Relevant bibliographies by topics / Oxytocin and Vasopressin

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Academic literature on the topic 'Oxytocin and Vasopressin'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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Journal articles on the topic "Oxytocin and Vasopressin"

1

Elands, J., C. Barberis, and S. Jard. "[3H]-[Thr4,Gly7]OT: a highly selective ligand for central and peripheral OT receptors." American Journal of Physiology-Endocrinology and Metabolism 254, no. 1 (1988): E31—E38. http://dx.doi.org/10.1152/ajpendo.1988.254.1.e31.

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Oxytocin receptors in rat hippocampal synaptic plasma membranes were compared with mammary gland and uterine oxytocin receptors. For this purpose, a highly specific oxytocic agonist [Thr4,Gly7]oxytocin was tritiated. We demonstrated that this ligand labels oxytocin receptors selectively. Scatchard analyses revealed a high affinity for all the oxytocin receptors investigated, with equilibrium dissociation constants between 1.0 and 2.0 nM. Binding appeared to take place at a single population of receptor sites. Competition experiments confirmed the high affinity of arginine vasopressin for hippo
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Möller, Carolina, та Frank Marí. "A vasopressin/oxytocin-related conopeptide with γ-carboxyglutamate at position 8". Biochemical Journal 404, № 3 (2007): 413–19. http://dx.doi.org/10.1042/bj20061480.

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Vasopressins and oxytocins are homologous, ubiquitous and multifunctional peptides present in animals. Conopressins are vasopressin/oxytocin-related peptides that have been found in the venom of cone snails, a genus of marine predatory molluscs that envenom their prey with a complex mixture of neuroactive peptides. In the present paper, we report the purification and characterization of a unique conopressin isolated from the venom of Conus villepinii, a vermivorous cone snail species from the western Atlantic Ocean. This novel peptide, designated γ-conopressin-vil, has the sequence CLIQDCPγG*
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Bankowski, Krzysztof, Bernard Lammek, Marian Kruszynski, Maurice Manning, Janny Seto, and Wilbur H. Sawyer. "2-O-methyl and 2-O-ethyl-tyrosine derivatives of [8-arginine]vasopressin analogs: Highly specific antidiuretic agonists." Collection of Czechoslovak Chemical Communications 53, no. 11 (1988): 2617–26. http://dx.doi.org/10.1135/cccc19882617.

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The solid phase synthesis of seven 2-O-methyl- and 2-O-ethyl-tyrosine substituted analogs of [8-arginine]vasopressin (AVP) with enhanced antidiuretic agonistic specificity is reported. These peptides are: [2-O-ethyltyrosine, 8-arginine]vasopressin (I), [2-O-methyltyrosine, 8-D-arginine]vasopressin (II), [2-O-ethyltyrosine, 8-D-arginine]vasopressin (III), [2-O-methyltyrosine, 4-valine, 8-arginine]vasopressin (IV), [2-O-ethyltyrosine, 4-valine, 8-arginine]vasopressin (V), [2-O-methyltyrosine, 4-valine, 8-D-arginine]vasopressin (VI), [2-O-ethyltyrosine, 4-valine, 8-D-arginine]vasopressin (VII). A
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GAINER, HAROLD, and SUSAN WRAY. "Oxytocin and Vasopressin." Annals of the New York Academy of Sciences 652, no. 1 (1992): 14–28. http://dx.doi.org/10.1111/j.1749-6632.1992.tb34342.x.

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Han, J. S., Y. Maeda, and M. A. Knepper. "Dual actions of vasopressin and oxytocin in regulation of water permeability in terminal collecting duct." American Journal of Physiology-Renal Physiology 265, no. 1 (1993): F26—F34. http://dx.doi.org/10.1152/ajprenal.1993.265.1.f26.

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We conducted studies in isolated perfused terminal inner medullary collecting ducts (IMCD) from rats to investigate the roles of oxytocin and vasopressin in the regulation of osmotic water permeability. Vasopressin and oxytocin were found to have both stimulatory effects (at 0.1 nM) and inhibitory effects (at 10 nM) on osmotic water permeability. Measurements of adenosine 3',5'-cyclic monophosphate (cAMP) production demonstrated that both vasopressin and oxytocin increase cAMP production. Both the selective oxytocin-receptor agonist [Thr4,Gly7]oxytocin (10 nM) and the selective V1b agonist [de
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Kasting, Norman W. "Simultaneous and independent release of vasopressin and oxytocin in the rat." Canadian Journal of Physiology and Pharmacology 66, no. 1 (1988): 22–26. http://dx.doi.org/10.1139/y88-004.

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The relative dependence or independence of the secretion of the neurohypophysial hormones, arginine vasopressin and oxytocin, was investigated using a wide variety of stimuli reported to cause the secretion of one or the other hormone. Differences in species, animal preparations, sampling techniques, assays, and other factors make comparison of many previous studies difficult. The aim of this study was to overcome these problems by using the same methodology, animal species, and assays to compare vasopressin and oxytocin release. To further strengthen the analysis, determinations of vasopressi
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Erickson, Elise N., C. Sue Carter, and Cathy L. Emeis. "Oxytocin, Vasopressin and Prolactin in New Breastfeeding Mothers: Relationship to Clinical Characteristics and Infant Weight Loss." Journal of Human Lactation 36, no. 1 (2019): 136–45. http://dx.doi.org/10.1177/0890334419838225.

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Background: Maternal milk production requires the neuropeptide oxytocin. Individual variation in oxytocin function is a compelling target for understanding low milk production, a leading cause of breastfeeding attrition. Complicating the understanding of oxytocin pathways is that vasopressin may interact with oxytocin receptors, yet little is known about the role of vasopressin in lactation. Research aims: The aims of this study were (1) to describe maternal plasma oxytocin, vasopressin, and prolactin patterns during breastfeeding following low-risk spontaneous labor and birth in healthy first
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Procházka, Zdenko, and Jiřina Slaninová. "The 1- and 2-Naphthylalanine Analogs of Oxytocin and Vasopressin." Collection of Czechoslovak Chemical Communications 60, no. 12 (1995): 2170–77. http://dx.doi.org/10.1135/cccc19952170.

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Solid phase technique on p-methylbenzhydrylamine resin was used for the synthesis of four analogs of oxytocin and four analogs of vasopressin with the non-coded amino acids L- or D- and 1- or 2-naphthylalanine and D-homoarginine. [L-1-Nal2]oxytocin, [D-1-Nal2]oxytocin, [L-2-Nal2]oxytocin, [D-2-Nal2]oxytocin, [L-1-Nal2, D-Har8]vasopressin, [D-1-Nal2, D-Har8]vasopressin, [L-2-Nal2, D-Har8]vasopressin and [D-2-Nal2, D-Har8]vasopressin were synthesized. All eight analogs were found to be uterotonic inhibitors in vitro and in vivo. Analogs with 2-naphthylalanine are stronger inhibitors, particularl
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Stoeckel, M. E., M. J. Freund-Mercier, J. M. Palacios, Ph Richard, and A. Porte. "Autoradiographic localization of binding sites for oxytocin and vasopressin in the rat kidney." Journal of Endocrinology 113, no. 2 (1987): 179—NP. http://dx.doi.org/10.1677/joe.0.1130179.

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ABSTRACT The distribution of [3H]vasopressin- and [3H]oxytocin-binding sites was examined, using an autoradiographical technique, in the kidney of Long–Evans and Brattleboro rats. Two types of binding sites with affinities in the nanomolar range were detected: one, located on glomeruli, bound both vasopressin and oxytocin; the other, on collecting ducts, bound vasopressin selectively. In the presence of 10 μmol oxytocin/1, [3H]vasopressin labelling was abolished in glomeruli, but only reduced in collecting ducts; [3H]oxytocin labelling was completely abolished by 10 μmol vasopressin/1. These o
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Zingg, Hans H. "Vasopressin and oxytocin receptors." Baillière's Clinical Endocrinology and Metabolism 10, no. 1 (1996): 75–96. http://dx.doi.org/10.1016/s0950-351x(96)80314-4.

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Dissertations / Theses on the topic "Oxytocin and Vasopressin"

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Lefebvre, Diana Lynn. "Extrahypothalamic vasopressin and oxytocin gene expression." Thesis, McGill University, 1992. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=41031.

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Considerable evidence supports a role for vasopressin (VP) as a local regulator of steroidogenesis in rat testes. I show that rat testes contain three distinct VP gene-related transcripts differing in size from the hypothalamic VP mRNA. Two of these transcripts contain exons B and C, but not the exon that encodes the nonapeptide VP. Hence, these transcripts are incapable of generating testicular irVP. The third transcript possesses exon A-like sequences, probably originating from expression of a VP-related gene. This transcript may encode the VP-like peptide that has been detected in testicula
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MacLean, Evan L., Laurence R. Gesquiere, Margaret E. Gruen, Barbara L. Sherman, W. Lance Martin, and C. Sue Carter. "Endogenous Oxytocin, Vasopressin, and Aggression in Domestic Dogs." FRONTIERS MEDIA SA, 2017. http://hdl.handle.net/10150/625986.

