Exocrine scent marking: coordinative role of arginine vasopressin in the systemic regulation of social signaling behaviors

Limbic system mechanisms of stress regulation: Hypothalamo-pituitary-adrenocortical axis

Herman, J. P., Ostrander, M. M., Mueller, N. K., & Figueiredo, H. (2005) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.08.006 · Cited by 1,322 · see citing works

Immunohistochemical identification of neurons in the paraventricular nucleus of the hypothalamus that project to the medulla or to the spinal cord in the rat

Sawchenko, P. E., & Swanson, L. W. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902050306 · Cited by 1,150 · see citing works

The oxytocin receptor: from intracellular signaling to behavior

Jurek, B., & Neumann, I. D. (2018) · Physiological Reviews · doi:10.1152/physrev.00031.2017 · Cited by 999 · see citing works

Balance of brain oxytocin and vasopressin: implications for anxiety, depression, and social behaviors

Neumann, I. D., & Landgraf, R. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.08.004 · Cited by 954 · see citing works

Dendritic peptide release and peptide-dependent behaviours

Ludwig, M., & Leng, G. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1845 · Cited by 945 · see citing works

Social behavior functions and related anatomical characteristics of vasotocin/vasopressin systems in vertebrates

Goodson, J. L., & Bass, A. H. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00043-1 · Cited by 632 · see citing works

Neuropeptides — an overview

Hökfelt, T. G. M., Broberger, C., Xu, Q., Sergeyev, V., Ubink, R., & Diez, M. (2000) · Neuropharmacology · doi:10.1016/s0028-3908(00)00010-1 · Cited by 607 · see citing works

Profound Impairment in Social Recognition and Reduction in Anxiety-Like Behavior in Vasopressin V1a Receptor Knockout Mice

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

Cloning and characterization of a vasopressin V2 receptor and possible link to nephrogenic diabetes insipidus

Lolait, S. J., O'Carroll, A.-M., McBride, O. W., Konig, M., Morel, A., & Brownstein, M. J. (1992) · Nature · doi:10.1038/357336a0 · Cited by 524 · see citing works

Vasopressin and oxytocin receptor systems in the brain: Sex differences and sex-specific regulation of social behavior

Dumais, K. M., & Veenema, A. H. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2015.04.003 · Cited by 520 · see citing works

Mammalian Scent Marking

Ralls, K. (1971) · Science · doi:10.1126/science.171.3970.443 · Cited by 514 · see citing works

Mammalian social odours: attraction and individual recognition

Brennan, P., & Kendrick, K. M. (2006) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2006.1931 · Cited by 510 · see citing works

Neuromodulation by Oxytocin and Vasopressin

Stoop, R. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.025 · Cited by 506 · see citing works

Vasopressin: Behavioral roles of an “original” neuropeptide

Caldwell, H. K., Lee, H.-J., Macbeth, A. H., & Young, W. S. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.10.007 · Cited by 504 · see citing works

Exocrine Gland Dysfunction in MC5-R-Deficient Mice: Evidence for Coordinated Regulation of Exocrine Gland Function by Melanocortin Peptides

Chen, W., Kelly, M. A., Opitz-Araya, X., Thomas, R. E., Low, M. J., & Cone, R. D. (1997) · Cell · doi:10.1016/s0092-8674(00)80467-5 · Cited by 488 · see citing works

Pheromonal communication in vertebrates

Brennan, P., & Zufall, F. (2006) · Nature · doi:10.1038/nature05404 · Cited by 485 · see citing works

Molecular cloning and expression of a rat Via arginine vasopressin receptor

Morel, A., O'Carroll, A.-M., Brownstein, M. J., & Lolaft, S. J. (1992) · Nature · doi:10.1038/356523a0 · Cited by 477 · see citing works

Scent wars: the chemobiology of competitive signalling in mice

Hurst, J. L., & Beynon, R. J. (2004) · BioEssays · doi:10.1002/bies.20147 · Cited by 474 · see citing works

The melanocortin system

Gantz, I., & Fong, T. M. (2003) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00434.2002 · Cited by 466 · see citing works

Patterns of brain vasopressin receptor distribution associated with social organization in microtine rodents

Insel, T., Wang, Z., & Ferris, C. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-09-05381.1994 · Cited by 454 · see citing works

Social Rank in House Mice: Differentiation Revealed by Ultraviolet Visualization of Urinary Marking Patterns

Desjardins, C., MARUNIAK, J. A., & Bronson, F. H. (1973) · Science · doi:10.1126/science.182.4115.939 · Cited by 449 · see citing works

Scent marking in mammals

Johnson, R. P. (1973) · Animal Behaviour · doi:10.1016/s0003-3472(73)80012-0 · Cited by 439 · see citing works

Oxytocin and Vasopressin Agonists and Antagonists as Research Tools and Potential Therapeutics

Manning, M., Misicka, A., Olma, A., Bankowski, K., Stoev, S., Chini, B., Durroux, T., Mouillac, B., Corbani, M., & Guillon, G. (2012) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2012.02303.x · Cited by 423 · see citing works

Information Processing in the Mammalian Olfactory System

Lledo, P., Gheusi, G., & Vincent, J. (2004) · Physiological Reviews · doi:10.1152/physrev.00008.2004 · Cited by 391 · see citing works

Attraction of kestrels to vole scent marks visible in ultraviolet light

Viitala, J., Korplmäki, E., Palokangas, P., & Koivula, M. (1995) · Nature · doi:10.1038/373425a0 · Cited by 377 · see citing works

Sexual differentiation of central vasopressin and vasotocin systems in vertebrates: different mechanisms, similar endpoints

De Vries, G. J., & Panzica, G. C. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.07.050 · Cited by 346 · see citing works

Vasopressin Receptors

Birnbaumer, M. (2000) · Trends in Endocrinology and Metabolism · doi:10.1016/s1043-2760(00)00304-0 · Cited by 343 · see citing works

Individual Odors among Mammals: Origins and Functions

Halpin, Z. T. (1986) · Advances in the study of behavior · doi:10.1016/s0065-3454(08)60187-4 · Cited by 330 · see citing works

