Oxytocin and vasopressin: genetics and behavioral implications

Caldwell, H. K.; Young, W. S.

doi:10.1007/978-0-387-30381-9_25

Cited by 114Neuroendocrine regulation and behaviorNeuropeptides and Animal PhysiologyNeurotransmitter Receptor Influence on Behavior

Oxytocin and vasopressin: genetics and behavioral implications

Caldwell, H. K., Young, W. S.·2006·Handbook of Neurochemistry and Molecular Neurobiology

DOI 10.1007/978-0-387-30381-9_25

Open this paper in CoChat — free account

Integrity signals

Registry

Crossref · 10.1007/978-0-387-30381-9_25

Cites

384 of 384 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Androgens and progesterone modulate oxytocin and oxytocin receptor expression, while estrogens seem to have the greatest impact on the oxytocin system.
“While androgens and progesterone modulate Oxt and Oxtr expression (72–75), it is the estrogens that seem to have the greatest impact on the Oxt system (68, 70, 74, 76–78).”
From Oxytocin during Development: Possible Organizational Effects on Behavior (2015) · cites this paper as [70]
Gonadal steroids play a significant role in regulating oxytocin activity.
“It is well established that gonadal steroids play a significant role in regulating Oxt activity (68–71).”
From Oxytocin during Development: Possible Organizational Effects on Behavior (2015) · cites this paper as [70]

