Differential Involvement of the Basolateral Amygdala and Mediodorsal Thalamus in Instrumental Action Selection
Open accessAbstract
Although it has been shown that the basolateral amygdala (BLA) and the mediodorsal thalamus (MD) are critical for goal-directed instrumental performance, much remains unknown about the respective contributions of these structures to action selection. The current study assessed the effects of post-training BLA and MD lesions on several tests of instrumental action selection. We found that MD damage disrupted the influence of pavlovian cues over action selection but left intact rats' ability to select actions based on either the expected value or the discriminative stimulus properties of the outcome. In contrast, BLA lesions impaired performance on all three tests of action selection. Because both lesion types disrupted the influence of cues that signal reward over instrumental performance, we then investigated the involvement of these structures in pavlovian contingency learning using a task in which the predictive status of one of two cues is degraded by delivering its outcome noncontingently during the intertrial interval. As expected, the sham group selectively suppressed their conditioned approach performance to the cue that no longer signaled its outcome but continued to respond to the control stimulus. In contrast, both lesioned groups were impaired on this task. Interestingly, whereas the MD group displayed a nonspecific reduction in responding to both cues, the BLA group continued to show high levels of responding to both cues as if their performance was completely insensitive to this contingency manipulation. These findings demonstrate that the BLA and MD make important yet distinct contributions to instrumental action selection.
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?
BLA lesion or BLA/DMS disconnection disrupts goal-directed behavior.
“BLA→DMS pathway function in action-outcome learning is consistent with evidence that BLA lesion or BLA/DMS disconnection disrupts goal-directed behavior29,48,49.”
From A dual-pathway architecture for stress to disrupt agency and promote habit (2025) · cites this paper as [49]
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
Hebb, D. O. (2005) · doi:10.4324/9781410612403 · Cited by 9,825 · see citing works
AChE-stained horizontal sections of the rat brain in stereotaxic coordinates
Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,501 · see citing works
Ongur, D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.206 · Cited by 2,627 · see citing works
Goal-directed instrumental action: contingency and incentive learning and their cortical substrates
Balleine, B. W., & Dickinson, A. (1998) · Neuropharmacology · doi:10.1016/s0028-3908(98)00033-1 · Cited by 1,541 · see citing works
Self-citationThe role of the dorsomedial striatum in instrumental conditioning
Yin, H. H., Ostlund, S. B., Knowlton, B. J., & Balleine, B. W. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04218.x · Cited by 1,099 · see citing works
Self-citationCoordination of Actions and Habits in the Medial Prefrontal Cortex of Rats
Killcross, S. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.4.400 · Cited by 748 · see citing works
Parallel incentive processing: an integrated view of amygdala function
Balleine, B. W., & Killcross, S. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.03.002 · Cited by 622 · see citing works
Self-citationCorbit, L. H., & Balleine, B. W. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4507-04.2005 · Cited by 589 · see citing works
Self-citationHatfield, T., Han, J.-S., Conley, M., Gallagher, M., & Holland, P. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05256.1996 · Cited by 555 · see citing works
Theories of Associative Learning in Animals
Pearce, J. M., & Bouton, M. E. (2001) · Annual Review of Psychology · doi:10.1146/annurev.psych.52.1.111 · Cited by 493 · see citing works
The role of prelimbic cortex in instrumental conditioning
Corbit, L. H., & Balleine, B. W. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.023 · Cited by 423 · see citing works
Self-citationOrbitofrontal cortex, associative learning and expectancies
Schoenbaum, G., & Roesch, M. (2005) · Neuron · doi:10.1016/j.neuron.2005.07.018 · Cited by 404 · see citing works
Amygdala–frontal interactions and reward expectancy
Holland, P. C., & Gallagher, M. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.03.007 · Cited by 390 · see citing works
Relations between Pavlovian-instrumental transfer and reinforcer devaluation
Holland, P. C. (2004) · Journal of Experimental Psychology: Animal Behavior Processes · doi:10.1037/0097-7403.30.2.104 · Cited by 388 · see citing works
Different Roles for Orbitofrontal Cortex and Basolateral Amygdala in a Reinforcer Devaluation Task
Pickens, C. L., Saddoris, M. P., Setlow, B., Gallagher, M., Holland, P. C., & Schoenbaum, G. M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11078.2003 · Cited by 379 · 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
Self-citationPostconditioning devaluation of a reinforcer affects instrumental responding.
