Hippocampal noradrenergic activation is necessary for object recognition memory consolidation and can promote BDNF increase and memory persistence

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works

Memory - A century of consolidation

McGaugh, J. L. (2000) · Science · doi:10.1126/science.287.5451.248 · Cited by 4,250 · 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

Memory Formation: The Sequence of Biochemical Events in the Hippocampus and Its Connection to Activity in Other Brain Structures

Izquierdo, I., & Medina, J. H. (1997) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1997.3799 · Cited by 959 · see citing works

BDNF is essential to promote persistence of long-term memory storage

Bekinschtein, P., Cammarota, M., Katche, C., Slipczuk, L. N., Rossato, J. I., Goldin, A. P., Izquierdo, I., & Medina, J. H. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711863105 · Cited by 658 · see citing works

Persistence of Long-Term Memory Storage Requires a Late Protein Synthesis- and BDNF- Dependent Phase in the Hippocampus

Bekinschtein, P., Cammarota, M., Igaz, L. M., Bevilaqua, L. R. M., Izquierdo, I., & Medina, J. H. (2007) · Neuron · doi:10.1016/j.neuron.2006.11.025 · Cited by 633 · see citing works

Assessing rodent hippocampal involvement in the novel object recognition task. A review

Cohen, S. J., & Stackman, R. W. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.08.002 · Cited by 592 · see citing works

Different molecular cascades in different sites of the brain control memory consolidation

Izquierdo, I., Bevilaqua, L. R., Rossato, J. I., Bonini, J. S., Medina, J. H., & Cammarota, M. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.07.005 · Cited by 452 · see citing works

Noradrenergic innervation of the adult rat hippocampal formation

Loy, R., Koziell, D. A., Lindsey, J. D., & Moore, R. Y. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901890406 · Cited by 443 · see citing works

Efferent projections of nucleus locus coeruleus: Morphologic subpopulations have different efferent targets

Loughlin, S. E., Foote, S. L., & Grzanna, R. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90156-9 · Cited by 437 · see citing works

Conditioned and Unconditioned Stimuli Increase Frontal Cortical and Hippocampal Acetylcholine Release: Effects of Novelty, Habituation, and Fear

Acquas, E., Wilson, C., & Fibiger, H. C. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-09-03089.1996 · Cited by 318 · see citing works

Plastic modifications induced by object recognition memory processing

Clarke, J. R., Cammarota, M., Gruart, A., Izquierdo, I., & Delgado-García, J. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0915059107 · Cited by 273 · see citing works

Consolidating memories

McGaugh, J. L. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-014954 · Cited by 271 · see citing works

BDNF activates mTOR to regulate GluR1 expression required for memory formation

Slipczuk, L., Bekinschtein, P., Katche, C., Cammarota, M., Izquierdo, I., & Medina, J. H. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006007 · Cited by 246 · see citing works

Noradrenergic activation of the basolateral amygdala modulates consolidation of object recognition memory

Roozendaal, B., Castello, N. A., Vedana, G., Barsegyan, A., & McGaugh, J. L. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.06.010 · Cited by 216 · see citing works

Locus Coeruleus Activation Facilitates Memory Encoding and Induces Hippocampal LTD that Depends on -Adrenergic Receptor Activation

Lemon, N., Aydın-Abidin, S., Funke, K., & Manahan‐Vaughan, D. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp065 · Cited by 147 · see citing works

Glucocorticoid receptor activation in the rat nucleus of the solitary tract facilitates memory consolidation: involvement of the basolateral amygdala

Roozendaal, B., Williams, C. L., & McGaugh, J. L. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00537.x · Cited by 140 · see citing works

The learning of fear extinction

Furini, C., Myskiw, J., & Izquierdo, I. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.10.016 · Cited by 124 · see citing works

The Nucleus of the Solitary Tract→Nucleus Paragigantocellularis→Locus Coeruleus→CA1 region of dorsal hippocampus pathway is important for consolidation of object recognition memory

Mello‐Carpes, P. B., & Izquierdo, I. (2012) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2012.12.002 · Cited by 123 · see citing works

Reversible lesions of the nucleus of the solitary tract attenuate the memory-modulating effects of posttraining epinephrine.

Williams, C. L., & McGaugh, J. L. (1993) · Behavioral Neuroscience · doi:10.1037/0735-7044.107.6.955 · Cited by 122 · see citing works

On the participation of mTOR in recognition memory.