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Aggressive behavior in dogs poses public health and animal welfare concerns, however the biological mechanisms regulating dog aggression are not well understood. We investigated the relationships between endogenous plasma oxytocin (OT) and vasopressin (AVP)-neuropeptides that have been linked to affiliative and aggressive behavior in other mammalian species-and aggression in domestic dogs. We first validated enzyme-linked immunosorbent assays (ELISAs) for the measurement of free (unbound) and total (free + bound) OT and AVP in dog plasma. In Experiment 1 we evaluated behavioral and neuroendocr
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McCurdy, Richard Douglas. "Postnatal growth of the porcine vasopressin/oxytocin-containing nucleus." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ33252.pdf.

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Epton, Matthew James. "Somatic cross-over mutations between vasopressin and oxytocin genes." Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365287.

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Gouin, Jean-Philippe. "MARITAL QUALITY AND PLASMA LEVELS OF OXYTOCIN AND VASOPRESSIN." The Ohio State University, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=osu1236184248.

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Haley, Gwendolen E. "Contribution of neurokinin 3 receptor signaling to systemic vasopressin and oxytocin release." Laramie, Wyo. : University of Wyoming, 2008. http://proquest.umi.com/pqdweb?did=1594497031&sid=1&Fmt=2&clientId=18949&RQT=309&VName=PQD.

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La-Borde, Penelope Jane. "Activation of the vasopressin and oxytocin receptor family : structural and mechanistic insights." Thesis, University of Birmingham, 2017. http://etheses.bham.ac.uk//id/eprint/7639/.

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G-protein-coupled receptors (GPCRs) are major pharmaceutical drug targets due to their crucial role in cell signalling. The neurohypophysial peptide hormones [Arg⁸] vasopressin (AVP) and oxytocin (OT) signal through a subfamily of GPCRs, comprising the AVP receptors (V₁a R, V₁bR and V₂R) and the OT receptor (OTR). The aim of this work was to understand the molecular basis of receptor activation by defining exact contacts between agonist and receptor. Molecular modelling suggested that two conserved negatively-charged residues may be important for agonist binding and receptor activation. Intera
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Aulino, Elizabeth Ann Morningstar. "The Impact of the Oxytocin and Vasopressin Systems on Sex-Specific Brain Development." Kent State University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=kent161965288538867.

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Karpenko, Iuliia. "Conception, synthesis and evaluation of fluorescent probes and PET radioligands for the oxytocin and vasopressin receptors." Thesis, Strasbourg, 2014. http://www.theses.fr/2014STRAF045/document.

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Les récepteurs de l’ocytocine (OTR) et de la vasopressine (AVPR) sont connus pour être impliqués dans la modulation d’effets centraux complexes. Récemment l’OTR a été proposé comme une cible thérapeutique pour le traitement des troubles du spectre autistique (TSA).Afin de mieux comprendre le rôle de l’OTR et des AVPR dans les TSA, d’éclaircir des nouveaux traits de sa pharmacologie et d’établir des méthodes du criblage sur les récepteurs sauvages, nous avons développé des traceurs pour la tomographie par émission des positons ainsi que des sondes fluorescentes pour la famille OT/AVP des RCPG.
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Linfoot, Ian. "Naturally occurring variations in defensive burying behavior are associated with differences in central neuropeptide expression in the male rat." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/793.

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The shock prod defensive burying test has proven incredibly reliable and instrumental in determining the underpinnings of normal anxiety in rodents. Largely ignored in tests of defensive burying, however, is the capacity for individual animals to display marked variations in active and passive coping behaviors. To unmask the neurobiological correlates of this behavioral differentiation, rats were exposed to a mousetrap that was remotely triggered upon approach to remove the quality of pain. This design invited striking variations in defensive burying behavior levels, in which some rats eith
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Books on the topic "Oxytocin and Vasopressin"

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Zingg, Hans H., Charles W. Bourque, and Daniel G. Bichet, eds. Vasopressin and Oxytocin. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4871-3.

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Neumann, Inga D. Advances in vasopressin and oxytocin: From genes to behaviour to disease. Elsevier, 2008.

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Advances in vasopressin and oxytocin: From genes to behaviour to disease. Elsevier, 2008.

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Edinburgh), World Congress on Neurohypophysial Hormones (1999. Oxytocin and vasopressin: From molecules to function. Published for the Physiological Society by Cambridge University Press, 2000.

