A double dissociation within the hippocampus of dopamine D1/D5 receptor and β-adrenergic receptor contributions to the persistence of long-term potentiation
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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The D1-like antagonist SCH does not block early LTP produced by tetanization, but does block late phase LTP.
“The D1-like antagonist, SCH, does not block early LTP produced by tetanization, but does block late phase LTP (Swanson-Park et al., 1999).”
From Dopamine regulates aversive contextual learning and associated in vivo synaptic plasticity in the Hippocampus (2016) · cites this paper as Swanson-Park et al., 1999
Cites
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 · see citing works
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 · see citing works
Aston-Jones, G., & Bloom, F. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00876.1981 · Cited by 1,960 · see citing works
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 · see citing works
Aston-Jones, G., & Bloom, F. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00887.1981 · Cited by 1,033 · see citing works
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 · see citing works
Hippocampal sharp waves: Their origin and significance
Buzsáki, G. (1986) · Brain Research · doi:10.1016/0006-8993(86)91483-6 · Cited by 925 · see citing works
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 · see citing works
Huang, Y.-Y., & Kandel, E. R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.7.2446 · Cited by 544 · see citing works
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 495 · see citing works
Bergson, C. M., Mrzljak, L., Smiley, J., Pappy, M., Levenson, R. G., & Goldman-Rakic, P. S. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-12-07821.1995 · Cited by 488 · see citing works
Localization of transmitter candidates in the brain: the hippocampal formation as a model
Storm‐Mathisen, J. (1977) · Progress in Neurobiology · doi:10.1016/0301-0082(77)90013-2 · Cited by 415 · see citing works
Madison, D. V., & Nicoll, R. A. (1986) · The Journal of Physiology · doi:10.1113/jphysiol.1986.sp016006 · Cited by 391 · see citing works
Otmakhova, N. A., & Lisman, J. E. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-23-07478.1996 · Cited by 377 · see citing works
Frey, U., Schroeder, H., & Matthies, H. (1990) · Brain Research · doi:10.1016/0006-8993(90)91578-5 · Cited by 333 · see citing works
Origin of dopaminergic innervation of the rat hippocampal formation
Scatton, B., Simon, H., Le Moal, M., & Bischoff, S. (1980) · Neuroscience Letters · doi:10.1016/0304-3940(80)90314-6 · Cited by 323 · see citing works
Stanton, P. K., & Sarvey, J. M. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-08-02169.1985 · Cited by 314 · see citing works
Frey, U., Matthies, H., Reymann, K. G., & Matthies, H. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90732-9 · Cited by 314 · see citing works
Correlations between immediate early gene induction and the persistence of long-term potentiation
Abraham, W. C., Mason, S. E., Demmer, J., Williams, J. M., Richardson, C. L., Tate, W. P., Lawlor, P. A., & Dragunow, M. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90369-q · Cited by 303 · see citing works
Self-citationBliss, T. V. P., Goddard, G. V., & Riives, M. L. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014507 · Cited by 293 · see citing works
Gray, R. G. F., & Johnston, D. (1987) · Nature · doi:10.1038/327620a0 · Cited by 285 · see citing works
Bortolotto, Z. A., & Collingridge, G. L. (1993) · Neuropharmacology · doi:10.1016/0028-3908(93)90123-k · Cited by 264 · see citing works
Frequency-Dependent Noradrenergic Modulation of Long-Term Potentiation in the Hippocampus
Hopkins, W. F., & Johnston, D. (1984) · Science · doi:10.1126/science.6091272 · Cited by 256 · see citing works
Sah, P., & Bekkers, J. M. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-15-04537.1996 · Cited by 253 · see citing works
LTP saturation and spatial learning disruption: effects of task variables and saturation levels
Barnes, C. A., Jung, M., McNaughton, B. L., Korol, D., Andreasson, K. I., & Worley, P. F. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-10-05793.1994 · Cited by 219 · see citing works
Blaha, C. D., Yang, C. R., Floresco, S., Barr, A. M., & Phillips, A. G. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01441.x · Cited by 207 · see citing works
Huang, Y.-Y., & Kandel, E. R. (1996) · Neuron · doi:10.1016/s0896-6273(00)80080-x · Cited by 199 · see citing works
D1/D5 Dopamine Receptors Inhibit Depotentiation at CA1 Synapses via cAMP-Dependent Mechanism
Otmakhova, N. A., & Lisman, J. E. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-04-01270.1998 · Cited by 176 · see citing works
Dahl, D. R., & Sarvey, J. M. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.12.4776 · Cited by 171 · see citing works
Seidenbecher, T., Reymann, K. G., & Balschun, D. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.4.1494 · Cited by 154 · see citing works
