Vasopressin and oxytocin receptors in the central nervous system

The oxytocin receptor system: structure, function, and regulation

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Nitric oxide in the central nervous system: neuroprotection versus neurotoxicity

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Neuroendocrine perspectives on social attachment and love

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Vasopressin and oxytocin release within the brain: a dynamic concept of multiple and variable modes of neuropeptide communication

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Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function

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Oxytocin is required for nursing but is not essential for parturition or reproductive behavior.

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Enhanced partner preference in a promiscuous species by manipulating the expression of a single gene.

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Synaptic Control of Motoneuronal Excitability

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A neurobiological basis of social attachment.

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Activity-dependent structural and functional plasticity of astrocyte-neuron interactions

Theodosis, D. T., Poulain, D. A., & Oliet, S. H. R. (2008) · Physiological Reviews · doi:10.1152/physrev.00036.2007 · Cited by 531 · see citing works

Effects of Partner Support on Resting Oxytocin, Cortisol, Norepinephrine, and Blood Pressure Before and After Warm Partner Contact

Grewen, K. M., Girdler, S. S., Amico, J., & Light, K. C. (2005) · Psychosomatic Medicine · doi:10.1097/01.psy.0000170341.88395.47 · Cited by 513 · see citing works

The effects of oxytocin and vasopressin on partner preferences in male and female prairie voles (Microtus ochrogaster)

Cho, M. M., DeVries, A. C., Williams, J. R., & Carter, C. S. (1999) · Behavioral Neuroscience · doi:10.1037/0735-7044.113.5.1071 · Cited by 529 · see citing works

Increased affiliative response to vasopressin in mice expressing the V1a receptor from a monogamous vole

Young, L. J., Nilsen, R., Waymire, K. G., MacGregor, G. R., & Insel, T. R. (1999) · Nature · doi:10.1038/23475 · Cited by 488 · see citing works

More frequent partner hugs and higher oxytocin levels are linked to lower blood pressure and heart rate in premenopausal women

Light, K. C., Grewen, K. M., & Amico, J. A. (2005) · Biological Psychology · doi:10.1016/j.biopsycho.2004.11.002 · Cited by 470 · see citing works

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 · see citing works

Sex differences in oxytocin and vasopressin: Implications for autism spectrum disorders?

CARTER, C. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.08.025 · Cited by 432 · see citing works

The neurobiology of pair bonding: Insights from a socially monogamous rodent

Young, K. A., Gobrogge, K. L., Liu, Y., & Wang, Z. (2011) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.07.006 · Cited by 389 · see citing works

Vasopressin V1a and V1b Receptors: From Molecules to Physiological Systems

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Neurochemistry in the pathophysiology of autism.

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Oxytocin Attenuates Stress-Induced c-<i>fos</i>mRNA Expression in Specific Forebrain Regions Associated with Modulation of Hypothalamo–Pituitary–Adrenal Activity

Windle, R. J., Kershaw, Y. M., Shanks, N., Wood, S. A., Lightman, S. L., & Ingram, C. D. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.3432-03.2004 · Cited by 408 · see citing works

The neuropeptide oxytocin facilitates pro-social behavior and prevents social avoidance in rats and mice

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 V1a Vasopressin Receptor Is Necessary and Sufficient for Normal Social Recognition: A Gene Replacement Study

Bielsky, 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

Developmental consequences of oxytocin

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Central 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

Evidence that paraventricular nucleus oxytocin neurons link hypothalamic leptin action to caudal brain stem nuclei controlling meal size

Blevins, J. E., Schwartz, M. W., & Baskin, D. G. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00604.2003 · Cited by 332 · see citing works

Oxytocin and Vasopressin V1a and V2 Receptors Form Constitutive Homo- and Heterodimers during Biosynthesis

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Neurochemical correlates of autistic disorder: a review of the literature

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Structural bases of vasopressin/oxytocin receptor function

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Comparative Distribution of Vasopressin V1b and Oxytocin Receptor Messenger Ribonucleic Acids in Brain ¹

