The DOI matches its Crossref record.
Noradrenergic enhancement of long-term potentiation at mossy fiber synapses in the hippocampus
Abstract
1. We tested several hypotheses related to the modulation of long-term potentiation (LTP) by norepinephrine (NE) at the mossy fiber synapses in the rat hippocampal slice preparation using extracellular and intracellular recording techniques. 2. NE exerted frequency-dependent effects on mossy fiber synaptic transmission. It had little effect on extracellular population excitatory postsynaptic potentials (pEPSPs) sampled during low-frequency stimulation, whereas it had marked effects on the duration, magnitude, and probability of induction of LTP at these synapses. 3. The beta-adrenoceptor agonist isoproterenol mimicked all of the effects of NE, whereas the beta-adrenoceptor antagonists propranolol and timolol reversibly blocked the induction of LTP, suggesting the effects of NE are mediated by a beta-adrenoceptor and that beta-adrenoceptor activation may be an important constituent for the expression of LTP at these synapses. 4. Frequency-dependent effects of NE and isoproterenol on mossy fiber pEPSPs were also observed in the presence of the gamma-aminobutyric acid (GABA) antagonist, picrotoxin, suggesting that NE can enhance LTP by a mechanism that does not depend on intact inhibition. However, propranolol did not block LTP in these disinhibited slices and did not affect LTP magnitude. 5. The adenylate cyclase activator forskolin augmented pEPSPs sampled during low-frequency stimulation in disinhibited slices and significantly enhanced LTP. Forskolin, however, did not produc…
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
“Moreover, neuromodulators can change the induction rules and time course of mossy fiber plasticity [101,102].”
From Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons (2024) · cites this paper as [101]
In the citing paper
“For example, high levels of noradrenaline acting at α1- and β-receptors enhance memory consolidation processes in the hippo-campus82,83 and increase the signal/noise ratio in primary sensory cortices84–86.”
From Stress signalling pathways that impair prefrontal cortex structure and function (2009) · cites this paper as [82]
Citations
Cites
Still being checked.
Cited by
Sorted by citations
Items 101–200 of 309
Long-term potentiation in mice lacking synapsins
Spillane, D. M., Rosahl, T. W., Südhof, T. C., & Malenka, R. C. (1995) · Neuropharmacology · doi:10.1016/0028-3908(95)00107-h · Cited by 65
Sakai, N., & Tanaka, C. (1993) · Brain Research · doi:10.1016/0006-8993(93)90921-9 · Cited by 66
Schimanski, L. A., & Nguyen, P. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.04.002 · Cited by 66
Modulation of Vigilance and Behavioral Activation by Alpha-1 Adrenoceptors in the Rat
Puumala, T., Riekkinen, P. J., & Sirviö, J. (1997) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(96)00408-x · Cited by 65
Dopamine selectively potentiates hippocampal mossy fiber to CA3 synaptic transmission
Kobayashi, K., & Suzuki, H. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.08.026 · Cited by 63
Mouse α1B‐adrenergic receptor is expressed in neurons and NG2 oligodendrocytes
Papay, R. S., Gaivin, R. J., McCune, D. F., Rorabaugh, B. R., Macklin, W. B., McGrath, J. C., & Perez, D. M. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20215 · Cited by 61
Cai, Z., Saugstad, J. A., Sorensen, S. D., Ciombor, K. J., Zhang, C., Schaffhauser, H., Hubálek, F., Pohl, J., Duvoisin, R. M., & Conn, P. J. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00468.x · Cited by 61
Impey, S., Wayman, G. A., Wu, Z., & Storm, D. R. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.12.8272 · Cited by 60
Exercise–Cognition Interaction
McMorris, T. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800778-5.00022-0 · Cited by 60
Herrero, I., & Sánchez‐Prieto, J. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.48.30554 · Cited by 59
Central Nervous System Agents in Medicinal Chemistry
(2019) · Central Nervous System Agents in Medicinal Chemistry · doi:10.2174/cnsamc-18715249-613 · Cited by 57
Villacres, E. C., Wu, Z., Hua, W., Nielsen, M. D., Watters, J. J., Yan, C., Beavo, J., & Storm, D. R. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.24.14352 · Cited by 61
Adrenergic modulation of sharp wave‐ripple activity in rat hippocampal slices
Haq, R. U., Liotta, A., Kovacs, R., Rösler, A., Jarosch, M. J., Heinemann, U., & Behrens, C. (2011) · Hippocampus · doi:10.1002/hipo.20918 · Cited by 57
Jenson, D., Yang, K., Acevedo-Rodriguez, A., Levine, A., Broussard, J. I., Tang, J., & Dani, J. A. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.10.029 · Cited by 52
Neuromodulation of the Feedforward Dentate Gyrus-CA3 Microcircuit
Prince, L. Y., Bacon, T., Tigaret, C. M., & Mellor, J. R. (2016) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2016.00032 · Cited by 53
Maeda, T., Kaneko, S., & Satoh, M. (1994) · Neuroscience Research · doi:10.1016/0168-0102(94)90163-5 · Cited by 54
Langdon, R. B., Johnson, J. W., & Barrionuevo, G. (1995) · Journal of Neurobiology · doi:10.1002/neu.480260309 · Cited by 52
McCauslin, C. S., Heath, V. L., Colangelo, A. M., Malı́k, R., Lee, S., Mallei, A., Mocchetti, I., & Johnson, P. F. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600207200 · Cited by 52
Kim, Q., Benz, B., Sorg, O., Pellerin, L., & Magistretti, P. J. (1997) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1997.68062386.x · Cited by 51
Serotonin inhibits induction of long-term potentiation at commissural synapses in hippocampus
Villani, F. S., & Johnston, D. (1993) · Brain Research · doi:10.1016/0006-8993(93)90998-3 · Cited by 50
Self-citationMethylphenidate 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
Hagena, H., & Manahan‐Vaughan, D. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00023 · Cited by 54
Cyclic AMP and long-term potentiation in the CA1 region of rat hippocampus
Pockett, S., Slack, J. R., & Peacock, S. J. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90151-5 · Cited by 47
Waterhouse, B. D., Mouradian, R., Sessler, F. M., & Lin, R. C. S. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02261-7 · Cited by 45
Booze, R. M., Crisostomo, E. A., & Davis, J. N. (1993) · Synapse · doi:10.1002/syn.890130303 · Cited by 44
Rudolphi, K. A., & Schubert, P. (1997) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)86055-x · Cited by 44
Ludvig, N., Ribak, C. E., Scott, J. D., & Rubin, C. S. (1990) · Brain Research · doi:10.1016/0006-8993(90)91694-c · Cited by 44
DISC1 as a therapeutic target for mental illnesses
Hikida, T., Gamo, N. J., & Sawa, A. (2012) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2012.719879 · Cited by 42
Duncan, G. E., Little, K. Y., Koplas, P. A., Kirkman, J. A., Breese, G. R., & Stumpf, W. E. (1991) · Brain Research · doi:10.1016/0006-8993(91)90752-h · Cited by 43
Long‐term potentiation and the mechanisms of memory
Izquierdo, I. (1993) · Drug Development Research · doi:10.1002/ddr.430300102 · Cited by 44
Correlation of phenotype with genotype in inherited retinal degeneration
Daiger, S. P., Sullivan, L. S., & Rodriguez, J. A. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00039212 · Cited by 43
Fukaya, R., Maglione, M., Sigrist, S. J., & Sakaba, T. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2016754118 · Cited by 42
Cocaine inhibits hippocampal long-term potentiation.
Smith, D., Browning, M., & Dunwiddie, T. (1993) · Brain Research · doi:10.1016/0006-8993(93)91466-6 · Cited by 39
Kamiya, H., & Yamamoto, C. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00098-5 · Cited by 40
Stimulation of alpha-1 adrenergic receptors facilitates spatial learning in rats
Puumala, T., Greijus, S., Narinen, K., Haapalinna, A., Riekkinen, P. J., & Sirviö, J. (1998) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(97)00040-0 · Cited by 41
Sizemore, M., & Perkel, D. J. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01212.2007 · Cited by 41
Milusheva, E. A., Baranyi, M., Zelles, T., Mike, Á., & Vizi, E. S. (1994) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1994.tb00260.x · Cited by 41
Williams, S. H., & Johnston, D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-11-03652.1996 · Cited by 40
Self-citationSynaptic Plasticity: Stairway to Memory
Jódar, L., & Kaneto, H. (1995) · The Japanese Journal of Pharmacology · doi:10.1254/jjp.68.359 · Cited by 44
Santschi, L. A., Reyes-Harde, M., & Stanton, P. K. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.3.1577 · Cited by 40
Lynn, B. D., Li, X., & Nagy, J. I. (2012) · The Journal of Membrane Biology · doi:10.1007/s00232-012-9451-5 · Cited by 39
Biochemical Correlates of Long-Term Potentiation in Hippocampal Synapses
Otani, S., & Ben‐Ari, Y. (1993) · International review of neurobiology · doi:10.1016/s0074-7742(08)60567-x · Cited by 40
Dexamphetamine effects on separate constructs in the rubber hand illusion test
Albrecht, M. A., Martin-Iverson, M. T., Price, G. W., Lee, J. J., Iyyalol, R., & Waters, F. (2011) · Psychopharmacology · doi:10.1007/s00213-011-2255-y · Cited by 39
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
Zoladz, P. R., & Diamond, D. M. (2008) · Dose-Response · doi:10.2203/dose-response.08-015.zoladz · Cited by 37
Gean, P., Huang, C., Lin, J.-H., & Tsai, J. (1992) · Brain Research · doi:10.1016/0006-8993(92)91146-6 · Cited by 36
Moriwaki, A. (1991) · Brain Research · doi:10.1016/0006-8993(91)90061-y · Cited by 36
Soto‐Moyano, R., Valladares, L., Sierralta, W. D., Pérez, H., Mondaca, M., Fernández, V., Burgos, H., & Hernández, A. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03094.x · Cited by 36
Evans, D. I., Jones, R. S. G., & Woodhall, G. L. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.2.571 · Cited by 36
Mercan, D., & Heneka, M. T. (2022) · Biology · doi:10.3390/biology11121822 · Cited by 34
Noradrenaline activation of hippocampal dopamine D 1 receptors promotes antidepressant effects
Kobayashi, K., Shikano, K., Kuroiwa, M., Horikawa, M., Ito, W., Nishi, A., Segi-Nishida, E., & Suzuki, H. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2117903119 · Cited by 34
Adenosine depresses induction of LTP at the mossy fiber-CA3 synapse in vitro
Alzheimer, C., Röhrenbeck, J., & ten Bruggencate, G. (1991) · Brain Research · doi:10.1016/0006-8993(91)91061-5 · Cited by 33
Xu, T., Ma, Q., Spealman, R. D., & Yao, W. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.07073.x · Cited by 33
Riekkinen, M., Stefański, R., Kuitunen, J., & Riekkinen, P. J. (1996) · European Journal of Pharmacology · doi:10.1016/0014-2999(95)00842-x · Cited by 33
Warren, R. A., & Dykes, R. W. (1996) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y95-225 · Cited by 33
Son, H., & Carpenter, D. O. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00532-3 · Cited by 31
Chida, N., Saitō, H., & Abe, K. (1992) · Brain Research · doi:10.1016/0006-8993(92)91263-e · Cited by 33
Development of dopamine‐beta hydroxylase—positive fiber innervation of the rat hippocampus
Moudy, A. M., Kunkel, D. D., & Schwartzkroin, P. A. (1993) · Synapse · doi:10.1002/syn.890150407 · Cited by 32
Powell, C. M., Johnston, D., & Sweatt, J. D. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)46880-9 · Cited by 32
Self-citationEffect of xanthine derivatives on hippocampal long-term potentiation
Tanaka, Y., Sakurai, M., Goto, M., & Hayashi, S. (1990) · Brain Research · doi:10.1016/0006-8993(90)91577-4 · Cited by 29
Maeda, T., Kaneko, S., & Satoh, M. (1993) · Brain Research · doi:10.1016/0006-8993(93)91628-6 · Cited by 29
Libri, V., Constanti, A., Zibetti, M., & Postlethwaite, M. (1997) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0701021 · Cited by 29
Altered hippocampal network excitability in the hypernoradrenergic mutant mousetottering
Noebels, J. L., & Rutecki, P. A. (1990) · Brain Research · doi:10.1016/0006-8993(90)90695-8 · Cited by 29
Galván, E. J., Cosgrove, K. E., Mauna, J. C., Card, J. P., Thiels, E., Meriney, S. D., & Barrionuevo, G. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5269-09.2010 · Cited by 28
Goldenstein, B., Nelson, B., Xu, K., Luger, E., Pribula, J. A., Wald, J. M., O'Shea, L., Weinshenker, D., Charbeneau, R. A., Huang, X., et al. (2009) · Molecular Pharmacology · doi:10.1124/mol.108.054296 · Cited by 28
Nowicky, A. V., Christofi, G., & Bindman, L. J. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90420-c · Cited by 28
Naparstek, S., Yeh, A. K., & Mills‐Finnerty, C. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1145207 · Cited by 27
Jin, S., Liu, L., Li, S., Meunier, A. L., & Selkoe, D. J. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105816 · Cited by 27
Lashgari, R., Khakpour-Taleghani, B., Motamedi, F., & Shahidi, . (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.05.012 · Cited by 27
α2-Adrenoceptor modulation of long-term potentiation elicited in vivo in rat occipital cortex
Mondaca, M., Hernández, A., Pérez, H., Valladares, L., Sierralta, W. D., Fernández, V., & Soto‐Moyano, R. (2004) · Brain Research · doi:10.1016/j.brainres.2004.07.020 · Cited by 27
Wang, J., Yeckel, M. F., Johnston, D., & Zucker, R. S. (2004) · Journal of Neurophysiology · doi:10.1152/jn.01073.2003 · Cited by 29
Self-citationFlores, O., Pérez, H., Valladares, L., Morgan, C., Gatica, A., Burgos, H., Olivares, R., & Hernández, A. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07429.x · Cited by 28
Cognitive enhancers and hippocampal long-term potentiation in vitro
Kaneko, S., Maeda, T., & Satoh, M. (1997) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)86044-5 · Cited by 25
Bronzino, J. D., Kehoe, P., Mallinson, K., & Fortin, D. A. (2001) · Hippocampus · doi:10.1002/hipo.1057 · Cited by 26
Imamura, K., Kasamatsu, T., Shirokawa, T., & Ohashi, T. (1999) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1999.0808 · Cited by 26
Katsuki, H., Saitō, H., & Satoh, M. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90384-j · Cited by 26
α2A Adrenergic Receptor Activation Inhibits Epileptiform Activity in the Rat Hippocampal CA3 Region
Jurgens, C., Hammad, H. M., Lichter, J. A., Boese, S., Nelson, B., Goldenstein, B., Davis, K. L., Xu, K., Hillman, K. L., Porter, J. E., et al. (2007) · Molecular Pharmacology · doi:10.1124/mol.106.031773 · Cited by 25
Morphine Induces Synchronous Oscillatory Discharges in the Rat Locus Coeruleus
Zhu, H., & Zhou, W. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-21-j0003.2001 · Cited by 25
Engineered synaptic tools reveal localized cAMP signaling in synapse assembly
Sando, R. C., Ho, M., Liu, X., & Südhof, T. C. (2021) · The Journal of Cell Biology · doi:10.1083/jcb.202109111 · Cited by 25
Noradrenergic Regulation of Hippocampus-Dependent Memory
Nguyen, P., & Connor, S. A. (2019) · Central Nervous System Agents in Medicinal Chemistry · doi:10.2174/1871524919666190719163632 · Cited by 22
Norepinephrine as a spatial memory reset signal
Grella, S. L., Gomes, S. M., Lackie, R. E., Renda, B., & Marrone, D. F. (2021) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000648 · Cited by 25
Neuromodulation of activity-dependent synaptic enhancement at crayfish neuromuscular junction
Qian, S., & Delaney, K. R. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00812-3 · Cited by 23
Immunohistochemical localization of the neural cannabinoid receptor in rat brain
Pettit, D. A. D., Harrison, M. P., Olson, J. M., Spencer, R. F., & Cabral, G. A. (1998) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19980201)51:3 · Cited by 228
Haq, R. U., Anderson, M., Liotta, A., Shafiq, M., Sherkheli, M. A., & Heinemann, U. (2016) · Hippocampus · doi:10.1002/hipo.22665 · Cited by 23
Clorgyline-mediated reversal of neurological deficits in a Complexin 2 knockout mouse
Glynn, D., Gibson, H. E., Harte, M., Reim, K., Jones, S., Reynolds, G. P., & Morton, A. J. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq252 · Cited by 21
Niittykoski, M., Ruotsalainen, S., Haapalinna, A., Larson, J., & Sirviö, J. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00447-3 · Cited by 21
Maeda, T., Kaneko, S., & Satoh, M. (1994) · Neuroscience Research · doi:10.1016/0168-0102(94)90023-x · Cited by 21
Miles, R. (1991) · The Journal of Physiology · doi:10.1113/jphysiol.1991.sp018857 · Cited by 21
Moody, T. D., Thomas, M. J., Makhinson, M., & O’Dell, T. J. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00217-0 · Cited by 20
Hebbian synapses in cortical and hippocampal pathways
Skrebitsky, V. G., & Chepkova, A. N. (1998) · Reviews in the Neurosciences · doi:10.1515/revneuro.1998.9.4.243 · Cited by 19
β-Adrenoceptors and synaptic plasticity in the perirhinal cortex
Laing, M., & Bashir, Z. I. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.04.070 · Cited by 19
Riekkinen, M., Kemppainen, S., & Riekkinen, P. J. (1997) · Psychopharmacology · doi:10.1007/s002130050264 · Cited by 19
Presynaptic Facilitation of Synaptic Transmission in the Hippocampus
Capogna, M. (1998) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(97)00162-9 · Cited by 18
Urban, I. J. A., Ontskul, A. H., Croiset, G., Cheng, Y., & de Wied, D. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(94)00172-c · Cited by 19
Norepinephrine, beyond the Synapse: Coordinating Epigenetic Codes for Memory
Maity, S., Abbaspour, R., Nahabedian, D., & Connor, S. A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23179916 · Cited by 18
Zhang, J. J., Okutani, F., Huang, G., Taniguchi, M., Murata, Y., & Kaba, H. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.06.002 · Cited by 18
Later Developments: Molecular Keys to Age-Related Memory Impairment
Barad, M. (2003) · Alzheimer Disease & Associated Disorders · doi:10.1097/00002093-200307000-00009 · Cited by 18
Noradrenaline and Kindling Revisited
Corcoran, M. E., & Weiss, G. K. (1990) · Advances in behavioral biology · doi:10.1007/978-1-4684-5796-4_11 · Cited by 18
Puumala, T., Sirviö, J., Ruotsalainen, S., & Riekkinen, P. J. (1996) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(95)02231-7 · Cited by 18
Ludvig, N., Mishra, P. K., & Jobe, P. C. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90891-a · Cited by 18
Metadata
- Authors
- Hopkins, W. F., & Johnston, D.
- Affiliations
- Baylor College of Medicine (US)
- Venue
- Journal of Neurophysiology
- Publisher
- American Physiological Society
- Published
- 1988-02-01
- Volume
- 59
- Issue
- 2
- Pages
- 667-687
- ISSN
- 0022-3077 (ISSN-L)
- 1522-1598
- OpenAlex
- W2403704540
- Cited by
- 310
- References
- 0
- Citations by year
- 2025: 1 · 2024: 2 · 2023: 2 · 2022: 5 · 2021: 5 · 2020: 1 · 2019: 3 · 2018: 4 · 2016: 4 · 2015: 4 · 2014: 8 · 2012: 7
- FWCI
- 5.37
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurophysiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (HL-31164)
- National Institute of Neurological Disorders and Stroke (NS-11535, NS-15772)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- norepinephrine, long-term potentiation, mossy fiber synapses, hippocampus, beta-adrenergic receptors, isoproterenol, propranolol, timolol, cyclic AMP, forskolin, 8-bromo-cAMP, synaptic transmission, GABAergic inhibition, tetanic stimulation, synaptic plasticity
- MeSH terms
- Animals, Colforsin, Hippocampus, Isoproterenol, Male, Nerve Fibers, Neural Inhibition, Norepinephrine, Picrotoxin, Rats, Inbred Strains, Receptors, Adrenergic, beta, Synapses, Time Factors, 8-Bromo Cyclic Adenosine Monophosphate, 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