Cited by 399Neuroendocrine regulation and behaviorNeuropeptides and Animal PhysiologyCardiovascular, Neuropeptides, and Oxidative Stress Research

The DOI matches its Crossref record.

Vasopressin and Oxytocin Receptors in the Central Nervous System

Tribollet, Eliane, Barberis, Claude·1996·Critical Reviews™ in Neurobiology

DOI 10.1615/critrevneurobiol.v10.i1.60

Open this paper in CoChat — free account

Abstract

This review concentrates on the pharmacological properties and the regional distribution of the arginine vasopressin (AVP) and oxytocin (OT) receptors that are present in the central nervous system. Of particular interest are the kinetics and the pharmacological profiles of these receptors that resemble those present at the periphery. However, their transduction mechanisms need to be further investigated. This should be rendered easier by molecular biology technology. The current knowledge of the anatomical distribution of AVP and OT receptors in the brain is reviewed. Also of great interest for double labeling studies will be the receptor antibodies, now being developed. The existence of additional receptors (AVP4-9) is examined, and aspects of the regulation of the receptors' expression in relation to the age, the species, and the hormonal status or following injury are also discussed.

Integrity signals

Registry

Crossref · 10.1615/critrevneurobiol.v10.i1.60

Cites

Statistics

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

Claims the paper makes

This paper’s full text isn’t openly available, 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?

Still being checked.

