The amygdala: vigilance and emotion
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Holland PC, Gallagher M . Amygdala circuitry in attentional and representational processes [Review] Trends Cogn Sci 1999 3: 65–73
Baldwin AE, Holahan MR, Sadeghian K, Kelley AE . N-methyl-D-aspartate receptor-dependent plasticity within a distributed corticostriatal network mediates appetitive instrumental learning Behav Neurosci 2000 114: 84–98
Miserendino MJD, Sananes CB, Melia KR, Davis M . Blocking of acquisition but not expression of conditioned fear-potentiated startle by NMDA antagonists in the amygdala Nature 1990 345: 716–718
Davis M, Walker DL, Lee Y . Roles of the amygdala and bed nucleus of the stria terminalis in fear and anxiety measured with the acoustic startle reflex: possible relevance to PTSD Ann NY Acad Sci 1997 821: 305–331
Davis M . Neurobiology of fear responses: the role of the amygdala J Neuropsy Clin Neurosci 1997 9: 382–402
Gray TS . Autonomic neuropeptide connections of the amygdala. In: Tache Y, Morley JE, Brown MR (eds) Neuropeptides and Stress Springer Verlag: New York 1989 pp 92–106
Gloor P . Amygdala. In: Field J (ed) Handbook of Physiology: Sec. I. Neurophysiology American Physiological Society: Washington, DC 1960 pp 1395–1420
Kapp BS, Pascoe JP, Bixler MA . The amygdala: a neuroanatomical systems approach to its contribution to aversive conditioning. In: Butters N, Squire LS (eds) The Neuropsychology of Memory The Guilford Press: New York 1984 pp 473–488
Kapp BS, Pascoe JP . Correlation aspects of learning and memory: vertebrate model systems. In: Martinez JL, Kesner RP (eds) Learning and Memory: A Biological View Academic Press: New York 1986 pp 399–440
Kapp BS, Wilson A, Pascoe JP, Supple WF, Whalen PJ . A neuroanatomical systems analysis of conditioned bradycardia in the rabbit. In: Gabriel M, Moore J (eds) Neurocomputation and Learning: Foundations of Adaptive Networks Bradford Books: New York 1990 pp 55–90
LeDoux JE. Emotion. In: Plum F (ed) . Handbook of Physiology, Sec. 1, Neurophysiology: Vol. 5. Higher Functions of the Brain American Psychological Society: Bethesda 1987 pp 416–459
Sarter M, Markowitsch HJ . Involvement of the amygdala in learning and memory: a critical review, with emphasis on anatomical relations Behav Neurosci 1985 99: 342–380
Davis M . The role of the amygdala in conditioned and unconditioned fear and anxiety. In: Aggleton JP (ed) The Amygdala, A Functional Analysis Oxford University Press: Oxford, UK 2000 213–287
Alheid G, deOlmos JS, Beltramino CA . Amygdala and extended amygdala. In: Paxinos G (ed) The Rat Nervous System Academic Press: New York 1995 pp 495–578
LeDoux JE, Iwata J, Cicchetti P, Reis DJ . Different projections of the central amygdaloid nucleus mediate autonomic and behavioral correlates of conditioned fear J Neurosci 1988 8: 2517–2529
Schwaber JS, Kapp BS, Higgins GA, Rapp PR . Amygdaloid basal forebrain direct connections with the nucleus of the solitary tract and the dorsal motor nucleus J Neurosci 1982 2: 1424–1438
Goldstein LE, Rasmusson AM, Bunney BS, Roth RH . Role of the amygdala in the coordination of behavioral, neuroendocrine, and prefrontal cortical monoamine responses to psychological stress in the rat J Neurosci 1996 16: 4787–4798
Aston-Jones G, Rajkowski J, Kubiak P, Valentino RJ, Shipley MT . Role of the locus coeruleus in emotional activation Prog Brain Res 1996 107: 379–402
Redmond DE Jr . Alteration in the function of the nucleus locus: a possible model for studies on anxiety. In: Hanin IE, Usdin E (eds) Animal Models in Psychiatry and Neurology Pergamon Press: Oxford UK 1977 pp 292–304
Kapp BS, Whalen PJ, Supple WF, Pascoe JP . Amygdaloid contributions to conditioned arousal and sensory information processing. In: Aggleton JP (ed) The Amygdala: Neurobiological Aspects of Emotion, Memory, and Mental Dysfunction Wiley-Liss: New York 1992 pp 229–254
McCall RB, Aghajanian GK . Serotonergic facilitation of facial motoneuron excitation Brain Res 1979 169: 11–27
White SR, Neuman RS . Facilitation of spinal motoneuron excitability by 5-hydroxytryptamine and noradrenaline Brain Res 1980 185: 1–9
Bandler R, Carrive P . Integrated defence reaction elicted by excitatory amino acid microinjection in the midbrain periaqueductal grey region of the unrestrained cat Brain Res 1988 439: 95–106
Blanchard DC, Williams G, Lee EMC, Blanchard RJ . Taming of wild Rattus norvegicus by lesions of the mesencephalic central gray Physiol Psychol 1981 9: 157–163
Fanselow MS . The midbrain periaqueductal gray as a coordinator of action in response to fear and anxiety. In: Depaulis A, Bandler R (eds) The Midbrain Periaqueductal Gray Matter: Functional, Anatomical and Neurochemical Organization Plenum Publishing: New York 1991 pp 151–173
Graeff FG . Animal models of aversion. In: Simon P, Soubrie P, Wildlocher D (eds) Selected Models of Anxiety, Depression and Psychosis Karger: Basel, Switzerland 1988 pp 115–141
Helmstetter FJ, Tershner SA, Poore LH, Bellgowan PSF . Antinociception following opioid stimulation of the basolateral amygdala is expressed through the periaqueductal gray and rostral ventromedial medulla Brain Res 1998 779: 104–118
Gloor P . Role of the amygdala in temporal lobe epilepsy. In: Aggleton JP (ed) The Amygdala: Neurobiological Aspects of Emotion, Memory and Mental Dysfunction Wiley-Liss: New York 1992 pp 505–538
Chapman WP, Schroeder HR, Guyer G, Brazier MAB, Fager C, Poppen JL et al. Physiological evidence concerning the importance of the amygdaloid nuclear region in the integration of circulating function and emotion in man Science 1954 129: 949–950
Gloor P, Olivier A, Quesney LF . The role of the amygdala in the expression of psychic phenomena in temporal lobe seizures. In: Ben-Ari Y (ed) The Amygdaloid Complex Elsevier/North Holland: New York 1981 pp 489–507
Sanders SK, Shekhar A . Blockade of GABAA receptors in the region of the anterior basolateral amygdala of rats elicits increases in heart rate and blood pressure Brain Res 1991 576: 101–110
Soltis RP, Cook JC, Gregg AE, Sanders BJ . Interaction of GABA and excitatory amino acids in the basolateral amygdala: role in cardiovascular regulation J Neurosci 1997 17: 9367–9374
Sajdyk TJ, Shekhar A . Excitatory amino acid receptor antagonists block the cardiovascular and anxiety responses elicited by γ-aminobutyric acid—a receptor blockade in the basolateral amygdala of rats J Pharmacol Exp Therapeut 1997 283: 969–977
