Dissociable Contributions of the Orbitofrontal and Infralimbic Cortex to Pavlovian Autoshaping and Discrimination Reversal Learning: Further Evidence for the Functional Heterogeneity of the Rodent Frontal Cortex
Open accessAbstract
To examine possible heterogeneity of function within the ventral regions of the rodent frontal cortex, the present study compared the effects of excitotoxic lesions of the orbitofrontal cortex (OFC) and the infralimbic cortex (ILC) on pavlovian autoshaping and discrimination reversal learning. During the pavlovian autoshaping task, in which rats learn to approach a stimulus predictive of reward [conditional stimulus (CS+)], only the OFC group failed to acquire discriminated approach but was unimpaired when preoperatively trained. In the visual discrimination learning and reversal task, rats were initially required to discriminate a stimulus positively associated with reward. There was no effect of either OFC or ILC lesions on discrimination learning. When the stimulus-reward contingencies were reversed, both groups of animals committed more errors, but only the OFC-lesioned animals were unable to suppress the previously rewarded stimulus-reward association, committing more "stimulus perseverative" errors. In contrast, the ILC group showed a pattern of errors that was more attributable to "learning" than perseveration. These findings suggest two types of dissociation between the effects of OFC and ILC lesions: (1) OFC lesions impaired the learning processes implicated in pavlovian autoshaping but not instrumental simultaneous discrimination learning, whereas ILC lesions were unimpaired at autoshaping and their reversal learning deficit did not reflect perseveration, and (2) OFC lesions induced perseverative responding in reversal learning but did not disinhibit responses to pavlovian CS-. In contrast, the ILC lesion had no effect on response inhibitory control in either of these settings. The findings are discussed in the context of dissociable executive functions in ventral sectors of the rat prefrontal cortex.
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The lateral and medial orbitofrontal cortex have been linked to associative learning, decision making, and reversal learning.
“Consistent with the idea that the OFC unites internal and external sensory information, the lateral OFC and the medial OFC have been linked to associative learning (Rolls et al. 1994; 1996) decision making (e.g., Bechara et al. 1996; 2000; Koenigs et al. 2007) and reversal learning, in which the reward values associated with choice options are reversed and animals must learn the current reward”
From The brain basis of emotion: a meta-analytic review (2012) · cites this paper as Chudasama & Robbins 2003
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Cites
Insensitivity to future consequences following damage to human prefrontal cortex
Bechara, A., Damasio, A. R., Damasio, H., & Anderson, S. W. (1994) · Cognition · doi:10.1016/0010-0277(94)90018-3 · Cited by 6,128 · see citing works
Different contributions of the human amygdala and ventromedial prefrontal cortex to decision-making
Bechara, A., Damasio, H., Damasio, A. R., & Lee, G. P. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05473.1999 · Cited by 2,001 · see citing works
Dissociation in prefrontal cortex of affective and attentional shifts
Dias, R., Robbins, T. W., & Roberts, A. C. (1996) · Nature · doi:10.1038/380069a0 · Cited by 1,527 · see citing works
Self-citationA developmental functional MRI study of prefrontal activation during performance of a go-no-go task
Casey, B. J., Trainor, R. J., Orendi, J. L., Schubert, A. B., Nystrom, L. E., Giedd, J. N., Castellanos, F. X., Haxby, J. V., Noll, D. C., Cohen, J. D., et al. (1997) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1997.9.6.835 · Cited by 1,106 · see citing works
Rolls, E. T., Hornak, J., Wade, D., & McGrath, J. (1994) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.57.12.1518 · Cited by 1,005 · see citing works
Motivational control of goal-directed action
Dickinson, A., & Balleine, B. (1994) · Animal Learning & Behavior · doi:10.3758/bf03199951 · Cited by 995 · see citing works
Efferent projections of the infralimbic cortex of the rat
Hurley, K. M., Herbert, H., Moga, M. M., & Saper, C. B. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903080210 · Cited by 777 · see citing works
Cardinal, R. N., Parkinson, J. A., Lachenal, G., Halkerston, K. M., Rudarakanchana, N., Hall, J., Morrison, C. H., Howes, S. R., Robbins, T. W., & Everitt, B. J. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.4.553 · Cited by 201 · see citing works
Self-citation
Flagged first, then by citations
Research works printed but not linked: 6
- Brutkowski S (1964) Prefrontal cortex and drive inhibition. In: The frontal granular cortex and behaviour (Warren JM, Akert K, eds), pp 242-270. New York: McGraw-Hill.