The oxytocin receptor system: structure, function, and regulation
Gimpl, G., & Fahrenholz, F. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.2.629 · Cited by 3,089 · see citing works
The neurobiology of pair bonding.
Young, L. J., & Wang, Z. (2004) · Nature Neuroscience · doi:10.1038/nn1327 · Cited by 1,523 · see citing works
Monogamy in Mammals
Kleiman, D. G. (1977) · The Quarterly Review of Biology · doi:10.1086/409721 · Cited by 1,436 · see citing works
The neurobiology of attachment
Insel, T. R., & Young, L. J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35053579 · Cited by 1,173 · 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
Microsatellites Within Genes: Structure, Function, and Evolution
Li, Y. (2004) · Molecular Biology and Evolution · doi:10.1093/molbev/msh073 · Cited by 1,132 · see citing works
Social amnesia in mice lacking the oxytocin gene
Ferguson, J. N., Young, L. J., Hearn, E. F., Matzuk, M. M., Insel, T. R., & Winslow, J. T. (2000) · Nature Genetics · doi:10.1038/77040 · Cited by 1,130 · see citing works
Vasopressin and oxytocin release within the brain: a dynamic concept of multiple and variable modes of neuropeptide communication
Landgraf, R., & Neumann, I. D. (2004) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2004.05.001 · Cited by 1,059 · see citing works
Oxytocin in the Medial Amygdala is Essential for Social Recognition in the Mouse
Ferguson, J. N., Aldag, J. M., Insel, T. R., & Young, L. J. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-20-08278.2001 · Cited by 1,043 · see citing works
Intra- and extrahypothalamic vasopressin and oxytocin pathways in the rat
Buijs, R. M., Swaab, D. F., Dogterom, J., & van Leeuwen, F. W. (1978) · Cell and Tissue Research · doi:10.1007/bf00224932 · Cited by 1,029 · see citing works
On some physiological actions of ergot
Dale, H. H. (1906) · The Journal of Physiology · doi:10.1113/jphysiol.1906.sp001148 · Cited by 1,011 · see citing works
A role for central vasopressin in pair bonding in monogamous prairie voles
Winslow, J. T., Hastings, N., Carter, C. S., Harbaugh, C. R., & Insel, T. R. (1993) · Nature · doi:10.1038/365545a0 · Cited by 948 · see citing works
Handbook of chemical neuroanatomy
(2005) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(05)80001-6 · Cited by 906 · see citing works
A Molecular Mechanism Regulating Rhythmic Output from the Suprachiasmatic Circadian Clock
Jin, X., Shearman, L. P., Weaver, D. R., Zylka, M. J., Vries, G. J. D., & Reppert, S. M. (1999) · Cell · doi:10.1016/s0092-8674(00)80959-9 · Cited by 891 · see citing works
Induction of maternal behavior in virgin rats after intracerebroventricular administration of oxytocin
Pedersen, C. A., & Prange, A. J. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.12.6661 · Cited by 841 · see citing works
Synthesis, transport, and release of posterior pituitary hormones
Brownstein, M. J., Russell, J. T., & Gainer, H. (1980) · Science · doi:10.1126/science.6153132 · Cited by 838 · see citing works
Oxytocin receptor distribution reflects social organization in monogamous and polygamous voles
Insel, T. R., & Shapiro, L. E. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.5981 · Cited by 833 · see citing works
Intra- and extrahypothalamic vasopressin and oxytocin pathways in the rat
Buijs, R. M. (1978) · Cell and Tissue Research · doi:10.1007/bf00212323 · Cited by 830 · see citing works
Oxytocin induces maternal behavior in virgin female rats
Pedersen, C. A., Ascher, J. A., Monroe, Y. L., & Prange, A. J. (1982) · Science · doi:10.1126/science.7071605 · Cited by 770 · see citing works
Oxytocin is required for nursing but is not essential for parturition or reproductive behavior.
Nishimori, K., Young, L. J., Guo, Q., Wang, Z., Insel, T. R., & Matzuk, M. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11699 · Cited by 734 · see citing works
Naturally occurring variations in maternal behavior in the rat are associated with differences in estrogen-inducible central oxytocin receptors
Champagne, F., Diorio, J., Sharma, S., & Meaney, M. J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.221224598 · Cited by 707 · see citing works
Neuropsychopharmacology
Mathur, R. (2004) · Jaypee Brothers Medical Publishers (P) Ltd. eBooks · doi:10.5005/jp/books/10243_6 · Cited by 669 · see citing works
Vasopressinergic control of pituitary adrenocorticotropin secretion comes of age
Antoni, F. A. (1993) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1993.1004 · Cited by 636 · see citing works
Structure and expression of a human oxytocin receptor
Kimura, T., Tanizawa, O., Mori, K., Brownstein, M., & Okayama, H. (1992) · Nature · doi:10.1038/356526a0 · Cited by 631 · see citing works
Enhanced partner preference in a promiscuous species by manipulating the expression of a single gene.
Lim, M. M., Wang, Z., Olazábal, D. E., Ren, X., Terwilliger, E. F., & Young, L. J. (2004) · Nature · doi:10.1038/nature02539 · Cited by 628 · see citing works
THE SEQUENCE OF AMINO ACIDS IN OXYTOCIN, WITH A PROPOSAL FOR THE STRUCTURE OF OXYTOCIN
du Vigneaud, V., Ressler, C., & Trippett, S. (1953) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)49238-1 · Cited by 603 · see citing works
Nucleus accumbens oxytocin and dopamine interact to regulate pair bond formation in female prairie voles
Liu, Y., & Wang, Z. X. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00555-4 · Cited by 580 · see citing works
HOW THE BRAIN PROCESSES SOCIAL INFORMATION: Searching for the Social Brain
Insel, T. R., & Fernald, R. D. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144148 · Cited by 556 · see citing works
Plasma oxytocin increases in the human sexual response
CARMICHAEL, M. S., HUMBERT, R., DIXEN, J., PALMISANO, G., GREENLEAF, W., & DAVIDSON, J. M. (1987) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-64-1-27 · Cited by 554 · see citing works
Pharmacology of penile erection.
Andersson, K. (2001) · Pharmacological Reviews · doi:10.1016/s0031-6997(24)01503-5 · Cited by 533 · 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
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
A gender-specific mechanism for pair bonding: oxytocin and partner preference formation in monogamous voles
Insel, T. R., & Hulihan, T. J. (1995) · Behavioral Neuroscience · doi:10.1037/0735-7044.109.4.782 · Cited by 528 · see citing works
The origin of the vasopressinergic and oxytocinergic innervation of the rat brain with special reference to the lateral septum
de Vries, G. J., & Buijs, R. M. (1983) · Brain Research · doi:10.1016/0006-8993(83)90855-7 · Cited by 524 · see citing works
The vasopressinergic innervation of the brain in normal and castrated rats
DeVries, G. J., Buijs, R. M., van Leeuwen, F. W., Caffé, A. R., & Swaab, D. F. (1985) · Journal of Comparative Neurology · doi:10.1002/cne.902330206 · Cited by 522 · see citing works
Vasopressin/serotonin interactions in the anterior hypothalamus control aggressive behavior in golden hamsters
Ferris, C. F., Melloni Jr, R. H., Koppel, G., Perry, K. W., Fuller, R. W., & Delville, Y. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-11-04331.1997 · Cited by 495 · 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
Co-expression of corticotropin-releasing factor and vasopressin immunoreactivity in parvocellular neurosecretory neurons of the adrenalectomized rat.
Sawchenko, P. E., Swanson, L. W., & Vale, W. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.6.1883 · Cited by 485 · see citing works
Oxytocin Administered Centrally Facilitates Formation of a Partner Preference in Female Prairie Voles (Microtus ochrogaster)
Williams, J. R., Insel, T. R., Harbaugh, C. R., & Carter, C. S. (1994) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1994.tb00579.x · Cited by 483 · see citing works
Anxiolytic- and antidepressant-like effects of the non-peptide vasopressin V 1b receptor antagonist, SSR149415, suggest an innovative approach for the treatment of stress-related disorders
Griebel, G., Simiand, J., Serradeil-Le Gal, C., Wagnon, J., Pascal, M., Scatton, B., Maffrand, J.-P., & Soubrié, P. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.092012099 · Cited by 471 · 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
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
CNS region-specific oxytocin receptor expression: importance in regulation of anxiety and sex behavior
Bale, T. L., Davis, A. M., Auger, A. P., Dorsa, D. M., & McCarthy, M. M. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-07-02546.2001 · Cited by 446 · see citing works
Hormonal Stimulation of Phosphatidylinositol Breakdown, with Particular Reference to the Hepatic Effects of Vasopressin
Michell, R. H., Kirk, C. J., & BILLAH, M. M. (1979) · Biochemical Society Transactions · doi:10.1042/bst0070861 · Cited by 440 · 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
Is social attachment an addictive disorder?
Insel, T. R. (2003) · Physiology & Behavior · doi:10.1016/s0031-9384(03)00148-3 · Cited by 430 · see citing works
Modulation of social memory in male rats by neurohypophyseal peptides
Dantzer, R., Bluthe, R. M., Koob, G. F., & Le Moal, M. (1987) · Psychopharmacology · doi:10.1007/bf00518192 · Cited by 423 · see citing works
The Synthesis of Oxytocin1
du Vigneaud, V., Ressler, C., SWAN, J. M., Roberts, C. W., & Katsoyannis, P. G. (1954) · Journal of the American Chemical Society · doi:10.1021/ja01641a004 · Cited by 422 · see citing works
Structure and comparison of the oxytocin and vasopressin genes from rat.
Ivell, R., & Richter, D. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.7.2006 · Cited by 419 · see citing works
Naturally Occurring Differences in Maternal Care are Associated with the Expression of Oxytocin and Vasopressin (V1a) Receptors: Gender Differences
Francis, D. D., Young, L. J., Meaney, M. J., & Insel, T. R. (2002) · Journal of Neuroendocrinology · doi:10.1046/j.0007-1331.2002.00776.x · Cited by 415 · see citing works
Brain oxytocin: differential inhibition of neuroendocrine stress responses and anxiety-related behaviour in virgin, pregnant and lactating rats
Neumann, I. D., Torner, L., & Wigger, A. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00433-9 · Cited by 402 · see citing works
Vasopressin V1b receptor knockout reduces aggressive behavior in male mice
Wersinger, S. R., Ginns, E. I., O'Carroll, A.-M., Lolait, S. J., & Young III, W. S. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4001195 · Cited by 397 · see citing works
Self-citation
Progress in comparative endocrinology
(1991) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(91)90143-s · Cited by 391 · see citing works
An estrogen-dependent four-gene micronet regulating social recognition: A study with oxytocin and estrogen receptor-α and -β knockout mice
Choleris, E., Gustafsson, J.-Å., Korach, K. S., Muglia, L. J., Pfaff, D. W., & Ogawa, S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0631699100 · Cited by 386 · see citing works