Soltis RP, Cook JC, Gregg AE, Stratton JM, Flickinger KA . EAA receptors in the dorsomedial hypothalamic area mediate the cardiovascular response to activation of the amygdala Am J Physiol 1998 275: R624–R631
Sanders SK, Shekhar A . Regulation of anxiety by GABAA receptors in the rat amygdala Pharmacol Biochem Behav 1995 52: 701–706
Sajdyk TJ, Schober DA, Gehlert DR, Shekhar A . Role of corticotropin-releasing factor and urocortin within the basolateral amygdala of rats in anxiety and panic responses Behav Brain Res 1999 100: 207–215
Adamec R . Transmitter systems involved in neural plasticity underlying increased anxiety and defense—implications for understanding anxiety following traumatic stress Neurosci Biobehav Rev 1997 21: 755–765
Feldman S, Weidenfeld J . The excitatory effects of the amygdala on hypothalamo-pituitary-adrenocortical responses are mediated by hypothalamic norepinephrine, serotonin, and CRF-41 Brain Res Bull 1998 45: 389–393
Kapp BS, Supple WF, Whalen PJ . Effects of electrical stimulation of the amygdaloid central nucleus on neocortical arousal in the rabbit Behav Neurosci 1994 108: 81–93
Dringenberg HC, Vanderwolf CH . Cholinergic activation of the electrocorticogram: an amygdaloid activating system Exp Brain Res 1996 108: 285–296
Applegate CD, Kapp BS, Underwood MD, McNall CL . Autonomic and somatomotor effects of amygdala central n. stimulation in awake rabbits Physiol Behav 1983 31: 353–360
Ursin H, Kaada BR . Functional localization within the amygdaloid complex in the cat Electroencephalogr Clin Neurophysiol 1960 12: 109–122
McKernan MG, Shinnick-Gallagher P . Fear conditioning induces a lasting potentiation of synaptic currents in vitro Nature 1997 390: 607–611
Quirk GJ, Repa JC, LeDoux JE . Fear conditioning enhances short-latency auditory responses of lateral amygdala neurons: parallel recordings in the freely behaving rat Neuron 1995 15: 1029–1039
Rogan MT, Staubli UV, LeDoux JE . Fear conditioning induces associative long-term potentiation in the amygdala Nature 1997 390: 604–607
Clugnet MC, LeDoux JE . Synaptic plasticity in fear conditioning circuits: induction of LTP in the lateral nucleus of the amygdala by stimulation of the medial geniculate body J Neurosci 1990 10: 2818–2824
Chapman PF, Kairiss EW, Keenan CL, Brown TH . Long-term synaptic potentiation in the amygdala Synapse 1990 6: 271–278
Chapman PF, Bellavance LL . Induction of long-term potentiation in the basolateral amygdala does not depend on NMDA receptor activation Synapse 1992 11: 310–318
Gean PW, Chang FC, Huang CC, Lin JH, Way LJ . Long-term enhancement of EPSP and NMDA receptor-mediated synaptic transmission in the amygdala Brain Res Bull 1993 31: 7–11
Huang YY, Kandel ER . Postsynaptic induction and PKA-dependent expression of LTP in the lateral amygdala Neuron 1998 21: 169–178
Shindou T, Watanabe S, Yamamoto K, Nakanishi H . NMDA receptor-dependent formation of long-term potentiation in the rat medial amygdala neuron in an in vitro slice preparation Brain Res Bull 1993 31: 667–672
Rogan MT, LeDoux JE . LTP is accompanied by commensurate enhancement of auditory-evoked responses in a fear conditioning circuit Neuron 1995 15: 127–136
Kluver H, Bucy PC . Preliminary analysis of functions of the temporal lobes in monkeys Arch Neurol Psychiatry 1939 42: 979–1000
Kling AS, Brothers LA . The amygdala and social behavior. In: Aggleton J (ed) The Amygdala: Neurobiological Aspects of Emotion, Memory and Mental Dysfunction John Wiley & Sons: New York 1992 pp 353–377
Dicks D, Meyers RE, Kling A . Uncus and amygdala lesions: effects on social behavior in the free-ranging rhesus monkey Science 1969 165: 69–71
Kling A, Lancaster J, Benitone J . Amygdalectomy in the free-ranging vervet J Psychiatr Res 1970 7: 191–199
Horel JA, Keating EG, Misantone LJ . Partial Kluver–Bucy syndrome produced by destroying termporal neocortex and amygdala Brain Res 1975 94: 347–359
Meyers RE, Swett C . Social behaviour deficits of free-ranging monkeys after anterior temporal cortex removals: a preliminary report Brain Res 1970 19: 39
Mishkin M, Pribram KH . Visual discrimination performance following partial ablations of the temporal lobe. I. Ventral vs lateral J Comp Physiol Psychol 1954 47: 14–20
Pribram KH, Bagshaw M . Further analysis of the temporal lobe syndrome utilizing fronto-temporal ablations J Comp Neurol 1953 99: 347–374
Schwartzbaum JS . Discrimination behavior after amygdalectomy in monkeys: learning set and discrimination reversals J Comp Physiol Psychol 1965 60: 314–319
Weiskrantz L . Behavioral changes associated with ablation of the amygdaloid complex in monkeys J Comp Physiol Psychol 1956 49: 381–391
Aggleton JP, Passingham RE . Syndrome produced by lesions of the amygdala in monkeys (Macaca mulatta) J Comp Physiol Psychol 1981 95: 961–977
Zola-Morgan S, Squire LR, Alvarez-Royo P, Clower RP . Independence of memory functions and emotional behavior: separate contributions of the hippocampal formation and the amygdala Hippocampus 1991 1: 207–220
Nelson EE, Shelton SE, Kelley AE, Kalin NH . Innate snake fear in rhesus monkeys: role of the amygdala Soc Neurosci Abs 1999 25: 2151
Aggleton J . The contribution of the amygdala to normal and abnormal emotional states Trends Neurosci 1993 8: 328–333
Kromer Vogt LJ, Hyman BT, Van Hoesen GW, Damasio AR . Pathological alterations in the amygdala in Alzheimer's disease Neuroscience 1990 37: 377–385
Kirkpatrick B, Buchanan RW . The neural basis of the deficit syndrome of schizophrenia J Nerv Ment Dis 1990 178: 545–555
Leonard CM, Rolls ET, Wilson FAW, Baylis GC . Neurons in the amygdala of the monkey with responses selective for faces Behav Brain Res 1985 15: 159–176
Nakamura K, Mikami A, Kubota K . Activity of single neurons in the monkey amygdala during performance of a visual discrimination task J Neurophysiol 1992 67: 1447–1463
Rolls ET . Neurons in the cortex of the temporal lobe and in the amygdala of the monkey with responses selective for faces Hum Neurobiol 1984 3: 209–222
Allison T, McCarthy G, Nobre A, Puce A, Belger A . Human extrastriate visual cortex and the perception of faces, words, numbers, and colors Cereb Cortex 1994 4: 544–554
Heit G, Smith ME, Halgren E . Neural encoding of individual words and faces by the human hippocampus and amygdala Nature 1988 333: 773–775
Brothers L, Ring B . Mesial temporal neurons in the macaque monkey with responses selective for aspects of social stimuli Behav Brain Res 1993 57: 53–61