Sorted by citations

Items 101–200 of 398

Paternal behavior is associated with central neurohormone receptor binding patterns in meadow voles (Microtus pennsylvanicus).
Parker, K. J., Kinney, L. F., Phillips, K. M., & Lee, T. M. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.6.1341 · Cited by 82
Oxytocin receptor agonists enhance inhibitory synaptic transmission in the rat hippocampus by activating interneurons in stratum pyramidale
Zaninetti, M., & Raggenbass, M. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00290.x · Cited by 82
Oxytocin in the medial prefrontal cortex attenuates anxiety: Anatomical and receptor specificity and mechanism of action
Sabihi, S., Dong, S. M., Maurer, S., Goodpaster, C. M., & Leuner, B. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.06.024 · Cited by 87
OXYTOCIN RECEPTOR mRNA EXPRESSION IN RAT BRAIN: IMPLICATIONS FOR BEHAVIORAL INTEGRATION AND REPRODUCTIVE SUCCESS
Ostrowski, N. L. (1998) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(98)00070-5 · Cited by 81
The Vasopressin Receptors Colocalize with Vasopressin in the Magnocellular Neurons of the Rat Supraoptic Nucleus and Are Modulated by Water Balance
Hurbin, A., Orcel, H., Alonso, G., Moos, F., & Rabié, A. (2002) · Endocrinology · doi:10.1210/endo.143.2.8643 · Cited by 80
Oxytocin Maintains as Well as Initiates Female Sexual Behavior: Effects of a Highly Selective Oxytocin Antagonist
Pedersen, C. A., & Boccia, M. L. (2002) · Hormones and Behavior · doi:10.1006/hbeh.2001.1736 · Cited by 81
Role of oxytocin receptors in modulation of fear by social memory
Guzmán, Y. F., Tronson, N. C., Sato, K., Mesic, I., Guedea, A. L., Nishimori, K., & Radulović, J. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3356-6 · Cited by 86
Developmental effects of oxytocin on stress response: Single versus repeated exposure
KRAMER, K., CUSHING, B., & CARTER, C. (2003) · Physiology & Behavior · doi:10.1016/s0031-9384(03)00175-6 · Cited by 79
Oxytocin microinjected into the central amygdaloid nuclei exerts anti-aggressive effects in male rats
Calcagnoli, F., Stubbendorff, C., Meyer, N., de Boer, S. F., Althaus, M., & Koolhaas, J. M. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.11.012 · Cited by 77
Remodeling of astrocytes, a prerequisite for synapse turnover in the adult brain? Insights from the oxytocin system of the hypothalamus
Theodosis, D. T., Trailin, A., & Poulain, D. A. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00755.2005 · Cited by 77
Vasopressin in the forebrain of common marmosets (Callithrix jacchus): studies with in situ hybridization, immunocytochemistry and receptor autoradiography
Wang, Z., Toloczko, D., Young, L. J., Moody, K., Newman, J. D., & Insel, T. R. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00636-7 · Cited by 75
[1-deamino-4-cyclohexylalanine] arginine vasopressin: a potent and specific agonist for vasopressin V1b receptors
Derick, S., Cheng, L. L., Voirol, M. J., Stoev, S., Giacomini, M., Wo, N. C., Szeto, H. H., Ben Mimoun, M., Andres, M., Gaillard, R. C., et al. (2002) · Endocrinology · doi:10.1210/en.2002-220363 · Cited by 76
Distribution of vasopressin and oxytocin receptors in the rat spinal cord: sex-related differences and effect of castration in pudendal motor nuclei
Tribollet, E., Barberis, C., & Arsenijévic, Y. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00591-x · Cited by 76
New insights into the regulation of synaptic plasticity from an unexpected place: Hippocampal area CA2Preprint
Caruana, D. A., Alexander, G. M., & Dudek, S. M. (2012) · Learning & Memory · doi:10.1101/lm.025304.111 · Cited by 81
Arginine vasopressin, fever and temperature regulation
Pittman, Q. J., Chen, X., Mouihate, A., Hirasawa, M., & Martin, S. M. (1999) · Progress in brain research · doi:10.1016/s0079-6123(08)61582-4 · Cited by 75
DIFFERENTIAL EFFECTS OF VASOPRESSINERGIC AND OXYTOCINERGIC PRE‐AUTONOMIC NEURONS ON CIRCULATORY CONTROL: REFLEX MECHANISMS AND CHANGES DURING EXERCISE
Michelini, L. C. (2007) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2007.04589.x · Cited by 72
Stimulation of the hypothalamic paraventricular nucleus modulates cardiorespiratory responses via oxytocinergic innervation of neurons in pre-Bötzinger complex
Mack, S. O., Wu, M., Kc, P., & Haxhiu, M. A. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00522.2006 · Cited by 73
Arginine vasopressin stimulation of cerebral microvascular endothelial cell Na-K-Cl cotransporter activity is V1 receptor and [Ca] dependent
O’Donnell, M. E., Duong, V., Suvatne, J., Foroutan, S., & Johnson, D. M. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00001.2005 · Cited by 73
Oxytocin and social cognition in rhesus macaques: Implications for understanding and treating human psychopathology
Chang, S. W. C., & Platt, M. L. (2014) · Brain Research · doi:10.1016/j.brainres.2013.11.006 · Cited by 71
