Role of the basolateral amygdala in memory consolidation

Progress in Neurobiology

Volumn 70, Issue 5, 2003, Pages 409-420

  Paré, Denis ^a  

^a RUTGERS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLCHOLINE; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; FORSKOLIN; ISOPRENALINE; LIDOCAINE; MUSCARINIC RECEPTOR BLOCKING AGENT; NORADRENALIN; TETRODOTOXIN;

ADRENAL GLAND; AMYGDALOID NUCLEUS; AROUSAL; BEHAVIOR; BRAIN; BRAIN NERVE CELL; CELL POPULATION; CELL STRUCTURE; CONCENTRATION (PARAMETERS); DATA ANALYSIS; DRUG ACTIVITY; DRUG EFFECT; EMOTION; FACILITATION; FUNCTIONAL ANATOMY; HIPPOCAMPUS; HORMONE ACTION; HUMAN; HYPOTHESIS; INJECTION; LEARNING; LONG TERM MEMORY; MEMORY CONSOLIDATION; MENTAL TASK; MICRODIALYSIS; NERVE CELL PLASTICITY; NERVE CONDUCTION; NERVE EXCITABILITY; NERVE FIBER; NEUROMODULATION; NONHUMAN; NORADRENALIN RELEASE; PRIORITY JOURNAL; REVIEW; STRESS; STRUCTURE ANALYSIS; SYNAPSE; TARGET CELL; TASK PERFORMANCE; TEMPORAL LOBE; TIME;

EID: 0141429116     PISSN: 03010082     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0301-0082(03)00104-7     Document Type: Review

References (175)

1. Abercrombie E.D., Jacobs B.L. Single-unit response of noradrenergic neurons in the locus coeruleus of freely moving cats. I. Acutely presented stressful and non-stressful stimuli. J. Neurosci. 7:1987a;2837-2843.
2. Abercrombie E.D., Jacobs B.L. Single-unit response of noradrenergic neurons in the locus coeruleus of freely moving cats. II. Adaptation to chronically presented stressful stimuli. J. Neurosci. 7:1987b;2844-2848.
3. Adolphs R., Cahill L., Schul R., Babinsky R. Impaired declarative memory for emotional stimuli following bilateral amygdala damage in humans. Learn. Mem. 4:1997;291-300.
4. Agranoff B.W., Davis R.E., Brink J.J. Chemical studies on memory fixation in goldfish. Brain Res. 1:1966;303-309.
5. Akirav I., Richter-Levin G. Biphasic modulation of hippocampal plasticity by behavioral stress and basolateral amygdala stimulation in the rat. J. Neurosci. 19:1999;10530-10535.
6. Alonso A., Garcia-Austt E. Neuronal sources of theta rhythm in the entorhinal cortex of the rat. Exp. Brain Res. 67:1987;493-501.
7. Amaral, D.G., Price, J.L., Pitkänen, A., Carmichael, S.T., 1992. Anatomical organization of the primate amygdaloid complex. In: Aggleton, J.P. (Ed.), The Amygdala: Neurobiological Aspects of Emotion, Memory, and Mental Dysfunction. Wiley-Liss, New York, pp. 1-66.
8. Amat J., Matus-Amat P., Watkins L.R., Maier S.F. Escapable and inescapable stress differentially alter extracellular levels of 5-HT in the basolateral amygdala of the rat. Brain Res. 812:1998;113-120.
9. + current in mammalian neurons. Proc. Natl. Acad. Sci. U.S.A. 92:1995;6635-6639.
10. Bakin J.S., Weinberger N.M. Induction of a physiological memory in the cerebral cortex by stimulation of the nucleus basalis. Proc. Natl. Acad. Sci. U.S.A. 93:1996;11219-11224.
11. Barazangi N., Role L.W. Nicotine-induced enhancement of glutamatergic and GABAergic synaptic transmission in the mouse amygdala. J. Neurophysiol. 86:2001;463-474.
12. Benington J.H., Frank M.G. Cellular and molecular connections between sleep and synaptic plasticity. Prog. Neurobiol. 69:2003;71-101.
13. Berridge C.W., Abercrombie E.D. Relationship between locus coeruleus discharge rates and rates of norepinephrine release within neocortex as assessed by in vivo microdialysis. Neuroscience. 93:1999;1263-1270.
14. Bjordahl T.S., Dimyan M.A., Weinberger N.M. Induction of long-term receptive field plasticity in the auditory cortex of the waking guinea pig by stimulation of the nucleus basalis. Behav. Neurosci. 112:1998;467-479.