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Preliminary Research on Plasma Oxytocin in Normal Cycling Women: Investigating Emotion and Interpersonal Distress

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Vasopressin in the lateral septum regulates pair bond formation in male prairie voles (Microtus ochrogaster)

Liu, Y., Curtis, J. T., & Wang, Z. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.4.910 · Cited by 282 · see citing works

Immunohistochemical Localization of the Vasopressin V1b Receptor in the Rat Brain and Pituitary Gland: Anatomical Support for Its Involvement in the Central Effects of Vasopressin

Hernando, F., Schoots, O., Lolait, S. J., & Burbach, J. P. H. (2001) · Endocrinology · doi:10.1210/endo.142.4.8067 · Cited by 275 · see citing works

Neuroendocrine bases of monogamy

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Cross-talk among oxytocin and arginine-vasopressin receptors: Relevance for basic and clinical studies of the brain and periphery

Song, Z., & Albers, H. E. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.10.004 · Cited by 244 · see citing works

Oxytocin, vasopressin, and autism: Is there a connection?

Insel, T. R., O’Brien, D. J., & Leckman, J. F. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(98)00142-5 · Cited by 226 · see citing works

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

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

Oxytocin-Secreting Neurons: A Physiological Model of Morphological Neuronal and Glial Plasticity in the Adult Hypothalamus

Theodosis, D. T. (2002) · Frontiers in Neuroendocrinology · doi:10.1006/frne.2001.0226 · Cited by 219 · see citing works

Both oxytocin and vasopressin may influence alloparental behavior in male prairie voles

Bales, K. L., Kim, A. J., Lewis-Reese, A. D., & Sue Carter, C. (2004) · Hormones and Behavior · doi:10.1016/j.yhbeh.2004.01.004 · Cited by 217 · see citing works

Oxytocin and Vasopressin Receptors and Species-Typical Social Behaviors

Young, L. J. (1999) · Hormones and Behavior · doi:10.1006/hbeh.1999.1548 · Cited by 211 · see citing works

Sensory circumventricular organs: central roles in integrated autonomic regulation

Cottrell, G. T., & Ferguson, A. V. (2003) · Regulatory Peptides · doi:10.1016/j.regpep.2003.09.004 · Cited by 210 · see citing works

Selective amnesic effects of oxytocin on human memory

Heinrichs, M., Meinlschmidt, G., Wippich, W., Ehlert, U., & Hellhammer, D. H. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.07.020 · Cited by 205 · see citing works

Sex differences and developmental effects of oxytocin on aggression and social behavior in prairie voles (Microtus ochrogaster)

Bales, K. L., & Carter, C. S. (2003) · Hormones and Behavior · doi:10.1016/s0018-506x(03)00154-5 · Cited by 195 · see citing works

Oxytocin and mutual communication in mother-infant bonding

Nagasawa, M., Okabe, S., Mogi, K., & Kikusui, T. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00031 · Cited by 202 · see citing works

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

Release of Oxytocin in the Rat Central Amygdala Modulates Stress-Coping Behavior and the Release of Excitatory Amino Acids

Ebner, K., Bosch, O. J., Krömer, S. A., Singewald, N., & Neumann, I. D. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300607 · Cited by 200 · see citing works

Oxytocin-Induced Analgesia and Scratching Are Mediated by the Vasopressin-1A Receptor in the Mouse

Schorscher-Petcu, A., Sotocinal, S., Ciura, S., Dupre, A., Ritchie, J., Sorge, R. E., Crawley, J. N., Hu, S.-B., Nishimori, K., Young, L. J., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1594-10.2010 · Cited by 189 · see citing works

Maternal separation interferes with developmental changes in brain vasopressin and oxytocin receptor binding in male rats

Lukas, M., Bredewold, R., Neumann, I. D., & Veenema, A. H. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.06.020 · Cited by 183 · see citing works

The biology of trust: Integrating evidence from genetics, endocrinology, and functional brain imaging.