The oxytocin receptor

Zingg, H. H., & Laporte, S. A. (2003) · Trends in Endocrinology and Metabolism · doi:10.1016/s1043-2760(03)00080-8 · Cited by 316 · see citing works

Pheromones and their Effect on Aggression in Mice

Mugford, R. A., & Nowell, N. W. (1970) · Nature · doi:10.1038/226967a0 · Cited by 300 · see citing works

SOCIAL ORGANIZATION AND TERRITORIAL BEHAVIOUR IN THE

CROWCROFT, P., & ROWE, F. P. (1963) · Proceedings of the Zoological Society of London · doi:10.1111/j.1469-7998.1963.tb01871.x · Cited by 286 · see citing works

Alterations in Central Neuropeptide Expression, Release, and Receptor Binding in Rats Bred for High Anxiety: Critical Role of Vasopressin

Wigger, A., Sánchez, M. M., Mathys, K. C., Ebner, K., Frank, E., Liu, D., Kresse, A. E., Neumann, I. D., Holsboer, F., Plotsky, P. M., et al. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300290 · Cited by 263 · see citing works

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 · see citing works

Vasopressin injected into the hypothalamus triggers a stereotypic behavior in golden hamsters

Ferris, C. F., Albers, H. E., Wesolowski, S. M., Goldman, B. D., & Luman, S. E. (1984) · Science · doi:10.1126/science.6538700 · Cited by 255 · see citing works

CHEMICAL COMMUNICATION IN RODENTS: FROM PHEROMONES TO INDIVIDUAL RECOGNITION

Johnston, R. E. (2003) · Journal of Mammalogy · doi:10.1644/ble-010 · Cited by 249 · see citing works

Vasopressin cells in the bed nucleus of the stria terminalis of the rat: sex differences and the influence of androgens

van Leeuwen, F. W., Caffe, A. R., & Vries, G. J. D. (1985) · Brain Research · doi:10.1016/0006-8993(85)90348-8 · Cited by 248 · see citing works

Potentiation by Vasopressin of Corticotropin Release Induced by Corticotropin-Releasing Factor1

Yates, F. E., Russell, S. M., Dallman, M. F., Hedge, G. A., McCann, S. M., & DHARIWAL, A. P. S. (1971) · Endocrinology · doi:10.1210/endo-88-1-3 · Cited by 245 · see citing works

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

Release of Vasopressin within the Rat Paraventricular Nucleus in Response to Emotional Stress: A Novel Mechanism of Regulating Adrenocorticotropic Hormone Secretion?

Wotjak, C. T., Kubota, M., Liebsch, G., Montkowski, A., Holsboer, F., Neumann, I. D., & Landgraf, R. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-23-07725.1996 · Cited by 231 · see citing works

Scent marking behavior as an odorant communication in mice

Arakawa, H., Blanchard, D. C., Arakawa, K., Dunlap, C., & Blanchard, R. J. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.05.012 · Cited by 229 · see citing works

Gonadal hormone actions on the morphology of the vasopressinergic innervation of the adult rat brain

De Vries, G. J., Buijs, R. M., & Sluiter, A. A. (1984) · Brain Research · doi:10.1016/0006-8993(84)91157-0 · Cited by 224 · see citing works

The vasopressin 1b receptor is prominent in the hippocampal area CA2 where it is unaffected by restraint stress or adrenalectomy

Young, W. S., Li, J., Wersinger, S. R., & Palkovits, M. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.08.040 · Cited by 222 · see citing works

An intrinsic vasopressin system in the olfactory bulb is involved in social recognition

Tobin, V. A., Hashimoto, H., Wacker, D. W., Takayanagi, Y., Langnaese, K., Caquineau, C., Noack, J., Landgraf, R., Onaka, T., Leng, G., et al. (2010) · Nature · doi:10.1038/nature08826 · Cited by 213 · see citing works

Cyto- and chemoarchitecture of the hypothalamic paraventricular nucleus in the C57BL/6J male mouse: a study of immunostaining and multiple fluorescent tract tracing

Biag, J., Huang, Y., Gou, L., Hintiryan, H., Askarinam, A., Hahn, J. D., Toga, A. W., & Dong, H. (2012) · Journal of Comparative Neurology · doi:10.1002/cne.22698 · Cited by 205 · see citing works

Expression of Estrogen Receptor- Messenger Ribonucleic Acid in Oxytocin and Vasopressin Neurons of the Rat Supraoptic and Paraventricular Nuclei

Hrabovszky, E., Kalló, I., Hajszán, T., Shughrue, P. J., Merchenthaler, I. J., & Liposits, Z. (1998) · Endocrinology · doi:10.1210/endo.139.5.6024 · Cited by 193 · see citing works

Sex differences in the effects of testosterone and its metabolites on vasopressin messenger RNA levels in the bed nucleus of the stria terminalis of rats

De Vries, G., Wang, Z., Bullock, N., & Numan, S. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-03-01789.1994 · Cited by 193 · see citing works

Vasopressin and the Output of the Hypothalamic Biological Clock

Kalsbeek, A., Fliers, E., Hofman, M. A., Swaab, D. F., & Buijs, R. M. (2010) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2010.01956.x · Cited by 192 · 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

A Specialized Neural Circuit Gates Social Vocalizations in the Mouse

Tschida, K., Michael, V., Takatoh, J., Han, B.-X., Zhao, S., Sakurai, K., MOONEY, R. D., & Wang, F. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.025 · Cited by 186 · see citing works

The Proopiomelanocortin System

Hadley, M. E., & Haskell‐Luevano, C. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb08662.x · Cited by 180 · see citing works

Distinct correlations of vasopressin release within the lateral septum and the bed nucleus of the stria terminalis with the display of intermale aggression

Veenema, A. H., Beiderbeck, D. I., Lukas, M., & Neumann, I. D. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.03.006 · Cited by 180 · see citing works

Anterior hypothalamic vasopressin regulates pair-bonding and drug-induced aggression in a monogamous rodent

Gobrogge, K. L., Liu, Y., Young, L. J., & Wang, Z. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908620106 · Cited by 178 · see citing works

Functional properties and projections of neurons in the medial amygdala

Keshavarzi, S., Sullivan, R. K. P., Ianno, D. J., & Sah, P. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1176-14.2014 · Cited by 176 · see citing works