15. Blair H.T., Schafe G.E., Bauer E.P., Rodrigues S.M., LeDoux J.E. Synaptic plasticity in the lateral amygdala: a cellular hypothesis of fear conditioning. Learn. Mem. 8:2001;229-242.
16. Burke A., Heuer F., Reisberg D. Remembering emotional events. Mem. Cognit. 20:1992;277-290.
17. Buzsáki G. Two-stage model of memory formation: a role for noisy brain states. Neuroscience. 31:1989;551-570.
18. Buzsáki G., Leung L., Vanderwolf C.H. Cellular bases of hippocampal EEG in the behaving rat. Brain Res. Rev. 6:1983;139-171.
19. Cahill, L., 2000. Modulation of long-term memory storage in humans by emotional arousal: adrenergic activation and the amygdala. In: Aggleton, J.P. (Ed.), The Amygdala: A Functional Analysis. Oxford University Press, Oxford, pp. 425-445.
20. Cahill L., Alkire M.T. Epinephrine enhancement of human memory consolidation: interaction with arousal at encoding. Neurobiol. Learn. Mem. 79:2003;194-198.
21. Cahill L., McGaugh J.L. Mechanisms of emotional arousal and lasting declarative memory. Trends Neurosci. 21:1998;294-299.
22. Cahill L., Prins B., Weber M., McGaugh J.L. Beta-adrenergic activation and memory for emotional events. Nature. 371:1994;702-704.
23. Cahill L., Babinsky R., Markowitsch H., McGaugh J.L. The amygdala and emotional memory. Nature. 377:1995;295-296.
24. Cahill L., Haier R., Fallon J., Alkire M., Tang C., Keator D., Wu J., McGaugh J.L. Amygdala activity at encoding correlated with long-term, free recall of emotional information. Proc. Natl. Acad. Sci. U.S.A. 93:1996;8016-8021.
25. Canli T., Zhao Z., Brewer J., Gabrieli J., Cahill L. Event-related activation in the human amygdala associates with later memory for individual emotional experience. J. Neurosci. 20:2000;NIL10-NIL14.
26. Castellano C., Brioni J.D., Nagahara A.H., McGaugh J.L. Post-training systemic and intra-amygdala administration of the GABA-B agonist baclofen impairs retention. Behav. Neural Biol. 52:1989;170-179.
27. Chafee M.V., Goldman-Rakic P.S. Matching patterns of activity in primate prefrontal area 8a and parietal area 7ip neurons during a spatial working memory task. J. Neurophysiol. 79:1998;2919-2940.
28. Chen J., Lang E.J. Inhibitory role of K(Ca) channels in the lateral amygdaloid (LAT) nucleus. Soc. Neurosci. Abstr. 26:2000;1726.
29. Christianson, S.A., 1992. Handbook of Emotion and Memory: Current Research and Theory. Erlbaum, Hillsdale, NJ.
30. Clayton E.C., Williams C.L. Adrenergic activation of the nucleus tractus solitarius potentiates amygdala norepinephrine release and enhances retention performance in emotionally arousing and spatial memory tasks. Behav. Brain Res. 112:2000;151-158.
31. Coleman M.K., McGaugh J.L. Muscimol injected into the right or left amygdaloid complex differentially affects retention performance following aversively motivated training. Brain Res. 676:1995;183-188.
32. Collins D.R., Lang E.J., Paré D. Spontaneous activity of the perirhinal cortex in behaving cats. Neuroscience. 89:1999;1025-1039.
33. Collins D.R., Pelletier J.G., Paré D. Slow and fast (gamma) neuronal oscillations in the perirhinal cortex and lateral amygdala. J. Neurophysiol. 85:2001;1661-1672.
34. Danober L., Pape H.C. Mechanisms and functional significance of a slow inhibitory potential in neurons of the lateral amygdala. Eur. J. Neurosci. 10:1998;853-867.
35. Dickinson A.H., Mesches M.H., Coleman K., McGaugh J.L. Bicuculline administered into the amygdala blocks benzodiazepine-induced amnesia. Behav. Neural Biol. 60:1993;1-4.
36. Dringenberg H.C., Vanderwolf C.H. Cholinergic activation of the electrocorticogram: an amygdaloid activating system. Exp. Brain Res. 108:1996;285-296.
37. Duncan C.P. The retroactive effect of electroshock on learning. J. Comp. Physiol. Psychol. 42:1949;32-44.
38. Duque A., Balatoni B., Detari L., Zaborszky L. EEG correlation of the discharge properties of identified neurons in the basal forebrain. J. Neurophysiol. 84:2000;1627-1635.
39. + current in colliculi neurons via activation of a cyclic AMP-dependent protein kinase. Br. J. Pharmacol. 105:1992;973-979.