Riedl‬, R., & Javor, A. (2011) · Journal of Neuroscience Psychology and Economics · doi:10.1037/a0026318 · Cited by 180 · see citing works

Consequences of Early Experiences and Exposure to Oxytocin and Vasopressin Are Sexually Dimorphic

Carter, C. S., Boone, E. M., Pournajafi-Nazarloo, H., & Bales, K. L. (2009) · Developmental Neuroscience · doi:10.1159/000216544 · Cited by 176 · see citing works

Oxytocin, Vasopressin, and the Neuroendocrine Basis of Pair Bond Formation

Insel, T. R., Winslow, J. T., Wang, Z., & Young, L. J. (1998) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4871-3_28 · Cited by 170 · see citing works

Reduction of Hypothalamic Vasopressinergic Hyperdrive Contributes to Clinically Relevant Behavioral and Neuroendocrine Effects of Chronic Paroxetine Treatment in a Psychopathological Rat Model

Keck, M. E., Welt, T., Müller, M. B., Uhr, M., Ohl, F., Wigger, A., Toschi, N., Holsboer, F., & Landgraf, R. (2002) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300040 · Cited by 168 · see citing works

Oxytocin innervation of caudal brainstem nuclei activated by cholecystokinin

Blevins, J. E., Eakin, T. J., Murphy, J. A., Schwartz, M. W., & Baskin, D. G. (2003) · Brain Research · doi:10.1016/j.brainres.2003.08.036 · Cited by 164 · see citing works

Neonatal manipulations of oxytocin alter expression of oxytocin and vasopressin immunoreactive cells in the paraventricular nucleus of the hypothalamus in a gender-specific manner

Yamamoto, Y., Cushing, B. S., Kramer, K. M., Epperson, P. D., Hoffman, G. E., & Carter, C. S. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.02.028 · Cited by 155 · see citing works

Baroreflex control of heart rate by oxytocin in the solitary-vagal complex

Higa, K. T., Mori, E., Viana, F. F., Morris, M., & Michelini, L. C. (2002) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00806.2000 · Cited by 157 · see citing works

Toward understanding how early-life social experiences alter oxytocin- and vasopressin-regulated social behaviors

Veenema, A. H. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.12.002 · Cited by 157 · see citing works

Developmental exposure to oxytocin facilitates partner preferences in male prairie voles (Microtus ochrogaster)

Bales, K. L., & Carter, C. S. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.4.854 · Cited by 155 · see citing works

Sex, parturition and motherhood without oxytocin?

Russell, J., & Leng, G. (1998) · Journal of Endocrinology · doi:10.1677/joe.0.1570343 · Cited by 150 · see citing works

Neonatal oxytocin manipulations have long-lasting, sexually dimorphic effects on vasopressin receptors

Bales, K. L., Plotsky, P. M., Young, L. J., Lim, M. M., Grotte, N., Ferrer, E., & Carter, C. S. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.09.009 · Cited by 150 · see citing works

Chapter 22 Cardiovascular effects of oxytocin

Petersson, M. (2002) · Progress in brain research · doi:10.1016/s0079-6123(02)39024-1 · Cited by 147 · see citing works

Localization of Vasopressin (V_1a) Receptor Binding and mRNA in the Rhesus Monkey Brain

Young, Toloczko, & Insel (1999) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1999.00332.x · Cited by 139 · see citing works

Vasopressin 1a receptor knockout mice have a subtle olfactory deficit but normal aggression

Wersinger, S. R., Caldwell, H. K., Martinez, L. A., Gold, P. W., Hu, S.-B., & Young, W. S. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00281.x · Cited by 139 · see citing works

Oxytocin enhances cranial visceral afferent synaptic transmission to the solitary tract nucleus

Peters, J. H., McDougall, S. J., Kellett, D. O., Jordan, D., Llewellyn-Smith, I. J., & Andresen, M. C. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.3419-08.2008 · Cited by 135 · see citing works

Species differences in vasopressin receptor binding are evident early in development: Comparative anatomic studies in prairie and montane voles

Wang, Z., Young, L. J., Liu, Y., & Insel, T. R. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970224)378:4 · Cited by 135 · see citing works

