The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.
Oxytocin mediates rodent social memory within the lateral septum and the medial amygdala depending on the relevance of the social stimulus: Male juvenile versus female adult conspecifics
Abstract
Brain oxytocin (OXT) plays an important role in short-term social memory in laboratory rodents. Here we monitored local release of OXT and its functional involvement in the maintenance and retrieval of social memory during the social discrimination test. We further assessed, if the local effects of OXT within the medial amygdala (MeA) and lateral septum (LS) on social discrimination abilities were dependent on the biological relevance of the social stimulus, thus comparing male juvenile versus adult female conspecifics. OXT release was increased in the LS of male rats during the retrieval, but not during the acquisition or maintenance, of social memory for male juvenile stimuli. Blockade of OXT activity by intracerebroventricular (ICV) administration of a specific OXT receptor antagonist (OXTR-A, rats: 0.75 μg/5 μl, mice: 2 μg/2 μl) immediately after acquisition of social memory impaired the maintenance of social memory, and consequently discrimination abilities during retrieval of social memory. In contrast, ICV OXTR-A was without effect when administered 20 min prior to retrieval of social memory in both species. Non-social memory measured in the object discrimination test was not affected by ICV OXTR-A in male mice, indicating that brain OXT is mainly required for memory formation in a social context. The biological relevance of the social stimulus seems to importantly determine social memory abilities, as male rats recognized a previously encountered female adult stimulus for at least 2h (versus 60 min for male juveniles), with a region-dependent contribution of endogenous OXT; while bilateral administration of OXTR-A into the MeA (0.1 μg/1 μl) impaired social memory for adult females only, administration of OXTR-A into the LS via retrodialysis (10 μg/ml, 1.0 μl/min) impaired social memory for both male juveniles and female adults. Overall, these results indicate that brain OXT is a critical mediator of social memory in male rodents and that, depending on the biological relevance of the social stimulus, distinct brain regions are recruited to mediate its effects.
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
“Likewise, the same dose of OTR-A impaired social recognition when injected into the lateral septum (Lukas et al., 2013)”
From Sex-specific modulation of juvenile social play behavior by vasopressin and oxytocin depends on social context (2014) · cites this paper as Lukas et al., 2013
In the citing paper
“even though the dose that we used impaired social recognition in adult male rats (Lukas et al., 2013) and in juvenile male rats (Veenema, unpublished observation).”
From Sex-specific modulation of juvenile social play by vasopressin (2013) · cites this paper as Lukas et al., 2013
In the citing paper
“ICV administration of an OTR antagonist impaired social recognition in both male (Lukas et al., 2013) and female (Engelmann et al., 1998) rats.”
From Vasopressin and oxytocin receptor systems in the brain: Sex differences and sex-specific regulation of social behavior (2016) · cites this paper as Lukas et al., 2013
In the citing paper
“Utilizing the three-chamber social memory assay in rodents, it was found that OXT activity in the septum and amygdala is required for social memory [43,70].”
From Neural circuits regulating prosocial behaviors (2023) · cites this paper as [70]
In the citing paper
“OXT is released within the brain as relationships form and it facilitates experience-dependent social adaptations including the formation of social memories 14,15, the establishment of mating-induced pair bonds 2 and maternal responsiveness 16.”
From Social experience alters oxytocinergic modulation in the nucleus accumbens of female prairie voles (2022) · cites this paper as [15]
In the citing paper
“and the well-established role of oxytocin in social behaviors and social recognition (13, 21, 34; 39-44).”
