The DOI matches its Crossref record; 92 of the 92 references it cites were found in a registry or an index.
PHA-L analysis of projections from the supramammillary nucleus in the rat
Abstract
The projections of the supramammillary nucleus (SUM) were examined in the rat by the anterograde anatomical tracer Phaseolus vulgaris leucoagglutinin (PHA-L). The majority of labeled fibers from SUM ascended through the forebrain within the medial forebrain bundle. SUM fibers were found to terminate heavily in the hippocampal formation, specifically within the granule cell layer and immediately adjoining molecular layer of the dentate gyrus. In addition, SUM fibers were shown to distribute densely to several structures with strong connections with the hippocampus, namely, the nucleus reunions of the thalamus, the medial and lateral septum, the entorhinal cortex, and the endopiriform nucleus. SUM fibers were also shown to project significantly to several additional subcortical and cortical sites. The subcortical sites were the dorsal raphe nucleus, the midbrain central gray, the fields of Forel/zona incerta, the dorsomedial hypothalamic area, midline/intralaminar nuclei of the thalamus (posterior paraventricular, rhomboid, central medial, intermediodorsal, and mediodorsal), the medial and lateral preoptic areas, the bed nucleus of the stria terminalis, the substantia innominata, the vertical limb of the diagonal band nucleus, and the claustrum. The cortical sites were the occipital, temporal, parietal, and frontal cortices. Some notable differences were observed in projections from the lateral as compared to the medial SUM. For example, fibers originating from the lateral SUM distributed heavily to the hippocampal formation and parts of the cortex, whereas those from the medial SUM projected sparsely to these two regions. The SUM projections to the hippocampal formation and associated structures may serve as the substrate for a SUM involvement in the generation of the theta rhythm of the hippocampus and the gating of information flow through the hippocampal formation.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“which also receives innervations from the posterior hypothalamic area including the supramammillary nucleus”
From Dopamine reward circuitry: Two projection systems from the ventral midbrain to the nucleus accumbens–olfactory tubercle complex (2007) · cites this paper as Vertes, 1992
Citations
Cites
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
Handbook of Chemical Neuroanatomy
Stern, C. D. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90021-5 · Cited by 4,160
Ledent, C. A., Valverde, O., Cossu, G., Petitet, F., Aubert, J.-F., Beslot, F., Böhme, G. A., Impérato, A., Pedrazzini, T., Roques, B. P., et al. (1999) · Science · doi:10.1126/science.283.5400.401 · Cited by 3,628
Central cholinergic pathways in the rat: An overview based on an alternative nomenclature (Ch1–Ch6)
Mesulam, M. M., Mufson, E. J., Wainer, B. H., & Levey, A. I. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90108-2 · Cited by 2,329
Swanson, L. W. (1982) · Brain Research Bulletin · doi:10.1016/0361-9230(82)90145-9 · Cited by 1,718
Gerfen, C. R., & Sawchenko, P. E. (1984) · Brain Research · doi:10.1016/0006-8993(84)90940-5 · Cited by 1,205
Zilles, K. (1985) · Springer eBooks · doi:10.1007/978-3-642-70573-1 · Cited by 1,066
The physiology and pharmacology of hippocampal formation theta rhythms
Bland, B. H. (1986) · Progress in Neurobiology · doi:10.1016/0301-0082(86)90019-5 · Cited by 1,039
Steward, O. (1976) · The Journal of Comparative Neurology · doi:10.1002/cne.901670303 · Cited by 883
A PHA-L analysis of ascending projections of the dorsal raphe nucleus in the rat
Vertes, R. P. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903130409 · Cited by 842
Flagged first, then by citations
Research works printed but not linked: 2
- Bland B. H., 1991, Dorsomedial‐posterior hypothalamic influences on the septo‐hippocampal pathway in the generation of hippocampal theta, Neurosci. Abstr., 17, 1036
- Zilles K., 1985, The Rat Nervous System, 375
Cited by
Sorted by citations
Items 201–296 of 296
GABAergic axons in the ventral forebrain of the rat: An electron microscopic study
Chang, H. T., Tian, Q., & Herron, P. (1995) · Neuroscience · doi:10.1016/0306-4522(95)00109-v · Cited by 14
Noncanonical circuits, states, and computations of the hippocampus
Farrell, J. S., & Soltész, I. (2025) · Science · doi:10.1126/science.adv4420 · Cited by 14
Aguggia, J. P., Cornejo, M. P., Fernández, G., Francesco, P. N. D., Mani, B. K., Cassano, D., Cabral, A., Valdivia, S., Romero, G. G., Reynaldo, M. B., et al. (2022) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2022.105716 · Cited by 13
Smiley, J. F., Bleiwas, C., Canals‐Baker, S., Williams, S. Z., Sears, R. M., Teixeira, C. M., Wilson, D. A., & Saito, M. (2021) · Alcohol · doi:10.1016/j.alcohol.2021.08.005 · Cited by 13
Hippocampal fields in the hedgehog tenrec
Künzle, H., & Radtke‐Schuller, S. (2001) · Neuroscience Research · doi:10.1016/s0168-0102(01)00288-7 · Cited by 13
Serotonergic Regulation of Rhythmical Activity of the Brain, Concentrating on the Hippocampus
Vertes, R. P. (2010) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(10)70084-9 · Cited by 12
“The DRN receives descending theta-related input from forebrain structures such as the supramammillary nucleus ( Vertes, 1992 ), which may rhythmically drive DRN neurons at theta frequencies ( Kocsis and Vertes, 1992, 1996 ; Kocsis et al ., 2006 ).”
BackgroundMethodHayakawa, T., & Zyo, K. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903460109 · Cited by 12
Hirai, H., Sakaba, T., & Hashimotodani, Y. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111871 · Cited by 11
Interhippocampal transfer in passive avoidance task modifies metabolic activity in limbic structures
Cimadevilla, J. M., Méndez-López, M., Méndez, M., & Árias, J. (2009) · Hippocampus · doi:10.1002/hipo.20720 · Cited by 11
“On the other hand, the suprammamillary nucleus is a part of the hypothalamic region that sends a large and direct projection to the hippocampal system (Vertes, 1992), playing an important role in the control of the rhythmic firing of hippocampal cells (theta rhythm).”
BackgroundPosterior hypothalamic GABAergic mediation of hippocampal theta in the cat
Bocian, R., & Konopacki, J. (2007) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2007.04.003 · Cited by 11
Léránth, C., & Vertes, R. P. (2000) · Springer eBooks · doi:10.1007/978-1-4612-1302-4_2 · Cited by 11
Hypothalamic regulation of hippocampal CA1 interneurons by the supramammillary nucleus
Jiang, Y., Lee, D. K., Guo, W., Li, M., & Sun, Q. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114898 · Cited by 10
Du, W., Li, E., Guo, J. Q., Arano, R., Kim, Y., Chen, Y.-T., Thompson, A., Oh, S. J., Samuel, A., Li, Y., et al. (2023) · Cell Reports Methods · doi:10.1016/j.crmeth.2023.100506 · Cited by 12
Young, C. K., Ruan, M., & McNaughton, N. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00072 · Cited by 8
“…HPC theta oscillations in vivo (Lawson and Bland, 1993), it is believed that SuM contributes to HPC theta exclusively through the MS despite its direct HPC innervations to the dentate gyrus and CA2 subregion (Vertes, 1992; Magloczky et al., 1994; Vertes and McKenna, 2000; Cui et al., 2013).”
