Brain networks activated to form object recognition memory
Open accessAbstract
Object recognition memory allows discrimination of familiar and novel objects. Previous studies have shown the importance of several brain regions for object recognition memories; however, the mechanisms underlying the consolidation of object recognition (OR) memory at the anatomic level remain unknown. Here, we analyzed the brain network for the generation of OR memory in mice by measuring the expression of the immediate-early gene c-fos. We found that c-fos expression was induced in the hippocampus (CA1 and CA3 regions), insular cortex (IC), perirhinal cortex (PRh), and medial prefrontal cortex (mPFC) when OR memory was generated, suggesting that gene expression in these brain regions contributes to the formation of OR memory. Consistently, inhibition of protein synthesis in the mPFC blocked the formation of long-term OR memory. Importantly, network analyses suggested that the hippocampus, IC, PRh and mPFC show increased connectivity with other brain regions when OR memory is formed. Thus, we suggest that a brain network composed of the hippocampus, IC, PRh, and mPFC is required for the generation of OR memory by connecting with other brain regions.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
Pre- or post-sample infusions of anisomycin into the mPFC disrupt long-term NOP memory in mice.
“Pre- (Nagai et al., 2007) or post-sample (Tanimizu et al., 2018) infusions of anisomycin, a protein synthesis inhibitor, into the mPFC disrupted long-term NOP memory in mice.”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Tanimizu et al., 2018
Increased functional connectivity of hippocampal CA1, CA3, insular cortex, perirhinal cortex and mPFC was formed by the NOP test.
“increased functional connectivity of hippocampal CA1, CA3, insular cortex, perirhinal cortex and mPFC formed by the NOP test”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Tanimizu et al., 2018
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The mouse brain in stereotaxic coordinates
Konsman, J. (2003) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(03)00088-x · Cited by 16,796 · see citing works
The Mouse Brain in Stereotaxic Coordinates
Paxinos, G. (2001) · Cited by 12,859 · see citing works
Handbook of Chemical Neuroanatomy
Stern, C. D. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90021-5 · Cited by 4,159 · see citing works
A new one-trial test for neurobiological studies of memory in rats. 1: behavioral data
Ennaceur, A., & Delacour, J. (1988) · Behavioural Brain Research · doi:10.1016/0166-4328(88)90157-x · Cited by 3,223 · see citing works
The novel object recognition memory: neurobiology, test procedure, and its modifications
Antunes, M., & Biala, G. (2012) · Cognitive Processing · doi:10.1007/s10339-011-0430-z · Cited by 2,390 · see citing works
Bourtchuladze, R., Frenguelli, B., Blendy, J., Cioffi, D., Schutz, G., & Silva, A. J. (1994) · Cell · doi:10.1016/0092-8674(94)90400-6 · Cited by 1,800 · see citing works
A cortical–hippocampal system for declarative memory
Eichenbaum, H. (2000) · Nature reviews. Neuroscience · doi:10.1038/35036213 · Cited by 1,725 · see citing works
Protein synthesis and memory: A review.