40. Fallon, J.H., Ciofi, P., 1992. Distribution of monoamines within the amygdala. In: Aggleton, J.P. (Ed.), The Amygdala. Wiley-Liss, New York, pp. 97-114.
41. Fallon J.H., Koziell D.A., Moore R.Y. Catecholamine innervation of the basal forebrain. II. Amygdala, suprarhinal cortex and entorhinal cortex. J. Comp. Neurol. 180:1978;509-531.
42. Ferry B., McGaugh J.L. Clenbuterol administration into the basolateral amygdala post-training enhances retention in an inhibitory avoidance task. Neurobiol. Learn. Mem. 72:1999;8-12.
43. Ferry B., McGaugh J.L. Role of amygdala norepinephrine in mediating stress hormone regulation of memory storage. Acta Pharmacol. Sin. 21:2000;481-493.
44. Ferry B., Magistretti P.J., Pralong E. Noradrenaline modulates glutamate-mediated neurotransmission in the rat basolateral amygdala in vitro. Eur. J. Neurosci. 9:1997;1356-1364.
45. Ferry B., Roozendaal B., McGaugh J.L. Basolateral amygdala noradrenergic influences on memory storage are mediated by an interaction between beta- and alpha1-adrenoceptors. J. Neurosci. 19:1999;5119-5123.
46. Frank M.G., Issa N.P., Stryker M.P. Sleep enhances plasticity in the developing visual cortex. Neuron. 30:2001;275-287.
47. Freund T.F., Martin K.A.C., Smith A.D., Somogyi P. Glutamate decarboxylase-immunoreactive terminals of Golgi-impregnated axoaxonic cells and of presumed basket cells in synaptic contact with pyramidal neurons of the cat's visual cortex. J. Comp. Neurol. 221:1983;263-278.
48. Frey U., Morris R.G. Synaptic tagging: implications for late maintenance of hippocampal long-term potentiation. Trends Neurosci. 21:1998;181-188.
49. Frey S., Bergado-Rosado J., Seidenbecher T., Pape H.C., Frey J.U. Reinforcement of early long-term potentiation (early-LTP) in dentate gyrus by stimulation of the basolateral amygdala: heterosynaptic induction mechanisms of late-LTP. J. Neurosci. 21:2001;3697-3703.
50. Fuster J.M., Alexander G.E. Neuron activity related to short-term memory. Science. 173:1971;652-654.
51. Gais S., Plihal W., Wagner U., Born J. Early sleep triggers memory for early visual discrimination skills. Nat. Neurosci. 3:2000;1335-1339.
52. Gao E., Suga N. Experience-dependent plasticity in the auditory cortex and the inferior colliculus of bats: role of the corticofugal system. Proc. Natl. Acad. Sci. U.S.A. 97:2000;8081-8086.
53. Gerard R.W. Physiology and psychiatry. Am. J. Psychiatry. 106:1949;161-173.
54. Girod R., Barazangi N., McGehee D., Role L.W. Facilitation of glutamatergic neurotransmission by presynaptic nicotinic acetylcholine receptors. Neuropharmacology. 39:2000;2715-2725.
55. Goddard G.V. Amygdaloid stimulation and learning in the rat. J. Comp. Physiol. Psychol. 58:1964;23-30.
56. Gold, P.E., McGaugh, J.L., 1975. A single-trace, two process view of memory storage processes. In: Deutsch, D., Deutsch, J.A. (Eds.), Short-Term Memory. Academic Press, New York, pp. 355-378.
57. Gold P.E., van Buskirk R.B. Effects of alpha- and beta-adrenergic receptor antagonists on post-trial epinephrine modulation of memory: relationship to post-training brain norepinephrine concentrations. Behav. Biol. 24:1978a;168-184.
58. Gold P.E., van Buskirk R.B. Posttraining brain norepinephrine concentrations: correlation with retention performance of avoidance training and with peripheral epinephrine modulation of memory processing. Behav. Biol. 23:1978b;509-520.
59. Gold P.E., van Buskirk R.B., McGaugh J.L. Effects of hormones on time-dependent memory storage processes. Prog. Brain Res. 42:1975a;210-211.
60. Gold P.E., Hankins L., Edwards R.M., Chester J., McGaugh J.L. Memory interference and facilitation with post-trial amygdala stimulation: effects on memory varies with footshock level. Brain Res. 86:1975b;509-513.
61. Gray P.C., Scott J.D., Catterall W.A. Regulation of ion channels by cAMP-dependent protein kinase and A-kinase anchoring proteins. Curr. Opin. Neurobiol. 8:1998;330-334.