Role of septal vasopressin innervation in paternal behavior in prairie voles (Microtus ochrogaster).
Wang, Z., Ferris, C. F., & De Vries, G. J. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.1.400 · Cited by 381 · see citing works
The influence of the posterior and inter-mediate lobe of the pituitary and pituitary peptides on the maintenance of a conditioned avoidance response in rats
Wled, D. D. (1965) · International Journal of Neuropharmacology · doi:10.1016/0028-3908(65)90005-5 · Cited by 377 · see citing works
On the Physiological Action of Extracts of Pituitary Body and certain other Glandular Organs
Oliver, G. D., & Schäfer, E. A. (1895) · The Journal of Physiology · doi:10.1113/jphysiol.1895.sp000565 · Cited by 374 · see citing works
Oxytocin improves long-lasting spatial memory during motherhood through MAP kinase cascade
Tomizawa, K., Iga, N., Lü, Y.-F., Moriwaki, A., Matsushita, M., Li, S., Miyamoto, O., Itano, T., & Matsui, H. (2003) · Nature Neuroscience · doi:10.1038/nn1023 · Cited by 372 · see citing works
Morphology of vasopressin and oxytocin neurones and their central and vascular projections
Sofroniew, M. V. (1983) · Progress in Brain Research · doi:10.1016/s0079-6123(08)64378-2 · Cited by 370 · see citing works
Behavioral effects of intraventricularly administered vasopressin and vasopressin fragments
de Wied, D. (1976) · Life Sciences · doi:10.1016/0024-3205(76)90165-x · Cited by 362 · see citing works
A critical role for nucleus accumbens dopamine in partner-preference formation in male prairie voles
Aragona, B. J., Liu, Y., Curtis, J. T., Stephan, F. K., & Wang, Z. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03483.2003 · Cited by 351 · see citing works
Infant vocalization, adult aggression, and fear behavior of an oxytocin null mutant mouse
Winslow, J. T., Hearn, E. F., Ferguson, J., Young, L. J., Matzuk, M. M., & Insel, T. R. (2000) · Hormones and Behavior · doi:10.1006/hbeh.1999.1566 · Cited by 348 · see citing works
Dendritic Release of Vasopressin and Oxytocin
Ludwig (1998) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1998.00279.x · Cited by 342 · see citing works
V1 vasopressin receptor antisense oligodeoxynucleotide into septum reduces vasopressin binding, social discrimination abilities, and anxiety-related behavior in rats
Landgraf, R., Gerstberger, R., Montkowski, A., Probst, J., Wotjak, C., Holsboer, F., & Engelmann, M. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-06-04250.1995 · Cited by 341 · see citing works
Dopamine D2 receptors in the nucleus accumbens are important for social attachment in female prairie voles (Microtus ochrogaster)
Gingrich, B., Liu, Y., Cascio, C., Wang, Z., & Insel, T. R. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.1.173 · Cited by 339 · see citing works
The human vasopressin gene is linked to the oxytocin gene and is selectively expressed in a cultured lung cancer cell line.
Sausville, E., Carney, D., & Battey, J. (1985) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)39236-0 · Cited by 338 · see citing works
Gene Regulation in the Magnocellular Hypothalamo-Neurohypophysial System
Burbach, J. P. H., Luckman, S. M., Murphy, D., & Gainer, H. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.3.1197 · Cited by 338 · see citing works
Extrapituitary expression of the rat V1b vasopressin receptor gene.
Lolait, S. J., O’Carroll, A., Mahan, L. C., Felder, C. C., Button, D. C., Young, W. S., Mezey, É., & Brownstein, M. J. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.15.6783 · Cited by 337 · see citing works
Self-citation
An Anxiolytic Action of Oxytocin is Enhanced by Estrogen in the Mouse
MCCARTHY, M. M., MCDONALD, C. H., BROOKS, P. J., & GOLDMAN, D. (1996) · Physiology & Behavior · doi:10.1016/s0031-9384(96)00212-0 · Cited by 328 · see citing works
Central Nervous System Effects of the Neurohypophyseal Hormones and Related Peptides
de Wied, D., Diamant, M., & Fodor, M. (1993) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1993.1009 · Cited by 327 · see citing works
Possible Role for Endogenous Oxytocin in Estrogen-Facilitated Maternal Behavior in Rats
Fahrbach, S. E., Morrell, J. I., & Pfaff, D. W. (2008) · Neuroendocrinology · doi:10.1159/000124125 · Cited by 322 · see citing works
Changes in oxytocin and vasopressin secretion during sexual activity in men
MURPHY, M. R., SECKL, J. R., BURTON, S., CHECKLEY, S. A., & LIGHTMAN, S. L. (1987) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-65-4-738 · Cited by 318 · 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
Neural control of maternal behaviour and olfactory recognition of offspring
Kendrick, K. M., Da Costa, A. P. C., Broad, K. D., Ohkura, S., Guevara, R., Lévy, F., & Keverne, E. B. (1997) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00218-9 · Cited by 311 · see citing works
Comparative Distribution of Vasopressin V1b and Oxytocin Receptor Messenger Ribonucleic Acids in Brain 1
Vaccari, C., Lolait, S. J., & Ostrowski, N. L. (1998) · Endocrinology · doi:10.1210/endo.139.12.6382 · Cited by 308 · see citing works
The social deficits of the oxytocin knockout mouse
Winslow, J. T., & Insel, T. R. (2002) · Neuropeptides · doi:10.1054/npep.2002.0909 · Cited by 307 · see citing works
Corticotropin-releasing factor-immunoreactive neurons of the paraventricular nucleus become vasopressin positive after adrenalectomy.
Kiss, J. Z., Mezey, É., & Skirboll, L. R. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.6.1854 · Cited by 304 · see citing works
Antidiuretic action of vasopressin: quantitative aspects and interaction between V1a and V2 receptor-mediated effects
Bankir, L. (2001) · Cardiovascular Research · doi:10.1016/s0008-6363(01)00328-5 · Cited by 300 · see citing works
Inhibition of post-partum maternal behaviour in the rat by injecting an oxytocin antagonist into the cerebral ventricles
van Leengoed, E., Kerker, E., & Swanson, H. H. (1987) · Journal of Endocrinology · doi:10.1677/joe.0.1120275 · Cited by 300 · see citing works
Vasopressin cells in the medial amygdala of the rat project to the lateral septum and ventral hippocampus
Caffé, A. R., van Leeuwen, F. W., & Luiten, P. G. M. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902610206 · Cited by 286 · see citing works
Cellular localization of vasopressin V1a receptor messenger ribonucleic acid in adult male rat brain, pineal, and brain vasculature.
Ostrowski, N. L., Lolait, S. J., & Young, W. S. (1994) · Endocrinology · doi:10.1210/endo.135.4.7925112 · Cited by 284 · see citing works
Self-citation
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
Vasopressin antagonists allow demonstration of a novel type of vasopressin receptor in the rat adenohypophysis.
Jard, S., Gaillard, R. C., Guillon, G., Marie, J., Schoenenberg, P., Muller, A. F., Manning, M., & Sawyer, W. H. (1986) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)10336-2 · Cited by 276 · 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
ENZYMATIC CLEAVAGE OF GLYCINAMIDE FROM VASOPRESSIN AND A PROPOSED STRUCTURE FOR THIS PRESSOR-ANTIDIURETIC HORMONE OF THE POSTERIOR PITUITARY
du Vigneaud, V., Lawler, H. C., & Popenoe, E. A. (1953) · Journal of the American Chemical Society · doi:10.1021/ja01115a554 · Cited by 275 · see citing works
Transmission disequilibrium testing of arginine vasopressin receptor 1A (AVPR1A) polymorphisms in autism
Kim, S.-J., Young, L. J., Gonen, D., Veenstra-VanderWeele, J., Courchesne, R., Courchesne, E., Lord, C., Leventhal, B. L., Cook Jr, E. H., & Insel, T. R. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4001125 · Cited by 265 · 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
Vasopressin receptor blockade in the anterior hypothalamus suppresses aggression in hamsters
Ferris, C. F., & Potegal, M. (1988) · Physiology & Behavior · doi:10.1016/0031-9384(88)90144-8 · Cited by 259 · 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
Manipulations of the AVT System Shift Social Status and Related Courtship and Aggressive Behavior in the Bluehead Wrasse
Semsar, K., Kandel, F. L. M., & Godwin, J. (2001) · Hormones and Behavior · doi:10.1006/hbeh.2001.1663 · Cited by 252 · see citing works
Evidence supporting a role for endogenous vasopressin in natural suppression of fever in the sheep.
Cooper, K., Kasting, N. W., Lederis, K. P., & Veale, W. L. (1979) · The Journal of Physiology · doi:10.1113/jphysiol.1979.sp012953 · Cited by 251 · see citing works
Neural Connections of the Anterior Hypothalamus and Agonistic Behavior in Golden Hamsters
Delville, Y., Vries, G. J. D., & Ferris, C. F. (2000) · Brain Behavior and Evolution · doi:10.1159/000006642 · Cited by 251 · see citing works
Lesions of the hypothalamic paraventricular nucleus disrupt the initiation of maternal behavior
Insel, T. R., & Harbaugh, C. R. (1989) · Physiology & Behavior · doi:10.1016/0031-9384(89)90234-5 · Cited by 250 · 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
Genomic screen and follow‐up analysis for autistic disorder
Shao, Y., Wolpert, C. M., Raiford, K. L., Menold, M. M., Donnelly, S. L., Ravan, S. A., Bass, M. P., McClain, C., von Wendt, L., Vance, J. M., et al. (2001) · American Journal of Medical Genetics · doi:10.1002/ajmg.10153 · Cited by 248 · see citing works
Clock genes, oscillators, and cellular networks in the suprachiasmatic nuclei
Hastings, M. H., & Herzog, E. D. (2004) · Journal of Biological Rhythms · doi:10.1177/0748730404268786 · Cited by 246 · see citing works
The human oxytocin gene promoter is regulated by estrogens
Richard, S., & Zingg, H. H. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)39297-x · Cited by 242 · see citing works
Oxytocin and Social Bondinga
CARTER, C. S., WILLIAMS, J. R., WITT, D. M., & INSEL, T. R. (1992) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1992.tb34356.x · Cited by 237 · see citing works
Distribution of V1a and V2 vasopressin receptor messenger ribonucleic acids in rat liver, kidney, pituitary and brain
Ostrowski, N. L., Lolait, S. J., Bradley, D. J., O’Carroll, A., Brownstein, M. J., & Young, W. S. (1992) · Endocrinology · doi:10.1210/endo.131.1.1535312 · Cited by 236 · see citing works
Self-citation
Species differences in V-sub-1a receptor gene expression in monogamous and nonmonogamous voles: Behavioral consequences.
Young, L. J., Winslow, J., Nilsen, R., & Insel, T. R. (1997) · Behavioral Neuroscience · doi:10.1037//0735-7044.111.3.599 · Cited by 235 · see citing works
Structural organization of the human oxytocin receptor gene
Inoue, T., Kimura, T., Azuma, C., Inazawa, J., Takemura, M., Kikuchi, T., Kubota, Y., Ogita, K., & Saji, F. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)31656-9 · Cited by 234 · see citing works
Physiology of Reproduction
Hammond, J. (1960) · Nature · doi:10.1038/185492a0 · Cited by 234 · see citing works
Evolution and tumour pathology of the neuroendocrine system