Davis, H. P., & Squire, L. R. (1984) · Psychological Bulletin · doi:10.1037/0033-2909.96.3.518 · Cited by 1,505 · see citing works
Silva, A. J., Kogan, J. H., Frankland, P. W., & Kida, S. (1998) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.21.1.127 · Cited by 1,462 · see citing works
Self-citationRetrograde amnesia and memory consolidation: a neurobiological perspective
Squire, L. R., & Alvarez, P. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80023-9 · Cited by 1,412 · see citing works
Sheng, M., McFadden, G., & Greenberg, M. E. (1990) · Neuron · doi:10.1016/0896-6273(90)90115-v · Cited by 1,076 · see citing works
The Involvement of the Anterior Cingulate Cortex in Remote Contextual Fear Memory
Frankland, P., Bontempi, B., Talton, L., Kaczmarek, L., & Silva, A. J. (2004) · Science · doi:10.1126/science.1094804 · Cited by 952 · see citing works
Handbook of chemical neuroanatomy
(2005) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(05)80001-6 · Cited by 906 · see citing works
Hippocampal damage and exploratory preferences in rats: memory for objects, places, and contexts
Mumby, D. G., Gaskin, S., Glenn, M. J., Schramek, T. E., & Lehmann, H. (2002) · Learning & Memory · doi:10.1101/lm.41302 · Cited by 714 · see citing works
Guzowski, J. F., Setlow, B., Wagner, E. K., & McGaugh, J. L. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05089.2001 · Cited by 700 · see citing works
Barker, G. R. I., Bird, F., Alexander, V., & Warburton, E. C. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5289-06.2007 · Cited by 691 · see citing works
CREB required for the stability of new and reactivated fear memories
Kida, S., Josselyn, S. A., de Ortı́z, S. P., Kogan, J. H., Chévere-Torres, I., Masushige, S., & Silva, A. J. (2002) · Nature Neuroscience · doi:10.1038/nn819 · Cited by 624 · see citing works
Self-citationConsolidation of Fear Extinction Requires Protein Synthesis in the Medial Prefrontal Cortex
Santini, E., Ge, H., Ren, K., de Ortiz, S. P., & Quirk, G. J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0786-04.2004 · Cited by 479 · see citing works
On the delay-dependent involvement of the hippocampus in object recognition memory
HAMMOND, R. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.03.005 · Cited by 476 · see citing works
Modulation of long-term memory for object recognition via HDAC inhibition
Stefanko, D. P., Barrett, R. M., Ly, A. R., Reolon, G. K., & Wood, M. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903964106 · Cited by 402 · see citing works
Mapping Cognition to the Brain Through Neural Interactions
McIntosh, A. R. (1999) · Memory · doi:10.1080/096582199387733 · Cited by 374 · see citing works
MAPK, CREB and zif268 are all required for the consolidation of recognition memory
Bozon, B., Kelly, A. M., Josselyn, S. A., Silva, A. J., Davis, S., & Laroche, S. (2003) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1224 · Cited by 327 · see citing works
The rodent hippocampus is essential for nonspatial object memory
Cohen, S. J., Munchow, A. H., Rios, L. M., Zhang, G., Ásgeirsdóttir, H. N., & Stackman, R. W. (2013) · Current Biology · doi:10.1016/j.cub.2013.07.002 · Cited by 325 · see citing works
Identification of a Functional Connectome for Long-Term Fear Memory in Mice
Wheeler, A. L., Teixeira, C. M., Wang, A. H., Xiong, X., Kovacevic, N., Lerch, J. P., McIntosh, A. R., Parkinson, J., & Frankland, P. W. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002853 · Cited by 315 · see citing works
Taste memory: The role of protein synthesis in gustatory cortex
