Unique regulation of long term potentiation in the rat ventral hippocampus

A synaptic model of memory: long-term potentiation in the hippocampus

Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566 · see citing works

The rat nervous system

Paxinos, G. (1985) · Cited by 3,715 · see citing works

The medial temporal lobe

Squire, L. R., Stark, C. E. L., & Clark, R. E. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144130 · Cited by 2,680 · see citing works

Regional dissociations within the hippocampus-memory and anxiety

Bannerman, D. M., Rawlins, J. N. P., McHugh, S. B., Deacon, R. M. J., Yee, B. K., Bast, T., Zhang, W.-N., Pothuizen, H. H. J., & Feldon, J. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.03.004 · Cited by 1,462 · see citing works

Inhibition of Postsynaptic PKC or CaMKII Blocks Induction But Not Expression of LTP

Malinow, R., Schulman, H., & Tsien, R. W. (1989) · Science · doi:10.1126/science.2549638 · Cited by 1,325 · see citing works

Reduced fear expression after lesions of the ventral hippocampus

Kjelstrup, K. G., Tuvnes, F. A., Steffenach, H.-A., Murison, R., Moser, E. I., & Moser, M.-B. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152112399 · Cited by 912 · see citing works

Metabotropic glutamate receptors: electrophysiological properties and role in plasticity

Anwyl, R. (1999) · Brain Research Reviews · doi:10.1016/s0165-0173(98)00050-2 · Cited by 776 · see citing works

Calcium- and activity-dependent synaptic plasticity

Zucker, R. S. (1999) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)80045-2 · Cited by 618 · see citing works

Bidirectional long-term modification of synaptic effectiveness in the adult and immature hippocampus

Dudek, S. M., & Bear, M. F. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-07-02910.1993 · Cited by 595 · see citing works

Metabotropic Glutamate Receptors 1 and 5 Differentially Regulate CA1 Pyramidal Cell Function

Mannaioni, G., Marino, M. J., Valenti, O., Traynelis, S. F., & Conn, P. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-16-05925.2001 · Cited by 441 · see citing works

The LTP Program: a data acquisition program for on-line analysis of long-term potentiation and other synaptic events

Anderson, W. W., & Collingridge, G. L. (2001) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(01)00374-0 · Cited by 423 · see citing works

Double dissociation of function within the hippocampus: A comparison of dorsal, ventral, and complete hippocampal cytotoxic lesions

Bannerman, D. M., Yee, B. K., Good, M. A., Heupel, M. J., Iversen, S. D., & Rawlins, J. N. P. (1999) · Behavioral Neuroscience · doi:10.1037/0735-7044.113.6.1170 · Cited by 397 · see citing works

Cellular mechanisms of neuronal population oscillations in the hippocampus in vitro

Traub, R. D., Bibbig, A., LeBeau, F. E. N., Buhl, E. H., & Whittington, M. A. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144303 · Cited by 358 · see citing works

Hippocampal Formation

Witter, M. P., & Amaral, D. G. (2004) · Elsevier eBooks · doi:10.1016/b978-012547638-6/50022-5 · Cited by 344 · see citing works

Segregating the functions of human hippocampus

Strange, B. A., Fletcher, P. C., Henson, R. N., Friston, K. J., & Dolan, R. J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.7.4034 · Cited by 332 · see citing works

Dissociation of function between the dorsal and the ventral hippocampus in spatial learning abilities of the rat: a within‐subject, within‐task comparison of reference and working spatial memory

Pothuizen, H. H. J., Zhang, W., Jongen‐Rêlo, A. L., Feldon, J., & Yee, B. K. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03170.x · Cited by 274 · see citing works

Induction of sharp wave–ripple complexes in vitro and reorganization of hippocampal networks

Behrens, C. J., van den Boom, L. P., de Hoz, L., Friedman, A., & Heinemann, U. (2005) · Nature Neuroscience · doi:10.1038/nn1571 · Cited by 262 · see citing works

Stores Not Just for Storage

Rose, C. R., & Konnerth, A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00402-0 · Cited by 225 · see citing works

Gamma-frequency oscillations: a neuronal population phenomenon, regulated by synaptic and intrinsic cellular processes, and inducing synaptic plasticity

Traub, R. D., Spruston, N., Soltész, I., Konnerth, A., Whittington, M. A., & Jefferys, J. G. R. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00020-3 · Cited by 189 · see citing works

A characterisation of long‐term depression induced by metabotropic glutamate receptor activation in the rat hippocampus in vitro

Fitzjohn, S. M., Palmer, M. J., May, J. E. R., Neeson, A., Morris, S. A. C., & Collingridge, G. L. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.00421.x · Cited by 175 · see citing works

Functional Differentiation Along the Anterior-Posterior Axis of the Hippocampus in Monkeys

Colombo, M., Fernandez, T., Nakamura, K., & Gross, C. G. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.2.1002 · Cited by 167 · see citing works

Thapsigargin blocks the induction of long-term potentiation in rat hippocampal slices

