rodents: neural and neurochemical substrates
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.
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“Like in primates, the PFC in rodents is considered to participate in functions such as attention, decision making and memory (Chudasama, 2011; Dalley et al., 2004; Preston and Eichenbaum, 2013).”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Dalley et al., 2004
In the citing paper
“The rodent mPFC can be anatomically divided into three subareas, namely the anterior cingulate cortex (ACC), prelimbic cortex (PLC) and infralimbic cortex (ILC), which are located along the dorsal – ventral axis (Dalley et al., 2004; Gabbott et al., 2005), and are reciprocally interconnected (Heidbreder and Groenewegen, 2003).”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Dalley et al., 2004
Citations
Cites
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
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
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-citationEvenden, 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
Research works printed but not linked: 1
- Sagvolden, 1998, Attention deficit/hyperactivity disorder—from brain dysfunctions to behavior, Behav Brain Res, 94, 1
Cited by
Sorted by citations
Items 601–700 of 998
Hockley, A. D., Bohórquez, L. H., & Malmierca, M. S. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115538 · Cited by 27
Increases of theta–low gamma coupling in rat medial prefrontal cortex during working memory task
Li, S., Bai, W., Liu, T., Hu, Y., & Tian, X. (2012) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2012.07.012 · Cited by 29
Amygdala afferents monosynaptically innervate corticospinal neurons in rat medial prefrontal cortex
Gabbott, P. L. A., Warner, T., Brown, J. Y., Salway, P., Gabbott, T., & Busby, S. J. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23047 · Cited by 29
Ramon‐Duaso, C., Gener, T., Consegal, M., Fernández-Avilés, C., Gallego, J., Castarlenas, L., Swanson, M. S., de la Torre, R., Maldonado, R. J., Puig, M. V., et al. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy164 · Cited by 32
Peng, X., & Burwell, R. D. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107520 · Cited by 29
Li, X., Hong, F.-F., Tu, Y., Li, Y., Ma, C., Yu, C., Li, F., Chen, J., Li, Z., Bao, S.-J., et al. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113929 · Cited by 29
Tian, M. K., Bailey, C. D. C., Biasi, M. D., Picciotto, M. R., & Lambe, E. K. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3600-11.2011 · Cited by 29
Impact of anxiety profiles on cognitive performance in BALB/c and 129P2 mice
Salomons, A. R., Arndt, S. S., & Ohl, F. (2012) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-012-0109-7 · Cited by 29
Effects of methamphetamine on sexual performance and compulsive sex behavior in male rats
Frohmader, K. S., Bateman, K. L., Lehman, M. N., & Coolen, L. M. (2010) · Psychopharmacology · doi:10.1007/s00213-010-1930-8 · Cited by 29
Dominguez, G., Belzung, C., Piérard, C., David, V., Henkous, N., Decorte, L., Mons, N. E., & Béracochéa, D. (2016) · Addiction Biology · doi:10.1111/adb.12371 · Cited by 31
Shinohara, F., Kamii, H., Minami, M., & Kaneda, K. (2017) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b17-00614 · Cited by 28
Novick, A. M., Forster, G. L., Hassell, J. E., Davies, D. R., Scholl, J. L., Renner, K. J., & Watt, M. J. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.05.032 · Cited by 29
Claustral Projections to Anterior Cingulate Cortex Modulate Engagement with the External WorldPreprint
Atlan, G., Matosevich, N., Peretz‐Rivlin, N., Marsh‐Yvgi, I., Chen, E., Kleinman, T., Bleistein, N., Sheinbach, E., Groysman, M., Nir, Y., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.06.17.448649 · Cited by 29
Moorman, D. E., & Aston‐Jones, G. (2022) · Psychopharmacology · doi:10.1007/s00213-022-06287-2 · Cited by 31
Dulka, B. N., Bress, K. S., Grizzell, J. A., & Cooper, M. A. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.07.042 · Cited by 27
Electroencephalogram-Based Brain-Computer Interface for Internet of Robotic Things
Katona, J., Ujbányi, T., Sziládi, G., & Kővári, A. (2018) · Topics in intelligent engineering and informatics · doi:10.1007/978-3-319-95996-2_12 · Cited by 28
Chronic oral methylphenidate treatment increases microglial activation in rats
Carias, E., Hamilton, J., Robison, L. S., Delis, F., Eiden, R. D., Quattrin, T., Hadjiargyrou, M., Komatsu, D. E., & Thanos, P. K. (2018) · Journal of Neural Transmission · doi:10.1007/s00702-018-1931-z · Cited by 30