Identification of Residues Responsible for the Selective Binding of Peptide Antagonists and Agonists in the V2 Vasopressin Receptor
de la Cotte, N., Balestre, M., Phalipou, S., Hibert, M., Manning, M., Barberis, C., & Mouillac, B. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.45.29462 · Cited by 72
Neonatal manipulation of oxytocin affects expression of estrogen receptor alpha
Yamamoto, Y., Carter, C. S., & Cushing, B. S. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.08.065 · Cited by 70
The S cience of Interpersonal Trust
Borum, R. (2010) · Digital Commons - University of South Florida (University of South Florida) · Cited by 69
Vasopressin and pair-bond formation: genes to brain to behavior.
Nair, H. P., & Young, L. J. (2006) · Physiology · doi:10.1152/physiol.00049.2005 · Cited by 68
Genomic and membrane actions of progesterone: implications for reproductive physiology and behavior
Schumacher, M., Coirini, H., Robert, F., Guennoun, R., & El‐Etr, M. (1999) · Behavioural Brain Research · doi:10.1016/s0166-4328(99)00081-9 · Cited by 68
Binding of the Non-Peptide Vasopressin V1a Receptor Antagonist SR-49059 in the Rat Brain: An in vitro and in vivo Autoradiographic Study
Tribollet, E., Raufaste, D., Maffrand, J., & Gal, C. S. (1999) · Neuroendocrinology · doi:10.1159/000054409 · Cited by 66
Vasopressin, Central Autonomic Control and Blood Pressure Regulation
Lozić, M., Šarenac, O., Murphy, D., & Japundžić‐Žigon, N. (2018) · Current Hypertension Reports · doi:10.1007/s11906-018-0811-0 · Cited by 67
Neuropeptidergic regulation of pair-bonding and stress buffering: Lessons from voles
Gobrogge, K. L., & Wang, Z. (2015) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.08.010 · Cited by 64
Long-term effects on hypothalamic neuropeptides after developmental exposure to chlorpyrifos in mice
Tait, S., Ricceri, L., Venerosi, A., Maranghi, F., Mantovani, A., & Calamandrei, G. (2009) · Environmental Health Perspectives · doi:10.1289/ehp.11696 · Cited by 64
Intracellular calcium signalling in magnocellular neurones of the rat supraoptic nucleus: understanding the autoregulatory mechanisms
Dayanithi, G., Sabatier, N., & Widmer, H. (2000) · Experimental Physiology · doi:10.1111/j.1469-445x.2000.tb00010.x · Cited by 62
Central expression of c-Fos in neonatal male and female prairie voles in response to treatment with oxytocin
Cushing, B. S., Yamamoto, Y., Hoffman, G. E., & Carter, C. S. (2003) · Developmental Brain Research · doi:10.1016/s0165-3806(03)00105-6 · Cited by 62
Roles of the Oxytocin Receptor (OXTR) in Human Diseases
Pierzynowska, K., Gaffke, L., Żabińska, M., Cyske, Z., Rintz, E., Wiśniewska, K., Podlacha, M., & Węgrzyn, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043887 · Cited by 64
Mapping Peptide-binding Domains of the Human V1a Vasopressin Receptor with a Photoactivatable Linear Peptide Antagonist
Phalipou, S., de la Cotte, N., Carnazzi, E., Seyer, R., Mahé, E., Jard, S., Barberis, C., & Mouillac, B. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.42.26536 · Cited by 60
Effects of a Single Administration of Oxytocin or Vasopressin and Their Interactions with Two Selective Receptor Antagonists on Memory Storage in Mice
Boccia, M. M., Kopf, S. R., & Baratti, C. M. (1998) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1997.3817 · Cited by 59
Activation of multiple intracellular transduction signals by vasopressin in vasopressin‐sensitive neurones of the rat supraoptic nucleus
Sabatier, N., Richard, P., & Dayanithi, G. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.699ba.x · Cited by 57
Sex Differences in the Embryonic Development of the Central Oxytocin System in Mice
Tamborski, S., Mintz, E. M., & Caldwell, H. K. (2016) · Journal of Neuroendocrinology · doi:10.1111/jne.12364 · Cited by 55
V1a‐ and V2‐type vasopressin receptors mediate vasopressin‐induced Ca2+ responses in isolated rat supraoptic neurones
Gouzènes, L., Sabatier, N., Richard, P., Moos, F., & Dayanithi, G. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.0771s.x · Cited by 55
Abolition of Hypertension-Induced End-Organ Damage by Androgen Receptor Blockade in Transgenic Rats Harboring the Mouse Ren-2 Gene
Baltatu, O. C., Cayla, C., Iliescu, R., Andreev, D., Jordan, C. L., & Bäder, M. (2002) · Journal of the American Society of Nephrology · doi:10.1097/01.asn.0000033327.65390.ca · Cited by 55
Effects of α‐Melanocyte‐Stimulating Hormone on Magnocellular Oxytocin Neurones and their Activation at Intromission in Male Rats
Caquineau, C., Leng, G., Guan, X.-M., Jiang, M., der Ploeg, L. H. T. V., & Douglas, A. J. (2006) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2006.01465.x · Cited by 58
α‐Melanocyte‐Stimulating Hormone and Oxytocin: A Peptide Signalling Cascade in the Hypothalamus
