The regulation of social recognition, social communication and aggression: vasopressin in the social behavior neural network

Albers, H. Elliott

doi:10.1016/j.yhbeh.2011.10.007

Cited by 290Neuroendocrine regulation and behaviorNeuropeptides and Animal PhysiologyNeurotransmitter Receptor Influence on Behavior

The regulation of social recognition, social communication and aggression: vasopressin in the social behavior neural network

Albers, H. Elliott·2012·Hormones and Behavior

DOI 10.1016/j.yhbeh.2011.10.007

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Abstract

Neuropeptides in the arginine vasotocin/arginine vasopressin (AVT/AVP) family play a major role in the regulation of social behavior by their actions in the brain. In mammals, AVP is found within a circuit of recriprocally connected limbic structures that form the social behavior neural network. This review examines the role played by AVP within this network in controlling social processes that are critical for the formation and maintenance of social relationships: social recognition, social communication and aggression. Studies in a number of mammalian species indicate that AVP and AVP V1a receptors are ideally suited to regulate the expression of social processes because of their plasticity in response to factors that influence social behavior. The pattern of AVP innervation and V1a receptors across the social behavior neural network may determine the potential range and intensity of social responses that individuals display in different social situations. Although fundamental information on how social behavior is wired in the brain is still lacking, it is clear that different social behaviors can be influenced by the actions of AVP in the same region of the network and that AVP can act within multiple regions of this network to regulate the expression of individual social behaviors. The existing data suggest that AVP can influence social behavior by modulating the interpretation of sensory information, by influencing decision making and by triggering complex motor outputs. This article is part of a Special Issue entitled Oxytocin, Vasopressin, and Social Behavior.

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From Cross-talk among oxytocin and arginine-vasopressin receptors: Relevance for basic and clinical studies of the brain and periphery (2018) · cites this paper as [62]