Aggleton JP . The functional effects of amygdala lesions in humans: a comparison with findings from monkeys. In: Aggleton JP (ed) The Amygdala: Neurobiological Aspects of Emotion, Memory and Mental Dysfunction Wiley-Liss: New York 1992 pp 485–503
Jacobson R . Disorders of facial recognition, social behaviour and affect after combined bilateral amygdalotomy and subcaudate tractotomy—a clinical and experimental study Psychol Med 1986 16: 439–450
Tranel D, Hyman BT . Neuropsychological correlates of bilateral amygdala damage Arch Neurol 1990 47: 349–355
Young AW, Aggleton JP, Hellawell DJ, Johnson M, Broks P, Hanley JR . Face processing impairments after amygdalotomy Brain 1995 118: 15–24
Calder AJ, Young AW, Rowland D, Perrett DI, Hodges JR, Etcoff NL . Facial emotion recognition after bilateral amygdala damage: differentially severe impairment of fear Cogn Neuropsychol 1996 13: 699–745
Adolphs R, Tranel D, Damasio H, Damasio AR . Impaired recognition of emotion in facial expressions following bilateral damage to the human amygdala Nature 1994 372: 669–672
Adolphs R, Tranel D, Damasio H, Damasio AR . Fear and the human amygdala J Neurosci 1995 15: 5879–5891
Adolphs R, Russell JA, Tranel D . A role for the human amygdala in recognizing emotion arousal from unpleasant stimuli Psychol Sci 1999 10: 167–171
Hamann SB, Stefanacci L, Squire LR, Adolphs R, Tranel D, Damasio H et al. Recognizing facial emotion Nature 1996 379: 497
Adolphs R, Cahill L, Schul R, Babinsky R . Impaired declarative memory for emotional material following bilateral amygdala damage in humans Learning and Memory 1997 4: 291–300
Cahill L, Babinsky R, Markowitsch HJ, McGaugh JL . The amygdala and emotional memory Nature 1995 377: 295–296
Markowitsch HJ, Calabrese P, Wurker M, Durwen HF, Kessler J, Babinsky R et al. The amygdala's contribution to memory—a study on two patients with Urbach–Wiethe disease NeuroReport 1994 5: 1349–1352
McGaugh JL, Introini-Collison IB, Nagahara AH, Cahill L, Brioni JD, Castellano C . Involvement of the amygdaloid complex in neuromodulatory influences on memory storage Neurosci Biobehav Rev 1990 14: 425–432
Anderson AK, Phelps EA . Expression without recognition: contributions of the human amygdala to emotional communication Psychol Sci 2000 11: 106–111
Anderson AK, Phelps EA . Intact recognition of vocal expressions of fear following bilateral lesions of the human amygdala Neuroreport 1998 9: 3607–3613
Adolphs R, Tranel D . Intact recognition of emotional prosody following amygdala damage Neuropsychologia 1999 37: 1285–1292
LeBar KS, LeDoux JE, Spencer DD, Phelps EA . Impaired fear conditioning following unilateral temporal lobectomy in humans J Neurosci 1995 15: 6846–6855
Bechara A, Tranel D, Damasio H, Adolphs R, Rockland C, Damasio AR . Double dissociation of conditioning and declarative knowledge relative to the amygdala and hippocampus in humans Science 1995 269: 1115–1118
Bagshaw MH, Kimble DP, Pribram KH . The GSR of monkeys during orienting and habituation and after ablation of the amygdala, hippocampus and inferotemporal cortex Neuropsychologia 1965 3: 111–119
Bagshaw MH, Benzies S . Multiple measures of the orienting reaction and their dissociation after amygdalectomy in monkeys Exp Neurol 1968 20: 175–187
Blanchard DC, Blanchard RJ . Innate and conditioned reactions to threat in rats with amygdaloid lesions J Comp Physiol Psychol 1972 81: 281–290
Ursin H, Jellestad F, Cabrera IG . The amygdala, exploration and fear. In: Ben-Ari Y (ed) The Amygdaloid Complex Elsevier North Holland Press: Amsterdam 1981 pp 317–329
Lee GP, Bechara A, Adolphs R, Arena J, Meador KJ, Loring DW, et al. Clinical and physiological effects of stereotaxic bilateral amygdalotomy for intractable aggression J Neuropsy Clin Neurosci 1998 10: 413–420
Kaada BR . Stimulation and regional ablation of the amygdaloid complex with reference to functional representations. In: Eleftheriou BE (ed) The Neurobiology of the Amygdala Plenum Press: New York 1972 pp 205–281
McGaugh JL, Introini-Collison IB, Cahill L, Castellano C, Dalmaz C, Parent MB et al. Neuromodulatory systems and memory storage: role of the amygdala Behav Brain Res 1993 58: 81–90
McGaugh J, Cahill L, Parent MB, Mesches MH, Coleman-Mesches K, Salinas JA . Involvement of the amygdala in the regulation of memory storage. In: McGaugh J, Bermudez-Rattoni F, Praco-Alcala RA (eds) Plasticity in the Central Nervous System Lawrence Erlbaum Associates: Hillsdale, NJ 1995 pp 17–40
Bennett C, Liang KC, McGaugh JL . Depletion of adrenal catecholamines alters the amnestic effect of amygdala stimulation Behav Brain Res 1985 15: 83–91
Bresnahan E, Routtenberg A . Memory disruption by unilateral low level, sub-seizure stimulation of the medial amygdaloid nucleus Physiol Behav 1972 9: 513–525
Ellis ME, Kesner RP . The noradrenergic system of the amygdala and aversive information processing Behav Neurosci 1983 97: 399–415
Gallagher M, Kapp BS, Frysinger RC, Rapp PR . b-Adrenergic manipulation in amygdala central n. alters rabbit heart rate conditioning Pharmacol Biochem Behav 1980 12: 419–426
Gallagher M, Kapp BS . Effect of phentolamine administration into the amygdala complex of rats on time-dependent memory processes Behav Neural Biol 1981 31: 90–95
Gallagher M, Kapp BS, McNall CL, Pascoe JP . Opiate effects in the amygdala central nucleus on heart rate conditioning in rabbits Pharmacol Biochem Behav 1981 14: 497–505
Gallagher M, Kapp BS . Manipulation of opiate activity in the amygdala alters memory processes Life Sci 1978 23: 1973–1978
Gold PE, Hankins L, Edwards RM, Chester J, McGaugh JL . Memory inference and facilitation with post-trial amygdala stimulation: effect varies with footshock level Brain Res 1975 86: 509–513
Handwerker MJ, Gold PE, McGaugh JL . Impairment of active avoidance learning with posttraining amygdala stimulation Brain Res 1974 75: 324–327
Liang KC, Bennett C, McGaugh JL . Peripheral epinephrine modulates the effects of post-training amygdala stimulation on memory Behav Brain Res 1985 15: 93–100
Liang KC, Juler RG, McGaugh JL . Modulating effects of post-training epinephrine on memory: involvement of the amygdala noradrenergic systems Brain Res 1986 368: 125–133
Mishkin M, Aggleton J . Multiple function contributions of the amygdala in the monkey. In: Ben-Ari Y (ed) The Amygdaloid Complex Elsevier/North Holland: New York 1981 pp 409–420
