CD38/cyclic ADP-ribose system: a new player for oxytocin secretion and regulation of social behaviour

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

Sniffing neuropeptides: A transnasal approach to the human brain

Born, J., Lange, T., Kern, W., McGregor, G. P., Bickel, U., & Fehm, H. L. (2002) · Nature Neuroscience · doi:10.1038/nn0602-849 · Cited by 1,356 · see citing works

The genetics of autism

Muhle, R., Trentacoste, S. V., & Rapin, I. (2004) · Pediatrics · doi:10.1542/peds.113.5.e472 · Cited by 1,207 · 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

Dendritic peptide release and peptide-dependent behaviours

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

Oxytocin, vasopressin, and human social behavior

Heinrichs, M., von Dawans, B., & Domes, G. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.05.005 · Cited by 799 · see citing works

Brain oxytocin: A key regulator of emotional and social behaviours in both females and males

Neumann, I. D. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01726.x · Cited by 743 · see citing works

Functional Hemichannels in Astrocytes: A Novel Mechanism of Glutamate Release

Ye, Z., Wyeth, M. S., Tekkök, S. B., & Ransom, B. R. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-09-03588.2003 · Cited by 706 · see citing works

CD38 is critical for social behaviour by regulating oxytocin secretion

Jin, D., Liu, H.-X., Hirai, H., Torashima, T., Nagai, T., Lopatina, O., Shnayder, N. A., Yamada, K., Noda, M., Seike, T., et al. (2007) · Nature · doi:10.1038/nature05526 · Cited by 665 · see citing works

The Peptide That Binds: A Systematic Review of Oxytocin and its Prosocial Effects in Humans

MacDonald, K., & MacDonald, T. M. (2010) · Harvard Review of Psychiatry · doi:10.3109/10673220903523615 · Cited by 585 · see citing works

What Is the Role of Astrocyte Calcium in Neurophysiology?

Agulhon, C., Petravicz, J., McMullen, A. B., Sweger, E. J., Minton, S. K., Taves, S., Casper, K. B., Fiacco, T. A., & McCarthy, K. D. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.004 · Cited by 567 · see citing works

Physiological astrocytic calcium levels stimulate glutamate release to modulate adjacent neurons

Parpura, V., & Haydon, P. G. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.15.8629 · Cited by 527 · see citing works

The hypothalamic-neurohypophysial system regulates the hypothalamic–pituitary–adrenal axis under stress: an old concept revisited

Engelmann, M., Landgraf, R., & Wotjak, C. T. (2004) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2004.09.001 · Cited by 450 · 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

Developmental consequences of oxytocin

Carter, C. S. (2003) · Physiology & Behavior · doi:10.1016/s0031-9384(03)00151-3 · Cited by 367 · see citing works

Regulation of intracellular levels of NAD: A novel role for CD38

Aksoy, P., White, T. A., Thompson, M., & Chini, E. N. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.05.042 · Cited by 353 · see citing works

Intracellular calcium stores regulate activity-dependent neuropeptide release from dendrites

Ludwig, M., Sabatier, N., Bull, P. M., Landgraf, R., Dayanithi, G., & Leng, G. (2002) · Nature · doi:10.1038/nature00822 · Cited by 346 · see citing works

Dissociated central and peripheral release of vasopressin, but not oxytocin, in response to repeated swim stress: New insights into the secretory capacities of peptidergic neurons

Wotjak, C. T., Ganster, J., Kohl, G., Holsboer, F., Landgraf, R., & Engelmann, M. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00683-0 · Cited by 345 · see citing works

Dopaminergic-neuropeptide interactions in the social brain

Skuse, D. H., & Gallagher, L. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2008.09.007 · Cited by 340 · see citing works

Central vasopressin and oxytocin release: regulation of complex social behaviours

VEENEMA, A., & NEUMANN, I. (2008) · Progress in Brain Research · doi:10.1016/s0079-6123(08)00422-6 · Cited by 338 · 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

Gene expression analysis in N‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine mice model of Parkinson's disease using cDNA microarray: effect of R‐apomorphine

Grünblatt, E., Mandel, S. A., Maor, G., & Youdim, M. B. H. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00397.x · Cited by 246 · see citing works