Scent marks as reliable signals of the competitive ability of mates

Rich, T. J., & Hurst, J. L. (1998) · Animal Behaviour · doi:10.1006/anbe.1998.0803 · Cited by 176 · see citing works

Sex differences in vasopressin and oxytocin innervation of the brain

DEVRIES, G. (2008) · Progress in Brain Research · doi:10.1016/s0079-6123(08)00402-0 · Cited by 169 · see citing works

60 YEARS OF POMC: Biosynthesis, trafficking, and secretion of pro-opiomelanocortin-derived peptides

Cawley, N. X., Li, Z., & Loh, Y. P. (2016) · Journal of Molecular Endocrinology · doi:10.1530/jme-15-0323 · Cited by 167 · see citing works

Viral vector‐mediated gene transfer of the vole V1a vasopressin receptor in the rat septum: improved social discrimination and active social behaviour

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

Central Control Circuit for Context-Dependent Micturition

Hou, X. H., Hyun, M., Taranda, J., Huang, K. W., Emmalee, T., Feng, D. D., Atwater, E., Croney, D. M., Zeidel, M. L., Osten, P., et al. (2016) · Cell · doi:10.1016/j.cell.2016.08.073 · Cited by 158 · see citing works

The physiological and pathophysiological functions of renal and extrarenal vasopressin V2 receptors

Juul, K. V., Bichet, D. G., Nielsen, S., & Nørgaard, J. P. (2014) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00604.2013 · Cited by 156 · see citing works

Impaired Repression at a Vasopressin Promoter Polymorphism Underlies Overexpression of Vasopressin in a Rat Model of Trait Anxiety

Murgatroyd, C., Wigger, A., Frank, E., Singewald, N., Bunck, M., Holsboer, F., Landgraf, R., & Spengler, D. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1614-04.2004 · Cited by 154 · see citing works

Scent Marking by Male Golden Hamsters (Mesocricetus auratus)

Johnston, R. E. (2010) · Zeitschrift für Tierpsychologie · doi:10.1111/j.1439-0310.1975.tb01128.x · Cited by 153 · see citing works

Unravelling the chemical basis of competitive scent marking in house mice

Humphries, R. E., Robertson, D. H. L., Beynon, R. J., & Hurst, J. L. (1999) · Animal Behaviour · doi:10.1006/anbe.1999.1252 · Cited by 148 · see citing works

Regulation of bone remodeling by vasopressin explains the bone loss in hyponatremia

Tamma, R., Sun, L., Cuscito, C., Lü, P., Corcelli, M., Li, J., Colaianni, G., Moonga, S. S., Benedetto, A. D., Grano, M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1318257110 · Cited by 141 · see citing works

Vasopressin receptor V1a regulates circadian rhythms of locomotor activity and expression of clock-controlled genes in the suprachiasmatic nuclei

Li, J., Burton, K. J., Zhang, C., Hu, S.-B., & Zhou, Q. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.90463.2008 · Cited by 135 · see citing works

Vasopressin innervation of the mouse ( <i>Mus musculus</i> ) brain and spinal cord

Rood, B. D., & De Vries, G. J. (2011) · Journal of Comparative Neurology · doi:10.1002/cne.22635 · Cited by 134 · see citing works

From models to mechanisms: Odorant communication as a key determinant of social behavior in rodents during illness-associated states

Arakawa, H., Cruz, S., & Deak, T. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.03.007 · Cited by 131 · 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

Proopiomelanocortin (POMC): the cutaneous roles of its melanocortin products and receptors

Millington, G. W. M. (2006) · Clinical and Experimental Dermatology · doi:10.1111/j.1365-2230.2006.02128.x · Cited by 131 · see citing works

The involvement of the vasopressin system in stress-related disorders

Landgraf, R. (2006) · CNS &amp; Neurological Disorders - Drug Targets · doi:10.2174/187152706776359664 · Cited by 127 · see citing works

Sex differences in vasopressin neurons in the bed nucleus of the stria terminalis by in situ hybridization

MILLER, M. A., Vician, L. J., Clifton, D. K., & Dorsa, D. M. (1989) · Peptides · doi:10.1016/0196-9781(89)90152-6 · Cited by 126 · see citing works

Organization of the neural switching circuitry underlying reflex micturition

de Groat, W. C., & Wickens, C. (2012) · Acta Physiologica · doi:10.1111/apha.12014 · Cited by 126 · see citing works

Behavioral and electrophysiological responses of female mice to male urine odors

Scott, J. W., & Pfaff, D. W. (1970) · Physiology & Behavior · doi:10.1016/0031-9384(70)90243-x · Cited by 125 · see citing works

Sexual differentiation of vasopressin projections of the bed nucleus of the stria terminals and medial amygdaloid nucleus in rats.

Wang, Z., Bullock, N. A., & De Vries, G. J. (1993) · Endocrinology · doi:10.1210/endo.132.6.8504734 · Cited by 123 · see citing works

Decline of vasopressin immunoreactivity and mRNA levels in the bed nucleus of the stria terminalis following castration

Miller, M., DeVries, G., al-Shamma, H., & Dorsa, D. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-08-02881.1992 · Cited by 122 · see citing works

A GABAergic cell type in the lateral habenula links hypothalamic homeostatic and midbrain motivation circuits with sex steroid signaling

Zhang, L., Hernández, V. S., Swinny, J. D., Verma, A. K., Giesecke, T., Emery, A. C., Mutig, K., García‐Segura, L. M., & Eiden, L. E. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0099-5 · Cited by 121 · see citing works

Site of origin of and sex differences in the vasopressin innervation of the mouse ( <i>Mus musculus</i> ) brain

Rood, B. D., Stott, R. T., You, S., Smith, C. J. W., Woodbury, M. E., & De Vries, G. J. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23288 · Cited by 120 · see citing works

Evolution of the vasopressin/oxytocin superfamily: characterization of a cDNA encoding a vasopressin-related precursor, preproconopressin, from the mollusc Lymnaea stagnalis.

