The ventral hippocampus and the lateral septum work in tandem to regulate rats' open-arm exploration in the elevated plus-maze
Abstract
Lesions or pharmacological inhibition of the ventral hippocampus or the lateral septum suppress rats' defensive responses in various rat models of anxiety. Although these two structures are extensively connected, it was not clear whether they regulate anxiety in a parallel (independent) or serial (integrated) fashion. In Experiment 1, bilateral infusions of the GABA-A receptor agonist muscimol (5 ng/side) into the lateral septum increased rats' open-arm exploration in the elevated plus-maze test, whereas unilateral infusions of muscimol did not. Similar anxiolytic-like effects were observed in Experiment 2, following bilateral infusions of muscimol (500 ng/side) into the ventral hippocampus. In Experiment 3, we confirmed that unilateral infusions of muscimol into either the lateral septum (5 ng) or the ventral hippocampus (500 ng) did not alter rats' normal open-arm avoidance. Importantly, dramatic increases in open-arm exploration were evident when muscimol was co-infused into one side of the lateral septum (5 ng) and the contralateral ventral hippocampus (500 ng). By contrast, open-arm exploration was not altered when these same doses of muscimol were co-infused into one side of the lateral septum and the ipsilateral ventral hippocampus. These results support the contention that the ventral hippocampus and the lateral septum regulate rats' open-arm exploration in a serial fashion, and that this involves ipsilateral projections from the former to the latter site.
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Ipsilateral projections from vHPC to lateral septum convey an anxiety signal; bilateral blockade of activity in either structure using muscimol increases open-arm exploration in the EPM, as does disconnection of the two using pharmacological inactivation of vHPC in one hemisphere and concurrent inactivation of the contralateral lateral septum.
“Ipsilateral projections from vHPC to lateral septum convey an anxiety signal; bilateral blockade of activity in either structure using muscimol increases open-arm exploration in the EPM, as does disconnection of the two using pharmacological inactivation of vHPC in one hemisphere and concurrent inactivation of the contralateral lateral septum95.”
From Resolving the neural circuits of anxiety (2015) · cites this paper as [95]
Cites
The rat brain in stereotaxic coordinates
Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959 · see citing works
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
Validation of open:closed arm entries in an elevated plus-maze as a measure of anxiety in the rat
Pellow, S., Chopin, P., File, S. E., & Briley, M. (1985) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(85)90031-7 · Cited by 5,822 · see citing works
Gray, J. A. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00013066 · Cited by 4,477 · see citing works
The Neuropsychology of Anxiety
Gray, J. A., & McNaughton, N. (2003) · doi:10.1093/acprof:oso/9780198522713.001.0001 · Cited by 1,933 · see citing works
Genetics of Mouse Behavior: Interactions with Laboratory Environment
Crabbe, J. C., Wahlsten, D., & Dudek, B. C. (1999) · Science · doi:10.1126/science.284.5420.1670 · Cited by 1,666 · 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
GABAA receptors: immunocytochemical distribution of 13 subunits in the adult rat brain
Pirker, S., Schwarzer, C., Wieselthaler, A., Sieghart, W., & Sperk, G. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00442-5 · Cited by 1,344 · see citing works
Opioid-receptor mRNA expression in the rat CNS: anatomical and functional implications
Mansour, A., Fox, C. A., Akil, H., & Watson, S. J. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93946-u · Cited by 1,297 · see citing works
Ethological and temporal analyses of anxiety-like behavior: The elevated plus-maze model 20 years on
Carobrez, A. P., & Bertoglio, L. J. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.04.017 · Cited by 993 · 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
Rodgers, R. J., & Johnson, N. J. (1995) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(95)00138-m · Cited by 793 · see citing works
Connections of the rat lateral septal complex 1Published on the World Wide Web on 2 June 1997. 1
Risold, P. Y., & Swanson, L. W. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00009-x · Cited by 671 · see citing works
Anxiogenic stimuli in the elevated plus-maze
Treit, D., Menard, J., & Royan, C. (1993) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(93)90492-c · Cited by 628 · see citing works
Self-citationVentral hippocampal lesions affect anxiety but not spatial learning
Bannerman, D. M., Grubb, M., Deacon, R. M. J., Yee, B. K., Feldon, J., & Rawlins, J. N. P. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00268-1 · Cited by 530 · see citing works
Regulation of affect by the lateral septum: implications for neuropsychiatry
Sheehan, T. P., Chambers, R. A., & Russell, D. S. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.04.009 · Cited by 514 · see citing works
The medial hypothalamic defensive system: Hodological organization and functional implications
Canteras, N. S. (2002) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(01)00685-2 · Cited by 463 · see citing works
The neuropsychology of anxiety
LADER, M. H. (1983) · Personality and Individual Differences · doi:10.1016/0191-8869(83)90137-x · Cited by 418 · see citing works
Double dissociation of function within the hippocampus: Spatial memory and hyponeophagia.
