Memory deficits associated with senescence: A neurophysiological and behavioral study in the rat.
Abstract
Neurophysiological and behavioral measures were obtained from 32 senescent (28--34 mo) and 32 mature adult (10--16 mo) rats. Extracellularly recorded synaptic responses were obtained from electrodes chronically implanted in the fascia dentata and perforant path. The rats were first tested on a circular platform, which favored the use of spatial cues for its solution, and the senescent rats were shown to exhibit poorer memory for the rewarded place. When granule cell synaptic responses were recorded after a single session of very brief high-frequency stimulation, the amount of elevation and time course of decline were equivalent between age groups. Af ter three repetitions, however, the young rats maintained the increased synaptic strength for at least 14 days, whereas the old rats declined after the first session. The amount of synaptic enhancement was statistically correlated with the ability to perform the circular platform task both within and between groups. Furthermore, the aftereffects of the high-frequency stimulation selectively impaired the old rats' spontaneous alternation behavior on a T-maze. Certain other neurophysiological and electroencephalographic measures did not distinguish between age groups. The results are discussed in terms of the synaptic theory of memory formation and of their relevance to the aging process.
Integrity signals
Registry
Cites
Statistics
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?
Assays thought to rely on hippocampal related behaviors.
“Assays thought to rely on hippocampal related behaviors43–45 were performed two months post ASO delivery to test the functionality of PTB ASO generated new neurons in the dentate gyri of 1.5 year old control or PTB ASO ICV injected mice.”
From Therapeutically viable generation of neurons with antisense oligonucleotide suppression of PTB (2021) · cites this paper as [44]
The Barnes maze examines spatial learning and memory by testing the ability to learn and remember the location of a target zone.
“This test is similar to the water maze navigation task in that it examines the ability of the mouse to learn and remember the location of a target zone (spatial learning and memory) (42).”
From Perivascular macrophages mediate the neurovascular and cognitive dysfunction associated with hypertension (2016) · cites this paper as [42]
Other common tasks of murine spatial working memory are the Radial Arm Water Maze and the Barnes Maze.
“Other common tasks of murine spatial working memory are the Radial Arm Water Maze (RAWM) and the Barnes Maze (Barnes, 1979; Diamond et al., 1999; Alamed et al., 2006).”
From Using mice to model Alzheimer's dementia: an overview of the clinical disease and the preclinical behavioral changes in 10 mouse models (2014) · cites this paper as Barnes, 1979
Cites
Hebb, D. O. (2005) · doi:10.4324/9781410612403 · Cited by 9,825 · see citing works
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010 · see citing works
Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,460 · see citing works
Handbook of the Psychology of Aging
Schaie, K. W., Willis, S. L., Knight, B. G., & Park, D. C. (2016) · Elsevier eBooks · doi:10.1016/c2012-0-07221-3 · Cited by 3,436 · see citing works
Simple memory: a theory for archicortex
Marr, D. (1971) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1971.0078 · Cited by 2,771 · see citing works
Place units in the hippocampus of the freely moving rat
O'Keefe, J. (1976) · Experimental Neurology · doi:10.1016/0014-4886(76)90055-8 · Cited by 1,836 · see citing works
Lamellar organization of hippocampal excitatory pathways
Andersen, P. N., Bliss, T. V. P., & Skrede, K. K. (1971) · Experimental Brain Research · doi:10.1007/bf00234087 · Cited by 943 · see citing works
Hippocampal connections and spatial discrimination
Olton, D. S., Walker, J. A., & Gage, F. H. (1978) · Brain Research · doi:10.1016/0006-8993(78)90930-7 · Cited by 848 · see citing works
Cells of origin of entorhinal cortical afferents to the hippocampus and fascia dentata of the rat
Steward, O., & Scoville, S. A. (1976) · The Journal of Comparative Neurology · doi:10.1002/cne.901690306 · Cited by 837 · see citing works
Kramis, R., Vanderwolf, C. H., & Bland, B. H. (1975) · Experimental Neurology · doi:10.1016/0014-4886(75)90195-8 · Cited by 791 · see citing works
Origin and termination of the hippocampal perforant path in the rat studied by silver impregnation
Hjorth‐Simonsen, A., & Jeune, B. (1972) · The Journal of Comparative Neurology · doi:10.1002/cne.901440206 · Cited by 680 · see citing works
Synaptic enhancement in fascia dentata: Cooperativity among coactive afferents
McNaughton, B. L., Douglas, R. M., & Goddard, G. V. (1978) · Brain Research · doi:10.1016/0006-8993(78)90030-6 · Cited by 647 · see citing works
Unit analysis of hippocampal population spikes
Andersen, P. N., Bliss, T. V. P., & Skrede, K. K. (1971) · Experimental Brain Research · doi:10.1007/bf00234086 · Cited by 606 · see citing works
A Fourier method for the analysis of exponential decay curves
Provencher, S. W. (1976) · Biophysical Journal · doi:10.1016/s0006-3495(76)85660-3 · Cited by 594 · see citing works
Long-term potentiation of the perforant path-granule cell synapse in the rat hippocampus
Douglas, R. M., & Goddard, G. V. (1975) · Brain Research · doi:10.1016/0006-8993(75)90697-6 · Cited by 507 · see citing works
Spontaneous alternation behavior.
