Microdialysis administration of vasopressin into the septum improves social recognition in Brattleboro rats

The rat brain in stereotaxic coordinates

Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585

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

Single base deletion in the vasopressin gene is the cause of diabetes insipidus in Brattleboro rats

Schmale, H., & Richter, D. (1984) · Nature · doi:10.1038/308705a0 · Cited by 397

Septal vasopressin modulates social memory in male rats

Dantzer, R., Koob, G. F., Bluthe´, R.-M., & Le Moal, M. (1988) · Brain Research · doi:10.1016/0006-8993(88)90066-2 · Cited by 262

Memory deficit in rats with hereditary diabetes insipidus

de Wied, D., Bohus, B., & Greidanus, T. B. V. W. (1975) · Brain Research · doi:10.1016/0006-8993(75)91022-7 · Cited by 223

Vasopressin and oxytocin release in the brain – a synaptic event

Buijs, R. M., & Heerikhuize, J. J. V. (1982) · Brain Research · doi:10.1016/0006-8993(82)90979-9 · Cited by 218

Behavioral and endocrine responses of rats with hereditary hypothalamic diabetes insipidus (Brattleboro strain)

Bohus, B., Greidanus, T. B. V. W., & de Wied, D. (1975) · Physiology & Behavior · doi:10.1016/0031-9384(75)90189-4 · Cited by 165

Androgen-dependent vasopressinergic neurons are involved in social recognition in rats

Bluthe, R.-M., Schoenen, J., & Dantzer, R. (1990) · Brain Research · doi:10.1016/0006-8993(90)90073-k · Cited by 164

Social recognition does not involve vasopressinergic neurotransmission in female rats

Bluthe´, R.-M., & Dantzer, R. (1990) · Brain Research · doi:10.1016/0006-8993(90)91613-l · Cited by 147

Social investigation in a memory task relates to natural variation in septal expression of oxytocin receptor and vasopressin receptor 1a in prairie voles (Microtus ochrogaster).

Ophir, A. G., Zheng, D.-J., Eans, S. O., & Phelps, S. M. (2009) · Behavioral Neuroscience · doi:10.1037/a0016663 · Cited by 46

The Septal Region and Social Behavior

Sheehan, T. P., & Numan, M. (2000) · Springer eBooks · doi:10.1007/978-1-4612-1302-4_8 · Cited by 46

Rodent models for autism: A critical review

Belzung, C., Leman, S., Vourc’h, P., & Andres, C. R. (2005) · Drug Discovery Today Disease Models · doi:10.1016/j.ddmod.2005.05.004 · Cited by 43

Sex‐Dependent Effects of Prenatal Stress on Social Memory in Rats: A Role for Differential Expression of Central Vasopressin‐1a Receptors

Grundwald, N. J., Benítez, D. P., & Brunton, P. J. (2015) · Journal of Neuroendocrinology · doi:10.1111/jne.12343 · Cited by 46

Subchronic phencyclidine administration alters central vasopressin receptor binding and social interaction in the rat

Tanaka, K., Suzuki, M., Sumiyoshi, T., Murata, M., Tsunoda, M., & Kurachi, M. (2003) · Brain Research · doi:10.1016/j.brainres.2003.08.050 · Cited by 42

The effects of chronic administration of established and putative antipsychotics on natural prepulse inhibition deficits in Brattleboro rats

Feifel, D., Melendez, G., Priebe, K., & Shilling, P. D. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.04.020 · Cited by 42

Neuroendocrine underpinning of social recognition in males and females

Aspesi, D., & Choleris, E. (2022) · Journal of Neuroendocrinology · doi:10.1111/jne.13070 · Cited by 41

Genetic Overexpression of NR2B Subunit Enhances Social Recognition Memory for Different Strains and Species

Jacobs, S., & Tsien, J. Z. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036387 · Cited by 40

Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders

Kim, K. C., Gonzales, E. L., Lázaro, M. T., Choi, C. S., Bahn, G. H., Yoo, H. J., & Shin, C. Y. (2016) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2016.061 · Cited by 44

Depressive- and anxiety-like behaviors and stress-related neuronal activation in vasopressin-deficient female Brattleboro rats

Fodor, A., Kovács, K., Balázsfi, D., Klausz, B., Pintér, O., Demeter, K., Daviu, N., Rabasa, C., Rotllant, D., Nadal, R. A., et al. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.02.041 · Cited by 39

Intranasal application of vasopressin fails to elicit changes in brain immediate early gene expression, neural activity and behavioural performance of rats

Ludwig, M., Tobin, V. A., Callahan, M. F., Papadaki, E., Becker, A., Engelmann, M., & Leng, G. (2013) · Journal of Neuroendocrinology · doi:10.1111/jne.12046 · Cited by 37

Vasopressin infusion into the lateral septum of adult male rats rescues progesterone-induced impairment in social recognition

Bychowski, M. E., Mena, J. D., & Auger, C. J. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.04.047 · Cited by 37

Facilitation of short-term social memory by ethanol in rats is mediated by dopaminergic receptors

Prediger, R. D., Batista, L. C., Miyoshi, E., & Takahashi, R. N. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.11.009 · Cited by 37

Endothelin neurotransmitter signalling controls zebrafish social behaviour

Gutiérrez, H. C., Colanesi, S., Cooper, B., Reichmann, F., Young, A. M. J., Kelsh, R. N., & Norton, W. (2019) · Scientific Reports · doi:10.1038/s41598-019-39907-7 · Cited by 36

Species Differences in the Immunoreactive Expression of Oxytocin, Vasopressin, Tyrosine Hydroxylase and Estrogen Receptor Alpha in the Brain of Mongolian Gerbils (Meriones unguiculatus) and Chinese Striped Hamsters (Cricetulus barabensis)

Wang, Y., Xu, L., Pan, Y., Wang, Z., & Zhang, Z. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065807 · Cited by 33

Role of frontal cortex in social odor discrimination and scent-marking in female golden hamsters (Mesocricetus auratus).

Petrulis, A., deSouza, I. S., Schiller, M., & Johnston, R. E. (1998) · Behavioral Neuroscience · doi:10.1037//0735-7044.112.1.199 · Cited by 33

Atypical Social Development in Vasopressin-Deficient Brattleboro Rats

Paul, M. J., Peters, N. V., Holder, M. K., Kim, A. M., Whylings, J., Terranova, J. I., & Vries, G. J. D. (2016) · eNeuro · doi:10.1523/eneuro.0150-15.2016 · Cited by 32

AVP(4-8) Improves Cognitive Behaviors and Hippocampal Synaptic Plasticity in the APP/PS1 Mouse Model of Alzheimer’s Disease

Zhang, X., Zhao, F., Wang, C., Zhang, J., Bai, Y., Zhou, F., Wang, Z.-J., Wu, M., Yang, W., Guo, J., et al. (2019) · Neuroscience Bulletin · doi:10.1007/s12264-019-00434-0 · Cited by 31

Plasma vasopressin and interpersonal functioning

Gouin, J.-P., Carter, C. S., Pournajafi‐Nazarloo, H., Malarkey, W. B., Loving, T. J., Stowell, J. R., & Kiecolt‐Glaser, J. K. (2012) · Biological Psychology · doi:10.1016/j.biopsycho.2012.07.003 · Cited by 33

Early locomotor and social effects in vasopressin deficient neonatal rats

Schank, J. C. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.08.019 · Cited by 33

Effects of arginine vasotocin (AVT) on the behavioral, cardiovascular, and corticosterone responses of starlings (Sturnus vulgaris) to crowding

Nephew, B. C., Aaron, R. S., & Romero, L. M. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2004.11.007 · Cited by 32

Oxytocin and Fear Memory Extinction: Possible Implications for the Therapy of Fear Disorders?