Colwill, R., & Rescorla, R. (1985) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.11.1.120 · Cited by 375 · see citing works
The effect of lesions of the basolateral amygdala on instrumental conditioning
Balleine, B. W., Killcross, A. S., & Dickinson, A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-02-00666.2003 · Cited by 355 · see citing works
Self-citationNeural bases of food-seeking: affect, arousal and reward in corticostriatolimbic circuits
BALLEINE, B. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.08.061 · Cited by 326 · see citing works
Self-citationOstlund, S. B., & Balleine, B. W. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1921-05.2005 · Cited by 291 · see citing works
Self-citationPostconditioning devaluation of a reinforcer affects instrumental responding.
Colwill, R. M., & Rescorla, R. A. (1985) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037//0097-7403.11.1.120 · Cited by 273 · see citing works
Associations between the discriminative stimulus and the reinforcer in instrumental learning.
Colwill, R., & Rescorla, R. (1988) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.14.2.155 · Cited by 259 · see citing works
Corbit, L. H., Janak, P. H., & Balleine, B. W. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05934.x · Cited by 231 · see citing works
Self-citationPavlovian conditioned stimulus effects upon instrumental choice behavior are reinforcer specific
Kruse, J. M., Overmier, J., Konz, W., & Rokke, E. (1983) · Learning and Motivation · doi:10.1016/0023-9690(83)90004-8 · Cited by 226 · see citing works
Lesions of the Basolateral Amygdala Disrupt Selective Aspects of Reinforcer Representation in Rats
Blundell, P., Hall, G., & Killcross, S. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-22-09018.2001 · Cited by 219 · see citing works
Corbit, L. H., Muir, J. L., & Balleine, B. W. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02833.x · Cited by 186 · see citing works
Self-citationStill at the Choice‐Point: Action Selection and Initiation in Instrumental Conditioning
BALLEINE, B. W., & OSTLUND, S. B. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1390.006 · Cited by 184 · see citing works
Self-citationTransfer of instrumental control mediated by a devalued outcome
Rescorla, R. A. (1994) · Animal Learning & Behavior · doi:10.3758/bf03199953 · Cited by 141 · see citing works
GABA<sub>A</sub>-Mediated Inhibition of Basolateral Amygdala Blocks Reward Devaluation in Macaques
Wellman, L. L., Gale, K., & Malkova, L. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2257-04.2005 · Cited by 126 · see citing works
Consolidation and Reconsolidation of Incentive Learning in the Amygdala
Wang, S., Ostlund, S. B., Nader, K., & Balleine, B. W. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4716-04.2005 · Cited by 126 · see citing works
Self-citationEncoding of the unconditioned stimulus in Pavlovian conditioning
Colwill, R. M., & Motzkin, D. K. (1994) · Animal Learning & Behavior · doi:10.3758/bf03209158 · Cited by 107 · see citing works
Ostlund, S. B., & Balleine, B. W. (2007) · Animal Learning & Behavior · doi:10.3758/bf03196073 · Cited by 82 · see citing works
Self-citationPreserved Sensitivity to Outcome Value after Lesions of the Basolateral Amygdala
Blundell-Birtill, P., Hall, G., & Killcross, S. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-20-07702.2003 · Cited by 81 · see citing works
Associative Representations of Instrumental Contingencies
Colwill, R. (1994) · The Psychology of learning and motivation/The psychology of learning and motivation · doi:10.1016/s0079-7421(08)60408-9 · Cited by 67 · see citing works
Delamater, A. R. (1995) · Animal Learning & Behavior · doi:10.3758/bf03198013 · Cited by 61 · see citing works
Burns, L. H., Everitt, B. J., & Robbins, T. W. (1999) · Behavioural Brain Research · doi:10.1016/s0166-4328(98)00119-3 · Cited by 57 · see citing works
Outcome-specific conditioned inhibition in Pavlovian backward conditioning
Delamater, A. R., Sosa, W., & LoLordo, V. M. (2003) · Learning & Behavior · doi:10.3758/bf03196000 · Cited by 53 · see citing works
Actions and responses: The dual psychology of behaviour
Dickinson, A., & Balleine, B. W. (1999) · doi:10.1093/oso/9780198238874.003.0017 · Cited by 37 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Bardo, M. T., & Hammer, R. P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90226-e · Cited by 3,229 · see citing works
Balleine, B. W., & O'Doherty, J. P. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.131 · Cited by 1,775 · see citing works
Self-citationNeuronal Reward and Decision Signals: From Theories to Data
Schultz, W. (2015) · Physiological Reviews · doi:10.1152/physrev.00023.2014 · Cited by 1,126 · see citing works
The transition to compulsion in addiction
Lüscher, C., Robbins, T. W., & Everitt, B. J. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-0289-z · Cited by 475 · see citing works
Yin, H. H., Ostlund, S. B., & Balleine, B. W. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06422.x · Cited by 416 · see citing works
Self-citationThe integrative function of the basal ganglia in instrumental conditioning
Balleine, B. W., Liljeholm, M., & Ostlund, S. B. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.10.034 · Cited by 356 · see citing works
Self-citationThe Cognitive Thalamus as a Gateway to Mental Representations
Wolff, M., & Vann, S. D. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0479-18.2018 · Cited by 340 · see citing works
Pavlovian to instrumental transfer: a neurobehavioural perspective.
