Cited by 175Neuroscience and Neuropharmacology ResearchMemory and Neural MechanismsNeurotransmitter Receptor Influence on Behavior

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A double dissociation within the hippocampus of dopamine D1/D5 receptor and β-adrenergic receptor contributions to the persistence of long-term potentiation

Swanson-Park, J.L, Coussens, C.M, Mason-Parker, S.E, Raymond, C.R, Hargreaves, E.L, Dragunow, M, Cohen, A.S, Abraham, W.C·1999·Neuroscience

DOI 10.1016/s0306-4522(99)00010-x

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Abstract

We compared the effects of the D1/D5 receptor antagonist SCH-23390 with the beta-adrenergic receptor antagonist propranolol on the persistence of long-term potentiation in the CA1 and dentate gyrus subregions of the hippocampus. In slices, SCH-23390 but not propranolol reduced the persistence of long-term potentiation in area CA1 without affecting its induction. The drugs exerted reverse effects in the dentate gyrus, although in this case the induction of long-term potentiation was also affected by propranolol. The lack of effect of SCH-23390 on the induction and maintenance of long-term potentiation in the dentate gyrus was confirmed in awake animals. The drug also had little or no effect on the expression of inducible transcription factors. In area CA1 of awake animals, SCH-23390 blocked persistence of long-term potentiation beyond 3 h, confirming the results in slices. To rule out a differential release of catecholamines induced by our stimulation protocols between brain areas, we compared the effects of the D1/D5 agonist SKF-38393 with the beta-adrenergic agonist isoproterenol on the persistence of a weakly induced, decremental long-term potentiation in CA1 slices. SKF-38393 but not isoproterenol promoted greater persistence of long-term potentiation over a 2-h period. In contrast, isoproterenol but not SKF-38392 facilitated the induction of long-term potentiation. These data demonstrate that there is a double dissociation of the catecholamine modulation of long-term potentiation between CA1 and the dentate gyrus, suggesting that long-term potentiation in these brain areas may be differentially consolidated according to the animal's behavioural state.

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A synaptic model of memory: long-term potentiation in the hippocampus
Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566
Why there are complementary learning systems in the hippocampus and neocortex: insights from the successes and failures of connectionist models of learning and memory
McClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256
Activity of norepinephrine-containing locus coeruleus neurons in behaving rats anticipates fluctuations in the sleep-waking cycle
Aston-Jones, G., & Bloom, F. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00876.1981 · Cited by 1,960
Effects of cAMP simulate a late stage of LTP in hippocampal CA1 neurons
Frey, U., Huang, Y.-Y., & Kandel, E. R. (1993) · Science · doi:10.1126/science.8389057 · Cited by 1,218
Nonrepinephrine-containing locus coeruleus neurons in behaving rats exhibit pronounced responses to non-noxious environmental stimuli
Aston‐Jones, G., & Bloom, F. E. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00887.1981 · Cited by 1,072
Responses of monkey dopamine neurons during learning of behavioral reactions
Ljungberg, T., Apicella, P., & Schultz, W. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.1.145 · Cited by 987
Hippocampal sharp waves: Their origin and significance
Buzsáki, G. (1986) · Brain Research · doi:10.1016/0006-8993(86)91483-6 · Cited by 925
Neuronal activity in monkey ventral striatum related to the expectation of reward
Schultz, W., Apicella, P., Scarnati, E., & Ljungberg, T. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-12-04595.1992 · Cited by 744
D1/D5 receptor agonists induce a protein synthesis-dependent late potentiation in the CA1 region of the hippocampus.
Huang, Y.-Y., & Kandel, E. R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.7.2446 · Cited by 544
The locus coeruleus: neurobiology of a central noradrenergic nucleus
Amaral, D. G., & Sinnamon, H. M. (1977) · Progress in Neurobiology · doi:10.1016/0301-0082(77)90016-8 · Cited by 497

Show all 45 references

Research works printed but not linked: 3

Buzsáki G. and Gage F. H. (1991) Long-term potentiation: does it happen in the normal brain? When and how? In Memory Mechanisms: A Tribute to G. V. Goddard (eds Abraham W. C., Corballis M. C. and White K. G.), pp. 79–102. Lawrence Erlbaum, Hillsdale.
Swanson, 1997, Role of the D1 dopamine receptor in the maintenance of long-term potentiation, Int. J. Neurosci., 89, 94
Swanson L., Kohler C. and Bjorklund A. (1987) The limbic region. I. The septohippocampal system. In Integrated Systems of the CNS (eds Bjorklund A., Hokfelt T. and Swanson L.), pp. 125–269. Elsevier Science, Amsterdam.

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Authors: Swanson-Park, J. L., Coussens, C. M., Mason-Parker, S. E., Raymond, C. R., Hargreaves, E. L., Dragunow, M., Cohen, A. S., & Abraham, W. C.
Affiliations: University of Otago (NZ)
University of Auckland (NZ)
Corresponding author: Abraham, W.C
ORCID: Hargreaves, E.L
Dragunow, M
Cohen, A.S
Abraham, W.C
Venue: Neuroscience
Publisher: Elsevier BV
Published: 1999-05
Volume: 92
Issue: 2
Pages: 485-497
ISSN: 0306-4522 (ISSN-L)
DOI: 10.1016/s0306-4522(99)00010-x
OpenAlex: W1992084781
Cited by: 175
References: 45
Citations by year: 2026: 2 · 2025: 1 · 2024: 5 · 2023: 6 · 2022: 6 · 2021: 1 · 2020: 2 · 2019: 3 · 2018: 6 · 2017: 3 · 2016: 6 · 2015: 9 · 2014: 12 · 2013: 15 · 2012: 9
FWCI: 1.21
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Neuroscience (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Keywords: long-term potentiation, dopamine D1/D5 receptors, beta-adrenergic receptors, hippocampus, CA1, dentate gyrus, SCH 23390, propranolol, SKF 38393, isoproterenol, synaptic consolidation, behavioral state
MeSH terms: Adrenergic beta-Antagonists, Animals, Benzazepines, Hippocampus, Male, Propranolol, Receptors, Adrenergic, beta, Rats, Sprague-Dawley, Receptors, Dopamine D1, Long-Term Potentiation, Dopamine Antagonists, Excitatory Postsynaptic Potentials, Receptors, Dopamine D5, Rats

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A double dissociation within the hippocampus of dopamine D1/D5 receptor and β-adrenergic receptor contributions to the persistence of long-term potentiation

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