Baldi, E., Costa, A., Rani, B., Passani, M. B., Blandina, P., Romano, A., & Provensi, G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810000 · Cited by 35

Resident–Intruder Trait Aggression is Associated with Differences in Lysine Vasopressin and Serotonin Receptor 1A (5‐HT1A) mRNA Expression in the Brain of Pre‐Pubertal Female Domestic Pigs (Sus scrofa)

D’Eath, R. B., Ormandy, E., Lawrence, A. B., SUMNER, B. E. H., & Meddle, S. (2005) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2005.01359.x · Cited by 30

The molecular neurobiology of stress – evidence from genetic and epigenetic models

Steckler, T. (2001) · Behavioural Pharmacology · doi:10.1097/00008877-200111000-00002 · Cited by 30

Vasopressin in the septum: not important versus causally involved in learning and memory — two faces of the same coin?

Engelmann, M. (2008) · Progress in brain research · doi:10.1016/s0079-6123(08)00432-9 · Cited by 29

Social recognition is context dependent in single male prairie voles

Zheng, D., Foley, L., Rehman, A., & Ophir, A. G. (2013) · Animal Behaviour · doi:10.1016/j.anbehav.2013.09.015 · Cited by 28

Autism: a large unmet medical need and a complex research problem

Gerlai, J., & Gerlai, R. T. (2003) · Physiology & Behavior · doi:10.1016/s0031-9384(03)00165-3 · Cited by 29

Pair bond formation leads to a sustained increase in global cerebral glucose metabolism in monogamous male titi monkeys (Callicebus cupreus)

Maninger, N., Hinde, K., Mendoza, S. P., Mason, W. A., Larke, R. H., Ragen, B., Jarcho, M. R., Cherry, S. R., Rowland, D. J., Ferrer, E. E., et al. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.02.028 · Cited by 27

Prenatal alcohol exposure disrupts male adolescent social behavior and oxytocin receptor binding in rodents

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

Gene Regulation as a Modulator of Social Preference in Voles

Hammock, E. A. D. (2007) · Advances in genetics · doi:10.1016/s0065-2660(07)59004-8 · Cited by 26

Possible contribution of epigenetic changes in the development of schizophrenia-like behavior in vasopressin-deficient Brattleboro rats

Demeter, K., Török, B., Fodor, A., Varga, J. M., Ferenczi, S., Kovács, K., Eszik, I., Szegedi, V., & Zelena, D. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.12.007 · Cited by 25

Vasopressinergic Neurocircuitry Regulating Social Attachment in a Monogamous Species

Tickerhoof, M. C., & Smith, A. S. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00265 · Cited by 26

Microdialysis of the brain structures: application in behavioral research on vasopressin and oxytocin

Orłowska-Majdak, M. (2004) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2004-1504 · Cited by 25

Long-term social recognition memory in adult male rats: factor analysis of the social and non-social behaviors

de Moura, P. J., Meirelles, S. T., & Xavier, G. F. (2010) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2010007500047 · Cited by 24

WAY 267,464, a non-peptide oxytocin receptor agonist, impairs social recognition memory in rats through a vasopressin 1A receptor antagonist action

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

Intranasal desmopressin as an adjunct to risperidone for negative symptoms of schizophrenia: A randomized, double-blind, placebo-controlled, clinical trial

Hosseini, S. M. R., Farokhnia, M., Rezaei, F., Gougol, A., Yekehtaz, H., Iranpour, N., Salehi, B., Tabrizi, M. H., Tajdini, M., Ghaleiha, A., et al. (2014) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2014.02.001 · 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

Examining the Role of Vasopressin in the Modulation of Parental and Sexual Behaviors

Zimmermann-Peruzatto, J. M., Lazzari, V. M., de Moura, A. C., Almeida, S., & Giovenardi, M. (2015) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00130 · Cited by 23

Naturally Occurring Variation in Vasopressin Immunoreactivity Is Associated with Maternal Behavior in Female Peromyscus Mice

Bester‐Meredith, J. K., & Marler, C. A. (2012) · Brain Behavior and Evolution · doi:10.1159/000341899 · Cited by 23

Autism: a target of pharmacotherapies?

Gerlai, R. T., & Gerlai, J. (2004) · Drug Discovery Today · doi:10.1016/s1359-6446(04)03039-9 · Cited by 23

Untitled work

McEwen (2004) · doi:10.1016/s1054-3589(04)50016-9 · Cited by 22

Restoration of peripheral V2 receptor vasopressin signaling fails to correct behavioral changes in Brattleboro rats

Balázsfi, D., Pintér, O., Klausz, B., Kovács, K., Fodor, A., Török, B., Engelmann, M., & Zelena, D. (2014) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2014.09.011 · Cited by 21

Investigation of social, affective, and locomotor behavior of adolescent Brattleboro rats reveals a link between vasopressin's actions on arousal and social behavior

Schatz, K. C., Kyne, R. F., Parmeter, S. L., & Paul, M. J. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2018.08.015 · Cited by 21

Sevoflurane-Induced Down-regulation of Hippocampal Oxytocin and Arginine Vasopressin Impairs Juvenile Social Behavioral Abilities

Zhou, Z., Yang, X., Yuan, B.-L., Niu, L., Zhou, X. P., Huang, W., Feng, X., & Zhou, L. (2014) · Journal of Molecular Neuroscience · doi:10.1007/s12031-014-0468-3 · Cited by 20

Oxytocin and vasopressin in the hippocampus

Zăgrean, A., Georgescu, I.-A., Ieșanu, M. I., Ionescu, R.-B., Haret, R. M., Panaitescu, A. M., & Zăgrean, L. (2022) · Vitamins and hormones · doi:10.1016/bs.vh.2021.11.002 · Cited by 20

The promiscuity of the oxytocin–vasopressin systems and their involvement in autism spectrum disorder

Borie, A. M., Theofanopoulou, C., & Andari, E. (2021) · Handbook of clinical neurology · doi:10.1016/b978-0-12-819973-2.00009-5 · Cited by 19

Food competition and social experience effects on V1a receptor binding in the forebrain of male Long–Evans hooded rats

Askew, A., González, F., Stahl, J. M., & Karom, M. C. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.08.001 · Cited by 19

Increase in Alzheimer's related markers preceeds memory disturbances: Studies in vasopressin-deficient Brattleboro rat

Varga, J. M., Klausz, B., Domokos, Á., Kálmán, S., Pákáski, M., Szücs, S., Garab, D., Zvara, Á., Puskás, L. G., Kalman, J. L., et al. (2013) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2013.10.010 · Cited by 19

Genetic Vasopressin Deficiency Facilitates Performance of a Lateralized Reaction-Time Task: Altered Attention and Motor Processes

Jentsch, J. D. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-03-01066.2003 · Cited by 18

Septal vasopressin induced preservation of social recognition in rats was abolished by pinealectomy

Appenrodt, E., Juszczak, M., & Schwarzberg, H. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00450-8 · Cited by 18

Extrahippocampal Contributions to Social Memory: The Role of Septal Nuclei

Shivakumar, A. B., Mehak, S. F., Jijimon, F., & Gangadharan, G. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.04.018 · Cited by 18

Selective breeding of rats for high (HAB) and low (LAB) anxiety-related behaviour: A unique model for comorbid depression and social dysfunctions

Gryksa, K., Schmidtner, A. K., Masís-Calvo, M., Rodríguez‐Villagra, O. A., Havasi, A., Wirobski, G., Maloumby, R., Jägle, H., Bosch, O. J., Slattery, D. A., et al. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105292 · Cited by 20

The Role of the Oxytocin/Arginine Vasopressin System in Animal Models of Autism Spectrum Disorder

Zhang, R., Xu, X., Zhang, H.-F., Han, S., & Han, J. (2017) · Advances in anatomy, embryology and cell biology · doi:10.1007/978-3-319-52498-6_8 · Cited by 17

Selective deletion of Caspase-3 gene in the dopaminergic system exhibits autistic-like behaviour

García-Domínguez, I., Suárez‐Pereira, I., Santiago, M., Pérez-Villegas, E. M., Bravo, L., López‐Martín, C., Roca-Ceballos, M. A., García‐Revilla, J., Espinosa‐Oliva, A. M., Rodríguez‐Gómez, J. A., et al. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110030 · Cited by 16

Circadian phase and intertrial interval interfere with social recognition memory

de Moura, P. J., Gimenes-Júnior, J. A., Valentinuzzi, V. S., & Xavier, G. F. (2008) · Physiology & Behavior · doi:10.1016/j.physbeh.2008.08.012 · Cited by 16

Finger release sequence for fastball and curveball pitches.

Stevenson, J. M. (1985) · PubMed · Cited by 16

Neurobehavioral Profiles of Six Genetically-based Rat Models of Schizophrenia- related Symptoms

Oliveras, I., Cañete, T., Sampedro-Viana, D., Río-Álamos, C., Tobeña, A., Corda, M. G., Giorgi, O., & Fernández‐Teruel, A. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230221093644 · Cited by 15

A potential cardiovascular mechanism for the behavioral effects of central and peripheral arginine vasotocin

Nephew, B. C., Romero, L. M., & Romero, L. M. (2005) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2005.05.010 · Cited by 14

Socio-behavioral dysfunction in disorders of hypothalamic-pituitary involvement: The potential role of disease-induced oxytocin and vasopressin signaling deficits

Clarke, L., Zyga, O., Pineo-Cavanaugh, P. L., Jeng, M., Fischbein, N. J., Partap, S., Katznelson, L. J., & Parker, K. J. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104770 · Cited by 13

Vasopressin as Possible Treatment Option in Autism Spectrum Disorder

László, K., Vörös, D., Correia, P., Fazekas, C. L., Török, B., Plangár, I., & Zelena, D. (2023) · Biomedicines · doi:10.3390/biomedicines11102603 · Cited by 13

Animal models of autism with a particular focus on the neural basis of changes in social behaviour: An update article

Olexová, L., Talarovičová, A., Lewis-Evans, B., Borbélyová, V., & Kršková, L. (2012) · Neuroscience Research · doi:10.1016/j.neures.2012.10.004 · Cited by 13

Mutation in the vasopressin gene eliminates the sex difference in social reinforcement in adolescent rats

Schatz, K. C., Martin, C. D., Ishiwari, K., George, A. M., Richards, J. B., & Paul, M. J. (2019) · Physiology & Behavior · doi:10.1016/j.physbeh.2019.04.004 · Cited by 13

The prepulse inhibition deficit appearance is largely independent on the circadian cycle, body weight, and the gender of vasopressin deficient Brattleboro rat

Fodor, A., Klausz, B., Tóth, B. I., & Zelena, D. (2016) · Endocrine Regulations · doi:10.1515/enr-2016-0004 · Cited by 13

Oxytocin in the regulation of social behaviours in medial amygdala‐lesioned mice via the inhibition of the extracellular signal‐regulated kinase signalling pathway

Wang, Y., Zhao, S., Wu, Z., Feng, Y., Zhao, C., & Zhang, C. (2015) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12378 · Cited by 13

Effects of arginine vasopressin on musical working memory

Granot, R., Uzefovsky, F., Bogopolsky, H., & Ebstein, R. P. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00712 · Cited by 12

The Neurobiology and Genetics of Affiliation and Social Bonding in Animal Models

Donaldson, Z. R., & Young, L. J. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3777-6_4 · Cited by 12

Electroencephalographic and early communicative abnormalities in Brattleboro rats

Lin, R. E., Ambler, L., Billingslea, E. N., Suh, J., Batheja, S., Tatard-Leitman, V. M., Featherstone, R. E., & Siegel, S. J. (2013) · Physiological Reports · doi:10.1002/phy2.100 · Cited by 11

Sociability trait and regional cerebral oxidative metabolism in rats: Predominantly nonlinear relations

Kanarik, M., & Harro, J. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.08.049 · Cited by 9

Ameliorating schizophrenia-like symptoms in vasopressin deficient male Brattleboro rat by chronic antipsychotic treatment

Török, B., Fodor, A., Klausz, B., Varga, J. M., & Zelena, D. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174383 · Cited by 9

Pubertal exposure to bisphenol-A affects social recognition and arginine vasopressin in the brain of male mice

Wang, J., Jin, S., Fu, W., Liang, Y., Yang, Y., & Xu, X. (2021) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2021.112843 · Cited by 9

The effects of lactation on impulsive behavior in vasopressin-deficient Brattleboro rats

Aliczki, M., Fodor, A., Balogh, Z., Haller, J., & Zelena, D. (2014) · Hormones and Behavior · doi:10.1016/j.yhbeh.2014.08.002 · Cited by 9

Viral rescue of magnocellular vasopressin cells in adolescent Brattleboro rats ameliorates diabetes insipidus, but not the hypoaroused phenotype

Schatz, K. C., Brown, L. M., Barrett, A., Roth, L. C., Grinevich, V., & Paul, M. J. (2019) · Scientific Reports · doi:10.1038/s41598-019-44776-1 · Cited by 9

Impaired vasopressin neuromodulation of the lateral septum leads to social behavior deficits in Shank3B+/- male mice

Bortolozzo-Gleich, M. H., Bouisset, G., Geng, L., Pino, A. R., Nomura, Y., Han, S., Li, Y., & Leroy, F. (2025) · Nature Communications · doi:10.1038/s41467-025-61994-6 · Cited by 10

Hippocampal gene expression patterns in oxytocin male knockout mice are related to impaired social interaction

Lazzari, V. M., Zimmermann-Peruzatto, J. M., Agnes, G., Becker, R. O., de Moura, A. C., Almeida, S., Guedes, R. P., & Giovenardi, M. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.10.034 · Cited by 8

Pinealectomy blocks modulation of active avoidance by central vasopressin application in rats

Appenrodt, E., & Schwarzberg, H. (2003) · Peptides · doi:10.1016/s0196-9781(02)00285-1 · Cited by 8

Altered cerebral glucose metabolism in an animal model of diabetes insipidus: A micro-PET study

Idbaïh, A., Burlet, A. J., Adle‐Biassette, H., Boisgard, R., Coulon, C., Paris, S., Marie, Y., Donadieu, J., Hoang‐Xuan, K., & Ribeiro, M. J. (2007) · Brain Research · doi:10.1016/j.brainres.2007.05.016 · Cited by 8

Social behavior in laboratory rats: Applications for psycho‐neuroethology studies

Yamamuro, Y. (2006) · Animal Science Journal · doi:10.1111/j.1740-0929.2006.00363.x · Cited by 8

Simultaneous Knockouts of the Oxytocin and Vasopressin 1b Receptors in Hippocampal CA2 Impair Social MemoryPreprint

Cymerblit‐Sabba, A., Walsh, C., Duan, K., Song, J., Holmes, O. W., & Young, W. S. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.30.526271 · Cited by 11

The involvement of oxytocin and vasopressin in social recognition and social learning

Dore, R., Phan, A., Clipperton‐Allen, A. E., Kavaliers, M., & Choleris, E. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139017855.016 · Cited by 7

Species differences in behavior and cell proliferation/survival in the adult brains of female meadow and prairie voles

Pan, Y., Liu, Y., Lieberwirth, C., Zhang, Z., & Wang, Z. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.12.026 · Cited by 7

Modeling Schizophrenia in Animals

Feifel, D., & Shilling, P. D. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-415894-8.00030-0 · Cited by 8