Amygdala and bed nucleus of the stria terminalis circuitry: Implications for addiction-related behaviors

Stamatakis, A. M., Sparta, D. R., Jennings, J. H., McElligott, Z. A., Decot, H., & Stuber, G. D. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.05.046 · Cited by 132 · see citing works

The neurobiology of parenting: A neural circuit perspective

Kohl, J., Autry, A. E., & Dulac, C. G. (2016) · BioEssays · doi:10.1002/bies.201600159 · Cited by 131 · see citing works

Voles and vasopressin: A review of molecular, cellular, and behavioral studies of pair bonding and paternal behaviors

Wang, Z., Young, L. J., Vries, G. J. D., & Insel, T. R. (1999) · Progress in brain research · doi:10.1016/s0079-6123(08)61589-7 · Cited by 132 · see citing works

A single social defeat experience selectively stimulates the release of oxytocin, but not vasopressin, within the septal brain area of male rats

Ebner, K., Wotjak, C. T., Landgraf, R., & Engelmann, M. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02464-1 · Cited by 129 · see citing works

The Neurobiology of Social Affiliation and Pair Bonding

Carter, C. S., & Keverne, E. B. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00004-8 · Cited by 128 · see citing works

Developmental exposure to vasopressin increases aggression in adult prairie voles

Stribley, J. M., & Carter, C. S. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.22.12601 · Cited by 123 · see citing works

Vasotocin and vasopressin stimulation of the chloride secretion in the human bronchial epithelial cell line, 16HBE14o‐

Bernard, K. F., Bogliolo, S., & Ehrenfeld, J. (2005) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706103 · Cited by 122 · see citing works

Vasopressin- and oxytocin-induced activity in the central nervous system: electrophysiological studies using in-vitro systems

Raggenbass, M. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(00)00064-2 · Cited by 120 · see citing works

Vasopressin Regulation of the Proestrous Luteinizing Hormone Surge in Wild-Type and Clock Mutant Mice1

Miller, B. H., Olson, S. L., Levine, J. E., Turek, F. W., Horton, T. H., & Takahashi, J. S. (2006) · Biology of Reproduction · doi:10.1095/biolreprod.106.052845 · Cited by 117 · see citing works

The vasopressin Avpr1b receptor: Molecular and pharmacological studies

Roper, J. A., O'Carroll, A.-M., Young, W. S., & Lolait, S. (2010) · Stress · doi:10.3109/10253890.2010.512376 · Cited by 116 · see citing works

Neuroendocrine mechanisms of innate states of attenuated responsiveness of the hypothalamo-pituitary adrenal axis to stress

Tilbrook, A. J., & Clarke, I. J. (2006) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2006.06.002 · Cited by 113 · see citing works

The Prairie Vole (Microtus ochrogaster): An Animal Model for Behavioral Neuroendocrine Research on Pair Bonding

Aragona, B. J., & Wang, Z. (2004) · ILAR Journal · doi:10.1093/ilar.45.1.35 · Cited by 112 · see citing works

Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic disorder

Keck, M. E., Kern, N., Erhardt, A., Unschuld, P. G., Ising, M., Salyakina, D., Müller, M. B., Knorr, C. C., Lieb, R., Hohoff, C., et al. (2008) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30750 · Cited by 113 · see citing works

Neural correlates of pair-bonding in a monogamous primate

Bales, K. L., Mason, W. A., Catana, C., Cherry, S. R., & Mendoza, S. P. (2007) · Brain Research · doi:10.1016/j.brainres.2007.09.087 · Cited by 112 · see citing works

Distribution of vasopressin and oxytocin binding sites in the brain and upper spinal cord of the common marmoset

Schorscher-Petcu, A., Dupré, A., & Tribollet, E. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.06.016 · Cited by 111 · see citing works

The Neurobiology of Social Affiliation and Pair Bonding

Carter, C. S., & Keverne, E. B. (2002) · Elsevier eBooks · doi:10.1016/b978-012532104-4/50006-8 · Cited by 109 · see citing works