van Kesteren, R. E., Smit, A. B., Dirks, R. W., de With, N. D., Geraerts, W. P., & Joosse, J. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.10.4593 · Cited by 120 · see citing works

Scent marking and the maintenance of dominant/subordinate status in male golden hamsters

Ferris, C. F., Axelson, J. F., Shinto, L. H., & Albers, H. E. (1987) · Physiology & Behavior · doi:10.1016/0031-9384(87)90114-4 · Cited by 119 · see citing works

Extraordinary diversity in vasopressin (V1a) receptor distributions among wild prairie voles (<i>Microtus ochrogaster</i>): Patterns of variation and covariation

Phelps, S. M., & Young, L. J. (2003) · Journal of Comparative Neurology · doi:10.1002/cne.10902 · Cited by 116 · see citing works

Organizational effects of testosterone, estradiol, and dihydrotestosterone on vasopressin mRNA expression in the bed nucleus of the stria terminalis

Han, T. M., & De Vries, G. J. (2003) · Journal of Neurobiology · doi:10.1002/neu.10157 · Cited by 116 · see citing works

Oxytocin and vasopressin in the medial amygdala differentially modulate approach and avoidance behavior toward illness-related social odor

Arakawa, H., Arakawa, K., & Terrence Deak, B. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.10.013 · Cited by 114 · see citing works

The olfactory thalamus: unanswered questions about the role of the mediodorsal thalamic nucleus in olfaction

Courtiol, E., & Wilson, D. A. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00049 · Cited by 113 · see citing works

A V1-like receptor mediates vasopressin-induced flank marking behavior in hamster hypothalamus

Albers, H., Pollock, J., Simmons, W., & Ferris, C. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-07-02085.1986 · Cited by 112 · see citing works

Vasopressin-like peptide and its receptor function in an indirect diuretic signaling pathway in the red flour beetle

Aikins, M. J., Schooley, D. A., Begum, K., Detheux, M., Beeman, R. W., & Park, Y. (2008) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2008.04.006 · Cited by 110 · see citing works

A comparison of the aversive and female attractant properties of urine from dominant and subordinate male mice

Jones, R. B., & Nowell, N. W. (1974) · Animal Learning & Behavior · doi:10.3758/bf03199141 · Cited by 106 · see citing works

Vasopressin in the septal area of the golden hamster controls scent marking and grooming

Irvin, R. W., Szot, P., Dorsa, D. M., Potegal, M., & Ferris, C. F. (1990) · Physiology &amp; Behavior · doi:10.1016/0031-9384(90)90213-n · Cited by 105 · see citing works

Selective and potent agonists and antagonists for investigating the role of mouse oxytocin receptors

Busnelli, M., Bulgheroni, E., Manning, M., Kleinau, G., & Chini, B. (2013) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.113.202994 · Cited by 102 · see citing works

Coping with stress in rats and mice: Differential peptidergic modulation of the amygdala-lateral septum complex

Koolhaas, J. M., Everts, H., de Ruiter, A. J. H., de Boer, S. F., & Bohus, B. (1999) · Progress in Brain Research · doi:10.1016/s0079-6123(08)61586-1 · Cited by 100 · see citing works

Modulation of anxiety behavior in the elevated plus maze using peptidic oxytocin and vasopressin receptor ligands in the rat

Mak, P., Broussard, C., Vacy, K., & Broadbear, J. H. (2011) · Journal of Psychopharmacology · doi:10.1177/0269881111416687 · Cited by 95 · see citing works

Putative Chemical Signals about Sex, Individuality, and Genetic Background in the Preputial Gland and Urine of the House Mouse (Mus musculus)

Zhang, J.-X., Rao, X.-P., Sun, L., Zhao, C., & Qin, X.-W. (2007) · Chemical Senses · doi:10.1093/chemse/bjl058 · Cited by 94 · see citing works

Sexual dimorphism in the vasopressin system: Lack of an altered behavioral phenotype in female V1a receptor knockout mice

Bielsky, I. F., Hu, S.-B., & Young, L. J. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.06.005 · Cited by 91 · see citing works

The Melanocortin 5 Receptor is Expressed in Human Sebaceous Glands and Rat Preputial Cells

Thiboutot, D., Sivarajah, A., Gilliland, K., Cong, Z., & Clawson, G. (2000) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2000.00094.x · Cited by 90 · see citing works

Vasopressin (V_1a) Receptor Binding, mRNA Expression and Transcriptional Regulation by Androgen in the Syrian Hamster Brain

Young, L. J., Wang, Z., Cooper, T. T., & Albers, H. E. (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00573.x · Cited by 88 · see citing works

Vasopressin Release in Male and Female Rats: Effects of Gonadectomy and Treatment with Gonadal Steroid Hormones*

Crofton, J. T., Baer, P. G., Share, L., & Brooks, D. P. (1985) · Endocrinology · doi:10.1210/endo-117-3-1195 · Cited by 85 · see citing works

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

Terranova, J. I., Ferris, C. F., & Albers, H. E. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00308 · Cited by 85 · see citing works

Glucose dependency of arginine vasopressin[ndash ]induced insulin and glucagon release from the perfused rat pancreas

Abu-Basha, E. A., Yibchok-anun, S., & Hsu, W. H. (2002) · Metabolism · doi:10.1053/meta.2002.34052 · Cited by 80 · see citing works

A new test paradigm for social recognition evidenced by urinary scent marking behavior in C57BL/6J mice

Arakawa, H., Arakawa, K., Blanchard, D. C., & Blanchard, R. J. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.02.009 · Cited by 80 · see citing works

Wiring olfaction: the cellular and molecular mechanisms that guide the development of synaptic connections from the nose to the cortex

de Castro, F. (2009) · Frontiers in Neuroscience · doi:10.3389/neuro.22.004.2009 · Cited by 78 · see citing works

Localization and characterization of vasopressin binding sites in the rat brain using an iodinated linear AVP antagonist

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

The effect of strange male odor on aggressive behavior in male mice.

Archer, J. (1968) · Journal of Mammalogy · doi:10.2307/1378238 · Cited by 77 · see citing works

Distribution of oxytocin and co-localization with arginine vasopressin in the brain of mice

Otero‐García, M., Agustín‐Pavón, C., Lanuza, E., & Martínez‐Garciá, F. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1111-y · Cited by 76 · see citing works

Thirst Is Associated with Suppression of Habenula Output and Active Stress Coping: Is there a Role for a Non-canonical Vasopressin-Glutamate Pathway?