Gallagher M, Graham PW, Holland PC . The amygdala central nucleus and appetitive pavlovian conditioning: lesions impair one class of conditioned behavior J Neurosci 1990 10: 1906–1911
Holland PC, Gallagher M . The effects of amygdala central nucleus lesions on blocking and unblocking Behav Neurosci 1993 107: 235–245
Holland PC, Gallagher M . Amygdala central nucleus lesions disrupt increments, but not decrement, in conditioned stimulus processing Behav Neurosci 1993 107: 246–253
Bermudez-Rattoni F, Grijalva CV, Kiefer SW, Garcia J . Flavor-illness aversion: the role of the amygdala in acquisition of taste-potentiated odor aversions Physiol Behav 1986 38: 503–508
Hatfield T, Graham PW, Gallagher M . Taste-potentiated odor aversion: role of the amygdaloid basolateral complex and central nucleus Behav Neurosci 1992 106: 286–293
Fernandez-Ruiz J, Miranda MI, Bermudez-Rattoni F, Drucker-Colin R . Effects of catecholaminergic depletion of the amygdala and insular cortex on the potentiation of odor by taste aversions Behav Neural Biol 1993 60: 189–191
Hatfield T, Gallagher M . Taste-potentiated odor conditioning: impairment produced by infusion of an N-methyl-D-aspartate antagonist into basolateral amygdala Behav Neurosci 1995 109: 663–668
Hatfield T, Han J-S, Conley M, Gallagher M, Holland P . Neurotoxic lesions of basolateral, but not central, amygdala interfere with Pavlovian second-order conditioning and reinforcer devaluation effects J Neurosci 1996 16: 5256–5265
Halgren E . Emotional neurophysiology of the amygdala within the context of human cognition. In: Aggleton JP (ed) The Amygdala: Neurobiological Aspects of Emotion, Memory, and Mental Dysfunction Wiley-Liss: New York 1992 pp 191–228
Crandall PH, Walter RD, Dymond A . The ictal electroencephalographic signal identifying limbic system seizure foci Proc Am Assoc Neurol Surg 1971 1: 1
DeSouza EB, Insel TR, Perrin MH, Rivier J, Vale WW, Kuhar MJ . Corticotropin-releasing factor receptors are widely distributed within the rat central nervous system: an autoradiographic study J Neurosci 1985 5: 3189–3203
Uryu K, Okumura T, Shibasaki T, Sakanaka M . Fine structure and possible origins of nerve fibers with corticotropin-releasing factor-like immunoreactivity in the rat central amygdaloid nucleus Brain Res 1992 577: 175–179
Sullivan RM, Henke PG, Ray A, Hebert MA, Trimper JM . The GABA/benzodiazepine receptor complex in the central amygdalar nucleus and stress ulcers in rats Behav Neural Biol 1989 51: 262–269
Green S, Vale AL . Role of amygdaloid nuclei in the anxiolytic effects of benzodiazepines in rats Behav Pharmacol 1992 3: 261–264
Hodges H, Green S, Glenn B . Evidence that the amygdala is involved in benzodiazepine and serotonergic effects on punished responding but not on discrimination Psychopharmacology 1987 92: 491–504
Petersen EN, Braestrup C, Scheel-Kruger J . Evidence that the anticonflict effect of midazolam in amygdala is mediated by the specific benzodiazepine receptor Neuroscience Lett 1985 53: 285–288
Scheel-Kruger J, Petersen EN . Anticonflict effect of the benzodiazepines mediated by a GABAergic mechanism in the amygdala Eur J Pharmacol 1982 82: 115–116
Thomas SR, Lewis ME, Iversen SD . Correlation of [3H]diazepam binding density with anxiolytic locus in the amygdaloid complex of the rat Brain Res 1985 342: 85–90
Shibata K, Kataoka Y, Yamashita K, Ueki S . An important role of the central amygdaloid nucleus and mammillary body in the mediation of conflict behavior in rats Brain Res 1986 372: 159–162
Takao K, Nagatani T, Kasahara K-I, Hashimoto S . Role of the central serotonergic system in the anticonflict effect of d-AP159 Pharmacol Biochem Behav 1992 43: 503–508
Pesold C, Treit D . The central and basolateral amygdala differentially mediate the anxiolytic effects of benzodiazepines Brain Res 1995 671: 213–221
Helmstetter FJ . Stress-induced hypoalgesia and defensive freezing are attenuated by application of diazepam to the amygdala Pharmacol Biochem Behav 1993 44: 433–438
Young BJ, Helmstetter FJ, Rabchenuk SA, Leaton RN . Effects of systemic and intra-amygdaloid diazepam on long-term habituation of acoustic startle in rats Pharmacol Biochem Behav 1991 39: 903–909
Costall B, Kelly ME, Naylor RJ, Onaivi ES, Tyers MB . Neuroanatomical sites of action of 5-HT3 receptor agonist and antagonists for alteration of aversive behaviour in the mouse Br J Pharmacol 1989 96: 325–332
Boadle-Biber MC, Singh VB, Corley KC, Phan TH, Dilts RP . Evidence that corticotropin-releasing factor within the extended amygdala mediates the activation of tryptophan hydroxylase produced by sound stress in the rat Brain Res 1993 628: 105–114
Heinrichs SC, Pich EM, Miczek KA, Britton KT, Koob GF . Corticotropin-releasing factor antagonist reduces emotionality in socially defeated rats via direct neurotropic action Brain Res 1992 581: 190–197
Rassnick S, Heinrichs SC, Britton KT, Koob GF . Microinjection of a corticotropin-releasing factor antagonist into the central nucleus of the amygdala reverses anxiogenic-like effects of ethanol withdrawal Brain Res 1993 605: 25–32
Heinrichs SC, Menzaghi F, Schulteis G, Koob GF, Stinus L . Suppression of corticotropoin-releasing factor in the amygdala attenuates aversive consequences of morphine withdrawal Behav Pharmacol 1995 6: 74–80
Liebsch G, Landgraf R, Gerstberger R, Probst JC, Wotjak CT, Engelmann M et al. Chronic infusion of a CRH1 receptor antisense oligodeoxynucleotide into the central nucleus of the amygdala reduced anxiety-related behavior in socially defeated rats Regul Peptides 1995 59: 229–239
Swiergiel AH, Takahashi LK, Kalin NH . Attenuation of stress-induced behavior by antagonism of corticotropin-releasing factor in the central amygdala of the rat Brain Res 1993 623: 229–234
Wiersma A, Baauw AD, Bohus B, Koolhaas JM . Behavioural activation produced by CRH but not a-helical CRH (CRH-receptor antagonist) when microinfused into the central nucleus of the amygdala under stress-free conditions Psychoneuroendocrinology 1995 20: 423–432
Ray A, Sullivan RM, Henke PG . Interactions of thyrotropin-releasing hormone (TRH) with neurotensin and dopamine in the central nucleus of the amygdala during stress ulcer formation in rats Neurosci Lett 1988 91: 95–100
Ray A, Henke PG . Enkephalin-dopamine interactions in the central amygdalar nucleus during gastric stress ulcer formation in rats Behav Brain Res 1990 36: 179–183