Sabatier, N. (2006) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2006.01464.x · Cited by 54
Neuropeptides involved in the pathophysiology of schizophrenia and major depression
de Wied, D., & Sigling, H. O. (2002) · Neurotoxicity Research · doi:10.1080/10298420290031432 · Cited by 52
Control of the Estradiol-Induced Prolactin Surge by the Suprachiasmatic Nucleus
Palm, I. F., van der Beek, E. M., Swarts, H. J. M., van der Vliet, J., Wiegant, V. M., Buijs, R. M., & Kalsbeek, A. (2001) · Endocrinology · doi:10.1210/endo.142.6.8219 · Cited by 53
Localization of leptin receptor immunoreactivity in the lean and obese Zucker rat brain
Yarnell, D. O., Knight, D. S., Hamilton, K. A., Tulp, O. L., & Tso, P. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01388-7 · Cited by 53
Imaging, Behavior and Endocrine Analysis of “Jealousy” in a Monogamous Primate
Maninger, N., Mendoza, S. P., Williams, D. R., Mason, W. A., Cherry, S. R., Rowland, D. J., Schaefer, T., & Bales, K. L. (2017) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2017.00119 · Cited by 51
Complementary Role of Oxytocin and Vasopressin in Cardiovascular Regulation
Szczepanska‐Sadowska, E. K., Wsół, A., Cudnoch‐Jędrzejewska, A., & Żera, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111465 · Cited by 55
Apelin‐13 and APJ in paraventricular nucleus contribute to hypertension via sympathetic activation and vasopressin release in spontaneously hypertensive rats
Zhang, F., Sun, H., Xiong, X., Chen, Q., Li, Y., Kang, Y., Wang, J., Gao, X., & Zhu, G. (2014) · Acta Physiologica · doi:10.1111/apha.12342 · Cited by 51
Neuropeptides as neuroprotective agents: oxytocin a forefront developmental player in the mammalian brain
Vargas-Martínez, F., Uvnäs-Moberg, K., Petersson, M., Olausson, H. A., & Jiménez-Estrada, I. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.10.001 · Cited by 51
Oxytocin in the NTS
Michelini, L. C. (2001) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2001.tb03678.x · Cited by 51
Vasopressin Receptors
Jard, S. (1998) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4871-3_1 · Cited by 49
Vasopressin Preferentially Depresses Excitatory Over Inhibitory Synaptic Transmission in the Rat Supraoptic Nucleus In Vitro
Kombian, Mouginot, Hirasawa, & Pittman, Q. J. (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00462.x · Cited by 49
The importance of mother–infant communication for social bond formation in mammals
Okabe, S., Nagasawa, M., Mogi, K., & Kikusui, T. (2012) · Animal Science Journal · doi:10.1111/j.1740-0929.2012.01014.x · Cited by 49
Short- and long-term consequences of different early environmental conditions on central immunoreactive oxytocin and arginine vasopressin levels in male rats
Oreland, S., Gustafsson-Ericson, L., & Nylander, I. (2010) · Neuropeptides · doi:10.1016/j.npep.2010.06.001 · Cited by 48
Vasopressin and oxytocin excite MCH neurons, but not other lateral hypothalamic GABA neurons
Yao, Y., Fu, L., Zhang, X., & van den Pol, A. N. (2012) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00452.2011 · Cited by 48
Vasopressin in vascular regulation and water homeostasis in the brain.
Koźniewska, E., & Romaniuk, K. (2008) · PubMed · Cited by 48
Vasopressin receptors. A historical survey.
Jard, S. (1998) · PubMed · Cited by 48
Effects of neonatal oxytocin manipulations on male reproductive potential in prairie voles
BALES, K., ABDELNABI, M., CUSHING, B., OTTINGER, M., & CARTER, C. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.02.016 · Cited by 47
Variations in the expression of vasotocin and isotocin receptor genes in the gilthead sea bream Sparus aurata during different osmotic challenges
Martos-Sitcha, J. A., Fuentes, J., Mancera, J. M., & Martı́nez-Rodrı́guez, G. (2013) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2013.11.026 · Cited by 47
Coping Style of Pigs Is Associated With Different Behavioral, Neurobiological and Immune Responses to Stressful Challenges
Kanitz, E., Tuchscherer, M., Otten, W., Tuchscherer, A., Zebunke, M., & Puppe, B. (2019) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00173 · Cited by 49
Challenges to the Pair Bond: Neural and Hormonal Effects of Separation and Reunion in a Monogamous Primate
Hinde, K., Muth, C., Maninger, N., Ragen, B., Larke, R. H., Jarcho, M. R., Mendoza, S. P., Mason, W. A., Ferrer, E. E., Cherry, S. R., et al. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00221 · Cited by 46
The Brain Oxytocin Receptor(s?)
Verbalis, J. G. (1999) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1999.0178 · Cited by 47
Gene and cDNA cloning and characterization of the mouse V3/V1b pituitary vasopressin receptor
Ventura, M., René, P., de Keyzer, Y., BERTAGNA, X. Y., & Clauser, É. (1999) · Journal of Molecular Endocrinology · doi:10.1677/jme.0.0220251 · Cited by 45
The Septal Region and Social Behavior