Zhang, L., Hernández, V. S., Vázquez‐Juárez, E., Chay, F. K., & Barrio, R. A. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00013 · Cited by 76 · see citing works

Ventral premammillary nucleus as a critical sensory relay to the maternal aggression network

Motta, S. C., Guimarães, C. C., Furigo, I. C., Sukikara, M. H., Baldo, M. V. C., Lonstein, J. S., & Canteras, N. S. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1305581110 · Cited by 75 · see citing works

Inhibition of vasopressin-stimulated flank marking behavior by V1-receptor antagonists

Ferris, C. F., Singer, E. A., Meenan, D. M., & Elliott Albers, H. (1988) · European Journal of Pharmacology · doi:10.1016/0014-2999(88)90092-1 · Cited by 74 · see citing works

A Hypomorphic Vasopressin Allele Prevents Anxiety-Related Behavior

Bunck, M., Czibere, L., Horvath, C., Graf, C., Frank, E., Kessler, M. S., Murgatroyd, C., Müller‐Myhsok, B., Gonik, M., Weber, P., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005129 · Cited by 73 · see citing works

Oxytocin and vasopressin: signalling, behavioural modulation and potential therapeutic effects

Rae, M., Lemos Duarte, M., Gomes, I., Camarini, R., & Devi, L. A. (2022) · British Journal of Pharmacology · doi:10.1111/bph.15481 · Cited by 72 · see citing works

The rodent accessory olfactory system

Mucignat‐Caretta, C. (2010) · Journal of Comparative Physiology A · doi:10.1007/s00359-010-0555-z · Cited by 62 · see citing works

The coagulating glands as a source of aversive and aggression-inhibiting pheromone(s) in the male albino mouse

Jones, R. B., & Nowell, N. W. (1973) · Physiology & Behavior · doi:10.1016/0031-9384(73)90031-0 · 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

Regulation of ACTH Secretion from Corticotrophs: The Interaction of Vasopressin and CRFa

Bilezikjian, L. M., & Vale, W. (1987) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1987.tb24952.x · Cited by 60 · see citing works

Neural circuitry controlling vasopressin-stimulated scent marking in Syrian hamsters (Mesocricetus auratus)

Bamshad, M., & Albers, E. H. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960527)369:2 · Cited by 59 · 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

Role of melanocortin signaling in the regulation of the hypothalamic–pituitary–thyroid (HPT) axis

Lechan, R. M., & Fekete, C. (2005) · Peptides · doi:10.1016/j.peptides.2005.01.033 · Cited by 59 · see citing works

The vomeronasal cortex – afferent and efferent projections of the posteromedial cortical nucleus of the amygdala in mice

Gutiérrez‐Castellanos, N., Pardo‐Bellver, C., Martínez‐Garciá, F., & Lanuza, E. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12393 · Cited by 59 · see citing works

The urinary aversive pheromone of mice: Species, strain and grouping effects

Jones, R. B., & Nowell, N. W. (1974) · Animal Behaviour · doi:10.1016/s0003-3472(74)80068-0 · Cited by 58 · see citing works

Vasopressin receptors in the mouse (Mus musculus) brain: sex-related expression in the medial preoptic area and hypothalamus

Dubois-Dauphin, M., Barberis, C., & de Bilbao, F. (1996) · Brain Research · doi:10.1016/s0006-8993(96)01019-0 · Cited by 57 · see citing works

Extra-neurohypophyseal axonal projections from individual vasopressin-containing magnocellular neurons in rat hypothalamus

Hernández, V. S., Vázquez‐Juárez, E., Márquez, M. M., Jáuregui-Huerta, F., Barrio, R. A., & Zhang, L. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00130 · Cited by 57 · 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

Ancient role of vasopressin/oxytocin-type neuropeptides as regulators of feeding revealed in an echinoderm

Odekunle, E., Semmens, D. C., Martynyuk, N., Tinoco, A. B., Garewal, A., Patel, R., Blowes, L. M., Zandawala, M., Delroisse, J., Slade, S. E., et al. (2019) · BMC Biology · doi:10.1186/s12915-019-0680-2 · Cited by 54 · see citing works

Distribution and chemical composition of estrogen receptor β neurons in the paraventricular nucleus of the female and male mouse hypothalamus

Oyola, M. G., Thompson, M. K., Handa, A. Z., & Handa, R. J. (2017) · Journal of Comparative Neurology · doi:10.1002/cne.24295 · Cited by 53 · see citing works

Vasopressin and social odor processing in the olfactory bulb and anterior olfactory nucleus

Wacker, D. W., Engelmann, M., Tobin, V. A., Meddle, S., & Ludwig, M. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05885.x · Cited by 51 · see citing works

Enhancement of [3H-Methyl]Thymidine Incorporation and Replication of Rat Chondrocytes Grown in Tissue Culture by Plasma, Tissue Extracts and Vasopressin1

Miller, R. P., HUSAIN, F., SVENSSON, M., & Lohin, S. (1977) · Endocrinology · doi:10.1210/endo-100-5-1365 · Cited by 49 · see citing works

Vasopressin Receptors

Jard, S. (1998) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4871-3_1 · Cited by 49 · see citing works

Molecular evolution of the neurohypophysial hormone precursors in mammals: Comparative genomics reveals novel mammalian oxytocin and vasopressin analogues

Wallis, M. (2012) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2012.07.030 · Cited by 48 · see citing works

Sex differences in vasopressin 1a receptor regulation of social communication within the lateral habenula and dorsal raphe of mice

Rigney, N., Beaumont, R., & Petrulis, A. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104715 · Cited by 47 · see citing works

Comparative and Evolutionary Physiology of Vasopressin/ Oxytocin-Type Neuropeptide Signaling in Invertebrates

Odekunle, E., & Elphick, M. R. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00225 · Cited by 47 · see citing works

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 44 · see citing works

Melanocortin-5 Receptor Deficiency in Mice Blocks a Novel Pathway Influencing Pheromone-Induced Aggression

Morgan, C., & Cone, R. (2006) · Behavior Genetics · doi:10.1007/s10519-005-9024-9 · Cited by 43 · see citing works

Melanocortin-5 Receptor Deficiency Reduces a Pheromonal Signal for Aggression in Male Mice

Morgan, C. (2004) · Chemical Senses · doi:10.1093/chemse/bjh011 · Cited by 43 · see citing works

Sex differences in the control of social investigation and anxiety by vasopressin cells of the paraventricular nucleus of the hypothalamus

Rigney, N., Whylings, J., de Vries, G. J., & Petrulis, A. (2021) · Neuroendocrinology · doi:10.1159/000509421 · Cited by 42 · see citing works

Central oxytocin regulates social familiarity and scent marking behavior that involves amicable odor signals between male mice

Arakawa, H., Blanchard, D. C., & Blanchard, R. J. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.04.016 · Cited by 41 · see citing works

Persistent Increase in Hypothalamic Arginine Vasopressin Gene Expression During Protracted Withdrawal from Chronic Escalating-Dose Cocaine in Rodents

Zhou, Y., Litvin, Y., Piras, A. P., Pfaff, D. W., & Kreek, M. J. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.97 · Cited by 41 · see citing works

Role of neuropeptides in learning versus performance: Focus on vasopressin

Koob, G. F., Lebrun‐Frénay, C., Bluthé, R.-M., Dantzer, R., & Moal, M. L. (1989) · Brain Research Bulletin · doi:10.1016/0361-9230(89)90222-0 · Cited by 41 · see citing works

Gonadal Steroid Modulation of Vasopressin Pathwaysa

Vries, G. J. D., Crenshaw, B. J., & AL‐SHAMMA, H. A. (1992) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1992.tb34369.x · Cited by 38 · see citing works

Sexually dimorphic role of BNST vasopressin cells in sickness and social behavior in male and female mice

Whylings, J., Rigney, N., Peters, N. V., de Vries, G. J., & Petrulis, A. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.09.015 · Cited by 37 · see citing works

The role of vasopressin in olfactory and visual processing

Wacker, D. W., & Ludwig, M. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2867-1 · Cited by 36 · see citing works

Vasopressin regulates daily rhythms and circadian clock circuits in a manner influenced by sex

Rohr, K. E., Telega, A., Savaglio, A., & Evans, J. A. (2021) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104888 · Cited by 35 · see citing works

An oxytocin/vasopressin-related neuropeptide modulates social foraging behavior in the clonal raider ant

Fetter-Pruneda, I., Hart, T., Ulrich, Y., Gal, A., Oxley, P. R., Olivos-Cisneros, L., Ebert, M. S., Kazmi, M. A., Garrison, J. L., Bargmann, C. I., et al. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001305 · Cited by 35 · see citing works

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

Behavioral effects of vasopressin and oxytocin within the medial preoptic area of the golden hamster

Albers, H. E., & Ferris, C. F. (1985) · Regulatory Peptides · doi:10.1016/0167-0115(85)90067-9 · Cited by 33 · see citing works

Evolutionary patterns of major urinary protein scent signals in house mice and relatives

Sheehan, M. J., Polly Campbell, A., & Miller, C. H. (2019) · Molecular Ecology · doi:10.1111/mec.15155 · Cited by 33 · 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

Social isolation uncovers a circuit underlying context-dependent territory-covering micturition

Hyun, M., Taranda, J., Radeljic, G., Miner, L. E., Wang, W., Ochandarena, N. E., Huang, K. W., Osten, P., & Sabatini, B. L. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2018078118 · Cited by 31 · see citing works

Chemosensory cues from the lacrimal and preputial glands stimulate production of IP3 in the vomeronasal organ and aggression in male mice

Thompson, R. N., Napier, A., & Wekesa, K. S. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.01.008 · Cited by 30 · see citing works

Absence of progestin receptors alters distribution of vasopressin fibers but not sexual differentiation of vasopressin system in mice

Rood, B. D., Murray, E. K., Laroche, J., Yang, M. K., Blaustein, J. D., & De Vries, G. J. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.03.087 · Cited by 30 · see citing works

Relationships between Scent Marking by Male Mice and the Pheromone-Induced Secretion of the Gonadotropic and Ovarian Hormones that Accompany Puberty in Female Mice

Bronson, F. H., & Desjardins, C. (1974) · Advances in behavioral biology · doi:10.1007/978-1-4684-3069-1_7 · Cited by 29 · see citing works

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 · see citing works

Social features of scent-donor mice modulate scent marking of C57BL/6J recipient males

Arakawa, H., Arakawa, K., Blanchard, D. C., & Blanchard, R. J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.07.007 · Cited by 29 · see citing works

Knockdown of sexually differentiated vasopressin expression in the bed nucleus of the stria terminalis reduces social and sexual behaviour in male, but not female, mice

Rigney, N., Zbib, A., de Vries, G. J., & Petrulis, A. (2022) · Journal of Neuroendocrinology · doi:10.1111/jne.13083 · Cited by 29 · see citing works

Anatomical and functional evidence for a role of arginine-vasopressin (AVP) in rat olfactory epithelium cells

Levasseur, G., Baly, C., Grébert, D., Durieux, D., Salesse, R., & Caillol, M. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03516.x · Cited by 28 · see citing works

Serotonin inhibits GABA synaptic transmission in presympathetic paraventricular nucleus neurons

Lee, K. S., Han, T. H., Jo, J. Y., Kang, G., Lee, S. Y., Ryu, P. D., Im, J. H., Jeon, B. H., & Park, J. B. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.05.012 · Cited by 27 · see citing works

Integrating resource defence theory with a neural nonapeptide pathway to explain territory-based mating systems

Oldfield, R. G., Harris, R. M., & Hofmann, H. A. (2015) · Frontiers in Zoology · doi:10.1186/1742-9994-12-s1-s16 · Cited by 27 · see citing works

Vasopressin and oxytocin : molecular, cellular, and clinical advances

Zingg, H. H., Bourque, C. W., & Bichet, D. G. (1998) · Plenum eBooks · Cited by 25 · see citing works

