Neural correlates to both emotion and cognitive functions in the monkey amygdala

Behavioural Brain Research

Volumn 188, Issue 1, 2008, Pages 14-23

  Nishijo, Hisao ^a   Hori, Etsuro ^a   Tazumi, Toru ^a   Ono, Taketoshi ^a  

^a UNIVERSITY OF TOYAMA   (Japan)

Author keywords

Amygdala; Biological significance; Emotion; Monkey; Prefrontal cortex; Schizophrenia; Single neuron; Working memory

Indexed keywords

AMYGDALOID NUCLEUS; ANALYTIC METHOD; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; AUDITORY DISCRIMINATION; AVERSION; COGNITION; CONTROLLED STUDY; EMOTION; MONKEY; NERVE CELL; NONHUMAN; PRIORITY JOURNAL; REWARD; SENSORY STIMULATION; SHORT TERM MEMORY; VISUAL DISCRIMINATION; WORKING MEMORY;

ACOUSTIC STIMULATION; AMYGDALA; ANIMALS; AROUSAL; ATTENTION; AVOIDANCE LEARNING; COGNITION; CONDITIONING, OPERANT; DISCRIMINATION LEARNING; EMOTIONS; EVOKED POTENTIALS; MACACA; MEMORY, SHORT-TERM; NEURONS; PHOTIC STIMULATION; TIME PERCEPTION;

EID: 38749128045     PISSN: 01664328     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbr.2007.10.013     Document Type: Article

References (91)

1. Aalto S., Brück A., Laine M., Någren K., and Rinne J.O. Frontal and temporal dopamine release during working memory and attention tasks in healthy humans: a positron emission tomography study using the high-affinity dopamine D receptor ligand [C]FLB 457. J Neurosci 25 (2005) 2471-2477
2. Adolphs R., Denburg N.L., and Tranel D. The amygdala's role in long-term declarative memory for gist and detail. Behav Neurosci 115 (2001) 983-992
3. Aggleton J.P., Burton M.J., and Passingham R.E. Cortical and subcortical afferents to the amygdala of the rhesus monkey (Macaca mulatta). Brain Res 190 (1980) 347-368
4. Aggleton J.P., and Passingham R.E. Syndrome produced by lesions of the amygdala in monkeys. J Comp Physiol Psychol 95 (1981) 961-977
5. Amaral D.G., and Price J.L. Amygdalo-cortical projections in the monkey (Macaca fascicularis). J Comp Neurol 230 (1984) 465-496
6. Amaral D.G., Veazey R.B., and Cowan W.M. Some observations on hypothalamo-amygdaloid connections in the monkey. Brain Res 252 (1982) 13-27
7. Barbas H. Connections underlying the synthesis of cognition, memory, and emotion in primate prefrontal cortices. Brain Res Bull 52 (2000) 319-330
8. Cahill L., and McGaugh J.L. Amygdaloid complex lesions differentially affect retention of tasks using appetitive and aversive reinforcement. Behav Neurosci 104 (1990) 532-543
9. Cirillo R.A., Horel J.A., and George P.J. Lesions of the anterior temporal stem and the performance of delayed match-to-sample and visual discriminations in monkeys. Behav Brain Res 34 (1989) 55-69
10. Cotter D., Landau S., Beasley C., Stevenson R., Chana G., MacMillan L., et al. The density and spatial distribution of GABAergic neurons, labelled using calcium binding proteins, in the anterior cingulate cortex in major depressive disorder, bipolar disorder, and schizophrenia. Biol Psychiatry 51 (2002) 377-386
11. Cunningham M.G., Bhattacharyya S., and Benes F.M. Amygdalo-cortical sprouting continues into early adulthood: implications for the development of normal and abnormal function during adolescence. J Comp Neurol 453 (2002) 116-130
12. Das P., Kemp A.H., Flynn G., Harris A.W.F., Liddell B.J., Whitford T.J., et al. Functional disconnections in the direct and indirect amygdala pathways for fear processing in schizophrenia. Schizophrenia Res 90 (2007) 284-294
13. Duyckaerts C., Derouesne C., Signoret J.L., Gray F., Escourolle R., and Castaigne P. Bilateral and limited amygdalohippocampal lesions causing a pure amnesic syndrome. Ann Neurol 18 (1985) 314-319
14. Elvevåg B., and Goldberg T.E. Cognitive impairment in schizophrenia is the core of the disorder. Crit Rev Neurobiol 14 (2000) 1-21
15. Fried I., Wilson C.L., Morrow J.W., Cameron K.A., Behnke E.D., Ackerson L.C., et al. Increased dopamine release in the human amygdala during performance of cognitive tasks. Nat Neurosci 4 (2001) 201-206
16. Funahashi S., Bruce C.J., and Goldman-Rakic P.S. Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex. J Neurophysiol 61 (1989) 331-349
17. Fuster J.M. Unit activity of pre-frontal cortex during delayed-response performance: neuronal correlates of transient memory. J Neurophysiol 36 (1973) 61-78
18. Fuster J.M. Inferotemporal units in selective visual attention and short-term memory. J Neurophysiol 64 (1990) 681-697
19. Fuster J.M., and Alexander G. Neuron activity related to short-term memory. Science 173 (1971) 652-654
20. Fuster J.M., and Jervey J.P. Inferotemporal neurons distinguish and retain behaviorally relevant features of visual stimuli. Science 212 (1981) 952-955
21. Fuster J.M., and Jervey J.P. Neuronal firing in the inferotemporal cortex of the monkey in a visual memory task. J Neurosci 2 (1982) 361-375
22. Gabbott P.L.A., Warner T.A., and Busby S.J. Amygdala input monosynaptically innervates parvalbumin immunoreactive local circuit neurons in rat medial prefrontal cortex. Neuroscience 139 (2006) 1039-1048
23. Geschwind N. Disconnexion syndromes in animals and man. Brain 88 (1965) 237-294
24. Ghashghaei H.T., Hilgetag C.C., and Barbas H. Sequence of information processing for emotions based on the anatomic dialogue between prefrontal cortex and amygdala. NeuroImage 34 (2007) 905-923
25. Gottleib Y., Vaadia E., and Abeles M. Single unit activity in the auditory cortex of a monkey performing a short term memory task. Exp Brain Res 74 (1989) 139-148
26. Gloor P. Amygdala. In: Field J. (Ed). Handbook of physiology, neurophysiology vol. 2 (1960), American Physiological Society, Washington 1395-1420
27. Guillem F., N'Kaoua B., Rougier A., and Claverie B. Differential involvement of the human temporal lobe structures in short- and long-term memory processes assessed by intracranial ERPs. Psychophysiology 33 (1996) 720-730
28. Horel J.A., Keating E.G., and Misantone L.J. Partial Klüver-Bucy syndrome produced by destroying temporal neocortex or amygdala. Brain Res 94 (1975) 347-359
29. Howard M.W., Rizzuto D.S., Caplan J.B., Madsen J.R., Lisman J., Aschenbrenner-Scheibe R., et al. Gamma oscillations correlate with working memory load in humans. Cereb Cortex 13 (2003) 1369-1374
30. Irle E., and Markowitsch H.J. Basal forebrain-lesioned monkeys are severely impaired in tasks of association and recognition memory. Ann Neurol 22 (1987) 735-743
31. Iwai E., and Yukie M. Amygdalofugal and amygdalopetal connections with modality-specific visual cortical areas in Macaques (Macaca fuscata, M. mulatta, and M. fascicularis). J Comp Neurol 261 (1987) 362-387
32. Jacobs B.L., and McGinty D.J. Participation of the amygdala in complex stimulus recognition and behavioral inhibition: evidence from unit studies. Brain Res 36 (1972) 431-436
33. Javanbakht A. Sensory gating deficits, pattern completion, and disturbed fronto-limbic balance, a model for description of hallucinations and delusions in schizophrenia. Med Hypotheses 67 (2006) 1173-1184
34. Jones B., and Mishkin M. Limbic lesions and the problem of stimulus-reinforcement associations. Exp Neurol 36 (1972) 362-377
35. Johnston J.B. Further contributions to the study of the evolution of the forebrain. J Comp Neurol 35 (1923) 337-481
36. Klüver H., and Bucy P.C. Preliminary analysis of functions of the temporal lobes in monkeys. Arch Neurol Psychiatry 42 (1939) 979-1000
37. Koch K.W., and Fuster J.M. Unit activity in monkey parietal cortex related to haptic perception and temporary memory. Exp Brain Res 76 (1989) 292-306
38. Komatsu H. Prefrontal unit activity during color discrimination task with go and No-go responses in the monkey. Brain Res 244 (1982) 269-277
39. Kreczmanski P., Heinsen H., Mantua V., Woltersdorf F., Masson T., Ulfig N., et al. Volume, neuron density and total neuron number in five subcortical regions in schizophrenia. Brain 130 (2007) 678-692
40. Krettek J.E., and Price J.L. Amygdaloid projections to subcortical structures within the basal forebrain and brainstem in the rat and cat. J Comp Neurol 178 (1978) 225-254
41. Kubota K., and Niki H. Prefrontal cortical unit activity and delayed alternation performance in monkeys. J Neurophysiol 34 (1971) 337-347
42. Kubota K., Tonoike M., and Mikami A. Neuronal activity in the monkey dorsolateral prefrontal cortex during discrimination task with delay. Brain Res 183 (1980) 29-42
43. Kusama T., and Mabuchi M. Stereotaxic atlas of the brain of Macaca fuscata (1970), Tokyo University Press, Tokyo
44. LeDoux J.E. Representation of affect in neural circuits. In: Squire L.R., Mishkin M., and Shimamura A. (Eds). Learning and memory, discussion in neuroscience vol. 6 (1990), Elsevier, Amsterdam 64-68
45. Lewis D.A., Hashimoto T., and Volk D.W. Cortical inhibitory neurons and schizophrenia. Nat Rev Neurosci 6 (2005) 312-324
46. McGaugh J.L. Memory-a century of consolidation. Science 287 (2000) 248-2451
47. Mesulam M., Mufson E.J., Levey A.I., and Wainer B.H. Cholinergic innervation of cortex by the fasal forebrain: cytochemistry and cortical connections of the septal area, diagonal band nuclei, nucleus basalis (substantia innominata), and hypothalamus in the rhesus monkey. J Comp Neurol 214 (1983) 170-197
48. Mikami A., and Kubota K. Inferotemporal neuron activities and color discrimination with delay. Brain Res 182 (1980) 229-244
49. Miserendino M.D.J., Sananes C.B., Melia K.R., and Davis M. Blocking of acquisition but not expression of conditioned fear-potentiated startle by NMDA antagonists in the amygdala. Nature 345 (1990) 716-718
50. Mishkin M. Memory in monkeys severely impaired by combined but not by separate removal of amygdala and hippocampus. Nature 273 (1978) 297-298
51. Mishkin M. A memory system in the monkey. Philos Trans R Soc Lond [Biol] 298 (1982) 85-95
52. Mishkin M., and Aggleton J. Multiple functional contributions of the amygdala in the monkey. In: Ben Ari Y. (Ed). The amygdala complex (1981), Elsevier/North-Holland Biomedical, Amsterdam 409-420
53. Miyashita Y., and Chang H.S. Neuronal correlate of pictorial short-term memory in the primate temporal cortex. Nat Lond 331 (1988) 68-70
54. Muramoto K., Ono T., Nishijo H., and Fukuda M. Rat amygdaloid neuron responses during auditory discrimination. Neuroscience 52 (1993) 621-636
55. Niki H. Prefrontal unit activity during delayed alternation in the monkey. I. Relation to direction of response. Brain Res 68 (1974) 185-196
56. Niki H. Differential activity of prefrontal units during right and left delayed response trials. Brain Res 70 (1974) 340-349
57. Niki H., and Watanabe M. Prefrontal unit activity and delayed response relation to cue location versus direction of response. Brain Res 105 (1976) 79-88
58. Nishijo H., Ono T., and Nishino H. Single neuron responses in amygdala of alert monkey during complex sensory stimulation with affective significance. J Neurosci 8 (1988) 3570-3583
59. Nishijo H., Ono T., and Nishino H. Topographic distribution of modality-specific amygdalar neurons in alert monkey. J Neurosci 8 (1988) 3556-3569
60. O'Keefe J., and Bouma H. Complex sensory properties of certain amygdala units in the freely moving cat. Exp Neurol 23 (1969) 384-398
61. Ono T., Luiten P.G.M., Nishijo H., Fukuda M., and Nishino H. Topographic organization of projections from the amygdala to the hypothalamus of the rat. Neurosci Res 21 (1985) 221-239
62. Ono T., Nakamura H., Nishijo H., and Fukuda M. Hypothalamic neuron involvement in integration of reward, aversion, and cue signals. J Neurophysiol 56 (1986) 63-79
63. Ono T., Nishino H., Sasaki K., Fukuda M., and Muramoto K. Role of the lateral hypothalamus and the amygdala in feeding behavior. Brain Res Bull 5 Suppl. 4 (1980) 143-149
64. Ono T., Nishino H., Sasaki K., Fukuda M., and Muramoto K. Monkey lateral hypothalamic neuron response to sight of food, and during bar press and ingestion. Neurosci Lett 21 (1981) 99-104
65. Penfield W., and Milner B. Memory deficit produced by bilateral lesions in the hippocampal zone. Arch Neurol Psychiatry (Chic) 79 (1958) 475-497
66. Perrett D.I., Rolls E.T., and Caan W. Visual neurons responsive to faces in the monkey temporal cortex. Exp Brain Res 47 (1982) 329-342
67. Pizlo I., Murray E.A., and Mishkin M. The role of limbic and prefrontal cortical areas iri concept formation and immediate memory in rhesus monkeys. Soc Neurosci Abst 16 (1990) 617
68. Pons T.P., Garraghty P.E., Friedman D.P., and Mishkin M. Physiological evidence for serial processing in somatosensory cortex. Science 237 (1987) 417-420
69. Price J.L. Toward a consistent terminology for the amygdaloid complex. In: Ben-Ari Y. (Ed). The amygdaloid complex (1981), Elsevier/North Holland Biomedical, Amsterdam 13-18
70. Price J.L., and Amaral D.G. An autoradiographic study of the projections of the central nucleus of the monkey amygdala. J Neurosci 1 (1981) 1242-1259
71. Rosenkilde C.E., Bauer R.H., and Fuster J.M. Single cell activity in ventral prefrontal cortex of behaving monkeys. Brain Res 209 (1981) 375-394
72. Russchen F.T., Amaral D.G., and Price J.L. The afferent connections of the substantia innominata in the monkey, Macaca fascicularis. J Comp Neurol 242 (1985) 1-27
73. Sakurai Y. Hippocampal cells have behavioral correlates during the performance of an auditory working task in the rat. Behav Neurosci 104 (1990) 252-263
74. Sawa M., and Delgado J.M.R. Amygdala unitary activity in the unrestrained cat. Electroencephalogr Clin Neurophysiol 15 (1963) 637-650
75. Schaefer A., Braver T.S., Reynolds J.R., Burgess G.C., Yarkoni T., and Gray J.R. Individual differences in amygdala activity predict response speed during working memory. J Neurosci 26 (2006) 10120-10128
76. Scoville W.B., and Milner B. Loss of recent memory after bilateral hippocampal lesions. J Neurol Neurosurg Psychiatry 20 (1957) 11-21
77. Sidman M., Stoddard T., and Mohr J.P. Some additional quantitative observations of immediate memory in a patient with bilateral hippocampal lesions. Neuropsychology 6 (1968) 245-254
78. Spencer K.M., Nestor P.G., Niznikiewicz M.A., Salisbury D.F., Shenton M.E., and McCarley R.W. Abnormal neural synchrony in schizophrenia. J Neurosci 23 (2003) 7407-7411
79. Spiegler B.J., and Mishkin M. Evidence for the sequential participation of inferior temporal cortex and amygdala in the acquisition of stimulus--reward associations. Behav Brain Res 3 (1981) 307-317
80. Squire L.R., Amaral D.G., Zola-Morgan S., Kritchevsky M., and Press G. Description of brain injury in the amnesic patient N.A. based on magnetic resonance imaging. Exp Neurol 105 (1989) 23-35
81. Struble R.G., Lekmann J.L., Mitchell S.J., Mcl∼nney M., Price D.L., Coyle J.T., et al. Basal forebrain neurons provide major cholinergic innervation of primate neocortex. Neurosci Lett 66 (1986) 215-220
82. Tallon-Baudry C., Bertrand O., Peronnet F., and Pernier J. Induced gamma-band activity during the delay of a visual short-term memory task in humans. J Neurosci 18 (1998) 4244-4254
83. Toyomitsu Y., Nishijo H., Uwano T., Kuratsu J., and Ono T. Neuronal responses of the rat amygdala during extinction and reassociation learning in elementary and configural associative tasks. Eur J Neurosci 15 (2002) 753-768
84. Turner B.H., Mishkin M., and Knapp M. Organization of the amygdalopetal projections from modality-specific cortical association areas in the monkey. J Comp Neurol 191 (1980) 515-543
85. Watanabe M. Prefrontal unit activity during delayed conditional golno-go discrimination in the monkey. I. Relation to the stimulus. Brain Res 382 (1986) 1-14
86. Weiskrantz L. Behavioral changes associated with ablation of the amygdaloid complex in monkeys. J Comp Physiol Psychol 49 (1956) 381-391
87. Wozniak D.F., Stewart G.R., Finger S., Olney J.W., and Cozzari C. Basal forebrain lesions impair tactile discrimination and working memory. Neurobiol Aging 10 (1989) 173-179
88. Yamatani K., Ono T., Nishijo H., and Takaku A. Activity and distribution of learning-related neurons in monkey prefrontal cortex. Behav Neurosci 104 (1990) 503-531
89. Zola-Morgan S.M., and Squire L.R. The primate hippocampal formation: evidence for a time-limited role in memory storage. Science 250 (1990) 288-289
90. Zola-Morgan S., Squire L.R., and Amaral D.G. Human amnesia and the medial temporal region: enduring memory impairment following a bilateral lesion limited to field CA1 of the hippocampus. J Neurosci 6 (1986) 2950-2967
91. Zola-Morgan S., Squire L.R., and Mishkin M. The neuroanatomy of amnesia: amygdala-hippocampus versus temporal stem. Science 218 (1982) 1337-1339