Pedarzani, P., & Storm, J. F. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.74.6.2749 · Cited by 122 · see citing works
Stanton, P. K., & Sarvey, J. M. (1987) · Brain Research Bulletin · doi:10.1016/0361-9230(87)90039-6 · Cited by 121 · see citing works
Matthies, H., Becker, A., Schröeder, H., Kraus, J., Höllt, V., & Krug, M. (1997) · Neuroreport · doi:10.1097/00001756-199711100-00023 · Cited by 106 · see citing works
LTP in the lateral perforant path is β-adrenergic receptor-dependent
Bramham, C. R., Bacher-Svendsen, K., & Sarvey, J. M. (1997) · Neuroreport · doi:10.1097/00001756-199702100-00028 · Cited by 95 · see citing works
Heginbotham, L., & Dunwiddie, T. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-08-02519.1991 · Cited by 80 · see citing works
Modulation of long-term potentiation: Effects of adrenergic and neuroleptic drugs
Dunwiddie, T. V., Roberson, N. L., & Worth, T. S. (1982) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(82)90130-7 · Cited by 78 · see citing works
Dopaminergic modulation of LTP induction in the dentate gyrus of intact brain
Kusuki, T., Imahori, Y., Ueda, S., & Inokuchi, K. (1997) · Neuroreport · doi:10.1097/00001756-199705260-00046 · Cited by 66 · see citing works
Glutamatergic control over brain dopamine release in vivo and in vitro
Whitton, P. S. (1997) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(96)00034-6 · Cited by 63 · see citing works
Kerr, D. S., & Abraham, W. C. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.25.11637 · Cited by 60 · see citing works
Self-citationAction of norepinephrine in the dentate gyrus. II. Iontophoretic studies
Winson, J., & Dahl, D. R. (1985) · Experimental Brain Research · doi:10.1007/bf00261340 · Cited by 59 · see citing works
Long-term potentiation in the dentate gyrus: Effects of noradrenaline depletion in the awake rat
Robinson, G. B., & Racine, R. J. (1985) · Brain Research · doi:10.1016/0006-8993(85)90303-8 · Cited by 38 · see citing works
Parfitt, K. D., Doze, V. A., Madison, D. V., & Browning, M. D. (1992) · Hippocampus · doi:10.1002/hipo.450020108 · Cited by 38 · see citing works
Grover, L. M., & Teyler, T. J. (1990) · Brain Research · doi:10.1016/0006-8993(90)91198-p · Cited by 29 · see citing works
Yanagihashi, R., & Ishikawa, T. (1992) · Brain Research · doi:10.1016/0006-8993(92)90744-t · Cited by 26 · see citing works
Mailleux, P., Zhang, F., & Vanderhaeghen, J. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90590-4 · Cited by 24 · see citing works
Flagged first, then by citations
Cited by
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Dopamine, learning and motivation.
Wise, R. A. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1406 · Cited by 3,379 · see citing works
The hippocampal-VTA loop: controlling the entry of information into long-term memory
Lisman, J. E., & Grace, A. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.002 · Cited by 1,983 · see citing works
BDNF function in adult synaptic plasticity: The synaptic consolidation hypothesis
Bramham, C. R., & Messaoudi, E. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.06.003 · Cited by 1,193 · see citing works
The synaptic plasticity and memory hypothesis: encoding, storage and persistence
Takeuchi, T., Duszkiewicz, A. J., & Morris, R. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0288 · Cited by 664 · see citing works
Dopamine: a potential substrate for synaptic plasticity and memory mechanisms
Jay, T. M. (2003) · Progress in Neurobiology · doi:10.1016/s0301-0082(03)00085-6 · Cited by 576 · see citing works
Dopamine-dependent facilitation of LTP induction in hippocampal CA1 by exposure to spatial novelty
Li, S., Cullen, W. K., Anwyl, R., & Rowan, M. J. (2003) · Nature Neuroscience · doi:10.1038/nn1049 · Cited by 568 · see citing works
Morris, R., Moser, E. I., Riedel, G., Martin, S. J., Sandin, J., Day, M., & O’Carroll, C. (2003) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1264 · Cited by 480 · see citing works
A neoHebbian framework for episodic memory; role of dopamine-dependent late LTP
Lisman, J., Grace, A. A., & Duzel, E. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.07.006 · Cited by 465 · see citing works
Lisman, J. E., & Otmakhova, N. A. (2001) · Hippocampus · doi:10.1002/hipo.1071 · Cited by 402 · see citing works
Is Heterosynaptic modulation essential for stabilizing hebbian plasiticity and memory
Bailey, C. H., Giustetto, M., Huang, Y.-Y., Hawkins, R. D., & Kandel, E. R. (2000) · Nature Reviews Neuroscience · doi:10.1038/35036191 · Cited by 382 · see citing works
Gurden, H., Takita, M., & Jay, T. M. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-j0003.2000 · Cited by 366 · see citing works
The Dendritic Branch Is the Preferred Integrative Unit for Protein Synthesis-Dependent LTP
Govindarajan, A., Israely, I., Huang, S.-Y., & Tonegawa, S. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.008 · Cited by 349 · see citing works
A clustered plasticity model of long-term memory engrams.
Govindarajan, A., Kelleher, R. J., & Tonegawa, S. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1937 · Cited by 355 · see citing works
Lemon, N., & Manahan‐Vaughan, D. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1454-06.2006 · Cited by 345 · see citing works
Late-associativity, synaptic tagging, and the role of dopamine during LTP and LTD
Sajikumar, S. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.03.003 · Cited by 341 · see citing works
Hippocampal long-term depression: master or minion in declarative memory processes?
Kemp, A., & Manahan-Vaughan, D. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.01.002 · Cited by 336 · see citing works
Pathways of the Past: the Imprint of Memory
Horn, G. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1324 · Cited by 308 · see citing works
Novelty and Dopaminergic Modulation of Memory Persistence: A Tale of Two Systems
Duszkiewicz, A. J., McNamara, C. G., Takeuchi, T., & Genzel, L. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.10.002 · Cited by 307 · see citing works
Dahan, L., Astier, B., Vautrelle, N., Urbain, N., Kocsis, B., & Chouvet, G. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301251 · Cited by 289 · see citing works
Bethus, I., Tse, D., & Morris, R. G. M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2721-09.2010 · Cited by 270 · see citing works
Hippocampal theta rhythm: A tag for short‐term memory
Vertes, R. P. (2005) · Hippocampus · doi:10.1002/hipo.20118 · Cited by 319 · see citing works
How long will long-term potentiation last?
Abraham, W. C. (2003) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1222 · Cited by 258 · see citing works
Self-citationSmith, W. B., Starck, S. R., Roberts, R. W., & Schuman, E. M. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.015 · Cited by 252 · see citing works
Granado, N., Ortiz, Ó., Suárez, L. M., Martín, E. D., Ceña, V., Solís, J. M., & Moratalla, R. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm026 · Cited by 249 · see citing works
Dopaminergic modulation of the persistence of one-trial hippocampus-dependent memoryPreprint
O’Carroll, C., Martin, S. J., Sandin, J., Frenguelli, B. G., & Morris, R. G. M. (2006) · Learning & Memory · doi:10.1101/lm.321006 · Cited by 236 · see citing works
The roles of the reward system in sleep and dreaming
Perogamvros, L., & Schwartz, S. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.05.010 · Cited by 239 · see citing works
Calabresi, P., Castrioto, A., Filippo, M. D., & Picconi, B. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(13)70118-2 · Cited by 211 · see citing works
Gelinas, J. N., & Nguyen, P. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4175-04.2005 · Cited by 205 · see citing works
Hansen, N., & Manahan‐Vaughan, D. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs362 · Cited by 185 · see citing works
Broussard, J. I., Yang, K., Levine, A. T., Tsetsenis, T., Jenson, D., Cao, F., Garcia, I., Arenkiel, B. R., Zhou, F.-M., De Biasi, M., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.01.070 · Cited by 180 · see citing works
“The D1-like antagonist, SCH, does not block early LTP produced by tetanization but does block late phase LTP (Swanson-Park et al., 1999).”
BackgroundInsights into the Role of Dopamine Receptor Systems in Learning and Memory
El-Ghundi, M., O’Dowd, B. F., & George, S. R. (2007) · Reviews in the Neurosciences · doi:10.1515/revneuro.2007.18.1.37 · Cited by 169 · see citing works
Behavioral characterization of dopamine D-sub-5 receptor null mutant mice.
Holmes, A., Hollon, T. R., Gleason, T., Liu, Z., Dreiling, J. L., Sibley, D. R., & Crawley, J. N. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.5.1129 · Cited by 166 · see citing works
O'Dell, T. J., Connor, S. A., Guglietta, R., & Nguyen, P. V. (2015) · Learning & Memory · doi:10.1101/lm.031088.113 · Cited by 163 · see citing works
Hagena, H., Hansen, N., & Manahan‐Vaughan, D. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv330 · Cited by 163 · see citing works
Straube, T., Korz, V., Balschun, D., & Frey, J. U. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.049452 · Cited by 152 · see citing works
Navakkode, S., Sajikumar, S., & Frey, J. U. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2007.02.010 · Cited by 149 · see citing works
Li, M., Long, C., & Yang, L. (2015) · BioMed Research International · doi:10.1155/2015/810548 · Cited by 137 · see citing works
Gao, C., Sun, X., & Wolf, M. E. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03999.x · Cited by 132 · see citing works
Norepinephrine and Dopamine as Learning Signals
Harley, C. W. (2004) · Neural Plasticity · doi:10.1155/np.2004.191 · Cited by 119 · see citing works
Nobiletin treatment improves motor and cognitive deficits seen in MPTP-induced Parkinson model mice
Yabuki, Y., Ohizumi, Y., Yokosuka, A., Mimaki, Y., & Fukunaga, K. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.11.051 · Cited by 118 · see citing works
Dopaminergic innervation and modulation of hippocampal networks
Edelmann, E., & Leßmann, V. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2800-7 · Cited by 115 · see citing works
Hammerschmidt, T., Kummer, M. P., Terwel, D., Martinez, A., Gorji, A., Pape, H., Rommelfanger, K. S., Schroeder, J. P., Stoll, M., Schultze, J. L., et al. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.06.013 · Cited by 114 · see citing works
Goh, J. J., & Manahan‐Vaughan, D. (2013) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2013.00001 · Cited by 101 · see citing works
Septo-hippocampo-septal loop and memory formation.
Khakpai, F., Nasehi, M. M., Haeri-Rohani, A., Eidi, A., & Zarrindast, M. (2013) · Europe PMC (PubMed Central) · Cited by 105 · see citing works
Pralong, É. (2002) · Progress in Neurobiology · doi:10.1016/s0301-0082(02)00017-5 · Cited by 99 · see citing works
Vago, D. R., Bevan, A., & Kesner, R. P. (2007) · Hippocampus · doi:10.1002/hipo.20329 · Cited by 94 · see citing works
Hansen, N., & Manahan‐Vaughan, D. (2015) · Hippocampus · doi:10.1002/hipo.22436 · Cited by 92 · see citing works
Locus Coeruleus and Dopamine-Dependent Memory Consolidation
Yamasaki, M., & Takeuchi, T. (2017) · Neural Plasticity · doi:10.1155/2017/8602690 · Cited by 91 · see citing works
Structural Plasticity of the Hippocampus in Neurodegenerative Diseases
Weerasinghe-Mudiyanselage, P. D. E., Ang, M. J., Kang, S., Kim, J.-S., & Moon, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063349 · Cited by 79 · see citing works
Relationship of hippocampal theta and gamma oscillations to potentiation of synaptic transmission
Bikbaev, A. F. (2008) · Frontiers in Neuroscience · doi:10.3389/neuro.01.010.2008 · Cited by 87 · see citing works
Dopaminergic Modulation of Auditory Cortex-Dependent Memory Consolidation through mTOR
Schicknick, H., Schott, B. H., Budinger, E., Smalla, K., Riedel, A., Seidenbecher, C. I., Scheich, H., Gundelfinger, E. D., & Tischmeyer, W. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn026 · Cited by 88 · see citing works
-Adrenoreceptors Comprise a Critical Element in Learning-Facilitated Long-Term Plasticity
Kemp, A., & Manahan‐Vaughan, D. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm164 · Cited by 84 · see citing works
Mori, K., Togashi, H., Ueno, K., Matsumoto, M., & Yoshioka, M. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00371-5 · Cited by 77 · see citing works
Regulation of AMPA Receptor Trafficking in the Nucleus Accumbens by Dopamine and Cocaine
Wolf, M. E. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9176-0 · Cited by 76 · see citing works
Synaptic tagging and capture in the living rat
Shires, K. L., Silva, B. M. D., Hawthorne, J. P., Morris, R., & Martin, S. J. (2012) · Nature Communications · doi:10.1038/ncomms2250 · Cited by 72 · see citing works
Initial memory consolidation and the synaptic tagging and capture hypothesis
Okuda, K., Højgaard, K., Privitera, L., Bayraktar, G., & Takeuchi, T. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14902 · Cited by 71 · see citing works
Trial Outcome and Associative Learning Signals in the Monkey Hippocampus
Wirth, S., Avşar, E., Chiu, C. C., Sharma, V., Smith, A. C., Brown, E. N., & SUZUKI, W. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.012 · Cited by 71 · see citing works
Stramiello, M., & Wagner, J. J. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.06.053 · Cited by 71 · see citing works
Molecular Genetics of Monoamine Transporters: Relevance to Brain Disorders
Haddley, K., Vasiliou, A. S., Ali, F. R., Paredes, U. M., Bubb, V. J., & Quinn, J. P. (2007) · Neurochemical Research · doi:10.1007/s11064-007-9521-8 · Cited by 70 · see citing works
Bramham, C. R. (2007) · Progress in Brain Research · doi:10.1016/s0079-6123(07)63025-8 · Cited by 69 · see citing works
O’Dell, T. J., Connor, S. A., Gelinas, J. N., & Nguyen, P. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2009.12.004 · Cited by 69 · see citing works
Mnemonic functions of dorsal striatum and hippocampus in aversive conditioning
White, N. M., & Salinas, J. A. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00402-3 · Cited by 65 · see citing works
Cocaine-induced modulation of long-term potentiation in the CA1 region of rat hippocampus
THOMPSON, A., Swant, J., & Wagner, J. J. (2005) · Neuropharmacology · doi:10.1016/j.neuropharm.2005.03.005 · Cited by 67 · see citing works
Hodas, J. J. L., Nehring, A., Höche, N., Sweredoski, M. J., Pielot, R., Hess, S. Y., Tirrell, D. A., Dieterich, D. C., & Schuman, E. M. (2012) · PROTEOMICS · doi:10.1002/pmic.201200112 · Cited by 66 · see citing works
Swant, J., & Wagner, J. J. (2006) · Learning & Memory · doi:10.1101/lm.63806 · Cited by 66 · see citing works
Straube, T., & Frey, J. U. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00151-9 · Cited by 65 · see citing works
Goodman, A. M., Langner, B. M., Jackson, N. L., Alex, C., & McMahon, L. L. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0119-21.2021 · Cited by 61 · see citing works
Dahl, M. J., Kulesza, A., Werkle‐Bergner, M., & Mather, M. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105358 · Cited by 62 · see citing works
Roggenhofer, E., Fidzinski, P., Bartsch, J., Kurz, F. T., Shor, O., & Behr, J. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07312.x · Cited by 62 · see citing works
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Tran, A. H., Uwano, T., Kimura, T., Hori, E., Katsuki, M., Nishijo, H., & Ono, T. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2680-08.2008 · Cited by 61 · see citing works
Central Nervous System Agents in Medicinal Chemistry
(2019) · Central Nervous System Agents in Medicinal Chemistry · doi:10.2174/cnsamc-18715249-613 · Cited by 57 · see citing works
LTP in cultured hippocampal–entorhinal cortex slices from young adult (P25-30) rats
Leutgeb, J. K., Frey, J. U., & Behnisch, T. (2003) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(03)00228-0 · Cited by 52 · see citing works
Savanthrapadian, S., Wolff, A. R., Logan, B. J., Eckert, M. J., Bilkey, D. K., & Abraham, W. C. (2013) · Hippocampus · doi:10.1002/hipo.22193 · Cited by 51 · see citing works
Self-citationEdelmann, E., & Leßmann, V. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00025 · Cited by 51 · see citing works
Mori, K., Togashi, H., Kojima, T., Matsumoto, M., Ohashi, S., Ueno, K.-I., & Yoshioka, M. (2001) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(01)00546-9 · Cited by 49 · see citing works
Edelmann, E., & Leßmann, V. (2011) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2011.00006 · Cited by 50 · see citing works
The Role of PKA, CaMKII, and PKC in Avoidance Conditioning: Permissive or Instructive?
Shobe, J. L. (2002) · Neurobiology of Learning and Memory · doi:10.1006/nlme.2001.4022 · Cited by 49 · see citing works
Inhibition of Perforant Path Input to the CA1 Region by Serotonin and Noradrenaline
Otmakhova, N. A., Lewey, J., Asrican, B., & Lisman, J. E. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00217.2005 · Cited by 49 · see citing works
Methylphenidate amplifies long-term plasticity in the hippocampus via noradrenergic mechanismsPreprint
Dommett, E. J., Henderson, E. L., Westwell, M. S., & Greenfield, S. A. (2008) · Learning & Memory · doi:10.1101/lm.1092608 · Cited by 48 · see citing works
Suárez, L. M., Bustamante, J., Orensanz, L. M., del Rı́o, R. M., & Solís, J. M. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.10.035 · Cited by 46 · see citing works
Mockett, B. G., Guévremont, D., Williams, J. M., & Abraham, W. C. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0838-06.2007 · Cited by 46 · see citing works
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Hammad, H. M., & Wagner, J. J. (2005) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.105.091579 · Cited by 46 · see citing works
Huang, X., Lawler, C. P., Lewis, M. M., Nichols, D. E., & Mailman, R. B. (2001) · International review of neurobiology · doi:10.1016/s0074-7742(01)48014-7 · Cited by 47 · see citing works
Navakkode, S., Sajikumar, S., Sacktor, T. C., & Frey, J. U. (2010) · Learning & Memory · doi:10.1101/lm.1991910 · Cited by 46 · see citing works
Roggenhofer, E., Fidzinski, P., Shor, O., & Behr, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062520 · Cited by 43 · see citing works
Mockett, B. G., Brooks, W. M., Tate, W. P., & Abraham, W. C. (2004) · Brain Research · doi:10.1016/j.brainres.2004.06.039 · Cited by 43 · see citing works
Self-citationPsychoneurochemical Investigations to Reveal Neurobiology of Memory Deficit in Epilepsy
Mishra, A., & Goel, R. K. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1163-4 · Cited by 38 · see citing works
Pezze, M. A., & Bast, T. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.05.036 · Cited by 39 · see citing works
De Bundel, D., Femenía, T., DuPont, C. M., Konradsson-Geuken, Å., Feltmann, K., Schilström, B., & Lindskog, M. (2013) · International Journal of Neuropsychopharmacology · doi:10.1017/s1461145713000370 · Cited by 37 · see citing works
Impaired hippocampal LTP in inbred mouse strains can be rescued by β‐adrenergic receptor activation
Schimanski, L. A., Ali, D. W., Baker, G. B., & Nguyen, P. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05376.x · Cited by 37 · see citing works
Papaleonidopoulos, V., Kouvaros, S., & Papatheodoropoulos, C. (2018) · Synapse · doi:10.1002/syn.22033 · Cited by 34 · see citing works
Brzdąk, P., Wójcicka, O., Zaręba-Kozioł, M., Minge, D., Henneberger, C., Włodarczyk, J., Mozrzymas, J. W., & Wójtowicz, T. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx324 · Cited by 34 · see citing works
Gangarossa, G., Ceolin, L., Paucard, A., Lerner‐Natoli, M., Perroy, J., Fagni, L., & Valjent, E. (2014) · Hippocampus · doi:10.1002/hipo.22327 · Cited by 35 · see citing works
Moraga‐Amaro, R., González, H., Ugalde, V., Donoso-Ramos, J. P., Quintana-Donoso, D., Lara, M., Morales, B., Rojas, P., Pacheco, R., & Stehberg, J. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.12.018 · Cited by 35 · see citing works
Protein Kinase A and Anxiety-Related Behaviors: A Mini-Review
Keil, M. F., Briassoulis, G. C., Stratakis, C. A., & Wu, T. J. (2016) · Frontiers in Endocrinology · doi:10.3389/fendo.2016.00083 · Cited by 34 · see citing works
Contrasting roles for β1, β2 and β3-adrenoceptors in memory formation in the chick
Gibbs, M. E., & Summers, R. J. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2004.10.036 · Cited by 33 · see citing works
Gibbs, M. E., Bowser, D. N., Hutchinson, D. S., Loiacono, R. E., & Summers, R. J. (2008) · Neuropsychopharmacology · doi:10.1038/npp.2008.5 · Cited by 32 · see citing works
Stramiello, M., & Wagner, J. J. (2010) · Synapse · doi:10.1002/syn.20764 · Cited by 32 · see citing works
Rozas, C., Carvallo, C., Contreras, D., Carreño, M., Ugarte, G., Delgado, R., Zeise, M. L., & Morales, B. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.07.003 · Cited by 31 · see citing works
β-adrenergic signaling broadly contributes to LTP induction
Jędrzejewska‐Szmek, J., Luczak, V., Abel, T. G., & Blackwell, K. T. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005657 · Cited by 30 · see citing works
- 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
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 1999-05
- Volume
- 92
- Issue
- 2
- Pages
- 485-497
- ISSN
- 0306-4522 (ISSN-L)
- 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
- 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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