Autocrine and Paracrine Calcium Signaling by the CD38/NAD+/Cyclic ADP‐Ribose System

FLORA, A. D., Zocchi, E., Guida, L., Franco, L., & Bruzzone, S. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1322.021 · Cited by 235 · see citing works

Endogenous opiates regulate oxytocin but not vasopressin secretion from the neurohypophysis

Bicknell, R. J., & Leng, G. (1982) · Nature · doi:10.1038/298161a0 · Cited by 229 · see citing works

Oxytocin induces morphological plasticity in the adult hypothalamo-neurohypophysial system

Theodosis, D. T., Montagnese, C. M., Rodriguez, F., Vincent, J., & Poulain, D. A. (1986) · Nature · doi:10.1038/322738a0 · Cited by 211 · see citing works

Gap junctions and neurological disorders of the central nervous system

Nakase, T., & Naus, C. C. G. (2004) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2004.01.009 · Cited by 205 · see citing works

A rise in the intracellular Ca2+ concentration of isolated rat supraoptic cells in response to oxytocin.

Lambert, R. C., Dayanithi, G., Moos, F., & Richard, P. (1994) · The Journal of Physiology · doi:10.1113/jphysiol.1994.sp020249 · Cited by 202 · see citing works

Organelle Selection Determines Agonist-specific Ca2+ Signals in Pancreatic Acinar and β Cells

Yamasaki, M., Masgrau, R., Morgan, A. J., Churchill, G. C., Patel, S., Ashcroft, S. J. H., & Galione, A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m311088200 · Cited by 201 · see citing works

Consequences of Early Experiences and Exposure to Oxytocin and Vasopressin Are Sexually Dimorphic

Carter, C. S., Boone, E. M., Pournajafi-Nazarloo, H., & Bales, K. L. (2009) · Developmental Neuroscience · doi:10.1159/000216544 · Cited by 176 · see citing works

Emotional Stress Triggers Intrahypothalamic But Not Peripheral Release of Oxytocin in Male Rats

Engelmann, Ebner, Landgraf, Holsboer, & Wotjak (1999) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1999.00403.x · Cited by 170 · 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

Molecular mechanisms of autism: a possible role for Ca2+ signaling

Krey, J. F., & Dolmetsch, R. E. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.01.010 · Cited by 169 · see citing works

Neurotransmitters and peptides: Whispered secrets and public announcements

Leng, G., & Ludwig, M. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.159103 · Cited by 168 · see citing works

Synaptic modulation by astrocytes via Ca2+-dependent glutamate release

Santello, M., & Volterra, A. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.03.039 · Cited by 163 · see citing works

Stimuli and consequences of dendritic release of oxytocin within the brain

Neumann, I. D. (2007) · Biochemical Society Transactions · doi:10.1042/bst0351252 · Cited by 161 · see citing works

Oxytocin and the maternal brain

LENG, G., MEDDLE, S., & DOUGLAS, A. (2008) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2008.07.001 · Cited by 158 · see citing works

Noradrenergic Excitation of Magnocellular Neurons in the Rat Hypothalamic Paraventricular Nucleus via Intranuclear Glutamatergic Circuits

Daftary, S. S., Boudaba, C., Szabó, K., & Tasker, J. G. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-24-10619.1998 · Cited by 145 · see citing works

Neural Pathways Controlling Central and Peripheral Oxytocin Release During Stress

Onaka, T. (2004) · Journal of Neuroendocrinology · doi:10.1111/j.0953-8194.2004.01186.x · Cited by 130 · see citing works

Evidence of a role for cyclic ADP‐ribose in calcium signalling and neurotransmitter release in cultured astrocytes

Verderio, C., Bruzzone, S., Zocchi, E., Fedele, E., Schenk, U., FLORA, A. D., & Matteoli, M. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00455.x · Cited by 128 · see citing works

Evidence that multiple P2X purinoceptors are functionally expressed in rat supraoptic neurones

Shibuya, I., Tanaka, K., Hattori, Y., Uezono, Y., Harayama, N., Noguchi, J., Ueta, Y., Izumi, F., & Yamashita, H. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.351ae.x · Cited by 123 · see citing works

Regulation of activity‐dependent dendritic vasopressin release from rat supraoptic neurones

