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Intramyometrial vasopressin as a haemostatic agent during myomectomy

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A Randomized Comparison of Vasopressin and Tourniquet as Hemostatic Agents During Myomectomy

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Separate Agonist and Peptide Antagonist Binding Sites of the Oxytocin Receptor Defined by Their Transfer into the V2 Vasopressin Receptor

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Molecular neurobiology and pharmacology of the Vasopressin/Oxytocin receptor family

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Two aromatic residues regulate the response of the human oxytocin receptor to the partial agonist arginine vasopressin

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Human Myometrium during Pregnancy Contains and Responds to VI Vasopressin Receptors as well as Oxytocin Receptors*

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Effects of vasopressin administration during hysteroscopic surgery.

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PRIMARY DYSMENORRHOEA AND VASOPRESSIN

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Molecular characterization of a cloned human oxytocin receptor

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Vasopressin and Oxytocin Receptors in Vagina, Myometrium, and Oviduct of Rabbits*

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Receptor‐mediated uterine effects of vasopressin and oxytocin in nonpregnant women

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Effect of SR49059, an orally active V1a vasopressin receptor antagonist, in the prevention of dysmenorrhoea

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Sex steroid modulation of neurohypophysial hormone receptors in human nonpregnant myometrium

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Oxytocin and vasopressin 1a receptor gene expression in the cycling or pregnant human uterus

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Gene and cDNA cloning and characterization of the mouse V3/V1b pituitary vasopressin receptor

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The role of oxytocin receptors and vasopressin V1a receptors in uterine contractions in rats: Implications for tocolytic therapy with oxytocin antagonists

Chan, W. Y., Wo, N. C., & Manning, M. (1996) · American Journal of Obstetrics and Gynecology · doi:10.1016/s0002-9378(96)70050-9 · Cited by 31 · see citing works

Effects of SR 49059, an orally active V1a vasopressin receptor antagonist, on vasopressin‐induced uterine contractions

Bossmar, T., Brouard, R., Döberl, A., & Åkerlund, M. (1997) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.1997.tb11500.x · Cited by 25 · see citing works

Effectiveness of Hormonal Tourniquet by Vasopressin during Myomectomy through Vasopressin V1a Receptor Ubiquitously Expressed in Myometrium

Kimura, T., Kusui, C., Matsumura, Y., Ogita, K., Isaka, S., Nakajima, A., Ohashi, K., Koyama, M., Azuma, C., & Murata, Y. (2002) · Gynecologic and Obstetric Investigation · doi:10.1159/000067881 · Cited by 25 · see citing works

Maturation of Spontaneous and Agonist-Induced Uterine Contractions in the Peripartum Mouse Uterus1

Mackler, A. M., Ducsay, C. A., Veldhuis, J. D., & Yellon, S. M. (1999) · Biology of Reproduction · doi:10.1095/biolreprod61.4.873 · Cited by 24 · see citing works

Photoaffinity labelling of the oxytocin receptor in plasma membranes from rat mammary gland

Müller, M., Soloff, M. S., & Fahrenholz, F. (1989) · FEBS Letters · doi:10.1016/0014-5793(89)80496-x · Cited by 23 · see citing works

A nonpeptide oxytocin receptor antagonist radioligand highly selective for human receptors

Lemaire, W., O’Brien, J. A., Burno, M., Chaudhary, A., Dean, D. C., Williams, P. D., Freidinger, R. M., Pettibone, D. J., & Williams, D. L. (2002) · European Journal of Pharmacology · doi:10.1016/s0014-2999(02)02048-4 · Cited by 22 · see citing works

Quantitative reverse transcription and polymerase chain reaction analysis of oxytocin and vasopressin receptor mRNAs in the rat uterus near parturition1M.S. Clerget was a recipient of a doctoral fellowship from the Ministère Chargé de la Recherche (Paris) during this work.1

Clerget-Froidevaux, M.-S., Elalouf, J., & Germain, G. (1997) · Molecular and Cellular Endocrinology · doi:10.1016/s0303-7207(97)00218-9 · Cited by 13 · see citing works