62. Green J.D., Arduini A.A. Hippocampal electrical activity in arousal. J. Neurophysiol. 17:1954;533-557.
63. Hamann S.B., Ely T.D., Grafton S.T., Kilts C.D. Amygdala activity related to enhanced memory for pleasant and aversive stimuli. Nat. Neurosci. 2:1999;289-293.
64. Hatfield T., McGaugh J.L. Norepinephrine infused into the basolateral amygdala Post-training enhances retention in a spatial water maze task. Neurobiol. Learn. Mem. 71:1999;232-239.
65. Heuer F., Reisberg D. Vivid memories of emotional events: the accuracy of remembered minutiae. Mem. Cognit. 5:1990;496-506.
66. Honkaniemi J., Pelto-Huikko M., Richardt L., Isola J., Lammi A., Fuxi K., Gustafsson J.A., Wikstruom A.C., Hokfelt T. Colocalization of peptide and glucocorticoid receptor immunoreactivities in rat central amygdaloid nucleus. Neuroendocrinology. 55:1992;451-459.
67. Hori K., Tanaka J., Nomura M. Effects of discrimination learning on the rat amygdala dopamine release: a microdialysis study. Brain Res. 621:1993;296-300.
68. Huang Y.Y., Kandel E.R. Postsynaptic induction and PKA-dependent expression of LTP in the lateral amygdala. Neuron. 21:1998;169-178.
69. Huang C.C., Hsu K.S., Gean P.W. Isoproterenol potentiates synaptic transmission primarily by enhancing presynaptic calcium influx via P- and/or Q-type calcium channels in the rat amygdala. J. Neurosci. 16:1996;1026-1033.
70. Huang Y.Y., Martin K.C., Kandel E.R. Both protein kinase a and mitogen-activated protein kinase are required in the amygdala for the macromolecular synthesis-dependent late phase of long-term potentiation. J. Neurosci. 20:2000;6317-6325.
71. Ikegaya Y., Saito H., Abe K. Attenuated hippocampal long-term potentiation in basolateral amygdala-lesioned rats. Brain Res. 656:1994;157-164.
72. Ikegaya Y., Saito H., Abe K. High-frequency stimulation of the basolateral amygdala facilitates the induction of long-term potentiation in the dentate gyrus in vivo. Neurosci. Res. 22:1995;203-207.
73. Ikegaya Y., Saito H., Abe K. The basomedial and basolateral amygdaloid nuclei contribute to the induction of long-term potentiation in the dentate gyrus in vivo. Eur. J. Neurosci. 8:1996;1833-1839.
74. Ikegaya Y., Nakanishi K., Saito H., Abe K. Amygdala beta-noradrenergic influence on hippocampal long-term potentiation in vivo. NeuroReport. 8:1997;3143-3146.
75. Inglis F.M., Moghaddam B. Dopaminergic innervation of the amygdala is highly responsive to stress. J. Neurochem. 72:1999;1088-1094.
76. Ji W.Q., Gao E.Q., Suga N.B. Effects of acetylcholine and atropine on plasticity of central auditory neurons caused by conditioning in bats. J. Neurophysiol. 86:2001;211-225.
77. Jolkkonen E., Meittinen R., Pikkarainen M., Pitkänen A. Projections from the amygdaloid complex to the magnocellular cholinergic basal forebrain in rat. Neuroscience. 111:2002;133-149.
78. Kandel E.R., Schwartz J.H. Molecular biology of learning: modulation of transmitter release. Science. 218:1982;433-443.
79. Kawahara H., Yoshida M., Yokoo H., Nishi M., Tanaka M. Psychological stress increases serotonin release in the rat amygdala and prefrontal cortex assessed by in vivo microdialysis. Neurosci. Lett. 162:1993;81-84.
80. Kilgard M.P., Merzenich M.M. Cortical map reorganization enabled by nucleus basalis activity. Science. 279:1998;1714-1718.
81. Kita H., Kitai S.T. Amygdaloid projections to the frontal cortex and the striatum in the rat. J. Comp. Neurol. 298:1990;40-49.
82. Klein M., Camardo J., Kandel E.R. Serotonin modulates a specific potassium current in the sensory neurons that show presynaptic facilitation in aplysia. Proc. Natl. Acad. Sci. U.S.A. 79:1982;5713-5717.
83. Krasne F.B. Extrinsic control of intrinsic neuronal plasticity: an hypothesis from work on simple systems. Brain Res. 140:1978;197-216.
84. Krettek J.E., 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.
85. Lang E.J., Paré D. Similar inhibitory processes dominate the responses of cat lateral amygdaloid projection neurons to their various afferents. J. Neurophysiol. 77:1997a;341-352.