Bannerman, D. M., Deacon, R. M. J., Offen, S., Friswell, J., Grubb, M. S., & Rawlins, J. N. P. (2002) · Behavioral Neuroscience · doi:10.1037//0735-7044.116.5.884 · Cited by 357 · see citing works
Double dissociation of function within the hippocampus: Spatial memory and hyponeophagia.
Bannerman, D. M., Deacon, R. M. J., Offen, S., Friswell, J., Grubb, M., & Rawlins, J. N. P. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.5.884 · Cited by 357 · see citing works
Rodent foraging is affected by indirect, but not by direct, cues of predation risk
Orrock, J. L. (2004) · Behavioral Ecology · doi:10.1093/beheco/arh031 · Cited by 352 · see citing works
Neuroanatomical characterization of Fos induction in rat behavioral models of anxiety
Duncan, G. E., Knapp, D. J., & Breese, G. R. (1996) · Brain Research · doi:10.1016/0006-8993(95)01486-1 · Cited by 326 · see citing works
Severe Reduction of Rat Defensive Behavior to a Predator by Discrete Hypothalamic Chemical Lesions
Canteras, N. S., Chiavegatto, S., do Valle, L. E. R., & Swanson, L. W. (1997) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00141-x · Cited by 274 · see citing works
Maren, S., & Holt, W. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.97 · Cited by 272 · see citing works
The role of hippocampus in anxiety: intracerebral infusion studies
Engin, E., & Treit, D. (2007) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e3282de7929 · Cited by 267 · see citing works
Effects of lesions to the dorsal and ventral hippocampus on defensive behaviors in rats
Pentkowski, N. S., Blanchard, D. C., Lever, C., Litvin, Y., & Blanchard, R. J. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04754.x · Cited by 244 · see citing works
McGregor, I. S., Hargreaves, G. A., Apfelbach, R., & Hunt, G. E. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0187-04.2004 · Cited by 231 · see citing works
Motta, S. C., Goto, M., Gouveia, F. V., Baldo, M. V. C., Canteras, N. S., & Swanson, L. W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900939106 · Cited by 209 · see citing works
The ventral hippocampus and fear conditioning in rats
Bast, T., Zhang, W., & Feldon, J. (2001) · Experimental Brain Research · doi:10.1007/s002210100746 · Cited by 197 · see citing works
Blanchard, D. C., Canteras, N. S., Markham, C. M., Pentkowski, N. S., & Blanchard, R. J. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.04.019 · Cited by 179 · see citing works
Trivedi, M. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.02.005 · Cited by 179 · see citing works
GABAergic influences on plus-maze behaviour in mice
Dalvi, A., & Rodgers, R. J. (1996) · Psychopharmacology · doi:10.1007/s002130050148 · Cited by 170 · see citing works
Behavior of hippocampal lesioned rats in home cage and novel situations
Jarrard, L. E. (1968) · Physiology & Behavior · doi:10.1016/0031-9384(68)90033-4 · Cited by 157 · 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 · see citing works
Preoptic and hypothalamic neurons and the initiation of locomotion in the anesthetized rat
Sinnamon, H. M. (1993) · Progress in Neurobiology · doi:10.1016/0301-0082(93)90003-b · Cited by 150 · see citing works
Rudy, J. W., & Matus-Amat, P. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.1.154 · Cited by 147 · see citing works
Lateral and Medial Septal Lesions Reduce Anxiety in the Plus-Maze and Probe-Burying Tests
Menard, J. L., & Treit, D. (1996) · Physiology & Behavior · doi:10.1016/0031-9384(96)00138-2 · Cited by 140 · see citing works
Self-citationBitran, D., Dugan, M., Renda, P., Ellis, R. C., & Foley, M. (1999) · Brain Research · doi:10.1016/s0006-8993(99)02150-2 · Cited by 132 · see citing works
Hippocampal lesions in rats and their effect on activity, avoidance, and aggression.