Rosenblum, K., Meiri, N., & Dudai, Y. (1993) · Behavioral and Neural Biology · doi:10.1016/0163-1047(93)91145-d · Cited by 288 · see citing works
Rossato, J. I., Bevilaqua, L. R. M., Myskiw, J. C., Medina, J. H., Izquierdo, I., & Cammarota, M. (2007) · Learning & Memory · doi:10.1101/lm.422607 · Cited by 282 · see citing works
Mamiya, N., Fukushima, H., Suzuki, A. Z., Matsuyama, Z., Homma, S., Frankland, P. W., & Kida, S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4639-08.2009 · Cited by 276 · see citing works
Self-citationRoozendaal, B., Hernandez, A., Cabrera, S. M., Hagewoud, R., Malvaez, M., Stefanko, D. P., Haettig, J., & Wood, M. A. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5717-09.2010 · Cited by 233 · see citing works
Tanimizu, T., Kenney, J. W., Okano, E., Kadoma, K., Frankland, P. W., & Kida, S. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.3451-16.2017 · Cited by 214 · see citing works
Self-citationBalderas, I., Rodriguez-Ortiz, C. J., Salgado-Tonda, P., Chavez-Hurtado, J., McGaugh, J. L., & Bermudez-Rattoni, F. (2008) · Learning & Memory · doi:10.1101/lm.1028008 · Cited by 213 · see citing works
Consolidation: Fragility on the Road to the Engram
Dudai, Y. (1996) · Neuron · doi:10.1016/s0896-6273(00)80168-3 · Cited by 135 · see citing works
Insular cortex is involved in consolidation of object recognition memoryPreprint
Bermúdez‐Rattoni, F., Okuda, S., Roozendaal, B., & McGaugh, J. L. (2005) · Learning & Memory · doi:10.1101/lm.97605 · Cited by 121 · see citing works
Mumby, D. G., Glenn, M. J., Nesbitt, C., & Kyriazis, D. A. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00444-2 · Cited by 120 · see citing works
Morrow, B. A., Elsworth, J. D., Inglis, F. M., & Roth, R. H. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05666.1999 · Cited by 114 · see citing works
Memory and cerebral protein synthesis in mice as affected by graded amounts of puromycin
Flexner, L. B., Flexner, J. B., & Stellar, E. (1965) · Experimental Neurology · doi:10.1016/0014-4886(65)90114-7 · Cited by 90 · see citing works
Network analysis of brain cognitive function using metabolic and blood flow data
Horwitz, B., McIntosh, A. R., Haxby, J. V., & Grady, C. L. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(94)00139-7 · Cited by 81 · see citing works
PARP-1 activity is required for the reconsolidation and extinction of contextual fear memory
Inaba, H., Tsukagoshi, A., & Kida, S. (2015) · Molecular Brain · doi:10.1186/s13041-015-0153-7 · Cited by 45 · see citing works
Self-citationSavalli, G., Bashir, Z. I., & Warburton, E. C. (2015) · Learning & Memory · doi:10.1101/lm.036921.114 · Cited by 19 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
The extracellular matrix and perineuronal nets in memory
Fawcett, J. W., Fyhn, M., Jendelova, P., Kwok, J. C. F., Ruzicka, J., & Sorg, B. A. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01634-3 · Cited by 169 · see citing works
Chao, O. Y., de Souza Silva, M. A., Yang, Y.-M., & Huston, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158 · see citing works
Lissner, L. J., Wartchow, K. M., Toniazzo, A. P., Gonçalves, C., & Rodrigues, L. (2021) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2021.173273 · Cited by 133 · see citing works
Hippocampus–Prefrontal Coupling Regulates Recognition Memory for Novelty Discrimination
Wang, C., Furlong, T. M., Stratton, P. G., Lee, C. C. Y., Xu, L., Merlin, S., Nolan, C. R., Arabzadeh, E., Marek, R., & Sah, P. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1202-21.2021 · Cited by 73 · see citing works