Sheehan, T. P., & Numan, M. (2000) · Springer eBooks · doi:10.1007/978-1-4612-1302-4_8 · Cited by 46
Reduced binding of oxytocin in the rat brain during aging
Arsenijevic, Y., Dreifuss, J. J., Vallet, P., Marguerat, A., & Tribollet, E. (1995) · Brain Research · doi:10.1016/0006-8993(95)01020-v · Cited by 36
The Oxytocin‐induced Inward Current in Vagal Neurons of the Rat is Mediated by G Protein Activation but not by an Increase in the lntracellular Calcium Concentration
Alberi, S., Dreifuss, J. J., & Raggenbass, M. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01690.x · Cited by 44
Exposure to chronic isolation modulates receptors mRNAs for oxytocin and vasopressin in the hypothalamus and heart
Pournajafi‐Nazarloo, H., Kenkel, W. M., Mohsenpour, S. R., Sanzenbacher, L., Saadat, H., Partoo, L., Yee, J. R., Azizi, F., & Carter, C. S. (2013) · Peptides · doi:10.1016/j.peptides.2013.02.007 · Cited by 43
The neurobiology of collective action
Zak, P. J., & Barraza, J. A. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00211 · Cited by 46
Oxytocin, but not vassopressin, modulates nociceptive responses in dorsal horn neurons
Rojas‐Piloni, G., Mejía-Rodríguez, R., Martı́nez-Lorenzana, G., & Condés‐Lara, M. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.03.076 · Cited by 43
Neural Regulation of Paternal Behavior in Mammals: Sensory, Neuroendocrine, and Experiential Influences on the Paternal Brain
Horrell, N. D., Hickmott, P. W., & Wendy Saltzman, A. (2018) · Current topics in behavioral neurosciences · doi:10.1007/7854_2018_55 · Cited by 45
Oxytocin actions within the supraoptic and paraventricular nuclei: differential effects on peripheral and intranuclear vasopressin release
Neumann, I. D., Torner, L., Toschi, N., & Veenema, A. H. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00763.2005 · Cited by 43
Attenuated Stress Response to Acute Lipopolysaccharide Challenge and Ethanol Administration in Vasopressin V1b Receptor Knockout Mice
Lolait, S. J., Stewart, L. Q., Roper, J. A., Harrison, G., Jessop, D., Young, W. S., & O’Carroll, A. (2007) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2007.01560.x · Cited by 43
The role of the arginine vasopressin Avp1b receptor in the acute neuroendocrine action of antidepressants
Stewart, L. Q., Roper, J. A., Young, W. S., O’Carroll, A., & Lolait, S. J. (2008) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2007.12.009 · Cited by 42
V 2 Receptor–Mediated Autocrine Role of Somatodendritic Release of AVP in Rat Vasopressin Neurons Under Hypo-Osmotic Conditions
Sato-Numata, K., Numata, T., Saito, T., Ueta, Y., & Okada, Y. (2011) · Science Signaling · doi:10.1126/scisignal.2001279 · Cited by 42
The neurobiological link between compassion and love
Esch, T., & Stefano, G. B. (2011) · Medical Science Monitor · doi:10.12659/msm.881441 · Cited by 44
Comparative and developmental perspectives on oxytocin and vasopressin.
Bales, K. L. (2013) · American Psychological Association eBooks · doi:10.1037/14250-002 · Cited by 40
Central oxytocin modulation of acute stress-induced cardiovascular responses after myocardial infarction in the rat
Wsół, A., Cudnoch‐Jędrzejewska, A., Szczepanska‐Sadowska, E. K., Kowalewski, S., & Dobruch, J. T. (2009) · Stress · doi:10.3109/10253890802687688 · Cited by 40
Neuropeptides as mediators of the early-life impact on the brain; implications for alcohol use disorders
Nylander, I., & Roman, E. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00077 · Cited by 40
Central release of oxytocin and the ventromedial hypothalamus
Sabatier, N., Rowe, I. C. M., & Leng, G. (2007) · Biochemical Society Transactions · doi:10.1042/bst0351247 · Cited by 40
Endocrine‐Autonomic Linkages
Sladek, C. D., Michelini, L. C., Stachenfeld, N. S., Stern, J. E., & Urban, J. H. (2015) · Comprehensive physiology · doi:10.1002/cphy.c140028 · Cited by 51
Heterotrimeric G Proteins of the Gq/11 Family Are Crucial for the Induction of Maternal Behavior in Mice
Wettschureck, N., Moers, A., Hamalainen, T., Lemberger, T., Schütz, G., & Offermanns, S. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.18.8048-8054.2004 · Cited by 46
Involvement of Central Cholinergic Mechanisms in the Effects of Oxytocin and an Oxytocin Receptor Antagonist on Retention Performance in Mice
Boccia, M. M., & Baratti, C. M. (2000) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1999.3954 · Cited by 39
Oxytocin Signaling Pathway: From Cell Biology to Clinical Implications
Iovino, M., Messana, T., Tortora, A., Giusti, C., Lisco, G., Giagulli, V. A., Guastamacchia, E., Pergola, G. D., & Triggiani, V. (2020) · Endocrine Metabolic & Immune Disorders - Drug Targets · doi:10.2174/1871530320666200520093730 · Cited by 39
Presence of functional vasopressin receptors in spinal ventral horn neurons of young rats: a morphological and electrophysiological study
