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Unique Neural Circuitry for Neonatal Olfactory Learning
Open accessAbstract
Imprinting ensures that the infant forms the caregiver attachment necessary for altricial species survival. In our mammalian model of imprinting, neonatal rats rapidly learn the odor-based maternal attachment. This rapid learning requires reward-evoked locus ceruleus (LC) release of copious amounts of norepinephrine (NE) into the olfactory bulb. This imprinting ends at postnatal day 10 (P10) and is associated with a dramatic reduction in reward-evoked LC NE release. Here we assess whether the functional emergence of LC alpha2 inhibitory autoreceptors and the downregulation of LC alpha1 excitatory autoreceptors underlie the dramatic reduction in NE release associated with termination of the sensitive period. Postsensitive period pups (P12) were implanted with either LC or olfactory bulb cannulas, classically conditioned with intracranial drug infusions (P14), and tested for an odor preference (P15). During conditioning, a novel odor was paired with either olfactory bulb infusion of abeta-receptor agonist (isoproterenol) to assess the target effects of NE or direct LC cholinergic stimulation combined with alpha2 antagonists and alpha1 agonists in a mixture to reinstate neonatal levels of LC autoreceptor activity to assess the source of NE. Pups learned an odor preference when the odor was paired with either olfactory bulb isoproterenol infusion or reinstatement of neonatal LC receptor activity. These results suggest that LC autoreceptor functional changes rather than olfactory bulb changes underlie sensitive period termination.
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“odors associated with early-life experiences acquire a rewarding value that promotes behaviors essential for survival [65].”
From Positive early-life olfactory memory is rooted in the olfactory bulb and triggers large-scale changes beyond the olfactory system (2026) · cites this paper as [65]
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Citations
Cites
(1969) · Cited by 18,340
Attachment and Loss. Vol. 1. Attachment
Rever, G. W. (1972) · Psychosomatic Medicine · doi:10.1097/00006842-197211000-00011 · Cited by 8,446
Berridge, C. W., & Waterhouse, B. D. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00143-7 · Cited by 2,529
The Pharmacological Basis of Therapeutics
Goodman, L., & Gilhan, A. (1941) · Anesthesiology · doi:10.1097/00000542-194105000-00013 · Cited by 2,148
The neurobiological consequences of early stress and childhood maltreatment
Teicher, M. H., Andersen, S. L., Polcari, A., Anderson, C. M., Navalta, C. P., & Kim, D. M. (2003) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(03)00007-1 · Cited by 1,465
Handbook of Developmental Cognitive Neuroscience
(2008) · The MIT Press eBooks · doi:10.7551/mitpress/7437.001.0001 · Cited by 1,191
The neurobiology of attachment
Insel, T. R., & Young, L. J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35053579 · Cited by 1,173
Modulation of visual cortical plasticity by acetylcholine and noradrenaline
Bear, M. F., & Singer, W. (1986) · Nature · doi:10.1038/320172a0 · Cited by 858
Foote, S. L., Aston-Jones, G., & Bloom, F. E. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.5.3033 · Cited by 857
Child abuse and neglect and the brain–a review
Glaser, D. (2000) · Journal of Child Psychology and Psychiatry · doi:10.1017/s0021963099004990 · Cited by 827
Involvement of the amygdala in memory storage: Interaction with other brain systems
McGaugh, J. L., Cahill, L. F., & Roozendaal, B. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.13508 · Cited by 747
Locus coeruleus neurons in monkey are selectively activated by attended cues in a vigilance task
Aston-Jones, G., Rajkowski, J., Kubiak, P., & Alexinsky, T. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-07-04467.1994 · Cited by 637
Selden, N. R. W., Everitt, B. J., Jarrard, L. E., & Robbins, T. W. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90379-3 · Cited by 578
The ontogeny of behaviour in the albino rat
Bolles, R. C., & Woods, P. J. (1964) · Animal Behaviour · doi:10.1016/0003-3472(64)90062-4 · Cited by 570