Ludwig, M., Bull, P. M., Tobin, V. A., Sabatier, N., Landgraf, R., Dayanithi, G., & Leng, G. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.083931 · Cited by 122 · see citing works

Paracrine Roles of NAD+ and Cyclic ADP-ribose in Increasing Intracellular Calcium and Enhancing Cell Proliferation of 3T3 Fibroblasts

Franco, L., Zocchi, E., Usai, C., Guida, L., Bruzzone, S., Costa, A., & FLORA, A. D. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m010536200 · Cited by 115 · see citing works

Simultaneous and independent release of vasopressin and oxytocin in the rat

Kasting, N. W. (1988) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y88-004 · Cited by 104 · see citing works

Nitric oxide and homeostatic control: an intercellular signalling molecule contributing to autonomic and neuroendocrine integration?

Stern, J. E. (2004) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2003.11.015 · Cited by 102 · see citing works

Neuronal localization of CD38 antigen in the human brain

Mizuguchi, M., Otsuka, N., Sato, M., Ishii, Y., Kon, S.-I., Yamada, M., Nishina, H., Katada, T., & Ikeda, K. (1995) · Brain Research · doi:10.1016/0006-8993(95)00885-t · Cited by 97 · see citing works

Astrocytic Plasticity and Patterned Oxytocin Neuronal Activity: Dynamic Interactions

Wang, Y., & Hatton, G. I. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4669-08.2009 · Cited by 97 · see citing works

ATP acts as fast neurotransmitter in rat habenula: neurochemical and enzymecytochemical evidence

Sperlágh, B., Kittel, Á., Lajtha, Á., et al. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00588-v · Cited by 93 · see citing works

Purinergic and Adrenergic Agonists Synergize in Stimulating Vasopressin and Oxytocin Release

Kapoor, J. R., & Sladek, C. D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-23-08868.2000 · Cited by 90 · see citing works

ATP‐evoked increases in [Ca2+]i and peptide release from rat isolated neurohypophysial terminals via a P2X2 purinoceptor

Troadec, J., Thirion, S., Nicaise, G., et al. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.089bi.x · Cited by 86 · see citing works

Ca2+Syntillas, Miniature Ca2+Release Events in Terminals of Hypothalamic Neurons, Are Increased in Frequency by Depolarization in the Absence of Ca2+Influx

Crescenzo, V. D., ZhuGe, R., Velázquez‐Marrero, C., Lifshitz, L. M., Custer, E. E., Carmichael, J. D., Lai, F. A., Tuft, R. A., Fogarty, K. E., Lémos, J. R., et al. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4286-03.2004 · Cited by 85 · see citing works

Morphological evidence for vesicular glutamate release from astrocytes

Bergersen, L. H., & Gundersen, V. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.03.074 · Cited by 84 · see citing works

Cyclic ADP-ribose as a universal calcium signal molecule in the nervous system

Higashida, H., Salmina, A. B., Olovyannikova, R. Y., Hashii, M., Yokoyama, S., Koizumi, K., Jin, D., Liu, H.-X., Lopatina, O. L., Amina, S., et al. (2007) · Neurochemistry International · doi:10.1016/j.neuint.2007.06.023 · Cited by 84 · see citing works

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 · see citing works

CD38 at the junction between prognostic marker and therapeutic target

Deaglio, S., Aydin, S., Vaisitti, T., Bergui, L., & Malavasi, F. (2008) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2008.02.005 · Cited by 74 · see citing works

Evidence for Stimulatory Noradrenergic and Inhibitory Dopaminergic Regulation of Oxytocin Release in the Lactating Rat*

Crowley, W. R., SHYR, S. W., Kacsoh, B. Z., & GROSVENOR, C. E. (1987) · Endocrinology · doi:10.1210/endo-121-1-14 · Cited by 71 · see citing works

Local regulation of vasopressin and oxytocin secretion by extracellular ATP in the isolated posterior lobe of the rat hypophysis

Sperlágh, B., Mergl, Z., Jurányi, Z., et al. (1999) · Journal of Endocrinology · doi:10.1677/joe.0.1600343 · Cited by 71 · see citing works

Psychopharmacologic Interventions for Repetitive Behaviors in Autism Spectrum Disorders