Swaab, D. F. (1985) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(85)90014-0 · Cited by 233 · see citing works
A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27
Auranen, M., Vanhala, R., Varilo, T., Ayers, K. L., Kempas, E., Ylisaukko‐oja, T., Sinsheimer, J. S., Peltonen, L., & Järvelä, I. E. (2002) · The American Journal of Human Genetics · doi:10.1086/342720 · Cited by 233 · see citing works
Suprachiasmatic Nucleus Vasopressin Messenger RNA: Circadian Variation in Normal and Brattleboro Rats
Uhl, G. R., & Reppert, S. M. (1986) · Science · doi:10.1126/science.3961487 · Cited by 228 · 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
Testosterone facilitates aggression by modulating vasopressin receptors in the hypothalamus
Delville, Y., Mansour, K. M., & Ferris, C. F. (1996) · Physiology & Behavior · doi:10.1016/0031-9384(95)02246-5 · Cited by 218 · see citing works
Differential colocalization of estrogen receptor β (ERβ) with oxytocin and vasopressin in the paraventricular and supraoptic nuclei of the female rat brain: An immunocytochemical study
Alves, S. E., López, V., McEwen, B. S., & Weiland, N. G. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.6.3281 · Cited by 217 · see citing works
Vasopressin, oxytocin and social behaviour
Keverne, E. B., & Curley, J. P. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.10.006 · Cited by 215 · see citing works
Examination of AVPR1a as an autism susceptibility gene
Wassink, T. H., Piven, J., Vieland, V. J., Pietila, J., Goedken, R. J., Folstein, S. E., & Sheffield, V. C. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001503 · Cited by 212 · see citing works
Interaction of colocalized neuropeptides: functional significance in the circadian timing system
Albers, H. E., Liou, S. Y., Stopa, E., & Zoeller, R. T. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-03-00846.1991 · Cited by 204 · see citing works
Gonadal steroids regulate oxytocin receptors but not vasopressin receptors in the brain of male and female rats. An autoradiographical study
Tribollet, E., Audigier, S., Dubois-Dauphin, M., & Dreifuss, J. J. (1990) · Brain Research · doi:10.1016/0006-8993(90)90232-z · Cited by 203 · see citing works
Female oxytocin-deficient mice display enhanced anxiety-related behavior
Mantella, R. C., Vollmer, R. R., Li, X., & Amico, J. A. (2003) · Endocrinology · doi:10.1210/en.2002-0197 · Cited by 200 · see citing works
Diversity in the mechanisms of gene regulation by estrogen receptors
Sánchez, R., Nguyen, D., Rocha, W., White, J. H., & Mader, S. (2002) · BioEssays · doi:10.1002/bies.10066 · Cited by 200 · see citing works
Vasopressin-immunoreactive cells in the dorsomedial hypothalamic region, medial amygdaloid nucleus and locus coeruleus of the rat
Caffe´, A. R., & van Leeuwen, F. W. (1983) · Cell and Tissue Research · doi:10.1007/bf00222229 · Cited by 199 · see citing works
Estradiol Modulates Density of Putative Oxytocin Receptors’ in Discrete Rat Brain Regions
de Kloet, R., Voorhuis, D. A. M., Boschma, Y., & Elands, J. (2008) · Neuroendocrinology · doi:10.1159/000124680 · Cited by 198 · see citing works
Species differences in V₁a receptor gene expression in monogamous and nonmonogamous voles: Behavioral consequences.
Young, L. J., Winslow, J. T., Nilsen, R., & Insel, T. R. (1997) · Behavioral Neuroscience · doi:10.1037/0735-7044.111.3.599 · Cited by 196 · see citing works
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
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
A SYNTHETIC PREPARATION POSSESSING BIOLOGICAL PROPERTIES ASSOCIATED WITH ARGININEVASOPRESSIN
du Vigneaud, V., Gish, D. T., & Katsoyannis, P. G. (1954) · Journal of the American Chemical Society · doi:10.1021/ja01647a089 · Cited by 192 · see citing works
Structure, characterization, and expression of the rat oxytocin receptor gene.
Rozen, F., Russo, C., Banville, D. L., & Zingg, H. H. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.1.200 · Cited by 191 · see citing works
Distribution of androgen receptor immunoreactivity in vasopressin- and oxytocin-immunoreactive neurons in the male rat brain.
Zhou, L., Blaustein, J. D., & De Vries, G. J. (1994) · Endocrinology · doi:10.1210/endo.134.6.8194487 · Cited by 189 · see citing works
Recent gene conversion involving bovine vasopressin and oxytocin precursor genes suggested by nucleotide sequence
Ruppert, S., Scherer, G., & Schütz, G. (1984) · Nature · doi:10.1038/308554a0 · Cited by 188 · see citing works
Agonistic Behaviour Between Pairs of Hamsters of the Same and Opposite Sex in a Neutral Observation Area
Payne, P., & Swanson, H. H. (1970) · Behaviour · doi:10.1163/156853970x00402 · Cited by 186 · see citing works
Ability of the CRF Immunoreactive Neurons of the Paraventricular Nucleus to Produce a Vasopressin-Like Material
Tramu, G., Croix, C., & Pillez, A. (2008) · Neuroendocrinology · doi:10.1159/000123595 · Cited by 180 · see citing works
The role of oxytocin and the paraventricular nucleus in the sexual behaviour of male mammals
Argiolas, A., & Melis, M. R. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.08.019 · Cited by 177 · see citing works
THE PURIFICATION AND THE AMINO ACID CONTENT OF VASOPRESSIN PREPARATIONS
Turner, R. A., Pierce, J. G., & du Vigneaud, V. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)50947-9 · Cited by 172 · see citing works
Vasopressin and serotonin interactions in the control of agonistic behavior
Ferris, C. F., & Delville, Y. (1994) · Psychoneuroendocrinology · doi:10.1016/0306-4530(94)90043-4 · Cited by 172 · see citing works
Oxytocin Control of Maternal Behavior Regulation by Sex Steroids and Offspring Stimulia
PEDERSEN, C. A. (1997) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1997.tb51916.x · Cited by 172 · see citing works
Effect of Intraseptal Vasotocin and Vasoactive Intestinal Polypeptide Infusions on Courtship Song and Aggression in the Male Zebra Finch ( Taeniopygia guttata )
Goodson, & Adkins‐Regan (1999) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1999.00284.x · Cited by 171 · see citing works
Central Oxytocin Administration Reduces Stress-Induced Corticosterone Release and Anxiety Behavior in Rats1
Windle, R. J., Shanks, N., Lightman, S. L., & Ingram, C. D. (1997) · Endocrinology · doi:10.1210/en.138.7.2829 · Cited by 170 · see citing works
Chapter 10 Alterations in behavioral and neuroendocrine stress coping strategies in pregnant, parturient and lactating rats
Neumann, I. D. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)33011-x · Cited by 169 · see citing works
The effects of infusion of arginine vasopressin, oxytocin, or their antagonists into the olfactory bulb upon social recognition responses in male rats
Dluzen, D. E., Muraoka, S., Engelmann, M., & Landgraf, R. (1998) · Peptides · doi:10.1016/s0196-9781(98)00047-3 · Cited by 169 · see citing works
Regulatory Mechanisms of Corticotropin‐Releasing Hormone and Vasopressin Gene Expression in the Hypothalamus
Itoi, K., Jiang, Y. ‐., Iwasaki, Y., & Watson, S. J. (2004) · Journal of Neuroendocrinology · doi:10.1111/j.0953-8194.2004.01172.x · Cited by 169 · see citing works
Estrogen receptor-β regulates transcript levels for oxytocin and arginine vasopressin in the hypothalamic paraventricular nucleus of male mice
Nomura, M., McKenna, E., Korach, K. S., Pfaff, D. W., & Ogawa, S. (2002) · Molecular Brain Research · doi:10.1016/s0169-328x(02)00525-9 · Cited by 167 · see citing works
Vasopressin and oxytocin: distribution and putative functions in the brain
Buijs, R. M., De Vries, G. J., Van Leeuwen, F. W., & Swaab, D. F. (1983) · Progress in Brain Research · doi:10.1016/s0079-6123(08)64379-4 · Cited by 167 · see citing works
The action of infundibulin upon the mammary secretion
Ott, I., & Scott, J. C. (1910) · Experimental Biology and Medicine · doi:10.3181/00379727-8-27 · Cited by 165 · see citing works
Chapter 16 Neurohypophyseal hormone receptor systems in brain and periphery
Jard, S., Barberis, C., Audigier, S., & Tribollet, E. (1987) · Progress in brain research · doi:10.1016/s0079-6123(08)60206-x · Cited by 164 · 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
Oxytocin, But Not Oxytocin Receptor, is Regulated by Oestrogen Receptor β in the Female Mouse Hypothalamus
Patisaul, H. B., Scordalakes, E. M., Young, L. J., & Rissman, E. F. (2003) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2003.01061.x · Cited by 160 · see citing works
Comparative Distribution of Vasopressin and Oxytocin Neurons in the Rat Brain Using a Double-Label Procedure
Hou-Yu, A., Lamme, A., Zimmerman, E. A., & Silverman, A. (2008) · Neuroendocrinology · doi:10.1159/000124651 · Cited by 160 · see citing works
Changes in Oxytocin Receptor mRNA in Rat Brain During Pregnancy and the Effects of Estrogen and Interleukin‐6
Young, L. J., Muns, S., Wang, Z., & Insel, T. R. (1997) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1997.00654.x · Cited by 160 · see citing works
Novel Ligand Specificity of Pituitary Vasopressin Receptors in the Rat
Antoni, F. A. (2008) · Neuroendocrinology · doi:10.1159/000123976 · Cited by 159 · 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
Sensory processing in the main and accessory olfactory systems: Comparisons and contrasts
Meredith, M. (1991) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(91)90258-7 · Cited by 155 · 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
Effects of androgens and estrogens on the vasopressin and oxytocin innervation of the adult rat brain
De Vries, G. J., Duetz, W., Buijs, R. M., van Heerikhuize, J., & Vreeburg, J. T. M. (1986) · Brain Research · doi:10.1016/0006-8993(86)91519-2 · Cited by 153 · see citing works
The Vasopressin mRNA Poly(A) Tract is Unusually Long and Increases during Stimulation of Vasopressin Gene Expression in Vivo
Carrazana, E. J., Pasieka, K. B., & Majzoub, J. A. (1988) · Molecular and Cellular Biology · doi:10.1128/mcb.8.6.2267-2274.1988 · Cited by 149 · see citing works
Differential modulation of lateral septal vasopressin receptor blockade in spatial learning, social recognition, and anxiety-related behaviors in rats
Everts, H. G. J., & Koolhaas, J. M. (1999) · Behavioural Brain Research · doi:10.1016/s0166-4328(98)00004-7 · Cited by 148 · see citing works
Neuropeptides and sexual behaviour
Argiolas, A. (1999) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(99)00068-8 · Cited by 148 · see citing works
Oxytocin stimulates myometrial guanosine triphosphatase and phospholipase-C activities via coupling to G alpha q/11
Ku, C.-Y., Qian, A., Wen, Y., Anwer, K., & Sanborn, B. M. (1995) · Endocrinology · doi:10.1210/endo.136.4.7895660 · Cited by 146 · see citing works
An oxytocin antagonist infused into the central nucleus of the amygdala increases maternal aggressive behavior
Lubin, D. A., Elliot, J. C., Black, M. C., & Johns, J. M. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.2.195 · Cited by 145 · see citing works
A critique of the vasopressin-memory hypothesis