Developmental consequences and biological significance of mother–infant bonding

Mogi, K., Nagasawa, M., & Kikusui, T. (2010) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2010.08.024 · Cited by 106 · see citing works

Sex differences and developmental effects of manipulations of oxytocin on alloparenting and anxiety in prairie voles

Bales, K. L., Pfeifer, L. A., & Carter, C. S. (2004) · Developmental Psychobiology · doi:10.1002/dev.10165 · Cited by 107 · see citing works

Oxytocin infusion increases charitable donations regardless of monetary resources

Barraza, J. A., McCullough, M. E., Ahmadi, S., & Zak, P. J. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.04.008 · Cited by 106 · see citing works

Gene targeting approaches to neuroendocrinology: oxytocin, maternal behavior, and affiliation

Young, L. J., Winslow, J. T., Wang, Z., Gingrich, B., Guo, Q., Matzuk, M. M., & Insel, T. R. (1997) · Hormones and Behavior · doi:10.1006/hbeh.1997.1377 · Cited by 105 · see citing works

Forced swimming triggers vasopressin release within the amygdala to modulate stress‐coping strategies in rats

Ebner, K., Wotjak, C. T., Landgraf, R., & Engelmann, M. (2002) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01869.x · Cited by 104 · see citing works

Overview of cellular electrophysiological actions of vasopressin

Raggenbass, M. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.11.074 · Cited by 102 · see citing works

Stress Responsiveness of the Hypothalamic–Pituitary–Adrenal Axis: Age-Related Features of the Vasopressinergic Regulation

Goncharova, N. D. (2013) · Frontiers in Endocrinology · doi:10.3389/fendo.2013.00026 · Cited by 99 · see citing works

The V1a and V1b, But Not V2, Vasopressin Receptor Genes Are Expressed in the Supraoptic Nucleus of the Rat Hypothalamus, and the Transcripts Are Essentially Colocalized in the Vasopressinergic Magnocellular Neurons

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The vasopressin 1b receptor and the neural regulation of social behavior

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Excitatory action of hypocretin/orexin on neurons of the central medial amygdala

Bisetti, A., Cvetkovic, V., Serafin, M., Bayer, L., Machard, D., Jones, B. E., & Mühlethaler, M. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.07.018 · Cited by 97 · see citing works

Synaptic innervation to rat hippocampus by vasopressin-immuno-positive fibres from the hypothalamic supraoptic and paraventricular nuclei

Zhang, L., & Hernández, V. S. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2012.10.010 · Cited by 96 · see citing works

The stimulatory effect of vasopressin on the luteinizing hormone surge in ovariectomized, estradiol-treated rats is time-dependent

Palm, I. F., van der Beek, E. M., Wiegant, V. M., Buijs, R. M., & Kalsbeek, A. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02309-5 · Cited by 97 · see citing works

Species and sex differences in brain distribution of corticotropin‐releasing factor receptor subtypes 1 and 2 in monogamous and promiscuous vole species

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The physiology of moral sentiments

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Oxytocin-induced excitation of neurones in the rat central and medial amygdaloid nuclei

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Corticotropin-releasing factor, vasopressin and receptor systems in depression and anxiety

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Sex differences in the regulation of offensive aggression and dominance by arginine-vasopressin

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Estrogen receptors in the medial amygdala inhibit the expression of male prosocial behavior

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Leptin Activates Oxytocin Neurons of the Hypothalamic Paraventricular Nucleus in Both Control and Diet-Induced Obese Rodents

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Role of corticotropin-releasing factor, vasopressin and the autonomic nervous system in learning and memory

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Pharmacology of Oxytocin and Vasopressin Receptors in the Central and Peripheral Nervous Systema

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Mapping and Analysis of Receptors for Neurohypophyseal Peptides Present in the Brain

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Printed in U.S.A. Copyright © 1998 by The Endocrine Society Comparative Distribution of Vasopressin V1b and Oxytocin Receptor Messenger Ribonucleic Acids in Brain*

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Chapter 16 Neurohypophyseal hormone receptor systems in brain and periphery

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