- Chudasama Y, Passetti F, Rhodes SEV, Lopian D, Desai A, Robbins TW (2003) Dissociable aspects of performance on the 5 choice serial reaction time task following lesions of the dorsal anterior cingulate, infralimbic, and orbitofrontal cortex in the rat: differential effects on selectivity, im- pulsivity, and compulsivity. Behav Brain Res, in press.
- Mackintosh NJ (1983) Conditioning and associative learning. Oxford: Clarendon.
- Macmillan NA, Creelman CD (1991) Detection theory: a user's guide. Cam- bridge, UK: Cambridge UP.
- Mishkin M (1964) Perseveration of central sets after frontal lesions in man. In: The frontal granular cortex and behaviour (Warren JM, Akert K, eds), pp 313-334. New York: McGraw-Hill.
- Winer BJ (1971) Statistical principles in experimental design, Ed 2. New York: McGraw-Hill.
Cited by
Sorted by citations
The brain basis of emotion: a meta-analytic review
Lindquist, K. A., Wager, T. D., Kober, H., Bliss-Moreau, E., & Barrett, L. F. (2012) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000446 · Cited by 2,320 · see citing works
“…1994; 1996) decision making (e.g., Bechara et al. 1996; 2000; Koenigs et al. 2007) and reversal learning, in which the reward values associated with choice options are reversed and animals must learn the current reward value (Chudasama & Robbins 2003; Hornak et al. 2004; Rudebeck & Murray 2008).”
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Bari, A., & Robbins, T. W. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.06.005 · Cited by 1,921 · see citing works
Self-citationPrefrontal executive and cognitive functions in rodents: neural and neurochemical substrates
Dalley, J. W., Cardinal, R. N., & Robbins, T. W. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.09.006 · Cited by 1,329 · see citing works
Self-citationGalvan, A., Hare, T. A., Parra, C. E., Penn, J., Voss, H., Glover, G., & Casey, B. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1062-06.2006 · Cited by 1,282 · see citing works
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Everitt, B. J., & Robbins, T. W. (2016) · Annual Review of Psychology · doi:10.1146/annurev-psych-122414-033457 · Cited by 1,225 · see citing works
Self-citationPrefrontal cortex in the rat: Projections to subcortical autonomic, motor, and limbic centers
Gabbott, P. L. A., Warner, T. A., Jays, P. R. L., Salway, P., & Busby, S. J. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20738 · Cited by 1,227 · see citing works
Menzies, L., Chamberlain, S. R., Laird, A. R., Thelen, S. M., Sahakian, B. J., & Bullmore, E. T. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.09.005 · Cited by 1,190 · see citing works
Orbitofrontal Cortex as a Cognitive Map of Task Space
Wilson, R. C., Takahashi, Y. K., Schoenbaum, G., & Niv, Y. (2014) · Neuron · doi:10.1016/j.neuron.2013.11.005 · Cited by 885 · see citing works
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Self-citationChamberlain, S. R., Blackwell, A. D., Fineberg, N. A., Robbins, T. W., & Sahakian, B. J. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.11.006 · Cited by 830 · see citing works
Self-citationThe neural basis of reversal learning: An updated perspective
Izquierdo, A., Brigman, J. L., Radke, A. K., Rudebeck, P. H., & Holmes, A. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2016.03.021 · Cited by 670 · see citing works
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Everitt, B. J., & Robbins, T. W. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.02.010 · Cited by 675 · see citing works
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Winstanley, C. A., Theobald, D. E. H., Cardinal, R. N., & Robbins, T. W. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.5606-03.2004 · Cited by 675 · see citing works
Self-citationIzquierdo, A., Suda, R. K., & Murray, E. A. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1921-04.2004 · Cited by 588 · see citing works
A new perspective on the role of the orbitofrontal cortex in adaptive behaviour
Schoenbaum, G., Roesch, M. R., Stalnaker, T. A., & Takahashi, Y. K. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2753 · Cited by 585 · see citing works
Separate neural pathways process different decision costs
Rudebeck, P. H., Walton, M. E., Smyth, A. N., Bannerman, D. M., & Rushworth, M. F. S. (2006) · Nature Neuroscience · doi:10.1038/nn1756 · Cited by 580 · see citing works