Effects of arginine-vasopressin and parathyroid hormone-related protein (1–34) on cell proliferation and production of YKL-40 in cultured chondrocytes from patients with rheumatoid arthritis and osteoarthritis

Petersson, M., Bucht, E., Granberg, B., & Stark, A. (2006) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2006.01.003 · Cited by 25 · see citing works

The Vasopressin 1b Receptor Antagonist A-988315 Blocks Stress Effects on the Retrieval of Object-Recognition Memory

Barsegyan, A., Atsak, P., Hornberger, W., Jacobson, P. B., van Gaalen, M. M., & Roozendaal, B. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.48 · Cited by 25 · see citing works

Inactivation of the lateral septum blocks fox odor-induced fear behavior

Endres, T., & Fendt, M. (2008) · Neuroreport · doi:10.1097/wnr.0b013e3282fb78d9 · Cited by 25 · see citing works

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 25 · see citing works

Medial Amygdala Arginine Vasopressin Neurons Regulate Innate Aversion to Cat Odors in Male Mice

Tong, W. H., Abdulai-Saiku, S., & Vyas, A. (2020) · Neuroendocrinology · doi:10.1159/000508862 · Cited by 25 · see citing works

Ionotropic glutamate receptors in hypothalamic paraventricular and supraoptic nuclei mediate vasopressin and oxytocin release in unanesthetized rats

Busnardo, C., Crestani, C. C., Resstel, L. B. M., Tavares, R. F., Antunes-Rodrigues, J., & Corrêa, F. M. A. (2012) · Endocrinology · doi:10.1210/en.2011-2079 · Cited by 24 · see citing works

Neural correlates of scent marking behavior in C57BL/6J mice: detection and recognition of a social stimulus

Borelli, K. G., Blanchard, D. C., Javier, L. K., Defensor, E. B., Brandão, M. L., & Blanchard, R. J. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.05.047 · Cited by 24 · see citing works

Who Plays the Strings in Newborn Analgesia at Birth, Vasopressin or Oxytocin?

Wellmann, S. M., & Bührer, C. (2012) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00078 · Cited by 24 · see citing works

Scent Marking With Urine in Two Races of the Bank Vole (Clethrionomys Glareolus)

Johnson, R. P. (1975) · Behaviour · doi:10.1163/156853975x00425 · Cited by 23 · see citing works

Vasopressin: An output signal from the suprachiasmatic nucleus to prepare physiology and behaviour for the resting phase

Buijs, R. M., Hurtado‐Alvarado, G., & Soto‐Tinoco, E. (2021) · Journal of Neuroendocrinology · doi:10.1111/jne.12998 · Cited by 23 · see citing works

Two ancient neuropeptides, PACAP and AVP, modulate motivated behavior at synapses in the extrahypothalamic brain: a study in contrast

Zhang, L., & Eiden, L. E. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2958-z · Cited by 21 · see citing works

Involvement of ventral pallidal vasopressin in the sex-specific regulation of sociosexual motivation in rats

DiBenedictis, B. T., Cheung, H. K., Nussbaum, E. R., & Veenema, A. H. (2019) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2019.104462 · Cited by 20 · see citing works

Roles for learning in mammalian chemosensory responses

Griffiths, P. R., & Brennan, P. (2014) · Hormones and Behavior · doi:10.1016/j.yhbeh.2014.08.010 · Cited by 19 · see citing works

Vasopressin eliminates the expression of familiar odor bias in neonatal female mice through V1aR

Hammock, E. A. D., Law, C. S., & Levitt, P. R. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.12.006 · Cited by 18 · see citing works

The bed nucleus of the stria terminalis in the Syrian hamster (Mesocricetus auratus): absence of vasopressin expression in standard and wild-derived hamsters and galanin regulation by seasonal changes in circulating sex steroids

Bolborea, M., Ansel-Bollepalli, L., Weinert, D., Steinlechner, S., Pévet, P., & Klosen, P. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.11.006 · Cited by 18 · see citing works

Scent-marking behaviour in response to conspecific odours by the rat, Rattus norvegicus

Birke, L. I. A., & Sadler, D. (1984) · Animal Behaviour · doi:10.1016/s0003-3472(84)80286-9 · Cited by 17 · see citing works

A RELATIONSHIP BETWEEN SOCIAL EXPERIENCE AND PREPUTIAL GLAND FUNCTION IN THE ALBINO MOUSE

Hucklebridge, F. H., Nowell, N. W., & Wouters, A. (1972) · Journal of Endocrinology · doi:10.1677/joe.0.0550449 · Cited by 17 · see citing works

Scent Marking, Sexual Behavior and Aggression in Male Gerbils: Comparative Analysis of Endocrine Control

Yahr, P. (1981) · American Zoologist · doi:10.1093/icb/21.1.143 · Cited by 16 · see citing works

Vasopressin: more than just an output of the circadian pacemaker? Focus on “Vasopressin receptor V1a regulates circadian rhythms of locomotor activity and expression of clock-controlled genes in the suprachiasmatic nuclei”

Bittman, E. L. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.90991.2008 · Cited by 15 · see citing works

Reduction in vasopressin cells in the suprachiasmatic nucleus in mice increases anxiety and alters fluid intake

Whylings, J., Rigney, N., Vries, G. J. D., & Petrulis, A. (2021) · Hormones and Behavior · doi:10.1016/j.yhbeh.2021.104997 · Cited by 15 · see citing works

Ethopharmacological studies on the effects of antihormones on rodent agonistic behavior with especial emphasis on progesterone

Brain, P. F., Simón, V. M., & Martı́nez, M. (1991) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(05)80143-5 · Cited by 14 · see citing works

Chronic ethanol exposure uncouples vasopressin synthesis and secretion in rats

Hoffman, P. (1991) · Neuropharmacology · doi:10.1016/0028-3908(91)90172-8 · Cited by 14 · see citing works

Activation of arginine vasopressin receptor 1a facilitates the induction of long-term potentiation in the accessory olfactory bulb of male mice

Namba, T., Taniguchi, M., Murata, Y., Tong, J., Wang, Y., Okutani, F., Yamaguchi, M., & Kaba, H. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2016.09.056 · Cited by 12 · see citing works

