The place of the hippocampus in fear conditioning

Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning.

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Neurobiology of Pavlovian fear conditioning

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The lateral amygdaloid nucleus: sensory interface of the amygdala in fear conditioning

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Why We Think Plasticity Underlying Pavlovian Fear Conditioning Occurs in the Basolateral Amygdala

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Conjunctive representations in learning and memory: Principles of cortical and hippocampal function.

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Fear conditioning enhances short-latency auditory responses of lateral amygdala neurons: Parallel recordings in the freely behaving rat

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Neurotoxic lesions of the dorsal hippocampus and Pavlovian fear conditioning in rats

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Contextual fear, gestalt memories, and the hippocampus

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The global record of memory in hippocampal neuronal activity

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Long-Term Memory Deficits in Pavlovian Fear Conditioning in Ca2+/Calmodulin Kinase Kinase α-Deficient Mice

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Agmatine Potentiates Morphine-Induced Conditioned Place Preference in Mice: Modulation by Alpha(2)-Adrenoceptors

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CRTC1 Function During Memory Encoding Is Disrupted in Neurodegeneration

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Brain STAT5 signaling modulates learning and memory formation

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Effects of pre or posttraining dorsal hippocampus D‐AP5 injection on fear conditioning to tone, background, and foreground context

Schenberg, E. E., & Oliveira, M. G. M. (2008) · Hippocampus · doi:10.1002/hipo.20475 · Cited by 40

A magnetic resonance imaging study of cortical thickness in animal phobia

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Cdk5: A Novel Role in Learning and Memory

Fischer, A., Sananbenesi, F., Spiess, J., & Radulović, J. (2003) · Neurosignals · doi:10.1159/000074621 · Cited by 40

Spatial exploration is required for the formation of contextual fear memory.

McHugh, T. J., & Tonegawa, S. (2007) · Behavioral Neuroscience · doi:10.1037/0735-7044.121.2.335 · Cited by 39

II. Cognitive performance of middle-aged female rats is influenced by capacity to metabolize progesterone in the prefrontal cortex and hippocampus

Paris, J. J., Walf, A. A., & Frye, C. A. (2010) · Brain Research · doi:10.1016/j.brainres.2010.10.099 · Cited by 38

Infusion of lidocaine into the dorsal hippocampus before or after the shock training phase impaired conditioned freezing in a two-phase training task of contextual fear conditioning

Chang, S., Chen, D.-Y., & Liang, K. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.07.012 · Cited by 38

Behavioral Defects in Chaperone-Deficient Alzheimer's Disease Model Mice

Ojha, J., Veeranan‐Karmegam, R., Masilamoni, J. G., Terry, A. V., & Cashikar, A. G. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016550 · Cited by 41

Amygdala conditioning modulates sensory input to the cerebellum.

Taub, A., & Mintz, M. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.09.004 · Cited by 38

What’s in a context? Cautions, limitations, and potential paths forward

Stark, S. M., Reagh, Z. M., Yassa, M. A., & Stark, C. E. L. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.05.022 · Cited by 42

Contextual processing elicits sex differences in dorsal hippocampus activation following footshock and context fear retrieval

Colón, L. M., & Poulos, A. M. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112771 · Cited by 40

Role of L-type Ca2+channel isoforms in the extinction of conditioned fearPreprint

Busquet, P., Hetzenauer, A., Sinnegger-Brauns, M. J., Striessnig, J., & Singewald, N. (2008) · Learning & Memory · doi:10.1101/lm.886208 · Cited by 36

Behavioral characterization of mice lacking the neurite outgrowth inhibitor Nogo‐A

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Comparison of Evoked vs. Spontaneous Tics in a Patient with Trigeminal Neuralgia (Tic Doloureux)

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Toward a framework for defective emotion processing in social phobia

Hermans, E. J., & van Honk, J. (2006) · Cognitive Neuropsychiatry · doi:10.1080/13546800500213993 · Cited by 35

Dorsal hippocampus is necessary for novel learning but sufficient for subsequent similar learning

Wang, S., Finnie, P. S. B., Hardt, O. M., & Nader, K. (2012) · Hippocampus · doi:10.1002/hipo.22036 · Cited by 34

Disconnection of the Perirhinal and Postrhinal Cortices Impairs Recognition of Objects in Context But Not Contextual Fear Conditioning

Heimer‐McGinn, V., Poeta, D. L., Aghi, K., Udawatta, M., & Burwell, R. D. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0254-17.2017 · Cited by 34