Holmes, N. M., Marchand, A., & Coutureau, E. (2010) · Neuroscience and Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.03.007 · Cited by 327 · see citing works
Morrison, S. E., & Salzman, C. D. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.02.007 · Cited by 341 · see citing works
Emotion, decision making, and the amygdala.
Seymour, B., & Dolan, R. (2008) · Neuron · doi:10.1016/j.neuron.2008.05.020 · Cited by 324 · see citing works
Mitchell, A. S. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.03.001 · Cited by 323 · see citing works
Appetitive Pavlovian-instrumental Transfer: A review.
Cartoni, E., Balleine, B., & Baldassarre, G. (2016) · Neuroscience and Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.09.020 · Cited by 284 · see citing works
Self-citationThe basolateral amygdala in reward learning and addiction
Wassum, K. M., & Izquierdo, A. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.08.017 · Cited by 306 · see citing works
Orbitofrontal Cortex: A Neural Circuit for Economic Decisions
Padoa‐Schioppa, C., & Conen, K. E. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.031 · Cited by 296 · see citing works
The Mediodorsal Thalamus: An Essential Partner of the Prefrontal Cortex for Cognition
Parnaudeau, S., Bolkan, S. S., & Kellendonk, C. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.11.008 · Cited by 283 · see citing works
What does the mediodorsal thalamus do?
Mitchell, A. S., & Chakraborty, S. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00037 · Cited by 267 · see citing works
Potential Vulnerabilities of Neuronal Reward, Risk, and Decision Mechanisms to Addictive Drugs
Schultz, W. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.014 · Cited by 219 · see citing works
Associative learning mechanisms underpinning the transition from recreational drug use to addiction
Hogarth, L., Balleine, B. W., Corbit, L. H., & Killcross, S. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06768.x · Cited by 204 · see citing works
Self-citationOptimizing exposure therapy with an inhibitory retrieval approach and the OptEx Nexus
Craske, M. G., Treanor, M., Zbozinek, T. D., & Vervliet, B. (2022) · Behaviour Research and Therapy · doi:10.1016/j.brat.2022.104069 · Cited by 195 · see citing works
The Meaning of Behavior: Discriminating Reflex and Volition in the Brain
Balleine, B. W. (2019) · Neuron · doi:10.1016/j.neuron.2019.09.024 · Cited by 172 · see citing works
Self-citationDistinct opioid circuits determine the palatability and the desirability of rewarding events
Wassum, K. M., Ostlund, S. B., Maidment, N. T., & Balleine, B. W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905874106 · Cited by 182 · see citing works
Self-citationAmygdala Central Nucleus Interacts with Dorsolateral Striatum to Regulate the Acquisition of Habits
Lingawi, N. W., & Balleine, B. W. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4806-11.2012 · Cited by 172 · see citing works
Self-citationBasolateral amygdala to orbitofrontal cortex projections enable cue-triggered reward expectations
Lichtenberg, N. T., Pennington, Z. T., Holley, S. M., Greenfield, V. Y., Cepeda, C., Levine, M. S., & Wassum, K. M. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.0486-17.2017 · Cited by 171 · see citing works
Shiflett, M. W., & Balleine, B. W. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07439.x · Cited by 170 · see citing works
Self-citationIndividual variation in resisting temptation: Implications for addiction
Saunders, B. T., & Robinson, T. E. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.02.008 · Cited by 165 · see citing works
Hart, G., Leung, B. K., & Balleine, B. W. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.11.003 · Cited by 166 · see citing works
Self-citationMannella, F., Gurney, K., & Baldassarre, G. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00135 · Cited by 166 · see citing works
Advances in Understanding Mechanisms of Thalamic Relays in Cognition and Behavior
Mitchell, A. S., Sherman, S. M., Sommer, M. A., Mair, R. G., Vertes, R. P., & Chudasama, Y. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3289-14.2014 · Cited by 164 · see citing works