Blanchard, R. J., Blanchard, D. C., & Fial, R. A. (1970) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0028958 · Cited by 130 · see citing works
Effects of hippocampal lesions on the rat's reaction to a cat.
Blanchard, R. J., & Blanchard, D. C. (1972) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0032176 · Cited by 128 · see citing works
Lammers, J. H. C. M., Kruk, M. R., Meelis, W., & van der Poel, A. M. (1988) · Brain Research · doi:10.1016/0006-8993(88)91045-1 · Cited by 121 · see citing works
Degroot, A., Kashluba, S., & Treit, D. (2001) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(01)00541-x · Cited by 109 · see citing works
Pesold, C., & Treit, D. (1992) · Physiology & Behavior · doi:10.1016/0031-9384(92)90431-z · Cited by 106 · see citing works
Blanchard, D. C., Li, C. I., Hubbard, D. T., Markham, C. M., Yang, M., Takahashi, L. K., & Blanchard, R. J. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00415-4 · Cited by 101 · see citing works
Medial Septal Lesions Mimic Effects of Both Selective Dorsal and Ventral Hippocampal Lesions.
Bannerman, D. M., Matthews, P. M., Deacon, R. M. J., & Rawlins, J. N. P. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.5.1033 · Cited by 98 · see citing works
Engin, E., & Treit, D. (2008) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2008.03.020 · Cited by 90 · see citing works
Bakshi, V. P., Newman, S. M., Smith‐Roe, S. L., Jochman, K. A., & Kalin, N. H. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3044-06.2007 · Cited by 86 · see citing works
Canteras, N. S., Ribeiro-Barbosa, É. R., & Comoli, E. (2001) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(01)00048-3 · Cited by 86 · see citing works
γ‐Aminobutyric acid and inhibition in the septal nuclei of the rat
McLennan, H., & Miller, J. J. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010501 · Cited by 85 · see citing works
The neuroanatomical specificity of the anxiolytic effects ofintra-septal infusions of midazolam
Pesold, C., & Treit, D. (1996) · Brain Research · doi:10.1016/0006-8993(95)01359-8 · Cited by 84 · see citing works
Rezayat, M., Roohbakhsh, A., Zarrindast, M.-R., Massoudi, R., & Djahanguiri, B. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.03.002 · Cited by 82 · see citing works
Septal lesions inhibit fear reactions in two animal models of anxiolytic drug action
Treit, D., & Pesold, C. (1990) · Physiology & Behavior · doi:10.1016/0031-9384(90)90155-w · Cited by 79 · see citing works
Häckl, L. P. N., & Carobrez, A. P. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.04.007 · Cited by 73 · see citing works
The anxiolytic effects of intra-hippocampal midazolam are antagonized by intra-septal l-glutamate
Menard, J. L., & Treit, D. (2001) · Brain Research · doi:10.1016/s0006-8993(00)03046-8 · Cited by 73 · see citing works
Self-citationModulation of predatory odor processing following lesions to the dorsal premammillary nucleus
Markham, C. M., Blanchard, D. C., Canteras, N. S., Cuyno, C. D., & Blanchard, R. J. (2004) · Neuroscience Letters · doi:10.1016/j.neulet.2004.09.006 · Cited by 64 · see citing works
Effects of intra-hippocampal infusion of WAY-100635 on plus-maze behavior in mice
Nunes‐de‐Souza, R. L., Canto‐de‐Souza, A., & Rodgers, R. J. (2002) · Brain Research · doi:10.1016/s0006-8993(01)03335-2 · Cited by 56 · see citing works
Jones, M. E., & Dayan, T. (2000) · Journal of Chemical Ecology · doi:10.1023/a:1005417707588 · Cited by 56 · see citing works
Modulation of anxiety by μ-opioid receptors of the lateral septal region in mice
Merrer, J. L., Cagniard, B., & Cazala, P. (2006) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2006.03.008 · Cited by 46 · see citing works
Low doses of muscimol produce anticonflict actions in the lateral septum of the rat
Drugan, R. C., Skolnick, P., Paul, S. M., & CRAWLEY, J. (1986) · Neuropharmacology · doi:10.1016/0028-3908(86)90042-0 · Cited by 45 · see citing works
Parada, M. A., Hernandez, L., de Parada, M. P., Páez, X., & Hoebel, B. G. (1990) · Brain Research Bulletin · doi:10.1016/0361-9230(90)90195-6 · Cited by 41 · see citing works
French, E. D., & Siggins, G. R. (1980) · Regulatory Peptides · doi:10.1016/0167-0115(80)90016-6 · Cited by 41 · see citing works
Schwerdtfeger, R. M. H., & Menard, J. L. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.11.011 · Cited by 39 · see citing works
Self-citationThe role of the dorsal and ventral hippocampus in fear and memory of a shock-probe experience
McEown, K., & Treit, D. (2008) · Brain Research · doi:10.1016/j.brainres.2008.11.041 · Cited by 39 · see citing works
Pentkowski, N. S., Litvin, Y., Blanchard, D. C., Vasconcellos, A., King, L. B., & Blanchard, R. J. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.02.007 · Cited by 34 · see citing works
Effects of lateral and medial septal lesions on exploratory behavior in the albino rat
̈hler, C. K., & Srebro, B. (1980) · Brain Research · doi:10.1016/0006-8993(80)91199-3 · Cited by 33 · see citing works
Engin, E., & Treit, D. (2008) · Neuropeptides · doi:10.1016/j.npep.2008.04.004 · Cited by 32 · see citing works
de Carvalho, M. C., Masson, S., Brandão, M. L., & Silva, M. A. D. S. (2008) · Peptides · doi:10.1016/j.peptides.2008.02.014 · Cited by 27 · see citing works
Inactivation of the lateral septum blocks fox odor-induced fear behavior
Endres, T., & Fendt, M. (2008) · Neuroreport · doi:10.1097/wnr.0b013e3282fb78d9 · Cited by 25 · see citing works
Improvement of shuttle-box performance by anterodorsal medial septal lesions in rats
Torras-García, M., Costa‐Miserachs, D., Morgado-Bernal, I., & Portell-Cortés, I. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00346-7 · Cited by 25 · see citing works
Dopamine–Acetylcholine Interaction in the Rat Lateral Hypothalamus in the Control of Locomotion
de Parada, M. P., Parada, M. A., Rada, P. V., Hernandez, L., & Hoebel, B. G. (2000) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(99)00244-0 · Cited by 18 · see citing works
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Resolving the neural circuits of anxiety
Calhoon, G. G., & Tye, K. M. (2015) · Nature Neuroscience · doi:10.1038/nn.4101 · Cited by 766 · see citing works
Neuromodulation by Oxytocin and Vasopressin
Stoop, R. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.025 · Cited by 506 · see citing works
Tests of unconditioned anxiety — Pitfalls and disappointments
Ennaceur, A. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.05.032 · Cited by 265 · see citing works
Parfitt, G. M., Nguyen, R., Bang, J. Y., Aqrabawi, A. J., Tran, M. M., Seo, D. K., Richards, B. A., & Kim, J. C. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.56 · Cited by 229 · see citing works
The microbiome regulates amygdala-dependent fear recall
Hoban, A. E., Stilling, R. M., Moloney, G., Shanahan, F., Dinan, T. G., Clarke, G., & Cryan, J. F. (2018) · Molecular Psychiatry · doi:10.1038/mp.2017.100 · Cited by 197 · see citing works
Pentkowski, N. S., Rogge-Obando, K., Donaldson, T. N., Bouquin, S. J., & Clark, B. J. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.05.005 · Cited by 169 · see citing works
Hippocampus: Molecular, Cellular, and Circuit Features in Anxiety
Shi, H., Wang, S., Wang, X., Zhang, R.-X., & Zhu, L. (2023) · Neuroscience Bulletin · doi:10.1007/s12264-023-01020-1 · Cited by 151 · see citing works
Lateral septum as a nexus for mood, motivation, and movement
Wirtshafter, H. S., & Wilson, M. A. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.03.029 · Cited by 122 · see citing works
Lateral septum-lateral hypothalamus circuit dysfunction in comorbid pain and anxiety
Wang, D., Pan, X., Zhou, Y., Wu, Z., Ren, K., Liu, H., Huang, C., Yu, Y., He, T., Zhang, X., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-022-01922-y · Cited by 117 · see citing works
Septo-hippocampo-septal loop and memory formation.
Khakpai, F., Nasehi, M. M., Haeri-Rohani, A., Eidi, A., & Zarrindast, M. (2013) · Europe PMC (PubMed Central) · Cited by 105 · see citing works
Anxiety and Nicotine Dependence: Emerging Role of the Habenulo-Interpeduncular Axis
Molas, S., DeGroot, S. R., Zhao-Shea, R., & Tapper, A. R. (2016) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2016.11.001 · Cited by 100 · see citing works
Vasciaveo, V., Iadarola, A., Casile, A., Dante, D., Morello, G., Minotta, L., Tamagno, E., Cicolin, A., & Guglielmotto, M. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-022-01498-2 · Cited by 96 · see citing works
Neuronal Responses to Conspecifics in the Ventral CA1
Rao, R. P., von Heimendahl, M., Bahr, V., & Brecht, M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.05.081 · Cited by 85 · see citing works
Current Understanding of the Neural Circuitry in the Comorbidity of Chronic Pain and Anxiety
Chen, T., Wang, J., Wang, Y.-Q., & Chu, Y. (2022) · Neural Plasticity · doi:10.1155/2022/4217593 · Cited by 80 · see citing works
Hunsaker, M. R., & Kesner, R. P. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.11.012 · Cited by 68 · 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
Locomotor and Hippocampal Processing Converge in the Lateral Septum
Wirtshafter, H. S., & Wilson, M. A. (2019) · Current Biology · doi:10.1016/j.cub.2019.07.089 · Cited by 65 · see citing works
Sampedro‐Piquero, P., Begega, A., & Arias, J. L. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.02.048 · Cited by 59 · see citing works
Wang, D., Guo, Q., Zhou, Y., Xu, Z., Hu, S.-W., Kong, X.-X., Yu, Y., Yang, J., Zhang, H., Ding, H., et al. (2021) · Anesthesiology · doi:10.1097/aln.0000000000003868 · Cited by 56 · see citing works
Dissecting the Function of Hippocampal Oscillations in a Human Anxiety Model
Khemka, S., Barnes, G. R., Dolan, R. J., & Bach, D. R. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1834-16.2017 · Cited by 53 · see citing works
Ventral hippocampus-lateral septum circuitry promotes foraging-related memory
Décarie-Spain, L., Liu, C. M., Lauer, L. T., Subramanian, K. S., Bashaw, A. G., Klug, M. E., Gianatiempo, I. H., Suarez, A. N., Noble, E. E., Donohue, K. N., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111402 · Cited by 45 · see citing works
Prenatal stress-induced programming of genome-wide promoter DNA methylation in 5-HTT-deficient mice
Schraut, K., Jakob, S., Weidner, M. T., Schmitt, A. G., Scholz, C. J., Strekalova, T. V., Hajj, N. E., Eijssen, L., Domschke, K., Reif, A., et al. (2014) · Translational Psychiatry · doi:10.1038/tp.2014.107 · Cited by 45 · see citing works
Social status alters defeat-induced neural activation in Syrian hamsters
Morrison, K. E., Curry, D. W., & Cooper, M. A. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.03.002 · Cited by 44 · see citing works
Interdependence between dorsal and ventral hippocampus during spatial navigation
Lee, S. L. T., Lew, D., Wickenheisser, V. A., & Markus, E. J. (2019) · Brain and Behavior · doi:10.1002/brb3.1410 · Cited by 41 · see citing works
Faure, J., Akimana, G., da Silva, J. E. M. C., Cosquer, B., Ferrandon, A., Geiger, K., Koning, E., Penazzi, L., Cassel, J., & Nehlig, A. (2013) · Epilepsia · doi:10.1111/epi.12219 · Cited by 42 · see citing works
Yeates, D. C. M., Leavitt, D., Sujanthan, S., Khan, N., Alushaj, D., Lee, A. C. H., & Ito, R. (2022) · Nature Communications · doi:10.1038/s41467-022-31082-0 · Cited by 39 · see citing works
Wang, D., Wang, W., Jiang, S., Ma, H., Lian, H., Meng, F., Liu, J., Cui, M., You, J., Liu, C., et al. (2021) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2021.02.043 · Cited by 36 · see citing works
DeVuono, M. V., Nashed, M. G., Sarikahya, M. H., Kocsis, A., Lee, K., Vanin, S., Hudson, R., Lonnee, E. P., Rushlow, W. J., Hardy, D. B., et al. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106588 · Cited by 34 · see citing works
Shoji, H., Ikeda, K., & Miyakawa, T. (2023) · Molecular Brain · doi:10.1186/s13041-023-01020-2 · Cited by 34 · see citing works
Jiang, J., Liu, H., Huang, Z., Cui, Y., Zhang, X., Zhang, X., Cui, Y., & Xin, W. (2016) · Addiction Biology · doi:10.1111/adb.12468 · Cited by 33 · see citing works
Infusions of neuropeptide Y into the lateral septum reduce anxiety-related behaviors in the rat
Trent, N. L., & Menard, J. L. (2011) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.06.009 · Cited by 32 · see citing works
Self-citationThe lateral septum as a regulator of hippocampal theta oscillations and defensive behavior in rats
Chee, S. A., Menard, J. L., & Dringenberg, H. C. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00806.2014 · Cited by 31 · see citing works
Self-citationVahid-Ansari, F., & Albert, P. R. (2017) · Neurotherapeutics · doi:10.1007/s13311-017-0590-3 · Cited by 30 · see citing works
Stubbendorff, C., Hale, E., Cassaday, H. J., Bast, T., & Stevenson, C. W. (2019) · Psychopharmacology · doi:10.1007/s00213-018-5162-7 · Cited by 30 · see citing works
van der Veldt, S., Etter, G., Mosser, C., Manseau, F., & Williams, S. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001383 · Cited by 32 · see citing works
Troyano‐Rodriguez, E., Wirsig‐Wiechmann, C. R., & Ahmad, M. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.01.022 · Cited by 29 · see citing works
Pattern of forebrain activation in high novelty-seeking rats following aggressive encounter
Clinton, S. M., Kerman, I. A., Orr, H. R., Bedrosian, T. A., Abraham, A. D., Simpson, D. N., Watson, S. J., & Akil, H. (2011) · Brain Research · doi:10.1016/j.brainres.2011.08.033 · Cited by 24 · see citing works
Central metabolite changes and activation of microglia after peripheral interleukin-2 challenge
Schneider, P., Weber‐Fahr, W., Schweinfurth, N., Ho, Y., Sartorius, A., Spanagel, R., & Pawlak, C. R. (2011) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2011.09.011 · Cited by 25 · see citing works
Neuronal diversity and reciprocal connectivity between the vertebrate hippocampus and septum
Iyer, A., & Tole, S. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.370 · Cited by 24 · see citing works
Theta frequency prefrontal–hippocampal driving relationship during free exploration in mice
Zhan, Y. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.05.063 · Cited by 24 · see citing works
Vila-Merkle, H., González-Martínez, A., Campos-Jiménez, R., Martínez‐Ricós, J., Teruel‐Martí, V., Lloret, A., Blasco‐Serra, A., & Cervera‐Ferri, A. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1122163 · Cited by 22 · see citing works
Brockway, E. T., Simon, S., & Drew, M. R. (2023) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2023.107832 · Cited by 20 · see citing works
Chee, S. A., & Menard, J. L. (2013) · Physiology & Behavior · doi:10.1016/j.physbeh.2013.03.016 · Cited by 19 · see citing works
Self-citationTalishinsky, A., & Rosen, G. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044236 · Cited by 17 · see citing works
Trent, N. L., & Menard, J. L. (2012) · Physiology & Behavior · doi:10.1016/j.physbeh.2012.12.011 · Cited by 14 · see citing works
Self-citationAstrocyte specification in the mouse septum is shaped by both developmental origin and local signals
Xie, Y., Reid, C. M., Garcίa, M. T., Dale-Huang, F., Granados, A. A., Lu, Y., Li, J., Hanson, S. M., Mancia, W., Liu, J., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-02007-z · Cited by 13 · see citing works
Chee, S. A., & Menard, J. L. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.02.027 · Cited by 13 · see citing works
Self-citationKingsbury, M. A., Miller, K. M., & Goodson, J. L. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.07.004 · Cited by 12 · see citing works
“…several studies implicate circuitry of the hippocampus and LS in reactions to novelty and exploration of novel environments, but without a social component (Belzung, 1992; Poucet, 1989; Trent and Menard, 2010), whereas our effects to contextual novelty were only observed in a social context.”
Lamontagne, S. J., Olmstead, M. C., & Menard, J. L. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.07.034 · Cited by 11 · see citing works
Self-citationAversive Contexts Reduce Activity in the Ventral Subiculum- BNST Pathway
Urien, L., Cohen, S., Howard, S., Yakimov, A., Nordlicht, R., & Bauer, E. P. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.06.019 · Cited by 11 · see citing works
The regulative role and mechanism of BNST in anxiety disorder
Xie, M., Xiong, Y., & Wang, H. (2024) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2024.1437476 · Cited by 7 · see citing works
Developmental origin and local signals cooperate to determine septal astrocyte identityPreprint
Xie, Y., Reid, C. M., Granados, A. A., Garcίa, M. T., Dale-Huang, F., Hanson, S. M., Mancia, W., Liu, J., Adam, M. A., Mosto, O., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.08.561428 · Cited by 6 · see citing works
Zarrabian, S., Nasehi, M., Farrahizadeh, M., & Zarrindast, M. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.08.007 · Cited by 5 · see citing works
Ventral hippocampus-lateral septum circuitry promotes foraging-related memoryPreprint
Décarie-Spain, L., Liu, C. M., Lauer, L. T., Subramanian, K., Bashaw, A. G., Klug, M. E., Gianatiempo, I. H., Suarez, A. N., Noble, E. E., Donohue, K. N., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.16.155721 · Cited by 4 · see citing works
Ventral hippocampus-lateral septum circuitry promotes foraging-related memoryPreprint
Décarie-Spain, L. (2022) · doi:10.17605/osf.io/rb2w8 · Cited by 3 · see citing works
Theta cycle dynamics of spatial representations in the lateral septumPreprint
Bzymek, K., & Kloosterman, F. (2023) · doi:10.7554/elife.90207.1 · Cited by 3 · see citing works
George, K., & Ahmad, M. (2024) · Journal of Neurophysiology · doi:10.1152/jn.00322.2024 · Cited by 2 · see citing works
Chaikovska, O. V., Dovhan, O. V., Rokunets, I. L., Nechiporuk, V. M., & Власенко, О. В. (2021) · Reports of Vinnytsia National Medical University · doi:10.31393/reports-vnmedical-2021-25(3)-03 · Cited by 2 · see citing works
vCA1 SST neurons represent avoidance states that guide anxiety-related behavioral choicesPreprint
Bratsch-Prince, J. X., Wei, M., Sureshbabu, S., Chhaya, V., Cano-Adamuz, N., Logas, K. R., & Kheirbek, M. A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.02.709156 · Cited by 2 · see citing works
Benson, A. A., & Gao, W. (2026) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.106762 · Cited by 1 · see citing works
Chodari, L., Oryan, S., Ahmadi, R., & Ashabi, G. (2014) · El Mednifico Journal · doi:10.18035/emj.v2i2.119 · Cited by 1 · see citing works
Zarrabian, S., Nasehi, M., & Zarrindast, M. (2016) · Archives of Advances in Biosciences · doi:10.22037/jps.v7i1.11098 · Cited by 1 · see citing works
van der Veldt, S., Etter, G., Mosser, C., Manseau, F., & Williams, S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.03.366849 · Cited by 1 · see citing works
The Lateral Septum and the Regulation of Anxiety
Chee, S. A. (2013) · QSpace (Queen's University Library)
Lateral Septal Regulation of Anxiety
Trent, N. L. (2012) · QSpace (Queen's University Library)
Self-citationKhakpai, F., Zarrindast, M., Nasehi, M., Haeri-Rohani, A., & Eidi, A. (2013)
Yoon, S. (2015) · QSpace (Queen's University Library)
Weidner, M. T., Zöller, J. E. M., Hamann, C. S., Schraut, K., Ali, M., Lardenoije, R., Eijssen, L., Foerstner, K. U., Gorbunov, N., Strekalova, T. V., et al. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1633386
Vasciaveo, V., Iadarola, A., Casile, A., Dante, D., Morello, G., Minotta, L., Tamagno, E., Cicolin, A., & Guglielmotto, M. (2024) · Figshare · doi:10.6084/m9.figshare.26562571
Re-evaluation of the medial hypothalamic defence system through a cell-type lens
Hong, C. Y., & Kim, J. C. (2026) · Trends Open · doi:10.1016/j.treopn.2026.08.008
Melleu, F. F., Domingues, K., Tassinari, I. D., & Canteras, N. S. (2026) · Hippocampus · doi:10.1002/hipo.70128
- Authors
- Trent, N. L., & Menard, J. L.
- Affiliations
- Queen's University (CA)
- Corresponding author
- Menard, Janet L.
- Venue
- Physiology & Behavior
- Publisher
- Elsevier BV
- Published
- 2010-08
- Volume
- 101
- Issue
- 1
- Pages
- 141-152
- ISSN
- 0031-9384 (ISSN-L)
- OpenAlex
- W1991416612
- Cited by
- 76
- References
- 69
- Citations by year
- 2026: 4 · 2025: 2 · 2024: 4 · 2023: 8 · 2022: 6 · 2021: 8 · 2020: 2 · 2019: 6 · 2017: 6 · 2016: 4 · 2015: 5 · 2014: 6 · 2013: 6 · 2012: 5
- FWCI
- 2.90
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Physiology & Behavior (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Natural Sciences and Engineering Research Council of Canada
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- ventral hippocampus, lateral septum, anxiety, open arm exploration, elevated plus maze, muscimol, GABAA receptor, ipsilateral projection, serial processing, anxiolytic effects, avoidance behavior
- MeSH terms
- Animals, Brain Mapping, Exploratory Behavior, Hippocampus, Functional Laterality, Male, Microinjections, Muscimol, Neural Pathways, GABA Agonists, Maze Learning, Rats, Long-Evans, Septum of Brain, Rats, GABA-A Receptor Agonists
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