“Green odor” inhalation by rats down-regulates stress-induced increases in Fos expression in stress-related forebrain regions

Ito, A., Miyoshi, M., Ueki, S., Fukada, M., Komaki, R., & Watanabe, T. (2009) · Neuroscience Research · doi:10.1016/j.neures.2009.06.012 · Cited by 34

Long-term cilostazol administration ameliorates memory decline in senescence-accelerated mouse prone 8 (SAMP8) through a dual effect on cAMP and blood-brain barrier

Yanai, S., Toyohara, J., Ishiwata, K., Ito, H., & Endo, S. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.12.006 · Cited by 35

Neurological sequelae induced by alphavirus infection of the CNS are attenuated by treatment with the glutamine antagonist 6-diazo-5-oxo-l-norleucine

Potter, M. C., Baxter, V. K., Mathey, R. W., Alt, J., Rojas, C., Griffin, D. E., & Slusher, B. S. (2015) · Journal of NeuroVirology · doi:10.1007/s13365-015-0314-6 · Cited by 32

Anxiety in synucleinopathies: neuronal circuitry, underlying pathomechanisms and current therapeutic strategies

Lai, T. T., Gericke, B., Feja, M., Conoscenti, M. A., Zelikowsky, M., & Richter, F. (2023) · npj Parkinson s Disease · doi:10.1038/s41531-023-00547-4 · Cited by 34

Behavioural, neurochemical and neuroendocrine effects of the endogenous β-carboline harmane in fear-conditioned rats

Smith, K. L., Ford, G. K., Jessop, D. S., & Finn, D. P. (2012) · Journal of Psychopharmacology · doi:10.1177/0269881112460108 · Cited by 31

Ablation of STAT3 in Purkinje cells reorganizes cerebellar synaptic plasticity in long-term fear memory network

Han, J.-K., Kwon, S., Kim, Y. G., Choi, J., Kim, J., Lee, Y., Ye, S.-K., & Kim, S. J. (2021) · eLife · doi:10.7554/elife.63291 · Cited by 32

The fear circuitry in panic disorder and its modulation by cognitive-behaviour therapy interventions

de Carvalho, M. R., Rozenthal, M., & Nardi, A. E. (2009) · The World Journal of Biological Psychiatry · doi:10.1080/15622970903178176 · Cited by 31

The fear circuitry in panic disorder and its modulation by cognitive-behaviour therapy interventions

de Carvalho, M. R., Rozenthal, M., & Nardi, A. E. (2010) · The World Journal of Biological Psychiatry · doi:10.3109/15622970903178176 · Cited by 30

From Age-Related Cognitive Decline to Alzheimer’s Disease: A Translational Overview of the Potential Role for Phosphodiesterases

Heckman, P. R. A., Blokland, A., & Prickaerts, J. (2017) · Advances in neurobiology · doi:10.1007/978-3-319-58811-7_6 · Cited by 30

A neurobehavioral account for individual differences in resilience to chronic military stress

Lin, T., Vaisvaser, S., Fruchter, E., Admon, R., Wald, I., Pine, D. S., Bar‐Haim, Y., & Hendler, T. (2014) · Psychological Medicine · doi:10.1017/s0033291714002013 · Cited by 29

Microtubule-Actin Cross-Linking Factor 1: Domains, Interaction Partners, and Tissue-Specific Functions.

Goryunov, D., & Liem, R. (2016) · Methods in Enzymology · doi:10.1016/bs.mie.2015.05.022 · Cited by 26

The neural correlates of attachment security in typically developing children

Choi, E. J., Taylor, M. J., Hong, S.-B., Kim, C.-D., & Yi, S.-H. (2018) · Brain and Cognition · doi:10.1016/j.bandc.2018.04.003 · Cited by 31

Emergence of spatial impairment in rats following specific cholinergic depletion of the medial septum combined with chronic stress

Craig, L. A., Hong, N. S., Kopp, J., & McDonald, R. J. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06179.x · Cited by 29

Impaired extinction of cued fear memory and abnormal dendritic morphology in the prelimbic and infralimbic cortices in VPAC2 receptor (VIPR2)-deficient mice

Ago, Y., Hayata‐Takano, A., Kawanai, T., Yamauchi, R., Takeuchi, S., Cushman, J. D., Rajbhandari, A. K., Fanselow, M. S., Hashimoto, H., & Waschek, J. A. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.10.010 · Cited by 28

Chronic reduction in dietary tryptophan leads to a selective impairment of contextual fear memory in mice

Uchida, S., Umeeda, H., Kitamoto, A., Masushige, S., & Kida, S. (2007) · Brain Research · doi:10.1016/j.brainres.2007.02.049 · Cited by 30

Fear conditioning enhances spontaneous AMPA receptor‐mediated synaptic transmission in mouse hippocampal CA1 area

Zhou, M., Conboy, L., Sandi, C., Joëls, M., & Krugers, H. J. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06951.x · Cited by 28

Fear conditioning is impaired in adult rats by ethanol doses that do not affect periadolescents

Land, C. L., & Spear, N. E. (2004) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2004.04.008 · Cited by 28

Neurotrophin-mediated neuroprotection of hippocampal neurons following traumatic brain injury is not associated with acute recovery of hippocampal function.

Royo, N., Lebold, D., Magge, S. N., Chen, I., Hauspurg, A., Cohen, A. S., & Watson, D. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.06.014 · Cited by 27

Social modulation of fear: Facilitation vs buffering

Morozov, A., & Ito, W. (2018) · Genes Brain & Behavior · doi:10.1111/gbb.12491 · Cited by 32

Neurobiological Pathways between Chronic Stress and Depression: Dysregulated Adaptive Mechanisms?

Sharpley, C. F. (2009) · Clinical Medicine Insights Psychiatry · doi:10.4137/cmpsy.s3658 · Cited by 26

Impaired P50 suppression in fear extinction in obsessive–compulsive disorder

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Sexual behavior modulates contextual fear memory through dopamine D1/D5 receptors

Bai, H., Cao, J., Liu, N., Xu, L., & Luo, J. (2008) · Hippocampus · doi:10.1002/hipo.20505 · Cited by 24

Age differences in fear retention and extinction in male Sprague-Dawley rats: Effects of ethanol challenge during conditioning

Broadwater, M., & SPEAR, L. P. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.06.029 · Cited by 26

Roles for the Dorsal Striatum in Aversive Behavior

Stanley, A. T., Lippiello, P., Sulzer, D. L., & Miniaci, M. C. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.634493 · Cited by 26

Inhibition of PKA anchoring to A-kinase anchoring proteins impairs consolidation and facilitates extinction of contextual fear memories

Nijholt, I. M., Ostroveanu, A., Scheper, W. A., Penke, B., Luiten, P. G. M., van der Zee, E. A., & Eisel, U. L. M. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.03.008 · Cited by 27

Neurotoxic lesions of the dorsal and ventral hippocampus impair acquisition and expression of trace-conditioned fear-potentiated startle in rats

Trivedi, M. A., & Coover, G. D. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.11.029 · Cited by 24

Comparison of the performance of DBA/2 and C57BL/6 mice in transitive inference and foreground and background contextual fear conditioning.

André, J. M., Cordero, K. A., & Gould, T. J. (2012) · Behavioral Neuroscience · doi:10.1037/a0027048 · Cited by 24

Behavioral Pharmacogenetic Analysis on the Role of the α4 GABAA Receptor Subunit in the Ethanol-Mediated Impairment of Hippocampus-Dependent Contextual Learning

Cushman, J. D., Moore, M. D., Jacobs, N. S., Olsen, R. W., & Fanselow, M. S. (2011) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2011.01546.x · Cited by 24

Limbic system development underlies the emergence of classical fear conditioning during the third and fourth weeks of life in the rat.

Deal, A. L., Erickson, K. J., Shiers, S. I., & Burman, M. A. (2016) · Behavioral Neuroscience · doi:10.1037/bne0000130 · Cited by 25

Protein Profiles Associated With Context Fear Conditioning and Their Modulation by Memantine

Ahmed, M. M., Dhanasekaran, A. R., Block, A., Tong, S., Costa, A. C. S., & Gardiner, K. (2014) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m113.035568 · Cited by 23

Exercise and Implicit Memory: A Brief Systematic Review

Loprinzi, P. D., & Edwards, M. K. (2017) · Psychological Reports · doi:10.1177/0033294117745563 · Cited by 23

Cortico-hippocampal Schemas Enable NMDAR-Independent Fear Conditioning in Rats

Finnie, P. S. B., Gamache, K., Protopoulos, M., Sinclair, E., Baker, A. G., Wang, S., & Nader, K. (2018) · Current Biology · doi:10.1016/j.cub.2018.07.037 · Cited by 23

Frontal Norepinephrine Represents a Threat Prediction Error Under Uncertainty

Basu, A., Yang, J.-H., Yu, A. L., Glaeser-Khan, S., Rondeau, J. A., Feng, J., Krystal, J. H., Li, Y., & Kaye, A. P. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.01.025 · Cited by 37

Disruption of the NF-κB/IκBα Autoinhibitory Loop Improves Cognitive Performance and Promotes Hyperexcitability of Hippocampal Neurons

Shim, D. J., Li, Y., Reed, J. G., Noebels, J. L., Chiao, P. J., & Zheng, H. (2011) · Molecular Neurodegeneration · doi:10.1186/1750-1326-6-42 · Cited by 23

Distinct but overlapping roles of LRRTM1 and LRRTM2 in developing and mature hippocampal circuits

Dhume, S. H., Connor, S. A., Mills, F., Tari, P. K., Au-Yeung, S. H., Karimi, B., Oku, S., Roppongi, R. T., Kawabe, H., Bamji, S. X., et al. (2022) · eLife · doi:10.7554/elife.64742 · Cited by 22

Induction of c-Fos expression in the mammillary bodies, anterior thalamus and dorsal hippocampus after fear conditioning

Conejo, N. M., González‐Pardo, H., López, M., Cantora, R., & Arias, J. L. (2007) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2007.06.006 · Cited by 22

Doublecortin Knockout Mice Show Normal Hippocampal-Dependent Memory Despite CA3 Lamination Defects

Germain, J., Bruel‐Jungerman, E., Grannec, G., Denis, C., Lepousez, G., Bruno Giros, A., Francis, F., & Nosten‐Bertrand, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074992 · Cited by 22

Magnetic resonance spectroscopy reveals N-acetylaspartate reduction in hippocampus and cingulate cortex after fear conditioning

Zhou, I. Y., Ding, A. Y., Li, Q., McAlonan, G. M., & Wu, E. X. (2012) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2012.09.010 · Cited by 22

Age-specific threats induce CRF expression in the paraventricular nucleus of the hypothalamus and hippocampus of young rats

Wiedenmayer, C. P., Magariños, A. M., McEwen, B. S., & Barr, G. A. (2004) · Hormones and Behavior · doi:10.1016/j.yhbeh.2004.09.001 · Cited by 23

Abnormal spontaneous neural activity in hippocampal–cortical system of patients with obsessive–compulsive disorder and its potential for diagnosis and prediction of early treatment response

Yan, H., Shan, X., Li, H., Liu, F., & Guo, W. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.906534 · Cited by 23

Median raphe region stimulation alone generates remote, but not recent fear memory traces

Balázsfi, D., Zelena, D., Farkas, L., Demeter, K., Barna, I., Cserép, C., Takács, V. T., Nyíri, G., Gölöncsér, F., Sperlágh, B., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0181264 · Cited by 22

Effects of glucocorticoids on emotion and cognitive processes in animals

Prickaerts, J., & Steckler, T. (2005) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(05)80021-5 · Cited by 25

Anxiolytic-like effects of DOI microinjections into the hippocampus (but not the amygdala nor the PAG) in the mice four plates test

Massé, F., Petit‐Demoulière, B., Dubois, I., Hascoët, M., & Bourin, M. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.11.005 · Cited by 21

Cognitive Sequelae and Hippocampal Dysfunction in Chronic Kidney Disease following 5/6 Nephrectomy

Yu, Y. H., Kim, S.-W., Im, H., Oh, S. W., Cho, N., Park, S., Park, D., Kim, D., & Gil, H. (2022) · Brain Sciences · doi:10.3390/brainsci12070905 · Cited by 19

Contextual learning increases dendrite complexity and EphrinB2 levels in hippocampal mouse neurons

Trabalza, A., Colazingari, S., Sgobio, C., & Bevilacqua, A. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.11.008 · Cited by 20

Effects of pre- or post-training entorhinal cortex AP5 injection on fear conditioning

Schenberg, E. E., Soares, J. C. K., & MENEZESOLIVEIRA, M. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.08.032 · Cited by 20

Genes and neurons: molecular insights to fear and anxiety

Stoppel, C. M., Albrecht, A., Pape, H., & Stork, O. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00229.x · Cited by 21

Systemic Cellular Activation Mapping of an Extinction-Impaired Animal Model

Park, K., & Chung, C. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00099 · Cited by 19

Resolving conflict between aversive and appetitive learning of views: how ants shift to a new route during navigation

Lionetti, V. A. G., Deeti, S., Murray, T., & Cheng, K. (2023) · Learning & Behavior · doi:10.3758/s13420-023-00595-z · Cited by 19

A cAMP analog reverses contextual and tone memory deficits induced by a PKA inhibitor in Pavlovian fear conditioning

Nassireslami, E., Nikbin, P., Payandemehr, B., Amini, E., Mohammadi, M., Vakilzadeh, G., Ghadiri, T., Noorbakhsh, F., & Sharifzadeh, M. S. (2013) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.02.016 · Cited by 18

Stress enhancement of fear learning in mice is dependent upon stressor type: Effects of sex and ovarian hormones

Sanders, M. J., Stevens, S., & Boeh, H. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.06.003 · Cited by 19

Central CRF receptor antagonist α-helical CRF9-41 blocks reinstatement of extinguished fear: The role of the bed nucleus of the stria terminalis.

Waddell, J., Bouton, M. E., & Falls, W. A. (2008) · Behavioral Neuroscience · doi:10.1037/a0013136 · Cited by 19

LARGE, an intellectual disability-associated protein, regulates AMPA-type glutamate receptor trafficking and memory

Seo, B. A., Cho, T., Lee, D. Z., Lee, J., Lee, B., Kim, S.-W., Shin, H., & Kang, M. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1805060115 · Cited by 18

Cued Fear Conditioning in Carioca High- and Low-Conditioned Freezing Rats

Macêdo-Souza, C., Maisonnette, S. S., Filgueiras, C. C., Landeira-Fernández, J., & Krahe, T. E. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00285 · Cited by 18

Midazolam reduces the selective activation of the rhinal cortex by contextual fear stimuli

Albrechet‐Souza, L., Borelli, K. G., Almada, R. C., & Brandão, M. L. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.09.006 · Cited by 17

Sevoflurane Impairs Short-Term Memory by Affecting PSD-95 and AMPA Receptor in the Hippocampus of a Mouse Model

Yuan, J., Fan, H., Wang, K., & Lu, S. (2019) · Behavioural Neurology · doi:10.1155/2019/1068260 · Cited by 17

Involvement of the dopaminergic system in the consolidation of fear conditioning in hippocampal CA3 subregion

Wen, J.-L., Li, X., Wang, R., Chen, Z.-X., Shi, Y., & Zhao, H. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.10.049 · Cited by 17

The dorsal hippocampus mediates synaptic destabilization and memory lability in the amygdala in the absence of contextual novelty

Ferrara, N. C., Trask, S., Pullins, S. E., & Helmstetter, F. J. (2019) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2019.107089 · Cited by 17

Emotional and learning behaviour in mice overexpressing heat shock protein 70

Ammon-Treiber, S., Grecksch, G., Angelidis, C. E., Vezyraki, P., Höllt, V., & Becker, A. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.04.006 · Cited by 17

Effects of a Flavonoid-Rich Fraction on the Acquisition and Extinction of Fear Memory: Pharmacological and Molecular Approaches

de Oliveira, D. R., Zamberlam, C. R., Rêgo, G. M., Cavalheiro, A. J., Cerutti, J. M., & Cerutti, S. M. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00345 · Cited by 16

Functional ultrasound imaging of recent and remote memory recall in the associative fear neural network in mice

Grohs, G., Smausz, R., Gigg, J., Boeckers, T. M., & Hengerer, B. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.113862 · Cited by 18

Early‐life exposure to high‐fat diet influences brain health in aging mice

Meco, A. D., & Praticò, D. (2019) · Aging Cell · doi:10.1111/acel.13040 · Cited by 16

Alcohol and Vaporized Nicotine Co-exposure During Adolescence Contribute Differentially to Sex-Specific Behavioral Effects in Adulthood

Ruffolo, J., Frie, J. A., Thorpe, H. H. A., Talhat, M. A., & Khokhar, J. Y. (2022) · Nicotine & Tobacco Research · doi:10.1093/ntr/ntab250 · Cited by 16

Contextual exploration previous to an aversive event predicts long-term emotional consequences of severe stress

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Chronic up-regulation of the SHH pathway normalizes some developmental effects of trisomy in Ts65Dn mice

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