Corrigendum to “Touch-screen visual reversal learning is mediated by value encoding and signal propagation in the orbitofrontal cortex” [Neurobiol. Learn. Mem. 139 (2017) 179–188] (Neurobiology of Learning and Memory (2017) 139 (179–188), (S107474271630301X), (10.1016/j.nlm.2017.01.006));Touch-screen visual reversal learning is mediated by value encoding and signal propagation in the orbitofrontal cortex

Neurobiology of Learning and Memory

Volumn 139, Issue , 2017, Pages 179-188

  Marquardt, Kristin ^a   Sigdel, Rahul ^a   Brigman, Jonathan L ^a,b  

^a UNIVERSITY OF NEW MEXICO SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF NEW MEXICO HEALTH SCIENCES CENTER   (United States)

Author keywords

Behavioral flexibility; In vivo electrophysiology; Local field potential; Perseveration; Spike firing

Indexed keywords

ANIMAL EXPERIMENT; ELECTROPHYSIOLOGICAL PROCEDURES; ERROR; LEARNING; MEDICAL DECISION MAKING; MODEL; NERVE CELL; NONHUMAN; ORBITAL CORTEX; PERSEVERATION; PRECLINICAL STUDY; REWARD; SPIKE WAVE; TOUCH; ACTION POTENTIAL; ANIMAL; DISCRIMINATION LEARNING; INSTRUMENTAL CONDITIONING; MALE; MOUSE; PHYSIOLOGY; PREFRONTAL CORTEX; REVERSAL LEARNING;

ACTION POTENTIALS; ANIMALS; CONDITIONING, OPERANT; DISCRIMINATION LEARNING; MALE; MICE; NEURONS; PREFRONTAL CORTEX; REVERSAL LEARNING; REWARD;

EID: 85013151748     PISSN: 10747427     EISSN: 10959564     Source Type: Journal    
DOI: 10.1016/j.nlm.2021.107380     Document Type: Erratum

References (61)