Dember, W. N., & Fowler, H. (1958) · Psychological Bulletin · doi:10.1037/h0045446 · Cited by 482 · see citing works
L�mo, T. (1971) · Experimental Brain Research · doi:10.1007/bf00234414 · Cited by 477 · see citing works
Entorhinal Activation of Dentate Granule Cells
Andersen, P. N., Holmqvist, B., & Voorhoeve, P. E. (1966) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1966.tb03223.x · Cited by 440 · see citing works
Alzheimer's Neurofibrillary Changes: A Topographic Study
HIRANO, A. (1962) · Archives of Neurology · doi:10.1001/archneur.1962.04210030065009 · Cited by 402 · see citing works
Discrimination of cues in mazes: A resolution of the "place-vs.-response" question.
Restle, F. (1957) · Psychological Review · doi:10.1037/h0040678 · Cited by 386 · see citing works
Prolongation of hippocampal inhibitory postsynaptic potentials by barbiturates
Nicoll, R. A., Eccles, J. C., OSHIMA, T., & Rubia, F. J. (1975) · Nature · doi:10.1038/258625a0 · Cited by 373 · see citing works
Fornix lesions selectively abolish place learning in the rat
O'Keefe, J. M., Nadel, L., Keightley, S. J., & Kill, D. (1975) · Experimental Neurology · doi:10.1016/0014-4886(75)90230-7 · Cited by 337 · see citing works
Impaired synaptic potentiation processes in the hippocampus of aged, memory-deficient rats
Landfield, P. W., McGaugh, J. L., & LYNCH, G. S. (1978) · Brain Research · doi:10.1016/0006-8993(78)90655-8 · Cited by 296 · see citing works
Harreveld, A. V., & Fifkova´, E. (1975) · Experimental Neurology · doi:10.1016/0014-4886(75)90055-2 · Cited by 280 · see citing works
McNaughton, B. L., & Barnes, C. A. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901750404 · Cited by 280 · see citing works
Self-citationHandbook of psychological research on the rat
Munn, N. L. (1950) · Cited by 260 · see citing works
The Regulation of Physiological Changes During Mammalian Aging
Finch, C. E. (1976) · The Quarterly Review of Biology · doi:10.1086/409053 · Cited by 242 · see citing works
Loesche, J., & Steward, O. (1977) · Brain Research Bulletin · doi:10.1016/0361-9230(77)90022-3 · Cited by 232 · see citing works
Does the Engram of Kindling Model the Engram of Normal Long Term Memory?
Goddard, G. V., & Douglas, R. M. (1975) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100020539 · Cited by 223 · see citing works
Hippocampal function in avoidance learning and punishment.