Ray A, Henke PG . TRH-enkephalin interactions in the amygdaloid complex during gastric stress ulcer formation in rats Regul Peptides 1991 35: 11–17
Gallagher M, Kapp BS, Pascoe JP . Enkephalin analogue effects in the amygdala central nucleus on conditioned heart rate Pharmacol Biochem Behav 1982 17: 217–222
File SE, Rodgers RJ . Partial anxiolytic actions of morphine sulphate following microinjection into the central nucleus of the amygdala in rats Pharmacol Biochem Behav 1979 11: 313–318
Sajdyk TJ, Vandergriff MG, Gehlert DR . Amygdalar neuropeptide Y Y-1 receptors mediate the anxiolytic-like actions of neuropeptide Y in the social interaction test Eur J Pharmacol 1999 368: 143–147
Heilig M, McLeod S, Brot M, Henrichs SC, Menzaghi F, Koob GF et al. Anxiolytic-like action of neuropeptide Y: mediation by Y1 receptors in amygdala, and dissociation from food intake effects Neuropsychopharmacology 1993 8: 357–363
Roozendaal B, Wiersma A, Driscoll P, Koolhaas JM, Bohus B . Vasopressinergic modulation of stress responses in the central amygdala of the Roman high-avoidance and low-avoidance rat Brain Res 1992 596: 35–40
Lamont EW, Kokkinidis L . Infusion of the dopamine D1 receptor antagonist SCH 23390 into the amygdala blocks fear expression in a potentiated startle paradigm Brain Res 1998 795: 128–136
Guarraci FA, Frohardt RJ, Kapp BS . Amygdaloid D1 dopamine receptor involvement in Pavlovian fear conditioning Brain Res 1999 827: 28–40
Kim M, Campeau S, Falls WA, Davis M . Infusion of the non-NMDA receptor antagonist CNQX into the amygdala blocks the expression of fear-potentiated startle Behav Neural Biol 1993 59: 5–8
Walker DL, Davis M . Double dissociation between the involvement of the bed nucleus of the stria terminalis and the central nucleus of the amygdala in light-enhanced versus fear-potentiated startle J Neurosci 1997 17: 9375–9383
Shors TJ, Mathew PR . NMDA receptor antagonism in the lateral/basolateral but not central nucleus of the amygdala prevents the induction of facilitated learning in response to stress Learning and Memory 1998 5: 220–230
Sajdyk TJ, Shekhar A . Excitatory amino acid receptors in the basolateral amygdala regulate anxiety responses in the social interaction test Brain Res 1997 764: 262–264
Taylor JR, Punch LJ, Elsworth JD . A comparison of the effects of clonidine and CNQX infusion into the locus coeruleus and the amygdala on naloxone-precipitated opiate withdrawal in the rat Psychopharmacology 1998 138: 133–142
Wiersma A, Bohus B, Koolhaas JM . Corticotropin-releasing hormone microinfusion in the central amygdala diminishes a cardiac parasympathetic outflow under stress-free conditions Brain Res 1993 625: 219–227
Brown MR, Gray TS . Peptide injections into the amygdala of conscious rats: effects on blood pressure, heart rate and plasma catecholamines Regul Peptides 1988 21: 95–106
Wiersma A, Tuinstra T, Koolhaas JM . Corticotropin-releasing hormone microinfusion into the basolateral nucleus of the amygdala does not induce any changes in cardiovascular, neuroendocrine or behavioural output in a stress-free condition Unpublished dissertation, University of Groningen, The Netherlands 1997
Wiersma A, Bohus B, Koolhaas JM . Corticotropin-releasing hormone microinfusion in the central amygdala enhances active behaviour responses in the conditioned burying paradigm Stress 1997 1: 113–122
Roozendaal B, Schoorlemmer GH, Koolhaas JM, Bohus B . Cardiac, neuroendocrine, and behavioral effects of central amygdaloid vasopressinergic and oxytocinergic mechanisms under stress-free conditions in rats Brain Res Bull 1993 32: 573–579
Willcox BJ, Poulin P, Veale WL, Pittman QJ . Vasopressin-induced motor effects: localization of a sensitive site in the amygdala Brain Res 1992 596: 58–64
Ray A, Henke PG, Sullivan RM . Effects of intra-amygdalar thyrotropin releasing hormone (TRH) and its antagonism by atropine and benzodiazepines during stress ulcer formation in rats Pharmacol Biochem Behav 1990 36: 597–601
Morrow NS, Hodgson DM, Garrick T . Microinjection of thyrotropin-releasing hormone analogue into the central nucleus of the amygdala stimulates gastric contractility in rats Brain Res 1996 735: 141–148
Hernandez DE, Salaiz AB, Morin P, Moreira MA . Administration of thyrotropin-releasing hormone into the central nucleus of the amygdala induces gastric lesions in rats Brain Res Bull 1990 24: 697–699
Ishikawa T, Yang H, Tache Y . Medullary sites of action of the TRH analogue, RX 77368, for stimulation of gastric acid secretion in the rat Gastroenterology 1988 95: 1470–1476
Calvino B, Lagowska J, Ben-Ari Y . Morphine withdrawal syndrome: differential participation of structures located within the amygdaloid complex and striatum of the rat Brain Res 1979 177: 19–34
Stinus L, LeMoal M, Koob GF . Nucleus accumbens and amygdala are possible substrates for the aversive stimulus effects of opiate withdrawal Neuroscience 1990 37: 767–773
Maldonado R, Stinus L, Gold LH, Koob GF . Role of different brain structures in the expression of the physical morphine withdrawal syndrome J Pharmacol Exp Therapeut 1992 261: 669–677
Fendt M, Koch M, Schnitzler HU . Amygdaloid noradrenaline is involved in the sensitization of the acoustic startle response in rats Pharmacol Biochem Behav 1994 48: 307–314
Belcheva I, Belcheva S, Petkov VV, Petkov VD . Asymmetry in behavioral responses to cholecystokinin microinjected into rat nucleus accumbens and amygdala Neuropharmacology 1994 33: 995–1002
Frankland PW, Josselyn SA, Bradwejn J, Vaccarino FJ, Yeomans JS . Activation of amygdala cholecystokininB receptors potentiates the acoustic startle response in the rat J Neurosci 1997 17: 1838–1847
McDonald J . Topographic organization of amgdaloid projections to the caudatoputamen, nucleus accumbens, and related striateal-like areas of the rat brain Neuroscience 1991 44: 15–33
Everitt BJ, Robbins TV . Amygdala-ventral striatal interactions and reward related processes. In: Aggleton JP (ed) The Amygdala: Neurobiological Aspects of Emotion, Memory and Mental Dysfunction Wiley-Liss: New York 1992 p 401–429
Morgenson GM . Limbic-motor intergration. In: Epstein A, Morrison AR (eds) Progress in Psychobiology and Physiological Psychology Academic Press: New York 1987 pp 117–170
Taylor JR, Robbins TW . Enhanced behavioral control by conditioned reinforcers following microinjections of d-amphetamine into the nucleus accumbens Psychopharmacology 1984 84: 405–412