On habits and addiction: an associative analysis of compulsive drug seeking
Ostlund, S. B., & Balleine, B. W. (2008) · Drug Discovery Today: Disease Models · doi:10.1016/j.ddmod.2009.07.004 · Cited by 147 · see citing works
Self-citationMediodorsal Thalamus Hypofunction Impairs Flexible Goal-Directed Behavior
Parnaudeau, S., Taylor, K., Bolkan, S., Ward, R. D., Balsam, P., & Kellendonk, C. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.03.020 · Cited by 156 · see citing works
Johnson, A. W., Gallagher, M., & Holland, P. C. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.3758-08.2009 · Cited by 132 · see citing works
Parkes, S. L., & Balleine, B. W. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5071-12.2013 · Cited by 136 · see citing works
Self-citationConnectivity characterization of the mouse basolateral amygdalar complex
Hintiryan, H., Bowman, I., Johnson, D. L., Korobkova, L., Zhu, M.-Y., Khanjani, N., Gou, L., Gao, L., Yamashita, S., Bienkowski, M., et al. (2019) · Nature Communications · doi:10.1038/s41467-021-22915-5 · Cited by 129 · see citing works
The Origins and Organization of Vertebrate Pavlovian ConditioningPreprint
Fanselow, M., & Wassum, K. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021717 · Cited by 123 · see citing works
Corbit, L. H., & Balleine, B. W. (2015) · Current topics in behavioral neurosciences · doi:10.1007/7854_2015_388 · Cited by 118 · see citing works
Self-citationJones, J. L., Day, J. J., Aragona, B. J., Wheeler, R. A., Wightman, R. M., & Carelli, R. M. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.11.006 · Cited by 113 · see citing works
A thalamic bridge from sensory perception to cognition
Wolff, M., Morceau, S., Folkard, R., Martín-Cortecero, J., & Groh, A. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.11.013 · Cited by 114 · see citing works
Courtiol, E., & Wilson, D. A. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00049 · Cited by 113 · see citing works
The amygdala: securing pleasure and avoiding pain
Fernando, A. B. P., Murray, J. E., & Milton, A. L. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00190 · Cited by 110 · see citing works
Alcaraz, F., Fresno, V., Marchand, A. R., Kremer, E. J., Coutureau, É., & Wolff, M. (2018) · eLife · doi:10.7554/elife.32517 · Cited by 97 · see citing works
Rhodes, S. E. V., & Murray, E. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4374-12.2013 · Cited by 96 · see citing works
Acute high-intensity sound exposure alters responses of place cells in hippocampus
Goble, T., Møller, A. R., & Thompson, L. T. (2009) · Hearing Research · doi:10.1016/j.heares.2009.03.002 · Cited by 96 · see citing works
The role of the anterior, mediodorsal, and parafascicular thalamus in instrumental conditioning
Bradfield, L. A., Hart, G., & Balleine, B. W. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00051 · Cited by 89 · see citing works
Self-citationThe mediodorsal thalamus in executive control
Wolff, M., & Halassa, M. M. (2024) · Neuron · doi:10.1016/j.neuron.2024.01.002 · Cited by 96 · see citing works
Laurent, V., Leung, B. K., Maidment, N. T., & Balleine, B. W. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4688-11.2012 · Cited by 85 · see citing works
Self-citationThe orbitofrontal cortex, predicted value and choice
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
Self-citationThe Role of Orbitofrontal–Amygdala Interactions in Updating Action–Outcome Valuations in Macaques
Fiuzat, E. C., Rhodes, S. E. V., & Murray, E. A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1839-16.2017 · Cited by 85 · see citing works
Interpreting the role of the striatum during multiple phases of motor learning
Cataldi, S., Stanley, A. T., Miniaci, M. C., & Sulzer, D. (2021) · FEBS Journal · doi:10.1111/febs.15908 · Cited by 77 · see citing works
On the Nature of CS and US Representations in Pavlovian Learning
Delamater, A. (2011) · Learning & Behavior · doi:10.3758/s13420-011-0036-4 · Cited by 88 · see citing works
Peak, J. N., Hart, G., & Balleine, B. W. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13964 · Cited by 80 · see citing works
Self-citationFunctional heterogeneity of the limbic thalamus: From hippocampal to cortical functions
Wolff, M., Alcaraz, F., Marchand, A. R., & Coutureau, É. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.11.011 · Cited by 80 · see citing works
Altered hypothalamic response to food in smokers
Geha, P., Aschenbrenner, K., Felsted, J. A., O’Malley, S. S., & Small, D. M. (2012) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.112.043307 · Cited by 80 · see citing works
Chakraborty, S., Kolling, N., Walton, M. E., & Mitchell, A. S. (2016) · eLife · doi:10.7554/elife.13588 · Cited by 75 · see citing works
Food cue reactivity: Neurobiological and behavioral underpinnings
Kanoski, S. E., & Boutelle, K. N. (2022) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-022-09724-x · Cited by 78 · see citing works
Amygdala-cortical collaboration in reward learning and decision making
Wassum, K. M. (2022) · eLife · doi:10.7554/elife.80926 · Cited by 76 · see citing works
Izquierdo, A., & Murray, E. A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3795-09.2010 · Cited by 77 · see citing works
Bertran‐Gonzalez, J., Laurent, V., Chieng, B. C. H., Christie, M. J., & Balleine, B. W. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1927-13.2013 · Cited by 75 · see citing works
Self-citationLeung, B. K., & Balleine, B. W. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4837-14.2015 · Cited by 74 · see citing works
Self-citationThe thalamus as a relay station and gatekeeper: relevance to brain disorders
Moustafa, A. A., McMullan, R. D., Rostron, B., Hewedi, D. H., & Haladjian, H. H. (2017) · Reviews in the Neurosciences · doi:10.1515/revneuro-2016-0067 · Cited by 70 · see citing works
Pavlovian to instrumental transfer of control in a human learning task.
Nadler, N., Delgado, M. R., & Delamater, A. R. (2011) · Emotion · doi:10.1037/a0022760 · Cited by 71 · see citing works
Testosterone during puberty shifts emotional control from pulvinar to anterior prefrontal cortex
Tyborowska, A., Volman, I., Smeekens, S., Toni, I., & Roelofs, K. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.3874-15.2016 · Cited by 67 · see citing works
Cui, B., Zhu, L., She, X., Wu, M., Ma, Q., Wang, T., Zhang, N., Xu, C.-X., Chen, X., An, G., et al. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.08.028 · Cited by 68 · see citing works
The role of opioid processes in reward and decision-making
Laurent, V., Morse, A. K., & Balleine, B. W. (2015) · British Journal of Pharmacology · doi:10.1111/bph.12818 · Cited by 64 · see citing works
Self-citationWassum, K. M., Cely, I., Balleine, B. W., & Maidment, N. T. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3102-10.2011 · Cited by 67 · see citing works
Self-citationCoutureau, É., Marchand, A. R., & Scala, G. D. (2009) · Behavioral Neuroscience · doi:10.1037/a0014818 · Cited by 66 · see citing works
Bradfield, L. A., Hart, G., & Balleine, B. W. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.09.008 · Cited by 64 · see citing works
Self-citationParallel inputs from the mediodorsal thalamus to the prefrontal cortex in the rat
Alcaraz, F., Marchand, A. R., Courtand, G., Coutureau, É., & Wolff, M. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13316 · Cited by 62 · see citing works
Rosas-Vidal, L. E., Lozada-Miranda, V., Cantres-Rosario, Y. M., Vega-Medina, A., Meléndez, L. M., & Quirk, G. J. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0176-8 · Cited by 62 · see citing works
Eyes on me: an fMRI study of the effects of social gaze on action control
Schilbach, L., Eickhoff, S. B., Cieslik, E. C., Shah, N. J., Fink, G. R., & Vogeley, K. T. (2010) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsq067 · Cited by 60 · see citing works
Malvaez, M., Greenfield, V. Y., Wang, A. S., Yorita, A. M., Feng, L., Linker, K. E., Monbouquette, H. G., & Wassum, K. M. (2015) · Scientific Reports · doi:10.1038/srep12511 · Cited by 61 · see citing works
Stimulus-response and response-outcome learning mechanisms in the striatum