From Social Interaction Elicits Activity in Glutamatergic Neurons in the Posterior Intralaminar Complex of the Thalamus (2024) · cites this paper as [40]
Citations
Cites
The Mouse Brain in Stereotaxic Coordinates
Paxinos, G. (2001) · Cited by 12,859
A new one-trial test for neurobiological studies of memory in rats. 1: behavioral data
Ennaceur, A., & Delacour, J. (1988) · Behavioural Brain Research · doi:10.1016/0166-4328(88)90157-x · Cited by 3,223
Oxytocin, vasopressin, and the neurogenetics of sociality
Donaldson, Z. R., & Young, L. J. (2008) · Science · doi:10.1126/science.1158668 · Cited by 1,645
Social amnesia in mice lacking the oxytocin gene
Ferguson, J. N., Young, L. J., Hearn, E. F., Matzuk, M. M., Insel, T. R., & Winslow, J. T. (2000) · Nature Genetics · doi:10.1038/77040 · Cited by 1,130
Oxytocin in the Medial Amygdala is Essential for Social Recognition in the Mouse
Ferguson, J. N., Aldag, J. M., Insel, T. R., & Young, L. J. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-20-08278.2001 · Cited by 1,043
Pervasive social deficits, but normal parturition, in oxytocin receptor-deficient mice
Takayanagi, Y., Yoshida, M., Bielsky, I. F., Ross, H. E., Kawamata, M., Onaka, T., Yanagisawa, T., Kimura, T., Matzuk, M. M., Young, L. J., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505312102 · Cited by 806
Oxytocin, vasopressin, and social recognition in mammals
Bielsky, I. F., & Young, L. J. (2004) · Peptides · doi:10.1016/j.peptides.2004.05.019 · Cited by 460
Tribollet, E., Barberis, C., Jard, S., Dubois-Dauphin, M., & Dreifuss, J. J. (1988) · Brain Research · doi:10.1016/0006-8993(88)91437-0 · Cited by 442
Modulation of social memory in male rats by neurohypophyseal peptides
Dantzer, R., Bluthe, R. M., Koob, G. F., & Le Moal, M. (1987) · Psychopharmacology · doi:10.1007/bf00518192 · Cited by 423
Lukas, M., Toth, I., Reber, S. O., Slattery, D. A., Veenema, A. H., & Neumann, I. D. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.95 · Cited by 403
Self-citation
Cited by
Sorted by citations
The oxytocin receptor: from intracellular signaling to behavior
Jurek, B., & Neumann, I. D. (2018) · Physiological Reviews · doi:10.1152/physrev.00031.2017 · Cited by 999
Stress and the social brain: behavioural effects and neurobiological mechanisms
Sandi, C., & Haller, J. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn3918 · Cited by 657
Dumais, K. M., & Veenema, A. H. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2015.04.003 · Cited by 520
“However, ICV administration of an OTR antagonist impaired social recognition in both male (Lukas et al., 2013) and female (Engelmann et al., 1998) rats.”
BackgroundOxytocin enhances social recognition by modulating cortical control of early olfactory processing
Oettl, L.-L., Ravi, N., Schneider, M., Scheller, M. F., Schneider, P., Mitre, M., da Silva Gouveia, M., Froemke, R. C., Chao, M. V., Young, W. S., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.03.033 · Cited by 359
Hippocampal oxytocin receptors are necessary for discrimination of social stimuli
Raam, T., McAvoy, K. M., Besnard, A., Veenema, A. H., & Sahay, A. (2017) · Nature Communications · doi:10.1038/s41467-017-02173-0 · Cited by 292
Insular cortex mediates approach and avoidance responses to social affective stimuli
Rogers-Carter, M. M., Varela, J. A., Gribbons, K. B., Pierce, A. F., McGoey, M. T., Ritchey, M., & Christianson, J. P. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0071-y · Cited by 277
Prefrontal–amygdala circuits in social decision-making
Gangopadhyay, P., Chawla, M., Monte, O. D., & Chang, S. W. C. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-00738-9 · Cited by 260
Oxytocin Signaling in the Central Amygdala Modulates Emotion Discrimination in Mice
Ferretti, V., Maltese, F., Contarini, G., Nigro, M., Bonavia, A., Huang, H., Gigliucci, V., Morelli, G., Scheggia, D., Managò, F., et al. (2019) · Current Biology · doi:10.1016/j.cub.2019.04.070 · Cited by 212
Brain oxytocin: how puzzle stones from animal studies translate into psychiatry
Grinevich, V., & Neumann, I. D. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0802-9 · Cited by 201
Brain oxytocin in social fear conditioning and its extinction: involvement of the lateral septum
Zoicas, I., Slattery, D. A., & Neumann, I. D. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.156 · Cited by 189
Self-citationIntranasal administration of oxytocin: behavioral and clinical effects, a review
Veening, J. G., & Olivier, B. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.04.012 · Cited by 169
Sex-specific modulation of juvenile social play by vasopressin
Veenema, A. H., Bredewold, R., & De Vries, G. J. (2013) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2013.06.002 · Cited by 166
“…lateral ventricle of Ringer’s solution (vehicle) (pH 7.4; 5 ml Ringer; males n = 8; females n = 10), the specific V1aR antagonist d(CH2)5Tyr(Me2)AVP (Manning et al., 2008; 0.75 mg/5 ml Ringer; males n = 11; females n = 8), or the specific OTR antagonist des-GlyNH2,d(CH2)5[Tyr(Me) 2,Thr4]OVT…”
BackgroundInfluentialBredewold, R., Smith, C. J. W., Dumais, K. M., & Veenema, A. H. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00216 · Cited by 164
Self-citationSmith, C. J. W., Poehlmann, M. L., Li, S., Ratnaseelan, A. M., Bredewold, R., & Veenema, A. H. (2017) · Brain Structure and Function · doi:10.1007/s00429-016-1260-7 · Cited by 143
Neurobiology of the lateral septum: regulation of social behavior
Menon, R., Süß, T., Oliveira, V. E. D. M., Neumann, I. D., & Bludau, A. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.10.010 · Cited by 163
Oxytocin׳s role in anxiety: A critical appraisal
MacDonald, K., & Feifel, D. (2014) · Brain Research · doi:10.1016/j.brainres.2014.01.025 · Cited by 139
Gur, R., Tendler, A., & Wagner, S. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.03.022 · Cited by 144
Interplay between Oxytocin and Sensory Systems in the Orchestration of Socio-Emotional Behaviors
Grinevich, V., & Stoop, R. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.016 · Cited by 139
Putting Together Pieces of the Lateral Septum: Multifaceted Functions and Its Neural Pathways
Rizzi-Wise, C. A., & Wang, D. V. (2021) · eNeuro · doi:10.1523/eneuro.0315-21.2021 · Cited by 161
Stilling, R. M., Bordenstein, S. R., Dinan, T. G., & Cryan, J. F. (2014) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2014.00147 · Cited by 139
Lukas, M., & Neumann, I. D. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.08.011 · Cited by 141
Zanos, P., Georgiou, P., Wright, S. R., Hourani, S. M., Kitchen, I., Winsky-Sommerer, R., & Bailey, A. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2013.285 · Cited by 133
Oxytocin and social functioning
Jones, C., Barrera, I., Brothers, S., Ring, R., & Wahlestedt, C. (2017) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2017.19.2/cjones · Cited by 132
Filial responses as predisposed and learned preferences: Early attachment in chicks and babies
Giorgio, E. D., Loveland, J. L., Mayer, U., Salva, O. R., Versace, E., & Vallortígara, G. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.09.018 · Cited by 121
Bo, T., Zhang, X., Kohl, K. D., Wen, J., Tian, S.-J., & Wang, D. (2020) · The ISME Journal · doi:10.1038/s41396-020-0711-6 · Cited by 120
Nonsocial Functions of Hypothalamic Oxytocin
Yang, H.-P., Wang, L., Han, L., & Wang, S. C. (2013) · ISRN Neuroscience · doi:10.1155/2013/179272 · Cited by 116
From Autism to Eating Disorders and More: The Role of Oxytocin in Neuropsychiatric Disorders
Romano, A., Tempesta, B., Bonaventura, M. V. M. D., & Gaetani, S. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00497 · Cited by 106
Mayer, U., Salva, O. R., & Vallortígara, G. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.09.031 · Cited by 81
Stoop, R. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.09.012 · Cited by 84
Beery, A. K., McEwen, L. M., MacIsaac, J. L., Francis, D. D., & Kobor, M. S. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.05.022 · Cited by 81
Calcagnoli, F., de Boer, S. F., Beiderbeck, D. I., Althaus, M., Koolhaas, J. M., & Neumann, I. D. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.12.050 · Cited by 88
Distribution of oxytocin and co-localization with arginine vasopressin in the brain of mice
Otero‐García, M., Agustín‐Pavón, C., Lanuza, E., & Martínez‐Garciá, F. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1111-y · Cited by 80
Social Novelty Investigation in the Juvenile Rat: Modulation by the μ‐Opioid System
Smith, C. J. W., Wilkins, K. B., Mogavero, J. N., & Veenema, A. H. (2015) · Journal of Neuroendocrinology · doi:10.1111/jne.12301 · Cited by 77
DiBenedictis, B. T., Nussbaum, E. R., Cheung, H. K., & Veenema, A. H. (2017) · Journal of Comparative Neurology · doi:10.1002/cne.24216 · Cited by 74
Dumais, K. M., Alonso, A. G., Immormino, M. A., Bredewold, R., & Veenema, A. H. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.11.007 · Cited by 80
Havránek, T., Zatkova, M., Lestanova, Z., Bačová, Z., Mravec, B., Hodosy, J., Štrbák, V., & Bakoš, J. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23559 · Cited by 71
Neural circuits regulating prosocial behaviors
Walsh, J. J., Christoffel, D. J., & Malenka, R. C. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-022-01348-8 · Cited by 72
Neuropeptide diversity and the regulation of social behavior in New World primates
French, J. A., Taylor, J. H., Mustoe, A. C., & Cavanaugh, J. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.03.004 · Cited by 66
Oxytocin and Rodent Models of Addiction
Leong, K.-C., Cox, S. S., King, C. E., Becker, H. C., & Reichel, C. M. (2018) · International review of neurobiology · doi:10.1016/bs.irn.2018.07.007 · Cited by 72
The lateral septum mediates kinship behavior in the rat
Clemens, A. M., Wang, H., & Brecht, M. (2020) · Nature Communications · doi:10.1038/s41467-020-16489-x · Cited by 65
de León-Reyes, N. S., Díaz, P. S., Nogueira, R., Ruiz-Pino, A., Nomura, Y., de Solis, C. A., Schulkin, J. A., Asok, A., & Leroy, F. (2023) · Cell · doi:10.1016/j.cell.2023.08.010 · Cited by 67
Oxytocin and sex differences in behavior
Caldwell, H. K. (2018) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2018.02.002 · Cited by 68
Routing of Hippocampal Ripples to Subcortical Structures via the Lateral Septum
Tingley, D., & Buzsáki, G. (2019) · Neuron · doi:10.1016/j.neuron.2019.10.012 · Cited by 77
Neural systems that facilitate the representation of social rank
Dwortz, M. F., Curley, J. P., Tye, K. M., & Padilla-Coreano, N. (2022) · Philosophical Transactions of the Royal Society B · doi:10.1098/rstb.2020.0444 · Cited by 64
Bredewold, R., Schiavo, J. K., van der Hart, M., Verreij, M., & Veenema, A. H. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.08.052 · Cited by 64
Lukas, M., & Neumann, I. D. (2014) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2014.03.013 · Cited by 65
Song, T.-J., Lan, X.-Y., Wei, M., Zhai, F.-J., Boeckers, T. M., Wang, J., Yuan, S., Jin, M.-Y., Xie, Y., Dang, W.-W., et al. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00111 · Cited by 67
Janeček, M., & Dabrowska, J. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2889-8 · Cited by 63
A, T. R. D. J., Beiderbeck, D. I., & Neumann, I. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091701 · Cited by 62
Dynamic influences on the neural encoding of social valence
Padilla-Coreano, N., Tye, K. M., & Zelikowsky, M. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00609-1 · Cited by 59
Hoffmann, A., Özyurt, J., Lohle, K., Reichel, J. F., Thiel, C. M., & Muller, H. L. (2017) · Endocrine · doi:10.1007/s12020-017-1257-x · Cited by 60
Neuropeptide S Activates Paraventricular Oxytocin Neurons to Induce Anxiolysis
Grund, T., Goyon, S., Li, Y., Eliava, M., Liu, H., Charlet, A., Grinevich, V., & Neumann, I. D. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2161-17.2017 · Cited by 61
Smith, C. J. W., DiBenedictis, B. T., & Veenema, A. H. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.02.001 · Cited by 59
The modulation of emotional and social behaviors by oxytocin signaling in limbic network
Triana-Del Rio, R., Ranade, S., Guardado, J., LeDoux, J., Klann, E., & Shrestha, P. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1002846 · Cited by 58
Hodges, T. E., Baumbach, J. L., Marcolin, M. L., Bredewold, R., Veenema, A. H., & McCormick, C. M. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.07.032 · Cited by 61
Kompier, N. F., Keysers, C., Gazzola, V., Lucassen, P. J., & Krugers, H. J. (2019) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00143 · Cited by 53
Georgiou, P., Zanos, P., García-Carmona, J. A., Hourani, S. M. O., Kitchen, I., Laorden, M. L., & Bailey, A. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.02.012 · Cited by 53
Oxytocin as a Modulator of Synaptic Plasticity: Implications for Neurodevelopmental Disorders
Rajamani, K. T., Wagner, S., Grinevich, V., & Harony-Nicolas, H. (2018) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2018.00017 · Cited by 53
Maternal separation facilitates extinction of social fear in adult male mice.
Zoicas, I., & Neumann, I. D. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.10.034 · Cited by 50
Lee, W., Hiura, L. C., Yang, E., Denney, K. A., Ophir, A. G., & Curley, J. P. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.06.015 · Cited by 49
Calcagnoli, F., Meyer, N., de Boer, S. F., Althaus, M., & Koolhaas, J. M. (2014) · Hormones and Behavior · doi:10.1016/j.yhbeh.2014.03.008 · Cited by 53
Neurobiological Aspects of Face Recognition: The Role of Oxytocin
Lopatina, O. L., Komleva, Y. K., Gorina, Y. V., Higashida, H., & Salmina, A. B. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00195 · Cited by 53
Role of oxytocin in parental behaviour
Olazábal, D. E. (2018) · Journal of Neuroendocrinology · doi:10.1111/jne.12594 · Cited by 49
Seeley, S. H., Chou, Y., & O'Connor, M. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.011 · Cited by 43
Septal oxytocin administration impairs peer affiliation via V1a receptors in female meadow voles
Anacker, A. M. J., Christensen, J. D., LaFlamme, E. M., Grunberg, D. M., & Beery, A. K. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.02.025 · Cited by 44
Social Fear Conditioning as an Animal Model of Social Anxiety Disorder
Toth, I., Neumann, I. D., & Slattery, D. A. (2013) · Current Protocols in Neuroscience · doi:10.1002/0471142301.ns0942s63 · Cited by 44
Smith, C. J. W., Mogavero, J. N., Tulimieri, M. T., & Veenema, A. H. (2017) · Hormones and Behavior · doi:10.1016/j.yhbeh.2017.05.005 · Cited by 48
Oxytocin and Anxiety Disorders: Translational and Therapeutic Aspects
Naja, W., & Aoun, M. P. (2017) · Current Psychiatry Reports · doi:10.1007/s11920-017-0819-1 · Cited by 42
Social experience alters oxytocinergic modulation in the nucleus accumbens of female prairie voles
Borie, A. M., Agezo, S., Lunsford, P., Boender, A. J., Guo, J.-D., Zhu, H., Berman, G. J., Young, L. J., & Liu, R. C. (2022) · Current Biology · doi:10.1016/j.cub.2022.01.014 · Cited by 39
Dumais, K. M., Alonso, A. G., Bredewold, R., & Veenema, A. H. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.05.036 · Cited by 42
Smith, C. J. W., Kingsbury, M. A., Dziabis, J. E., Hanamsagar, R., Malacon, K. E., Tran, J. N., Norris, H. A., Gulino, M., Bordt, E. A., & Bilbo, S. D. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.08.013 · Cited by 47
The Neuroscience of Human and Artificial Intelligence Presence
Harris, L. T. (2023) · Annual Review of Psychology · doi:10.1146/annurev-psych-013123-123421 · Cited by 46
Rajamani, K. T., Barbier, M., Lefèvre, A., Niblo, K., Cordero, N., Netser, S., Grinevich, V., Wagner, S., & Harony‐Nicolas, H. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02336-0 · Cited by 44
Oettl, L., & Kelsch, W. (2017) · Current topics in behavioral neurosciences · doi:10.1007/7854_2017_8 · Cited by 39
Brain functional networks associated with social bonding in monogamous voles
López-Gutiérrez, M. F., Gracia-Tabuenca, Z., Ortiz, J. J., Camacho, F., Young, L. J., Paredes, R. G., Díaz, N. F., Portillo, W., & Alcauter, S. (2021) · eLife · doi:10.7554/elife.55081 · Cited by 42
Horiai, M., Otsuka, A., Hidema, S., Hiraoka, Y., Hayashi, R., Miyazaki, S., Furuse, T., Mizukami, H., Teruyama, R., Tamura, M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-79109-0 · Cited by 38
Oxytocin is implicated in social memory deficits induced by early sensory deprivation in mice
Zhang, J., Chen, L., Lv, Z.-M., Niu, X.-Y., Shao, C.-C., Zhang, C., Pruski, M., Huang, Y., Qi, C., Song, N., et al. (2016) · Molecular Brain · doi:10.1186/s13041-016-0278-3 · Cited by 33
The Role of Oxytocin in Abnormal Brain Development: Effect on Glial Cells and Neuroinflammation
Knoop, M. S., Possovre, M.-L., Jacquens, A., Charlet, A., Baud, O., & Darbon, P. (2022) · Cells · doi:10.3390/cells11233899 · Cited by 35
Dynorphins regulate the strength of social memory
Bilkei‐Gorzó, A., Mauer, D., Michel, K., & Zimmer, A. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.10.023 · Cited by 31
Mooney, S. J., Coen, C. W., Holmes, M. M., & Beery, A. K. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.06.043 · Cited by 30
Fish as a model in social neuroscience: conservation and diversity in the social brain network
Ogawa, S., Pfaff, D. W., & Parhar, I. S. (2021) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12689 · Cited by 32
Structure and function of the medial amygdala
(2020) · Handbook of Behavioral Neuroscience · doi:10.1016/b978-0-12-815134-1.00002-7 · Cited by 29
Kim, E. U., Varlinskaya, E. I., Dannenhoffer, C. A., & SPEAR, L. P. (2018) · Alcohol · doi:10.1016/j.alcohol.2018.05.002 · Cited by 30
Oxytocin signaling in the treatment of drug addiction: Therapeutic opportunities and challenges
Che, X., Cai, J., Liu, Y., Xu, T., Yang, J., & Wu, C. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107820 · Cited by 28
Joushi, S., Esmaeilpour, K., Masoumi‐Ardakani, Y., Esmaeili‐Mahani, S., & Sheibani, V. (2020) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2020.105044 · Cited by 28
Dissecting neural mechanisms of prosocial behaviors
Walsh, J. J., Christoffel, D. J., Wu, X., Pomrenze, M. B., & Malenka, R. C. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.11.006 · Cited by 30
Mikulecká, A., Druga, R., Stuchlı́k, A., Mareš, P., & Kubová, H. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113005 · Cited by 27
Holman, P. J., Ellis, L. A., Morgan, E., & Weinberg, J. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2018.08.004 · Cited by 29
Hodges, T. E., Eltahir, A. M., Patel, S. D., Bredewold, R., Veenema, A. H., & McCormick, C. M. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.104579 · Cited by 28
Frankiensztajn, L. M., Gur-Pollack, R., & Wagner, S. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.04.006 · Cited by 28
Kamrani-Sharif, R., Hayes, A. W., Gholami, M., Salehirad, M., Khani, M. A., Motaghinejad, M., & Emanuele, E. (2023) · Neuropeptides · doi:10.1016/j.npep.2023.102352 · Cited by 27
Administration of an oxytocin receptor antagonist attenuates sexual motivation in male rats
Blitzer, D. S., Wells, T. E., & Hawley, W. R. (2017) · Hormones and Behavior · doi:10.1016/j.yhbeh.2017.06.002 · Cited by 25
Role of Acid Sphingomyelinase in the Regulation of Social Behavior and Memory
Zoicas, I., Reichel, M., Gulbins, E., & Kornhuber, J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0162498 · Cited by 24
He, Z., Guo, Q., Yang, Y., Wang, L., Zhang, S., Yuan, W., Li, L., Zhang, J., Hou, W., Yang, J., et al. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.09.006 · Cited by 25
Albert‐Gascó, H., Sánchez‐Sarasúa, S., Ma, S., Díaz, C. G., Gundlach, A. L., Sánchez‐Pérez, A. M., & Olucha-Bordonau, F. E. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1763-5 · Cited by 25
Hicks, C., Ramos, L., Reekie, T. A., Narlawar, R., Kassiou, M., & McGregor, I. S. (2015) · Psychopharmacology · doi:10.1007/s00213-015-3902-5 · Cited by 23
Giving a good start to a new life via maternal brain allostatic adaptations in pregnancy
Russell, J. A., & Brunton, P. J. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.02.003 · Cited by 24
Hegoburu, C., Tang, Y., Niu, R., Ghosh, S., Rio, R. T. D., Salgado, I. D. A., Abatis, M., Caseiro, D. M., van den Burg, E. H., Grundschober, C., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-45626-z · Cited by 29
Neumann, I. D., & Landgraf, R. (2019) · Journal of Neuroendocrinology · doi:10.1111/jne.12695 · Cited by 23
Matricon, J., Seillier, A., & Giuffrida, A. (2016) · Neuroscience Research · doi:10.1016/j.neures.2016.04.004 · Cited by 22
Metadata
- Authors
- Lukas, M., Toth, I., Veenema, A. H., & Neumann, I. D.
- Affiliations
- University of Regensburg (DE)
- Venue
- Psychoneuroendocrinology
- Publisher
- Elsevier BV
- Published
- 2013-06
- Volume
- 38
- Issue
- 6
- Pages
- 916-926
- ISSN
- 0306-4530 (ISSN-L)
- OpenAlex
- W2105088884
- Cited by
- 211
- References
- 43
- Citations by year
- 2026: 9 · 2025: 9 · 2024: 26 · 2023: 18 · 2022: 19 · 2021: 12 · 2020: 15 · 2019: 18 · 2018: 21 · 2017: 13 · 2016: 18 · 2015: 14 · 2014: 11 · 2013: 7
- FWCI
- 15.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Psychoneuroendocrinology (publishedVersion)
- PubMed (publishedVersion)
- University of Regensburg Publication Server (University of Regensburg) (acceptedVersion)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Keywords
- oxytocin, social memory, lateral septum, medial amygdala, social discrimination, memory retrieval, memory maintenance, sex differences, retrodialysis, object discrimination, rats, mice
- MeSH terms
- Amygdala, Animals, Cues, Discrimination, Psychological, Female, Male, Memory, Short-Term, Ornipressin, Oxytocin, Septal Nuclei, Receptors, Oxytocin, Mice, Rats, Infusions, Intraventricular, Social Discrimination
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