Sahgal, A. (1984) · Psychopharmacology · doi:10.1007/bf00464785 · Cited by 145 · see citing works
Social status in pairs of male squirrel monkeys determines the behavioral response to central oxytocin administration
Winslow, J., & Insel, T. (1991) · The Journal of Neuroscience · doi:10.1523/jneurosci.11-07-02032.1991 · Cited by 145 · see citing works
Dendritically released transmitters cooperate via autocrine and retrograde actions to inhibit afferent excitation in rat brain
Hirasawa, M., Schwab, Y., Natah, S. S., Hillard, C. J., Mackie, K., Sharkey, K. A., & Pittman, Q. J. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.066159 · Cited by 143 · see citing works
The neurophysin-containing innervation of the forebrain of the mouse
Castel, M., & Morris, J. F. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90078-4 · Cited by 143 · see citing works
Infusion of Antisense Oligo-deoxynucleotides to the Oxytocin Receptor in the Ventromedial Hypothalamus Reduces Estrogen-Induced Sexual Receptivity and Oxytocin Receptor Binding in the Female Rat
McCarthy, M. M., Kleopoulos, S. P., Mobbs, C. V., & Pfaff, D. W. (2008) · Neuroendocrinology · doi:10.1159/000126689 · Cited by 142 · see citing works
The influence of androgens on the development of a sex difference in the vasopressinergic innervation of the rat lateral septum
Vries, G. J. D., Best, W., & Sluiter, A. A. (1983) · Developmental Brain Research · doi:10.1016/0165-3806(83)90019-6 · Cited by 141 · see citing works
Lateral and Medial Septal Lesions Reduce Anxiety in the Plus-Maze and Probe-Burying Tests
Menard, J. L., & Treit, D. (1996) · Physiology & Behavior · doi:10.1016/0031-9384(96)00138-2 · Cited by 140 · see citing works
Oxytocin receptor gene expression in the rat uterus during pregnancy and the estrous cycle and in response to gonadal steroid treatment
Larcher, A., Neculcea, J., Breton, C., Arslan, A., Rozen, F., Russo, C., & Zingg, H. H. (1995) · Endocrinology · doi:10.1210/endo.136.12.7588281 · Cited by 140 · see citing works
Mapping oxytocin receptor gene expression in the mouse brain and mammary gland using an oxytocin receptor-LacZ reporter mouse
Gould, B. R., & Zingg, H. H. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00283-5 · Cited by 138 · see citing works
The amino-acid sequence in oxytocin
Tuppy, H. (1953) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(53)90071-7 · Cited by 137 · see citing works
Vasopressinergic regulation of the hypothalamic pituitary adrenal axis and stress adaptation
Volpi, S., Rabadan-Diehl, C., & Aguilera, G. (2004) · Stress · doi:10.1080/10253890410001733535 · Cited by 136 · see citing works
The neurohypophysial endocrine regulatory cascade: precursors, mediators, receptors, and effectors
Acher, R., & Chauvet, J. (1995) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1995.1009 · Cited by 135 · see citing works
Hypothalamic Paraventricular Nucleus Modulates Maternal Aggression in Rats: Effects of Ibotenic Acid Lesion and Oxytocin Antisense
Giovenardi, M., Padoin, M. J., Cadore, L. P., & Lucion, A. B. (1998) · Physiology & Behavior · doi:10.1016/s0031-9384(97)00434-4 · Cited by 135 · see citing works
Differential lateral septal vasopressin innervation in aggressive and nonaggressive male mice
Compaan, J. C., Buijs, R. M., Pool, C. W., De Ruiter, A. J. H., & koolhaas, J. M. (1993) · Brain Research Bulletin · doi:10.1016/0361-9230(93)90032-7 · Cited by 135 · see citing works
Reduced aggressive behaviour in mice with targeted disruption of the oxytocin gene
DeVries, A. C., Young III, W. S., & Nelson, R. J. (1997) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1997.t01-1-00589.x · Cited by 134 · see citing works
Self-citation
Oxytocin potently enhances novelty-induced grooming behavior in the rat
Drago, F., Pedersen, C. A., Caldwell, J. D., & Prange, A. J. (1986) · Brain Research · doi:10.1016/0006-8993(86)90573-1 · Cited by 134 · see citing works
Effects of estrogen on oxytocin receptor messenger ribonucleic acid expression in the uterus, pituitary, and forebrain of the female rat
Quiñones-Jenab, V., Jenab, S., Ogawa, S., Adan, R. A. M., Burbach, P. H., & Pfaff, D. W. (2008) · Neuroendocrinology · doi:10.1159/000127160 · Cited by 134 · see citing works
Steroid Dependency of Vasopressin Neurons in the Bed Nucleus of the Stria Terminalis byin SituHybridization*
MILLER, M. A., URBAN, J. H., & DORSA, D. M. (1989) · Endocrinology · doi:10.1210/endo-125-5-2335 · Cited by 134 · see citing works
Social motivation is reduced in vasopressin 1b receptor null mice despite normal performance in an olfactory discrimination task
Wersinger, S. R., Kelliher, K. R., Zufall, F., Lolait, S. J., O’Carroll, A., & Young, W. S. (2004) · Hormones and Behavior · doi:10.1016/j.yhbeh.2004.07.004 · Cited by 132 · see citing works
Self-citation
Coexpression of Vasopressin and Oxytocin in Hypothalamic Supraoptic Neurons of Lactating Rats*
Mezey, É., & Kiss, J. Z. (1991) · Endocrinology · doi:10.1210/endo-129-4-1814 · Cited by 130 · see citing works
Structure of mouse vasopressin and oxytocin genes
Hara, Y., Battey, J. F., & Gainer, H. (1990) · Molecular Brain Research · doi:10.1016/0169-328x(90)90045-f · Cited by 129 · see citing works
Central oxytocin and reproductive behaviours
Insel, T. R. (1997) · Reviews of Reproduction · doi:10.1530/ror.0.0020028 · Cited by 129 · see citing works
The oxytocin antagonist d(CH2)5Tyr(Me)-Orn8-vasotocin inhibits male copulatory behaviour in rats
Argiolas, A., Collu, M., Gessa, G. L., Melis, M. R., & Serra, G. (1988) · European Journal of Pharmacology · doi:10.1016/0014-2999(88)90675-9 · Cited by 125 · see citing works
Distribution of messenger RNA for the vasopressin V1a receptor in the CNS of male and female rats
Szot, P., Bale, T. L., & Dorsa, D. M. (1994) · Molecular Brain Research · doi:10.1016/0169-328x(94)90111-2 · Cited by 125 · see citing works
Molecular Cloning and Characterization of Rat V1B Vasopressin Receptor: Evidence for Its Expression in Extrapituitary Tissues
Saito, M., Sugimoto, T., Tahara, A., & Kawashima, H. (1995) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1995.2033 · Cited by 124 · see citing works
Oxytocin in the Amygdala Facilitates Maternal Aggression
Ferris, C. F., FOOTE, K. B., Meltser, H., PLENBY, M. G., Smith, K. L., & Insel, T. R. (1992) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1992.tb34382.x · 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
Aggression and arginine vasopressin immunoreactivity regulation by androgen receptor and estrogen receptor α
Scordalakes, E. M., & Rissman, E. F. (2004) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2004.00036.x · Cited by 119 · see citing works
Oxytocin inhibits infanticide in female house mice (Mus domesticus)
McCarthy, M. J. (1990) · Hormones and Behavior · doi:10.1016/0018-506x(90)90015-p · Cited by 119 · see citing works
Cloning, Novel Promoter Sequence, and Estrogen Regulation of a Rat Oxytocin Receptor Gene
Bale, T. L., & Dorsa, D. M. (1997) · Endocrinology · doi:10.1210/endo.138.3.4998 · Cited by 118 · see citing works
Extraordinary diversity in vasopressin (V1a) receptor distributions among wild prairie voles (Microtus ochrogaster): 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
Estradiol induces oxytocin binding sites in rat hypothalamic ventromedial nucleus
de Kloet, E. R., Voorhuis, T. A. M., & Elands, J. (1985) · European Journal of Pharmacology · doi:10.1016/0014-2999(85)90679-x · Cited by 116 · see citing works
Oxytocin but not vasopressin facilities social recognition following injection into the medial preoptic area of the rat brain
Popik, P., & van Ree, J. M. (1991) · European Neuropsychopharmacology · doi:10.1016/0924-977x(91)90010-r · Cited by 114 · see citing works
Vasopressin- and neurophysin-immunoreactive neurons in the septal region, medial amygdala and locus coeruleus in colchicine-treated rats
Sofroniew, M. V. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90217-9 · Cited by 113 · see citing works
Gonadal steroids have paradoxical effects on brain oxytocin receptors
Insel, T. R., Young, L., Witt, D. M., & Crews, D. (1993) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1993.tb00531.x · Cited by 113 · see citing works
A composite hormone response element mediates the transactivation of the rat oxytocin gene by different classes of nuclear hormone receptors
Adan, R. A. H., Cox, J. J., Beischlag, T. V., & Burbach, J. P. H. (1993) · Molecular Endocrinology · doi:10.1210/mend.7.1.8383287 · 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
Evidence that the lateral septum is involved in the antidepressant-like effects of the vasopressin V1b receptor antagonist, SSR149415
Stemmelin, J., Lukovic, L., Salome, N., & Griebel, G. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300562 · Cited by 112 · 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
Chapter 15 Nonpeptide vasopressin receptor antagonists: development of selective and orally active V1a, V2 and V1b receptor ligands
Gal, C. S., Wagnon, J., Valette, G., Garcia, G., Pascal, M., Maffrand, J., & Fur, G. L. (2002) · Progress in brain research · doi:10.1016/s0079-6123(02)39017-4 · Cited by 111 · see citing works
Estradiol influences oxytocin-immunoreactive brain systems
Jirikowski, G. F., Caldwell, J. D., Pedersen, C. A., & Stumpf, W. E. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90022-x · Cited by 111 · see citing works
Single Cell Reverse Transcription-Polymerase Chain Reaction Analysis of Rat Supraoptic Magnocellular Neurons: Neuropeptide Phenotypes and High Voltage-Gated Calcium Channel Subtypes
Glasgow, E. F., Kusano, K., Chin, H. R., Mezey, É., Young, W. S., & Gainer, H. (1999) · Endocrinology · doi:10.1210/endo.140.11.7136 · Cited by 111 · see citing works
Self-citation
A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression
West, D. V., Del‐Favero, J., Aulchenko, Y. S., Oswald, P., Souery, D., Forsgren, T., Sluijs, S., Belkacem, S., Adolfsson, R., Mendlewicz, J., et al. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001420 · Cited by 110 · see citing works
Medial preoptic area oxytocin and female sexual receptivity.
Caldwell, J. D., Jirikowski, G. F., Greer, E. R., & Pedersen, C. A. (1989) · Behavioral Neuroscience · doi:10.1037//0735-7044.103.3.655 · Cited by 110 · see citing works
Oxytocin Inhibits Aggression in Female Syrian Hamsters
Harmon, A. C., Huhman, K. L., Moore, T. O., & Albers, H. E. (2002) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2002.00863.x · Cited by 108 · see citing works
Positive and negative regulation of the rat vasopressin gene promoter
Iwasaki, Y. (1997) · Endocrinology · doi:10.1210/en.138.12.5266 · Cited by 108 · see citing works
Molecular regulation of the oxytocin receptor in peripheral organs
Kimura, T., Saji, F., Nishimori, K., Ogita, K., Nakamura, H., Koyama, M., & Murata, Y. (2003) · Journal of Molecular Endocrinology · doi:10.1677/jme.0.0300109 · Cited by 103 · see citing works