Black, A. H., Nadel, L., & O'Keefe, J. M. (1977) · Psychological Bulletin · doi:10.1037/0033-2909.84.6.1107 · Cited by 221 · see citing works
Impaired Monosynaptic Potentiation in in Vitro Hippocampal Slices From Aged, Memory-deficient Rats
Landfield, P. W., & LYNCH, G. S. (1977) · Journal of Gerontology · doi:10.1093/geronj/32.5.523 · Cited by 181 · see citing works
Progressive dendritic changes in the aging human limbic system
Scheibel, M. E., Lindsay, R. D., Tomiyasu, U., & Scheibel, A. B. (1976) · Experimental Neurology · doi:10.1016/0014-4886(76)90082-0 · Cited by 158 · see citing works
Steward, O., Cotman, C. W., & LYNCH, G. S. (1976) · Brain Research · doi:10.1016/0006-8993(76)90665-x · Cited by 150 · see citing works
Age and the Measurement of Mental Health
Gaitz, C. M., & Scott, J. (1972) · Journal of Health and Social Behavior · doi:10.2307/2136973 · Cited by 142 · see citing works
Ebbesson, S. O. E. (1970) · Springer eBooks · doi:10.1007/978-3-642-85986-1_7 · Cited by 140 · see citing works
Lipofuscin Pigment Accumulation as a Function of Age and Distribution in Rodent Brain
Reichel, W., Hollander, J. E., Clark, J. H., & Strehler, B. L. (1968) · Journal of Gerontology · doi:10.1093/geronj/23.1.71 · Cited by 139 · see citing works
Circadian Rhythm of Synaptic Excitability in Rat And Monkey Central Nervous System
Barnes, C. A., McNaughton, B. L., Goddard, G. V., Douglas, R. M., & Adamec, R. E. (1977) · Science · doi:10.1126/science.194313 · Cited by 138 · see citing works
Self-citationThe recall of events through the learning of associations between their parts
Gardner-Medwin, A. R. (1976) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1976.0084 · Cited by 125 · see citing works
Age Differences in Recognition Memory
Erber, J. T. (1974) · Journal of Gerontology · doi:10.1093/geronj/29.2.177 · Cited by 125 · see citing works
Geinisman, Y., & Bondareff, W. (1976) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(76)90003-8 · Cited by 120 · see citing works
A study of forgetting in amnesic patients
Weiskrantz, L., & Warrington, E. K. (1970) · Neuropsychologia · doi:10.1016/0028-3932(70)90074-6 · Cited by 110 · see citing works
Goodrick, C. L. (1968) · Journal of Gerontology · doi:10.1093/geronj/23.3.298 · Cited by 107 · see citing works
Learning by Mature-young and Aged Wistar Albino Rats As a Function of Test Complexity
Goodrick, C. L. (1972) · Journal of Gerontology · doi:10.1093/geronj/27.3.353 · Cited by 103 · see citing works
Studies in the processes of aging: Electroencephalographic findings in 400 elderly subjects
Silverman, A. J., Busse, E. W., & Barnes, R. H. (1955) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(55)90060-2 · Cited by 100 · see citing works
Ultrastructural age changes in hippocampal neurons, synapses and neuroglia
Hasan, M. N., & Glees, P. (1973) · Experimental Gerontology · doi:10.1016/0531-5565(73)90017-x · Cited by 96 · see citing works
Rat hippocampus and memory for places of changing significance.