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Dominique, Poulain, Oliet, Stéphane H. R., 1965-, and Theodosis Dionysia, eds. Vasopressin and oxytocin: From genes to clinical applications. Elsevier, 2002.

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Choleris, Elena, Donald W. Pfaff, and Martin Kavaliers, eds. Oxytocin, Vasopressin and Related Peptides in the Regulation of Behavior. Cambridge University Press, 2013. http://dx.doi.org/10.1017/cbo9781139017855.

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1936-, Saitō Toshikazu, Kurokawa Kiyoshi, and Yoshida Shō, eds. Neurohypophysis: Recent progress of vasopressin and oxytocin research : proceedings of the 1st Joint World Congress of Neurohypophysis and Vasopressin, Nasu, Tochigi, Japan, 16-21 July 1995. Elsevier, 1995.

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Hu, Shuang-Bao. Corticothropin-releasing factor-41 (CRF-41), arginne vasopressin (AVP), and oxytocin regulation in hypothalamic cellsin culture. Brunel University, 1992.

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Shō, Yoshida, and Share Leonard, eds. Recent progress in posterior pituitary hormones 1988: Proceedings of the Satellite Symposium on Posterior Pituitary Hormones, Hakone, Japan, 14-16 July 1988. Excerpta Medica, 1988.

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Zingg, Hans H., Charles W. Bourque, and Daniel G. Bichet. Vasopressin and Oxytocin. Springer, 2012.

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Book chapters on the topic "Oxytocin and Vasopressin"

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Jard, Serge, and Etienne-Emile Baulieu. "Vasopressin and Oxytocin." In Hormones. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-3060-8_6.

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Mühlethaler, Michel, Mario Raggenbass, and J. J. Dreifuss. "Oxytocin and Vasopressin." In Neurotransmitter Actions in the Vertebrate Nervous System. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-4961-7_15.

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Richter, Dietmar. "Oxytocin and Vasopressin Genes." In Molecular Cloning of Hormone Genes. Humana Press, 1987. http://dx.doi.org/10.1007/978-1-4612-4824-8_8.

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Ferris, Craig F. "Vasopressin/oxytocin and aggression." In Novartis Foundation Symposia. John Wiley & Sons, Ltd, 2008. http://dx.doi.org/10.1002/0470010703.ch13.

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Burbach, J. P. H. "Proteolytic Conversion of Oxytocin, Vasopressin, and Related Peptides in the Brain." In Neurobiology of Oxytocin. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70414-7_3.

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Young, Larry J., and Thomas R. Insel. "Transgenic Models for Oxytocin and Vasopressin." In Transgenics in Endocrinology. Humana Press, 2001. http://dx.doi.org/10.1007/978-1-59259-102-2_12.

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Lincoln, Dennis W., and John A. Russell. "Oxytocin and Vasopressin Secretion: New Perspectives." In Neuroendocrine Molecular Biology. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5131-3_17.

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King, Lanikea B., and Larry J. Young. "Oxytocin, Vasopressin, and Diversity in Social Behavior." In Molecular Neuroendocrinology. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118760369.ch19.

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Kovács, Gábor L., Gyula Telegdy, Ferenc Laczi, and Ferenc A. László. "Oxytocin and Vasopressin in Memory and Amnesia." In Brain Plasticity, Learning, and Memory. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-5003-3_30.

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Caldwell, H. K., and W. S. Young. "Oxytocin and Vasopressin: Genetics and Behavioral Implications." In Handbook of Neurochemistry and Molecular Neurobiology. Springer US, 2006. http://dx.doi.org/10.1007/978-0-387-30381-9_25.

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Conference papers on the topic "Oxytocin and Vasopressin"

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Maixnerová, Jana, Lenka Klasová, Jana Barthová, Tomislav Barth, and Václav Kašička. "Fluorescent fragments of oxytocin, vasopressin and dDAVP." In VIIIth Conference Biologically Active Peptides. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2003. http://dx.doi.org/10.1135/css200306049.

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Mařík, Jan, Miloš Buděšínský, Jiřina Slaninová, and Jan Hlaváček. "Biologically inactive methylene-oxy analogs of oxytocin and vasopressin." In VIIth Conference Biologically Active Peptides. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2001. http://dx.doi.org/10.1135/css200104026.

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Koupilová, Marie, Jiří Patočka, and Tomislav Barth. "The effect of pyroglutamic fragments of vasopressin and oxytocin on the retention of memory after intoxication by neurotoxins QB and DSP-4 in rats." In VIth Conference Biologically Active Peptides. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 1999. http://dx.doi.org/10.1135/css199903034.

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