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Elliott Albers, H., Dean, A., Karom, M. C., Smith, D., & Huhman, K. L. (2006) · Brain Research · doi:10.1016/j.brainres.2005.12.081 · Cited by 78 · see citing works
Self-citation
Role of vasopressin and oxytocin in the control of social behavior in Syrian hamsters(Mesocricetus auratus
Albers, H. E., & Bamshad, M. (1999) · Progress in brain research · doi:10.1016/s0079-6123(08)61583-6 · Cited by 72 · see citing works
Self-citation
Adolescent exposure to anabolic/androgenic steroids and the neurobiology of offensive aggression: A hypothalamic neural model based on findings in pubertal Syrian hamsters
Melloni, R. H., & Ricci, L. A. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.11.002 · Cited by 72 · see citing works
Social Recognition in Ovariectomized and Estradiol-Treated Female Rats
Hliňáck, Z. (1993) · Hormones and Behavior · doi:10.1006/hbeh.1993.1012 · Cited by 72 · see citing works
Neurohypophysial hormones and sexual behavior in males of the domestic fowl (Gallus domesticus L.) and the pigeon (Columba livia Gmel.)
Kihlström, J. E., & Danninge, I. (1972) · General and Comparative Endocrinology · doi:10.1016/0016-6480(72)90087-1 · Cited by 69 · see citing works
Intraspecific aggression in male hamsters is inhibited by intrahypothalamic vasopressin‐receptor antagonist
Potegal, M., & Ferris, C. F. (1989) · Aggressive Behavior · doi:10.1002/ab.2480150406 · Cited by 69 · see citing works
Neural mechanisms of individual and sexual recognition in Syrian hamsters (Mesocricetus auratus)
Petrulis, A. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.10.027 · Cited by 69 · see citing works
Organization and expression of agonistic and socio-sexual behavior in golden hamsters over the estrous cycle and after ovariectomy
Takahashi, L. K., & Lisk, R. D. (1983) · Physiology & Behavior · doi:10.1016/0031-9384(83)90069-0 · Cited by 68 · see citing works
Behavioral and biochemical responses of mice to the intraventricular administration of ACTH analogs and lysine vasopressin
Rees, H. D., Dunn, A. J., & Iuvone, P. M. (1976) · Life Sciences · doi:10.1016/0024-3205(76)90212-5 · Cited by 67 · see citing works
Testosterone alters the behavioral response of the medial preoptic-anterior hypothalamus to microinjection of arginine vasopressin in the hamster
Albers, H. E., Liou, S. Y., & Ferris, C. F. (1988) · Brain Research · doi:10.1016/0006-8993(88)90244-2 · Cited by 65 · see citing works
Self-citation
Castration reduces vasopressin receptor binding in the hamster hypothalamus
Johnson, A. E., Barberis, C., & Elliott Albers, H. (1995) · Brain Research · doi:10.1016/0006-8993(95)00010-n · Cited by 65 · see citing works
Self-citation
ACTH and Vasopressin Treatments Immediately After a Defeat Increase Future Submissiveness in Male Mice
Roche, K. E., & Leshner, A. I. (1979) · Science · doi:10.1126/science.221973 · Cited by 64 · see citing works
Repeated agonistic encounters in hamsters modulate AVP V1a receptor binding
COOPER, M., KAROM, M., HUHMAN, K., & ELLIOTTALBERS, H. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.04.012 · Cited by 61 · see citing works
An iodinated vasopressin (V1) antagonist blocks flank marking and selectively labels neural binding sites in golden hamsters
Ferris, C. F., Delville, Y., Grzonka, Z., Luber‐Narod, J., & Insel, T. R. (1993) · Physiology & Behavior · doi:10.1016/0031-9384(93)90085-t · Cited by 61 · see citing works
Vasopressin mediates enhanced offspring protection in multiparous rats
Nephew, B. C., Byrnes, E. M., & Bridges, R. S. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.06.032 · Cited by 60 · see citing works
Arginine-vasopressin immunoreactivity is not altered by photoperiod or gonadal hormones in the Syrian hamster (Mesocricetus auratus)
Albers, H. E., Rowland, C. M., & Ferris, C. F. (1991) · Brain Research · doi:10.1016/0006-8993(91)90696-s · Cited by 59 · see citing works
Self-citation