Endothelial Piezo1 channel mediates mechano-feedback control of brain blood flow
Lim, X. R., Abd-Alhaseeb, M. M., Ippolito, M., Koide, M., Senatore, A. J., Plante, C., Hariharan, A., Weir, N., Longden, T. A., Laprade, K. A., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-52969-0 · Cited by 78 · see citing works
A survey of brain network analysis by electroencephalographic signals
Luo, C., Li, F., Li, P., Yi, C., Li, C., Tao, Q., Zhang, X., Si, Y., Yao, D., Yin, G., et al. (2021) · Cognitive Neurodynamics · doi:10.1007/s11571-021-09689-8 · Cited by 54 · see citing works
Brault, V., Nguyen, T. L., Gutiérrez, J. F., Iacono, G. L., Birling, M., Lalanne, V., Méziane, H., Manousopoulou, A., Pavlovic, G., Lindner, L., et al. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009777 · Cited by 41 · see citing works
Kuboyama, T., Hirotsu, K., Arai, T., Yamasaki, H., & Tohda, C. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00805 · Cited by 42 · see citing works
Peñasco, S., Rico-Barrio, I., Puente, N., Fontaine, C. J., Ramos, A., Reguero, L., Gerrikagoitia, I., de Fonseca, F. R., Suarez, J., Barrondo, S., et al. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-019-0530-5 · Cited by 37 · see citing works
Kjærgaard, K., Mikkelsen, A. C. D., Landau, A. M., Eriksen, P. L., Hamilton-Dutoit, S. J., Magnusson, N. E., Thomsen, M. B., Chen, F., Vilstrup, H., Mookerjee, R. P., et al. (2023) · JHEP Reports · doi:10.1016/j.jhepr.2023.100992 · Cited by 38 · see citing works
Conditional Dnmt3b deletion in hippocampal dCA1 impairs recognition memory
Kong, Q., Yu, M., Zhang, M., Wei, C., Gu, H., Yu, S., Sun, W., Li, N., & Zhou, Y. (2020) · Molecular Brain · doi:10.1186/s13041-020-00574-9 · Cited by 31 · see citing works
Muroi, Y., & Ishii, T. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.12.034 · Cited by 28 · see citing works
Wong, J. H., Muthuraju, S., Reza, F., Senik, M. H., Zhang, J., Yeo, N. A. B. M. Y., Chuang, H. G., Jaafar, H., Yusof, S. R., Mohamad, H., et al. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.11.044 · Cited by 28 · see citing works
Chakraborty, S., Tripathi, S. J., Srikumar, B. N., Raju, T. R., & Rao, B. S. S. (2019) · Brain stimulation · doi:10.1016/j.brs.2019.01.020 · Cited by 26 · see citing works
Arakawa, Y., Yokoyama, K., Tasaki, S., Kato, J., Nakashima, K., Takeyama, M., Nakatani, A., & Suzuki, M. (2019) · PLoS ONE · doi:10.1371/journal.pone.0220389 · Cited by 26 · see citing works
Characterizing age-related decline of recognition memory and brain activation profile in mice
Belblidia, H., Léger, M., Abdelmalek, A., Quiedeville, A., Calocer, F., Boulouard, M., Jozet‐Alves, C., Fréret, T., & Schumann‐Bard, P. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2018.03.006 · Cited by 25 · see citing works
Esaki, H., Izumi, S., Fukao, A., Ito, S., Nishitani, N., Deyama, S., & Kaneda, K. (2021) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b21-00314 · Cited by 25 · see citing works
Novel object recognition memory in REM sleep-deprived rats: Role of the cannabinoid CB1 receptor
Shahveisi, K., Farnia, V., Khazaie, H., Ghazvini, H., Nozari, M., & Khodamoradi, M. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112311 · Cited by 24 · see citing works
Liu, X., Guo, L., Duan, B., Wu, J., & Wang, E. (2022) · NeuroToxicology · doi:10.1016/j.neuro.2022.08.003 · Cited by 23 · see citing works
Chen, Y., Barsegyan, A., Kasri, N. N., & Roozendaal, B. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.08.018 · Cited by 23 · see citing works