Vasopressin as a Possible Link between Sleep-Disturbances and Memory Problems

Török, B., Varga, J. M., & Zelena, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232415467 · Cited by 6

Discovery and evaluation of a novel 18F-labeled vasopressin 1a receptor PET ligand with peripheral binding specificity

Hu, J., Li, Y., Dong, C., Wei, H., Liao, K., Wei, J., Zhao, C., Chaudhary, A. F., Chen, J., Xu, H., et al. (2024) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2024.05.033 · Cited by 6

The role of avpr1a microsatellite length on reproductive success of female Microtus ochrogaster

Harris, M. N., Alvarez, R. M., Keane, B., Talib, A. D., Eiswerth, M. J., & Solomon, N. G. (2014) · Behaviour · doi:10.1163/1568539x-00003178 · Cited by 5

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de Moura, P. J., Venkitaramani, D. V., Tashev, R. E., Lombroso, P. J., & Xavier, G. F. (2011) · Behavioural Processes · doi:10.1016/j.beproc.2011.06.008 · Cited by 4

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Hammock, E. A. D., & Young, L. J. (2006) · Springer eBooks · doi:10.1007/978-0-387-30405-2_6 · Cited by 4

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Cymerblit‐Sabba, A., Stackmann, M., Williams, S. K., Granovetter, M. C., Cliz, N. I., Pereira, F., Smith, A. S., Song, J., Lee, H., & Young, W. S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.11.078915 · Cited by 3

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Drozd, H. P., Karathanasis, S. F., Molosh, A. I., Lukkes, J. L., Clapp, D. W., & Shekhar, A. (2018) · Progress in brain research · doi:10.1016/bs.pbr.2018.10.003 · Cited by 3

Vasopressin selectively modulates the release of taurine within the septum of the rat brain

Singewald, N., Ebner, K., Landgraf, R., Wotjak, C. T., & Engelmann, M. (1999) · Neuroscience Letters · doi:10.1016/s0304-3940(99)00841-1 · Cited by 3

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Belokoskova, S. G., & Tsikunov, S. G. (2014) · Reviews on Clinical Pharmacology and Drug Therapy · doi:10.17816/rcf1233-12 · Cited by 2

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Zhang, W., Huang, C., Liu, J., Lu, L., Bai, Y., Sun, Y., Zhang, L., Ren, L., Huang, K., Yan, S., et al. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.115984 · Cited by 1

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Votinov, M., Wagels, L., Karges, W., & Habel, U. (2026) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2026.111657 · Cited by 1

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Lin, R. E., Suh, J., Ambler, L., Billingslea, E. N., Cho, M., Ciacci, A., Tatard-Leitman, V. M., Featherstone, R. E., & Siegel, S. J. (2014) · Journal of Psychiatry and Brain Functions · doi:10.7243/2055-3447-1-3

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Cordes, C. N., Fredricks, C. P., Liu, L., Brakey, D. J., Daniels, D., & Paul, M. J. (2024) · Physiology & Behavior · doi:10.1016/j.physbeh.2024.114699 · Cited by 1

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Omouessi, S. T., Boussera, B., Ongali, B., Fernette, B., Lémamy, G. J., Ndeboko, B., Mouécoucou, J., & Thornton, S. N. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.113308 · Cited by 1

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Popik, P., Vos, P. E., & Van Ree, J. M. (1992) · Behavioural Pharmacology · doi:10.1097/00008877-199208000-00011 · Cited by 93

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Bluthé, R.-M., & Dantzer, R. (1992) · Brain Research · doi:10.1016/0006-8993(92)90480-w · Cited by 47

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Bychowski, M. E., Mena, J. D., & Auger, C. J. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.04.047 · Cited by 37

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Engelmann, M., & Landgraf, R. (1994) · Max Planck Institute for Plasma Physics

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van Wimersma Greidanus, T. B., & Maigret, C. (1996) · Brain Research · doi:10.1016/0006-8993(95)01505-1 · Cited by 117