The amygdala, reward and emotion

Trends in Cognitive Sciences

Volumn 11, Issue 11, 2007, Pages 489-497

  Murray, Elisabeth A ^a  

^a NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BEHAVIORAL RESEARCH; MAMMALS; NEURONS; SENSORY AIDS;

AROUSING EFFECT; AUTONOMIC RESPONSES; PROCESSING POSITIVE REWARD;

NEUROPHYSIOLOGY;

AFFECT; AMYGDALOID NUCLEUS; ANIMAL BEHAVIOR; BRAIN FUNCTION; COGNITION; CONDITIONING; EMOTION; EXPERIMENTAL MODEL; FUNCTIONAL ANATOMY; HUMAN; LEARNING; MONKEY; NERVE CELL NETWORK; NEUROPSYCHOLOGY; NONHUMAN; PROCESSING; REINFORCEMENT; REVIEW; REWARD; STIMULUS RESPONSE;

AFFECT; AMYGDALA; ANIMALS; COGNITION; EMOTIONS; HAPLORHINI; HUMANS; RATS; REWARD;

EID: 36049028685     PISSN: 13646613     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tics.2007.08.013     Document Type: Review

References (82)

1. Murray E.A., and Wise S.P. What, if anything, is the medial temporal lobe, and how can the amygdala be part of it if there is no such thing?. Neurobiol. Learn. Mem. 82 (2004) 178-198
2. Herzog A.G., and Van Hoesen G.W. Temporal neocortical afferent connections to the amygdala in the rhesus monkey. Brain Res. 115 (1976) 57-69
3. Turner B.H., et al. Organization of the amygdalopetal projections from modality-specific cortical association areas in the monkey. J. Comp. Neurol. 191 (1980) 515-543
4. Aggleton J.P., et al. Cortical and subcortical afferents to the amygdala of the rhesus monkey (Macaca mulatta). Brain Res. 190 (1980) 347-386
5. Friedman D.P., et al. Cortical connections of the somatosensory fields of the lateral sulcus of macaques: evidence for a corticolimbic pathway for touch. J. Comp. Neurol. 252 (1986) 323-347
6. Stefanacci L., and Amaral D.G. Topographic organization of cortical inputs to the lateral nucleus of the macaque monkey amygdala: a retrograde tracing study. J. Comp. Neurol. 421 (2000) 52-79
7. Mufson E.J., et al. Insular interconnections with the amygdala in the rhesus monkey. Neuroscience 6 (1981) 1231-1248
8. Carmichael S.T., and Price J.L. Limbic connections of the orbital and medial prefrontal cortex in macaque monkeys. J. Comp. Neurol. 363 (1995) 615-641
9. Amaral D.G., and Price J.L. Amygdalo-cortical projections in the monkey (Macaca fascicularis). J. Comp. Neurol. 230 (1984) 465-496
10. Avendano C., et al. Evidence for an amygdaloid projection to premotor cortex but not to motor cortex in the monkey. Brain Res. 264 (1983) 111-117
11. Ghashghaei H.T., and Barbas H. Pathways for emotion: interactions of prefrontal and anterior temporal pathways in the amygdala of the rhesus monkey. Neuroscience 115 (2002) 1261-1279
12. Cardinal R.N., et al. Emotion and motivation: the role of the amygdala, ventral striatum, and prefrontal cortex. Neurosci. Biobehav. Rev. 26 (2002) 321-352
13. Berridge K.C., and Robinson T.E. Parsing reward. Trends Neurosci. 26 (2003) 507-513
14. Balleine B.W. Neural bases of food-seeking: affect, arousal and reward in corticostriatolimbic circuits. Physiol. Behav. 86 (2005) 717-730
15. Barrett L.F., et al. The experience of emotion. Annu. Rev. Psychol. 58 (2007) 373-403
16. Mason W.A., et al. Amygdalectomy and responsiveness to novelty in rhesus monkeys (Macaca mulatta): generality and individual consistency of effects. Emotion 6 (2006) 73-81
17. Ohman A., and Mineka S. Fears, phobias, and preparedness: toward an evolved module of fear and fear learning. Psychol. Rev. 108 (2001) 483-522