Myskiw, J., Rossato, J., Bevilaqua, L., Medina, J., Izquierdo, I., & Cammarota, M. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.10.002 · Cited by 118 · see citing works

A study of inputs to antidromically identified neurons of the locus coeruleus

Takigawa, M., & Mogenson, G. J. (1977) · Brain Research · doi:10.1016/0006-8993(77)91027-7 · Cited by 117 · see citing works

Adrenergic activation of the nucleus tractus solitarius potentiates amygdala norepinephrine release and enhances retention performance in emotionally arousing and spatial memory tasks

Clayton, E. C., & Williams, C. L. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00178-9 · Cited by 115 · see citing works

Differential distribution of locus coeruleus projections to the hippocampal formation: anatomical and biochemical evidence

Haring, J. H., & Davis, J. N. (1985) · Brain Research · doi:10.1016/0006-8993(85)90342-7 · Cited by 79 · see citing works

Adrenergic enhancement of consolidation of object recognition memory

Dornelles, A. D. S., de Lima, M. N. M., Grazziotin, M. M., Presti-Torres, J., Garcia, V. A., Scalco, F. S., Roesler, R., & Schröder, N. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.01.005 · Cited by 74 · see citing works

Facilitation of fear extinction by novelty depends on dopamine acting on D1-subtype dopamine receptors in hippocampus

Menezes, J., Alves, N., Borges, S., Roehrs, R., Myskiw, J. D. C., Furini, C. R. G., Izquierdo, I., & Mello‐Carpes, P. B. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1502295112 · Cited by 73 · see citing works

β‐Adrenergic receptors link NO/sGC/PKG signaling to BDNF expression during the consolidation of object recognition long‐term memory

Furini, C. R., Rossato, J. I., Bitencourt, L. L., Medina, J. H., Izquierdo, I., & Cammarota, M. (2010) · Hippocampus · doi:10.1002/hipo.20656 · Cited by 72 · see citing works

Moving beyond standard procedures to assess spontaneous recognition memory

Ameen‐Ali, K. E., Easton, A., & Eacott, M. J. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.03.013 · Cited by 59 · see citing works

Consolidation and reconsolidation of object recognition memory

Balderas, I., Rodríguez‐Ortiz, C. J., & Bermúdez‐Rattoni, F. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.08.049 · Cited by 58 · see citing works

From learning to forgetting: Behavioral, circuitry, and molecular properties define the different functional states of the recognition memory trace

Romero‐Granados, R., Fontán‐Lozano, Á., Delgado-Garcia, J. M., & Carrión, Á. M. (2009) · Hippocampus · doi:10.1002/hipo.20669 · Cited by 51 · see citing works

Peripheral arousal-related hormones modulate norepinephrine release in the hippocampus via influences on brainstem nuclei

Miyashita, T., & Williams, C. L. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.11.005 · Cited by 49 · see citing works

Novelty-induced arousal enhances memory for cued classical fear conditioning: Interactions between peripheral adrenergic and brainstem glutamatergic systemsPreprint

King, S. O., & Williams, C. L. (2009) · Learning & Memory · doi:10.1101/lm.1513109 · Cited by 44 · see citing works

Noradrenergic activation of the basolateral amygdala enhances object recognition memory and induces chromatin remodeling in the insular cortex

Beldjoud, H., Barsegyan, A., & Roozendaal, B. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00108 · Cited by 42 · see citing works

Paragigantocellularis stimulation induces β-adrenergic hippocampal potentiation

Babstock, D. M., & Harley, C. W. (1992) · Brain Research Bulletin · doi:10.1016/0361-9230(92)90250-2 · Cited by 26 · see citing works

Response of the rat brain β-endorphin system to novelty: Importance of the fornix connection

Netto, C. A., Cavalheiro, É. A., Carrasco, M. A., Volkmer, N., Dias, R. D., & Izquierdo, I. (1985) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(85)91468-2 · Cited by 25 · see citing works

Moderate stress enhances memory persistence: Are adrenergic mechanisms involved?

Parfitt, G. M., Barbosa, Â. K., Campos, R. C., Koth, A. P., & Barros, D. M. (2012) · Behavioral Neuroscience · doi:10.1037/a0029861 · Cited by 25 · see citing works

Glutamatergic influences on the nucleus paragigantocellularis: Contribution to performance in avoidance and spatial memory tasks.