BackgroundPiallat, B. (1995) · Physiology & Behavior · doi:10.1016/0031-9384(94)00351-5 · Cited by 10
Escobedo, A., Holloway, S.-A., Votoupal, M., Cone, A. L., Skelton, H. E., Legaria, A. A., Ndiokho, I., Floyd, T., Kravitz, A. V., Bruchas, M. R., et al. (2023) · eLife · doi:10.7554/elife.90972 · Cited by 11
Matulewicz, P., Orzeł-Gryglewska, J., Kuśmierczak, M., & Jurkowlaniec, E. (2014) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2014.06.001 · Cited by 9
Billwiller, F., Castillo, L., Elseedy, H., Ivanov, A. I., Scapula, J., Ghestem, A., Carponcy, J., Salin, P. A., Bras, H., Abdelmeguid, N. E., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/584862 · Cited by 9
“In rats, many studies have described the projections from SuM neurons to the hippocampus (Segal & Landis, 1974; Pasquier & Reinoso-Suarez, 1976, 1978; Wyss et al., 1979; Haglund et al., 1984; Saper et al., 1985; Vertes, 1992; Magloczky et al., 1994; Nitsch and Leranth 1996; Vertes & McKenna, 2000).”
BackgroundNucleus Reuniens: Circuitry, Function, and Dysfunction
Vertes, R. P., Linley, S. B., & Viena, T. D. (2022) · Neuromethods · doi:10.1007/978-1-0716-2631-3_4 · Cited by 8
Kobayashi, S., Ohno, K., Iwakuma, M., Kaneda, Y., & Saji, M. (2002) · Neuroscience Research · doi:10.1016/s0168-0102(02)00172-4 · Cited by 8
Vicente, A. F., Slézia, A., Ghestem, A., Bernard, C., & Quilichini, P. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2020.03.034 · Cited by 7
Ariffin, M. Z., Low, C., & Khanna, S. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00079 · Cited by 7
“Indeed, both the lSuM and septal neurons project to a range of cortical regions which, besides Cg, include the entorhinal cortex, the frontal cortex including the region of motor cortex, and the occipital cortex (Gaykema et al., 1990; Vertes, 1992).”
BackgroundInfluentialCaban, B., Staszelis, A., Kaźmierska, P., Kowalczyk, T., & Konopacki, J. (2018) · Developmental Neurobiology · doi:10.1002/dneu.22628 · Cited by 7
“It is also accepted that the PHa contributes to the process of controlling the HPC theta rhythm frequency, at least during animals’ immobility-related behavior (Vertes, 1992; Kirk and McNaughton, 1991, 1993 ; Bland et al., 1995; Kirk, 1998; Woodnorth et al., 2003; Woodnorth and McNaughton, 2005).”
BackgroundResultSynaptic organization of afferent projections to the supramammillary nucleus of the rat
Hayakawa, T., & Zyo, K. (1996) · Anatomy and Embryology · doi:10.1007/bf00198328 · Cited by 7
“There are reciprocal connections between the SUM and the preoptic area, the diagonal band nucleus, and the laterodorsal tegmental nucleus at the light microscopic level (Swanson 1982; Satoh and Fibiger 1986; Vertes 1992; Hayakawa et al. 1993).”
BackgroundŠust, M., Schmalz, T., Beyer, L., Rost, R., Hansen, E., & Weiß, T. (1997) · International Journal of Neuroscience · doi:10.3109/00207459708986394 · Cited by 7
Zhang, Y., Stoelzel, C. R., Ezrokhi, M., Tsai, T., & Cincotta, A. H. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.05.005 · Cited by 6
Bocian, R., Kłos‐Wojtczak, P., Caban, B., Kowalczyk, T., Kaźmierska, P., & Konopacki, J. (2016) · Hippocampus · doi:10.1002/hipo.22612 · Cited by 6
Sleep-wake dependent hippocampal regulation of fear memory
Wen, Y., Jiang, J., Zhai, F., Fan, F., & Lu, J. (2024) · Sleep Medicine · doi:10.1016/j.sleep.2024.02.022 · Cited by 5
Rajamani, K. T., Barbier, M., Lefèvre, A., Niblo, K., Cordero, N., Netser, S., Grinevich, V., Wagner, S., & Harony‐Nicolas, H. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.23.493099 · Cited by 4
Froula, J. M., Rose, J. J., Krook-Magnuson, C., & Krook-Magnuson, E. I. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0887-24.2024 · Cited by 4
Identifying SUM projections to claustrum is about knowing your limits
Qadir, H., & Mathur, B. N. (2019) · Claustrum · doi:10.1080/20023294.2019.1609865 · Cited by 3
“Vertes and colleagues (8) injected an anterograde anatomical tracer into the SUM and observed SUM fibers in the general region occupied by claustrum, the endopiriform nucleus, and the insular cortex.”