Taylor JR, Robbins TW . 6-hydroxydopamine lesions of the nucleus accumbens, but not the caudate nucleus, attenuate enhanced responding with reward-related stimuli produced by intra-accumbens d-amphetamine Psychopharmacology 1986 90: 390–397
Burns LH, Everitt BJ, Kelly AE, Robbins TW . Glutamate-dopamine interactions in the ventral striatum: role in locomotor activity and responding with conditioned reinforcement Psychopharmacology 1994 115: 516–528
Cador M, Robbins TW, Everitt BJ . Involvement of the amygdala in stimulus-reward associations: interactions with the ventral striatum Neuroscience 1989 30: 77–86
Koch M, Schmid A, Schnitzler H-U . Pleasure-attenuation of startle is disrupted by lesions of the nucleus accumbens Neuroreport 1996 7: 1442–1446
Everitt BJ, Morris KA, O'Brien A, Robbins TW . The basolateral amygdala-ventral striatal system and conditioned place preference: further evidence of limbic-striatal interactions underlying reward-related processes Neuroscience 1991 42: 1–18
Cahill L, McGaugh JL . Mechanisms of emotional arousal and lasting declarative memory Trends Neurosci 1998 21: 294–299
McGaugh JL, Introini-Collison IB, Cahill L, Kim M, Liang KC . Involvement of the amygdala in neuromodulatory influences on memory storage. In: Aggleton JP (ed) The Amygdala: Neurobiological Aspects of Emotion, Memory, and Mental Dysfunction Wiley-Liss: New York 1992 pp 431–451
Packard MG, Teather LA . Amygdala modulation of multiple memory systems: hippocampus and caudate-putamen Neurobiol Learning Memory 1998 69: 163–203
Packard MG, Cahill L, McGaugh JL . Amygdala modulation of hippocampal-dependent and caudate nucleus-dependent memory processes Proc Nat Acad Sci USA 1994 91: 8477–8481
Amorapanth P, LeDoux JE, Nader K . Different lateral amygdala outputs mediate reactions and actions elicited by a fear-arousing stimulus Nature Neurosci 2000 3: 74–79
Killcross S, Robbins TW, Everitt BJ . Different types of fear-conditioned behaviour mediated by separate nuclei within amygdala Nature 1997 388: 377–380
Hatfield T, McGaugh JL . Norepinephrine infused into the basolateral amygdala posttraining enhances retention in the spatial water maze task Neurobiol Learning Memory 1999 71: 232–239
Ikegaya Y, Saito H, Abe K . Attenuated hippocampal long-term potentiation in basolateral amygdala-lesioned rats Brain Res 1994 1994: 157–164
Ikegaya Y, Saito H, Abe K . Amygdala N-methyl-D-aspartate receptors participate in the induction of long-term potentiation in the dentate gyrus in vivo Neurosci Lett 1995 192: 193–196
Ikegaya Y, Saito H, Abe K . Requirement of basolateral amygdala neuron activity for the induction of long-term potentiation in the dentate gyrus in vivo Brain Res 1995 671: 351–354
Ikegaya Y, Abe K, Saito H, Nishiyama N . Medial amygdala enhances synaptic transmission and synaptic plasticity in the dentate gyrus of rats in vivo J Neurophysiol 1995 74: 2201–2203
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 Neuroscience Res 1995 22: 203–207
Gewirtz JC, Davis M . Application of Pavlovian higher-order conditioning to the analysis of the neural substrates of learning and memory Neuropharmacology 1998 37: 453–460
Akbari Y, Mongeau R, Maren S, Fanselow MS . Reversible inactivation of the basolateral amygdala prevents inflation of fear conditioning in rats In: Society for Neuroscience: New Orleans 1997
Everitt BJ, Cador M, Robbins TW . Interactions between the amygdala and ventral striatum in stimulus-reward associations: studies using a second-order schedule of sexual reinforcement Neuroscience 1989 30: 63–75
Gewirtz J, Davis M . Second order fear conditioning prevented by blocking NMDA receptors in the amygdala Nature 1997 388: 471–474
Anderson SW, Bechara A, Damasio H, Tranel D, Damasio AR . Impairment of social and moral behavior related to early damage in human prefrontal cortex Nature Neurosci 1999 2: 1032–1037
Damasio AR . Descartes’ Error Grosset/Putnam: New York 1994
Bechara A, Damasio H, Tranel D, Damasio AR . Deciding advantageously before knowing the advantageous strategy Science 1997 275: 1293–1294
Schoenbaum G, Chiba AA, Gallagher M . Orbitofrontal cortex and basolateral amygdala encode expected outcomes during learning Nature Neurosci 1998 1: 155–159
Schoenbaum G, Chiba AA, Gallagher M . Neural encoding in orbitofrontal cortex and basolateral amygdala during olfactory discrimination learning J Neurosci 1999 19: 1876–1884
Sanghera MK, Rolls ET, Roper-Hall A . Visual responses of neurons in the dorsolateral amygdala of the alert monkey Exp Neurol 1979 63: 610–626
Baxter MG, Parker A, Lindner CCC, Izquierdo AD, Murray EA . Control of response selection by reinforcer value requires interaction of amygdala and orbital prefrontal cortex J Neurosci 2000 20: 4311–4319
Breiter HC, Etcoff NL, Whalen PJ, Kennedy WA, Rauch SL, Buckner RL et al. Response and habituation of the human amygdala during visual processing of facial expression Neuron 1996 17: 875–887
Morris JS, Frith CD, Perrett DI, Rowland D, Young AW, Calder AJ et al. A differential neural response in the human amygdala to fearful and happy facial expressions Nature 1996 383: 812–815
Phillips ML, Young AW, Senior C, Brammer M, Andrew C, Calder AJ et al. A specific neural substrate for perceiving facial expressions of disgust Nature 1997 389: 495–498
Phillips ML, Young AW, Scott SK, Calderm AJ, Andrew C, Giampietro V et al. Neural responses to facial and vocal expressions of fear and disgust Proc R Soc Lond B 1998 265: 1809–1817
Whalen PJ, Rauch SL, Etcoff NL, McInerney SC, Lee MB, Jenike MA . Masked presentations of emotional facial expressions modulate amygdala activity without explicit knowledge J Neurosci 1998 18: 411–418
Baird AA, Gruber SA, Fein DA, Maas LC, Steingard RJ, Renshaw PF et al. Functional magnetic resonance imaging of facial affect recognition in children and adolescents J Am Acad Child Adolesc Psychiatry 1999 38: 195–199
Blair RJ, Morris JS, Frith CD, Perrett DI, Dolan RJ . Dissociable neural responses to facial expressions of sadness and anger Brain 1999 122: 883–893
Hariri AR, Bookheimer SY, Mazziotta JC . Modulating emotional responses: effects of a neocortical network on the limbic system Neuroreport 2000 11: 43–48
Critchley H, Daly E, Phillips M, Brammer M, Bullmore E, Williams S et al. Explicit and implicit neural mechanisms for processing of social information from facial expressions: a functional magnetic resonance imaging study Hum Brain Mapp 2000 9: 93–105