Arginine vasopressin V1a receptor antagonist impairs maternal memory in rats
Nephew, B. C., & Bridges, R. S. (2008) · Physiology & Behavior · doi:10.1016/j.physbeh.2008.05.016 · Cited by 57 · see citing works
Neuropeptide modulation of social and exploratory behaviors in laboratory rodents
Crawley, J. N., Hays, S. E., O’Donohue, T. L., Paul, S. M., & Goodwin, F. K. (1981) · Peptides · doi:10.1016/0196-9781(81)90066-8 · Cited by 57 · see citing works
Manipulations of vasopressin alter aggression differently across testing conditions in monogamous and non-monogamousPeromyscus mice
Bester‐Meredith, J. K., MARTIN, P. A., & Marler, C. A. (2005) · Aggressive Behavior · doi:10.1002/ab.20075 · Cited by 57 · see citing works
Vasopressin maintains long-term potentiation in rat lateral septum slices
van den Hooff, P., Urban, I. J. A., & de Wied, D. (1989) · Brain Research · doi:10.1016/0006-8993(89)91440-6 · Cited by 54 · see citing works
Gonadal steroids influence neurophysin II distribution in the forebrain of normal and mutant mice
Mayes, C. R., Watts, A. G., McQueen, J., Fink, G., & Charlton, H. M. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90054-1 · Cited by 54 · see citing works
Novel Mechanisms Underlying Neuroendocrine Regulation of Aggression: A Synthesis of Rodent, Avian, and Primate Studies
Demas, G. E., Cooper, M. A., Albers, H. E., & Soma, K. K. (2006) · Springer eBooks · doi:10.1007/978-0-387-30405-2_8 · Cited by 54 · see citing works
Self-citation
Activity of Vasopressinergic Neurones of the Human Supraoptic Nucleus os Age‐ and Sex‐Dependent
Ishunina, Salehi, A., Hofman, & Swaab, D. F. (1999) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1999.00318.x · Cited by 53 · see citing works
Microinjection of arginine-vasopressin into the periaqueductal gray stimulates flank marking in Syrian-hamsters (Mesocricetus-Auratus)
Hennessey, A. C., Carol Whitman, D., & elliott Albers, H. (1992) · Brain Research · doi:10.1016/0006-8993(92)90379-n · Cited by 52 · see citing works
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Effects of Gonadotropin-Releasing Hormones, Corticotropin-Releasing Hormone, and Vasopressin on Female Sexual Behavior
Schiml, P. A., & Rissman, E. F. (2000) · Hormones and Behavior · doi:10.1006/hbeh.2000.1575 · Cited by 50 · see citing works
Microinjection of Kainic Acid into the Hypothalamus of Golden Hamsters Prevents Vasopressin-Dependent Flank-Marking Behavior
Ferris, C. F., Meenan, D. M., & Albers, H. E. (2008) · Neuroendocrinology · doi:10.1159/000124631 · Cited by 48 · see citing works
Self-citation
Chronic intracerebral infusions of vasopressin and vasopressin antagonist modulate social recognition in rat
Bluthé, R.-M., & Dantzer, R. (1992) · Brain Research · doi:10.1016/0006-8993(92)90480-w · Cited by 47 · see citing works
The role of neurohypophyseal peptides in the central mediation of complex social processes — evidence from comparative studies
Insel, T. R., Winslow, J. T., WILLIAMS, J. R., Hastings, N., Shapiro, L. E., & Carter, C. S. (1993) · Regulatory Peptides · doi:10.1016/0167-0115(93)90194-d · Cited by 44 · see citing works
Serotonin and vasopressin interact in the hypothalamus to control communicative behavior
Albers, E. H., Karom, M. C., & Smith, D. (2002) · Neuroreport · doi:10.1097/00001756-200205240-00006 · Cited by 44 · see citing works
Septo-hypothalamic organization of a stereotyped behavior controlled by vasopressin in golden hamsters
Ferris, C. F., Delville, Y., Irvin, R. W., & Potegal, M. (1994) · Physiology & Behavior · doi:10.1016/0031-9384(94)90056-6 · Cited by 43 · see citing works
Sexual differences in the magnocellular vasopressinergic system in golden hamsters
Delville, Y., Koh, E. T., & Ferris, C. F. (1994) · Brain Research Bulletin · doi:10.1016/0361-9230(94)90080-9 · Cited by 39 · see citing works
Vasopressin and the Regulation of Hamster Social Behaviora
Albers, H. E., Hennessey, A. C., & Whitman, D. C. (1992) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1992.tb34358.x · Cited by 39 · see citing works
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Unique evolution of neurohypophysial hormones in cartilaginous fishes: Possible implications for urea-based osmoregulation
Acher, R., Chauvet, J., Chauvet, M. T., & Rouillé, Y. (1999) · Journal of Experimental Zoology · doi:10.1002/(sici)1097-010x(19991001)284:5 · Cited by 39 · see citing works
Memory for individuals: Hamsters (Mesocricetus auratus) require contact to develop multicomponent representations (concepts) of others.
Johnston, R. E., & Peng, A. (2008) · Journal of comparative psychology · doi:10.1037/0735-7036.122.2.121 · Cited by 38 · see citing works
Kin recognition by self-referent phenotype matching: weighing the evidence
Mateo, J. M., & Johnston, R. E. (2003) · Animal Cognition · doi:10.1007/s10071-003-0165-z · Cited by 38 · see citing works
Neurochemical responses of mice to ACTH and lysine vasopressin
Dudin, A. J., Iuvone, M., & Rees, H. D. (1976) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(76)90343-9 · Cited by 37 · see citing works
Central vasopressin V1a receptors modulate neural processing in mothers facing intruder threat to pups
Caffrey, M. K., Nephew, B. C., & Febo, M. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.06.023 · Cited by 36 · see citing works
Kainic Acid Lesion of Vasopressinergic Neurons in the Hypothalamus Disrupts Flank Marking Behavior in Golden Hamsters
Ferris, C. F., Irvin, R. W., Potegal, M., & Axelson, J. F. (1990) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1990.tb00841.x · Cited by 36 · see citing works
Anterior hypothalamic vasopressin modulates the aggression-stimulating effects of adolescent cocaine exposure in Syrian hamsters
Jackson, D., Burns, R., Trksak, G. H., Simeone, B. P., DeLeon, K. R., Connor, D. F., Harrison, R. J., & Melloni, R. H. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.02.047 · Cited by 34 · see citing works
Estradiol increases the behavioral response to arginine vasopressin (AVP) in the medial preoptic-anterior hypothalamus
Huhman, K. L., & Albers, H. E. (1993) · Peptides · doi:10.1016/0196-9781(93)90085-u · Cited by 34 · see citing works
Self-citation
Short‐Photoperiod Exposure Reduces Vasopressin (V1a) Receptor Binding But Not Arginine‐Vasopressin‐Induced Flank Marking in Male Syrian Hamsters
Caldwell, H. K., & Albers, H. E. (2003) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2003.01086.x · Cited by 33 · see citing works
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Effects of testosterone on the behavioral response to arginine vasopressin microinjected into the central gray and septum
Albers, H. E., & Cooper, T. T. (1995) · Peptides · doi:10.1016/0196-9781(94)00188-x · Cited by 33 · see citing works
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Vasopressin and sex differences in hamster flank marking
Hennessey, A. C., Huhman, K. L., & Albers, H. E. (1994) · Physiology & Behavior · doi:10.1016/0031-9384(94)90078-7 · Cited by 33 · see citing works
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Vasopressin and behavior: from memory to olfaction
Dantzer, R., & Bluthé, R.-M. (1993) · Regulatory Peptides · doi:10.1016/0167-0115(93)90193-c · Cited by 32 · see citing works
Sexual differences in vasopressin receptor binding within the ventrolateral hypothalamus in golden hamsters
Delville, Y., & Ferris, C. F. (1995) · Brain Research · doi:10.1016/0006-8993(95)00291-w · Cited by 31 · see citing works
Sex differences in odor-stimulated flank marking in the golden hamster (Mesocricetus auratus)
Albers, H. E. (1992) · Hormones and Behavior · doi:10.1016/0018-506x(92)90044-v · Cited by 31 · see citing works
Self-citation
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 · see citing works
Social experience and social context alter the behavioral response to centrally administered oxytocin in female Syrian hamsters
Harmon, A. C., Moore, T. O., Huhman, K. L., & Albers, H. E. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00523-1 · Cited by 30 · see citing works
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Coordination of hamster lordosis and flank marking behavior: Role of arginine vasopressin within the medial preoptic-anterior hypothalamus
Albers, H. E., & Rawls, S. (1989) · Brain Research Bulletin · doi:10.1016/0361-9230(89)90168-8 · Cited by 30 · see citing works
Self-citation
Regional differences in testosterone effects on vasopressin receptors and on vasopressin immunoreactivity in intact and castrated Siberian hamsters
Dubois‐Dauphin, M., Theler, J., Ouarour, A., Pévet, P., Barberis, C., & Dreifuss, J. J. (1994) · Brain Research · doi:10.1016/0006-8993(94)90659-9 · Cited by 28 · see citing works
Vasopressin impairs or enhances retention of learned submissive behavior in mice depending on the time of application
Siegfried, B., Frischknecht, H.-R., & Waser, P. G. (1984) · Behavioural Brain Research · doi:10.1016/0166-4328(84)90218-3 · Cited by 27 · see citing works
Communication
Johnston, R. E. (1985) · Springer eBooks · doi:10.1007/978-1-4757-0815-8_6 · Cited by 26 · see citing works
Glutamate and vasopressin interact to control scent marking in Syrian hamsters (Mesocricetus auratus)
Bamshad, M., Cooper, T. T., Karom, M. C., & Albers, H. E. (1996) · Brain Research · doi:10.1016/0006-8993(96)00670-1 · Cited by 24 · see citing works
Self-citation
Glutamate-vasopressin interactions and the neurobiology of anabolic steroid-induced offensive aggression
Carrillo, M., Ricci, L. A., & Melloni, R. H. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.03.056 · Cited by 22 · see citing works
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 · see citing works
Chronic intracerebral infusions of vasopressin and vasopressin antagonist modulate behavioral effects of interleukin-1 in rat
Bluthé, R.-M., & Dantzer, R. (1992) · Brain Research Bulletin · doi:10.1016/0361-9230(92)90162-q · Cited by 17 · see citing works
Photoperiodic mechanisms controlling scent marking: interactions of vasopressin and gonadal steroids
Caldwell, H. K., Smith, D. A., & Albers, H. E. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06071.x · Cited by 17 · see citing works
Self-citation
LACK OF THIRST, OSMORECEPTOR DYSFUNCTION, EARLY PUBERTY AND ABNORMALLY AGGRESSIVE BEHAVIOUR IN TWO BOYS
Dunger, D. B., Lightman, S. L., WILLIAMS, M., Preece, M. A., & Grant, D. (1985) · Clinical Endocrinology · doi:10.1111/j.1365-2265.1985.tb00146.x · Cited by 15 · see citing works
Ovarian hormones alter the behavioral response of the medial preoptic anterior hypothalamus to arginine-vasopressin
Albers, H. E., Karom, M. C., & Whitman, D. C. (1996) · Peptides · doi:10.1016/s0196-9781(96)00194-5 · Cited by 15 · see citing works
Self-citation
Arginine vasotocin and aggression in rats
Brown, R. A., & King, M. G. (1984) · Peptides · doi:10.1016/0196-9781(84)90179-7 · Cited by 13 · see citing works
Seasonal regulation of social communication by photoperiod and testosterone: Effects of arginine–vasopressin, serotonin and galanin in the medial preoptic area–anterior hypothalamus
Gutzler, S. J., Karom, M. C., Erwin, W. D., & Albers, H. E. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.07.042 · Cited by 13 · see citing works
Self-citation
Galanin antagonizes vasopressin-stimulated flank marking in male golden hamsters
Ferris, C. F., Delville, Y., Bonigut, S., & MILLER, M. A. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01432-8 · Cited by 13 · see citing works
Norepinephrine Inhibits Vasopressin‐Stimulated Flank Marking in the Syrian Hamster by Acting Within the Medial Preoptic‐Anterior Hypothalamus
Whitman, D. C., Hennessey, A. C., & Albers, H. E. (1992) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1992.tb00202.x · Cited by 10 · see citing works
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The Golden Hamster, Mesocricetus auratus
Robinson, R. (1975) · Springer eBooks · doi:10.1007/978-1-4613-4470-4_12 · Cited by 6 · see citing works

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Oxytocin pathways and the evolution of human behavior
Carter, C. S. (2014) · Annual Review of Psychology · doi:10.1146/annurev-psych-010213-115110 · Cited by 714 · see citing works
Neural mechanisms of mother–infant bonding and pair bonding: Similarities, differences, and broader implications
Numan, M., & Young, L. J. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.05.015 · Cited by 355 · 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
Sex differences in the neural and behavioral response to intranasal oxytocin and vasopressin during human social interaction
Rilling, 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
“For example, although AVP injections in the anterior hypothalamus of male hamsters stimulate aggression in the resident-intruder test, the same injections decrease aggression in females (Albers, 2012).”
Background
Stress, hypothalamic–pituitary–adrenal axis, hypothalamic–pituitary–gonadal axis, and aggression.
Mbiydzenyuy, N. E., & Qulu, L.-A. (2024) · Metabolic Brain Disease · doi:10.1007/s11011-024-01393-w · Cited by 255 · see citing works
Cross-talk among oxytocin and arginine-vasopressin receptors: Relevance for basic and clinical studies of the brain and periphery
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Oxytocin and vasopressin: powerful regulators of social behavior
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Species, sex and individual differences in the vasotocin/vasopressin system: relationship to neurochemical signaling in the social behavior neural network
Albers, H. E. (2015) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.07.001 · Cited by 200 · see citing works
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A randomized placebo-controlled pilot trial shows that intranasal vasopressin improves social deficits in children with autism
Parker, K. J., Oztan, O., Libove, R. A., Mohsin, N., Karhson, D. S., Sumiyoshi, R. D., Summers, J. E., Hinman, K. E., Motonaga, K. S., Phillips, J. M., et al. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aau7356 · Cited by 185 · see citing works
Developmental Perspectives on Oxytocin and Vasopressin
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The Oxytocin–Vasopressin Pathway in the Context of Love and Fear
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Oxytocin and vasopressin effects on the neural response to social cooperation are modulated by sex in humans
Feng, C., Hackett, P. D., DeMarco, A. C., Chen, X., Stair, S., Haroon, E., Ditzen, B., Pagnoni, G., & Rilling, J. K. (2015) · Brain Imaging and Behavior · doi:10.1007/s11682-014-9333-9 · Cited by 157 · see citing works
Neuroanatomical distribution of oxytocin and vasopressin 1a receptors in the socially monogamous coppery titi monkey (Callicebus cupreus)
Freeman, S. M., Walum, H., Inoue, K., Smith, A. L., Goodman, M. M., Bales, K. L., & Young, L. J. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.04.055 · Cited by 153 · see citing works
Social functions of individual vasopressin–oxytocin cell groups in vertebrates: What do we really know?
Kelly, A. M., & Goodson, J. L. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.04.005 · Cited by 141 · see citing works
The neuroscience of social feelings: mechanisms of adaptive social functioning
Eslinger, P. J., Anders, S., Ballarini, T., Boutros, S., Krach, S., Mayer, A. V., Moll, J., Newton, T. L., Schroeter, M. L., de Oliveira-Souza, R., et al. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.05.028 · Cited by 130 · see citing works
Oxytocin, vasopressin, and the motivational forces that drive social behaviors
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A phase 2 clinical trial of a vasopressin V1a receptor antagonist shows improved adaptive behaviors in men with autism spectrum disorder
Bolognani, F., del Valle Rubido, M., Squassante, L., Wandel, C., Derks, M., Murtagh, L., Sevigny, J., Khwaja, O., Umbricht, D., & Fontoura, P. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aat7838 · Cited by 128 · see citing works
DHEA effects on brain and behavior: Insights from comparative studies of aggression
Soma, K. K., Rendon, N. M., Boonstra, R., Albers, H. E., & Demas, G. E. (2014) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2014.05.011 · Cited by 128 · see citing works
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Intranasal administration of oxytocin increases human aggressive behavior
Ne'eman, R., Perach-Barzilay, N., Fischer-Shofty, M., Atias, A., & Shamay-Tsoory, S. G. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2016.01.015 · Cited by 121 · see citing works
Serotonin and arginine–vasopressin mediate sex differences in the regulation of dominance and aggression by the social brain
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Oxytocin induces social communication by activating arginine-vasopressin V1a receptors and not oxytocin receptors
Song, Z., McCann, K. E., McNeill, J. K., Larkin, T. E., Huhman, K. L., & Albers, H. E. (2014) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2014.08.005 · Cited by 111 · see citing works
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Social isolation impairs the prefrontal-nucleus accumbens circuit subserving social recognition in mice
Park, G., Ryu, C., Kim, S., Jeong, S. J., Koo, J. W., Lee, Y., & Kim, S. J. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109104 · Cited by 105 · see citing works
Behavioural, hormonal and neurobiological mechanisms of aggressive behaviour in human and nonhuman primates
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Hypothalamic oxytocin and vasopressin neurons exert sex-specific effects on pair bonding, gregariousness, and aggression in finches
Kelly, A. M., & Goodson, J. L. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1322554111 · Cited by 106 · see citing works
Activation of oxytocin receptors, but not arginine-vasopressin V1a receptors, in the ventral tegmental area of male Syrian hamsters is essential for the reward-like properties of social interactions
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Variation in vasopressin receptor (Avpr1a) expression creates diversity in behaviors related to monogamy in prairie voles
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Authors: Albers, H. E.
Affiliations: Georgia State University (US)
Corresponding author: Albers, H. Elliott
ORCID: Albers, H. Elliott
Venue: Hormones and Behavior
Publisher: Elsevier BV
Published: 2012-03
Volume: 61
Issue: 3
Pages: 283-292
ISSN: 0018-506X (ISSN-L)
DOI: 10.1016/j.yhbeh.2011.10.007
OpenAlex: W2008920507
Cited by: 288
References: 150
Citations by year: 2026: 18 · 2025: 19 · 2024: 17 · 2023: 16 · 2022: 24 · 2021: 27 · 2020: 15 · 2019: 27 · 2018: 18 · 2017: 23 · 2016: 19 · 2015: 15 · 2014: 23 · 2013: 18 · 2012: 9
FWCI: 2.14
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Hormones and Behavior (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health
Division of Integrative Organismal Systems
Topics: Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Keywords: vasopressin, arginine vasotocin, V1a receptor, social recognition, social communication, aggression, interpersonal relationships, limbic system, neuropeptides, social behavior regulation
MeSH terms: Aggression, Animals, Brain, Brain Chemistry, Communication, Humans, Nerve Net, Social Behavior, Vasopressins, Receptors, Vasopressin, Recognition, Psychology

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The regulation of social recognition, social communication and aggression: vasopressin in the social behavior neural network

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