86. Lang E.J., Paré D. Synaptic and synaptically activated intrinsic conductances underlie inhibitory potentials in cat lateral amygdaloid projection neurons in vivo. J. Neurophysiol. 77:1997b;353-363.
87. Lang E.J., Paré D. Synaptic responsiveness of interneurons of the cat lateral amygdaloid nucleus. Neuroscience. 83:1998;877-889.
88. Levitan I.B. Modulation of ion channels by protein phosphorylation and dephosphorylation. Annu. Rev. Physiol. 56:1994;193-212.
89. Liang, K.C., 2001. Epinephrine modulation of memory: amygdala activation and regulation of long-term memory storage. In: Gold, P.E., Greenough W.T. (Eds.), Memory Consolidation. American Psychological Association, Washington, DC, pp. 165-183.
90. Liang K.C., McGaugh J.L. Lesions of the stria terminals attenuate the enhancing effect of post-training epinephrine on retention of an inhibitory avoidance response. Behav. Brain Res. 9:1983;49-58.
91. Liang K.C., McGaugh J.L., Martinez J.L., Jensen R.A., Vasquez B.J., Messing R.B. Post-training amygdala lesions impair retention of an inhibitory avoidance response. Behav. Brain Res. 4:1982;237-249.
92. Liang K.C., McGaugh J.L., Yao H.Y. Involvement of amygdala pathways in the influence of post-training intra-amygdala norepinephrine and peripheral epinephrine on memory storage. Brain Res. 508:1990;225-233.
93. Malenka R.C. Synaptic plasticity in the hippocampus: LTP and LTD. Cell. 78:1994;535-538.
94. Manns I.D., Alonso A., Jones B.E. Discharge properties of juxtacellularly labeled and immunohistochemically identified cholinergic basal forebrain neurons recorded in association with the electroencephalogram in anesthetized rats. J. Neurosci. 20:2000;1505-1518.
95. Mark, V.H., Ervin, F.R., Sweet, W.H., 1972. Deep temporal lobe stimulation in man. In: Eleftheriou, B. (Ed.), The Neurobiology of the Amygdala. Plenum Press, New York, pp. 495-510.
96. Martina M., Royer S., Paré D. Cell-type-specific GABA responses and chloride homeostasis in the cortex and amygdala. J. Neurophysiol. 86:2001;2887-2895.
97. Mayr B., Montminy M. Transcriptional regulation by the phosphorylation-dependent factor CREB. Nat. Rev. Mol. Cell. Biol. 2:2001;599-609.
98. McDonald A.J. Cortical pathways to the mammalian amygdala. Prog. Neurobiol. 55:1998;257-332.
99. McDonough J.R., Kesner R.P. Amnesia produced by brief electrical stimulation of the amygdala or dorsal hippocampus is cats. J. Comp. Physiol. Psychol. 77:1971;171-178.
100. McGaugh J.L. Time-dependent processes in memory storage. Science. 153:1966;1351-1358.
101. McGaugh J.L. Drug facilitation of learning and memory. Ann. Rev. Pharmacol. 13:1973;229-241.
102. McGaugh J.L. Memory consolidation and the amygdala: a systems perspective. Trends Neurosci. 25:2002a;456.
103. McGaugh, J.L., 2002b. The amygdala regulates memory consolidation. In: Squire, L.R., Schacter, D.L. (Eds.), Neuropsychology of Memory, third ed. Guilford Press, New York, pp. 437-449.
104. McGaugh, J.L., Gold, P.E., 1976. Modulation of memory by electrical stimulation of the brain. In: Rosenzweig, M.R., Bennett, E.L. (Eds.), Neural Mechanisms of Learning and Memory. MIT Press, Cambridge, pp. 549-560.
105. McIntyre D.C., Wong R.K. Cellular and synaptic properties of amygdala-kindled pyriform cortex in vitro. J. Neurophysiol. 55:1986;1295-1307.
106. McIntyre C.K., Marriott L.K., Gold P.E. Cooperation between memory systems: acetylcholine release in the amygdala correlates positively with performance on a hippocampus dependent task. Behav. Neurosci. 117:2003;320-326.
107. Mesches M.H., Bianchin M., McGaugh J.L. The effects of intra-amygdala infusion of the AMPA receptor antagonist CNQX on retention performance following aversive training. Neurobiol. Learn. Mem. 66:1996;324-340.
108. + channels in cultured colliculi neurons. Pflugers Arch. 437:1998;74-78.
109. Mitchell S., Ranck J.B. Generation of theta rhythm in medial entorhinal cortex of freely moving rats. Brain Res. 189:1980;49-66.
