Oxytocin, vasopressin, and social recognition in mammals
Abstract
While pheromones may act as social memory signals, oxytocin and vasopressin acting in the brain appear to be critical for the neural processing of olfactory signatures used for social discrimination. Evidence from a variety of laboratories using a range of animal models, as well as an array of molecular and pharmacological techniques, have helped to determine the neuroanatomical and functional roles oxytocin and vasopressin play in social cognition. In this review we discuss the considerable evidence for the roles of oxytocin and vasopressin in social recognition in rats and mice, as well as in offspring recognition in sheep and mate preference in monogamous voles.
Integrity signals
Registry
Cites
Statistics
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?
AVP expression within the BST and CMA is involved in a number of social behaviors, including social play behavior.
“AVP expression within the bed nucleus of the striaterminalis (BST) and the centromedial amygdala (CMA) is known to be involved in a number of social behaviors, [18][19][20] including social play behavior.21”
From Neonatal MeCP2 is important for the organization of sex differences in vasopressin expression (2012) · cites this paper as [20]
The role of the OXT system has been investigated in rodent models, but uniquely using OXT-related mutant mice and giving OXT through intracerebroventricular (ICV), intraperitoneal (IP) and subcutaneous (SC) injections.
“The role of the OXT system has been investigated in rodent models, but uniquely using OXT-related mutant mice and giving OXT through intracerebroventricular (ICV), intraperitoneal (IP) and subcutaneous (SC) injections (Bielsky and Young, 2004;Jin et al, 2007;Popik et al, 1996;Sala et al, 2012;Sala et al, 2011;Takayanagi et al, 2005;Winslow and Insel, 2002).”
From Chronic and acute intranasal oxytocin produce divergent social effects in mice (2014) · cites this paper as Bielsky and Young, 2004
Chronic intranasal OXT treatment increased V1aR-binding sites in the lateral septum.
“Interestingly, we observed that chronic intranasal OXT treatment increased the V1aR-binding sites in the lateral septum, that is, þ 18% in OXT 0.15 IU-treated mice and þ 31% in OXT 0.3 IU-treated mice (Figure 3b).”
From Chronic and acute intranasal oxytocin produce divergent social effects in mice (2014) · cites this paper as Bielsky and Young, 2004
Oxytocin neurons in the PVH regulate a range of social behaviors, from parental care to social recognition of conspecifics.
“which are known to regulate a range of social behaviors, from parental care to social recognition of conspecifics (13-18).”
From Social Interaction Elicits Activity in Glutamatergic Neurons in the Posterior Intralaminar Complex of the Thalamus (2024) · cites this paper as [13]
Oxytocin has a well-established role in social behaviors and social recognition.
“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 [13]
Cites
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 · see citing works
Self-citationOxytocin 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 · see citing works
Self-citationThe differential projections of the olfactory bulb and accessory olfactory bulb in mammals
Scalia, F., & Winans, S. S. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901610105 · Cited by 983 · see citing works
A role for central vasopressin in pair bonding in monogamous prairie voles
Winslow, J. T., Hastings, N., Carter, C. S., Harbaugh, C. R., & Insel, T. R. (1993) · Nature · doi:10.1038/365545a0 · Cited by 948 · see citing works
Oxytocin receptor distribution reflects social organization in monogamous and polygamous voles
Insel, T. R., & Shapiro, L. E. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.5981 · Cited by 833 · see citing works
Oxytocin is required for nursing but is not essential for parturition or reproductive behavior.