Effect of the non‐peptide, vasopressin V1a receptor antagonist, SR 49059 and its enantiomer, SR 49770, on isolated human myometrium

Bossmar, T., Rasmussen, T., & Åkerlund, M. (1996) · Acta Obstetricia Et Gynecologica Scandinavica · doi:10.3109/00016349609054663 · Cited by 13 · see citing works

Pervasive social deficits, but normal parturition, in oxytocin receptor-deficient mice

Takayanagi, Y., Yoshida, M., Bielsky, I. F., Ross, H. E., Kawamata, M., Onaka, T., Yanagisawa, T., Kimura, T., Matzuk, M. M., Young, L. J., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505312102 · Cited by 806 · 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

New aspects of oxytocin receptor function revealed by knockout mice: sociosexual behaviour and control of energy balance

Nishimori, K., Takayanagi, Y., YOSHIDA, M., Kasahara, Y., YOUNG, L., & Kawamata, M. (2008) · Progress in brain research · doi:10.1016/s0079-6123(08)00408-1 · Cited by 98 · see citing works

Oxytocin Receptor in the Hypothalamus Is Sufficient to Rescue Normal Thermoregulatory Function in Male Oxytocin Receptor Knockout Mice

Kasahara, Y., Sato, K., Takayanagi, Y., Mizukami, H., Ozawa, K., Hidema, S., So, K.-H., Kawada, T., Inoue, N., Ikeda, I., et al. (2013) · Endocrinology · doi:10.1210/en.2012-2206 · Cited by 96 · see citing works

The Parental Brain

Numan, M. (2020) · doi:10.1093/oso/9780190848675.001.0001 · Cited by 101 · see citing works

Inhibitory Effect of Barusiban and Atosiban on Oxytocin-Induced Contractions of Myometrium From Preterm and Term Pregnant Women

Pierzyński, P., Lemancewicz, A., Reinheimer, T. M., Åkerlund, M., & LAUDAŃSKI, T. (2004) · Journal of the Society for Gynecologic Investigation · doi:10.1016/j.jsgi.2004.02.008 · Cited by 58 · see citing works

SSR126768A (4-Chloro-3-[(3 R)-(+)-5-chloro-1-(2,4-dimethoxybenzyl)-3-methyl-2- oxo-2,3-dihydro-1 H-indol-3-yl]-N-ethyl-N-(3-pyridylmethyl)-benzamide, Hydrochloride): A New Selective and Orally Active Oxytocin Receptor Antagonist for the Prevention of Preterm Labor

Gal, C. S., Valette, G., Foulon, L., Germain, G., Advenier, C., Naline, E., Bardou, M., Martinolle, J.-P., Pouzet, B., Raufaste, D., et al. (2004) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.103.061200 · Cited by 56 · see citing works

Oxytocin in Women’s Health and Disease

Liu, N., Yang, H.-P., Han, L., & Ma, M. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.786271 · Cited by 46 · see citing works

Mice deficient in Dmrt7 show infertility with spermatogenic arrest at pachytene stage

Kawamata, M., & Nishimori, K. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.10.066 · Cited by 44 · see citing works

Mutual regulation of vasopressin- and oxytocin-induced glucagon secretion in V1b vasopressin receptor knockout mice

Fujiwara, Y., Hiroyama, M., Sanbe, A., Yamauchi, J., Tsujimoto, G., & Tanoue, A. (2007) · Journal of Endocrinology · doi:10.1677/joe.1.06864 · Cited by 36 · see citing works

The Discovery of Novel Vasopressin V1b Receptor Ligands for Pharmacological, Functional and Structural Investigations

Guillon, G., Derick, S., Peña, A., Cheng, L., Stoev, S., Seyer, R., Morgat, J. L., Barberis, C., Gal, C. S., Wagnon, J., et al. (2004) · Journal of Neuroendocrinology · doi:10.1111/j.0953-8194.2004.01163.x · Cited by 35 · see citing works

Oxytocin and vasopressin signalling and myometrial contraction

Arrowsmith, S. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.10.006 · Cited by 33 · see citing works