110. Mueller G.E., Pilzecker A. Experimentelle beitrage zur lehre vom gedachtniss. Zeitschrift fuer Psychologie. 1:1900;1-288.
111. Myme C.I., Sugino K., Turrigiano G.G., Nelson S.B. The NMDA- to -AMPA ratio at synapses onto layer 2/3 pyramidal neurons is conserved across prefrontal and visual cortices. J. Neurophysiol. 90:2003;771-779.
112. Nielson K.A., Jensen R.A. Beta-adrenergic receptor antagonist antihypertensive medications impair arousal-induced modulation of working memory in elderly humans. Behav. Neural Biol. 62:1994;190-200.
113. Packard M.G., Teather L.A. Amygdala modulation of multiple sensory systems: hippocampus and caudate putamen. Neurobiol. Learn. Mem. 69:1998;163-203.
114. Packard M.G., Cahill L., McGaugh J.L. Amygdala modulation of hippocampal-dependent and caudate nucleus-dependent memory processes. Proc. Natl. Acad. Sci. U.S.A. 91:1994;8477-8481.
115. Pape H.C., Driesang R.B. Ionic mechanisms of intrinsic oscillations in neurons of the basolateral amygdaloid complex. J. Neurophysiol. 79:1998;217-226.
116. Pape H.C., Stork A. Genes and mechanisms in the amygdala involved in the formation of fear memory. Ann. N.Y. Acad. Sci. 985:2003;92-105.
117. Paré D., Collins D.R. Neuronal correlates of fear in the lateral amygdala: multiple extracellular recordings in conscious cats. J. Neurosci. 20:2000;2701-2710.
118. Paré D., Gaudreau H. Projection cells and interneurons of the lateral and basolateral amygdala: distinct firing patterns and differential relation to theta and delta rhythms in conscious cats. J. Neurosci. 16:1996;3334-3350.
119. Paré D., Dong J., Gaudreau H. Amygdalo-entorhinal relations and their reflection in the hippocampal formation: generation of sharp sleep potentials. J. Neurosci. 15:1995a;2482-2503.
120. Paré D., Pape H.C., Dong J. Physiological properties of cat basolateral amygdaloid neurons: intracellular recordings in barbiturate-anesthetized cats. J. Neurophysiol. 74:1995b;1179-1191.
121. Paré D., Smith Y., Paré J.F. Intra-amygdaloid projections of the basolateral and basomedial nuclei in the cat: phaseolus vulgaris-leucoagglutinin anterograde tracing at the light and electron microscopic level. Neuroscience. 69:1995c;567-583.
122. Parent M.B., McGaugh J.L. Posttraining infusion of lidocaine into the amygdala basolateral complex impairs retention of inhibitory avoidance training. Brain Res. 661:1994;97-103.
123. Parent M.B., Quirarte G.L., Cahill L., McGaugh J.L. Spared retention of inhibitory avoidance learning after post-training amygdala lesions. Behav. Neurosci. 109:1995;803-807.
124. Pelletier J.G., Paré D. Uniform range of conduction times from the lateral amygdala to distributed perirhinal sites. J. Neurophysiol. 87:2002;1213-1221.
125. Pickel V.M., Segal M., Bloom F.E. A radioautographic study of the efferent pathways of the nucleus locus coeruleus. J. Comp. Neurol. 154:1974;15-42.
126. Pikkarainen M., Rönkkö S., Savander V., Insausti R., Pitkänen A. Projections from the lateral, basal, and accessory basal nuclei of the amygdala to the hippocampal formation in rat. J. Comp. Neurol. 403:1999;229-260.
127. Pitkänen, A., 2000. Connectivity of the rat amygdaloid complex. In: Aggleton, J.P. (Ed.), The Amygdala: A Functional Analysis. Oxford University Press, Oxford, pp. 31-115.
128. Plihal W., Born J. Effects of early and late nocturnal sleep on priming and spatial memory. Psychophysiology. 36:1999;571-582.
129. Power A.E., McGaugh J.L. Phthalic acid amygdalopetal lesion of the nucleus basalis magnocellularis induces reversible memory deficits in rats. Neurobiol. Learn. Mem. 77:2002;372-388.
130. Power A.E., Roozendaal B., McGaugh J.L. Glucocorticoid enhancement of memory consolidation in the rat is blocked by muscarinic receptor antagonism in the basolateral amygdala. Eur. J. Neurosci. 12:2000;3481-3487.
131. Power A.E., Thal L.J., McGaugh J.L. Lesions of the nucleus basalis magnocellularis induced by 192 IgG-saporin block memory enhancement with Post-training norepinephrine in the basolateral amygdala. Proc. Natl. Acad. Sci. U.S.A. 99:2002;2315-2319.