Liu, X., Tribollet, E., Ogier, R., Barberis, C., & Raggenbass, M. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02625.x · Cited by 38
Physiological Roles of Aquaporins in the Choroid Plexus
Boassa, D., & Yool, A. J. (2005) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(05)67005-6 · Cited by 37
Association between a vasopressin receptor AVPR1A promoter region microsatellite and eating behavior measured by a self‐report questionnaire (Eating Attitudes Test) in a family‐based study of a nonclinical population
Bachner‐Melman, R., Zohar, A. H., Elizur, Y., Nemanov, L., Gritsenko, I., Konis, D., & Ebstein, R. P. (2004) · International Journal of Eating Disorders · doi:10.1002/eat.20049 · Cited by 38
Chapter 1.4 Vasopressin binding sites in the central nervous system: Distribution and regulation
Tribollet, E., Arsenijévic, Y., & Barberis, C. (1999) · Progress in brain research · doi:10.1016/s0079-6123(08)61561-7 · Cited by 37
The organizational effects of oxytocin on the central expression of estrogen receptor α and oxytocin in adulthood
Kramer, K. M., Yoshida, S., Papademetriou, E., & Cushing, B. S. (2007) · BMC Neuroscience · doi:10.1186/1471-2202-8-71 · Cited by 36
New Topics in Vasopressin Receptors and Approach to Novel Drugs: Vasopressin and Pain Perception
Koshimizu, T., & Tsujimoto, G. (2009) · Journal of Pharmacological Sciences · doi:10.1254/jphs.08r18fm · Cited by 36
Intracellular Calcium Increase and Somatodendritic Vasopressin Release by Vasopressin Receptor Agonists in the Rat Supraoptic Nucleus: Involvement of Multiple Intracellular Transduction Signals
Sabatier, N., Shibuya, I., & Dayanithi, G. (2004) · Journal of Neuroendocrinology · doi:10.1111/j.0953-8194.2004.01155.x · Cited by 36
Central Oxytocin, Vasopressin, and Corticotropin-Releasing Factor Receptor Densities in the Basal Forebrain Predict Isolation Potentiated Startle in Rats
Nair, H. P., Gutman, A. R., Davis, M., & Young, L. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2524-05.2005 · Cited by 36
Presynaptic actions of endocannabinoids mediate α-MSH-induced inhibition of oxytocin cells
Sabatier, N., & Leng, G. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00667.2005 · Cited by 52
Oxytocin And Individual Variation in Parental Care in Prairie Voles
Olazábal, D. E., & Young, L. J. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-374285-8.00021-4 · Cited by 35
Positive Social Interactions in a Lifespan Perspective with a Focus on Opioidergic and Oxytocinergic Systems: Implications for Neuroprotection
Colonnello, V., Petrocchi, N., Farinelli, M., & Ottaviani, C. (2016) · Current Neuropharmacology · doi:10.2174/1570159x14666160816120209 · Cited by 36
Oxytocin Increases Phasic and Tonic GABAergic Transmission in CA1 Region of Mouse Hippocampus
Maniezzi, C., Talpo, F., Spaiardi, P., Toselli, M., & Biella, G. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00178 · Cited by 35
Disulfide bond cleavages observed in SORI‐CID of three nonapeptides complexed with divalent transition‐metal cations
Mihalca, R., van der Burgt, Y. E. M., Heck, A. J. R., & Heeren, R. M. A. (2007) · Journal of Mass Spectrometry · doi:10.1002/jms.1175 · Cited by 35
RhoA inhibition is a key step in pituicyte stellation induced by A1‐type adenosine receptor activation
Rosso, L., Maison-Peteri, B., Vouret‐Craviari, V., Deroanne, C., Troadec, J., Thirion, S., Obberghen‐Schilling, E. V., & Mienville, J. (2002) · Glia · doi:10.1002/glia.10072 · Cited by 35
Magnocellular vasopressin system in ontogenesis: Development and regulation
Ugrumov, M. V. (2002) · Microscopy Research and Technique · doi:10.1002/jemt.10021 · Cited by 35
The Role of Oxytocin in Parenting and as Augmentative Pharmacotherapy: Critical Issues and Bold Conjectures
van IJzendoorn, M. H., & Bakermans‐Kranenburg, M. J. (2015) · Journal of Neuroendocrinology · doi:10.1111/jne.12355 · Cited by 33
Vasopressin and alcohol: a multifaceted relationship
Harper, K. M., Knapp, D. J., Criswell, H. E., & Breese, G. R. (2018) · Psychopharmacology · doi:10.1007/s00213-018-5099-x · Cited by 35
Characterisation of the biological effects of neurohypophysial peptides on seminiferous tubules
Harris, G., & Nicholson, H. (1998) · Journal of Endocrinology · doi:10.1677/joe.0.1560035 · Cited by 33
Analysis of interactions responsible for vasopressin binding to human neurohypophyseal hormone receptors—molecular dynamics study of the activated receptor–vasopressin–Gα systems
Ślusarz, M. J., Giełdoń, A., Ślusarz, R., & Ciarkowski, J. (2005) · Journal of Peptide Science · doi:10.1002/psc.714 · Cited by 32
Social experience and social context alter the behavioral response to centrally administered oxytocin in female Syrian hamsters
Harmon, A. C., Moore, T. O., Huhman, K. L., & Albers, H. E. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00523-1 · Cited by 30