DuBois S, Rossion B, Schlitz C, Bodart JM, Michel C, Bruyer R et al. Effect of familiarity on the processing of human faces Neuroimage 1999 9: 278–289
Kawashima R, Sugiura M, Kato T, Nakamura A, Hatano K, Ito K et al. The human amygdala plays an important role in gaze monitoring: a PET study Brain 1999 122: 779–783
Sprengelmeyer R, Rausch M, Eysel UT, Przuntek H . Neural structures associated with recognition of facial expressions of basic emotions Proc R Soc Lond B 1998 265: 1927–1931
Lane RD, Reiman EM, Bradley MM, Lang PJ, Ahern GL, Davidson RJ et al. Neuroanatomical correlates of pleasant and unpleasant emotion Neuropsychologia 1997 35: 1437–1444
Taylor SF, Liberzon I, Fig LM, Decker LR, Minoshima S, Koeppe RA . The effect of emotional content on visual recognition memory: a PET activation study Neuroimage 1998 8: 188–197
Reiman EM, Lane RD, Ahern GL, Schwartz GE, Davidson RJ, Friston KJ et al. Neuroanatomical correlates of externally and internally generated human emotion Am J Psychiatry 1997 54: 918–925
Paradiso S, Johnson DL, Andreasen NC, O'Leary DS, Watkins GL, Boles Ponto LL et al. Cerebral blood flow changes associated with attribution of emotional valence to pleasant, unpleasant, and neutral visual stimuli in a PET study of normal subjects Am J Psychiatry 1999 156: 1618–1629
Fischer H, Furmark T, Wik G, Fredrikson M . Brain representation of habituation to repeated complex visual stimulation studied with PET Neuroreport 2000 11: 123–126
Cahill L, Haier RJ, Fallon J, Alkire MT, Tang C, Keator D et al. Amygdala activity at encoding correlated with long-term, free recall of emotional information Proc Nat Acad Sci USA 1996 93: 8016–8021
Hamann SB, Ely TD, Grafton ST, Kilts CD . Amygdala activity related to enhanced memory for pleasant and aversive stimuli Nature Neurosci 1999 2: 289–293
Dolan RJ, Lane R, Chua P, Fletcher P . Dissociable temporal lobe activations during emotional episodic memory retrieval Neuroimage 2000 11: 203–209
Zald DH, Pardo JV . Emotion, olfaction, and the human amygdala: amygdala activation during aversive olfactory stimulation Proc Nat Acad Sci USA 1997 94: 4119–4124
Zald DH, Lee JT, Fluegel KW, Pardo JV . Aversive gustatory stimulation activates limbic circuits in humans Brain 1998 121: 1143–1154
Isenberg N, Silbersweig D, Engelien A, Emmerich S, Malavade K, Beattie B et al. Linguistic threat activates the human amygdala Proc Natl Acad Sci 1999 96: 10456–10459
Whalen PJ, Bush G, McNally RJ, Wilhelm S, McInerney SC, Jenike MA et al. The emotional counting Stroop paradigm: a functional magnetic resonance imaging probe of the anterior cingulate affective division Biol Psychiatry 1998 44: 1219–1228
Morris JS, Scott SK, Dolan RJ . Saying it with feeling: neural responses to emotional vocalizations Neuropsychologia 1999 37: 1155–1163
Schneider F, Gur RE, Alavi, A, Seligman MEP, Mozley LH, Smith RJ et al. Cerebral blood flow changes in limbic regions induced by unsolvable anagram tasks Am J Psychiatry 1996 153: 206–212
Bonda E, Petrides M, Ostry D, Evans A . Specific involvement of human parietal systems and the amygdala in the perception of biological motion J Neurosci 1996 16: 3737–3744
Furmark T, Fischer H, Wirk G, Larsson M, Fredrikson M . The amygdala and individual differences in human fear conditioning NeuroReport 1997 8: 3957–3960
LaBar KS, Gatenby JC, Gore JC, LeDoux JE, Phelps EA . Human amygdala activation during conditioned fear acquisition and extinction: a mixed-trial fMRI study Neuron 1998 20: 937–945
Büchel C, Morris J, Dolan RJ, Friston KJ . Brain systems mediating aversive conditioning: an event-related fMRI study Neuron 1998 20: 947–957
Morris JS, Öhman A, Dolan RJ . Conscious and unconscious emotional learning in the human amygdala Nature 1998 393: 467–470
Büchel C, Dolan RJ, Armony JL, Friston KJ . Amygdala-hippocampal involvement in human aversive trace conditioning revealed through event-related functional magnetic resonance imaging J Neurosci 1999 19: 10869–10876
Phelps EA, O'Connor KJ, Gatenby JC, Gore JC, Grillon C, Davis M . Activation of the left amygdala to a cognitive representation of fear Nature Neurosci (in press)
Schneider F, Gur RE, Harper Mozley L, Smith RJ, Mosley PD, Censits DM et al. Mood effects on limbic blood flow correlate with emotional self-rating: a PET study with oxygen-15 labeled water Psychiatry Res: Neuroimaging 1995 61: 265–283
Schneider F, Grodd W, Weiss U, Klos U, Mayer KR, Nagele T et al. Functional MRI reveals left amygdala activation during emotion Psychiatry Res 1997 76: 75–82
Grodd W, Schneider F, Klose U, Nägele T . Functional magnetic resonance tomography of psychological functions with experimentally induced emotions [German] Radiologe 1995 35: 283–289
Ketter TA, Andreason PJ, George MS, Lee C, Gill DS, Parekh PI et al. Anterior paralimbic mediation of procaine-induced emotional and psychosensory experiences Arch Gen Psychiatry 1996 53: 59–69
Servan-Schreiber DS, Perlstein WM, Cohen JD, Mintun M . Selective pharmacological activation of limbic structures in human volunteers: a positron emission tomography study J Neuropsychiatry Clin Neurosci 1998 10: 148–159
Hui KKS, Liu J, Makris N, Gollub RL, Chen AJW, Moore CI et al. Acupuncture modulates the limbic system and subcortical gray structures of the human brain: evidence from fMRI studies in normal subjects Hum Brain Mapp 2000 9: 13–25
Lazar SW, Bush G, Gollub RL, Fricchione GL, Khalsa G, Benson H . Functional brain mapping of the relaxation response and meditation Neuroreport 2000 11: 1581–1585
Becerra L, Breiter HC, Stojanovic M, Fishman S, Edwards A, Comite AR et al. Human brain activation under controlled thermal stimulation and habituation to noxious heat: an fMRI study Magn Reson Med 1999 41: 1044–1057
Derbyshire S, Jones A, Gyulai F, Clark S, Townsend D, Firestone L . Pain processing during three levels of noxious stimulation produces differential patterns of central activity Pain 1997 73: 431–445
Rauch SL, van der Kolk BA, Fisler RE, Alpert NM, Orr SP, Savage CR et al. A symptom provocation study of posttraumatic stress disorder using positron emission tomography and script-driven imagery Arch Gen Psychiatry 1996 53: 380–387
Shin LM, Kosslyn SM, McNally RJ, Alpert NM, Thompson WL, Rauch SL et al. Visual imagery and perception in posttraumatic stress disorder: a positron emission tomographic investigation Arch Gen Psychiatry 1997 54: 233–241
Liberzon I, Taylor SF, Amdur R, Jung TD, Chamberlain KR, Minoshima S et al. Brain activation in PTSD in response to trauma-related stimuli Biol Psychiatry 1999 45: 817–826