132. Quirarte G.L., Galvez R., Roozendaal B., McGaugh J.L. Norepinephrine release in the amygdala in response to footshock and opioid peptidergic drugs. Brain Res. 808:1998;134-140.
133. Ribak C.E. Aspinous and sparsely-spinous stellate neurons in the visual cortex of rats contain glutamic acid decarboxylase. J. Neurocytol. 7:1978;461-478.
134. Ricardo J.A., Koh E.T. Anatomical evidence of direct projections from the nucleus of the solitary tract to the hypothalamus, amygdala, and other forebrain structures in the rat. Brain Res. 153:1978;1-26.
135. Roesler R., Roozendaal B., McGaugh J.L. Basolateral amygdala lesions block the memory-enhancing effect of 8-Br-cAMP infused into the entorhinal cortex of rats after training. Eur. J. Neurosci. 15:2002;905-910.
136. Roozendaal B., McGaugh J.L. Amygdaloid nuclei lesions differentially affect glucocorticoid-induced memory enhancement in an inhibitory avoidance task. Neurobiol. Learn. Mem. 65:1996a;1-8.
137. Roozendaal B., McGaugh J.L. The memory-modulatory effects of glucocorticoids depend on an intact stria terminalis. Brain Res. 709:1996b;243-250.
138. Roozendaal B., McGaugh J.L. Basolateral amygdala lesions block the memory-enhancing effect of glucocorticoid administration in the dorsal hippocampus of rats. Eur. J. Neurosci. 9:1997;76-83.
139. Roozendaal B., Portillo-Marquez G., McGaugh J.L. Basolateral amygdala lesions block glucocorticoid-induced modulation of memory for spatial learning. Behav. Neurosci. 110:1996;1074-1083.
140. Roozendaal B., Sapolsky R.M., McGaugh J.L. Basolateral amygdala lesions block the disruptive effects of long-term adrenalectomy on spatial memory. Neuroscience. 84:1998;453-465.
141. Roozendaal B., Nguyen B.T., Power A.E., McGaugh J.L. Basolateral amygdala noradrenergic influence enables enhancement of memory consolidation induced by hippocampal glucocorticoid receptor activation. Proc. Natl. Acad. Sci. U.S.A. 96:1999;11642-11647.
142. Royce G.J. Cells of origin of subcortical afferents to the caudate nucleus: a horseradish peroxidase study in the cat. Brain Res. 153:1978;465-475.
143. Russchen F.T., Bakst I., Amaral D.G., Price J.L. The amygdalostriatal projections in the monkey. An anterograde tracing study. Brain Res. 329:1985;241-257.
144. Sacchetti B., Lorenzini C.A., Baldi E., Tassoni G., Bucherelli C. Auditory thalamus, dorsal hippocampus, basolateral amygdala, and perirhinal cortex role in the consolidation of conditioned freezing to context and to acoustic conditioned stimulus in the rat. J. Neurosci. 19:1999;9570-9578.
145. Salinas J.A., McGaugh J.L. Muscimol induces retrograde amnesia for changes in reward magnitude. Neurobiol. Learn. Mem. 63:1995;277-285.
146. Salinas J.A., McGaugh J.L. The amygdala modulates memory for changes in reward magnitude: involvement of the amygdaloid GABAergic system. Behav. Brain Res. 80:1996;87-98.
147. Salinas J.A., Packard M.G., McGaugh J.L. Amygdala modulates memory for changes in reward magnitude: reversible post-training inactivation with lidocaine attenuates the response to a reduction in reward. Behav. Brain Res. 59:1993;153-159.
148. Salinas J.A., Introini-Collison I.B., Dalmaz C., McGaugh J.L. Posttraining intraamygdala infusions of oxotremorine and propranolol modulate storage of memory for reductions in reward magnitude. Neurobiol. Learn. Mem. 68:1997;51-59.
149. Samson R.D., Dumont E.C., Paré D. Feedback inhibition defines transverse processing modules in the lateral amygdala. J. Neurosci. 23:2003;1966-1973.
150. Sarrieau A., Dussaillant M., Agid F., Philibert D., Agid Y., Rostene W. Autoradiographic localization of glucocorticosteroids and progesterone binding sites in the human post-mortem brain. J. Steroid Biochem. 25:1986;717-721.
151. Schreurs J., Seelig T., Schulman H. Beta2-adrenergic receptors on peripheral nerves. J. Neurochem. 46:1986;294-296.
152. Shen W.X., Mennerick S., Covey D.F., Zorumski C.F. Pregnenolone sulfate modulates inhibitory synaptic transmission by enhancing GABA A receptor desensitization. J. Neurosci. 20:2000;3571-3579.