Authors: Tribollet, E., & Barberis, C.
Affiliations: University of Geneva (CH)
Inserm (FR)
Venue: Critical Reviews™ in Neurobiology
Publisher: Begell House
Published: 1996
Volume: 10
Issue: 1
Pages: 119-154
ISSN: 0892-0915 (ISSN-L)
DOI: 10.1615/critrevneurobiol.v10.i1.60
OpenAlex: W1975731777
Cited by: 399
References: 0
Citations by year: 2026: 2 · 2025: 3 · 2024: 4 · 2023: 7 · 2022: 6 · 2021: 7 · 2020: 7 · 2019: 7 · 2018: 5 · 2017: 11 · 2016: 9 · 2015: 15 · 2014: 10 · 2013: 19 · 2012: 13
FWCI: 37.93
Type: journal article
Language: en
Open access: closed
Locations: Critical Reviews in Neurobiology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Health Sciences › Medicine › Surgery › Cardiovascular, Neuropeptides, and Oxidative Stress Research
Keywords: arginine vasopressin receptor, oxytocin receptor, central nervous system, receptor pharmacology, receptor kinetics, signal transduction, receptor antibodies, receptor regulation, age differences, species differences, hormonal status, brain injury
MeSH terms: Amino Acid Sequence, Animals, Central Nervous System, Humans, Molecular Sequence Data, Receptors, Vasopressin, Receptors, Oxytocin

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

Vasopressin and Oxytocin Receptors in the Central Nervous System

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks