Cited by 593Neural and Behavioral Psychology StudiesMemory and Neural MechanismsNeural dynamics and brain function

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Neural Activity in the Primate Prefrontal Cortex during Associative Learning

Open access

Abstract

The prefrontal (PF) cortex has been implicated in the remarkable ability of primates to form and rearrange arbitrary associations rapidly. This ability was studied in two monkeys, using a task that required them to learn to make specific saccades in response to particular cues and then repeatedly reverse these responses. We found that the activity of individual PF neurons represented both the cues and the associated responses, perhaps providing a neural substrate for their association. Furthermore, during learning, neural activity conveyed the direction of the animals' impending responses progressively earlier within each successive trial. The final level of activity just before the response, however, was unaffected by learning. These results suggest a role for the PF cortex in learning arbitrary cue-response associations, an ability critical for complex behavior.

Overview

Integrity signals

Registry

Crossref · 10.1016/s0896-6273(00)80658-3

Cites

3 of 3 references verified0 citation errors · 0 not checkable

Statistics

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

Verification

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Increased activity of bilateral ventrolateral prefrontal cortex (PMv/IFG) in the dual-task condition before training suggests that dual-task conditions may require greater control over stimulus-response mapping rules, even when the mappings are spatially compatible.

    “The increased activity of bilateral ventrolateral prefrontal cortex (PMv/IFG) in our dual-task condition before training suggests that dual-task conditions may require greater control over stimulus-response mapping rules, even in cases in which the mappings are spatially compatible.”

    From The Neural Correlates of Motor Skill Automaticity (2005) · cites this paper as Asaad et al., 1998

Citations

Cites

Flagged first, then by citations

Research works printed but not linked: 54

  1. Barbas, H., and Pandya, D. (1991). Patterns of connections of the prefrontal cortex in the rhesus monkey associated with cortical architecture. In Frontal Lobe Function and Dysfunction, H.S. Levin, H.M. Eisenberg, and A.L. Benton, eds. (New York: Oxford University Press), pp. 35–58. · DOI
  2. Berns, 1998, Brain regions responsive to novelty in the absence of awareness, Science, 276, 1272, 10.1126/science.276.5316.1272 · DOI
  3. Boussaoud, 1993, Primate frontal cortex, Exp. Brain Res, 95, 28
  4. Boussaoud, 1993, Primate frontal cortex, Exp. Brain Res, 95, 15
  5. Chen, 1995, Neuronal activity in the supplementary eye field during acquisition of conditional oculomotor associations, J. Neurophysiol, 73, 1101, 10.1152/jn.1995.73.3.1101 · DOI
  6. Chen, 1995, Supplementary eye field contrasted with the frontal eye field during acquisition of conditional oculomotor associations, J. Neurosci, 73, 1122
  7. Chen, 1996, Evolution of directional preferences in the supplementary eye field during acquisition of conditional oculomotor associations, J. Neurosci, 16, 3067, 10.1523/JNEUROSCI.16-09-03067.1996 · DOI
  8. Deadwyler, 1996, Hippocampal ensemble activity during spatial delayed-nonmatch-to-sample performance in rats, J. Neurosci, 16, 354, 10.1523/JNEUROSCI.16-01-00354.1996 · DOI
  9. di Pellegrino, 1991, A neurophysiological comparison of three distinct regions of the primate frontal lobe, Brain, 114, 951, 10.1093/brain/114.2.951 · DOI
  10. Eacott, 1992, Inferotemporal-frontal disconnection—the uncinate fascicle and visual associative learning in monkeys, Eur. J. Neurosci, 4, 1320, 10.1111/j.1460-9568.1992.tb00157.x · DOI
  11. Funahashi, 1993, Prefrontal neuronal activity in rhesus monkeys performing a delayed anti-saccade task, Nature, 365, 753, 10.1038/365753a0 · DOI
  12. Fuster, 1973, Unit activity in prefrontal cortex during delayed-response performance, J. Neurophysiol, 36, 61, 10.1152/jn.1973.36.1.61 · DOI · Paper page
  13. Fuster, 1981, Inferotemporal neurons distinguish and retain behaviorally relevant features of visual stimuli, Science, 212, 952, 10.1126/science.7233192 · DOI
  14. Fuster, 1982, Cellular discharge in the dorsolateral prefrontal cortex of the monkey in cognitive tasks, Exp. Neurol, 77, 679, 10.1016/0014-4886(82)90238-2 · DOI
  15. Gaffan, 1988, Inferotemporal-frontal disconnection and fornix transection in visuomotor conditional learning by monkeys, Behav. Brain Res, 31, 149, 10.1016/0166-4328(88)90018-6 · DOI
  16. Halsband, 1985, Premotor cortex and the conditions for movement in monkeys, Behav. Brain Res, 18, 269, 10.1016/0166-4328(85)90035-X · DOI
  17. Hasegawa, 1998, Monkey prefrontal neuronal activity coding the forthcoming saccade in an oculomotor delayed matching-to-sample task, J. Neurophysiol, 79, 322, 10.1152/jn.1998.79.1.322 · DOI
  18. Judge, 1980, Vision during saccadic eye movements. I. Visual interactions in striate cortex, J. Neurophysiol, 43, 1133, 10.1152/jn.1980.43.4.1133 · DOI
  19. Kojima, 1982, Delay-related activity of prefrontal neurons in rhesus monkeys performing delayed response, Brain Res, 248, 43, 10.1016/0006-8993(82)91145-3 · DOI
  20. Li, 1993, The representation of stimulus familiarity in anterior inferior temporal cortex, J. Neurophysiol, 69, 1918, 10.1152/jn.1993.69.6.1918 · DOI · Paper page
  21. Miller, 1991, Habituation-like decrease in the responses of neurons in inferior temporal cortex of the macaque, Vis. Neurosci, 7, 357, 10.1017/S0952523800004843 · DOI
  22. Miller, 1993, Activity of neurons in anterior inferior temporal cortex during a short-term memory task, J. Neurosci, 13, 1460, 10.1523/JNEUROSCI.13-04-01460.1993 · DOI
  23. Miller, 1996, Neural mechanisms of visual working memory in prefrontal cortex of the macaque, J. Neurosci, 16, 5154, 10.1523/JNEUROSCI.16-16-05154.1996 · DOI
  24. Mitz, 1991, Learning-dependent neuronal activity in the premotor cortex, J. Neurosci, 11, 1855, 10.1523/JNEUROSCI.11-06-01855.1991 · DOI
  25. Murray, 1996, Role of the hippocampus plus subjacent cortex but not amygdala in visuomotor conditional learning in rhesus monkeys, Behav. Neurosci, 110, 1261, 10.1037/0735-7044.110.6.1261 · DOI
  26. Niki, 1976, Prefrontal unit activity and delayed response, Brain Res, 105, 79, 10.1016/0006-8993(76)90924-0 · DOI
  27. Pandya, D.N., and Barnes, C.L. (1987). Architecture and connections of the frontal lobe. In The Frontal Lobes Revisited, E. Perecman, ed. (New York: The IRBN Press), pp. 41–72.
  28. Pandya, 1990, Prefrontal cortex in relation to other cortical areas in rhesus monkey—architecture and connections, Prog. Brain Res, 85, 63, 10.1016/S0079-6123(08)62676-X · DOI
  29. Parker, 1998, Memory after frontal/temporal disconnection in monkeys, Neuropsychologia, 36, 259, 10.1016/S0028-3932(97)00112-7 · DOI
  30. Petrides, 1982, Motor conditional associative-learning after selective prefrontal lesions in the monkey, Behav. Brain Res, 5, 407, 10.1016/0166-4328(82)90044-4 · DOI
  31. Petrides, 1985, Deficits in nonspatial conditional associative learning after periarcuate lesions in the monkey, Behav. Brain Res, 16, 95, 10.1016/0166-4328(85)90085-3 · DOI
  32. Petrides, 1985, Deficits on conditional associative-learning tasks after frontal- and temporal-lobe lesions in man, Neuropsychologia, 23, 601, 10.1016/0028-3932(85)90062-4 · DOI
  33. Petrides, 1986, The effect of periarcuate lesions in the monkey on the performance of symmetrically and asymmetrically reinforced visual and auditory go, no-go tasks, J. Neurosci, 6, 2054, 10.1523/JNEUROSCI.06-07-02054.1986 · DOI
  34. Petrides, 1990, Nonspatial conditional learning impaired in patients with unilateral frontal but not unilateral temporal lobe excisions, Neuropsychologia, 28, 137, 10.1016/0028-3932(90)90096-7 · DOI
  35. Quintana, 1992, Mnemonic and predictive functions of cortical neurons in a memory task, Neuroreport, 3, 721, 10.1097/00001756-199208000-00018 · DOI
  36. Raichle, 1994, Practice-related changes in human brain functional anatomy during nonmotor learning, Cereb. Cortex, 4, 8, 10.1093/cercor/4.1.8 · DOI · Paper page
  37. Rainer, 1998, Memory fields of neurons in the primate prefrontal cortex, Proc. Natl. Acad. Sci. USA, in press
  38. Rainer, 1998, Selective representation of relevant information by neurons in the primate prefrontal cortex, Nature, 393, 577, 10.1038/31235 · DOI
  39. Rao, 1997, Integration of what and where in the primate prefrontal cortex, Science, 276, 821, 10.1126/science.276.5313.821 · DOI
  40. Riches, 1991, The effects of visual stimulation and memory on neurons of the hippocampal formation and the neighboring parahippocampal gyrus and inferior temporal cortex of the primate, J. Neurosci, 11, 1763, 10.1523/JNEUROSCI.11-06-01763.1991 · DOI
  41. Robinson, 1963, A method of measuring eye movement using a scleral search coil in a magnetic field, IEEE Trans. Bio-Med. Eng. BME-, 10, 137, 10.1109/TBMEL.1963.4322822 · DOI
  42. Rupniak, 1987, Monkey hippocampus and learning about spatially directed movements, J. Neurosci, 7, 2331
  43. Rushworth, 1997, Ventral prefrontal cortex is not essential for working memory, J. Neurosci, 17, 4829, 10.1523/JNEUROSCI.17-12-04829.1997 · DOI
  44. Sakagami, 1994, Encoding of behavioral significance of visual stimuli by primate prefrontal neurons, Exp. Brain Res, 97, 423, 10.1007/BF00241536 · DOI
  45. Sakagami, 1994, Spatial selectivity of go/no-go neurons in monkey prefrontal cortex, Exp. Brain Res, 100, 165, 10.1007/BF00227290 · DOI
  46. Schultz, 1993, Responses of monkey dopamine neurons to reward and conditioned stimuli during successive steps of learning a delayed response task, J. Neurosci, 13, 900, 10.1523/JNEUROSCI.13-03-00900.1993 · DOI · Paper page
  47. Schultz, 1997, A neural substrate of prediction and reward, Science, 275, 1593, 10.1126/science.275.5306.1593 · DOI · Paper page
  48. Schwartz, 1984, Callosal and intrahemispheric connectivity of the prefrontal association cortex in rhesus monkey, J. Comp. Neurol, 226, 403, 10.1002/cne.902260309 · DOI
  49. Sereno, 1998, Shape selectivity in primate lateral intraparietal cortex, Nature, 395, 500, 10.1038/26752 · DOI
  50. Spitzer, 1991, Task difficulty, Exp. Brain Res, 83, 340, 10.1007/BF00231157 · DOI
  51. Spitzer, 1988, Increased attention enhances both behavioral and neuronal performance, Science, 240, 338, 10.1126/science.3353728 · DOI
  52. Watanabe, 1986, Prefrontal unit activity during delayed conditional go/no-go discrimination in the monkey. II. Relation to go and no-go responses, Brain Res, 382, 15, 10.1016/0006-8993(86)90105-8 · DOI
  53. Watanabe, 1992, Frontal units of the monkey coding the associative significance of visual and auditory stimuli, Exp. Brain Res, 89, 233, 10.1007/BF00228241 · DOI
  54. Young, 1994, Correlates of hippocampal complex-spike cell activity in rats performing a nonspatial radial maze task, J. Neurosci, 14, 6553, 10.1523/JNEUROSCI.14-11-06553.1994 · DOI

Cited by

Sorted by citations

Metadata

Authors
Asaad, W. F., Rainer, G., & Miller, E. K.
Affiliations
  • Massachusetts Institute of Technology (US)
  • Max Planck Society (DE)
Corresponding author
Miller, Earl K
Venue
Neuron
Publisher
Elsevier BV
Published
1998-12
Volume
21
Issue
6
Pages
1399-1407
ISSN
0896-6273 (ISSN-L)
OpenAlex
W1993129834
Cited by
593
References
3
Citations by year
2026: 9 · 2025: 20 · 2024: 16 · 2023: 16 · 2022: 20 · 2021: 17 · 2020: 17 · 2019: 14 · 2018: 17 · 2017: 25 · 2016: 24 · 2015: 26 · 2014: 21 · 2013: 23 · 2012: 26
FWCI
11.68
Type
journal article
Language
en
Open access
Locations
  • Neuron (publishedVersion)
  • PubMed (publishedVersion)
  • MPG.PuRe (Max Planck Society) (submittedVersion)
Funders
National Institute of Neurological Disorders and Stroke (NS35145-02)
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Keywords
prefrontal cortex, associative learning, reversal learning, single-unit activity, neural coding, monkeys, response timing
MeSH terms
Animals, Association Learning, Brain Mapping, Eye Movements, Functional Laterality, Macaca mulatta, Neurons, Reaction Time, Restraint, Physical, Saccades, Prefrontal Cortex

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review