Horvitz, J. C. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.12.014 · Cited by 58 · see citing works
Leung, B. K., & Balleine, B. W. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1697-13.2013 · Cited by 60 · see citing works
Self-citationSavage, L., & Ramos, R. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.10.028 · Cited by 69 · see citing works
A bidirectional corticoamygdala circuit for the encoding and retrieval of detailed reward memories
Sias, A. C., Morse, A. K., Wang, S. C., Greenfield, V. Y., Goodpaster, C. M., Wrenn, T. M., Wikenheiser, A. M., Holley, S. M., Cepeda, C., Levine, M. S., et al. (2021) · eLife · doi:10.7554/elife.68617 · Cited by 60 · see citing works
Making habits measurable beyond what they are not: A focus on associative dual-process models
Watson, P., O’Callaghan, C., Perkes, I. E., Bradfield, L. A., & Turner, K. M. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104869 · Cited by 61 · see citing works
Evidence for Mediodorsal Thalamus and Prefrontal Cortex Interactions during Cognition in Macaques
Browning, P. G. F., Chakraborty, S., & Mitchell, A. S. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv093 · Cited by 59 · see citing works
Lichtenberg, N. T., Sepe-Forrest, L., Pennington, Z. T., Lamparelli, A. C., Greenfield, V. Y., & Wassum, K. M. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0901-21.2021 · Cited by 57 · see citing works
A neuronal mechanism for motivational control of behavior
Courtin, J., Bitterman, Y., Müller, S., Hinz, J., Hagihara, K. M., Müller, C. R., & Lüthi, A. (2022) · Science · doi:10.1126/science.abg7277 · Cited by 52 · see citing works
Jones, J. L., Day, J. J., Wheeler, R. A., & Carelli, R. M. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.05.073 · Cited by 55 · see citing works
Bermúdez, M. A., & Schultz, W. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00933.2009 · Cited by 52 · see citing works
Impaired executive function following ischemic stroke in the rat medial prefrontal cortex
Cordova, C. A., Jackson, D., Langdon, K. D., Hewlett, K. A., & Corbett, D. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.10.022 · Cited by 52 · see citing works
Okada, M., Fukuyama, K., Kawano, Y., Shiroyama, T., & Ueda, Y. (2019) · Pharmacology Research & Perspectives · doi:10.1002/prp2.457 · Cited by 51 · see citing works
Disruption of endogenous opioid activity during instrumental learning enhances habit acquisition
Wassum, K. M., Cely, I. C., Maidment, N. T., & Balleine, B. W. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.06.071 · Cited by 46 · see citing works
Self-citationWest, E. A., Forcelli, P. A., Murnen, A. T., McCue, D. L., Gale, K., & Málková, L. (2012) · Behavioral Neuroscience · doi:10.1037/a0029080 · Cited by 45 · see citing works
A thalamocortical circuit for updating action-outcome associations
Fresno, V., Parkes, S. L., Faugère, A., Coutureau, É., & Wolff, M. (2019) · eLife · doi:10.7554/elife.46187 · Cited by 42 · see citing works
Zhou, W., Zheng, H., Wang, M., Zheng, Y., Chen, S., Wang, M., & Dong, G. (2020) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2020.12.058 · Cited by 43 · see citing works
Apathy blunts neural response to money in Parkinson's disease
Lawrence, A. D., Goerendt, I. K., & Brooks, D. J. (2011) · Social Neuroscience · doi:10.1080/17470919.2011.556821 · Cited by 43 · see citing works
Ostlund, S. B., & Maidment, N. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2011.217 · Cited by 52 · see citing works
Self-citationNeural Representation of Odor-Guided Behavior in the Rat Olfactory Thalamus
Courtiol, E., & Wilson, D. A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0533-16.2016 · Cited by 40 · see citing works
Behavioral and cognitive changes after early postnatal lesions of the rat mediodorsal thalamus
Ouhaz, Z., Ba-M’hamed, S., Mitchell, A. S., Idrissi, A. E., & Bennis, M. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.06.017 · Cited by 39 · see citing works
Chronic noise exposure and Alzheimer disease: Is there an etiological association?