Modulation of male mouse sociosexual and anxiety-like behaviors by vasopressin receptors

Shimizu, K., Nakamura, K., Yokosuka, M., & Kondo, Y. (2018) · Physiology & Behavior · doi:10.1016/j.physbeh.2018.09.016 · Cited by 10 · see citing works

Differential Central and Peripheral Release of Vasopressin and Oxytocin in Response to Swim Stress in Rats

Engelmann, M., Wotjak, C. T., & Landgraf, R. (1998) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4871-3_20 · Cited by 10 · see citing works

Contrasting central and systemic effects of arginine-vasopressin on urinary marking behavior as a social signal in male mice

Higuchi, Y., & Arakawa, H. (2022) · Hormones and Behavior · doi:10.1016/j.yhbeh.2022.105128 · Cited by 9 · see citing works

Projections from the anteroventral part of the medial amygdaloid nucleus in the rat

Novaes, L. S., & Shammah‐Lagnado, S. J. (2011) · Brain Research · doi:10.1016/j.brainres.2011.09.021 · Cited by 8 · see citing works

EFFECTS OF CYPROTERONE ACETATE UPON URINARY AVERSIVE CUES AND ACCESSORY SEX GLANDS IN MALE ALBINO MICE

Jones, R. B., & Nowell, N. W. (1974) · Journal of Endocrinology · doi:10.1677/joe.0.0620167 · Cited by 8 · see citing works

Vasopressin Receptors in Voiding Dysfunction

Pisipati, S., & Hashim, H. (2011) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-16499-6_21 · Cited by 8 · see citing works

Vasopressin receptor antagonists: pharmacological tools and potential therapeutic agents

Streefkerk, J. O., & van Zwieten, P. A. (2006) · Autonomic and Autacoid Pharmacology · doi:10.1111/j.1474-8673.2006.00361.x · Cited by 6 · see citing works

A surgical approach in the treatment of preputial gland abscesses in mice

Bertrand, H. G. M. J., Thomas, A., Ellen, Y. C., Dorward, R. S., & Flecknell, P. A. (2016) · BMC Veterinary Research · doi:10.1186/s12917-016-0636-5 · Cited by 6 · see citing works

The Preputial Gland and its Role in Pheromone Production in Relation to Some Endocrine Factors

Merza, H. (2017) · HAL (Le Centre pour la Communication Scientifique Directe) · Cited by 6 · see citing works

The Preputial Gland and its Role in Pheromone Production in Relation to Some Endocrine Factors

Homady, M. H. (2018) · Journal of Stem Cell Biology and Transplantation · doi:10.21767/2575-7725.100004 · Cited by 4 · see citing works

AVPR1A distribution in the whole C57BL/6J mouse neonate

Day, K. R., Coleman, A., Greenwood, M. A., & Hammock, E. A. D. (2020) · Scientific Reports · doi:10.1038/s41598-020-71392-1 · Cited by 3 · see citing works

Untitled work

(1971) · PubMed

Oxytocin, Vasopressin, and Social Behavior: From Neural Circuits to Clinical Opportunities

Rigney, N., de Vries, G. J., Petrulis, A., & Young, L. J. (2022) · Endocrinology · doi:10.1210/endocr/bqac111 · Cited by 191 · see citing works

Faded neural projection from the posterior bed nucleus of the stria terminalis to the lateral habenula contributes to social signaling deficit in male BTBR mice as a mouse model of autism

Higuchi, Y., Tachigori, S.-I., & Arakawa, H. (2022) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2022.106004 · Cited by 12 · see citing works

From fundamental research to clinical translation: The neural modulation of social behavior by oxytocin and vasopressin

Zhao, W., Zhang, X., & Kendrick, K. M. (2026) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.106624 · Cited by 7 · see citing works

Adolescent social isolation disrupts developmental tuning of neuropeptide circuits in the hypothalamus to amygdala regulating social and defensive behavior

Arakawa, H., Tokashiki, M., Higuchi, Y., & Konno, T. (2024) · Peptides · doi:10.1016/j.peptides.2024.171178 · Cited by 4 · see citing works

Defending the self: The role of oxytocin in responses to psychological threat

Feng, C., Luo, W., & Zhu, R. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106406 · Cited by 3 · see citing works

Neural signature underlying the effect of intranasal vasopressin on emotional responses to spontaneous social comparison

Li, X., ZHENG, Z., Tian, X., Long, A., Yang, B., Gu, R., Ma, Y., Luo, W., & Feng, C. (2026) · NeuroImage · doi:10.1016/j.neuroimage.2026.121832 · Cited by 1 · see citing works

The Usability of Mouse Models to Study the Neural Circuity in Autism Spectrum Disorder: Regulatory Mechanisms of Core Behavioral Symptoms

Arakawa, H., & Higuchi, Y. (2023) · Springer eBooks · doi:10.1007/978-3-031-42383-3_6

Neuroendocrine Pathways in Skin Health and Homeostasis: A Systematic Review

Kream, E. J., Golpanian, R. S., Hosking, A., Boen, M., & Fabi, S. G. (2026) · Journal of Dermatology Research · doi:10.46889/jdr.2026.7119

Contrasting central and systemic effects of arginine-vasopressin on urinary marking behavior as a social signal in male mice

Higuchi, Y., & Arakawa, H. (2022) · Hormones and Behavior · doi:10.1016/j.yhbeh.2022.105128 · Cited by 9 · see citing works

Vasopressin: Roles in Modulating Social Behaviors

Williams, S. K., & Cymerblit‐Sabba, A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803592-4.00057-2 · Cited by 5 · see citing works

Vasopressin involvement in antipyresis, social communication, and social recognition: a synthesis.

Dantzer, R., & Bluthé, R.-M. (1992) · PubMed · Cited by 55 · see citing works

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

Albers, H. E. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.10.007 · Cited by 288 · see citing works

Neurohypophyseal principles and memory processes

van Ree, J. M., Bohus, B., Versteeg, D. H. G., & de Wied, D. (1978) · Biochemical Pharmacology · doi:10.1016/0006-2952(78)90021-7 · Cited by 153 · see citing works