Flagged first, then by citations

Research works printed but not linked: 8

Acher R, Chauvet J, Chauvet MT. 1995. Man and chimera: selective versus neutral oxytocin evolution. Adv Exp Med Biol 395: 615–627.
Aragona BJ, Liu Y, Cameron A, Perlman G, Wang ZX. 2003a. Opposite modulation of social attachment by D1‐ and D2‐type dopamine receptor activation in nucleus accumbens shell. Horm Behav 44, 37. [Abstract]
Burbach JP, Adan RA. 1993. The rat oxytocin gene. Physiological changes in expression in the hypothalamo‐neurohypophysial system and responsiveness of promoter activity. Ann N Y Acad Sci 689: 34–49.
Farini F. 1913. Diabete insipido ed opoterapia. Gazz Osped Clin 34: 1135–1139.
Koolhaas JM, Moor E, Hiemstra Y. 1991. The testosterone‐dependent vasopressinergic neurons in the medial amygdala and lateral septum: involvement in social behaviour in male rats. Proceedings of the Third International Vasopressin Conference. Jard S, Jamison R, editors. Paris, London: Colloque INSERM/John Libbey Eurotext Ltd; pp. 213–219.
Landgraf R, Malkinson TJ, Veale WL, Lederis K, Pittman QJ. 1990. Vasopressin and oxytocin in the rat brain in response to prostaglandin fever. Am J Physiol 259: R1056–R1062.
Manning M, Sawyer WH. 1991. Antagonists of vasopressin and oxytocin: current status and future perspective. Vasopressin. Jard S, Jamison R, editors. France: John Libbey Eurotext Ltd; pp. 297–309.
Vongraven D. 1913. Die nierenwirkung von hypophysenextrakten meschen. Berl Klin Wochenscgr 50: 2083–2086.