153. + channels in aplysia sensory neurons. Nature. 299:1982;413-417.
154. Smith Y., Paré D. Intra-amygdaloid projections of the lateral nucleus in the cat: PHA-L anterograde labeling combined with post-embedding GABA and glutamate immunocytochemistry. J. Comp. Neurol. 342:1994;232-248.
155. Soderling T.R., Derkach V.A. Postsynaptic protein phosphorylation and LTP. Trends Neurosci. 23:2000;75-80.
156. Squire L.R., Cohen N. Memory and amnesia: resistance to disruption develops for years after learning. Behav. Neural Biol. 25:1979;115-125.
157. Stickgold R., LaTanya J., Hobson J.A. Visual discrimination learning requires sleep after training. Nat. Neurosci. 3:2000;1237-1238.
158. Stoop R., Epiney S., Meier E., Pralong E. Modulation of epileptiform discharges in the rat limbic system in vitro by noradrenergic agents. Neurosci. Lett. 287:2000;5-8.
159. Tanaka T., Yokoo H., Mizoguchi K., Yoshida M., Tsuda A., Tanaka M. Noradrenaline release in the rat amygdala is increased by stress: studies with intracerebral microdialysis. Brain Res. 544:1991;174-176.
160. Teschemacher A., Kasparov S., Kravitz E.A., Rahamimoff R. Presynaptic action of the neurosteroid pregnenolone sulfate on inhibitory transmitter release in cultured hippocampal neurons. Brain Res. 772:1997;226-232.
161. Thomson A.M., Deuchars J. Synaptic interactions in neocortical local circuits: dual intracellular recordings in vitro. Cereb. Cortex. 7:1997;510-522.
162. Tomaz C., Dickinson-Anson H., McGaugh J.L. Basolateral amygdala lesions block diazepam-induced anterograde amnesia in an inhibitory avoidance task. Proc. Natl. Acad. Sci. U.S.A. 89:1992;3615-3619.
163. Van Bockstaele E.J., Peoples J., Telegan P. Efferent projections of the nucleus of the solitary tract to peri-locus coeruleus dendrites in rat brain: evidence for a monosynaptic pathway. J. Comp. Neurol. 412:1999;410-428.
164. Walker D.L., Davis M. The role of amygdala glutamate receptors in fear learning, fear-potentiated startle, and extinction. Pharmacol. Biochem. Behav. 71:2002;379-392.
165. Washburn M.S., Moises H.C. Muscarinic responses of rat basolateral amygdaloid neurons recorded in vitro. J. Physiol. (Lond.). 449:1992;121-154.
166. Weinberger N.M. Physiological memory in primary auditory cortex: characteristics and mechanisms. Neurobiol. Learn. Mem. 70:1998;226-251.
167. Williams C.L., McGaugh J.L. Reversible lesions of the nucleus of the solitary tract attenuate the memory-modulating effects of Post-training epinephrine. Behav. Neurosci. 107:1993;955-962.
168. Williams C.L., Men D., Clayton E.C. The effects of noradrenergic activation of the nucleus tractus solitarius on memory and in potentiating norepinephrine release in the amygdala. Behav. Neurosci. 114:2000;1131-1144.
169. Wilson M.A., McNaughton B.L. Reactivation of hippocampal ensemble memories during sleep. Science. 265:1989;676-679.
170. Wong M., Moss R.L. Patch-clamp analysis of direct steroidal modulation of glutamate receptor-channels. J. Neuroendocrinol. 6:1994;347-355.
171. Yajeya J., Juan A.D., Bajo V.M., Riolobos A.S., Heredia M., Criado J.M. Muscarinic activation of a non-selective cationic conductance in pyramidal neurons in rat basolateral amygdala. Neuroscience. 88:1999;159-167.
172. Yajeya J., De La Fuente A., Criado J.M., Bajo V., Sanchez-Riobolos A., Heredia M. Muscarinic agonist carbachol depresses excitatory synaptic transmission in the rat basolateral amygdala in vitro. Synapse. 38:2000;151-160.
173. Young A., Rees K.R. Dopamine release in the amygdaloid complex of the rat, studied by brain microdialysis. Neurosci. Lett. 249:1998;49-52.
174. Young M.P., Scannell J.W., Burns G.A., Blakemore C. Analysis of connectivity: neural systems in the cerebral cortex. Rev. Neurosci. 5:1994;227-249.
175. Zbrozyna, A.W., 1972. The organization of the defense reaction elicited from amygdala and its connections. In: Eleftheriou, B. (Ed.), The Neurobiology of the Amygdala. Plenum Press, New York, pp. 597-608.