1. Amodeo, L.R., McMurray, M.S., Roitman, J.D., Orbitofrontal cortex reflects changes in response-outcome contingencies during probabilistic reversal learning. Neuroscience 16 (2016), 30004–30005.
2. Bissonette, G.B., Martins, G.J., Franz, T.M., Harper, E.S., Schoenbaum, G., Powell, E.M., Double dissociation of the effects of medial and orbital prefrontal cortical lesions on attentional and affective shifts in mice. Journal of Neuroscience 28 (2008), 11124–11130.
3. Boulougouris, V., Dalley, J.W., Robbins, T.W., Effects of orbitofrontal, infralimbic and prelimbic cortical lesions on serial spatial reversal learning in the rat. Behavioural Brain Research 179 (2007), 219–228.
4. Brigman, J.L., Daut, R.A., Wright, T., Gunduz-Cinar, O., Graybeal, C., Davis, M.I., Holmes, A., GluN2B in corticostriatal circuits governs choice learning and choice shifting. Nature Neuroscience 16 (2013), 1101–1110.
5. Brigman, J.L., Mathur, P., Harvey-White, J., Izquierdo, A., Saksida, L.M., Bussey, T.J., Holmes, A., Pharmacological or genetic inactivation of the serotonin transporter improves reversal learning in mice. Cerebral Cortex 20 (2010), 1955–1963.
6. Brigman, J.L., Padukiewicz, K.E., Sutherland, M.L., Rothblat, L.A., Executive functions in the heterozygous reeler mouse model of schizophrenia. Behavioral Neuroscience 120 (2006), 984–988.
7. Brigman, J.L., Wright, T., Talani, G., Prasad-Mulcare, S., Jinde, S., Seabold, G.K., Holmes, A., Loss of GluN2B-containing NMDA receptors in CA1 hippocampus and cortex impairs long-term depression, reduces dendritic spine density, and disrupts learning. Journal of Neuroscience 30 (2010), 4590–4600.
8. Buzsaki, G., Anastassiou, C.A., Koch, C., The origin of extracellular fields and currents–EEG, ECoG, LFP and spikes. Nature Reviews Neuroscience 13 (2012), 407–420.
9. Buzsaki, G., Draguhn, A., Neuronal oscillations in cortical networks. Science 304 (2004), 1926–1929.
10. Cai, X., Padoa-Schioppa, C., Contributions of orbitofrontal and lateral prefrontal cortices to economic choice and the good-to-action transformation. Neuron 81 (2014), 1140–1151.
11. Calderone, D.J., Lakatos, P., Butler, P.D., Castellanos, F.X., Entrainment of neural oscillations as a modifiable substrate of attention. Trends in Cognitive Sciences 18 (2014), 300–309.
12. Cavanagh, J.F., Cohen, M.X., Allen, J.J., Prelude to and resolution of an error: EEG phase synchrony 20 reveals cognitive control dynamics during action monitoring. Journal of Neuroscience 29 (2009), 98–105.
13. Clarke, H.F., Robbins, T.W., Roberts, A.C., Lesions of the medial striatum in monkeys produce perseverative impairments during reversal learning similar to those produced by lesions of the orbitofrontal cortex. Journal of Neuroscience 28 (2008), 10972–10982.
14. Cohen, M. X. (2014a). Analyzing neural time series data theory and practice preface. Iss Clin Cogn Neurop (pp. Xvii–Xviii).
15. Cohen, M.X., Fluctuations in oscillation frequency control spike timing and coordinate neural networks. The Journal of neuroscience: The official journal of the Society for Neuroscience 34 (2014), 8988–8998.
16. Copping, N.A., Berg, E.L., Foley, G.M., Schaffler, M.D., Onaga, B.L., Buscher, N., Yang, M., Touchscreen learning deficits and normal social approach behavior in the Shank3B model of Phelan-McDermid Syndrome and autism. Neuroscience 16 (2016), 30165–30168.
17. Costa, V.D., Tran, V.L., Turchi, J., Averbeck, B.B., Reversal learning and dopamine: A Bayesian perspective. Journal of Neuroscience 35 (2015), 2407–2416.
18. DePoy, L., Daut, R., Brigman, J.L., MacPherson, K., Crowley, N., Gunduz-Cinar, O., Holmes, A., Chronic alcohol produces neuroadaptations to prime dorsal striatal learning. Proceedings of the National Academy of Sciences of the United States of America 110 (2013), 14783–14788.
19. Fries, P., Reynolds, J.H., Rorie, A.E., Desimone, R., Modulation of oscillatory neuronal synchronization by selective visual attention. Science 291 (2001), 1560–1563.