Rauch SL, Whalen PJ, Shin LM, McInerney SC, Macklin ML, Lasko NB et al. Exaggerated amygdala response to masked facial stimuli in posttraumatic stress disorder Biol Psychiatry 2000 47: 769–776
Semple WE, Goyer PF, McCormick R, Donovan B, Muzic RF, Rugle L et al. Higher brain blood flow at amygdala and lower frontal cortex blood flow in PTSD patients with comorbid cocaine and alcohol abuse compared with normals Psychiatry 2000 63: 65–74
Drevets WC, Videen TO, Price JL, Preskorn SH, Carmichael ST, Raichle ME . A functional anatomical study of unipolar depression J Neurosci 1992 12: 3628–3641
Abercrombie HC, Schaefer SM, Larson CL, Oakes TRL, Lindgren KA, Holden JE et al. Metabolic rate in the right amygdala predicts negative affect in depressed patients Neuroreport 1998 9: 3301–3307
Birbaumer N, Grodd W, Diedrich O, Klose U, Erb M, Lotze M et al. fMRI reveals amygdala activation to human faces in social phobics NeuroReport 1998 9: 1223–1226
Schneider F, Weiss U, Kessler C, Müller-Gärtner H-W, Posse S, Salloum JB et al. Subcortical correlates of differential classical conditioning of aversive emotional reactions in social phobia Biol Psychiatry 1999 45: 863–871
Whalen PJ . Fear, vigilance, and ambiguity: initial neuroimaging studies of the human amygdala Curr Direct Psychol Sci 1998 7: 177–188
Grillon C, Ameli R, Woods SW, Merikangas K, Davis M . Fear-potentiated startle in humans: effects of anticipatory anxiety on the acoustic blink reflex Psychophysiology 1991 28: 588–595
Irwin W, Davidson RJ, Lowe MJ, Mock BJ, Sorenson JA, Turski PA . Human amygdala activation detected with echo-planar functional magnetic resonance imaging NeuroReport 1996 7: 1765–1769
Morris JS, Friston KJ, Büchel C, Frith CD, Young AW, Calder AJ et al. A neuromodulatory role for the human amygdala in processing emotional facial expressions Brain 1998 121: 47–57
Drevets WC, Raichle M . Reciprocal suppression of regional cerebral blood flow during emotional versus higher cognitive processes: implications for interactions between emotion and cognition Cognition and Emotion 1998 12: 353–385
Esteves F, Öhman A . Masking the face: recognition of emotional facial expressions as a function of the parameters of backward masking Scand J Psychol 1993 34: 1–18
Kapp BS, Silvestri AJ, Guarraci FA . Amygdaloid central nucleus neuronal activity: correlations with EEG arousal Neurosci Abs 1996 22: 2049
Kapp BS, Silvestri AJ, Guarraci FA, Moynihan JE, Cain ME . Associative and EEG arousal-related characteristics of amygdaloid central nucleus neurons in the rabbit Neurosci Abs 1997 23: 787
Metherate R, Ashe JH . Basal forebrain stimulation modifies auditory cortex responsiveness by an action at muscarinic receptors Brain Res 1991 559: 163–167
Sillitto AM, Kemp JA . Cholinergic modulation of the functional organization of the cat visual cortex Brain Res 1983 289: 143–155
Weinberger NM, Ashe JH, Metherate R, McKenna TM, Diamond DM, Bakin JS et al. Neural adaptive information processing: a preliminary model of receptive-field plasticity in auditory cortex during Pavlovian conditioning. In: Gabriel M, Moore J (eds). Learning and Computational Neuroscience: Foundations of Adaptive Networks MIT Press: Cambridge MA 1990
Chiba AA, Bucci DJ, Holland PC, Gallagher M . Basal forebrain cholinergic lesions disrupt increments but not decrements in conditioned stimulus processing J Neurosci 1995 15: 7315–7322
Bucci DJ, Holland PC, Gallagher M . Removal of cholinergic input to rat posterior parietal cortex disrupts incremental processing of conditioned stimuli J Neurosci 1998 18: 8038–8046
Robbins TW, Everitt BJ, Marston HM, Wilkinson J, Jones GH, Page KJ . Comparative effects of ibotenic acid- and quisqualic acid-induced lesions of the substantia innominata on attentional function in the rat: further implications for the role of the cholinergic neurons of the nucleus basalis in cognitive processes Behav Brain Res 1989 35: 221–240
Whalen PJ, Shin LM, McInerney SC, Rauch SL . Greater fMRI activation to fearful vs angry facial expression in the amygdaloid region Neurosci Abs 1998 24: 692
Whalen PJ, Kapp BS . Contributions of the amygdaloid central nucleus to the modulation of the nictitating membrane reflex in the rabbit Behav Neurosci 1991 105: 141–153
Masur JD, Dienst FT, O'Neal EC . The acquisition of a Pavlovian conditioned response in septally damaged rabbits: role of a competing response Physiol Psychol 1974 2: 133–136
Schneiderman N . Response system divergencies in aversive classical conditioning. In: Black AH, Prokasy WF (eds). Classical Conditioning, Vol. III: Current Research and Theory Appleton-Century-Crofts: New York 1972
Weisz DJ, McInerney J . An associative process maintains reflex facilitation of the unconditioned nictitating membrane response during the early stages of training Behav Neurosci 1990 104: 21–27
Powell DA, Milligan WL . Effects of partial and continuous reinforcement on conditioned heart rate and corneoretinal potential responses in the rabbit (Oryctolagus cuniculus) Psychol Record 1975 25: 419–426
Fitzgerald RD, Vardaris RM, Brown JS . Classical conditioning of heart-rate deceleration in the rat with continuous and partial reinforcement Psychon Sci 1966 6: 437–438
Campeau S, Falls WA, Cullinan WE, Helmreich DL, Davis M, Watson SJ . Elicitation and reduction of fear: behavioral and neuroendocrine indices and brain induction of the immediate-early gene c-fos Neuroscience 1997 78: 1087–1104
Davis M, Schlesinger LS, Sorenson CA . Temporal specificity of fear-conditioning: effects of different conditioned stimulus-unconditioned stimulus intervals on the fear-potentiated startle effect J Exp Psychol: Anim Behav Proc 1989 15: 295–310
Kim M, Davis M . Electrolytic lesions of the amygdala block acquisition and expression of fear-potentiated startle even with extensive training, but do not prevent re-acquisition Behav Neurosci 1993 107: 580–595
Maren S . Overtraining does not mitigate contextual fear conditioning deficits produced by neurotoxic lesions of the basolateral amygdala J Neurosci 1998 18: 3088–3097
Scannell JW, Young MP . Neuronal population activity and functional imaging Proc Royal Soc London B 1999 266: 875–881
Lee Y, Davis M . Role of the hippocampus, bed nucleus of the stria terminalis and amygdala in the excitatory effect of corticotropin releasing (CRH) hormone on the acoustic startle reflex J Neurosci 1997 17: 6434–6446