Distribution of α2-adrenergic receptor subtype gene expression in rat brain
Scheinin, M., Lomasney, J. W., Hayden‐Hixson, D. M., Schambra, U. B., Caron, M. G., Lefkowitz, R. J., & Fremeau, R. T. (1994) · Molecular Brain Research · doi:10.1016/0169-328x(94)90386-7 · Cited by 430
Fleming, A. S., O’Day, D. H., & Kraemer, G. W. (1999) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(99)00011-1 · Cited by 429
Facilitation of time-dependent memory processes with posttrial epinephrine injections
Gold, P. E., & Buskirk, R. B. V. (1975) · Behavioral Biology · doi:10.1016/s0091-6773(75)91784-8 · Cited by 377
Restoration of visual cortical plasticity by local microperfusion of norepinephrine
Kasamatsu, T., Pettigrew, J. D., & Ary, M. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901850110 · Cited by 363
Atlas Of The Developing Rat Brain
Paxinos, G., & Fritchle, A. L. R. (1991) · Medical Entomology and Zoology · Cited by 345
NEURAL MECHANISMS OF MAMMALIAN OLFACTORY LEARNING
Brennan, P., & Keverne, E. B. (1997) · Progress in Neurobiology · doi:10.1016/s0301-0082(96)00069-x · Cited by 337
Good memories of bad events in infancy
Sullivan, R. M., Landers, M., Yeaman, B., & Wilson, D. A. (2000) · Nature · doi:10.1038/35024156 · Cited by 315
Self-citationKasamatsu, T., & Pettigrew, J. D. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901850109 · Cited by 314
Response to Novelty and its Rapid Habituation in Locus Coeruleus Neurons of the Freely Exploring Rat
Vankov, A., Hervé‐Minvielle, A., & Sara, S. J. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb01108.x · Cited by 309
Roozendaal, B., Nguyen, B. T., Power, A. E., & McGaugh, J. L. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.20.11642 · Cited by 293
Norepinephrine and learning-induced plasticity in infant rat olfactory system
Sullivan, R., Wilson, D., & Leon, M. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-11-03998.1989 · Cited by 261
Self-citationRudy, J. W., & Morledge, P. (1994) · Behavioral Neuroscience · doi:10.1037//0735-7044.108.2.227 · Cited by 253
Pieribone, V., Nicholas, A., Dagerlind, A., & Hokfelt, T. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-07-04252.1994 · Cited by 243
Mother's milk: A medium for transmission of cues reflecting the flavor of mother's diet.
Galef, B. G., & Sherry, D. F. (1973) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0034665 · Cited by 243
Gene Expression Profiling of the pH Response inEscherichia coli
Tucker, D. L., Tucker, N., & Conway, T. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.23.6551-6558.2002 · Cited by 232
Enhanced Neural Response to Familiar Olfactory Cues
Coopersmith, R., & Leon, M. (1984) · Science · doi:10.1126/science.6474157 · Cited by 210
Liang, K., McGaugh, J. L., & Yao, H.-Y. (1990) · Brain Research · doi:10.1016/0006-8993(90)90400-6 · Cited by 210
Neurobiology of associative learning in the neonate: Early olfactory learning
Wilson, D. A., & Sullivan, R. M. (1994) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(05)80039-1 · Cited by 206
Self-citationActivation of the noradrenergic system facilitates an attentional shift in the rat
Devauges, V., & Sara, S. J. (1990) · Behavioural Brain Research · doi:10.1016/0166-4328(90)90118-x · Cited by 202
Edeline, J. (1999) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00042-2 · Cited by 197
Multiple memory systems, development and conditioning
Stanton, M. E. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(99)00182-5 · Cited by 190
Infantile Experience with Suckling Odors Determines Adult Sexual Behavior in Male Rats
Fillion, T. J., & Blass, E. M. (1986) · Science · doi:10.1126/science.3945807 · Cited by 188
Sullivan, R. M., Stackenwalt, G., Nasr, F., Lemon, C. H., & Wilson, D. A. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.5.957 · Cited by 169
Self-citationGray, C. M., Freeman, W. J., & Skinner, J. E. (1986) · Behavioral Neuroscience · doi:10.1037//0735-7044.100.4.585 · Cited by 162
Early olfactory learning induces an enhanced olfactory bulb response in young rats
Sullivan, R. M., & Leon, M. (1986) · Developmental Brain Research · doi:10.1016/0165-3806(86)90256-7 · Cited by 151
Self-citationActivation and odor conditioning of suckling behavior in 3-day-old albino rats.
Pedersen, P. E., Williams, C. L., & Blass, E. M. (1982) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.8.4.329 · Cited by 149
Camp, L. L., & Rudy, J. W. (1988) · Developmental Psychobiology · doi:10.1002/dev.420210103 · Cited by 147
Donzella, B., Gunnar, M. R., Krueger, W. K., & Alwin, J. (2000) · Developmental Psychobiology · doi:10.1002/1098-2302(2000)37:4 · Cited by 142
Gray, C. M., Freeman, W. J., & Skinner, J. E. (1986) · Behavioral Neuroscience · doi:10.1037/0735-7044.100.4.585 · Cited by 142
Wilson, D. A., Sullivan, R. M., & Leon, M. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-10-03154.1987 · Cited by 141
Self-citationSullivan, R. M., Hofer, M. A., & Brake, S. (1986) · Developmental Psychobiology · doi:10.1002/dev.420190612 · Cited by 134
Self-citationPostnatal development of electrical activity in the locus ceruleus
Nakamura, S., Kimura, F., & Sakaguchi, T. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.58.3.510 · Cited by 130 · cited 7×
“…␣2 inhibitory noradrenergic autoreceptors, resulting in the LC autoinhibition within milliseconds of activation and the functional attenuation of LC ␣1 excitatory noradrenergic autoreceptors, which prolong LC neonatal responses (Nakamura et al., 1987; Pieribone et al., 1994; Scheinin et al., 1994).”
InfluentialToward a Neurobiology of Attachment
Insel, T. R. (2000) · Review of General Psychology · doi:10.1037/1089-2680.4.2.176 · Cited by 122
The role of olfactory bulb norepinephrine in early olfactory learning
Sullivan, R. M., Zyzak, D. R., Skierkowski, P., & Wilson, D. A. (1992) · Developmental Brain Research · doi:10.1016/0165-3806(92)90207-d · Cited by 119
Self-citationAppetitive conditioning in neonatal rats: Conditioned orientation to a novel odor
Johanson, I. B., & HALL, W. G. (1982) · Developmental Psychobiology · doi:10.1002/dev.420150410 · Cited by 115
Novelty seeking behavior in the rat is dependent upon the integrity of the noradrenergic system
Sara, S. J., Dyon-Laurent, C., & Hervé, A. (1995) · Cognitive Brain Research · doi:10.1016/0926-6410(95)90007-1 · Cited by 114
Localized changes in olfactory bulb morphology associated with early olfactory learning
Woo, C. C., Coopersmith, R., & Leon, M. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902630110 · Cited by 114
Nonnutritive, thermotactile induction of filial huddling in rat pups
Alberts, J. R., & May, B. J. (1984) · Developmental Psychobiology · doi:10.1002/dev.420170207 · Cited by 110
Importance of !b-noradrenergic receptors in the olfactory bulb of sheep for recognition of lambs.
Lévy, F., Gervais, R., Kindermann, U., Orgeur, P., & al, E. (1990) · Behavioral Neuroscience · doi:10.1037//0735-7044.104.3.464 · Cited by 109
Sullivan, R. M. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.130.013 · Cited by 104
Self-citationOlfactory bulbectomy and nursing behavior in rat pups (Wistar DAB)
Singh, P. J., & Tobach, E. (1975) · Developmental Psychobiology · doi:10.1002/dev.420080207 · Cited by 99
Sensitive period for neural and behavioral response development to learned odors
Woo, C. C., & Leon, M. (1987) · Developmental Brain Research · doi:10.1016/0165-3806(87)90038-1 · Cited by 99
McLean, J. H., & Shipley, M. T. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903040310 · Cited by 96
Importance of !b-noradrenergic receptors in the olfactory bulb of sheep for recognition of lambs.
Lévy, F., Gervais, R., Kindermann, U., et al. (1990) · Behavioral Neuroscience · doi:10.1037/0735-7044.104.3.464 · Cited by 96
Nakamura, S., & Sakaguchi, T. (1990) · Progress in Neurobiology · doi:10.1016/0301-0082(90)90018-c · Cited by 94
Corticosterone Influences on Mammalian Neonatal Sensitive-Period Learning.
Moriceau, S., & Sullivan, R. M. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.2.274 · Cited by 92
Self-citationA learned odor evokes an enhanced Fos-like glomerular response in the olfactory bulb of young rats
Johnson, B. A., Woo, C. C., Duong, H., Nguyen, V., & Leon, M. (1995) · Brain Research · doi:10.1016/0006-8993(95)00896-x · Cited by 91
Feenstra, M. G. P., Vogel, M., Botterblom, M. H. A., Joosten, R. N. J. M. A., & De Bruin, J. P. C. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01471.x · Cited by 90
McLean, J. H., Harley, C. W., Darby‐King, A., & Yuan, Q. (1999) · Learning & Memory · doi:10.1101/lm.6.6.608 · Cited by 90
Ontogenesis of trace conditioning in young rats: Dissociation of associative and memory processes
Moye, T. B., & Rudy, J. W. (1987) · Developmental Psychobiology · doi:10.1002/dev.420200405 · Cited by 86
Noradrenergic modulation of olfactory bulb excitability in the postnatal rat
Wilson, D. A., & Leon, M. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90202-7 · Cited by 84
Early odor preference training increases olfactory bulb norepinephrine
Rangel, S. J., & Leon, M. (1995) · Developmental Brain Research · doi:10.1016/0165-3806(94)00211-h · Cited by 84
Sullivan, R. M., Wilson, D. A., Lemon, C. H., & Gerhardt, G. A. (1994) · Brain Research · doi:10.1016/0006-8993(94)90038-8 · Cited by 82
Self-citationEnhanced neural response by adult rats to odors experienced early in life
Coopersmith, R., & Leon, M. (1986) · Brain Research · doi:10.1016/0006-8993(86)90384-7 · Cited by 76
Freeman, J. H., & Nicholson, D. A. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-02-00813.2000 · Cited by 75
Adams, L. M., & Foote, S. L. (1988) · Brain Research Bulletin · doi:10.1016/0361-9230(88)90151-7 · Cited by 71
Developmental dissociation of the components of conditioned fear.
Hunt, P. S., & Campbell, B. A. (1997) · American Psychological Association eBooks · doi:10.1037/10223-003 · Cited by 71
Moye, T. B., & Rudy, J. W. (1985) · Developmental Psychobiology · doi:10.1002/dev.420180505 · Cited by 70
Pager, J. (1974) · Physiology & Behavior · doi:10.1016/0031-9384(74)90172-3 · Cited by 67
Sullivan, R. M., Brake, S. C., Hofer, M. A., & Williams, C. L. (1986) · Developmental Psychobiology · doi:10.1002/dev.420190613 · Cited by 67
Self-citationIvanov, A., & Aston‐Jones, G. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.74.6.2427 · Cited by 62
Harley, C., & Sara, S. (1992) · Experimental Brain Research · doi:10.1007/bf00229883 · Cited by 61
Neural correlates of conditioned odor avoidance in infant rats.
Sullivan, R. M., & Wilson, D. A. (1991) · Behavioral Neuroscience · doi:10.1037//0735-7044.105.2.307 · Cited by 59
Self-citationRole of the amygdala complex in early olfactory associative learning.
Sullivan, R. M., & Wilson, D. A. (1993) · Behavioral Neuroscience · doi:10.1037//0735-7044.107.2.254 · Cited by 57
Self-citationWinzer‐Serhan, U. H., Broide, R. S., Chen, Y.-L., & Leslie, F. M. (1999) · Brain Research Protocols · doi:10.1016/s1385-299x(98)00043-9 · Cited by 55
Optical Imaging of Odor Preference Memory in the Rat Olfactory Bulb
Yuan, Q., Harley, C. W., McLean, J. H., & Knöpfel, T. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00917.2001 · Cited by 55
Neural correlates of conditioned odor avoidance in infant rats.
Sullivan, R. M., & Wilson, D. A. (1991) · Behavioral Neuroscience · doi:10.1037/0735-7044.105.2.307 · Cited by 54
Self-citationRole of the amygdala complex in early olfactory associative learning.
Sullivan, R. M., & Wilson, D. A. (1993) · Behavioral Neuroscience · doi:10.1037/0735-7044.107.2.254 · Cited by 52
Self-citationSullivan, R. M. (2001) · Integrative Psychological and Behavioral Science · doi:10.1007/bf02688797 · Cited by 50
Self-citationKimura, F., & Nakamura, S. (1985) · Developmental Brain Research · doi:10.1016/0165-3806(85)90055-0 · Cited by 49
Passive avoidance learning in the young rat
Blozovski, D., & Cudennec, A. (1980) · Developmental Psychobiology · doi:10.1002/dev.420130510 · Cited by 46
Mouly, A., Elaagouby, A., & Ravel, N. (1995) · Brain Research · doi:10.1016/0006-8993(95)00280-4 · Cited by 44
Inhibitory learning and memory in newborn rats
Mysliveček, J. (1997) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00036-1 · Cited by 42
Shah, A. A., Oxley, G., Lovic, V., & Fleming, A. S. (2002) · Developmental Psychobiology · doi:10.1002/dev.10064 · Cited by 40
Harley, C. W., Lalies, M. D., & Nutt, D. (1996) · Brain Research · doi:10.1016/0006-8993(95)01443-8 · Cited by 39
The ontogeny of conditioned odor potentiation of startle.
Richardson, R., Paxinos, G., & Lee, J. (2000) · Behavioral Neuroscience · doi:10.1037//0735-7044.114.6.1167 · Cited by 39
Landers, M. S., & Sullivan, R. M. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-12-05131.1999 · Cited by 38
Self-citationThe ontogeny of conditioned odor potentiation of startle.
Richardson, R., Paxinos, G., & Lee, J. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.6.1167 · Cited by 35
Chaulk, P. C., & Harley, C. W. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01460-1 · Cited by 34
Wilson, D. A., & Sullivan, R. M. (1990) · Developmental Brain Research · doi:10.1016/0165-3806(90)90009-n · Cited by 33
Self-citationEarly Olfactory Experience, Novelty, and Choice of Sexual Partner by Male Rats
Moore, C., JORDAN, L., & Wong, L. (1996) · Physiology & Behavior · doi:10.1016/s0031-9384(96)00249-1 · Cited by 32
Approach-avoidance conflict in preweanling rats: A developmental study
Collier, A. C., Mast, J., Meyer, D. R., & Jacobs, C.-E. (1979) · Animal Learning & Behavior · doi:10.3758/bf03209712 · Cited by 32
Locus coeruleus involvement in the learning of classically conditioned bradycardia
Harris, G. C. M., & Fitzgerald, R. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-08-02314.1991 · Cited by 31
Thoman, E. B., Wetzel, A. B., & Levine, S. (1968) · Animal Behaviour · doi:10.1016/0003-3472(68)90108-5 · Cited by 31
Olfactory denervation: Its biological and behavioral effects in infant rats.
Hofer, M. A. (1976) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0077272 · Cited by 30
Postnatal development of α-adrenoceptor-mediated autoinhibition in the locus coeruleus
Kimura, F., & Nakamura, S. (1987) · Developmental Brain Research · doi:10.1016/0165-3806(87)90004-6 · Cited by 29
Electrode implantation in infant rats for kindling and chronic brain recording
Gilbert, M. E., & Cain, D. P. (1980) · Behavioural Brain Research · doi:10.1016/0166-4328(80)90010-8 · Cited by 25
Noradrenergic control of ocular dominance plasticity in the visual cortex of dark-reared cats
Shirokawa, T., Kasamatsu, T., Kuppermann, B. D., & Ramachandran, V. S. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90187-9 · Cited by 19
Norepinephrine and associative conditioning in the neonatal rat somatosensory system
Landers, M. S., & Sullivan, R. M. (1999) · Developmental Brain Research · doi:10.1016/s0165-3806(99)00026-7 · Cited by 19
Self-citationMansour, A. A. H., Babstock, D. M., Penney, J. H., Martin, G. M., McLean, J. H., & Harley, C. W. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.3.621 · Cited by 16
Conspecific odor preferences of male albino rats are reversed by intracerebral 6-hydroxydopamine
Cornwell‐Jones, C. A. (1981) · Brain Research · doi:10.1016/0006-8993(81)90242-0 · Cited by 11
Noradrenergic Long-Term Potentiation in the Dentate Gyrus
Harley, C. W. (1997) · Advances in pharmacology · doi:10.1016/s1054-3589(08)60905-9 · Cited by 10
Collins, P. L., Lopez, J. C., & Wood, H. B. (2001) · Nature reviews. Neuroscience · doi:10.1038/35049008 · Cited by 7
Changes in the electrical activity of locus coeruleus neurons in pregnant rats
Nakamura, S., Sakaguchi, T., Shirokawa, T., Yamatodani, A., Maeyama, K., & Wada, H. (1988) · Neuroscience Letters · doi:10.1016/0304-3940(88)90587-3 · Cited by 4
Dettling (1998) · doi:10.1002/(sici)1098-2302(199807)33:1
Schore, A. N. (2001) · Infant Mental Health Journal · doi:10.1002/1097-0355(200101/04)22:1
Research works printed but not linked: 12
- 1965, Anim Behav, 12, 427
- 1998, Adv Pharmacol, 42, 952
- 1992, Exp Brain Res, 89, 581
- 1976, J Comp Physiol, 90, 829
- 1987, Brain Res, 432, 21
- 10.1037/0735-7044.108.2.227 · DOI
- 1990, Neuroscience, 42, 335
- 2000, Nature, 407, 38
- 2002, J Bacteriol, 183, 6551
- 1987, Brain Res, 433, 309
- 2003, J Neurophysiol, 87, 3156
- 2003, Dev Psychobiol, 37, 246
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Metadata
- Authors
- Moriceau, S., & Sullivan, R. M.
- Affiliations
- University of Oklahoma (US)
- ORCID
- Sullivan, Regina M.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2004-02-04
- Volume
- 24
- Issue
- 5
- Pages
- 1182-1189
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC1868533
- OpenAlex
- W1963661711
- Cited by
- 141
- References
- 106
- Citations by year
- 2026: 4 · 2025: 2 · 2024: 3 · 2023: 3 · 2021: 4 · 2020: 2 · 2019: 7 · 2018: 6 · 2017: 5 · 2016: 10 · 2015: 6 · 2014: 9 · 2013: 6 · 2012: 9
- FWCI
- 4.00
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- Funders
- National Science Foundation (0117234)
- University of Oklahoma
- Oklahoma Center for the Advancement of Science and Technology
- National Institute of Child Health and Human Development
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD33402, R01HD033402)
- Topics
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Keywords
- locus coeruleus, noradrenaline release, olfactory bulb, neonatal rats, classical conditioning, isoproterenol, cholinergic stimulation
- MeSH terms
- Acetylcholine, Adrenergic alpha-Agonists, Animals, Animals, Newborn, Choice Behavior, Critical Period, Psychological, Drug Administration Routes, Female, Imprinting, Psychological, Infusion Pumps, Learning, Locus Coeruleus, Male, Nerve Net, Norepinephrine, Olfactory Bulb, Olfactory Pathways, Phenylephrine, Smell, Cholinergic Agents, Maze Learning, Rats, Long-Evans, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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