Role of the Oxytocin Receptor Expressed in the Rostral Medullary Raphe in Thermoregulation During Cold Conditions

Kasahara, Y., Tateishi, Y., Hiraoka, Y., Otsuka, A., Mizukami, H., Ozawa, K., Sato, K., Hidema, S., & Nishimori, K. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00180 · Cited by 32 · see citing works

Effects of vasopressin V1b receptor deficiency on adrenocorticotropin release from anterior pituitary cells in response to oxytocin stimulation

Nakamura, K., Fujiwara, Y., Mizutani, R., Sanbe, A., Miyauchi, N., Hiroyama, M., Yamauchi, J., Yamashita, T., Nakamura, S., Mori, T., et al. (2008) · Endocrinology · doi:10.1210/en.2007-1528 · Cited by 25 · 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

Oxytocin-induced phasic and tonic contractions are modulated by the contractile machinery rather than the quantity of oxytocin receptor

Kawamata, M., Tonomura, Y., Kimura, T., Sugimoto, Y., Yanagisawa, T., & Nishimori, K. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00492.2006 · Cited by 18 · see citing works

Functional Hierarchy of Uterotonics Required for Successful Parturition in Mice

Yoshida, M., Takayanagi, Y., Ichino-Yamashita, A., Sato, K. A., Sugimoto, Y., Kimura, T., & Nishimori, K. (2019) · Endocrinology · doi:10.1210/en.2019-00499 · Cited by 12 · see citing works

Infusion of oxytocin induces successful delivery in prostanoid FP-receptor-deficient mice

Kawamata, M., Yoshida, M., Sugimoto, Y., Kimura, T., Tonomura, Y., Takayanagi, Y., Yanagisawa, T., & Nishimori, K. (2008) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2007.10.012 · Cited by 11 · see citing works

Morphofunctional alterations of the nonpregnant murine uterus in response to intense and exhaustive exercise are not related to oxidative stress

Costa, A. E. A., da Silva, J. L. V., Simões, M. D. J., & Nouailhetas, V. L. A. (2014) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01342.2012 · Cited by 10 · see citing works

Vasopressin-to-oxytocin receptor crosstalk in the preoptic area underlying parental behaviors in male mice

Inada, K., Hagihara, M., Yaguchi, K., Irie, S., Inoue, Y., Inoue, T., & Miyamichi, K. (2025) · Nature Communications · doi:10.1038/s41467-025-66908-0 · Cited by 12 · see citing works

The differential coupling of oxytocin receptors to uterine contractions in murine estrous cycle

Kawamata, M., Tonomura, Y., Kimura, T., Yanagisawa, T., & Nishimori, K. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.07.019 · Cited by 9 · see citing works

Critical role of V1a vasopressin receptor in murine parturition†

Tsuchiya, H., Fujimura, S., Fujiwara, Y., & Koshimizu, T. (2019) · Biology of Reproduction · doi:10.1093/biolre/ioz220 · Cited by 7 · see citing works

Synthesis and pharmacological profile of non-peptide vasopressin antagonists

Galanski, M. E., Erker, T., Studenik, C. R., Kamyar, M.-R., Rawnduzi, P., Pabstova, M., & Lemmens‐Gruber, R. (2005) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2004.12.008 · Cited by 6 · see citing works

Cu(II) complexation does not affect oxytocin action on pregnant human myometrium in vitro

Kleszczewski, T., Modzelewska, B., Bal, W., Sipowicz, M. A., Kleszczewska, E., & Kostrzewska, A. (2015) · Reproductive Toxicology · doi:10.1016/j.reprotox.2015.11.004 · Cited by 5 · see citing works

New research models and novel signal analysis in studies on preterm labor: a key to progress?

Pierzyński, P., Oczeretko, E., Laudański, P., & LAUDAŃSKI, T. (2007) · BMC Pregnancy and Childbirth · doi:10.1186/1471-2393-7-s1-s6 · Cited by 4 · see citing works

Nonapeptide Evolution and the Regulation of Social Behaviour in Teleost Fish: From Molecules to Sociality

Kareklas, K., Sorigue, P., & Oliveira, R. F. (2025) · Masterclass in neuroendocrinology · doi:10.1007/978-3-031-80209-6_15 · Cited by 3 · see citing works

The Parental Brain in Humans

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.003.0008 · Cited by 2 · see citing works

Hormonal Control of Maternal Behavior in Nonhuman Mammals

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.003.0003 · Cited by 2 · see citing works

Parental Behavior

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.003.0002 · Cited by 1 · see citing works

Regional differences in oxytocin and vasopressin 1a receptor functionality in mouse embryonic brain development

Sommer, E., & Caldwell, H. K. (2025) · Neuroscience Letters · doi:10.1016/j.neulet.2025.138409 · Cited by 1 · see citing works

Introduction

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.003.0001 · Cited by 1 · see citing works

Central Neural Circuits Regulating Maternal Behavior in Nonhuman Mammals

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.003.0005 · Cited by 1 · see citing works

Alloparental Behavior and Paternal Behavior in Nonhuman Mammals

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.003.0007 · Cited by 1 · see citing works

Modulation of Peripheral Taste Function by Glial-like Taste Cells

Sinclair, M. S. (2012)

Evolutionary Perspectives on the Parental Brain

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.003.0011

Anxiety Reduction and Maternal Aggression in Postpartum Nonhuman Mammals

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.003.0006

Development of the Parental Brain in Nonhuman Mammals

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.003.0009

Development of the Parental Brain in Humans

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.003.0010

Brain Mechanisms Regulating Maternal Behavior in Nonhuman Mammals

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.003.0004

Preface

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.002.0006

Copyright Page

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.002.0003

Abbreviations Used for Major Brain Regions

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.002.0007

Dedication

Numan, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190848675.002.0004

Kamikihito ameliorates social recognition in oxytocin gene deficient mice and environmentally induced autism spectrum disorder model mice

Hidema, S., Nishimori, K., Otsuka, A., Horiai, M., Mizuno, K., Ono, T., Maejima, Y., & Shimomura, K. (2025) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2025.120263

New regulators in oxytocin and vasopressin release : role of the endolysosomal two-pore channels

Martucci, L. L. (2021) · theses.fr (ABES) · doi:10.70675/027d1ae2zd2ebz4677za019ze6ccd94cafe9

Vasopressin signaling and vasopressin-to-oxytocin receptor crosstalk in the regulation of parental caregiving behavior

Inada, K. (2026) · Neuroscience Research · doi:10.1016/j.neures.2026.105109

CME Test Questions Advances in cardiometabolic health

(2007) · Clinical cornerstone · doi:10.1016/s1098-3597(07)80013-5

Comparison of vasopressin and oxytocin receptors in the rat uterus and vascular tissue

Anouar, A., Clerget-Froidevaux, M.-S., Durroux, T., Barberis, C., & Germain, G. (1996) · European Journal of Pharmacology · doi:10.1016/0014-2999(96)00258-0 · Cited by 13 · see citing works

Receptors for and myometrial responses to oxytocin and vasopressin in preterm and term human pregnancy: Effects of the oxytocin antagonist atosiban

Bossmar, T., Åkerlund, M., Fantoni, G., Szamatowicz, J., Melin, P., & Maggi, M. (1994) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(94)90415-4 · Cited by 112 · see citing works

The role of oxytocin receptors and vasopressin V1a receptors in uterine contractions in rats: Implications for tocolytic therapy with oxytocin antagonists

Chan, W. Y., Wo, N. C., & Manning, M. (1996) · American Journal of Obstetrics and Gynecology · doi:10.1016/s0002-9378(96)70050-9 · Cited by 31 · see citing works

Receptor binding of oxytocin and vasopressin antagonists and inhibitory effects on isolated myometrium from preterm and term pregnant women

Åkerlund, M., Bossmar, T., Brouard, R., Kostrzewska, A., Laudanski, T., Lemancewicz, A., Gal, C. S., & Steinwall, M. (1999) · BJOG: An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.1999.tb08112.x · Cited by 123 · see citing works