Ramos-Prats, A., Kölldorfer, J., Paolo, E., Zeidler, M., Schmid, G., & Ferraguti, F. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00030 · Cited by 21 · see citing works
Role of dopamine neurons in familiarity
Fleury, S., Kolaric, R., Espera, J., Ha, Q. H., Tomaio, J. N., Gether, U., Sørensen, A. T., & Mingote, S. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16326 · Cited by 21 · see citing works
Peripheral ERK modulates acupuncture-induced brain neural activity and its functional connectivity
Park, J.-Y., Cho, S.-J., Lee, S. H., Ryu, Y., Jang, J., Kim, S., & Park, H. (2021) · Scientific Reports · doi:10.1038/s41598-021-84273-y · Cited by 20 · see citing works
Sosa, M. A. G., Gasperi, R. D., Pryor, D., Garcia, G. S. P., Perez, G. M., Abutarboush, R., Kawoos, U., Hogg, S., Ache, B., Sowa, A., et al. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01553-6 · Cited by 20 · see citing works
Kermath, B. A., Vanderplow, A. M., Bjornson, K. J., Seablom, E. N., Novak, A., Bernhardt, C. R., & Cahill, M. E. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0835-0 · Cited by 17 · see citing works
Pradhan, G., Melugin, P. R., Wu, F., Fang, H. M., Weber, R. E., & Kroener, S. (2018) · Psychopharmacology · doi:10.1007/s00213-018-4900-1 · Cited by 19 · see citing works
Song, L., Pei, L., Hu, L., Pan, S., Xiong, W., Liu, M., Wu, Y., Shang, Y., & Yao, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-27842-y · Cited by 20 · see citing works
Neuron-specific deletion of VEGF or its receptor Flk-1 impairs recognition memory
Deyama, S., Li, X., & Duman, R. S. (2020) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2019.11.002 · Cited by 17 · see citing works
Lin, B., Zhang, L., Yin, X., Chen, X., Ruan, C., Wu, T., Liu, Z., & Huang, J. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.968767 · Cited by 15 · see citing works
Object Recognition and Object Location Recognition Memory – The Role of Dopamine and Noradrenaline
Moreno‐Castilla, P., Guzmán-Ramos, K. R., & Bermúdez‐Rattoni, F. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00028-8 · Cited by 16 · see citing works
Peripheral CB1 receptor blockade acts as a memory enhancer through a noradrenergic mechanism
Martínez‐Torres, S., Bergadà‐Martínez, A., Ortega, J. E., Galera-López, L., Hervera, A., Reyes‐Ramírez, L. D. L., Ortega-Álvaro, A., Remmers, F., Muñoz‐Moreno, E., Sòria, G., et al. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01436-9 · Cited by 15 · see citing works
Nagayoshi, T., Isoda, K., Mamiya, N., & Kida, S. (2017) · Molecular Brain · doi:10.1186/s13041-017-0341-8 · Cited by 15 · see citing works
Self-citationNovel object recognition in Octopus maya
Vergara-Ovalle, F., Ayala‐Guerrero, F., Rosas, C., & Sánchez-Castillo, H. (2023) · Animal Cognition · doi:10.1007/s10071-023-01753-6 · Cited by 14 · see citing works
Social Fear Affects Limbic System Neuronal Activity and Gene Expression
Hamann, C. S., Bankmann, J., Maza, H. M., Kornhuber, J., Zoicas, I., & Schmitt-Böhrer, A. G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158228 · Cited by 13 · see citing works
Tresserra, M. P., Galofré-López, N., Pallares, E., Gimenez-Montes, C., Barcia, C., Granero, R., Rojic-Becker, D., Vale-Martı́nez, A., Martí‐Nicolovius, M., & Guillazo‐Blanch, G. (2023) · Nutrients · doi:10.3390/nu15071572 · Cited by 13 · see citing works
Esaki, H., Deyama, S., Izumi, S., Katsura, A., Nishikawa, K., Nishitani, N., & Kaneda, K. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109672 · Cited by 13 · see citing works
Functional connectivity of anterior retrosplenial cortex in object recognition memory