Nishimori, K., Young, L. J., Guo, Q., Wang, Z., Insel, T. R., & Matzuk, M. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11699 · Cited by 734 · see citing works
Self-citationMolecular detection of pheromone signals in mammals: from genes to behaviour
Dulac, C. G., & Torello, A. T. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1140 · Cited by 662 · see citing works
Bielsky, I. F., Hu, S.-B., Szegda, K. L., Westphal, H., & Young, L. J. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300360 · Cited by 531 · see citing works
Self-citationInsel, T. R., & Hulihan, T. J. (1995) · Behavioral Neuroscience · doi:10.1037/0735-7044.109.4.782 · Cited by 528 · see citing works
de Vries, G. J., & Buijs, R. M. (1983) · Brain Research · doi:10.1016/0006-8993(83)90855-7 · Cited by 524 · see citing works
Cellular Mechanisms of Social Attachment
Young, L. J., Lim, M. M., Gingrich, B., & Insel, T. R. (2001) · Hormones and Behavior · doi:10.1006/hbeh.2001.1691 · Cited by 523 · see citing works
Self-citationThe vasopressinergic innervation of the brain in normal and castrated rats
DeVries, G. J., Buijs, R. M., van Leeuwen, F. W., Caffé, A. R., & Swaab, D. F. (1985) · Journal of Comparative Neurology · doi:10.1002/cne.902330206 · Cited by 522 · see citing works
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 · see citing works
Vasopressin and oxytocin receptors in the central nervous system
Tribollet, E., & Barberis, C. (1996) · Critical Reviews™ in Neurobiology · doi:10.1615/critrevneurobiol.v10.i1.60 · Cited by 399 · see citing works
Choleris, E., Gustafsson, J.-Å., Korach, K. S., Muglia, L. J., Pfaff, D. W., & Ogawa, S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0631699100 · Cited by 386 · see citing works
Social memory of the male laboratory rat.
Thor, D. H., & Holloway, W. R. (1982) · Journal of Comparative and Physiological Psychology · doi:10.1037/0735-7036.96.6.1000 · Cited by 375 · see citing works
Encoding pheromonal signals in the accessory olfactory bulb of behaving mice
Luo, M., Fee, M. S., & Katz, L. C. (2003) · Science · doi:10.1126/science.1082133 · Cited by 365 · see citing works
Landgraf, R., Gerstberger, R., Montkowski, A., Probst, J., Wotjak, C., Holsboer, F., & Engelmann, M. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-06-04250.1995 · Cited by 341 · see citing works
Vasopressin-dependent neural circuits underlying pair bond formation in the monogamous prairie vole
Lim, M. M., & Young, L. J. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2003.12.008 · Cited by 322 · see citing works
Self-citationNeural control of maternal behaviour and olfactory recognition of offspring
Kendrick, K. M., Da Costa, A. P. C., Broad, K. D., Ohkura, S., Guevara, R., Lévy, F., & Keverne, E. B. (1997) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00218-9 · Cited by 311 · see citing works
Vaccari, C., Lolait, S. J., & Ostrowski, N. L. (1998) · Endocrinology · doi:10.1210/endo.139.12.6382 · Cited by 308 · see citing works
Caffé, A. R., van Leeuwen, F. W., & Luiten, P. G. M. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902610206 · Cited by 286 · see citing works
Engelmann, M., Wotjak, C. T., & Landgraf, R. (1995) · Physiology & Behavior · doi:10.1016/0031-9384(95)00053-l · Cited by 274 · see citing works
Engelmann, M., Wotjak, C. T., Neumann, I. D., Ludwig, M., & Landgraf, R. (1996) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(95)00059-3 · Cited by 267 · see citing works
Neuroendocrine bases of monogamy
Young, L. J., Wang, Z., & Insel, T. R. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01167-3 · Cited by 265 · see citing works
Self-citationChanges in the sensory processing of olfactory signals induced by birth in sleep