Sorted by citations

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
Gregory, S. G., Connelly, J. J., Towers, A. J., Johnson, J., Biscocho, D., Markunas, C. A., Lintas, C., Abramson, R. K., Wright, H. H., Ellis, P., et al. (2009) · BMC Medicine · doi:10.1186/1741-7015-7-62 · Cited by 576 · see citing works
Acute effects of steroid hormones and neuropeptides on human social-emotional behavior: A review of single administration studies
Bos, P. A., Panksepp, J., Bluthé, R.-M., & Honk, J. V. (2012) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2011.01.002 · Cited by 429 · see citing works
Brain vasopressin is an important regulator of maternal behavior independent of dams’ trait anxiety
Bosch, O. J., & Neumann, I. D. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807412105 · Cited by 280 · see citing works
A conditional knockout mouse line of the oxytocin receptor
Lee, H.-J., Caldwell, H. K., Macbeth, A. H., Tolu, S. G., & Young, W. S. (2008) · Endocrinology · doi:10.1210/en.2007-1710 · Cited by 269 · see citing works
Self-citation
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 and vasopressin: powerful regulators of social behavior
Caldwell, H. K. (2017) · The Neuroscientist · doi:10.1177/1073858417708284 · Cited by 216 · see citing works
Self-citation
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
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
Low stress reactivity and neuroendocrine factors in the BTBR T+tf/J mouse model of autism
Silverman, J. L., Yang, M., Turner, S. M., Katz, A. M., Bell, D. B., Koenig, J. I., & Crawley, J. N. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.09.059 · Cited by 146 · 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
Self-citation
Oxytocin, vasopressin, and the motivational forces that drive social behaviors
Caldwell, H. K., & Albers, H. E. (2015) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2015_390 · Cited by 129 · see citing works
Self-citation
What do DNA methylation studies tell us about depression? A systematic review
Li, M., D’Arcy, C., Li, X., Zhang, T., Joober, R., & Meng, X. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0412-y · Cited by 125 · see citing works
Neurobiological correlates of social functioning in autism
Neuhaus, E., Beauchaine, T. P., & Bernier, R. (2010) · Clinical Psychology Review · doi:10.1016/j.cpr.2010.05.007 · Cited by 122 · see citing works
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
Shock – Classification and Pathophysiological Principles of Therapeutics
Kislitsina, O. N., Rich, J. D., Wilcox, J. E., Pham, D. T., Churyla, A., Vorovich, E. B., Ghafourian, K., & Yancy, C. W. (2018) · Current Cardiology Reviews · doi:10.2174/1573403x15666181212125024 · Cited by 115 · see citing works
Oxytocin as a natural antipsychotic: a study using oxytocin knockout mice
Caldwell, H. K., Stephens, S. L., & Young, W. S. (2008) · Molecular Psychiatry · doi:10.1038/sj.mp.4002150 · Cited by 108 · see citing works
Self-citation
Effects of Affiliative Human–Animal Interaction on Dog Salivary and Plasma Oxytocin and Vasopressin
MacLean, E. L., Gesquiere, L. R., Gee, N. R., Levy, K., Martin, W. L., & Carter, C. S. (2017) · Frontiers in Psychology · doi:10.3389/fpsyg.2017.01606 · Cited by 93 · see citing works
Effects of chronic social defeat on behavioral and neural correlates of sociality: Vasopressin, oxytocin and the vasopressinergic V1b receptor
Litvin, Y., Murakami, G., & Pfaff, D. W. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.03.007 · Cited by 90 · see citing works
Physiology of the vasopressin receptors
Maybauer, M. O., Maybauer, D. M., Enkhbaatar, P., & Traber, D. L. (2008) · Best practice & research. Clinical anaesthesiology · doi:10.1016/j.bpa.2008.03.003 · Cited by 90 · see citing works
Inactivation of the oxytocin and the vasopressin (Avp) 1b receptor genes, but not the Avp 1a receptor gene, differentially impairs the Bruce effect in laboratory mice (Mus musculus)
Wersinger, S. R., Temple, J. L., Caldwell, H. K., & Young, W. S. (2008) · Endocrinology · doi:10.1210/en.2007-1056 · Cited by 83 · see citing works
Self-citation
Oxytocin during Development: Possible Organizational Effects on Behavior
Miller, T. V., & Caldwell, H. K. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00076 · Cited by 79 · see citing works
Self-citation
Oxytocin: a therapeutic target for mental disorders
Matsuzaki, M., Matsushita, H., Tomizawa, K., & Matsui, H. (2012) · The Journal of Physiological Sciences · doi:10.1007/s12576-012-0232-9 · Cited by 79 · 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
Neuropeptide diversity and the regulation of social behavior in New World primates
French, J. A., Taylor, J. H., Mustoe, A. C., & Cavanaugh, J. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.03.004 · Cited by 66 · see citing works
Oxytocin - A Multifunctional Analgesic for Chronic Deep Tissue Pain
Goodin, B. R., Ness, T. J., & Robbins, M. T. (2014) · Current Pharmaceutical Design · doi:10.2174/1381612820666141027111843 · Cited by 66 · see citing works
Hyponatremia and the syndrome of inappropriate secretion of antidiuretic hormone (SIADH)
Peri, A., Pirozzi, N., Parenti, G., Festuccia, F., & Mené, P. (2010) · Journal of Endocrinological Investigation · doi:10.1007/bf03346668 · Cited by 62 · see citing works
Social plasticity in fish: integrating mechanisms and function
Oliveira, R. F. (2012) · Journal of Fish Biology · doi:10.1111/j.1095-8649.2012.03477.x · Cited by 61 · see citing works
Neurobiology of sociability
Caldwell, H. K. (2012) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4614-1704-0_12 · Cited by 58 · see citing works
Self-citation
The relative contribution of proximal 5′ flanking sequence and microsatellite variation on brain vasopressin 1a receptor (Avpr1a) gene expression and behavior
Donaldson, Z. R., & Young, L. J. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003729 · Cited by 52 · see citing works
Behavioural studies using temporal and spatial inactivation of the oxytocin receptor
LEE, H., CALDWELL, H., MACBETH, A., & YOUNGIII, W. (2008) · Progress in brain research · doi:10.1016/s0079-6123(08)00407-x · Cited by 49 · see citing works
Self-citation
Oxytocin/vasopressin and gonadotropin‐releasing hormone from cephalopods to vertebrates
Minakata, H. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05569.x · Cited by 47 · see citing works
New, Potent, Selective, and Short-Acting Peptidic V1aReceptor Agonists
Wiśniewski, K., Galyean, R., Tariga, H., Alagarsamy, S., Croston, G. E., Heitzmann, J., Kohan, A., Wiśniewska, H., Laporte, R., Rivière, P. J.-M., et al. (2011) · Journal of Medicinal Chemistry · doi:10.1021/jm200278m · Cited by 47 · see citing works
Housing conditions and stimulus females: a robust social discrimination task for studying male rodent social recognition
Macbeth, A. H., Edds, J. S., & Young, W. S. (2009) · Nature Protocols · doi:10.1038/nprot.2009.141 · Cited by 46 · see citing works
Self-citation
Vasopressin and copeptin release during sepsis and septic shock
Gomes, D. A., Beltrão, R. L. D. A., Junior, F. M. D. O., da Silva, J. C., de Arruda, E. P. C., Lira, E. C., & Rocha, M. J. A. (2020) · Peptides · doi:10.1016/j.peptides.2020.170437 · Cited by 42 · see citing works
Neuroendocrine underpinning of social recognition in males and females
Aspesi, D., & Choleris, E. (2022) · Journal of Neuroendocrinology · doi:10.1111/jne.13070 · Cited by 41 · see citing works
Balancing selection maintains polymorphisms at neurogenetic loci in field experiments
Lönn, E., Koskela, E., Mappes, T., Mökkönen, M., Sims, A. M., & Watts, P. C. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1621228114 · Cited by 39 · see citing works
Adaptive evolution of the osmoregulation-related genes in cetaceans during secondary aquatic adaptation
Xu, S., Yang, Y., Zhou, X., Xu, J., Zhou, K., & Yang, G. (2013) · BMC Evolutionary Biology · doi:10.1186/1471-2148-13-189 · Cited by 39 · see citing works
Specification of oxytocinergic and vasopressinergic circuits in the developing mouse brain
Madrigal, M. P., & Jurado, S. (2021) · Communications Biology · doi:10.1038/s42003-021-02110-4 · Cited by 38 · see citing works
Marmosets treated with oxytocin are more socially attractive to their long-term mate
Cavanaugh, J., Huffman, M. C., Harnisch, A. M., & French, J. A. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00251 · Cited by 36 · see citing works
De novo sequencing and initial annotation of the Mongolian gerbil (Meriones unguiculatus) genome
Zorio, D. A. R., Monsma, S. A., Sanes, D. H., Golding, N. L., Rubel, E. W., & Wang, Y. (2018) · Genomics · doi:10.1016/j.ygeno.2018.03.001 · Cited by 36 · see citing works
Social dominance in male vasopressin 1b receptor knockout mice
Caldwell, H. K., Dike, O. E., Stevenson, E. L., Storck, K. E., & Young, W. S. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.03.008 · Cited by 34 · see citing works
Self-citation
Long-term consumption of sugar-sweetened beverage during the growth period promotes social aggression in adult mice with proinflammatory responses in the brain
Choi, J.-Y., Park, M.-N., Kim, C.-S., Lee, Y.-K., Choi, E. Y., Chun, W. Y., & Shin, D.-M. (2017) · Scientific Reports · doi:10.1038/srep45693 · Cited by 32 · see citing works
Oxytocin Facilitates Allomaternal Behavior under Stress in Laboratory Mice
Tsuneoka, Y., Yoshihara, C., Ohnishi, R., Yoshida, S., Miyazawa, E., Yamada, M., Horiguchi, K., Young, W. S., Nishimori, K., Kato, T., et al. (2022) · eNeuro · doi:10.1523/eneuro.0405-21.2022 · Cited by 31 · see citing works
Self-citation
Vasopressin/oxytocin-related peptides influence long-term memory of a passive avoidance task in the cuttlefish, Sepia officinalis
Bardou, I., Leprince, J., Chichery, R., Vaudry, H., & Agin, V. (2009) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2009.10.004 · Cited by 30 · see citing works
Recent advances in oral delivery of peptide hormones
Varamini, P., & Tóth, I. (2016) · Expert Opinion on Drug Delivery · doi:10.1517/17425247.2016.1142526 · Cited by 29 · see citing works
Neural correlates of mating system diversity: oxytocin and vasopressin receptor distributions in monogamous and non-monogamous Eulemur
Grebe, N. M., Sharma, A., Freeman, S. M., Palumbo, M. C., Patisaul, H. B., Bales, K. L., & Drea, C. M. (2021) · Scientific Reports · doi:10.1038/s41598-021-83342-6 · Cited by 26 · see citing works
Solid-phase peptide synthesis and solid-phase fragment coupling mediated by isonitriles
Wang, T., & Danishefsky, S. J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1310431110 · Cited by 25 · see citing works
Oxytocin structure and function in New World monkeys: from pharmacology to behavior
Mustoe, A. C., Taylor, J. H., & French, J. A. (2018) · Integrative Zoology · doi:10.1111/1749-4877.12318 · Cited by 25 · see citing works
Efficacy of bleeding control using a large amount of highly diluted vasopressin in laparoscopic treatment for interstitial pregnancy
Moon, H. S., Kim, S. G., Park, G. S., Choi, J. K., Koo, J. S., & Joo, B. S. (2010) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2010.02.030 · Cited by 25 · see citing works
Peace-Making in Marsupials: The First Study in the Red-Necked Wallaby (Macropus rufogriseus)
Cordoni, G., & Norscia, I. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086859 · Cited by 24 · see citing works
Centrally administered ghrelin potently inhibits water intake induced by angiotensin II and hypovolemia in rats
Hashimoto, H., Otsubo, H., Fujihara, H., Suzuki, H., Ohbuchi, T., Yokoyama, T., Takei, Y., & Ueta, Y. (2009) · The Journal of Physiological Sciences · doi:10.1007/s12576-009-0062-6 · Cited by 24 · see citing works
Alcohol and endocannabinoids: Neuroendocrine interactions in the reproductive axis
Rettori, V., Laurentiis, A. D., & Fernández‐Solari, J. (2010) · Experimental Neurology · doi:10.1016/j.expneurol.2010.03.019 · Cited by 24 · see citing works
Expression of circadian clock genes and proteins in urothelial cancer is related to cancer-associated genes