Harvey, J., & Collingridge, G. L. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90551-h · Cited by 159 · see citing works

Anxiety is functionally segregated within the septo-hippocampal system

Degroot, A., & Treit, D. (2004) · Brain Research · doi:10.1016/j.brainres.2003.10.065 · Cited by 153 · cited 2× · see citing works

Facilitation of long-term potentiation by prior activation of metabotropic glutamate receptors

Cohen, A. S., & Abraham, W. C. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.2.953 · Cited by 134 · see citing works

Long-Lasting Increase in Cellular Excitability Associated With the Priming of LTP Induction in Rat Hippocampus

Cohen, A. S., Coussens, C. M., Raymond, C. R., & Abraham, W. C. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.6.3139 · Cited by 126 · see citing works

Decreased ability of rat temporal hippocampal CA1 region to produce long-term potentiation

Papatheodoropoulos, C., & Kostopoulos, G. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(99)01002-2 · Cited by 123 · see citing works

When Are Class I Metabotropic Glutamate Receptors Necessary for Long-Term Potentiation?

Wilsch, V. W., Behnisch, T., Jäger, T., Reymann, K. G., & Balschun, D. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-16-06071.1998 · Cited by 116 · see citing works

Long‐term potentiation is impaired in rat hippocampal slices that produce spontaneous sharp waves

Colgin, L. L., Kubota, D., Jia, Y., Rex, C. S., & LYNCH, G. S. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.068080 · Cited by 112 · see citing works

Homeostatic Maintenance of Neuronal Excitability by Burst Discharges In Vivo

Buzsáki, G. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.9.893 · Cited by 108 · see citing works

Distinct properties of carbachol- and DHPG-induced network oscillations in hippocampal slices

Pálhalmi, J., Paulsen, O., Freund, T. F., & Hájos, N. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.04.010 · Cited by 107 · see citing works

Differences in paired‐pulse facilitation and long‐term potentiation between dorsal and ventral CA1 regions in anesthetized rats

Maruki, K., Izaki, Y., Nomura, M., & Yamauchi, T. (2001) · Hippocampus · doi:10.1002/hipo.1080 · Cited by 102 · see citing works

Dorsal-ventral differentiation of short-term synaptic plasticity in rat CA1 hippocampal region

Papatheodoropoulos, C., & Kostopoulos, G. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)01084-3 · Cited by 88 · see citing works

Synchronized oscillations in hippocampal CA3 neurons induced by metabotropic glutamate receptor activation

Taylor, G., Merlin, L., & Wong, R. K. S. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-12-08039.1995 · Cited by 84 · see citing works

The regulation of hippocampal LTP by the molecular switch, a form of metaplasticity, requires mGlu5 receptors

Bortolotto, Z. A., Collett, V. J., Conquet, F., Jia, Z., van der Putten, H., & Collingridge, G. L. (2005) · Neuropharmacology · doi:10.1016/j.neuropharm.2005.05.020 · Cited by 76 · see citing works

Both mGluR1 and mGluR5 mediate Ca2+ release and inward currents in hippocampal CA1 pyramidal neurons

Rae, M. G., & Irving, A. J. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.02.002 · Cited by 71 · see citing works

Contingent versus incidental context processing during conditioning: Dissociation after excitotoxic hippocampal plus dentate gyrus lesions

Good, M. A., de Hoz, L., & Morris, R. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1998)8:2 · Cited by 67 · see citing works

Inhibition of long-term potentiation in the dentate gyrus of freely moving rats by the metabotropic glutamate receptor antagonist MCPG

Riedel, G., Casabona, G., & Reymann, K. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00087.1995 · Cited by 67 · see citing works

Metabotropic glutamate receptor subtype agonists facilitate long-term potentiation within a distinct time window in the dentate gyrus in vivo

Manahan‐Vaughan, D., & Reymann, K. G. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00162-5 · Cited by 56 · see citing works

Synaptically Activated Ca2+ Release From Internal Stores in CNS Neurons

Ross, W. N., Nakamura, T., Watanabe, S., Larkum, M. E., & Lasser‐Ross, N. (2005) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-005-3060-0 · Cited by 54 · see citing works

Weaker synaptic inhibition in CA1 region of ventral compared to dorsal rat hippocampal slices

Papatheodoropoulos, C., Asprodini, E. K., Nikita, I., Koutsona, C., & Kostopoulos, G. (2002) · Brain Research · doi:10.1016/s0006-8993(02)02958-x · Cited by 50 · see citing works

Activation of mGlu receptors induces LTD without affecting postsynaptic sensitivity of CA1 neurons in rat hippocampal slices

Rammes, G., Palmer, M. J., Eder, M., Dodt, H., Zieglgänsberger, W., & Collingridge, G. L. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.033514 · Cited by 49 · see citing works

Synchronous 20 Hz rhythmic activity in hippocampal networks induced by activation of metabotropic glutamate receptors in vitro.

Boddeke, H. W. G. M., Best, R., & Boeijinga, P. H. (1997) · PubMed · Cited by 40 · see citing works

Activation of metabotropic glutamate receptors induces gamma frequency oscillations in the rat dentate gyrus in vivo

Martin, S. J. (2001) · Neuropharmacology · doi:10.1016/s0028-3908(00)00190-8 · Cited by 17 · see citing works

Properties of long-term synaptic plasticity and metaplasticity in organotypic slice cultures of rat hippocampus

Mellentin, C., Møller, M., & Jahnsen, H. (2005) · Experimental Brain Research · doi:10.1007/s00221-005-0236-2 · Cited by 15 · see citing works

Effects of ventral hippocampal long-term potentiation and depression on the gamma-band local field potential in anesthetized rats

Izaki, Y., Takita, M., Nomura, M., & Akema, T. (2004) · Experimental Brain Research · doi:10.1007/s00221-004-1828-y · Cited by 8 · see citing works

Untitled work

(1998) · doi:10.1002/(sici)1098-1063(1998)8:6

Metaplasticity: tuning synapses and networks for plasticity

Abraham, W. C. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2356 · Cited by 1,119 · see citing works

Striking Variations in Corticosteroid Modulation of Long-Term Potentiation along the Septotemporal Axis of the Hippocampus

Maggio, N., & Segal, M. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.0155-07.2007 · Cited by 230 · see citing works

A ventral view on antidepressant action: roles for adult hippocampal neurogenesis along the dorsoventral axis

O’Leary, O. F., & Cryan, J. F. (2014) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2014.09.011 · Cited by 212 · see citing works

Differential environmental regulation of neurogenesis along the septo-temporal axis of the hippocampus

Tanti, A., Rainer, Q., Minier, F., Surget, A., & Belzung, C. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.04.022 · Cited by 161 · see citing works

Stress‐induced dynamic routing of hippocampal connectivity: A hypothesis

Segal, M., Richter‐Levin, G., & Maggio, N. (2010) · Hippocampus · doi:10.1002/hipo.20751 · Cited by 146 · see citing works

Are BDNF and glucocorticoid activities calibrated?

Jeanneteau, F. D., & Chao, M. V. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.09.017 · Cited by 141 · see citing works

Differential Corticosteroid Modulation of Inhibitory Synaptic Currents in the Dorsal and Ventral Hippocampus

Maggio, N., & Segal, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4399-08.2009 · Cited by 128 · see citing works

Mapping the electrophysiological and morphological properties of CA 1 pyramidal neurons along the longitudinal hippocampal axis

Malik, R., Dougherty, K. A., Parikh, K., Byrne, C. T., & Johnston, D. (2015) · Hippocampus · doi:10.1002/hipo.22526 · Cited by 119 · see citing works

Differential Modulation of Long-Term Depression by Acute Stress in the Rat Dorsal and Ventral Hippocampus

Maggio, N., & Segal, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1901-09.2009 · Cited by 119 · see citing works

Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress

Maras, P. M., Molet, J., Chen, Y., Rice, C., Ji, S. G., Solodkin, A., & Baram, T. Z. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.12 · Cited by 118 · see citing works

A role for the spine apparatus in LTP and spatial learning

Jedlička, P., Vlachos, A., Schwarzacher, S. W., & Deller, T. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.02.033 · Cited by 116 · see citing works

Electrophysiological Properties of CA1 Pyramidal Neurons along the Longitudinal Axis of the Mouse Hippocampus

Milior, G., Castro, M. A. D., Sciarria, L. P., Garofalo, S., Branchi, I., Ragozzino, D., Limatola, C., & Maggi, L. (2016) · Scientific Reports · doi:10.1038/srep38242 · Cited by 100 · see citing works

Behavioral profiling as a translational approach in an animal model of posttraumatic stress disorder.

Ardi, Z., Albrecht, A., Richter-Levin, A., Saha, R., & Richter-Levin, G. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.01.012 · Cited by 83 · see citing works

Dorsal and Ventral Hippocampus Differentiate in Functional Pathways and Differentially Associate with Neurological Disease-Related Genes during Postnatal Development

Lee, A.-R., Kim, J.-H., Cho, E., Kim, S., & Park, M. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00331 · Cited by 79 · see citing works

Differential expression of molecular markers of synaptic plasticity in the hippocampus, prefrontal cortex, and amygdala in response to spatial learning, predator exposure, and stress‐induced amnesia

Zoladz, P. R., Park, C. R., Halonen, J. D., Salim, S., Alzoubi, K. H., Srivareerat, M., Fleshner, M., Alkadhi, K. A., & Diamond, D. M. (2011) · Hippocampus · doi:10.1002/hipo.20922 · Cited by 79 · see citing works

Thrombin induces ischemic LTP (iLTP): implications for synaptic plasticity in the acute phase of ischemic stroke

Stein, E. S., Itsekson-Hayosh, Z., Aronovich, A., Reisner, Y., Bushi, D., Pick, C. G., Tanné, D., Chapman, J., Vlachos, A., & Maggio, N. (2015) · Scientific Reports · doi:10.1038/srep07912 · Cited by 76 · see citing works

The ventral hippocampus is necessary for expressing a spatial memory

Loureiro, M., Lecourtier, L., Engeln, M., Lopez, J., Cosquer, B., Geiger, K., Kelche, C. R., Cassel, J., & de Vasconcelos, A. P. (2011) · Brain Structure and Function · doi:10.1007/s00429-011-0332-y · Cited by 75 · see citing works

Persistent Changes in Ability to Express Long-Term Potentiation/Depression in the Rat Hippocampus After Juvenile/Adult Stress

Maggio, N., & Segal, M. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.11.026 · Cited by 72 · see citing works

Cellular, molecular, and genetic substrates underlying the impact of nicotine on learning

Gould, T. J., & Leach, P. T. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.08.004 · Cited by 68 · see citing works

Nicotinic receptors in the dorsal and ventral hippocampus differentially modulate contextual fear conditioning

Kenney, J. W., Raybuck, J. D., & Gould, T. J. (2012) · Hippocampus · doi:10.1002/hipo.22003 · Cited by 65 · see citing works

Tumor necrosis factor (TNF) modulates synaptic plasticity in a concentration-dependent manner through intracellular calcium stores

Maggio, N., & Vlachos, A. (2018) · Journal of Molecular Medicine · doi:10.1007/s00109-018-1674-1 · Cited by 65 · see citing works

Neurobiological consequences of juvenile stress: A GABAergic perspective on risk and resilience

Albrecht, A., Müller, I., Ardi, Z., Çalışkan, G., Gruber, D., Ivens, S., Segal, M., Behr, J., Heinemann, U., Stork, O., et al. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.01.005 · Cited by 63 · see citing works

Functional differentiation of adult-born neurons along the septotemporal axis of the dentate gyrus.Preprint

Wu, M. V., Sahay, A., Duman, R., & Hen, R. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a018978 · Cited by 56 · see citing works

Corticosteroid Regulation of Synaptic Plasticity in the Hippocampus

Maggio, N., & Segal, M. (2010) · The Scientific World JOURNAL · doi:10.1100/tsw.2010.48 · Cited by 58 · see citing works

Steroid modulation of hippocampal plasticity: switching between cognitive and emotional memories

Maggio, N., & Segal, M. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00012 · Cited by 60 · see citing works

Thrombin regulation of synaptic plasticity: Implications for physiology and pathology

Maggio, N., Itsekson, Z., Dominissini, D., Blatt, I., Amariglio, N., Rechavi, G., Tanné, D., & Chapman, J. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.02.011 · Cited by 60 · see citing works

Subchronic Peripheral Neuregulin-1 Increases Ventral Hippocampal Neurogenesis and Induces Antidepressant-Like Effects

Mahar, I., Tan, S., Davoli, M. A., Domínguez-López, S., Qiang, C., Rachalski, A., Turecki, G., & Mechawar, N. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026610 · Cited by 59 · see citing works

Dendritic GIRK Channels Gate the Integration Window, Plateau Potentials, and Induction of Synaptic Plasticity in Dorsal But Not Ventral CA1 Neurons

Malik, R., & Johnston, D. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2784-16.2017 · Cited by 60 · see citing works

Synaptic plasticity at the interface of health and disease: New insights on the role of endoplasmic reticulum intracellular calcium stores

Maggio, N., & Vlachos, A. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.09.041 · Cited by 57 · see citing works

Differential Regulation of NMDA Receptor-Mediated Transmission by SK Channels Underlies Dorsal-Ventral Differences in Dynamics of Schaffer Collateral Synaptic Function

Babiec, W. E., Jami, S. A., Guglietta, R., Chen, P. B., & O’Dell, T. J. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3196-16.2017 · Cited by 56 · see citing works

Differential lipid composition and regulation along the hippocampal longitudinal axis

Miranda, A. M., Bravo, F. V., Chan, R., Sousa, N., Paolo, G. D., & Oliveira, T. G. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0478-6 · Cited by 56 · see citing works

Less means more: The magnitude of synaptic plasticity along the hippocampal dorso‐ventral axis is inversely related to the expression levels of plasticity‐related neurotransmitter receptors

Dubovyk, V., & Manahan‐Vaughan, D. (2017) · Hippocampus · doi:10.1002/hipo.22816 · Cited by 55 · see citing works

Interplay of hippocampal long-term potentiation and long-term depression in enabling memory representations

Hagena, H., & Manahan‐Vaughan, D. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0229 · Cited by 54 · see citing works

Combined Fluoxetine and Metformin Treatment Potentiates Antidepressant Efficacy Increasing IGF2 Expression in the Dorsal Hippocampus

Poggini, S., Golia, M. T., Alboni, S., Milior, G., Sciarria, L. P., Viglione, A., Bon, G. M., Brunello, N., Puglisi‐Allegra, S., Limatola, C., et al. (2019) · Neural Plasticity · doi:10.1155/2019/4651031 · Cited by 50 · see citing works

Differential Dorso-ventral Distributions of Kv4.2 and HCN Proteins Confer Distinct Integrative Properties to Hippocampal CA1 Pyramidal Cell Distal Dendrites

Marcelin, B., Lugo, J. N., Brewster, A. L., Liu, Z., Lewis, A. S., McClelland, S., Chetkovich, D. M., Baram, T. Z., Anderson, A. E., Becker, A. J., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.c112.367110 · Cited by 49 · see citing works

Prolonged systemic inflammation persistently modifies synaptic plasticity in the hippocampus: modulation by the stress hormones

Maggio, N., Stein, E. S., Dori, A., Blatt, I., & Chapman, J. (2013) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2013.00046 · Cited by 48 · see citing works

Chronic Intermittent Ethanol Exposure Selectively Increases Synaptic Excitability in the Ventral Domain of the Rat Hippocampus

Ewin, S. E., Morgan, J. W., Niere, F., McMullen, N. P., Barth, S. H., Almonte, A. G., Raab‐Graham, K. F., & Weiner, J. L. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.11.028 · Cited by 45 · see citing works

Selective facilitation of LTP in the ventral hippocampus by calcium stores

Grigoryan, G., Korkotian, E., & Segal, M. (2012) · Hippocampus · doi:10.1002/hipo.22000 · Cited by 47 · see citing works

Juvenile stress alters LTP in ventral hippocampal slices: Involvement of noradrenergic mechanisms

Grigoryan, G., Ardi, Z., Albrecht, A., Richter‐Levin, G., & Segal, M. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.09.047 · Cited by 46 · see citing works

Differential activation of amygdala, dorsal and ventral hippocampus following an exposure to a reminder of underwater trauma

Ritov, G., Ardi, Z., & Richter‐Levin, G. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00018 · Cited by 44 · see citing works

Distinct Properties of Long-Term Potentiation in the Dentate Gyrus along the Dorsoventral Axis: Influence of Age and Inhibition

Schreurs, A., Sabanov, V., & Balschun, D. (2017) · Scientific Reports · doi:10.1038/s41598-017-05358-1 · Cited by 44 · see citing works

3D‐reconstruction and functional properties of GFP‐positive and GFP‐negative granule cells in the fascia dentata of the Thy1‐GFP mouse

Vukšić, M., Turco, D. D., Orth, C. B., Burbach, G. J., Feng, G., Müller, C. M., Schwarzacher, S. W., & Deller, T. (2008) · Hippocampus · doi:10.1002/hipo.20398 · Cited by 43 · see citing works

Hippocampal GABAergic interneurons and their co-localized neuropeptides in stress vulnerability and resilience

Albrecht, A., Redavide, E., Regev-Tsur, S., Stork, O., & Richter‐Levin, G. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.11.002 · Cited by 38 · see citing works

Cellular basis of a rapid effect of mineralocorticosteroid receptors activation on LTP in ventral hippocampal slices

Maggio, N., & Segal, M. (2010) · Hippocampus · doi:10.1002/hipo.20893 · Cited by 37 · see citing works

Transcriptome differentiation along the dorso–ventral axis in laser-captured microdissected rat hippocampal granular cell layer

Christensen, T. T., Bisgaard, C. F., Nielsen, H. B., & Wiborg, O. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.07.016 · Cited by 35 · see citing works

IgG accumulates in inhibitory hippocampal neurons of experimental antiphospholipid syndrome

Katzav, A., Menachem, A., Maggio, N., Pollak, L., Pick, C. G., & Chapman, J. (2014) · Journal of Autoimmunity · doi:10.1016/j.jaut.2014.07.006 · Cited by 33 · see citing works

A septo-temporal molecular gradient of sfrp3 in the dentate gyrus differentially regulates quiescent adult hippocampal neural stem cell activation

Sun, J., Bonaguidi, M. A., Jun, H., Guo, J. U., Sun, G. J., Will, B., Yang, Z., Jang, M., Song, H., Ming, G., et al. (2015) · Molecular Brain · doi:10.1186/s13041-015-0143-9 · Cited by 31 · see citing works

A Role for the Longitudinal Axis of the Hippocampus in Multiscale Representations of Large and Complex Spatial Environments and Mnemonic Hierarchies

Harland, B. C., Contreras, M., & Fellous, J. (2018) · InTech eBooks · doi:10.5772/intechopen.71165 · Cited by 28 · see citing works

Insulin differentially modulates GABA signalling in hippocampal neurons and, in an age‐dependent manner, normalizes GABA‐activated currents in the tg‐APPSwe mouse model of Alzheimer’s disease

Hammoud, H., Netsyk, O., Tafreshiha, A. S., Korol, S. V., Jin, Z., Li, J.-P., & Birnir, B. (2021) · Acta Physiologica · doi:10.1111/apha.13623 · Cited by 30 · see citing works

Activation of the CA2-ventral CA1 pathway reverses social discrimination dysfunction in Shank3B knockout mice

Cope, E. C., Wang, S. H., Waters, R. C., Gore, I. R., Vasquez, B., Laham, B. J., & Gould, E. (2023) · Nature Communications · doi:10.1038/s41467-023-37248-8 · Cited by 31 · see citing works

Lack of correlation between synaptopodin expression and the ability to induce LTP in the rat dorsal and ventral hippocampus

Vlachos, A., Maggio, N., & Segal, M. (2007) · Hippocampus · doi:10.1002/hipo.20373 · Cited by 30 · see citing works

Pilocarpine-Induced Status Epilepticus Is Associated with Changes in the Actin-Modulating Protein Synaptopodin and Alterations in Long-Term Potentiation in the Mouse Hippocampus

Lenz, M., Shimon, M. B., Deller, T., Vlachos, A., & Maggio, N. (2017) · Neural Plasticity · doi:10.1155/2017/2652560 · Cited by 29 · see citing works

Adenosine A1 and A2A receptors differently control synaptic plasticity in the mouse dorsal and ventral hippocampus

Reis, S. L., Silva, H. B. L., de Almeida, M. F., Cunha, R. A., Simões, A. P., & Canas, P. M. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14816 · Cited by 29 · see citing works

Enhanced ventral hippocampal synaptic transmission and impaired synaptic plasticity in a rodent model of alcohol addiction vulnerability

Almonte, A. G., Ewin, S. E., Mauterer, M. I., Morgan, J. W., Carter, E. S., & Weiner, J. L. (2017) · Scientific Reports · doi:10.1038/s41598-017-12531-z · Cited by 28 · see citing works

Increased thrombin activity following reperfusion after ischemic stroke alters synaptic transmission in the hippocampus

Bushi, D., Shimon, M. B., Stein, E. S., Chapman, J., Maggio, N., & Tanné, D. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13372 · Cited by 27 · see citing works

Ischemic LTP : NMDA ‐dependency and dorso/ventral distribution within the hippocampus

Maggio, N., Stein, E. S., & Segal, M. (2015) · Hippocampus · doi:10.1002/hipo.22467 · Cited by 26 · see citing works

Differential ability of the dorsal and ventral rat hippocampus to exhibit group I metabotropic glutamate receptor–dependent synaptic and intrinsic plasticity

Tidball, P., Burn, H. V., Teh, K. L., Volianskis, A., Collingridge, G. L., & Fitzjohn, S. M. (2017) · Brain and Neuroscience Advances · doi:10.1177/2398212816689792 · Cited by 25 · see citing works

D-type potassium channels normalize action potential firing between dorsal and ventral CA1 neurons of the mouse hippocampus

Ordemann, G. J., Apgar, C. J., & Brager, D. H. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00737.2018 · Cited by 25 · see citing works

A Novel and Selective Dopamine Transporter Inhibitor, (S)-MK-26, Promotes Hippocampal Synaptic Plasticity and Restores Effort-Related Motivational Dysfunctions

Kouhnavardi, S., Ecevitoglu, A., Dragačević, V., Sanna, F., Arias‐Sandoval, E., Kalaba, P., Kirchhofer, M., Lubec, J., Niello, M., Holy, M., et al. (2022) · Biomolecules · doi:10.3390/biom12070881 · Cited by 24 · see citing works

NMDA receptor-dependent synaptic plasticity in dorsal and intermediate hippocampus exhibits distinct frequency-dependent profiles

Kenney, J., & Manahan‐Vaughan, D. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.02.017 · Cited by 23 · see citing works

Repeated cocaine enhances ventral hippocampal‐stimulated dopamine efflux in the nucleus accumbens and alters ventral hippocampal NMDA receptor subunit expression

Barr, J. L., Forster, G. L., & Unterwald, E. M. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12764 · Cited by 23 · see citing works

Inhibition of endoplasmic reticulum Ca2+ ATPase in preBötzinger complex of neonatal rat does not affect respiratory rhythm generation

Beltrán‐Parrazal, L., Fernández-Ruíz, J., Toledo‐Cárdenas, M. R., Manzo, J. G., & Morgado‐Valle, C. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.08.016 · Cited by 22 · see citing works

Major dorsoventral differences in the modulation of the local CA1 hippocampal network by NMDA, mGlu5, adenosine A2A and cannabinoid CB1 receptors.

Kouvaros, S., & Papatheodoropoulos, C. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2015.12.059 · Cited by 24 · see citing works

Cannabidiol Regulates Long Term Potentiation Following Status Epilepticus: Mediation by Calcium Stores and Serotonin

Maggio, N., Stein, E. S., & Segal, M. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00032 · Cited by 21 · see citing works

Ryanodine-mediated conversion of STP to LTP is lacking in synaptopodin-deficient mice

Grigoryan, G., & Segal, M. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1026-7 · Cited by 20 · see citing works

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 18 · see citing works

GluN3A and Excitatory Glycine Receptors in the Adult Hippocampus

Hurley, E. P., Mukherjee, B., Fang, L. Z., Barnes, J. R., Barron, J. C., Nafar, F., Hirasawa, M., & Parsons, M. P. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0401-24.2024 · Cited by 19 · see citing works

Effects of a True Prophylactic Treatment on Hippocampal and Amygdala Synaptic Plasticity and Gene Expression in a Rodent Chronic Stress Model of Social Defeat

Winzenried, E. T., Everett, A. C., Saito, E. R., Miller, R. M., Johnson, T., Neal, E., Boyce, Z., Smith, C., Jensen, C., Kimball, S., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241311193 · Cited by 19 · see citing works

Tonic GABA ‐activated synaptic and extrasynaptic currents in dentate gyrus granule cells and CA3 pyramidal neurons along the mouse hippocampal dorsoventral axis

Netsyk, O., Hammoud, H., Korol, S. V., Jin, Z., Tafreshiha, A. S., & Birnir, B. (2020) · Hippocampus · doi:10.1002/hipo.23245 · Cited by 15 · see citing works

Protease Activated Receptor 2 (PAR2) Induces Long-Term Depression in the Hippocampus through Transient Receptor Potential Vanilloid 4 (TRPV4)

Stein, E. S., Artan-Furman, A., Feingold, E., Shimon, M. B., Itzekson-Hayosh, Z., Chapman, J., Vlachos, A., & Maggio, N. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00042 · Cited by 15 · see citing works

Recording Field Potentials and Synaptic Plasticity From Freely Behaving Rodents

Manahan‐Vaughan, D. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812028-6.00001-x · Cited by 14 · see citing works

Differential developmental refinement of the intrinsic electrophysiological properties of CA1 pyramidal neurons from the rat dorsal and ventral hippocampus

Dougherty, K. A. (2019) · Hippocampus · doi:10.1002/hipo.23152 · Cited by 14 · see citing works

Expression of p53 Target Genes in the Early Phase of Long-Term Potentiation in the Rat Hippocampal CA1 Area

Pustylnyak, V. O., Lisachev, P. D., & Shtark, M. B. (2015) · Neural Plasticity · doi:10.1155/2015/242158 · Cited by 12 · see citing works

False Opposing Fear Memories Are Produced as a Function of the Hippocampal Sector Where Glucocorticoid Receptors Are Activated

Kaouane, N., Ducourneau, E., Marighetto, A., Segal, M., & Desmedt, A. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.00144 · Cited by 9 · see citing works

Excitatory glycine receptors control ventral hippocampus synaptic plasticity and anxiety-related behaviors

Pizzamiglio, L., Morice, É., Cardoso, C., Bossi, S., Mailhes‐Hamon, C., von Heimendahl, M., Girardeau, G., & Paoletti, P. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2501118122 · Cited by 8 · see citing works

Prolonged Systemic Inflammation Alters Muscarinic Long-Term Potentiation (mLTP) in the Hippocampus

Stein, E. S., Dori, A., Shimon, M. B., Gofrit, S. G., & Maggio, N. (2021) · Neural Plasticity · doi:10.1155/2021/8813734 · Cited by 7 · see citing works

miRNA-132/212 Deficiency Disrupts Selective Corticosterone Modulation of Dorsal vs. Ventral Hippocampal Metaplasticity

Kouhnavardi, S., Cabatic, M., Mañas‐Padilla, M. C., Malabanan, M.-A., Smani, T., Cicvaric, A., Aranzalez, E. M., Koenig, X., Urban, E., Lübec, G., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119565 · Cited by 8 · see citing works

Increased Inhibition May Contribute to Maintaining Normal Network Function in the Ventral Hippocampus of a Fmr1-Targeted Transgenic Rat Model of Fragile X Syndrome

Leontiadis, L. J., Trompoukis, G., Felemegkas, P., Tsotsokou, G., Miliou, A., & Papatheodoropoulos, C. (2023) · Brain Sciences · doi:10.3390/brainsci13111598 · Cited by 6 · see citing works

Noncanonical, Dopamine-Dependent Long-Term Potentiation at Hippocampal Output Synapses in a Rodent Model of First-Episode Psychosis

Bartsch, J., & Behr, J. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00055 · Cited by 6 · see citing works

Female mice exhibit similar long-term plasticity and microglial properties between the dorsal and ventral hippocampal poles

Felice, E. D., Bobotis, B. C., Rigillo, G., Khakpour, M., de Andrade, E. G., Benatti, C., Vilella, A., Tascedda, F., Limatola, C., Tremblay, M., et al. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.11.034 · Cited by 5 · 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

Hippocampal Synaptic Plasticity: Integrating Memory and Anxiety Impairments in the Early Stages of Alzheimer’s Disease

Good, M. A., & Bannerman, D. M. (2024) · Current topics in behavioral neurosciences · doi:10.1007/7854_2024_565 · Cited by 4 · see citing works

Electrophysiological Investigation of Metabotropic Glutamate Receptor-Dependent Metaplasticity in the Hippocampus

Hegemann, R. U., & Abraham, W. C. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9077-1_7 · Cited by 4 · see citing works

Incremental induction of NMDAR-STP and NMDAR-LTP in the CA1 area of ventral hippocampal slices relies on graded activation of discrete NMDA receptors

Ingram, R., Volianskis, R., Georgiou, J., Jane, D. E., Michael-Titus, A. T., Collingridge, G. L., & Volianskis, A. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0239 · Cited by 3 · see citing works

Effects of Stress Factors on the Functioning of the Adult Hippocampus: Molecular-Cellular Mechanisms and the Dorsoventral Gradient

Gulyaeva, N. V. (2014) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-014-0012-5 · Cited by 3 · see citing works

Association of connexin36 with adherens junctions at mixed synapses and distinguishing electrophysiological features of those at mossy fiber terminals in rat ventral hippocampus

Thomas, D. (2024) · International Journal of Physiology Pathophysiology and Pharmacology · doi:10.62347/rtmh4490 · Cited by 2 · see citing works

Practical Considerations for In Vivo Electrophysiology Along the Dorsoventral Hippocampal Axis

Leasure, J. L., Triviño-Paredes, J., & Christie, B. R. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812028-6.00004-5 · Cited by 2 · see citing works

Comparing the synaptic potentiation in schaffer collateral-CA1 synapses in dorsal and intermediate regions of the hippocampus in normal and kindled rats

Sharifi, M., Oryan, S., Komaki‬, A., Barkley, V., Sarihi, A., & Mirnajafi‐Zadeh, J. (2023) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2023.09.010 · Cited by 1 · see citing works

Stress Modulation of Synaptic Plasticity in the Hippocampus

Segal, M., & Maggio, N. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1056-4_8

Brain circuit dynamics related to extremes in trait anxiety in mice

Avrabos, C. (2012) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.14994

Stress, Corticosteroids and Excitatory Neurotransmission

Groc, L., & Chaouloff, F. (2008) · Future Neurology · doi:10.2217/14796708.3.6.623

METAPLASTICITY IN A MOUSE MODEL OF ALZHEIMER’S DISEASE AND POSSIBLE THERAPEUTIC INTERVENTIONS

Megill, A. (2014)

Faculty Opinions recommendation of Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress.

Sandi, C. (2014) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718297966.793492714

Peer Review #1 of "CA1 pyramidal cells have diverse biophysical properties, affected by development, experience, and aging (v0.1)"

(2017) · PeerJ · doi:10.7287/peerj.3836v0.1/reviews/1

Peer Review #2 of "CA1 pyramidal cells have diverse biophysical properties, affected by development, experience, and aging (v0.1)"

(2017) · PeerJ · doi:10.7287/peerj.3836v0.1/reviews/2

Peer Review #2 of "CA1 pyramidal cells have diverse biophysical properties, affected by development, experience, and aging (v0.2)"

(2017) · PeerJ · doi:10.7287/peerj.3836v0.2/reviews/2

Transcriptomic analysis of PER and LEC regions in micePreprint

Aoyama, B. B., Lindo-Samanamud, S., Machado, J. P. D., de Araújo, H. N., Athie, M. C. P., & Vieira, A. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.18.643907

A Time-Sensitive Plasticity Distinguishes the Rapid and Sustained Synaptic Actions of Ketamine from Its (2 R ,6 R )-Hydroxynorketamine Metabolite

Brown, K. A., Morris, P. J., Thomas, C. J., & Gould, T. D. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.0958-25.2026 · Cited by 1 · see citing works

Mémoire émotionnelle normale et pathologique : implication des glucocorticoïdes intra-hippocampiques

Kaouane, N. (2010) · doi:10.70675/88cd8717zf87cz49ebz8438z628e6365997a

The how and why for multiple forms of hippocampal LTP

Gall, C. M., Le, A. A., & LYNCH, G. S. (2026) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2026.1855059

M (2007) Unique regulation of long term potentiation in the rat ventral hippocampus

Maggio, N., & Segal, M. (2014)

Long-term potentiation varies along the dorso-ventral axis in the mouse hippocampus

An, S., & Balschun, D. (2015) · Frontiers in Neuroscience · doi:10.3389/conf.fnins.2015.89.00075

High-frequency stimulation-induced synaptic potentiation in dorsal and ventral CA1 hippocampal synapses: the involvement of NMDA receptors, mGluR5, and (L-type) voltage-gated calcium channelsPreprint

Papatheodoropoulos, C., & Kouvaros, S. (2016) · Learning & Memory · doi:10.1101/lm.042531.116 · Cited by 17 · see citing works

Decreased ability of rat temporal hippocampal CA1 region to produce long-term potentiation

Papatheodoropoulos, C., & Kostopoulos, G. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(99)01002-2 · Cited by 123 · see citing works

Differential ability of the dorsal and ventral rat hippocampus to exhibit group I metabotropic glutamate receptor–dependent synaptic and intrinsic plasticity

Tidball, P., Burn, H. V., Teh, K. L., Volianskis, A., Collingridge, G. L., & Fitzjohn, S. M. (2017) · Brain and Neuroscience Advances · doi:10.1177/2398212816689792 · Cited by 25 · see citing works