Sinnamon, H. M., Freniere, S., & Kootz, J. P. (1978) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0077446 · Cited by 94 · see citing works
Another inexpensive headplug for the electrical recording and or stimulation of rats
Molino, A., & McIntyre, D. (1972) · Physiology & Behavior · doi:10.1016/0031-9384(72)90249-1 · Cited by 92 · see citing works
Retrieving Information from Korsakoff Patients Effects of Categorical Cues and Reference to the Task
Gardner, H., Boller, F., Moreines, J., & Butters, N. (1973) · Cortex · doi:10.1016/s0010-9452(73)80025-5 · Cited by 82 · see citing works
Application of Signal Detection Theory to Prose Recall and Recognition in Elderly and Young Adults
Gordon, S. K., & Clark, W. C. (1974) · Journal of Gerontology · doi:10.1093/geronj/29.1.64 · Cited by 81 · see citing works
Scheff, S. W., & Cotman, C. W. (1977) · Behavioral Biology · doi:10.1016/s0091-6773(77)90374-1 · Cited by 79 · see citing works
Douglas, R. M. (1977) · Brain Research · doi:10.1016/0006-8993(77)90733-8 · Cited by 78 · see citing works
Effects of age on learning ability: Contributions from the animal literature
Elias, P. K., & Elias, M. F. (1976) · Experimental Aging Research · doi:10.1080/03610737608257985 · Cited by 72 · see citing works
Barbiturate reversal of amino acid antagonism produced by convulsant agents
Bowery, N. G., & Dray, A. (1976) · Nature · doi:10.1038/264276a0 · Cited by 57 · see citing works
Behavioral Rigidity as a Mechanism for Facilitation of Problem Solving for Aged Rats
Goodrick, C. L. (1975) · Journal of Gerontology · doi:10.1093/geronj/30.2.181 · Cited by 48 · see citing works
Steward, O., White, W. F., Cotman, C., et al. (1976) · Experimental Brain Research · doi:10.1007/bf00234223 · Cited by 44 · see citing works
Age Differences in Retention of Concurrent Discrimination Problems in Monkeys
Medin, D. L., O'Neil, P., Smeltz, E., & Davis, R. T. (1973) · Journal of Gerontology · doi:10.1093/geronj/28.1.63 · Cited by 36 · see citing works
Discrimination Learning With Old and Young Rats
Kay, H., & Sime, M. E. (1962) · Journal of Gerontology · doi:10.1093/geronj/17.1.75 · Cited by 32 · see citing works
Memory Span, Practice, and Aging
Taub, H. A. (1973) · Journal of Gerontology · doi:10.1093/geronj/28.3.335 · Cited by 27 · see citing works
The Electroencephalogram of Healthy Aged Males.
Obrist, W. D. (1963) · doi:10.1037/10776-007 · Cited by 23 · see citing works
A comparison of long-term potentiation in the in vitro and in vivo hippocampal preparations
Teyler, T. J., Alger, B. E., Bergman, T., et al. (1977) · Behavioral Biology · doi:10.1016/s0091-6773(77)91303-7 · Cited by 20 · see citing works
Interaction of Learning and Memory with Age in the Rat
Ray, O. S., & Barrett, R. J. (1973) · Advances in behavioral biology · doi:10.1007/978-1-4684-7770-2_3 · Cited by 19 · see citing works
Thompson, C. I., & Fitzsimons, T. R. (1976) · Journal of Gerontology · doi:10.1093/geronj/31.1.47 · Cited by 14 · see citing works
Potentiation of Monosynaptic EPSPs in the Perforant Path- Dentate Granule Cell Synapse
Mo, T. (1971) · Cited by 10 · see citing works
Age-dependent changes in hippocampal theta
Cooper, R. L., Prinz, P. N., & Marsh, G. R. (1975) · Experimental Aging Research · doi:10.1080/03610737508257950 · Cited by 9 · see citing works
Effects of remote dendritic synapses on hippocampal pyramids [proceedings].
Andersen, P. N., SILFVENIUS, H., Sundberg, S. H., et al. (1977) · PubMed · Cited by 6 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Place navigation impaired in rats with hippocampal lesions
Morris, R. G. M., Garrud, P., Rawlins, J. N. P., & O'Keefe, J. (1982) · Nature · doi:10.1038/297681a0 · Cited by 6,340 · 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
Pattern separation in the hippocampus
Yassa, M. A., & Stark, C. E. L. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.06.006 · Cited by 1,544 · see citing works
Hippocampal synaptic enhancement and information storage within a distributed memory system
McNaughton, B. L., & Morris, R. G. M. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90011-7 · Cited by 1,304 · see citing works
Replay of neuronal firing sequences in rat hippocampus during sleep following spatial experience
Skaggs, W. E., & McNaughton, B. L. (1996) · Science · doi:10.1126/science.271.5257.1870 · Cited by 1,173 · see citing works
Goldstein, L. E., Fisher, A. M., Tagge, C. A., Zhang, X.-L., Velisek, L., Sullivan, J. A., Upreti, C., Kracht, J. M., Ericsson, M., Wojnarowicz, M. W., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003716 · Cited by 958 · see citing works
The hippocampus—what does it do?