BackgroundMethodInfluentialRajamani, K. T., Barbier, M., Lefèvre, A., Niblo, K., Cordero, N., Netser, S., Grinevich, V., Wagner, S., & Harony‐Nicolas, H. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4124625 · Cited by 3
Escobedo, A., Holloway, S.-A., Votoupal, M., Cone, A. L., Skelton, H. E., Legaria, A. A., Ndiokho, I., Floyd, T., Kravitz, A. V., Bruchas, M. R., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.22.507167 · Cited by 3
“Research on SuM has focused on connections to the hippocampus and septum, while SuM projections to other brain areas remain less understood ( Pan and McNaughton, 2004 ; Vertes, 1992 ; Kiss et al., 2002 ).”
BackgroundTop-down regulation of subcortical regions by hippocampal long-range inhibition
Kinney, J. L., Robinson, H. L., Wang, H., Jiang, Y., Zhou, M., Lee, D. K., Li, M., Oliva, A., & Sun, Q. (2025) · Current Biology · doi:10.1016/j.cub.2025.10.062 · Cited by 5
Hippocampo–supramammillary coupling across sleep and wake
Caneo, M., Espinosa, N., Lazcano, G., Aguilera, A., Lara-Vásquez, A., & Fuentealba, P. (2026) · Scientific Reports · doi:10.1038/s41598-026-37066-0 · Cited by 2
Kowalczyk, T., Staszelis, A., Bocian, R., Siwiec, M., Sowa, J. E., Tokarski, K., Kaźmierska, P., & Caban, B. (2023) · Hippocampus · doi:10.1002/hipo.23500 · Cited by 3
“As presented earlier, the PHa is considered a crucial part of the ascending brainstem-hippocampal synchronizing system and is involved in the emergence and control of theta appearance in the hippocampal formation (Bland & Oddie, 1998; Kowalczyk et al., 2021; Pignatelli et al., 2012; Vertes, 1992).”
BackgroundDiencephalic modulation of the hippocampus in affective and cognitive behavior
Vertes, R. P., Linley, S. B., Rojas, A. K. P., Lamothe, K., & Allen, T. A. (2024) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2024.101377 · Cited by 2
Duan, L., Cai, P., Li, Z.-S., Wang, Q., Zhang, L., Chen, Z.-L., Zhang, M.-J., Zhang, C.-W., Xu, Z., & Chen, L. (2025) · Anesthesiology · doi:10.1097/aln.0000000000005584 · Cited by 2
“10,11 Among these brain structures, medial septum (MS) is particularly noteworthy.”
Is electrical coupling involved in the generation of posterior hypothalamic theta rhythm?
Bocian, R., Caban, B., Kłos‐Wojtczak, P., Konopacki, J., & Kowalczyk, T. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13338 · Cited by 2
“…studies have revealed that the SuM receives direct connections from the nucleus reticularis pontis oralis (Vertes et al., 1986) and the septal complex (Gonzalo-Ruiz et al., 1999) and projects in turn into the septal nuclei (Borhegyi et al., 1998) and the hippocampal formation (Vertes, 1992).”
BackgroundHippocampal theta rhythm of REM sleep
Vertes, R. P. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511921179.018 · Cited by 2
Yamazaki, C., Shirao, T., Sasagawa, Y., Maruyama, Y., Akita, H., Saji, M., & Sekino, Y. (2011) · The Kitakanto Medical Journal · doi:10.2974/kmj.61.287 · Cited by 2
Serotonergic regulation of hippocampal rhythmical activity
Vertes, R. P., & Linley, S. B. (2020) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-444-64125-0.00019-0 · Cited by 2
Entorhinal Silencing Reveals Energy Cascade Organization of Hippocampal Oscillations
Zhao, B., Qin, Y. F., Burke, S. N., & Maurer, A. P. (2025) · Hippocampus · doi:10.1002/hipo.70050 · Cited by 1
Picón, L., & Francisco, R. (2008) · Cited by 1
Postnatal development of the relaxin-3 innervation of the rat medial septum
Ros‐Bernal, F., Gil‐Miravet, I., Morales, J. L., Navarro-Sánchez, M., Castillo-Gómez, E., Gundlach, A. L., & Olucha-Bordonau, F. E. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1176587 · Cited by 1
“In the adult rat, the MS receives ascending projections from the posterior hypothalamus, including the supramammillary nuclei (Vertes, 1992; Leranth and Kiss, 1996; Kiss et al., 2000; Vertes and McKenna, 2000), brainstem raphe nuclei (Kocsis and Vertes, 1992; Vertes et al., 1994; Vertes and Kocsis,…”
BackgroundCola, R. B., Roccaro-Waldmeyer, D. M., Naim, S., Babalian, A. L., Seebeck, P., Álvarez-Bolado, G., & Celio, M. R. (2023) · eLife · doi:10.7554/elife.86737.3 · Cited by 2
Silkis, I. G. (2021) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-021-01169-0 · Cited by 1
“In addition, SMN neurons monosynaptically innervate the thalamic reuniens nucleus [Vertes, 1992] (Fig.”
BackgroundDinâmica do sistema córtico-hipocampal durante o condicionamento contextual de medo
Kunicki, A. C. B. (2012) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2012.tde-11052012-113850 · Cited by 1
Influences of self-motion signals on the hippocampal neural code for space
Terrazas, A. (2003) · UA Campus Repository (The University of Arizona) · Cited by 1
Chauvière, L. (2010) · theses.fr (ABES) · doi:10.70675/2a39bc21zed63z4f59z9650zbd80d49c1e37 · Cited by 1
Septotemporal Variation in Theta Rhythm Dynamics: Effects of Speed and Habituation
Hinman, J. R. (2011) · OpenCommons - UConn (University of Connecticut)
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
Theta Dynamics: Speed, Acceleration and Contribution to Cognition
Long, L. L. (2012) · OpenCommons - UConn (University of Connecticut)
The Lateral Septum and the Regulation of Anxiety
Chee, S. A. (2013) · QSpace (Queen's University Library)
THE MEDIATION OF FORMALIN PAIN BY THE FOREBRAIN MEDIAL SEPTUM
Andy, L. T. H. (2013) · National University of Singapore
Influence of Brain Neurochemical Systems on Frequency Spectra of Hippocampal Theta Rhythm
Bagirova, R. M. (2015) · Journal of Pharmacy and Pharmacology · doi:10.17265/2328-2150/2015.07.005
Billwiller, F. (2016) · theses.fr (ABES) · doi:10.70675/005ea76cz4e3dz4be8z87aezb883d3b73c2a
“study (20), a large number of anterogradely labeled fibers was observed in the dentate gyrus in close vicinity of FOS+ neurons after CTb injection in the SUML in REM sleep hypersomniac rats (Fig.”
BackgroundAn investigation of the neural circuitry of cued alcohol behaviors in P and Wistar rats
McCane, A. M. (2017) · Purdue e-Pubs (Purdue University System) · doi:10.7912/c2f36s
The role of the supramammillary area of the hypothalamus in cognitive functions
Shim, H. S., Park, H.-J., Lee, M., Ye, M., & Shim, I. (2018) · Animal Cells and Systems · doi:10.1080/19768354.2018.1427627
Neurochemical Modulation Frequency Band of Hippocampal Theta Rhythm
Baghirova, R. M. (2019) · Biomedical Journal of Scientific & Technical Research · doi:10.26717/bjstr.2019.20.003410
Evaluation of Tranexamic Acid in Bleeding Control in Primary Total Knee Arthroplasty
Ramos, M. R. F. (2020) · Biomedical Journal of Scientific & Technical Research · doi:10.26717/bjstr.2020.29.004861
“ATX is an antifibrinolytic, inhibits the dissolution of clots by blocking the formation of plasma by not activating the coagulation cascade, reducing the intensity and risks of bleeding [8-10].”
BackgroundBaghirova, R. M. (2020) · Biomedical Journal of Scientific & Technical Research · doi:10.26717/bjstr.2020.29.004855
“The possibility of modulating the electrical activity of the hippocampus and especially its theta rhythm by changing the functional state of the extrahippocampal structures of the brain, including the hypothalamus and amygdala, is well known [5-8].”
BackgroundRola obszaru tylnego podwzgórza w generowaniu rytmu theta*
Staszelis, A., & Kowalczyk, T. (2021) · Postępy Higieny i Medycyny Doświadczalnej · doi:10.5604/01.3001.0014.9333
THE ROLE OF MICROTUBULE-ASSOCIATED PROTEIN TAU IN NEURONAL EXCITABILITY AND EPILEPTOGENESIS
Cloyd, R. (2021) · UKnowledge (University of Kentucky) · doi:10.13023/etd.2021.271
Hypothalamic supramammillary neurons that project to the medial septum control wakefulnessPreprint
Liang, M., Jian, T., Jin, W., Chen, Q., Yang, X., Wang, R., Xiao, J., Yang, Z., Liao, X., Chen, X., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.20.521335
Cola, R. B., Roccaro-Waldmeyer, D. M., Naim, S., Babalian, A. L., Seebeck, P., Álvarez-Bolado, G., & Celio, M. R. (2023) · eLife · doi:10.7554/elife.86737.1
Navarro-Sánchez, M., Gil‐Miravet, I., Montero-Caballero, D., Chaima, L., Es-Safi, S., & Olucha-Bordonau, F. E. (2023) · Àgora de salut · doi:10.6035/agorasalut.2023.9.8
Escobedo, A., Holloway, S.-A., Votoupal, M., Cone, A. L., Skelton, H. E., Legaria, A. A., Ndiokho, I., Floyd, T., Kravitz, A. V., Bruchas, M. R., et al. (2023) · eLife · doi:10.7554/elife.90972.1
(2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15596-3.16001-1
Escobedo, A., Holloway, S.-A., Votoupal, M., Cone, A. L., Skelton, H. E., Legaria, A. A., Ndiokho, I., Floyd, T., Kravitz, A. V., Bruchas, M. R., et al. (2024) · eLife · doi:10.7554/elife.90972.2
Aguiar, C. L. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2014.tde-06052024-112835
THE SMALL IRREGULAR ACTIVITY STATE IN THE RAT HIPPOCAMPUS
Jarosiewicz, B. (2004) · D-Scholarship@Pitt (University of Pittsburgh)
Moallem, S. (2015) · Scholarship@Western (Western University)
A hypothalamo-septo-hippocampal circuit for REM sleep-dependent consolidation of social memoryPreprint
Qin, H., Jin, W., Jin, W., Liang, M., Liao, X., Zhang, K., Liang, S., Zhang, C., He, C., Jia, H., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.13.699230 · Cited by 1
“From an anatomical perspective, the SuM can be subdivided into medial and lateral subregions, which differ in their cellular composition and in their efferent-afferent circuit organization(Pan and McNaughton, 2004; Vertes, 1992).”
A hypothalamo-septo-hippocampal circuit for REM sleep-dependent consolidation of social memoryPreprint
Jian, T., Jin, W., Liang, M., Liao, X., Zhang, K., Liang, S., Zhang, C., He, C., Jia, H., Wang, Y., et al. (2026) · eLife · doi:10.7554/elife.110519
A hypothalamo-septo-hippocampal circuit for REM sleep-dependent consolidation of social memoryPreprint
Jian, T., Jin, W., Liang, M., Liao, X., Zhang, K., Liang, S., Zhang, C., He, C., Jia, H., Wang, Y., et al. (2026) · eLife · doi:10.7554/elife.110519.1
Mécanismes responsables de l'activation corticale pendant le sommeil paradoxal
Renouard, L. (2011) · theses.fr (ABES) · doi:10.70675/fb03b5cez134bz4527zb76cz110ad804221c
Functional identification of GluN3A subunit-containing NMDA receptors in the adult brain
Gerges, S. A. (2020) · theses.fr (ABES) · doi:10.70675/396af5c3z01b5z4f37z8e98zd597406fe5ab
How hippocampal area CA2 activity is altered in a mouse model of the 22q11.2 deletion syndrome
Lepicard, E. (2023) · theses.fr (ABES) · doi:10.70675/27e30c9bz7d70z457bzb3afz56ac50bd6ee3
Salter, E. W., Kadia, A., Zhang, L., Thacker, J. S., Choi, S.-L., Ralph, L. T., Lei, G., Jin, F., Georgiou, J., & Collingridge, G. L. (2026) · Glia · doi:10.1002/glia.70154
“In the CA2 stratum pyramidale (CA2 SP) of the hippocampus, there is a separate set of VGLUT2 + inputs from the hypothalamus that form large perisomatic boutons (Haglund et al. 1984; Vertes 1992; Halasy et al. 2004).”
Barbier, M., & Risold, P. (2026) · Journal of Neuroendocrinology · doi:10.1111/jne.70212
“6 44 The SUM functions as a hypothalamic relay that influences hippocampal dynamics according to the animal's behavioral state (e.g., exploration, sleep).”
Vertes, R. P., Linley, S. B., & Mitchell, A. S. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-24078-2.00014-0
Wheeler, D. W., Witter, M. P., & Ascoli, G. A. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-24078-2.00019-x
Glassburn, L., Havener, E., Stangler, O., de Velasco, E. M. F., & Krook-Magnuson, E. I. (2026) · The Journal of Physiology · doi:10.1113/jp291809
Aurfan, Z., Fransson, A., Davidsson, J., Risling, M., Günther, M., & Thams, S. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2026.107612
Ikemoto, S., Arima, Y., Ye, Z., Calva, C., Min, X., Gibbons, J., Mendoza, J., Getachew, B., Johnson, S. A., & Belal, M. (2026) · Research Square · doi:10.21203/rs.3.rs-11156760/v1
The functional anatomy of hippocampal theta and gamma oscillations
Montgomery, S. M. (2009) · Rutgers University Community Repository (Rutgers University) · doi:10.7282/t3k937rc
“In addition to brainstem nuclei, hypothalamic nuclei, including the supramammilary nucleus, project predominantly to the dentate granule layer and inner third of the molecular layer (Vertes 1992).”
BackgroundNakagawa (1999) · doi:10.1002/(sici)1096-9861(19990830)411:3
Metadata
- Authors
- Vertes, R. P.
- Affiliations
- Florida Atlantic University (US)
- Corresponding author
- Vertes, Robert P.
- ORCID
- Vertes, Robert P.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1992-12-22
- Volume
- 326
- Issue
- 4
- Pages
- 595-622
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2029127832
- Cited by
- 299
- References
- 92
- Citations by year
- 2026: 11 · 2025: 4 · 2024: 9 · 2023: 14 · 2022: 14 · 2021: 10 · 2020: 7 · 2019: 10 · 2018: 6 · 2017: 10 · 2016: 8 · 2015: 10 · 2014: 9 · 2013: 7 · 2012: 11
- FWCI
- 3.82
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01mh045075-06)
- National Institute of Mental Health (MH-45075)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Keywords
- supramammillary nucleus, anterograde tracing, Phaseolus vulgaris leucoagglutinin, hippocampal formation, dentate gyrus, medial forebrain bundle, thalamic nuclei, septum, entorhinal cortex, endopiriform nucleus, dorsal raphe nucleus, thalamus, preoptic area, bed nucleus of the stria terminalis, substantia innominata, diagonal band of Brodmann, claustrum, theta oscillations
- MeSH terms
- Animals, Cerebral Cortex, Hippocampus, Male, Mammillary Bodies, Mesencephalon, Neural Pathways, Phytohemagglutinins, Prosencephalon, Rats, Sprague-Dawley, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review