Chudasama, Y., Passetti, F., Rhodes, S. E. V., Lopian, D., Desai, A., & Robbins, T. W. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.020 · Cited by 518 · see citing works
Self-citationWhat the orbitofrontal cortex does not do
Stalnaker, T. A., Cooch, N. K., & Schoenbaum, G. (2015) · Nature Neuroscience · doi:10.1038/nn.3982 · Cited by 531 · see citing works
Orbitofrontal cortex, decision-making and drug addiction
Schoenbaum, G., Roesch, M. R., & Stalnaker, T. A. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2005.12.006 · Cited by 499 · see citing works
RAGOZZINO, M. E. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.013 · Cited by 482 · see citing works
Chudasama, Y., & Robbins, T. W. (2006) · Biological Psychology · doi:10.1016/j.biopsycho.2006.01.005 · Cited by 484 · see citing works
Self-citationWalton, M. E., Behrens, T. E. J., Buckley, M. J., Rudebeck, P. H., & Rushworth, M. F. S. (2010) · Neuron · doi:10.1016/j.neuron.2010.02.027 · Cited by 397 · see citing works
Robbins, T. W. (2007) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2007.2097 · Cited by 413 · see citing works
Self-citationPrefrontal mechanisms of behavioral flexibility, emotion regulation and value updating
Rudebeck, P. H., Saunders, R. C., Prescott, A. T., Chau, L. S., & Murray, E. A. (2013) · Nature Neuroscience · doi:10.1038/nn.3440 · Cited by 383 · see citing works
Orbitofrontal Cortex Mediates Outcome Encoding in Pavlovian But Not Instrumental Conditioning
Ostlund, S. B., & Balleine, B. W. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5443-06.2007 · Cited by 379 · see citing works
“Several studies have shown that OFC lesions disrupt reversal learning (Jones and Mishkin, 1972; Dias et al., 1997; Schoenbaum et al., 2002; Chudasama and Robbins, 2003), suggesting that this structure may play an important role in the flexible modification of previously acquired stimulus– outcome associations.”
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Learning task-state representations
Niv, Y. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0470-8 · Cited by 356 · see citing works
Bissonette, G. B., Martins, G. J., Franz, T. M., Harper, E. S., Schoenbaum, G., & Powell, E. M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2820-08.2008 · Cited by 353 · see citing works
Bussey, T. J., Holmes, A., Lyon, L., Mar, A. C., McAllister, K. A. L., Nithianantharajah, J., Oomen, C. A., & Saksida, L. M. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.04.011 · Cited by 299 · see citing works
Cortico-limbic-striatal circuits subserving different forms of cost-benefit decision making
Floresco, S. B., Onge, J. R. S., Ghods-Sharifi, S., & Winstanley, C. A. (2008) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.8.4.375 · Cited by 305 · see citing works
Boulougouris, V., Dalley, J. W., & Robbins, T. W. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.02.005 · Cited by 297 · see citing works
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Dombrovski, A. Y., Szanto, K., Clark, L., Reynolds, C. F., & Siegle, G. J. (2013) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.75 · Cited by 289 · see citing works
Expectancy-related changes in firing of dopamine neurons depend on orbitofrontal cortex
Takahashi, Y. K., Roesch, M. R., Wilson, R. C., Toreson, K., O'Donnell, P., Niv, Y., & Schoenbaum, G. (2011) · Nature Neuroscience · doi:10.1038/nn.2957 · Cited by 280 · see citing works
Clarke, H. F., Robbins, T. W., & Roberts, A. C. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1521-08.2008 · Cited by 263 · see citing works
Self-citationSynaptic scaffold evolution generated components of vertebrate cognitive complexity
Nithianantharajah, J., Komiyama, N. H., McKechanie, A., Johnstone, M., Blackwood, D. H., Clair, D. S., Emes, R. D., van de Lagemaat, L. N., Saksida, L. M., Bussey, T. J., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3276 · Cited by 251 · see citing works
The touchscreen cognitive testing method for rodents: How to get the best out of your rat
Bussey, T. J., Padain, T. L., Skillings, E. A., Winters, B. D., Morton, A. J., & Saksida, L. M. (2008) · Learning & Memory · doi:10.1101/lm.987808 · Cited by 255 · see citing works
Value-guided remapping of sensory cortex by lateral orbitofrontal cortex
Banerjee, A., Parente, G., Teutsch, J., Lewis, C., Voigt, F. F., & Helmchen, F. (2020) · Nature · doi:10.1038/s41586-020-2704-z · Cited by 199 · see citing works
Does the orbitofrontal cortex signal value?