Eichenbaum, H., Otto, T., & Cohen, N. J. (1992) · Behavioral and Neural Biology · doi:10.1016/0163-1047(92)90724-i · Cited by 867 · see citing works
Webster, S. J., Bachstetter, A. D., Nelson, P. T., Schmitt, F. A., & Van Eldik, L. J. (2014) · Frontiers in Genetics · doi:10.3389/fgene.2014.00088 · Cited by 755 · see citing works
Yankner, B. A., Lu, T., & Loerch, P. (2008) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev.pathmechdis.2.010506.092044 · Cited by 677 · see citing works
A complement–microglial axis drives synapse loss during virus-induced memory impairment
Vasek, M. J., Garber, C., Dorsey, D., Durrant, D. M., Bollman, B., Soung, A., Yu, J., Perez-Torres, C., Frouin, A., Wilton, D. K., et al. (2016) · Nature · doi:10.1038/nature18283 · Cited by 671 · see citing works
Reactive Oxygen Species in the Regulation of Synaptic Plasticity and Memory
Massaad, C. A., & Klann, E. (2011) · Antioxidants & Redox Signaling · doi:10.1089/ars.2010.3208 · Cited by 635 · see citing works
Clinton, L. K., Blurton-Jones, M., Myczek, K., Trojanowski, J. Q., & LaFerla, F. M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.0490-10.2010 · Cited by 576 · see citing works
Associations across time: The hippocampus as a temporary memory store
Rawlins, J. N. P. (1985) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00001291 · Cited by 561 · see citing works
SIRT1 Is Essential for Normal Cognitive Function and Synaptic Plasticity
Michan, S., Li, Y., Chou, M. M.-H., Parrella, E., Ge, H., Long, J. M., Allard, J. S., Lewis, K., Miller, M., Xu, W., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0027-10.2010 · Cited by 541 · see citing works
Izquierdo, I., Furini, C. R. G., & Myskiw, J. C. (2016) · Physiological Reviews · doi:10.1152/physrev.00018.2015 · Cited by 453 · see citing works
Endogenous anxiety and stress responses in water maze and Barnes maze spatial memory tasks
Harrison, F. E., Hosseini, A. H., & McDonald, M. P. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.10.015 · Cited by 399 · see citing works
The dynamics of memory as a consequence of optimal adaptation to a changing body
Kording, K. P., Tenenbaum, J. B., & Shadmehr, R. (2007) · Nature Neuroscience · doi:10.1038/nn1901 · Cited by 393 · see citing works
Bifidobacteria modulate cognitive processes in an anxious mouse strain
Savignac, H. M., Tramullas, M., Kiely, B., Dinan, T. G., & Cryan, J. F. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.02.044 · Cited by 365 · see citing works
Murray, C. A., & Lynch, M. A. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-08-02974.1998 · Cited by 359 · see citing works
Arendash, G. W., King, D. L., Gordon, M. N., Morgan, D., Hatcher, J. M., Hope, C. E., & Diamond, D. M. (2001) · Brain Research · doi:10.1016/s0006-8993(00)03186-3 · Cited by 349 · see citing works
Faraco, G., Sugiyama, Y., Lane, D., Garcia-Bonilla, L., Chang, H., Santisteban, M. M., Racchumi, G., Murphy, M., Van Rooijen, N., Anrather, J., et al. (2016) · Journal of Clinical Investigation · doi:10.1172/jci86950 · Cited by 350 · see citing works
Dietary salt promotes neurovascular and cognitive dysfunction through a gut-initiated TH17 response
Faraco, G., Brea, D., Garcia-Bonilla, L., Wang, G., Racchumi, G., Chang, H., Buendia, I., Santisteban, M. M., Segarra, S. G., Koizumi, K., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-017-0059-z · Cited by 343 · see citing works
Caffé, A. R., van Leeuwen, F. W., & Luiten, P. G. M. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902610206 · Cited by 286 · see citing works
HDAC4 Governs a Transcriptional Program Essential for Synaptic Plasticity and Memory
Sando, R., Gounko, N., Pieraut, S., Liao, L., Yates, J., & Maximov, A. (2012) · Cell · doi:10.1016/j.cell.2012.09.037 · Cited by 274 · see citing works
Huang, Y.-Y., Kandel, E. R., Varshavsky, L., Brandont, E. P., Qi, M., Idzerda, R. L., Stanley McKnight, G., & Bourtchouladz, R. (1995) · Cell · doi:10.1016/0092-8674(95)90146-9 · Cited by 267 · see citing works
Wang, S.-H., Redondo, R. L., & Morris, R. G. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1008638107 · Cited by 251 · see citing works
Long-term potentiation and memory
Morris, R. G. M. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1230 · Cited by 232 · see citing works
A phenotypic and molecular characterization of the <i>fmr1‐tm1Cgr</i> Fragile X mouse
Yan, Q. J., Asafo‐Adjei, P. K., Arnold, H. M., Brown, R. E., & Bauchwitz, R. P. (2004) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2004.00087.x · Cited by 213 · see citing works
Intermittent fasting attenuates lipopolysaccharide-induced neuroinflammation and memory impairment.
Vasconcelos, A. R., Yshii, L. M., Viel, T. A., Buck, H. S., Mattson, M. P., Scavone, C., & Kawamoto, E. M. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-85 · Cited by 210 · see citing works
Scharf, M. T., Woo, N. H., Lattal, K. M., Young, J. Z., Nguyen, P. V., & Abel, T. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.87.6.2770 · Cited by 204 · see citing works
Single cell molecular alterations reveal target cells and pathways of concussive brain injury
Arneson, D., Zhang, G., Ying, Z., Zhuang, Y., Byun, H. R., Ahn, I. S., Gomez-Pinilla, F., & Yang, X. (2018) · Nature Communications · doi:10.1038/s41467-018-06222-0 · Cited by 193 · see citing works
The touchscreen operant platform for testing working memory and pattern separation in rats and mice.
Oomen, C. A., Hvoslef-Eide, M., Heath, C. J., Mar, A. C., Horner, A. E., Bussey, T. J., & Saksida, L. M. (2013) · Nature Protocols · doi:10.1038/nprot.2013.124 · Cited by 193 · see citing works
STEWART, J., MITCHELL, J., & KALANT, N. (1989) · Neurobiology of Aging · doi:10.1016/0197-4580(89)90003-1 · Cited by 177 · see citing works
Changes in Cortical Plasticity Across the Lifespan
Freitas, C., Perez, J., Knobel, M., Tormos, J. M., Oberman, L., Eldaief, M., Bashir, S., Vernet, M., Peña-Gómez, C., & Pascual-Leone, A. (2011) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2011.00005 · Cited by 172 · see citing works
Denis, I., Potier, B., Vancassel, S., Heberden, C., & Lavialle, M. (2013) · Ageing Research Reviews · doi:10.1016/j.arr.2013.01.007 · Cited by 150 · see citing works
Ortiz, O., Delgado-García, J. M., Espadas, I., Bahí, A., Trullas, R., Dreyer, J.-L., Gruart, A., & Moratalla, R. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2655-10.2010 · Cited by 143 · see citing works
Selective cognitive dysfunction in mice lacking histamine H1 and H2 receptors
Dai, H., Kaneko, K., Kato, H., Fujii, S., Jing, Y., Xu, A., Sakurai, E., Kato, M., Okamura, N., Kuramasu, A., et al. (2007) · Neuroscience Research · doi:10.1016/j.neures.2006.10.020 · Cited by 136 · see citing works
Larson, J., Jessen, R. E., Kim, D., Fine, A.-K. S., & du Hoffmann, J. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2638-05.2005 · Cited by 135 · see citing works
Elimination of GD3 synthase improves memory and reduces amyloid-β plaque load in transgenic mice
Bernardo, A., Harrison, F. E., McCord, M., Zhao, J., Bruchey, A., Davies, S. S., Jackson Roberts, L., Mathews, P. M., Matsuoka, Y., Ariga, T., et al. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.12.022 · Cited by 127 · see citing works
Trem2 deletion enhances tau dispersion and pathology through microglia exosomes
Zhu, B., Liu, Y., Hwang, S., Archuleta, K., Huang, H., Campos, A., Murad, R., Piña-Crespo, J., Xu, H., & Huang, T. Y. (2022) · Molecular Neurodegeneration · doi:10.1186/s13024-022-00562-8 · Cited by 127 · see citing works
Haure-Mirande, J.-V., Audrain, M., Fanutza, T., Kim, S. H., Klein, W. L., Glabe, C., Readhead, B., Dudley, J. T., Blitzer, R. D., Wang, M., et al. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1737-3 · Cited by 127 · see citing works
Merrill, D. A., Chiba, A. A., & Tuszynski, M. H. (2001) · Journal of Comparative Neurology · doi:10.1002/cne.1327 · Cited by 118 · see citing works
Pereira, A. C., Lambert, H. K., Grossman, Y. S., Dumitriu, D., Waldman, R., Jannetty, S. K., Calakos, K., Janssen, W. G., McEwen, B. S., & Morrison, J. H. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421285111 · Cited by 116 · see citing works
Levodopa ameliorates learning and memory deficits in a murine model of Alzheimer’s disease
Ambrée, O., Richter, H., Sachser, N., Lewejohann, L., Dere, E., de Souza Silva, M. A., Herring, A., Keyvani, K., Paulus, W., & Schäbitz, W.-R. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.11.010 · Cited by 115 · see citing works
Young bone marrow transplantation preserves learning and memory in old mice
Das, M. M., Godoy, M., Chen, S., Moser, V. A., Avalos, P., Roxas, K. M., Dang, I., Yáñez, A., Zhang, W., Bresee, C., et al. (2019) · Communications Biology · doi:10.1038/s42003-019-0298-5 · Cited by 98 · see citing works
Environmental enrichment is associated with rapid volumetric brain changes in adult mice
Scholz, J., Allemang-Grand, R., Dazai, J., & Lerch, J. P. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.01.027 · Cited by 90 · see citing works
Romcy‐Pereira, R., & Pavlides, C. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03808.x · Cited by 95 · see citing works
Le Grevès, M., Zhou, Q., Berg, M., Le Grevès, P., Fhölenhag, K., Meyerson, B., & Nyberg, F. (2006) · Experimental Brain Research · doi:10.1007/s00221-006-0438-2 · Cited by 92 · see citing works
Haure-Mirande, J.-V., Wang, M., Audrain, M., Fanutza, T., Kim, S. H., Heja, S., Readhead, B., Dudley, J. T., Blitzer, R. D., Schadt, E. E., et al. (2019) · Molecular Psychiatry · doi:10.1038/s41380-018-0255-6 · Cited by 84 · see citing works
Large-scale assessment of human navigation ability across the lifespan
van der Ham, I. J. M., Claessen, M. H. G., Evers, A. W. M., & van der Kuil, M. N. A. (2020) · Scientific Reports · doi:10.1038/s41598-020-60302-0 · Cited by 76 · see citing works
Neural ageing and synaptic plasticity: prioritizing brain health in healthy longevity
Navakkode, S., & Kennedy, B. K. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1428244 · Cited by 75 · see citing works
Whittemore, K., Derevyanko, A., Martinez, P., Serrano, R., Pumarola, M., Bosch, F., & Blasco, M. A. (2019) · Aging · doi:10.18632/aging.101982 · Cited by 69 · see citing works
Belur, L. R., Temme, A., Podetz-Pedersen, K. M., Riedl, M., Vulchanova, L., Robinson, N., Hanson, L. R., Kozarsky, K. F., Orchard, P. J., Frey, W. H., et al. (2017) · Human Gene Therapy · doi:10.1089/hum.2017.187 · Cited by 67 · see citing works
Therapeutically viable generation of neurons with antisense oligonucleotide suppression of PTB
Maimon, R., Chillon-Marinas, C., Snethlage, C. E., Singhal, S. M., McAlonis-Downes, M., Ling, K., Rigo, F., Bennett, C. F., Da Cruz, S., Hnasko, T. S., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00864-y · Cited by 62 · see citing works
Karabeg, M. M., Grauthoff, S., Kollert, S. Y., Weidner, M., Heiming, R. S., Jansen, F., Popp, S., Kaiser, S., Lesch, K.-P., Sachser, N., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078238 · Cited by 56 · see citing works
Mindspan: lessons from rat models of neurocognitive aging