20. Graybeal, C., Feyder, M., Schulman, E., Saksida, L.M., Bussey, T.J., Brigman, J.L., Holmes, A., Paradoxical reversal learning enhancement by stress or prefrontal cortical damage: Rescue with BDNF. Nature Neuroscience 14 (2011), 1507–1509.
21. Gregoriou, G.G., Gotts, S.J., Zhou, H., Desimone, R., High-frequency, long-range coupling between prefrontal and visual cortex during attention. Science 324 (2009), 1207–1210.
22. Hamilton, D.A., Brigman, J.L., Behavioral flexibility in rats and mice: Contributions of distinct frontocortical regions. Genes Brain and Behavior 14 (2015), 4–21.
23. Hoover, W.B., Vertes, R.P., Projections of the medial orbital and ventral orbital cortex in the rat. The Journal of comparative neurology 519 (2011), 3766–3801.
24. Hvoslef-Eide, M., Nilsson, S.R., Saksida, L.M., Bussey, T.J., Cognitive translation using the rodent touchscreen testing approach. Current Topics in Behavioral Neurosciences 28 (2016), 423–447.
25. Izquierdo, A., Brigman, J.L., Radke, A.K., Rudebeck, P.H., Holmes, A., The neural basis of reversal learning: An updated perspective. Neuroscience, 2016.
26. Jang, A.I., Costa, V.D., Rudebeck, P.H., Chudasama, Y., Murray, E.A., Averbeck, B.B., The role of frontal cortical and medial-temporal lobe brain areas in learning a bayesian prior belief on reversals. Journal of Neuroscience 35 (2015), 11751–11760.
27. Kennerley, S.W., Behrens, T.E., Wallis, J.D., Double dissociation of value computations in orbitofrontal and anterior cingulate neurons. Nature Neuroscience 14 (2011), 1581–1589.
28. Klanker, M., Post, G., Joosten, R., Feenstra, M., Denys, D., Deep brain stimulation in the lateral orbitofrontal cortex impairs spatial reversal learning. Behavioural Brain Research 245 (2013), 7–12.
29. Leach, P.T., Hayes, J., Pride, M., Silverman, J.L., Crawley, J.N., Normal performance of Fmr1 mice on a touchscreen delayed nonmatching to position working memory task. eNeuro, 3, 2016.
30. Mar, A.C., Horner, A.E., Nilsson, S.R., Alsio, J., Kent, B.A., Kim, C.H., Bussey, T.J., The touchscreen operant platform for assessing executive function in rats and mice. Nature Protocols 8 (2013), 1985–2005.
31. Marquardt, K., Sigdel, R., Caldwell, K., Brigman, J.L., Prenatal ethanol exposure impairs executive function in mice into adulthood. Alcoholism, Clinical and Experimental Research 38 (2014), 2962–2968.
32. McMurray, M.S., Amodeo, L.R., Roitman, J.D., Consequences of adolescent ethanol consumption on risk preference and orbitofrontal cortex encoding of reward. Neuropsychopharmacology 41 (2016), 1366–1375.
33. Mirenowicz, J., Schultz, W., Importance of unpredictability for reward responses in primate dopamine neurons. Journal of Neurophysiology 72 (1994), 1024–1027.
34. Moorman, D.E., Aston-Jones, G., Orbitofrontal cortical neurons encode expectation-driven initiation of reward-seeking. Journal of Neuroscience 34 (2014), 10234–10246.
35. Morris, S.E., Yee, C.M., Nuechterlein, K.H., Electrophysiological analysis of error monitoring in schizophrenia. Journal of Abnormal Psychology 115 (2006), 239–250.
36. Padoa-Schioppa, C., Orbitofrontal cortex and the computation of economic value. Annals of the New York Academy of Sciences 1121 (2007), 232–253.
37. Padoa-Schioppa, C., Assad, J.A., Neurons in the orbitofrontal cortex encode economic value. Nature 441 (2006), 223–226.
38. Paxinos, K.B.J., Franklin, G., The mouse brain in stereotaxic coordinates. 2001, Academic Press, London.
39. Porjesz, B., Almasy, L., Edenberg, H.J., Wang, K., Chorlian, D.B., Foroud, T., Begleiter, H., Linkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locus. Proceedings of the National Academy of Sciences of the United States of America 99 (2002), 3729–3733.
40. Riceberg, J.S., Shapiro, M.L., Reward stability determines the contribution of orbitofrontal cortex to adaptive behavior. Journal of Neuroscience 32 (2012), 16402–16409.
41. Rich, E.L., Wallis, J.D., Decoding subjective decisions from orbitofrontal cortex. Nature Neuroscience 19 (2016), 973–980.
42. Roesch, M.R., Calu, D.J., Schoenbaum, G., Dopamine neurons encode the better option in rats deciding between differently delayed or sized rewards. Nature Neuroscience 10 (2007), 1615–1624.
43. Saez, A., Rigotti, M., Ostojic, S., Fusi, S., Salzman, C.D., Abstract context representations in primate amygdala and prefrontal cortex. Neuron 87 (2015), 869–881.
44. Schilman, E.A., Uylings, H.B., Galis-de Graaf, Y., Joel, D., Groenewegen, H.J., The orbital cortex in rats topographically projects to central parts of the caudate-putamen complex. Neuroscience Letters 432 (2008), 40–45.
45. Schoenbaum, G., Chiba, A.A., Gallagher, M., Changes in functional connectivity in orbitofrontal cortex and basolateral amygdala during learning and reversal training. Journal of Neuroscience 20 (2000), 5179–5189.
46. Schoenbaum, G., Esber, G.R., How do you (estimate you will) like them apples? Integration as a defining trait of orbitofrontal function. Current Opinion in Neurobiology 20 (2010), 205–211.
47. Stalnaker, T.A., Cooch, N.K., Schoenbaum, G., What the orbitofrontal cortex does not do. Nature Neuroscience 18 (2015), 620–627.
48. Sul, J.H., Kim, H., Huh, N., Lee, D., Jung, M.W., Distinct roles of rodent orbitofrontal and medial prefrontal cortex in decision making. Neuron 66 (2010), 449–460.
49. Takahashi, Y.K., Roesch, M.R., Stalnaker, T.A., Haney, R.Z., Calu, D.J., Taylor, A.R., Schoenbaum, G., The orbitofrontal cortex and ventral tegmental area are necessary for learning from unexpected outcomes. Neuron 62 (2009), 269–280.
50. Talpos, J., Steckler, T., Touching on translation. Cell and Tissue Research 354 (2013), 297–308.
51. Thorpe, S.J., Rolls, E.T., Maddison, S., The orbitofrontal cortex: Neuronal activity in the behaving monkey. Experimental Brain Research 49 (1983), 93–115.
52. van der Meer, M.A., Johnson, A., Schmitzer-Torbert, N.C., Redish, A.D., Triple dissociation of information processing in dorsal striatum, ventral striatum, and hippocampus on a learned spatial decision task. Neuron 67 (2010), 25–32.
53. van Wingerden, M., Vinck, M., Lankelma, J., Pennartz, C.M., Theta-band phase locking of orbitofrontal neurons during reward expectancy. Journal of Neuroscience 30 (2010), 7078–7087.
54. van Wingerden, M., Vinck, M., Lankelma, J.V., Pennartz, C.M., Learning-associated gamma-band phase-locking of action-outcome selective neurons in orbitofrontal cortex. Journal of Neuroscience 30 (2010), 10025–10038.
55. Vinck, M., van Wingerden, M., Womelsdorf, T., Fries, P., Pennartz, C.M., The pairwise phase consistency: A bias-free measure of rhythmic neuronal synchronization. NeuroImage 51 (2010), 112–122.
56. Wilson, R.C., Takahashi, Y.K., Schoenbaum, G., Niv, Y., Orbitofrontal cortex as a cognitive map of task space. Neuron 81 (2014), 267–279.
57. Womelsdorf, T., Schoffelen, J.M., Oostenveld, R., Singer, W., Desimone, R., Engel, A.K., Fries, P., Modulation of neuronal interactions through neuronal synchronization. Science 316 (2007), 1609–1612.
58. Womelsdorf, T., Valiante, T.A., Sahin, N.T., Miller, K.J., Tiesinga, P., Dynamic circuit motifs underlying rhythmic gain control, gating and integration. Nature Neuroscience 17 (2014), 1031–1039.
59. Yang, M., Lewis, F.C., Sarvi, M.S., Foley, G.M., Crawley, J.N., 16p11.2 Deletion mice display cognitive deficits in touchscreen learning and novelty recognition tasks. Learning & Memory 22 (2015), 622–632.
60. Young, J.J., Shapiro, M.L., Double dissociation and hierarchical organization of strategy switches and reversals in the rat PFC. Behavioral Neuroscience 123 (2009), 1028–1035.
61. Young, J.J., Shapiro, M.L., Dynamic coding of goal-directed paths by orbital prefrontal cortex. The Journal of neuroscience: The official journal of the Society for Neuroscience 31 (2011), 5989–6000.