Linsenbardt, D. N., Timme, N. M., & Lapish, C. C. (2019) · eNeuro · doi:10.1523/eneuro.0489-18.2019 · Cited by 29
Savulich, G., Hezemans, F. H., Grothe, S. V. G., Dafflon, J., Schulten, N., Brühl, A. B., Sahakian, B. J., & Robbins, T. W. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0634-z · Cited by 29
Self-citationEvolution of stress responses refine mechanisms of social rank
Korzan, W. J., & Summers, C. H. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2021.100328 · Cited by 30
Cortical GluN2B deletion attenuates punished suppression of food reward-seeking
Radke, A. K., Nakazawa, K., & Holmes, A. (2015) · Psychopharmacology · doi:10.1007/s00213-015-4033-8 · Cited by 29
Stress-Induced Deficits in Cognition and Emotionality: A Role for Glutamate
Graybeal, C., Kiselycznyk, C., & Holmes, A. (2011) · Current topics in behavioral neurosciences · doi:10.1007/7854_2011_193 · Cited by 30
Locklear, M. N., Cohen, A. B., Jone, A., & Kritzer, M. F. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu222 · Cited by 28
Prior chronic cocaine exposure in mice induces persistent alterations in cognitive function
Krueger‐Burg, D., Howell, J. L., Oo, H., Olausson, P., Taylor, J. R., & Nairn, A. C. (2009) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e328333a2bb · Cited by 28
Plasse, G., Fors, S. S. B. M. L., Meerkerk, D. T. J., Joosten, R. N. J. M. A., Uylings, H. B. M., & Feenstra, M. G. P. (2007) · Psychopharmacology · doi:10.1007/s00213-007-0917-6 · Cited by 28
Thomsen, M. S., Mikkelsen, J. D., Timmermann, D. B., Peters, D., Hay‐Schmidt, A., Martens, H., & Hansen, H. H. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.03.083 · Cited by 28
Feja, M., & Koch, M. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3763-3 · Cited by 28
Sun, J., Han, X., Xianguo, R., Dongqi, Y., Rongyi, Z., Shuang, L., You, Y., Yuchen, S., & Jingnan, Y. (2017) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2017/2695903 · Cited by 28
Talpos, J. C., & Shoaib, M. C. (2015) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-16522-6_6 · Cited by 27
Bandyopadhya, R. S., Datta, S., & Saha, S. G. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2173-06.2006 · Cited by 28
Behavioral and Cognitive Testing Procedures in Animal Models of Epilepsy
Stafstrom, C. E. (2006) · Elsevier eBooks · doi:10.1016/b978-012088554-1/50051-7 · Cited by 28
Putative Microcircuit-Level Substrates for Attention Are Disrupted in Mouse Models of Autism
Luongo, F. J., Horn, M. E., & Sohal, V. S. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.04.014 · Cited by 28
Heidbreder, C. A. (2012) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-012-0803-6 · Cited by 28
Newland, M. C., Hoffman, D. J., Heath, J. C., & Donlin, W. D. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.05.038 · Cited by 29
Farooq, U., Rajkumar, R., Sukumaran, S., Wu, Y., Tan, W. H., & Dawe, G. S. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12242 · Cited by 27
Dopamine effects on stress-induced working memory deficits
Bahari, Z., Meftahi, G. H., & Meftahi, M. A. (2018) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000429 · Cited by 29
Oleson, E. B., Hamilton, L. R., & Gomez, D. M. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.660218 · Cited by 28
Souza, R., Bueno, D., Lima, L. B., Muchon, M. J., Gonçalves, L., Donato, J., Shammah‐Lagnado, S. J., & Metzger, M. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02538-2 · Cited by 30
Zheng, C., Quan, M., & Zhang, T. (2012) · Journal of Computational Neuroscience · doi:10.1007/s10827-012-0400-1 · Cited by 27
Hunter, D., Hazel, S. J., Kind, K. L., Liu, H., Marini, D., Owens, J. A., Pitcher, J. B., & Gatford, K. L. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.11.037 · Cited by 27
Auclair, A. L., Besnard, J., Newman‐Tancredi, A., & Depoortère, R. (2009) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2009.01.005 · Cited by 30
Dwyer, J. M., Platt, B. J., Rizzo, S. J. S., Pulicicchio, C. M., Wantuch, C., Zhang, M.-Y., Cummons, T. A., Leventhal, L., Bender, C. N., Zhang, J., et al. (2010) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145709991088 · Cited by 27
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Devilbiss, D. M., Spencer, R. C., & Berridge, C. W. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw140 · Cited by 30
Lipaus, I. F. S., Gomes, E. F., Martins, C. W., Martins-Silva, C., Pires, R. G. W., Malgarin, F., Schuck, P. F., Nakamura-Palacios, E. M., & Rodrigues, L. C. D. M. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.06.020 · Cited by 28
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Rodriguiz, R. M., & Wetsel, W. C. (2006) · Frontiers in neuroscience · doi:10.1201/9781420004335.ch12 · Cited by 27
Chauveau, F., Laudereau, K., Libourel, P., Gervasoni, D., Thomasson, J., Poly‐Thomasson, B., Piérard, C., & Béracochéa, D. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.04.017 · Cited by 27
Jiang, S., Li, H., Liu, L., Yao, D., & Luo, C. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210325130624 · Cited by 27
Sheynikhovich, D., Otani, S., Bai, J., & Arleo, A. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.1068271 · Cited by 31
Xue, X., Shao, S., Wang, W., & Shao, F. (2013) · Neuropsychobiology · doi:10.1159/000356188 · Cited by 26
Fitzgerald, P. J. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.04.003 · Cited by 29
Adams, W. K., Levesque, D. L., Cocker, P. J., Kaur, S., Bodnar, T. S., Young, A. H., & Winstanley, C. A. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.07.018 · Cited by 27
Camp, M., Mayfield, R. D., McCracken, M. L., McCracken, L. M., & Alcantara, A. A. (2006) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2006.00160.x · Cited by 26
Kristensen, S. E., Thomsen, M. S., Hansen, H. H., Timmermann, D. B., Hay‐Schmidt, A., & Mikkelsen, J. D. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.03.016 · Cited by 26
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Klarer, M., Weber-Stadlbauer, U., Arnold, M., Langhans, W., & Meyer, U. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.05.006 · Cited by 25
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Sidorov, M. S., Judson, M. C., Kim, H., Rougie, M., Ferrer, A. I., Nikolova, V. D., Riddick, N. V., Moy, S. S., & Philpot, B. D. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.2828-17.2018 · Cited by 25
Shah, D., Verhoye, M., Van der Linden, A., & D’Hooge, R. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhy329 · Cited by 25
Chen, X.-P., Chen, W.-Z., Wang, F.-S., & Liu, J. (2012) · Brain Research · doi:10.1016/j.brainres.2012.07.036 · Cited by 25
Flores-Martínez, E., & Peña‐Ortega, F. (2017) · International Journal of Peptides · doi:10.1155/2017/7386809 · Cited by 26
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Prouty, E. W., Chandler, D. J., & Waterhouse, B. D. (2017) · Brain Research · doi:10.1016/j.brainres.2017.08.031 · Cited by 25
Himmler, B. T., Mychasiuk, R., Nakahashi, A., Himmler, S. M., Pellis, S. M., & Kolb, B. E. (2017) · Synapse · doi:10.1002/syn.22022 · Cited by 25
Strauss, M. J., O’Donovan, B., Ma, Y., Xiao, Z., Lin, S., Bardo, M. T., Ortinski, P. I., McLaughlin, J. P., & Zhu, J. (2020) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.120.266023 · Cited by 25
Sánchez-León, C. A., Sánchez‐López, Á., Gómez‐Climent, M. Á., Cordones, I., Kadosh, R. C., & Márquez‐Ruiz, J. (2021) · Progress in brain research · doi:10.1016/bs.pbr.2021.01.017 · Cited by 29
Esaki, H., Izumi, S., Fukao, A., Ito, S., Nishitani, N., Deyama, S., & Kaneda, K. (2021) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b21-00314 · Cited by 25
Where Actions Meet Outcomes: Medial Prefrontal Cortex, Central Thalamus, and the Basal Ganglia
Mair, R. G., Francoeur, M. J., Krell, E. M., & Gibson, B. M. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.928610 · Cited by 38
Marquis, J., Goulet, S.-M., & Doré, F. Y. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.02.048 · Cited by 27
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Ehman, K. D., Phillips, P. M., McDaniel, K. L., Barone, S., & MOSER, V. C. (2007) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2007.07.004 · Cited by 25
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Bueno-Júnior, L. S., Lopes‐Aguiar, C., Ruggiero, R. N., Romcy-Pereira, R. N., & Leite, J. P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0047484 · Cited by 26
Humpston, C. S., Wood, C. M., & Robinson, E. S. J. (2012) · Journal of Psychopharmacology · doi:10.1177/0269881112466182 · Cited by 26
Linsenbardt, D. N., Smoker, M. P., Janetsian-Fritz, S. S., & Lapish, C. C. (2016) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-016-0475-7 · Cited by 25
Boomhower, S. R., & Newland, M. C. (2017) · Experimental and Clinical Psychopharmacology · doi:10.1037/pha0000107 · Cited by 25
Cannella, N., Cosa‐Linan, A., Roscher, M., Takahashi, T. T., Vogler, N., Wängler, B., & Spanagel, R. (2017) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2017.00218 · Cited by 25
Reichert, M. S., Crofts, S., Davidson, G. L., Firth, J. A., Kulahci, I. G., & Quinn, J. L. (2020) · Royal Society Open Science · doi:10.1098/rsos.192107 · Cited by 25
Altabella, L., Zoratto, F., Adriani, W., & Canese, R. (2014) · American Journal of Neuroradiology · doi:10.3174/ajnr.a3843 · Cited by 25
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Robbins, T. W. (2005) · Cited by 25
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Newland, M. C., Reed, M. N., & Rasmussen, E. B. (2015) · Behavioural Processes · doi:10.1016/j.beproc.2015.03.007 · Cited by 24
Miller, E. M., Quintero, J. E., Pomerleau, F., Huettl, P. F., Gerhardt, G. A., & Glaser, P. E. A. (2015) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2015.01.018 · Cited by 24
Navailles, S., Guillem, K., Vouillac‐Mendoza, C., & Ahmed, S. H. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu112 · Cited by 26
Theta frequency prefrontal–hippocampal driving relationship during free exploration in mice
Zhan, Y. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.05.063 · Cited by 24
Shtemberg, A. S., Kokhan, V. S., Кудрин, В. С., Матвеева, М. И., Lebedeva-Georgievskaya, K. D., Тимошенко, Г. Н., Molokanov, A. G., Krasavin, E. A., Наркевич, В. Б., Михайлович, К. П., et al. (2015) · Neurochemical Journal · doi:10.1134/s1819712415010109 · Cited by 24
Neuro-anatomic mapping of dopamine D1 receptor involvement in nicotine self-administration in rats
Hall, B. J., Slade, S. K., Allenby, C. E., Kutlu, M. G., & Levin, E. D. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.03.005 · Cited by 26
Milot, M. R., & Plamondon, H. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.02.017 · Cited by 24
The Habitual Brain: An “Adapted Habit” Theory of Substance Use Disorders
Newlin, D. B., & Strubler, K. A. (2007) · Substance Use & Misuse · doi:10.1080/10826080601144606 · Cited by 26
Rachidi, M., Delezoide, A., Delabar, J. M., & Lopes, C. (2009) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2009.02.001 · Cited by 24
Wood, C., Kohli, S., Malcolm, E. M., Allison, C., & Shoaib, M. C. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.01.006 · Cited by 27
Rathod, R. S., Khaire, A. A., Kale, A. A., & Joshi, S. (2016) · Biochimie · doi:10.1016/j.biochi.2016.08.009 · Cited by 27
Ventromedial prefrontal cortex mediates sex differences in persistent cognitive drive for food
Anderson, L. C., & Petrovich, G. D. (2018) · Scientific Reports · doi:10.1038/s41598-018-20553-4 · Cited by 24
Giangrasso, D. M., Furlong, T. M., & Keefe, K. A. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104673 · Cited by 24
Salimi, M., Ghazvineh, S., Nazari, M., Dehdar, K., Garousi, M., Zare, M., Tabasi, F., Jamaati, H., Salimi, A., Barkley, V., et al. (2021) · Brain Research · doi:10.1016/j.brainres.2021.147368 · Cited by 24
Selective dopamine D3receptor antagonists. A decade of progress: 1997 – 2007
Micheli, F., & Heidbreder, C. A. (2008) · Expert Opinion on Therapeutic Patents · doi:10.1517/13543776.18.8.821 · Cited by 24
Brain processes in discounting: consequences of adolescent methylphenidate exposure.
Adriani, W., Zoratto, F., & Laviola, G. (2012) · Current topics in behavioral neurosciences · doi:10.1007/7854_2011_156 · Cited by 23
Schmitz, F., Pierozan, P., Rodrigues, A. F., Biasibetti, H., Coelho, D. D. M., Mussulini, B. H. M., Pereira, M. S. L., Parisi, M. M., Barbé‐Tuana, F. M., de Oliveira, D. L., et al. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9219-x · Cited by 24
León-Domínguez, U., Vela‐Bueno, A., Froufe, M., & León‐Carrión, J. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.03.012 · Cited by 25
Wanchoo, S. J., Lee, M. J., Swann, A. C., & Dafny, N. (2009) · Brain Research · doi:10.1016/j.brainres.2009.11.035 · Cited by 23
Lejeune, S., Dourmap, N., Martres, M., Bruno Giros, A., Daugé, V., & Naudon, L. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.10.005 · Cited by 23
Finding prefrontal cortex in the rat
Leonard, C. M. (2016) · Brain Research · doi:10.1016/j.brainres.2016.02.002 · Cited by 23
Inhibitory Control and Drug Abuse Prevention
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Metadata
- Authors
- Dalley, J. W., Cardinal, R. N., & Robbins, T. W.
- Affiliations
- University of Cambridge (GB)
- Corresponding author
- Dalley, Jeffrey W.
- Venue
- Neuroscience & Biobehavioral Reviews
- Publisher
- Elsevier BV
- Published
- 2004-01
- Volume
- 28
- Issue
- 7
- Pages
- 771-784
- ISSN
- 0149-7634 (ISSN-L)
- 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
- 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
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