Clayton, E. C., & Williams, C. L. (2000) · Behavioral Neuroscience · doi:10.1037//0735-7044.114.4.707 · Cited by 21 · see citing works

Nucleus of the solitary tract chemical stimulation induces extracellular norepinephrine release in the lateral and basolateral amygdala

García-Medina, N. E., & Miranda, M. I. (2012) · Brain stimulation · doi:10.1016/j.brs.2012.03.020 · Cited by 19 · see citing works

Difference in the norepinephrine levels of experimental and non-experimental rats with age in the object recognition task

Nirogi, R. V. S., Abraham, R., Jayarajan, P., Medapati, R. B., Shanmuganathan, D., Kandikere, V. N., Irappanavar, S. M., Saralaya, R., Benade, V. S., Bhyrapuneni, G., et al. (2012) · Brain Research · doi:10.1016/j.brainres.2012.03.013 · Cited by 19 · see citing works

Glutamatergic influences on the nucleus paragigantocellularis: Contribution to performance in avoidance and spatial memory tasks.

Clayton, E. C., & Williams, C. L. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.4.707 · Cited by 19 · see citing works

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

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

Neuronal circuitry for recognition memory of object and place in rodent models

Chao, O. Y.-H., Nikolaus, S., Yang, Y., & Huston, J. P. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104855 · Cited by 157 · see citing works

Chemogenetic Silencing of the Locus Coeruleus–Basolateral Amygdala Pathway Abolishes Pain-Induced Anxiety and Enhanced Aversive Learning in Rats

Llorca-Torralba, M., Suárez‐Pereira, I., Bravo, L., Camarena-Delgado, C., Garcia-Partida, J. A., Micó, J. A., & Berrocoso, E. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.02.018 · Cited by 116 · see citing works

Trigeminal, Visceral and Vestibular Inputs May Improve Cognitive Functions by Acting through the Locus Coeruleus and the Ascending Reticular Activating System: A New Hypothesis

Cicco, V. D., Fantozzi, M. P. T., Cataldo, E., Barresi, M., Bruschini, L., Faraguna, U., & Manzoni, D. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00130 · Cited by 91 · see citing works

The Central Amygdala Corticotropin-releasing hormone (CRH) Neurons Modulation of Anxiety-like Behavior and Hippocampus-dependent Memory in Mice

Paretkar, T., & Dimitrov, E. L. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.08.019 · Cited by 73 · see citing works

Baroreceptor Modulation of the Cardiovascular System, Pain, Consciousness, and Cognition

Suárez-Roca, H., Mamoun, N. F., Sigurdsson, M. I., & Maixner, W. D. (2021) · Comprehensive physiology · doi:10.1002/cphy.c190038 · Cited by 95 · see citing works

The Importance of Ventral Hippocampal Dopamine and Norepinephrine in Recognition Memory

Titulaer, J., Björkholm, C., Feltmann, K., Malmlöf, T., Mishra, D., Gonzales, C. B., Schilström, B., & Konradsson‐Geuken, Å. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.667244 · Cited by 48 · see citing works

New Insights into the Role of the Locus Coeruleus-Noradrenergic System in Memory and Perception Dysfunction

Eschenko, O., Mello‐Carpes, P. B., & Hansen, N. (2017) · Neural Plasticity · doi:10.1155/2017/4624171 · Cited by 47 · see citing works

A single bout of exercise increases hippocampalBdnf: influence of chronic exercise and noradrenaline

Venezia, A. C., Quinlan, E. M., & Roth, S. M. (2017) · Genes Brain & Behavior · doi:10.1111/gbb.12394 · Cited by 43 · see citing works

One-single physical exercise session after object recognition learning promotes memory persistence through hippocampal noradrenergic mechanisms

de Vargas, L. D. S., das Neves, B.-H. S., Roehrs, R., Izquierdo, I., & Mello‐Carpes, P. B. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.04.050 · Cited by 41 · see citing works

Taraxerol as a possible therapeutic agent on memory impairments and Alzheimer’s disease: Effects against scopolamine and streptozotocin-induced cognitive dysfunctions

Berté, T. E., Dalmagro, A. P., Zimath, P. L., Gonçalves, A. E., Meyre‐Silva, C., Bürger, C., Weber, C. J., Santos, D., Filho, V. C., & de Souza, M. M. (2018) · Steroids · doi:10.1016/j.steroids.2018.01.002 · Cited by 41 · see citing works

Sexual differences in locus coeruleus neurons and related behavior in C57BL/6J mice

Mariscal, P., Bravo, L., Llorca-Torralba, M., Razquin, J., Miguélez, C., Suárez‐Pereira, I., & Berrocoso, E. (2023) · Biology of Sex Differences · doi:10.1186/s13293-023-00550-7 · Cited by 39 · see citing works

Baroreceptor Modulation of the Cardiovascular System, Pain, Consciousness, and Cognition

Suárez-Roca, H., Mamoun, N. F., Sigurdsson, M. I., & Maixner, W. D. (2021) · Comprehensive physiology · doi:10.1002/j.2040-4603.2021.tb00152.x · Cited by 39 · see citing works

Lactoferrin-conjugated pH and redox-sensitive polymersomes based on PEG-S-S-PLA-PCL-OH boost delivery of bacosides to the brain

Goyal, K., Konar, A., Kumar, B. S. H., & Koul, V. (2018) · Nanoscale · doi:10.1039/c8nr03828g · Cited by 38 · see citing works

Chronic Pain–Related Cognitive Deficits: Preclinical Insights into Molecular, Cellular, and Circuit Mechanisms

Han, S., Wang, J., Zhang, W., & Tian, X. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04073-z · Cited by 37 · see citing works

α-Synuclein and Noradrenergic Modulation of Immune Cells in Parkinson’s Disease Pathogenesis

Butkovich, L. M., Houser, M. C., & Tansey, M. G. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00626 · Cited by 37 · see citing works

Noradrenergic neuromodulation in ageing and disease

Krohn, F., Lancini, E., Ludwig, M., Leiman, M., Guruprasath, G., Haag, L., Panczyszyn, J., Düzel, E., Hämmerer, D., & Betts, M. J. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105311 · Cited by 36 · see citing works

Neural, Cellular and Molecular Mechanisms of Active Forgetting

Medina, J. H. (2018) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00003 · Cited by 33 · see citing works

A noradrenergic lesion aggravates the effects of systemic inflammation on the hippocampus of aged rats

Bharani, K., Derex, R., Granholm, A., & Ledreux, A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0189821 · Cited by 32 · see citing works

Matured Hop-Derived Bitter Components in Beer Improve Hippocampus-Dependent Memory Through Activation of the Vagus Nerve

Ayabe, T., Ohya, R., Taniguchi, Y., Shindo, K., Kondô, K., & Ano, Y. (2018) · Scientific Reports · doi:10.1038/s41598-018-33866-1 · Cited by 30 · see citing works

Peumus boldus (Boldo) Aqueous Extract Present Better Protective Effect than Boldine Against Manganese-Induced Toxicity in D. melanogaster

Bianchini, M. C., Gularte, C. A. O., Escoto, D. F., Pereira, G., Gayer, M. C., Roehrs, R., Soares, F. A. A., & Puntel, R. L. (2016) · Neurochemical Research · doi:10.1007/s11064-016-1984-z · Cited by 29 · see citing works

Hippocampal glucocorticoid target genes associated with enhancement of memory consolidation

Buurstede, J. C., van Weert, L. T. C. M., Colucci, P., Gentenaar, M., Viho, E. M. G., Koorneef, L. L., Schoonderwoerd, R. A., Lanooij, S. D., Moustakas, I., Balog, J., et al. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15226 · Cited by 28 · see citing works

The removal of percutaneous Kirschner wires used in the stabilisation of fractures in children.

Symons, S., Persad, R., & Paterson, M. (2005) · PubMed · Cited by 28 · see citing works

Catecholaminergic hippocampal activation is necessary for object recognition memory persistence induced by one-single physical exercise session

de Vargas, L. D. S., Lima, K. R., Ramborger, B. P., Roehrs, R., Izquierdo, I., & Mello‐Carpes, P. B. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112356 · Cited by 24 · see citing works

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 · see citing works

The path from trigeminal asymmetry to cognitive impairment: a behavioral and molecular study

Fantozzi, M. P. T., Lazzarini, G., Cicco, V. D., Briganti, A., Argento, S., Cicco, D. D., Barresi, M., Cataldo, E., Bruschini, L., D’Ascanio, P., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-82265-6 · Cited by 19 · see citing works

Short-term green tea supplementation prevents recognition memory deficits and ameliorates hippocampal oxidative stress induced by different stroke models in rats

Altermann, C. D. C., Souza, M. A., Schimidt, H. L., Izaguirry, A. P., Martins, A., Garcia, A., Cibin, F. W. S., & Mello‐Carpes, P. B. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.03.007 · Cited by 19 · see citing works

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 · see citing works

Improving Effects of Hop-Derived Bitter Acids in Beer on Cognitive Functions: A New Strategy for Vagus Nerve Stimulation

Ayabe, T., Fukuda, T., & Ano, Y. (2020) · Biomolecules · doi:10.3390/biom10010131 · Cited by 16 · see citing works

Differential effects of social isolation rearing on glutamate- and GABA-stimulated noradrenaline release in the rat prefrontal cortex and hippocampus

Atmore, K. H., Stein, D. J., Harvey, B. H., Russell, V. A., & Howells, F. M. (2020) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2020.05.007 · Cited by 16 · see citing works

Plasma brain-derived neurotrophic factor (BDNF) in Egyptian children with attention deficit hyperactivity disorder

El-Ghamry, R. H., El-Sheikh, M., Meguid, M. A., Nagib, S., & El‐Gabry, D. A. (2021) · Middle East Current Psychiatry · doi:10.1186/s43045-021-00099-4 · Cited by 16 · 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

Acute physical exercise improves recognition memory via locus coeruleus activation but not via ventral tegmental area activation

Lima, K. R., das Neves, B.-H. S., Carrazoni, G. S., da Rosa, A. C. D. S., Carriço, M. R. S., Roehrs, R., & Mello‐Carpes, P. B. (2023) · Physiology & Behavior · doi:10.1016/j.physbeh.2023.114370 · Cited by 15 · see citing works

Neuroprotective actions of norepinephrine in neurological diseases

Ghasemi, M., & Mehranfard, N. (2024) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-024-02999-w · Cited by 16 · see citing works

Cognitive Impairment in Alzheimer’s and Metabolic Diseases: A Catecholaminergic Hypothesis

Guzmán-Ramos, K. R., Osorio‐Gómez, D., & Bermúdez‐Rattoni, F. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.05.031 · Cited by 15 · see citing works

Chronic pain and cognitive dysfunction: clinical manifestations, underlying mechanisms, and emerging therapeutic strategies

Gong, T., Yu, W., Zhao, P., Wu, Z.-Y., Zhu, Y., Gong, Q., & Zhu, Z. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1641903 · Cited by 14 · see citing works

Roles of Rac1-Dependent Intrinsic Forgetting in Memory-Related Brain Disorders: Demon or Angel

Wang, W., Wang, Z., Cao, J., Dong, Y., & Chen, Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310736 · Cited by 11 · see citing works

Behavioral effects of 6-hydroxydopamine-induced damage to nigro-striatal pathway and Locus coeruleus as a rodent model of Parkinson’s disease

Bustelli, I. B., Oliveira, L. M., Correa-Netto, N. F., Stilhano, R. S., & Caetano, A. L. (2024) · Behavioural Brain Research · doi:10.1016/j.bbr.2024.114873 · Cited by 14 · see citing works

Light‐exercise‐induced dopaminergic and noradrenergic stimulation in the dorsal hippocampus: Using a rat physiological exercise model

Hiraga, T., Hata, T., Soya, S., Shimoda, R., Takahashi, K., Soya, M., Inoue, K., Johansen, J. P., Okamoto, M., & Soya, H. (2024) · The FASEB Journal · doi:10.1096/fj.202400418rrr · Cited by 13 · see citing works

Dopamine activity on the perceptual salience for recognition memory

Osorio‐Gómez, D., Guzmán-Ramos, K. R., & Bermúdez‐Rattoni, F. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.963739 · Cited by 13 · see citing works

Effects of age and social isolation on murine hippocampal biochemistry and behavior

Panossian, A., Cave, M. W., Patel, B. A., Brooks, E. L., Flint, M. S., & Yeoman, M. S. (2020) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2020.111337 · Cited by 13 · see citing works

BDNF as a Putative Target for Standardized Extract of Ginkgo biloba-Induced Persistence of Object Recognition Memory

Muratori, B. G., Zamberlam, C. R., Mendes, T. B., Nozima, B., Cerutti, J., & Cerutti, S. M. (2021) · Molecules · doi:10.3390/molecules26113326 · Cited by 12 · see citing works

Methylphenidate treatment increases hippocampal BDNF levels but does not improve memory deficits in hypoxic-ischemic rats

Miguel, P. M., Deniz, B. F., Confortim, H. D., de Almeida, W., Bronauth, L., Vieira, M. C., Bertoldi, K., Siqueira, I. R., Silveira, P. P., & Pereira, L. O. (2020) · Journal of Psychopharmacology · doi:10.1177/0269881120913153 · Cited by 12 · see citing works

Maternal Deprivation Induces Memory Deficits That Are Reduced by One Aerobic Exercise Shot Performed after the Learning Session

Sosa, P. M., das Neves, B.-H. S., Carrazoni, G. S., Gomes, G. C. M., Rosso, G. D., Ramborger, B. P., Rohers, R., & Mello‐Carpes, P. B. (2019) · Neural Plasticity · doi:10.1155/2019/3608502 · Cited by 10 · see citing works

A new inbred strain of Fawn-Hooded rats demonstrates mania-like behavioural and monoaminergic abnormalities

Azechi, H., Hakamada, K., & Yamamoto, T. (2019) · IBRO Reports · doi:10.1016/j.ibror.2019.11.001 · Cited by 8 · see citing works

Insulin enhances contextual fear memory independently of its effect in increasing plasma adrenaline

Oliveira, A., Seixas, R., Pereira, F., Azevedo, M., Martinho, R., Serrão, P., & Moreira-Rodrigues, M. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121881 · Cited by 6 · see citing works

Norepinephrine in the dentate gyrus is involved in spatial learning and memory alteration induced by chronic restraint stress in aged rats

Wang, F., Tang, R.-Q., Lv, J., Xiao, B., Li, Y.-S., & Jin, Q.-H. (2020) · Neuroreport · doi:10.1097/wnr.0000000000001547 · Cited by 6 · see citing works

Hormonal contraception and cognition: Considering the influence of endogenous ovarian hormones and genes for clinical translation.

Gravelsins, L., Zhao, S., & Einstein, G. (2023) · Frontiers in neuroendocrinology (Print) · doi:10.1016/j.yfrne.2023.101067 · Cited by 3 · see citing works

The dose-dependent neuroprotective effect of norepinephrine in improving memory retrieval in an experimental model of multiple sclerosis, experimental autoimmune encephalomyelitis

Taherian, N., Vaezi, G., Neamati, A., Hojjati, V., Ghorbani-Taherdehi, F., Sahebkar, A., & Valokola, M. G. (2024) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2024.110907 · Cited by 5 · see citing works

Novelty facilitates the persistence of aversive memory extinction by dopamine regulation in the hippocampus and ventral tegmental area

Lima, K. R., Alves, N., Lopes, L. F., Picua, S. S., de Vargas, L. D. S., Daré, L. R., Ramborger, B. P., Roehrs, R., de Gomes, M. G., & Mello‐Carpes, P. B. (2023) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2023.110832 · Cited by 5 · see citing works

Interregional phase-amplitude coupling between theta rhythm in the nucleus tractus solitarius and high-frequency oscillations in the hippocampus during REM sleep in rats

Atiwiwat, D., Aquilino, M. S., Devinsky, O., Bardakjian, B. L., & Carlen, P. L. (2023) · SLEEP · doi:10.1093/sleep/zsad027 · Cited by 4 · see citing works

Functional and phosphoproteomic analysis of β-adrenergic receptor signaling at excitatory synapses in the CA1 region of the ventral hippocampus

Jami, S. A., Wilkinson, B., Guglietta, R., Hartel, N. G., Babiec, W. E., Graham, N. A., Coba, M. P., & O’Dell, T. J. (2023) · Scientific Reports · doi:10.1038/s41598-023-34401-7 · Cited by 4 · see citing works

The Reduction of Seizure Intensity and Attenuation of Memory Deficiency and Anxiety-Like Behavior through Aerobic Exercise by Increasing the BDNF in Mice with Chronic Epilepsy

Sabaghi, A., Heirani, A., Kiani, A., Yousofvand, N., & Sabaghi, S. (2020) · Neurochemical Journal · doi:10.1134/s1819712420020105 · Cited by 3 · see citing works

Role of the hippocampus in memory functioning: modern view

Assonov, D. O., & Bozhuk, B. S. (2017) · Zaporozhye Medical Journal · doi:10.14739/2310-1210.2017.6.115318 · Cited by 3 · see citing works

Effects of NMDA glutamatergic receptors pharmacological stimulation of the ventral tegmental area on the memory deficits induced by maternal deprivation

das Neves, B.-H. S., Lima, K. R., da Rosa, A. C. D. S., Liao, G., Perretto, A. C., Carrazoni, G. S., & Mello‐Carpes, P. B. (2024) · Brain Research · doi:10.1016/j.brainres.2024.149316 · Cited by 2 · see citing works

β-adrenergic receptor-induced E-S potentiation in the dorsal and ventral hippocampus

Trompoukis, G., Miliou, A., & Papatheodoropoulos, C. (2024) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2024.1511485 · Cited by 2 · see citing works

Effects of Prenatal Seizures on Cognitive and Motor Performance in Mice Offspring (with Emphasis on BDNF and GDNF Levels)

Sabaghi, A., Heirani, A., Kiani, A., & Yosofvand, N. (2018) · Neurophysiology · doi:10.1007/s11062-019-09759-y · Cited by 2 · see citing works

Propranolol Administration During Morphine Addiction Attenuates Reinstatement of Drug-Aversive Memories Caused by Exposure to Stressful Stimuli

Cánovas, A., Teruel-Fernández, F.-J., Fernández-López, L., Martínez-Laorden, E., Navarro‐Zaragoza, J., & Almela, P. (2025) · Pharmaceuticals · doi:10.3390/ph19010033 · Cited by 1 · see citing works

Maternal egg yolk supplementation alters offspring liver choline status and is associated with functional network activation and monoamine metabolism in a sow-piglet model

Lee, S., Zukaitis, J. G., Malysheva, O., Dubrof, S., Hudson, B. T., Filipov, N. M., Ahmed, I., Zhao, Q., & Park, H. J. (2026) · Nutrition Research · doi:10.1016/j.nutres.2026.05.005 · Cited by 1 · see citing works

Argentinean Society of Experimental Pharmacology: Brief history and main scientific contributions to the discipline

Bruni, S. F. S., & Acosta, G. B. (2016) · Pharmacological Research · doi:10.1016/j.phrs.2016.01.014 · Cited by 1 · see citing works

Memory reactivation mediates emotional valence updating of contextual memory in mice with protracted morphine withdrawal

Correa-Netto, N. F., Masukawa, M. Y., Silva-Gomes, A. M., Linardi, A., & Santos-Junior, J. G. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.114212 · Cited by 1 · see citing works

Multiple Stages of Memory Formation and Persistence

Medina, J. H., & Cammarota, M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21099-7 · Cited by 1 · see citing works

The Roles of Neurotrophins in Novel Object Recognition

Kelly, Á. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00030-6

Effect of Seizure During Pregnancy on Cognitive and Motor Coordination Performances in Adult Male Offspring of Female Mice: The Role of Serum Corticosterone Level

Sabaghi, A., Heyrani, A., Kiani, A., Khazaee, H., Sabaghi, S., & Beygie, S. (2019) · The Neuroscience Journal of Shefaye Khatam · doi:10.29252/shefa.7.4.8

Brainstem Seizures and Associated Cardiorespiratory Depression Following Intrahippocampal 4-AP Application in Freely Moving Rats

Lertwittayanon, W. (2018) · TSpace (University of Toronto)

Effects of CA1 α2-adrenergic receptors on morphine-induced exploratory behaviors

Beirami, E., & Tamijani, S. M. S. (2024) · Physiology and Pharmacology · doi:10.61186/phypha.28.1.66

Ameliorative Effects of High‐Intensity Interval Training (HIIT) and Methylphenidate Against Tramadol‐Induced Cognitive Impairment: The Role of Hippocampal Oxidative Stress

Shirazpour, S., Taheri, F., Sepehri, G., Meymandi, M. S., Zangiabadizadeh, M., Zangiabadi, M., Hosseini, N. S., Rajizadeh, M. A., Sheikhi, S., & Sabet, N. (2025) · Brain and Behavior · doi:10.1002/brb3.70925

Acute ketamine withdrawal disrupts memory and monoaminergic neurotransmission in adolescent female rats

Pantoja, L. V. P. D. S., Soares, L. F. R., da Conceição, B. C., Carvalheiro-Simas, T. C. V. S., Luz, D. A., Prediger, R. D., de Andrade, G. M., Fontes-Júnior, E. A., Pinheiro, B. G., Cartágenes, S. D. C., et al. (2026) · Behavioural Brain Research · doi:10.1016/j.bbr.2026.116048

Short-term docosahexaenoic acid rich diet prevents cognitive deficits in human apolipoprotein E epsilon 4-targeted replacement mice

Raffoul, R., Lopez, J. A., Vachon, A., Laurent, B., & Plourde, M. (2026) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2026.102730

Scalp electroacupuncture targeting trigeminal nerve activation alleviates post‐traumatic stress disorder–induced depression and neuroinflammation in mice

Lee, B., Kim, Y., Kim, H., & Hahm, D. (2026) · Animal Models and Experimental Medicine · doi:10.1002/ame2.70164

Acute physical exercise enhances memory persistence in female rats via hippocampal catecholaminergic receptors

Lima, K. R., da Rosa, A. C. D. S., Gomes, G. C. M., Sigaran, G. J., Martinez, G. A., Dias, L. D. A., & Mello‐Carpes, P. B. (2026) · Physiology & Behavior · doi:10.1016/j.physbeh.2026.115426

Sex-specific exploration patterns and noradrenergic modulation in object recognition memory: Role of the perirhinal cortex

Roselló-Jiménez, L., Pastor, R., Miquel, M., & Font, L. (2026) · Psychopharmacology · doi:10.1007/s00213-026-07191-9

Locus coeruleus

Vreven, A., Chandler, D. J., Fan, W., Jordan, R., Krentzman, O. J., Lüthi, A., McCall, J. G., Sciolino, N. R., Tkaczynski, J., & Totah, N. K. B. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-24078-2.00010-3

Bioengineered microbiotic levodopa therapy improves cognition and reduces pathology in a rat model of Alzheimer's disease

Abdelhamid, M., Padhi, P., Gifani, M., Beck, J. S., Thomas, J. P., Khadse, G., Kudela, C., Phillips, G. J., Kanthasamy, A. G., & Counts, S. (2026) · British Journal of Pharmacology · doi:10.1111/bph.70670

Locus Coeruleus Stimulation Enhances Object Recognition Memory Persistence After Early-Life Stress Independent of Hippocampal Noradrenergic Signaling

das Neves, B.-H. S., Lima, K. R., da Rosa, A. C. D. S., Gomes, G. C. M., Perretto, A. C., Martinez, G. A., Coura, B. P., & Mello‐Carpes, P. B. (2026) · Archives of Medical Research · doi:10.1016/j.arcmed.2026.103537

The Nucleus of the Solitary Tract→Nucleus Paragigantocellularis→Locus Coeruleus→CA1 region of dorsal hippocampus pathway is important for consolidation of object recognition memory

Mello‐Carpes, P. B., & Izquierdo, I. (2012) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2012.12.002 · Cited by 123 · see citing works

β‐Adrenergic receptors link NO/sGC/PKG signaling to BDNF expression during the consolidation of object recognition long‐term memory

Furini, C. R., Rossato, J. I., Bitencourt, L. L., Medina, J. H., Izquierdo, I., & Cammarota, M. (2010) · Hippocampus · doi:10.1002/hipo.20656 · Cited by 72 · see citing works

Participação da via NTS-PGI-LC-hipocampo (núcleo do trato solitário- núcleo paragigantocelular-Locus coeruleus-hipocampo) na consolidação da memória de reconhecimento de objetos

Carpes, P. B. M. (2010) · Americanae (AECID Library)

Neuropeptide S interacts with the basolateral amygdala noradrenergic system in facilitating object recognition memory consolidation

Han, R.-W., Xu, H., Zhang, R., Wang, P., Chang, M., Peng, Y., Deng, K., & Wang, R. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.10.010 · Cited by 32 · see citing works

b-Adrenergic Receptors Link NO/sGC/PKG Signaling to BDNF Expression During the Consolidation of Object Recognition Long-Term Memory

Furini, C. R. G., Rossato, J. I., Bitencourt, L. L., & Medina, J. H. (2016)