18. LeDoux J. The emotional brain, fear, and the amygdala. Cell. Mol. Neurobiol. 23 (2003) 727-738
19. Fanselow M.S., and Gale G.D. The amygdala, fear, and memory. Ann. N. Y. Acad. Sci. 985 (2003) 125-134
20. Morris J.S., et al. A differential neural response in the human amygdala to fearful and happy facial expressions. Nature 383 (1996) 812-815
21. Paton J.J., et al. The primate amygdala represents the positive and negative value of visual stimuli during learning. Nature 439 (2006) 865-870
22. Nishijo H., et al. Single neuron responses in amygdala of alert monkey during complex sensory stimulation with affective significance. J. Neurosci. 8 (1988) 3570-3583
23. Sugase-Miyamoto Y., and Richmond B.J. Neuronal signals in the monkey basolateral amygdala during reward schedules. J. Neurosci. 25 (2005) 11071-11083
24. Sanghera M.K., et al. Visual responses of neurons in the dorsolateral amygdala of the alert monkey. Exp. Neurol. 63 (1979) 610-626
25. Wilson F.A., and Rolls E.T. The primate amygdala and reinforcement: a dissociation between rule-based and associatively-mediated memory revealed in neuronal activity. Neuroscience 133 (2005) 1061-1072
26. Braesicke K., et al. Autonomic arousal in an appetitive context in primates: a behavioural and neural analysis. Eur. J. Neurosci. 21 (2005) 1733-1740
27. Baxter M.G., and Murray E.A. The amygdala and reward. Nat. Rev. Neurosci. 3 (2002) 563-573
28. Wellman L.L., et al. GABAA-mediated inhibition of basolateral amygdala blocks reward devaluation in macaques. J. Neurosci. 25 (2005) 4577-4586
29. Everitt B.J., et al. Appetitive behavior: impact of amygdala-dependent mechanisms of emotional learning. Ann. N. Y. Acad. Sci. 985 (2003) 233-250
30. Hiroi N., and White N.W. The lateral nucleus of the amygdala mediates expression of the amphetamine-produced conditioned place preference. J. Neurosci. 11 (1991) 2107-2116
31. Schoenbaum G., et al. Orbitofrontal cortex and basolateral amygdala encode expected outcomes during learning. Nat. Neurosci. 1 (1998) 155-159
32. Schoenbaum G., et al. Neural encoding in orbitofrontal cortex and basolateral amygdala during olfactory discrimination learning. J. Neurosci. 19 (1999) 1876-1884
33. Somerville L.H., et al. Dissociable medial temporal lobe contributions to social memory. J. Cogn. Neurosci. 18 (2006) 1253-1265
34. Johnsrude I.S., et al. Impaired preference conditioning after anterior temporal lobe resection in humans. J. Neurosci. 20 (2000) 2649-2656
35. Rolls E.T. The Brain and Emotion (1999), Oxford University Press
36. Barrett T.W. Studies of the function of the amygdaloid complex in Macaca mulatta. Neuropsychologia 7 (1969) 1-12
37. Schwartzbaum J.S., and Poulos D.A. Discrimination behavior after amygdalectomy in monkeys: learning set and discrimination reversals. J. Comp. Physiol. Psychol. 60 (1965) 320-328
38. Jones B., and Mishkin M. Limbic lesions and the problem of stimulus-reinforcement associations. Exp. Neurol. 36 (1972) 362-377
39. 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) 303-317
40. Aggleton J.P., and Passingham R.E. Syndrome produced by lesions of the amygdala in monkeys (Macaca mulatta). J. Comp. Physiol. Psychol. 95 (1981) 961-977
41. Klüver H., and Bucy P.C. Preliminary analysis of functions of the temporal lobes in monkeys. Arch. Neurol. Psychiatry 42 (1939) 979-1000
42. Baxter M.G., and Murray E.A. Reinterpreting the behavioural effects of amygdala lesions in nonhuman primates. In: Aggleton J.P. (Ed). The Amygdala: A Functional Analysis (2000), Oxford University Press 545-568
43. Stefanacci L., et al. Selective neurotoxic amygdala lesions in monkeys disrupt reactivity to food and object stimuli and have limited effects on memory. Behav. Neurosci. 117 (2003) 1029-1043
44. Izquierdo A., and Murray E.A. Selective bilateral amygdala lesions in rhesus monkeys fail to disrupt object reversal learning. J. Neurosci. 27 (2007) 1054-1062
45. Goulet S., et al. Aspiration lesions of the amygdala disrupt the rhinal corticothalamic projection system in rhesus monkeys. Exp. Brain Res. 119 (1998) 131-140
46. Balleine B.W. Incentive processes in instrumental conditioning. In: Mowrer R.R., and Klein S.B. (Eds). Handbook of Contemporary Learning Theories (2001), Lawrence Erlbaum Associates 307-366
47. Blundell P., et al. Lesions of the basolateral amygdala disrupt selective aspects of reinforcer representation in rats. J. Neurosci. 21 (2001) 9018-9026
48. Mineka S. A primate model of phobic fears. In: Eysenck H.J., and Martin I. (Eds). Theoretical Foundations of Behavior Therapy (1987), Plenum Press 81-111
49. Nelson E.E., et al. Individual differences in the responses of naive rhesus monkeys to snakes. Emotion 3 (2003) 3-11
50. Izquierdo A., et al. Comparison of the effects of bilateral orbital prefrontal cortex lesions and amygdala lesions on emotional responses in rhesus monkeys. J. Neurosci. 25 (2005) 8534-8542
51. Corbit L.H., and Balleine B.W. Double dissociation of basolateral and central amygdala lesions on the general and outcome-specific forms of Pavlovian-instrumental transfer. J. Neurosci. 25 (2005) 962-970
52. Everitt B.J., et al. Differential involvement of amygdala subsystems in appetitive conditioning and drug addiction. In: Aggleton J.P. (Ed). The Amygdala: A Functional Analysis (2000), Oxford University Press 353-390
53. Holland P.C., et al. The effects of amygdala lesions on conditioned stimulus-potentiated eating in rats. Physiol. Behav. 76 (2002) 117-129
54. Balleine B.W., and Killcross S. Parallel incentive processing: an integrated view of amygdala function. Trends Neurosci. 29 (2006) 272-279
55. Holland P.C. Relations between Pavlovian-instrumental transfer and reinforcer devaluation. J. Exp. Psychol. Anim. Behav. Process. 30 (2004) 104-117
56. Schoenbaum G., and Roesch M. Orbitofrontal cortex, associative learning, and expectancies. Neuron 47 (2005) 633-636
57. Baxter M.G., et al. Control of response selection by reinforcer value requires interaction of amygdala and orbital prefrontal cortex. J. Neurosci. 20 (2000) 4311-4319
58. Holland P.C., and Gallagher M. Amygdala-frontal interactions and reward expectancy. Curr. Opin. Neurobiol. 14 (2004) 148-155
59. Pickens C.L., et al. Different roles for orbitofrontal cortex and basolateral amygdala in a reinforcer devaluation task. J. Neurosci. 23 (2003) 11078-11084
60. Schoenbaum G., et al. Encoding predicted outcome and acquired value in orbitofrontal cortex during cue sampling depends upon input from basolateral amygdala. Neuron 39 (2003) 855-867
61. Balleine B.W., et al. The effect of lesions of the basolateral amygdala on instrumental conditioning. J. Neurosci. 23 (2003) 666-675
62. Rushworth M.F., et al. Contrasting roles for cingulate and orbitofrontal cortex in decisions and social behaviour. Trends Cogn. Sci. 11 (2007) 168-176
63. Saddoris M.P., et al. Rapid associative encoding in basolateral amygdala depends on connections with orbitofrontal cortex. Neuron 46 (2005) 321-331
64. Murray, E.A. (2007) Neuropsychology of primate reward processes. In The New Encyclopedia of Neuroscience (Squire, L.R., ed.), Elsevier (in press)
65. Bussey T.J., et al. Interaction of ventral and orbital prefrontal cortex with inferotemporal cortex in conditional visuomotor learning. Behav. Neurosci. 116 (2002) 703-715
66. Browning P.G., et al. Frontal-temporal disconnection abolishes object discrimination learning set in macaque monkeys. Cereb. Cortex 17 (2007) 859-864
67. Murray E.A., et al. Monkeys with rhinal cortex damage or neurotoxic hippocampal lesions are impaired on spatial scene learning and object reversals. Behav. Neurosci. 112 (1998) 1291-1303
68. Paz R., et al. Emotional enhancement of memory via amygdala-driven facilitation of rhinal interactions. Nat. Neurosci. 9 (2006) 1321-1329
69. Packard M.G., and Teather L.A. Amygdala modulation of multiple memory systems: hippocampus and caudate-putamen. Neurobiol. Learn. Mem. 69 (1998) 163-203
70. Murray E.A., and Bussey T.J. Perceptual-mnemonic functions of the perirhinal cortex. Trends Cogn. Sci. 3 (1999) 142-151
71. Vuilleumier P. How brains beware: neural mechanisms of emotional attention. Trends Cogn. Sci. 9 (2005) 585-594
72. Anderson A.K., and Phelps E.A. Lesions of the human amygdala impair enhanced perception of emotionally salient events. Nature 411 (2001) 305-309
73. Butter C.M. Perseveration in extinction and in discrimination reversal tasks following selective frontal ablations in Macaca mulatta. Physiol. Behav. 4 (1969) 163-171
74. Meunier M., et al. Effects of aspiration versus neurotoxic lesions of the amygdala on emotional responses in monkeys. Eur. J. Neurosci. 11 (1999) 4403-4418
75. Kalin N.H., et al. The primate amygdala mediates acute fear but not the behavioral and physiological components of anxious temperament. J. Neurosci. 21 (2001) 2067-2074
76. Malkova L., et al. Excitotoxic lesions of the amygdala fail to produce impairment in visual learning for auditory secondary reinforcement but interfere with reinforcer devaluation effects in rhesus monkeys. J. Neurosci. 17 (1997) 6011-6020
77. Izquierdo A., et al. Bilateral orbital prefrontal cortex lesions in rhesus monkeys disrupt choices guided by both reward value and reward contingency. J. Neurosci. 24 (2004) 7540-7548
78. Weiskrantz L. Behavioral changes associated with ablation of the amygdaloid complex in monkeys. J. Comp. Physiol. Psychol. 49 (1956) 381-391
79. Butter C.M., et al. Conditioning and extinction of a food-rewarded response after selective ablations of frontal cortex in rhesus monkeys. Exp. Neurol. 7 (1963) 65-75
80. Mishkin M. Perseveration of central sets after frontal lesions in monkeys. In: Warren J.M., and Akert K. (Eds). The Frontal Granular Cortex & Behavior (1964), McGraw-Hill 219-241
81. Izquierdo A., and Murray E.A. Opposing effects of amygdala and orbital prefrontal cortex lesions on the extinction of instrumental responding in macaque monkeys. Eur. J. Neurosci. 22 (2005) 2341-2346
82. Rudebeck P.H., et al. A role for the macaque anterior cingulate gyrus in social valuation. Science 313 (2006) 1310-1312