Cui, B., & Li, K. (2013) · Medical Hypotheses · doi:10.1016/j.mehy.2013.07.017 · Cited by 39 · see citing works
Zimmermann, K. S., Li, C.-C., Rainnie, D. G., Ressler, K. J., & Gourley, S. L. (2018) · Neuropsychopharmacology · doi:10.1038/npp.2017.219 · Cited by 38 · see citing works
Neural Estimates of Imagined Outcomes in Basolateral Amygdala Depend on Orbitofrontal Cortex
Lucantonio, F., Gardner, M., Mirenzi, A., Newman, L. E., Takahashi, Y. K., & Schoenbaum, G. M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3126-15.2015 · Cited by 34 · see citing works
Zimmermann, K. S., Li, C.-C., Rainnie, D. G., Ressler, K. J., & Gourley, S. L. (2018) · Neuropsychopharmacology · doi:10.1038/npp.2017.139 · Cited by 37 · see citing works
Amygdala-Cortical Control of Striatal Plasticity Drives the Acquisition of Goal-Directed Action
Fisher, S. D., Ferguson, L. A., Bertran-Gonzalez, J., & Balleine, B. W. (2020) · Current Biology · doi:10.1016/j.cub.2020.08.090 · Cited by 36 · see citing works
Self-citationDissociable effects of anterior and mediodorsal thalamic lesions on spatial goal-directed behavior
Alcaraz, F., Naneix, F., Desfosses, E., Marchand, A. R., Wolff, M., & Coutureau, É. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0893-7 · Cited by 36 · see citing works
Salling, M. C., Hodge, C. J., Psilos, K. E., Eastman, V. R., Faccidomo, S., & Hodge, C. W. (2017) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2017.10.011 · Cited by 29 · see citing works
Parallel and hierarchical neural mechanisms for adaptive and predictive behavioral control
Macpherson, T., Matsumoto, M., Gomi, H., Morimoto, J., Uchibe, E., & Hikida, T. (2021) · Neural Networks · doi:10.1016/j.neunet.2021.09.009 · Cited by 30 · see citing works
A dual-pathway architecture for stress to disrupt agency and promote habit
Giovanniello, J. R., Paredes, N., Wiener, A., Ramírez-Armenta, K., Oragwam, C., Uwadia, H. O., Yu, A. L., Lim, K., Pimenta, J. S., Vilchez, G. E., et al. (2025) · Nature · doi:10.1038/s41586-024-08580-w · Cited by 30 · see citing works
Goal-Directed Behavior and Instrumental Devaluation: A Neural System-Level Computational Model
Mannella, F., Mirolli, M., & Baldassarre, G. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00181 · Cited by 30 · see citing works
- Authors
- Ostlund, S. B., & Balleine, B. W.
- Affiliations
- University of California, Los Angeles (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2008-04-23
- Volume
- 28
- Issue
- 17
- Pages
- 4398-4405
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC2652225
- OpenAlex
- W2002961865
- Cited by
- 198
- References
- 38
- Citations by year
- 2026: 5 · 2025: 7 · 2024: 8 · 2023: 12 · 2022: 12 · 2021: 11 · 2020: 7 · 2019: 10 · 2018: 11 · 2017: 14 · 2016: 12 · 2015: 15 · 2014: 8 · 2013: 16 · 2012: 10
- FWCI
- 6.72
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Public Health Service (NIMH 56446)
- National Institute of Mental Health (R29MH056446, 56446)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- basolateral amygdala, mediodorsal thalamus, classical conditioning, reward prediction, lesion studies, rats
- MeSH terms
- Amygdala, Animals, Conditioning, Operant, Female, Motivation, Reward, Rats, Long-Evans, Mediodorsal Thalamic Nucleus, 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 ›
Are you an author, or do you see a problem with this page? Request a review