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Aging and an Immune Challenge Interact to Produce Prolonged, but Not Permanent, Reductions in Hippocampal L-LTP and mBDNF in a Rodent Model with Features of Delirium

Tanaka, N., Cortese, G. P., Barrientos, R. M., Maier, S. F., & Patterson, S. L. (2018) · eNeuro · doi:10.1523/eneuro.0009-18.2018 · Cited by 22

Dose–Response Effect of Vibratory Stimulus on Synaptic and Muscle Plasticity in a Middle-Aged Murine Model

Cariati, I., Bonanni, R., Annino, G., Scimeca, M., Bonanno, E., D’Arcangelo, G., & Tancredi, V. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.678449 · Cited by 21

Neurotensin receptor levels as a function of brain aging and cognitive performance in the Morris water maze task in the rat

Rowe, W. B., Kar, S., Meaney, M. J., & Quirion, R. (2006) · Peptides · doi:10.1016/j.peptides.2006.03.036 · Cited by 21

CA1 pyramidal cells have diverse biophysical properties, affected by development, experience, and aging

McKiernan, E. C., & Marrone, D. F. (2017) · PeerJ · doi:10.7717/peerj.3836 · Cited by 20

Activation of NLRP3-Caspase-1 pathway contributes to age-related impairments in cognitive function and synaptic plasticity

Wang, T., Ruan, B., Wang, J., Zhou, Z., Zhang, X., Zhang, C., Zhao, H., Yang, Y., & Yuan, D. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105220 · Cited by 22

Decreased Response to Acetylcholine during Aging of Aplysia Neuron R15

Akhmedov, K., Rizzo, V., Kadakkuzha, B. M., Carter, C. J., Magoski, N. S., Capo, T. R., & Puthanveettil, S. V. (2013) · PLoS ONE · doi:10.1371/journal.pone.0084793 · Cited by 19

Dual Role of NMDAR Containing NR2A and NR2B Subunits in Alzheimer’s Disease

Raïch, I., Lillo, J., Rebassa, J. B., Capó, T., Cordomí, A., Reyes‐Resina, I., Pallàs, M., & Navarro, G. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094757 · Cited by 20

Learning impairments identified early in life are predictive of future impairments associated with aging

Hullinger, R., & Bürger, C. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.08.004 · Cited by 18

Effects of electromagnetic radiation on spatial memory and synapses in rat hippocampal CA1.

Li, Y., Shi, C., Lu, G., Xu, Q., & Liu, S. (2012) · Europe PMC (PubMed Central) · doi:10.3969/j.issn.1673-5374.2012.16.007 · Cited by 18

Long-term Memory Upscales Volume of Postsynaptic Densities in the Process that Requires Autophosphorylation of αCaMKII

Śliwińska, M. A., Cały, A., Borczyk, M., Ziółkowska, M., Skonieczna, E., Chilimoniuk, M., Bernaś, T., Giese, K.-P., & Radwańska, K. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz261 · Cited by 16

Spatial reference- (not working- or procedural-) memory performance of aged rats in the water maze predicts the magnitude of sulpiride-induced facilitation of acetylcholine release by striatal slices

Cassel, J., Lazaris, A., Birthelmer, A., & Jackisch, R. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.05.032 · Cited by 17

Adenylate Cyclase-Mediated Forms of Neuronal Plasticity in Hippocampal Area CA1 Are Reduced With Aging

Reis, G. F., Lee, M. B., Huang, A. S., & Parfitt, K. D. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00827.2003 · Cited by 15

Hallmarks of healthy cognitive aging: Inter-individual differences in aging trajectories

Abrous, D. N., Blin, N., Boraxbekk, C., Catheline, G., Fitzsimons, C. P., Hilscher, M. M., Lemoine, M., Lopes, L. V., Maass, A., Nilsson, M., et al. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103102 · Cited by 18

Age-dependent loss of cholinergic neurons in learning and memory-related brain regions and impaired learning in SAMP8 mice with trigeminal nerve damage

He, Y., Zhu, J., Huang, F. P., Liu, Q., Fan, W., & He, H. (2014) · Neural Regeneration Research · doi:10.4103/1673-5374.145380 · Cited by 14

Synaptic Commitment: Developmentally Regulated Reciprocal Changes in Hippocampal Granule Cell NMDA and AMPA Receptors Over the Lifespan

Yang, Z., Krause, M., Rao, G., McNaughton, B. L., & Barnes, C. A. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01276.2007 · Cited by 16

Age-related changes in theta frequency stimulation-induced long-term potentiation

Watabe, A. M., & O’Dell, T. J. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(02)00082-9 · Cited by 42

Aging Effects on the Limits and Stability of Long-Term Synaptic Potentiation and Depression in Rat Hippocampal Area CA1

Kumar, A., Thinschmidt, J. S., Foster, T. C., & King, M. A. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00249.2007 · Cited by 68

Reduced hippocampal CA1 Ca2+-induced long-term potentiation is associated with age-dependent impairment of spatial learning

Diana, G., Domenici, M. R., de Carolis, A. S., Loizzo, A., & Sagratella, S. (1995) · Brain Research · doi:10.1016/0006-8993(95)00440-2 · Cited by 45

Hippocampal synaptic plasticity is modulated by theta rhythm in the fascia dentata of adult and aged freely behaving rats

Orr, G. W., RAO, G. R., Houston, F. P., McNaughton, B. L., & Barnes, C. A. (2001) · Hippocampus · doi:10.1002/hipo.1079 · Cited by 125

An age comparison of the rates of acquisition and forgetting of spatial information in relation to long-term enhancement of hippocampal synapses.

Barnes, C. A., & McNaughton, B. L. (1985) · Behavioral Neuroscience · doi:10.1037//0735-7044.99.6.1040 · Cited by 337