de Landeta, A. B., Pereyra, M., Miranda, M., Bekinschtein, P., Medina, J. H., & Katche, C. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107544 · Cited by 13 · see citing works
Epigenetic mechanisms regulate cue memory underlying discriminative behavior
Shang, A., & Bieszczad, K. M. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104811 · Cited by 14 · see citing works
Doostdar, N., Kim, E., Grayson, B., Harte, M., Neill, J. C., & Vernon, A. C. (2019) · Journal of Psychopharmacology · doi:10.1177/0269881119844196 · Cited by 12 · see citing works
Takeda, K., Watanabe, K., Iijima, S., Nagahiro, T., Suzuki, H., Izumo, K., Ikegaya, Y., & Matsumoto, N. (2025) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2025.03.013 · Cited by 11 · see citing works
Object Novelty Recognition Memory
Ennaceur, A. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00001-x · Cited by 11 · see citing works
Robakiewicz, I., Polak, M., Rawska, M., Alberski, D., Polowy, R., Wytrychiewicz‐Pankowska, K., Syperek, M., Matysiak, J., & Filipkowski, R. K. (2019) · Acta Neurobiologiae Experimentalis · doi:10.21307/ane-2019-029 · Cited by 11 · see citing works
Borreca, A., Valeri, F., Luca, M. D., Ernst, L., Russo, A., Nobili, A., Cordella, A., Corsetti, V., Amadoro, G., Mercuri, N. B., et al. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104787 · Cited by 11 · see citing works
Shi, X., Barr, J. L., von Weltin, E., Wolsh, C. C., & Unterwald, E. M. (2019) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.119.259283 · Cited by 9 · see citing works
Kuedo, Z., Chotphruethipong, L., Raju, N., Reudhabibadh, R., Benjakul, S., Chonpathompikunlert, P., Klaypradit, W., & Hutamekalin, P. (2022) · Foods · doi:10.3390/foods11172673 · Cited by 9 · see citing works
Activation of the Gut–Brain Interaction by Urolithin A and Its Molecular Basis
Kubota, D., Sato, M., Udono, M., Kohara, A., Kudoh, M., Ukawa, Y., Teruya, K., & Katakura, Y. (2024) · Nutrients · doi:10.3390/nu16193369 · Cited by 8 · see citing works
Pistono, C., Zimmermann, A., Morel, C., Herbeaux, K., Héraud, C., Dumont, S., Pévet, P., Felder‐Schmittbuhl, M., & Mathis, C. (2021) · Hormones and Behavior · doi:10.1016/j.yhbeh.2021.105076 · Cited by 8 · see citing works
Hisaoka‐Nakashima, K., Tokuda, S., Goto, T., Yoshii, N., Nakamura, Y., Ago, Y., & Morioka, N. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.115590 · Cited by 7 · see citing works
Copper nanoclusters based short-term memory “eraser”
Hu, K., Liu, Y., Wang, Q., Xiong, Y., Guo, Z., Weng, Z., Liu, Y., Zhang, Y., Wu, H., Ai, F., et al. (2023) · Chemical Engineering Journal · doi:10.1016/j.cej.2023.142366 · Cited by 7 · see citing works
Qiu, Y., Bi, L., Huang, G., Li, Z., Wei, H., Li, G., Wei, J., Liao, K., Yang, M., Ye, P., et al. (2024) · Brain‐X · doi:10.1002/brx2.55 · Cited by 6 · see citing works
Ramli, N. Z., Yahaya, M. F., Fahami, N. A. M., Hamezah, H. S., Bakar, Z. H. A., Arrozi, A. P., Yanagisawa, D., Tooyama, I., Singh, M., & Damanhuri, H. A. (2024) · Experimental Gerontology · doi:10.1016/j.exger.2024.112607 · Cited by 6 · see citing works
Acid Sphingomyelinase Is a Modulator of Contextual Fear
Zoicas, I., & Kornhuber, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063398 · Cited by 6 · see citing works
The neurotoxicity of polychlorinated biphenyls (PCBs)
Badley, J. R., Wilson, R. J., Werner, A., Smiley‐Jewell, S. M., & Lein, P. J. (2023) · Advances in neurotoxicology · doi:10.1016/bs.ant.2023.09.001 · Cited by 5 · see citing works
Watanabe, K., Takeda, K., Nagahiro, T., Iijima, S., Ikegaya, Y., & Matsumoto, N. (2025) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2025.08.002 · Cited by 5 · see citing works
Miyata, S., Tsuda, M., & Mitsui, S. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03890-y · Cited by 5 · see citing works
Esaki, H., Izumi, S., Nishikawa, K., Nagayasu, K., Kaneko, S., Nishitani, N., Deyama, S., & Kaneda, K. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176790 · Cited by 4 · see citing works
Hippocampal CaMKII Regulates the Consolidation of Recognition Memory
Rossato, J. I., González, M. C., Apolinário, G., Radiske, A., Brisa, E., Carneiro, L. M., & Cammarota, M. (2025) · European Journal of Neuroscience · doi:10.1111/ejn.70049 · Cited by 4 · see citing works
Mbnl2 loss alters novel context processing and impairs object recognition memory
Khandelwal, A., Cushman, J. D., Choi, J., Zhuravka, I., Rajbhandari, A. K., Valiulahi, P., Li, X., Zhou, C., Comai, L., & Reddy, S. (2023) · iScience · doi:10.1016/j.isci.2023.106732 · Cited by 4 · see citing works
Urushihata, T., Goto, M., Kabetani, K., Kiyozuka, M., Maruyama, S., Tsuji, S., Tada, H., & Satoh, A. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1252689 · Cited by 4 · see citing works
Kobayashi, R., & Tohda, C. (2017) · Neurochemical Research · doi:10.1007/s11064-017-2394-6 · Cited by 4 · see citing works
Vorontsova, O. N., Аляева, А. Г., Колясникова, К. Н., Valdman, E. A., & Povarnina, P. Y. (2023) · Pharmacokinetics and Pharmacodynamics · doi:10.37489/2587-7836-2023-3-50-55 · Cited by 2 · see citing works
Ma, J.-C., Che, X., Zhu, X.-N., Ren, A.-X., Hu, Y., Yang, C.-L., Xu, Z.-T., Li, Y., Wu, C., & Yang, J. (2024) · Acta Pharmacologica Sinica · doi:10.1038/s41401-024-01321-9 · Cited by 2 · see citing works
Novel Object Recognition in Octopus maya.Preprint
Vergara-Ovalle, F., Guerrero, F. A., Rosas, C., & Sánchez-Castillo, H. (2022) · Research Square · doi:10.21203/rs.3.rs-1439375/v1 · Cited by 2 · see citing works
Mao, M., Yu, H.-L., Liu, Q., Wen, Y., Jiang, M., Yuan, H.-M., Zeng, H.-B., Zhang, L., & Feng, S. (2024) · Psychopharmacology · doi:10.1007/s00213-024-06728-0 · Cited by 1 · see citing works
Esaki, H., Imai, K., Nishikawa, K., Nishitani, N., Deyama, S., & Kaneda, K. (2025) · Neurochemistry International · doi:10.1016/j.neuint.2025.105963 · Cited by 1 · see citing works
A Survey on Computational Intelligence Techniques in Learning and Memory
Singh, A. K., & Tiwari, A. K. (2022) · Communications in computer and information science · doi:10.1007/978-3-031-10766-5_11 · Cited by 1 · see citing works
New mechanistic insights into memory processes
Giese, K.-P., & Kida, S. (2018) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2018.04.004 · Cited by 1 · see citing works
Self-citationThe Roles of Neurotrophins in Novel Object Recognition
Kelly, Á. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00030-6
Transient upregulation of translational efficiency in prodromal Tg2576 mice precipitates AD symptomsPreprint
Borreca, A., Valeri, F., Luca, M. D., Ernst, L., Russo, A., Cordella, A., Corsetti, V., Nobili, A., Amadoro, G., Mercuri, N. B., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/581652
Long-Lasting Memory Impairments after Subchronic Immune Challenge
Tchessalova, D. (2019) · Deep Blue (University of Michigan)
Peripheral CB1 receptor blockade acts as a memory enhancer through an adrenergic-dependent mechanismPreprint
Martínez‐Torres, S., Bergadà‐Martínez, A., Ortega, J. E., Galera-López, L., Hervera, A., Ortega-Álvaro, A., Remmers, F., Muñoz‐Moreno, E., Sòria, G., del Rı́o, J. A., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.06.16.448227