Schoenbaum, G., Takahashi, Y., Liu, T., & McDannald, M. A. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.06210.x · Cited by 232 · see citing works
Boulougouris, V., Glennon, J. C., & Robbins, T. W. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301584 · Cited by 219 · see citing works
Self-citationDalley, J. W., Lääne, K., Theobald, D. E. H., Armstrong, H. C., Corlett, P. R., Chudasama, Y., & Robbins, T. W. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0502080102 · Cited by 214 · see citing works
Self-citationDissociable effects of lesions to orbitofrontal cortex subregions on impulsive choice in the rat
Mar, A. C., Walker, A. L. J., Theobald, D. E., Eagle, D. M., & Robbins, T. W. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6620-10.2011 · Cited by 206 · see citing works
Self-citationFerguson, B. R., & Gao, W.-J. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.11.033 · Cited by 186 · see citing works
Reversal learning and dopamine: a Bayesian perspective
Costa, V. D., Tran, V. L., Turchi, J., & Averbeck, B. B. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.1989-14.2015 · Cited by 170 · see citing works
Brigman, J. L., Mathur, P., Harvey-White, J., Izquierdo, A., Saksida, L. M., Bussey, T. J., Fox, S., Deneris, E., Murphy, D. L., & Holmes, A. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp266 · Cited by 184 · see citing works
Perry, J. L., Joseph, J. E., Jiang, Y., Zimmerman, R. S., Kelly, T. H., Darna, M., Huettl, P., Dwoskin, L. P., & Bardo, M. T. (2011) · Brain Research Reviews · doi:10.1016/j.brainresrev.2010.09.001 · Cited by 180 · see citing works
Lapiz-Bluhm, M. D. S., Soto-Piña, A. E., Hensler, J. G., & Morilak, D. A. (2009) · Psychopharmacology · doi:10.1007/s00213-008-1224-6 · Cited by 163 · see citing works
Rudebeck, P. H., & Murray, E. A. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2272-08.2008 · Cited by 148 · see citing works
Rygula, R., Walker, S. C., Clarke, H. F., Robbins, T. W., & Roberts, A. C. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2631-10.2010 · Cited by 136 · see citing works
Self-citationThe long-term cognitive consequences of adolescent exposure to recreational drugs of abuse
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“…that various sub regions within the FC play a critical role in behavioral flexibility and attention (Dias and Aggleton 2000; Chudasama et al. 2003; Chudasama and Robbins 2003), whereas sub regions of the HC appear to be vital in spatial and contextual learning and memory (Stubley-Weatherly et al.…”
BackgroundBoulougouris, V., Castañé, A., & Robbins, T. W. (2009) · Psychopharmacology · doi:10.1007/s00213-008-1341-2 · Cited by 104 · see citing works
Self-citationAndrzejewski, M. E., Schochet, T. L., Feit, E. C., Harris, R., Mckee, B. L., & Kelley, A. E. (2011) · Behavioral Neuroscience · doi:10.1037/a0022038 · Cited by 96 · see citing works
Learning to Like: A Role for Human Orbitofrontal Cortex in Conditioned Reward
Cox, S. M. L., Andrade, A., & Johnsrude, I. S. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3360-04.2005 · Cited by 99 · see citing works
Reward-Guided Learning with and without Causal Attribution
Jocham, G., Brodersen, K. H., Constantinescu, A. O., Kahn, M. C., Ianni, A. M., Walton, M. E., Rushworth, M. F. S., & Behrens, T. E. J. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.018 · Cited by 92 · see citing works
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Balleine, B. W., Leung, B. K., & Ostlund, S. B. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.06270.x · Cited by 80 · see citing works
Effects of sex and COMT genotype on environmentally modulated cognitive control in mice
Papaleo, F., Erickson, L., Liu, G., Chen, J., & Weinberger, D. R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1214397109 · Cited by 81 · see citing works
Roberts, A. C., & Clarke, H. F. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902288116 · Cited by 79 · see citing works
Burke, K. A., Takahashi, Y. K., Correll, J., Leon Brown, P., & Schoenbaum, G. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06992.x · Cited by 76 · see citing works
TAIT, D. S., & BROWN, V. J. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.010 · Cited by 75 · see citing works
Shanahan, N. A., Velez, L. P., Masten, V. L., & Dulawa, S. C. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.07.032 · Cited by 72 · see citing works
Panayi, M. C., & Killcross, S. (2018) · eLife · doi:10.7554/elife.37357 · Cited by 69 · see citing works
Basolateral amygdala lesions facilitate reward choices after negative feedback in rats
Izquierdo, A., Darling, C., Manos, N., Pozos, H., Kim, C., Ostrander, S., Cazares, V., Stepp, H., & Rudebeck, P. H. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.4942-12.2013 · Cited by 63 · see citing works
Hervig, M. E., Fiddian, L., Piilgaard, L., Božič, T., Blanco-Pozo, M., Knudsen, C., Olesen, S. F., Alsiö, J., & Robbins, T. W. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhz144 · Cited by 65 · see citing works
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Dickson, P. E., Rogers, T. D., Mar, N. D., Martin, L. A., Heck, D., Blaha, C. D., Goldowitz, D., & Mittleman, G. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.05.010 · Cited by 59 · see citing works
Impaired reward learning and intact motivation after serotonin depletion in rats
Izquierdo, A., Carlos, K., Ostrander, S., Rodriguez, D., McCall-Craddolph, A., Yagnik, G., & Zhou, F. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.05.032 · Cited by 59 · see citing works
Brown, H. D., Amodeo, D. A., Sweeney, J. A., & Ragozzino, M. E. (2012) · Journal of Psychopharmacology · doi:10.1177/0269881111430749 · Cited by 56 · see citing works
van den Boom, B. J. G., Mooij, A. H., Misevičiūtė, I., Denys, D., & Willuhn, I. (2019) · Genes, Brain and Behavior · doi:10.1111/gbb.12557 · Cited by 55 · see citing works
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Dissociable roles of medial orbitofrontal cortex in human operant extinction learning
Finger, E. C., Mitchell, D. G. V., Jones, M., & Blair, R. J. R. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.08.021 · Cited by 45 · see citing works
Janhunen, S. K., Svärd, H., Talpos, J., Kumar, G., Steckler, T., Plath, N., Lerdrup, L., Ruby, T., Haman, M., Wyler, R., et al. (2015) · Psychopharmacology · doi:10.1007/s00213-015-3954-6 · Cited by 43 · see citing works
Ross, R. S., LoPresti, M. L., Schon, K., & Stern, C. E. (2013) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-013-0170-x · Cited by 28 · see citing works
Granseth, B., Andersson, F. K., & Lindström, S. H. (2015) · Genes, Brain and Behavior · doi:10.1111/gbb.12230 · Cited by 23 · see citing works
Adler, S. M., Girotti, M., & Morilak, D. A. (2020) · Neurobiology of Stress · doi:10.1016/j.ynstr.2020.100258 · Cited by 15 · see citing works
Cognitive inflexibility, obsessive-compulsive symptoms and traits and poor post-pandemic adjustment
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- Authors
- Chudasama, Y., & Robbins, T. W.
- Affiliations
- University of Cambridge (GB)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2003-09-24
- Volume
- 23
- Issue
- 25
- Pages
- 8771-8780
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6740430
- OpenAlex
- W2116813115
- Cited by
- 543
- References
- 8
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 13 · 2023: 12 · 2022: 23 · 2021: 22 · 2020: 24 · 2019: 28 · 2018: 20 · 2017: 21 · 2016: 23 · 2015: 34 · 2014: 21 · 2013: 32 · 2012: 26
- FWCI
- 9.14
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust
- Medical Research Council
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- orbitofrontal cortex, infralimbic cortex, discrimination reversal learning, perseverative responding, response inhibition, excitotoxic lesions, ventral prefrontal cortex, functional heterogeneity, stimulus-reward associations
- MeSH terms
- Animals, Behavior, Animal, Cerebral Cortex, Conditioning, Classical, Discrimination Learning, Frontal Lobe, Inhibition, Psychological, Limbic System, Male, Neurotoxins, Photic Stimulation, Rats, Inbred Strains, Reaction Time, Retention, Psychology, Reversal Learning, Reward, Sensitivity and Specificity, Rats
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 ›
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