Kendrick, K., Levy, F., & Keverne, E. (1992) · Science · doi:10.1126/science.1589766 · Cited by 244 · see citing works
Young, L. J., Winslow, J., Nilsen, R., & Insel, T. R. (1997) · Behavioral Neuroscience · doi:10.1037//0735-7044.111.3.599 · Cited by 235 · see citing works
Self-citationEngelmann, M., & Landgraf, R. (1994) · Physiology & Behavior · doi:10.1016/0031-9384(94)90022-1 · Cited by 225 · see citing works
Low doses of oxytocin facilitate social recognition in rats
Popik, P., Vetulani, J., & van Ree, J. M. (1992) · Psychopharmacology · doi:10.1007/bf02253591 · Cited by 212 · see citing works
Young, L. J., Winslow, J. T., Nilsen, R., & Insel, T. R. (1997) · Behavioral Neuroscience · doi:10.1037/0735-7044.111.3.599 · Cited by 196 · see citing works
Self-citationKendrick, K. M., Keverne, E. B., Baldwin, B. A., & Sharman, D. F. (2008) · Neuroendocrinology · doi:10.1159/000124638 · Cited by 187 · see citing works
Chapter 1.1 Anatomy and function of extrahypothalamic vasopressin systems in the brain
Vries, G. J. D., & MILLER, M. A. (1999) · Progress in brain research · doi:10.1016/s0079-6123(08)61558-7 · Cited by 183 · see citing works
Oxytocin Facilitation of Maternal Behavior in Sheepa
Keverne, E. B., & Kendrick, K. M. (1992) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1992.tb34348.x · Cited by 183 · see citing works
Lévy, F., Kendrick, K. M., Goode, J. A., Guevara‐Guzmán, R., & Keverne, E. B. (1995) · Brain Research · doi:10.1016/0006-8993(94)01236-b · Cited by 181 · see citing works
Multiple roles of major urinary proteins in the house mouse, Mus domesticus
Beynon, R. J., & Hurst, J. L. (2003) · Biochemical Society Transactions · doi:10.1042/bst0310142 · Cited by 173 · see citing works
Dluzen, D. E., Muraoka, S., Engelmann, M., & Landgraf, R. (1998) · Peptides · doi:10.1016/s0196-9781(98)00047-3 · Cited by 169 · see citing works
Landgraf, R., Frank, E., Aldag, J. M., Neumann, I. D., Sharer, C. A., Ren, X., Terwilliger, E. F., Niwa, M., Wigger, A., & Young, L. J. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02750.x · Cited by 164 · see citing works
Self-citationAndrogen-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 · see citing works
Endogenous oxytocin is involved in short-term olfactory memory in female rats
Engelmann, M., Ebner, K., Wotjak, C. T., & Landgraf, R. (1998) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)00084-3 · Cited by 156 · see citing works
Everts, H. G. J., & Koolhaas, J. M. (1999) · Behavioural Brain Research · doi:10.1016/s0166-4328(98)00004-7 · Cited by 148 · see citing works
Vasopressin and oxytocin receptors
Zingg, H. H. (1996) · Baillière s Clinical Endocrinology and Metabolism · doi:10.1016/s0950-351x(96)80314-4 · Cited by 137 · see citing works
Centrally injected arginine vasopressin (AVP) facilitates social memory in rats
Moal, M. L., Dantzer, R., Michaud, B., & Koob, G. F. (1987) · Neuroscience Letters · doi:10.1016/0304-3940(87)90527-1 · Cited by 131 · see citing works
Greidanus, T. B. V. W., van Ree, J. M., & de Wied, D. (1983) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(83)90036-0 · Cited by 130 · see citing works
Polymodal dose-response curve for oxytocin in the social recognition test
Benelli, A., Bertolini, A., Poggioli, R., Menozzi, B., Basaglia, R., & Arletti, R. (1995) · Neuropeptides · doi:10.1016/0143-4179(95)90029-2 · Cited by 128 · see citing works
The role of limbic vasopressin and oxytocin in social recognition
van Wimersma Greidanus, T. B., & Maigret, C. (1996) · Brain Research · doi:10.1016/0006-8993(95)01505-1 · Cited by 117 · see citing works
Dluzen, D. E., Muraoka, S., Engelmann, M., Ebner, K., & Landgraf, R. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00952.x · Cited by 100 · see citing works
Lateral septal vasopressin in rats: role in social and object recognition?
Everts, H. G. J., & Koolhaas, J. M. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00269-2 · Cited by 98 · see citing works
Roles of the basolateral amygdala and hippocampus in social recognition in rats
Maaswinkel, H., Baars, A. M., Gispen, W. H., & Spruijt, B. M. (1996) · Physiology & Behavior · doi:10.1016/0031-9384(95)02233-3 · Cited by 97 · see citing works
Daenen, E. W. P. M., Wolterink, G., Gerrits, M. A. F. M., & van Ree, J. M. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00223-1 · Cited by 93 · see citing works
Dluzen, D. E., Muraoka, S., & Landgraf, R. (1998) · Neuroscience Letters · doi:10.1016/s0304-3940(98)00691-0 · Cited by 89 · see citing works
Role of the vomeronasal system in vasopressinergic modulation of social recognition in rats
Bluthé, R.-M., & Dantzer, R. (1993) · Brain Research · doi:10.1016/0006-8993(93)90370-3 · Cited by 85 · see citing works
Ferris, C. F., Gold, L., Vries, G. J. D., & Potegal, M. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902930310 · Cited by 78 · see citing works
Impaired discrimination of and aversion to parasitized male odors by female oxytocin knockout mice
Kavaliers, M., Colwell, D. D., Choleris, E., Ågmo, A., Muglia, L. J., Ogawa, S., & Pfaff, D. W. (2003) · Genes, Brain and Behavior · doi:10.1034/j.1601-183x.2003.00021.x · Cited by 78 · see citing works
Opposite action of oxytocin and its peptide antagonists on social memory in rats
Popik, P., & Vetulani, J. (1991) · Neuropeptides · doi:10.1016/0143-4179(91)90159-g · Cited by 77 · see citing works
Johnson, A. E., Audigier, S., Rossi, F., Jard, S., Tribollet, E., & Barberis, C. (1993) · Brain Research · doi:10.1016/0006-8993(93)90795-o · Cited by 77 · see citing works
Engelmann, M., Ludwig, M., & Landgraf, R. (1994) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1994.tb00598.x · Cited by 76 · see citing works
Szot, P., & Dorsa, D. M. (1993) · Developmental Brain Research · doi:10.1016/0165-3806(93)90136-x · Cited by 65 · see citing works
Neural mechanisms underlying the action of primer pheromones in mice
Li, C.-S. R., Kaba, H., Saitô, H., & Seto, K. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90019-z · Cited by 48 · see citing works
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 44 · see citing works
Executive function of the hippocampus in social behavior in the rat.
Maaswinkel, H., Gispen, W. H., & Spruijt, B. M. (1997) · Behavioral Neuroscience · doi:10.1037//0735-7044.111.4.777 · Cited by 42 · see citing works
Facilitation and attenuation of social recognition in rats by different oxytocin-related peptides
Popik, P., Vetulani, J., & Van Ree, J. M. (1996) · European Journal of Pharmacology · doi:10.1016/0014-2999(96)00215-4 · Cited by 42 · see citing works
Androgenic regulation of chemoinvestigatory behaviors in male and female hamsters
Powers, J. B., & Bergondy, M. L. (1983) · Hormones and Behavior · doi:10.1016/0018-506x(83)90013-2 · Cited by 40 · see citing works
Executive function of the hippocampus in social behavior in the rat.
Maaswinkel, H., Gispen, W. H., & Spruijt, B. M. (1997) · Behavioral Neuroscience · doi:10.1037/0735-7044.111.4.777 · Cited by 37 · see citing works
Effects of small amygdala lesions on fear, but not aggression, in the rat
Oakes, M. E., & Coover, G. D. (1997) · Physiology & Behavior · doi:10.1016/s0031-9384(96)00348-4 · Cited by 36 · see citing works
DISTURBED BEHAVIOR AND MEMORY OF THE BRATTLEBORO RAT
Greidanus, T. B. V. W. (1982) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1982.tb37484.x · Cited by 34 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Social effects of oxytocin in humans: context and person matter
Bartz, J. A., Zaki, J., Bolger, N., & Ochsner, K. N. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.05.002 · Cited by 1,572 · see citing works
Assessment of positive emotions in animals to improve their welfare
Boissy, A., Manteuffel, G., Jensen, M. B., Moe, R. O., Spruijt, B., Keeling, L. J., Winckler, C., Forkman, B., Dimitrov, I., Langbein, J., et al. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.02.003 · Cited by 1,486 · see citing works
Neumann, I. D., & Landgraf, R. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.08.004 · Cited by 954 · see citing works
The science of interpersonal touch: An overview
Gallace, A., & Spence, C. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.10.004 · Cited by 879 · see citing works
Brain oxytocin: A key regulator of emotional and social behaviours in both females and males
Neumann, I. D. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01726.x · Cited by 743 · see citing works
Lebow, M. A., & Chen, A. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.1 · Cited by 660 · see citing works
Neuropeptidergic regulation of affiliative behavior and social bonding in animals
Lim, M. M., & Young, L. J. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.06.028 · Cited by 624 · see citing works
Self-citationThe Peptide That Binds: A Systematic Review of Oxytocin and its Prosocial Effects in Humans
MacDonald, K., & MacDonald, T. M. (2010) · Harvard Review of Psychiatry · doi:10.3109/10673220903523615 · Cited by 585 · see citing works
Microsatellite instability generates diversity in brain and sociobehavioral traits
Hammock, E. A. D., & Young, L. J. (2005) · Science · doi:10.1126/science.1111427 · Cited by 545 · see citing works
Self-citationNeuromodulation by Oxytocin and Vasopressin
Stoop, R. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.025 · Cited by 506 · see citing works
Bos, P. A., Panksepp, J., Bluthé, R.-M., & Honk, J. V. (2012) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2011.01.002 · Cited by 429 · see citing works
Oxytocin Attenuates Affective Evaluations of Conditioned Faces and Amygdala Activity
Petrovic, P., Kalisch, R., Singer, T., & Dolan, R. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4572-07.2008 · Cited by 424 · see citing works
“At first glance, this might seem to conflict with findings that oxytocin receptor knock-out mice have lower social recognition of conspecifics (Ferguson et al., 2002; Bielsky and Young, 2004).”
ResultAutism, oxytocin and interoception
Quattrocki, E., & Friston, K. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.09.012 · Cited by 393 · see citing works
Oxytocin Makes a Face in Memory Familiar
Rimmele, U., Hediger, K., Heinrichs, M., & Klaver, P. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.4260-08.2009 · Cited by 402 · see citing works
Bosch, O. J., & Neumann, I. D. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.11.002 · Cited by 400 · see citing works
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 · see citing works
The neural mechanisms and circuitry of the pair bond
Walum, H., & Young, L. J. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0072-6 · Cited by 353 · see citing works
Self-citationBielsky, I. F., Hu, S.-B., Ren, X., Terwilliger, E. F., & Young, L. J. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.031 · Cited by 367 · see citing works
Self-citationRilling, J. K., DeMarco, A. C., Hackett, P. D., Chen, X., Gautam, P., Stair, S., Haroon, E., Thompson, R., Ditzen, B., Patel, R., et al. (2014) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2013.09.022 · Cited by 343 · see citing works
“Given significant cross-reactivity between OT and AVP systems (Audigier & Barberis, 1985), coupled with evidence that OT and AVP can have similar effects on behavior (Bielsky & Young, 2004), it is important to determine whether intranasal OT and AVP activate similar or different brain regions.”
BackgroundCentral vasopressin and oxytocin release: regulation of complex social behaviours
VEENEMA, A., & NEUMANN, I. (2008) · Progress in Brain Research · doi:10.1016/s0079-6123(08)00422-6 · Cited by 338 · see citing works
Ring, R. H., Malberg, J. E., Potestio, L., Ping, J., Boikess, S., Luo, B., Schechter, L. E., Rizzo, S., Rahman, Z., & Rosenzweig-Lipson, S. (2006) · Psychopharmacology · doi:10.1007/s00213-005-0293-z · Cited by 319 · see citing works
Does Oxytocin Increase Trust in Humans? A Critical Review of Research
Nave, G., Camerer, C., & McCullough, M. (2015) · Perspectives on Psychological Science · doi:10.1177/1745691615600138 · Cited by 309 · see citing works
Burkett, J. P., & Young, L. J. (2012) · Psychopharmacology · doi:10.1007/s00213-012-2794-x · Cited by 307 · see citing works
“Taken together , these data demonstrate a role for OT and AVP in the selective processing of social aspects of memory ( for reviews , see Bielsky and Young 2004 ; Wacker and Ludwig 2012 ) .”
Self-citationAlbers, H. E. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.10.007 · Cited by 288 · see citing works
Mother–infant bonding and the evolution of mammalian social relationships
Broad, K. D., Curley, J. P., & Keverne, E. B. (2006) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2006.1940 · Cited by 283 · see citing works
Brain vasopressin is an important regulator of maternal behavior independent of dams’ trait anxiety
Bosch, O. J., & Neumann, I. D. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807412105 · Cited by 280 · see citing works
Israel, S., Lerer, E., Shalev, I., Uzefovsky, F., Riebold, M., Laiba, E., Bachner-Melman, R., Maril, A., Bornstein, G., Knafo, A., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005535 · Cited by 278 · see citing works
Post-learning intranasal oxytocin modulates human memory for facial identity
Savaskan, E., Ehrhardt, R., Schulz, A., Walter, M., & Schächinger, H. (2008) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2007.12.004 · Cited by 262 · see citing works
Targeted activation of the hippocampal CA2 area strongly enhances social memory
Smith, A. S., Williams Avram, S. K., Cymerblit-Sabba, A., Song, J., & Young, W. S. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.189 · Cited by 236 · see citing works
Lukas, M., Toth, I., Veenema, A. H., & Neumann, I. D. (2013) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.09.018 · Cited by 211 · see citing works
Dodhia, S., Hosanagar, A., Fitzgerald, D. A., Labuschagne, I., Wood, A. G., Nathan, P. J., & Phan, K. L. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.53 · Cited by 209 · see citing works
Chronic and acute intranasal oxytocin produce divergent social effects in mice
Huang, H., Michetti, C., Busnelli, M., Managò, F., Sannino, S., Scheggia, D., Giancardo, L., Sona, D., Murino, V., Chini, B., et al. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2013.310 · Cited by 199 · see citing works
Human neuroimaging of oxytocin and vasopressin in social cognition
Zink, C. F., & Meyer-Lindenberg, A. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.01.016 · Cited by 176 · see citing works
Neumann, I. D. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.04.012 · Cited by 162 · see citing works
Transgenerational effects of prenatal bisphenol A on social recognition
Wolstenholme, J. T., Goldsby, J. A., & Rissman, E. F. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.09.007 · Cited by 157 · see citing works
Anagnostou, E., Soorya, L., Brian, J., Dupuis, A., Mankad, D., Smile, S., & Jacob, S. (2014) · Brain Research · doi:10.1016/j.brainres.2014.01.049 · Cited by 155 · see citing works
Oxytocin facilitates accurate perception of competition in men and kinship in women
Fischer-Shofty, M., Levkovitz, Y., & Shamay-Tsoory, S. G. (2013) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsr100 · Cited by 132 · see citing works
Kas, M. J., Glennon, J. C., Buitelaar, J., Ey, E., Biemans, B., Crawley, J., Ring, R. H., Lajonchere, C., Esclassan, F., Talpos, J., et al. (2014) · Psychopharmacology · doi:10.1007/s00213-013-3268-5 · Cited by 132 · see citing works
Oxytocin, vasopressin, and the motivational forces that drive social behaviors
Caldwell, H. K., & Albers, H. E. (2015) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2015_390 · Cited by 129 · see citing works
Oxytocin and vasopressin: genetics and behavioral implications
Caldwell, H. K., & Young, W. S. (2006) · Handbook of Neurochemistry and Molecular Neurobiology · doi:10.1007/978-0-387-30381-9_25 · Cited by 113 · see citing works
A Review of Oxytocin’s Effects on the Positive, Negative, and Cognitive Domains of Schizophrenia
Feifel, D., Shilling, P. D., & MacDonald, K. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.07.025 · Cited by 110 · see citing works
Antiaggressive activity of central oxytocin in male rats
Calcagnoli, F., de Boer, S. F., Althaus, M., den Boer, J. A., & Koolhaas, J. M. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3124-7 · Cited by 90 · see citing works
Pup exposure facilitates retrieving behavior via the oxytocin neural system in female mice
Okabe, S., Tsuneoka, Y., Takahashi, A., Ooyama, R., Watarai, A., Maeda, S., Honda, Y., Nagasawa, M., Mogi, K., Nishimori, K., et al. (2017) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2017.01.036 · Cited by 82 · see citing works
Frijling, J. L., van Zuiden, M., Nawijn, L., Koch, S. B. J., Neumann, I. D., Veltman, D. J., & Olff, M. (2015) · Journal of Neuroendocrinology · doi:10.1111/jne.12300 · Cited by 74 · see citing works
Oxytocin and vasopressin: Social neuropeptides with complex neuromodulatory functions
Benarroch, E. E. (2013) · Neurology · doi:10.1212/wnl.0b013e31828cfb15 · Cited by 74 · see citing works
Donaldson, Z. R., Spiegel, L., & Young, L. J. (2010) · Behavioral Neuroscience · doi:10.1037/a0018094 · Cited by 71 · see citing works
Self-citationJarcho, M. R., Mendoza, S. P., Mason, W. A., Yang, X., & Bales, K. L. (2011) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2010.00677.x · Cited by 70 · see citing works
When Two Become One: The Role of Oxytocin in Interpersonal Coordination and Cooperation
Arueti, M., Perach-Barzilay, N., Tsoory, M. M., Berger, B., Getter, N., & Shamay-Tsoory, S. G. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00400 · Cited by 67 · see citing works
Long-term effects on hypothalamic neuropeptides after developmental exposure to chlorpyrifos in mice
Tait, S., Ricceri, L., Venerosi, A., Maranghi, F., Mantovani, A., & Calamandrei, G. (2009) · Environmental Health Perspectives · doi:10.1289/ehp.11696 · Cited by 64 · see citing works
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 · see citing works
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 · see citing works
Region Specific Up-Regulation of Oxytocin Receptors in the Opioid Oprm1−/− Mouse Model of Autism
Gigliucci, V., Leonzino, M., Busnelli, M., Luchetti, A., Palladino, V. S., D’Amato, F. R., & Chini, B. (2014) · Frontiers in Pediatrics · doi:10.3389/fped.2014.00091 · Cited by 56 · see citing works
Dissecting natural sensory plasticity: hormones and experience in a maternal context
Miranda, J. A., & Liu, R. C. (2009) · Hearing Research · doi:10.1016/j.heares.2009.04.014 · Cited by 52 · see citing works
Brain vasopressin signaling modulates aspects of maternal behavior in lactating rats
Bayerl, D. S., & Bosch, O. J. (2019) · Genes, Brain and Behavior · doi:10.1111/gbb.12517 · Cited by 46 · see citing works
Coburn, C. G., Curras-Collazo, M. C., & Kodavanti, P. R. S. (2007) · Toxicological Sciences · doi:10.1093/toxsci/kfm086 · Cited by 45 · see citing works
Neonatal MeCP2 is important for the organization of sex differences in vasopressin expression
Forbes-Lorman, R. M., Rautio, J. J., Kurian, J. R., Auger, A. P., & Auger, C. J. (2012) · Epigenetics · doi:10.4161/epi.7.3.19265 · Cited by 43 · see citing works
Vasopressin and oxytocin in CSF and plasma of patients with aneurysmal subarachnoid haemorrhage
Martin, J., Kagerbauer, S. M., Schuster, T., Blobner, M., Kochs, E. F., & Landgraf, R. (2014) · Neuropeptides · doi:10.1016/j.npep.2013.12.004 · Cited by 40 · see citing works
Engell, M. D., Godwin, J., Young, L. J., & Vandenbergh, J. G. (2006) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2005.10.002 · Cited by 40 · see citing works
Self-citationHypothalamic Supramammillary Control of Cognition and Motivation
Kesner, A. J., Mozaffarilegha, M., Thirtamara Rajamani, K., Arima, Y., Harony-Nicolas, H., Hashimotodani, Y., Ito, H. T., Song, J., & Ikemoto, S. (2023) · The Journal of Neuroscience · doi:10.1523/jneurosci.1320-23.2023 · Cited by 35 · see citing works
Helping behavior in prairie voles: a model of empathy and the importance of oxytocin
Kitano, K., Yamagishi, A., Horie, K., Nishimori, K., & Sato, N. (2022) · iScience · doi:10.1016/j.isci.2022.103991 · Cited by 31 · see citing works
Progesterone impairs social recognition in male rats
Bychowski, M. E., & Auger, C. J. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.02.009 · Cited by 25 · see citing works
“…a conspecific after an initial exposure typically lasts only 30 minutes; however, subcutaneous injections of AVP in rats and mice can facilitate social recognition by lengthening this social memory to 2 hours after initial exposure to a conspecific (Dantzer et al., 1987;Bielsky and Young, 2004).”
BackgroundCoria-Avila, G. A., Herrera-Covarrubias, D., García, L. I., Toledo, R., Hernández, M. E., Paredes-Ramos, P., Corona-Morales, A. A., & Manzo, J. (2022) · Animals · doi:10.3390/ani12243589 · Cited by 25 · see citing works
Development of a genetically-encoded oxytocin sensor
Mignocchi, N., Krüssel, S., Jung, K., Lee, D., & Kwon, H.-B. (2020) · doi:10.1101/2020.07.14.202598 · Cited by 22 · see citing works
Leithead, A. B., Godino, A., Barbier, M., & Harony-Nicolas, H. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.05.016 · Cited by 21 · see citing works
Socially-mediated activation in the snake social-decision-making network
Skinner, M., Daanish, D., Damphousse, C. C., Krohmer, R. W., Mallet, P. E., McKay, B. E., & Miller, N. (2024) · Behavioural Brain Research · doi:10.1016/j.bbr.2024.114965 · Cited by 3 · see citing works
- Authors
- Bielsky, I. F., & Young, L. J.
- Affiliations
- Emory University (US)
- Corresponding author
- Bielsky, Isadora F.
- ORCID
- Young, Larry J.
- Venue
- Peptides
- Publisher
- Elsevier BV
- Published
- 2004-09
- Volume
- 25
- Issue
- 9
- Pages
- 1565-1574
- ISSN
- 0196-9781 (ISSN-L)
- OpenAlex
- W2121134774
- Cited by
- 460
- References
- 66
- Citations by year
- 2026: 11 · 2025: 18 · 2024: 12 · 2023: 16 · 2022: 17 · 2021: 28 · 2020: 17 · 2019: 17 · 2018: 23 · 2017: 22 · 2016: 24 · 2015: 30 · 2014: 25 · 2013: 24 · 2012: 27
- FWCI
- 2.39
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Peptides (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Foundation
- National Institutes of Health (1f31mh070112-01)
- National Institute of Mental Health (MH-64692, K02MH064692, MH 56897, MH070112, R01MH056538, MH056538)
- National Center for Research Resources (RR-00 165, P51RR000165)
- Topics
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Human-Animal Interaction Studies
- Keywords
- oxytocin, vasopressin, social recognition, social memory, pheromones, social discrimination, social cognition, offspring recognition, mate preferences, rats, mice, sheep
- MeSH terms
- Animals, Brain, Arvicolinae, Female, Male, Models, Biological, Oxytocin, Peptides, Time Factors, Vasopressins, Receptors, Vasopressin, Receptors, Oxytocin, Mice, 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