Gallagher, M., Stocker, A. M., & Koh, M. T. (2011) · ILAR Journal · doi:10.1093/ilar.52.1.32 · Cited by 53 · see citing works
Hyer, M. M., Shaw, G. A., Goswamee, P., Dyer, S. K., Burns, C. M., Soriano, E., Sanchez, C. S., Rowson, S. A., McQuiston, A. R., & Neigh, G. N. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2021.100303 · Cited by 51 · see citing works
Tatsukawa, T., Ogiwara, I., Mazaki, E., Shimohata, A., & Yamakawa, K. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.01.009 · Cited by 47 · see citing works
Teixeira, A. M., Pase, C. S., Boufleur, N., Roversi, K., Barcelos, R. C. S., Benvegnú, D. M., Segat, H. J., Dias, V. T., Reckziegel, P., Trevizol, F., et al. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.055 · Cited by 44 · see citing works
Involvement of hippocampal CAMKII/CREB signaling in the spatial memory retention induced by creatine
Souza, M. A., Magni, D. V., Guerra, G. P., Oliveira, M. S., Furian, A. F., Pereira, L., Marquez, S. V., Ferreira, J., Fighera, M. R., & Royes, L. F. F. (2012) · Amino Acids · doi:10.1007/s00726-012-1329-4 · Cited by 42 · see citing works
Gökçek-Saraç, Ç., Wesierska, M., & Jakubowska-Doğru, E. (2015) · Learning & Behavior · doi:10.3758/s13420-014-0163-9 · Cited by 28 · see citing works
Seibenhener, M. L., Zhao, T., Du, Y., Calderilla-Barbosa, L., Yan, J., Jiang, J., Wooten, M. W., & Wooten, M. C. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.04.006 · Cited by 22 · see citing works
Illouz, T., Madar, R., Biragyn, A., & Okun, E. (2019) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2018.10.004 · Cited by 22 · see citing works
Hippocampal synaptic plasticity and NMDA receptors: a role in information storage?
MORRIS, R. G. M., DAVIS, S., & BUTCHER, S. P. (1991) · Behavioural and Neural Aspects of Learning and Memory · doi:10.1093/acprof:oso/9780198521983.003.0011 · Cited by 15 · see citing works
Jee, S.-C., Lee, K. M., Kim, M., Lee, Y.-J., Kim, S., Park, J.-O., & Sung, J.-S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21239202 · Cited by 15 · see citing works
- Authors
- Barnes, C. A.
- Affiliations
- University of Oslo (NO)
- Corresponding author
- Barnes, C. A.
- ORCID
- Barnes, C. A.
- Venue
- Journal of Comparative and Physiological Psychology
- Published
- 1979
- Volume
- 93
- Issue
- 1
- Pages
- 74-104
- ISSN
- 0021-9940 (ISSN-L)
- OpenAlex
- W2103861118
- Cited by
- 2,088
- References
- 65
- Citations by year
- 2026: 37 · 2025: 86 · 2024: 75 · 2023: 74 · 2022: 70 · 2021: 69 · 2020: 69 · 2019: 62 · 2018: 93 · 2017: 66 · 2016: 68 · 2015: 82 · 2014: 68 · 2013: 70 · 2012: 62
- FWCI
- 16.41
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Comparative and Physiological Psychology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- memory impairment, aging, senescence, synaptic plasticity, high-frequency stimulation, long-term potentiation, long-term depression, hippocampus, dentate gyrus, perforant path, spatial memory, spontaneous alternation, T-maze
- MeSH terms
- Age Factors, Aging, Animals, Brain Mapping, Electroencephalography, Evoked Potentials, Hippocampus, Humans, Limbic System, Male, Membrane Potentials, Memory Disorders, Neural Pathways, Synaptic Transmission, Reaction Time, 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