Gao, Y., Li, Y., Yang, X., Hao, J., Shen, X., Xu, L., Liu, Y., Liu, L., Tong, K., You, Y., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-670804/v1
Gao, Y., Yang, L., Yang, X. J., Hao, J., Shen, X., Wang, H.-Y., Li, X., Liu, Y., Liu, L., Tong, K., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-973050/v1
PKMζ drives spatial memory reconsolidation but not maintenance
de Oliveira, J. R., Rossato, J. I., Souza, J., Orvate, R., Carneiro, L., Baracho, A. L., & Cammarota, M. (2025) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2025.1638371
Additional file 1 of Conditional Dnmt3b deletion in hippocampal dCA1 impairs recognition memory
Kong, Q., Yu, M., Zhang, M., Wei, C., Gu, H., Yu, S., Sun, W., Li, N., & Zhou, Y. (2020) · Figshare · doi:10.6084/m9.figshare.11998743
Upstream CB1R Regulation of β‐Adrenergic Memory Consolidation
Rossato, J. I., Ribeiro, L., Lima‐Silva, T., Araújo, R. B. D. A., Orvate, R., Azevedo, A. L., Cammarota, N. B., Baracho, A. L., Carneiro, L. M., & Cammarota, M. (2026) · Hippocampus · doi:10.1002/hipo.70084
Zoicas, I., Sucu, B., Kornhuber, J., & Fejtová, A. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2026.107362 · Cited by 1 · see citing works
Pair bonding sex-specifically improves object recognition memory in monogamous prairie vole
Iwai, H., Otsuki, C., Kobayashi, Y., Okano, S., Sugimura, N., Kamura, E., Totsuka, A., Noguchi, R., Young, L. J., & Mitsui, S. (2026) · Physiology & Behavior · doi:10.1016/j.physbeh.2026.115333
Roselló-Jiménez, L., Pastor, R., Miquel, M., & Font, L. (2026) · Psychopharmacology · doi:10.1007/s00213-026-07191-9
- Authors
- Tanimizu, T., Kono, K., & Kida, S.
- Affiliations
- Tokyo University of Agriculture (JP)
- Corresponding author
- Kida, Satoshi
- ORCID
- Kida, Satoshi
- Venue
- Brain Research Bulletin
- Publisher
- Elsevier BV
- Published
- 2018-07
- Volume
- 141
- Pages
- 27-34
- ISSN
- 0361-9230 (ISSN-L)
- OpenAlex
- W2620787577
- Cited by
- 81
- References
- 39
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 9 · 2023: 11 · 2022: 10 · 2021: 11 · 2020: 7 · 2019: 10 · 2018: 10 · 2017: 3
- FWCI
- 4.71
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Brain Research Bulletin (acceptedVersion)
- PubMed (publishedVersion)
- Funders
- Grant-in-Aids for Scientific Research (15H02488)
- Scientific Research (23300120, 20380078)
- Challenging Exploratory Research (24650172, 26640014)
- Grant-in-Aids for Scientific Research on Priority Areas − Molecular Brain Science (18022038, 22022039)
- Grant-in-Aid for Scientific Research on Innovative Areas (24116008, 24116001, 23115716, 17H05961, 17H05581)
- Core Research for Evolutional Science and Technology (CREST), Japan
- The Science Research Promotion Fund
- The Promotion and Mutual Aid Corporation for Private Schools of Japan
- The Sumitomo Foundation
- The Naito Foundation
- The Uehara Memorial Foundation
- Takeda Science Foundation, Japan
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- object recognition memory, memory consolidation, Fos expression, hippocampus, insula, perirhinal cortex, medial prefrontal cortex, protein synthesis inhibition, long-term memory formation, brain network connectivity, mice
- MeSH terms
- Memory Consolidation, Animals, Brain, Computer Simulation, Immunohistochemistry, Male, Mice, Inbred C57BL, Neural Pathways, Neurons, Gene Expression, Proto-Oncogene Proteins c-fos, Recognition, Psychology
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