Litlekalsøy, J., Rostad, K., Kalland, K., Hostmark, J. G., & Lærum, O. D. (2016) · BMC Cancer · doi:10.1186/s12885-016-2580-y · Cited by 23 · see citing works
Putting it in Context: Linking Auditory Processing with Social Behavior Circuits in the Vertebrate Brain
Petersen, C. L., & Hurley, L. M. (2017) · Integrative and Comparative Biology · doi:10.1093/icb/icx055 · Cited by 23 · see citing works
Arg-Vasotocin Directly Activates Isotocin Receptors and Induces COX2 Expression in Ovoviviparous Guppies
Lyu, L. K., Li, J. S., Wang, X. J., Yao, Y. J., Li, J. F., Li, Y., Wen, H. S., & Qi, X. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.617580 · Cited by 20 · see citing works
Novel Vasoregulatory Aspects of Hereditary Angioedema: the Role of Arginine Vasopressin, Adrenomedullin and Endothelin-1
Kajdácsi, E., Jani, P. K., Csuka, D., Varga, L. Á., Prohászka, Z., Farkas, H., & Cervenak, L. (2016) · Journal of Clinical Immunology · doi:10.1007/s10875-016-0239-8 · Cited by 20 · see citing works
Oxytocin and vasopressin increase male-directed threats and vocalizations in female macaques
Jiang, Y., & Platt, M. L. (2018) · Scientific Reports · doi:10.1038/s41598-018-36332-0 · Cited by 19 · see citing works
Comparison of the distribution of oxytocin and vasopressin 1a receptors in rodents reveals conserved and derived patterns of nonapeptide evolution
Freeman, A. R., Aulino, E. A., Caldwell, H. K., & Ophir, A. G. (2020) · Journal of Neuroendocrinology · doi:10.1111/jne.12828 · Cited by 19 · see citing works
Self-citation
Using transgenic mouse models to study oxytocin's role in the facilitation of species propagation
Lee, H., Pagani, J. H., & Young, W. S. (2010) · Brain Research · doi:10.1016/j.brainres.2010.08.042 · Cited by 19 · see citing works
Self-citation
Militaries and the duty of care to enhanced veterans
Henschke, A. (2019) · Journal of the Royal Army Medical Corps · doi:10.1136/jramc-2018-001140 · Cited by 18 · see citing works
99mTc-Labeled Vasopressin Peptide as a Radiopharmaceutical for Small-Cell Lung Cancer (SCLC) Diagnosis
Gniazdowska, E., Koźmiński, P., Bańkowski, K., & Ochman, P. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm500272r · Cited by 17 · see citing works
Role of Oxytocin/Vasopressin-Like Peptide and Its Receptor in Vitellogenesis of Mud Crab
Lin, D., Wei, Y., & Ye, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21072297 · Cited by 15 · see citing works
Intranasal oxytocin decreases self-oriented learning
Liao, Z., Huang, L., & Luo, S. (2020) · Psychopharmacology · doi:10.1007/s00213-020-05694-7 · Cited by 14 · see citing works
Oxytocin/vasopressin-like neuropeptide signaling in insects
Muratspahić, E., Monjon, E., Duerrauer, L., Rogers, S. M., Cullen, D. A., Broeck, J. V., & Gruber, C. W. (2020) · Vitamins and hormones · doi:10.1016/bs.vh.2019.08.011 · Cited by 14 · see citing works
Behavioral Roles of Oxytocin and Vasopressin
Benjamin, C. (2012) · InTech eBooks · doi:10.5772/50422 · Cited by 14 · see citing works
Co-peptin: Role as a novel biomarker in clinical practice
Dabla, P. K., Dabla, V., & Arora, S. (2010) · Clinica Chimica Acta · doi:10.1016/j.cca.2010.09.034 · Cited by 14 · see citing works
Physiological/Neurophysiological Mechanisms Involved in the Formation of Stress Responses
Yaribeygi, H., & Sahraei, H. (2018) · Neurophysiology · doi:10.1007/s11062-018-9727-1 · Cited by 15 · see citing works
Identification of tumor differentiation factor (TDF) in select CNS neurons
Woods, A. G., Sokolowska, I., Deinhardt, K., Sandu, C., & Darie, C. C. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0571-1 · Cited by 13 · see citing works
Potential hypothalamic mechanisms in trigeminal neuropathic pain: a comparative analysis with migraine and cluster headache
Islam, J., Rahman, M. T., Ali, M., Elina, K. C., & Park, Y. S. (2024) · The Journal of Headache and Pain · doi:10.1186/s10194-024-01914-z · Cited by 12 · see citing works
Male Carollia perspicillata bats call more than females in a distressful context
González‐Palomares, E., López‐Jury, L., Wetekam, J., Kiai, A., García‐Rosales, F., & Hechavarría, J. C. (2021) · Royal Society Open Science · doi:10.1098/rsos.202336 · Cited by 11 · see citing works
Hormones
Hamid, A. A., Issa, M. B., & Nizar, N. N. A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-08-101892-7.00013-4 · Cited by 10 · see citing works
3T Renal 23Na-MRI: effects of desmopressin in patients with central diabetes insipidus
Haneder, S., Michaely, H. J., Konstandin, S., Schad, L. R., Morelli, J. N., Krämer, B. K., Schoenberg, S. O., & Lammert, A. (2013) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-013-0377-4 · Cited by 11 · see citing works
Development of a High-Sensitivity Quantitation Method for Arginine Vasopressin by High-Performance Liquid Chromatography Tandem Mass Spectrometry, and Comparison with Quantitative Values by Radioimmunoassay
Tsukazaki, Y., Senda, N., Kubo, K., Yamada, S., Kugoh, H., Kazuki, Y., & Oshimura, M. (2016) · Analytical Sciences · doi:10.2116/analsci.32.153 · Cited by 11 · see citing works
Closeness of all kinds: The role of oxytocin and vasopressin in the physiology of spiritual and religious behavior
Grigorenko, E. L. (2011) · Wiley eBooks · doi:10.1002/9781118092699.ch3 · Cited by 11 · see citing works
Vasotocin induces sexually dimorphic effects on acoustically-guided behavior in a tropical frog
Baugh, A. T., & Ryan, M. J. (2017) · Journal of Comparative Physiology A · doi:10.1007/s00359-017-1155-y · Cited by 10 · see citing works
Home seeking behavior in rat pups: Attachment vs. kin selection, oxytocin vs. vasopressin
Sigling, H. O., Wolterink‐Donselaar, I. G., & Spruijt, B. M. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.03.070 · Cited by 10 · see citing works
The Role of Vasopressin in Anxiety and Depression
Morales‐Medina, J. C., Witchey, S. K., & Caldwell, H. K. (2016) · Springer eBooks · doi:10.1007/978-81-322-2803-5_40 · Cited by 9 · see citing works
Self-citation
Neuroendocrinology and Behavior
Sumiyoshi, T. (2012) · InTech eBooks · doi:10.5772/1666 · Cited by 9 · see citing works
Female Mate Choice in Rodents
Fickel, J., & Weyrich, A. (2011) · Primatology monographs · doi:10.1007/978-4-431-53892-9_1 · Cited by 7 · see citing works
Ontogeny of Oxytocin-Like Immunoreactivity in the Cuttlefish, Sepia officinalis, Central Nervous System
Bardou, I., Maubert, E., Leprince, J., Chichery, R., Dallérac, G. M., Vaudry, H., & Agin, V. (2009) · Developmental Neuroscience · doi:10.1159/000235942 · Cited by 5 · see citing works
Vasopressin/Oxytocin and Receptors
Young, W. S., & Gainer, H. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.01475-3 · Cited by 5 · see citing works
Self-citation
TAKOTSUBO CARDIOMYOPATHY WITH HYPERVASOPRESSINEMIA
Urahama, N., Nakashima, H., Kurose, H., & Ohno, T. (2009) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.2009.02281.x · Cited by 4 · see citing works
Histidine analogues of oxytocin and vasopressin as efficient ligands for Zn2+ ions – Potentiometric and NMR studies
Brasuń, J., Cebrat, M., Jaremko, M., Jaremko, Ł., Gładysz, O., & Zhukov, I. (2009) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2009.04.016 · Cited by 3 · see citing works
The biological perspective on mother-infant bonding: the importance of oxytocin
Nagasawa, M., Okabe, S., Mogi, K., & Kikusui, T. (2013) · Japanese Journal of Animal Psychology · doi:10.2502/janip.63.1.4 · Cited by 3 · see citing works
Investigating a Novel Protein Using Mass Spectrometry: The Example of Tumor Differentiation Factor (TDF)
Woods, A. G., Sokolowska, I., Deinhardt, K., & Darie, C. C. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-06068-2_25 · Cited by 2 · see citing works
Renin, antidiuretic hormone (ADH), and ADH receptor levels in cerebral salt wasting associated with tuberculous meningitis
Tripathi, A., Kumar, M., Kalita, J., Kant, S., & Misra, U. K. (2022) · Neurological Sciences · doi:10.1007/s10072-021-05681-6 · Cited by 2 · see citing works
Synthesis of fluorenated analogues of self-assembling peptide P11-4 and study on P11-4 therapeutic effect on artificial initial enamel lesions
Uzunova, I., Dobrev, I. N., Danalev, D. L., Raycheva, R., Georgiev, K. G., Petrova, S., Nihtyanova, T., & Belcheva, A. (2023) · Journal of Chemical Technology and Metallurgy · doi:10.59957/jctm.v58i3.88 · Cited by 1 · see citing works
EFFECT OF AQUEOUS EXTRACT OF SEEDS OF LAGENARIA SICERARIA ON URINE VOLUME AND URINARY ELECTROLYTES IN SWISS ALBINO RATS
Jayasree, T., Naveen, A., Ubedulla, S., & Sekhar, N. C. (2014) · International Research Journal of Pharmacy · doi:10.7897/2230-8407.050582 · Cited by 1 · see citing works
Peptides and Glycopeptides
Owens, N. W., & Schweizer, F. (2011) · Elsevier eBooks · doi:10.1016/b978-0-08-088504-9.00012-x · Cited by 1 · see citing works
Duality of stochasticity and natural selection shape the ecology-driven pattern of social interactions: the fall of Hamilton's rule
Heininger, K. (2015) · doi:10.13140/rg.2.2.26412.95368 · Cited by 1 · see citing works
Oxytocin and obsessive–compulsive disorder
Soltan, M. (2022) · Egyptian Journal of Psychiatry · doi:10.4103/ejpsy.ejpsy_28_21 · Cited by 1 · see citing works
Testosterone and vasopressin in men's reproductive behavior
Steiner, E. T. (2020) · Digital Scholarship - UNLV (University of Nevada Reno) · doi:10.34917/2269036 · Cited by 1 · see citing works
Role of Mass Spectrometry in Investigating a Novel Protein: The Example of Tumor Differentiation Factor (TDF)
Sokolowska, I., Wetie, A. G. N., Woods, A. G., Jayathirtha, M., & Darie, C. C. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-15950-4_24 · Cited by 1 · see citing works
Children’s Education in The Story of Single Mothers in Qur’ȃn
Chaer, M. T., Wasim, A. T., & Khilmiyah, A. (2019) · International Journal of Education and Learning · doi:10.31763/ijele.v1i2.36 · Cited by 1 · see citing works
Pathophysiological mechanisms and pharmacological methods of prevention and treatment of bronchopulmonary dysplasia in preterm infants
Wątroba, S., & Bryda, J. (2019) · Journal of Pre-Clinical and Clinical Research · doi:10.26444/jpccr/114123 · Cited by 1 · see citing works
Characterizing Protein Conformational Spaces using Dimensionality Reduction and Algebraic TopologyPreprint
Joshi, A., Haspel, N., & González, E. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.16.468545 · Cited by 1 · see citing works
Optical Investigations of Neurohypophysial Excitability and Amyloid Fibril Formation
Foley, J. (2013) · Digital Commons - University of South Florida (University of South Florida)
Attachment behavior in rats
Sigling, H. O. (2009) · Utrecht University Repository (Utrecht University)
Kinetic Investigation and Anticoagulant Activity of Amide Analogues of Isoform 2 and 3 of Antistasin
Danalev, D. L., Marinkova, D., Raykova, R., Yotova, L. K., Tsibranska, I., Savov, K., & Obretenova, G. (2013) · International Journal of Peptide Research and Therapeutics · doi:10.1007/s10989-013-9381-9

Authors: Caldwell, H. K., & Young, W. S.
ORCID: Caldwell, H. K.
Young, W. S.
Venue: Handbook of Neurochemistry and Molecular Neurobiology
Publisher: Springer US
Published: 2006
Pages: 573-607
DOI: 10.1007/978-0-387-30381-9_25
OpenAlex: W2097309877
Cited by: 113
References: 383
Citations by year: 2026: 1 · 2025: 1 · 2024: 1 · 2023: 1 · 2022: 5 · 2021: 7 · 2020: 6 · 2019: 7 · 2018: 6 · 2017: 8 · 2016: 7 · 2015: 6 · 2014: 7 · 2013: 8 · 2012: 6
FWCI: 14.49
Type: book chapter
Language: en
Open access: closed
Locations: Springer eBooks (publishedVersion)
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: oxytocin, vasopressin, oxytocin receptor, vasopressin receptor, knockout mice, viral vectors, hormonal regulation, maternal behavior, social recognition, lateral septum, Microtus ochrogaster, golden hamster

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Oxytocin and vasopressin: genetics and behavioral implications

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks