The DOI matches its Crossref record.
Postnatal development of electrical activity in the locus ceruleus
Abstract
1. A method for adapting a standard stereotaxic frame for use with neonatal rats as young as postnatal day 1 (PD 1) was devised, and single-unit extracellular recordings were obtained from neurons in the locus ceruleus (LC) in urethan-anesthetized rats during different stages in development from PD 1 to PD 34. 2. The spontaneous firing pattern of neonatal LC neurons was characterized by long silent periods punctuated by brief epochs of sporadic firing. At PD 7-14, LC neurons exhibited periodic occurrences of irregular firing that lasted for 20-30 s. By PD 20, the pattern and rate of spontaneous activity were virtually indistinguishable from that of adults. 3. Conditioning stimulation of the dorsal noradrenergic bundle (DNB), given 10-200 ms prior to a test stimulus to the DNB, markedly reduced the amplitude of the antidromic action potentials to the test stimulus and sometimes resulted in spike decomposition. This refractoriness of the soma-dendritic membrane of LC cells was significantly attenuated with development and approached adult levels after PD 18. 4. Antidromic responses elicited by DNB stimulation were followed by a phase of inhibition or inhibition-excitation. Postactivation excitation was most prominent in cells that were not spontaneously active, and decreased steadily throughout development, probably because of the steady increase in spontaneous firing rate seen during maturation. 5. Although the conduction velocity of LC axons increased steadily from birth through PD 26, conduction time remained unchanged. 6. Neonatal LC neurons were equally sensitive to noxious and nonnoxious somatosensory stimuli. As development proceeded, LC neurons became less sensitive to innocuous somatosensory stimuli such as air puffs and tactile stimuli while simultaneously becoming more sensitive to noxious stimuli. Auditory and visual stimuli became effective for the first time at PD 14 and PD 12, respectively. 7. These results indicate that the electrical activity of LC neurons in the developing brain is intimately related to input from peripheral sensory sources. Therefore, the influence of the LC on the developing brain may occur predominantly through sensory input.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In particular, the large amounts of NE required for this attachment-related plasticity results from the failure of the infant LC to show habituation or to turn itself off via auto-inhibition (as occurs in older pups and adults) (Nakamura et al., 1987, Winzer-Serhan et al., 1996).”
From Early life adversity during the infant sensitive period for attachment: Programming of behavioral neurobiology of threat processing and social behavior (2017) · cites this paper as Nakamura et al., 1987
In the citing paper
“The mechanism for the prolonged neonatal LC response appears due to the lack of functional α2 inhibitory noradrenergic autoreceptors that terminate the LC response in older pups/adult (Nakamura et al., 1987; Pieribone et al., 1994; Scheinin et al., 1994; Winzer-Serhan et al., 1999).”
From Early-life stress disrupts attachment learning: the role of amygdala corticosterone, locus ceruleus corticotropin releasing hormone, and olfactory bulb norepinephrine (2009) · cites this paper as Nakamura et al., 1987
In the citing paper
“In contrast, in older pups and adult, the LC has different characteristics limiting NE release that is associated with α2 inhibitiory autoreceptors functional emergence (Nakamura et al., 1987; Nakamura and Sakaguchi, 1990; Scheinin et al., 1994).”
From Early-life stress disrupts attachment learning: the role of amygdala corticosterone, locus ceruleus corticotropin releasing hormone, and olfactory bulb norepinephrine (2009) · cites this paper as Nakamura et al., 1987
In the citing paper
“Indeed, developmental differences in LC activity are reflected during both noxious (electric shock) and nonnoxious (stroking) stimulus-evoked NE release in the olfactory bulb, with neonatal pups releasing significantly more NE than older pups/adult (Kimura and Nakamura, 1987; Nakamura et al., 1987; Nakamura and Sakaguchi, 1990; McLean and Shipley, 1991; Sullivan et al., 1992; Sullivan and Wilson,”
From Early-life stress disrupts attachment learning: the role of amygdala corticosterone, locus ceruleus corticotropin releasing hormone, and olfactory bulb norepinephrine (2009) · cites this paper as Nakamura et al., 1987
Citations
Cited by
Sorted by citations
Items 101–132 of 132
Hirao, K., Eto, K., Nakahata, Y., Ishibashi, H., Nagai, T., & Nabekura, J. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00813.2014 · Cited by 7
Ogawa, H., Ohgushi, M., Hasegawa, K., & Murayama, N. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90057-p · Cited by 7
Su, C.-W., Yang, F., Lai, R., Li, Y., Naeem, H., Yao, N., Zhang, S.-P., Zhang, H., Li, Y., & Huang, Z. (2025) · Cognitive Neurodynamics · doi:10.1007/s11571-024-10208-8 · Cited by 8
“The denser and longer dendrites in Increase of a 2-AR on LC (Nakamura et al. 1987; Nakamura and Sakaguchi 1990; Patel and Joshi 2015) The periodic pattern of discharge changes to a tonic pattern”
InfluentialMaternal separation disrupts noradrenergic control of adult coping behaviors
Vazquez, C. R., Becker, L. J., Kuo, C., Cariello, S. A., Hamdan, A. N., Al‐Hasani, R., Maloney, S. E., & McCall, J. G. (2025) · Neuropsychopharmacology · doi:10.1038/s41386-025-02201-4 · Cited by 7
Boulanger-Bertolus, J., White, A. M., & Dębiec, J. (2017) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-017-0112-y · Cited by 7
Autocrine Neuromodulation and Network Activity Patterns in the Locus Coeruleus of Newborn Rat Slices
Waselenchuk, Q., & Ballanyi, K. (2022) · Brain Sciences · doi:10.3390/brainsci12040437 · Cited by 4
“Due to its small size there is very sparse information on electrophysiological and pharmacological LC properties in intact newborn animals [6,28,29].”
BackgroundNicotinic Receptor Regulation of Developing Catecholamine Systems
Leslie, F. M., Azam, L., Gallardo, K. A., O’Leary, K. T., Franke, R. M., & Lotfipour, S. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195183139.003.0023 · Cited by 5
Neurobiology and programming capacity of attachment learning to nurturing and abusive caregivers
Roth, T. L., Barr, G. A., Lewis, M. J., & Sullivan, R. M. (2016) · Wiley eBooks · doi:10.1002/9781118931684.ch6 · Cited by 6
Learning-induced mRNA alterations in olfactory bulb mitral cells in neonatal ratsPreprint
Nartey, M. N., Peña‐Castillo, L., LeGrow, M., Doré, J. J. E., Bhattacharya, S., Darby‐King, A., Carew, S. J., Yuan, Q., Harley, C. W., & McLean, J. H. (2020) · Learning & Memory · doi:10.1101/lm.051177.119 · Cited by 5
“Forebrain NE release by locus coeruleus neurons occurs with tactile activation in rat pups (Kimura and Nakamura 1985; Nakamura et al. 1987).”
BackgroundKhilji, M. S., Tahir, M., & Jafari, F. H. (2010) · PubMed · Cited by 4
Chapter 53 Extracellular properties of cells within mesencephalon suspension grafts in rat striatum
Fisher, L. J., Young, S. J., Groves, P. M., et al. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)62636-9 · Cited by 4
Aoki, F., & Nakamura, S. (1991) · Experimental Neurology · doi:10.1016/0014-4886(91)90128-y · Cited by 4
Self-citationRelease of Noradrenaline in the Locus Coeruleus
Pudovkina, O. L., & Westerink, B. H. C. (2007) · Springer eBooks · doi:10.1007/0-387-23696-1_10 · Cited by 3
Meng, Q., Garcia‐García, Á. L., Dranovsky, A., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/287243 · Cited by 3
Developmental Aspects of Memory Processes
Stylianopoulou, F., & Stamatakis, A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21102-4 · Cited by 2
Intracranial dynamics in pre-term infants and neonates: implications for physiotherapists
Paratz, J. D., & BURNS, Y. R. (1993) · Australian Journal of Physiotherapy · doi:10.1016/s0004-9514(14)60479-7 · Cited by 2
Fujii, Y., Nakamura, S., & Ito, H. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00158-2 · Cited by 2
Self-citationIn Vivo Development of the Spontaneous Activity of Rat Nigrostriatal Dopaminergic Neurons
Tepper, J. M., Trent, F., & Nakamura, S. (1991) · Advances in behavioral biology · doi:10.1007/978-1-4684-5871-8_26 · Cited by 2
Self-citationFontaine, C. J., Mukherjee, B., Morrison, G. L., et al. (2014) · Journal of Visualized Experiments · doi:10.3791/51808 · Cited by 1
Silva, W. D. S. (2025) · Caderno Pedagógico · doi:10.54033/cadpedv22n11-179 · Cited by 1
Contemplating the GANE model using an extreme case paradigm
Geva, R. (2016) · Behavioral and Brain Sciences · doi:10.1017/s0140525x15001806 · Cited by 1
Peters, S. E. (2017) · doi:10.7282/t35142bt · Cited by 1
Elison, J. T., & Sera, M. D. (2018) · Wiley eBooks · doi:10.1002/9781119461746.ch2 · Cited by 1
Efeito da manipulação neonatal sobre o sinal de BDNF no bulbo olfatório de ratos
Reis, A. R. (2010) · Americanae (AECID Library)
The anterior piriform cortex as a locus for early odor preference learning in rats
Morrison, G. L. (2013) · Memorial University Research Repository (Memorial University)
The Noradrenergic Basis of Early Olfactory Plasticity
Leon, M. (1994) · Springer eBooks · doi:10.1007/978-4-431-68355-1_201
Ghosh, A. (2016) · Memorial University Research Repository (Memorial University)
Translational Model of Infant PTSD Induction: Methods for Infant Fear Conditioning
Zanca, R. M., Stanciu, S., Ahmed, I., Cain, C. K., & Sullivan, R. M. (2023) · Neuromethods · doi:10.1007/978-1-0716-3218-5_1
Maturation of social adaptation circuits from ontogeny to pathology
Gleske, M., Jeanneteau, F. D., Opendak, M. M., & Coutellier, L. D. (2026) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.106874
Marsland, P., Penta, P. T., Towner, T. T., Coleman, H. J., Liss, A., Varlinskaya, E. I., Werner, D. F., & Varodayan, F. P. (2026) · Neuropharmacology · doi:10.1016/j.neuropharm.2026.111203
Manipulação Neonatal, Aprendizado Olfatório e Reprodução em Ratos
Raineki, C. (2006) · Americanae (AECID Library)
Metadata
- Authors
- Nakamura, S., Kimura, F., & Sakaguchi, T.
- Affiliations
- The University of Osaka (JP)
- Venue
- Journal of Neurophysiology
- Publisher
- American Physiological Society
- Published
- 1987-09-01
- Volume
- 58
- Issue
- 3
- Pages
- 510-524
- ISSN
- 0022-3077 (ISSN-L)
- 1522-1598
- OpenAlex
- W2412072574
- Cited by
- 130
- References
- 0
- Citations by year
- 2026: 2 · 2025: 3 · 2023: 4 · 2022: 3 · 2021: 1 · 2020: 4 · 2019: 2 · 2018: 2 · 2017: 6 · 2016: 6 · 2015: 2 · 2014: 9 · 2013: 2 · 2012: 7
- FWCI
- 1.25
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurophysiology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroscience of respiration and sleep
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- locus coeruleus, postnatal development, spontaneous firing, neonatal rats, antidromic action potentials, dorsal noradrenergic bundle, sensory input, axonal conduction velocity, noradrenergic neurons
- MeSH terms
- Aging, Animals, Animals, Newborn, Electrophysiology, Locus Coeruleus, Neurons, Rats, Inbred Strains, 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 ›
Are you an author, or do you see a problem with this page? Request a review