Soorya, L. V., Kiarashi, J., & Hollander, E. (2008) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/j.chc.2008.06.003 · Cited by 69 · see citing works

CD38-dependent ADP-ribosyl cyclase activity in developing and adult mouse brain

Ceni, C., Pochon, N., Brun, V., Muller‐Steffner, H., Andrieux, A., Grünwald, D., Schuber, F. J., WAARD, M. M. D., Lund, F. E., Villaz, M., et al. (2003) · Biochemical Journal · doi:10.1042/bj20020604 · Cited by 66 · see citing works

Cyclic ADP-ribose as a second messenger revisited from a new aspect of signal transduction from receptors to ADP-ribosyl cyclase

Higashida, H., Hashii, M., Yokoyama, S., Hoshi, N., Chen, X.-L., Egorova, A., Noda, M., & Zhang, J.-S. (2001) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(01)00142-5 · Cited by 61 · see citing works

Uterine Contractile Activity Stimulates Supraoptic Neurons in Term Pregnant Rats Via a Noradrenergic Pathway**This work was supported by The Wellcome Trust (Project Grant 047318/Z/96/Z) and the Biotechnology and Biological Sciences Research Council.

Douglas, A. J., Scullion, S., Antonijevic, I. A., Brown, D., Russell, J. A., & Leng, G. (2001) · Endocrinology · doi:10.1210/endo.142.2.7962 · Cited by 59 · see citing works

Extracellular Application of Nicotinic Acid Adenine Dinucleotide Phosphate Induces Ca2+ Signaling in Astrocytes in Situ

Heidemann, A., Schipke, C. G., & Kettenmann, H. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m507338200 · Cited by 59 · see citing works

Locomotor activity, ultrasonic vocalization and oxytocin levels in infant CD38 knockout mice

Liu, H.-X., Lopatina, O., Higashida, C., Tsuji, T., Kato, I., Takasawa, S., Okamoto, H., Yokoyama, S., & Higashida, H. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.09.084 · Cited by 58 · see citing works

Neurotransmitter/Neuropeptide Interactions in the Regulation of Neurohypophyseal Hormone Release

Sladek, C. D., & Kapoor, J. R. (2001) · Experimental Neurology · doi:10.1006/exnr.2001.7779 · Cited by 58 · see citing works

Role of metabotropic glutamate receptors in the control of neuroendocrine function

Durand, D., Pampillo, M., Caruso, C. M., & Lasaga, M. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.06.022 · Cited by 58 · see citing works

Mechanism of nitric oxide action on inhibitory GABAergic signaling within the nucleus tractus solitarii

Wang, S., Teschemacher, A. G., Paton, J. F. R., et al. (2006) · The FASEB Journal · doi:10.1096/fj.05-5547fje · Cited by 58 · see citing works

Glutamate‐mediated overexpression of CD38 in astrocytes cultured with neurones

Bruzzone, S., Verderio, C., Schenk, U., Fedele, E., Zocchi, E., Matteoli, M., & FLORA, A. D. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2003.02326.x · Cited by 55 · see citing works

Ontogeny of Opioid Inhibition of Vasopressin and Oxytocin Release in Response to Osmotic Stimulation*

Hartman, R. D., Rosella-Dampman, L. M., Emmert, S. E., & Summy‐Long, J. Y. (1986) · Endocrinology · doi:10.1210/endo-119-1-1 · Cited by 55 · see citing works

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 · see citing works

Dendritic secretion of peptides from hypothalamic magnocellular neurosecretory neurones: a local dynamic control system and its functions

Morris, J. F., Christian, H., Ma, D., & Wang, H. (2000) · Experimental Physiology · doi:10.1111/j.1469-445x.2000.tb00016.x · Cited by 52 · see citing works

Role of Estrogen Receptor-β in Regulation of Vasopressin and Oxytocin Releasein Vitro

Somponpun, S. J., & Sladek, C. D. (2002) · Endocrinology · doi:10.1210/endo.143.8.8946 · Cited by 49 · see citing works

Dopamine D4 Receptor-Mediated Presynaptic Inhibition of GABAergic Transmission in the Rat Supraoptic Nucleus

Azdad, K., Piet, R., Poulain, D. A., & Oliet, S. H. R. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00226.2003 · Cited by 47 · see citing works

Substance P and NPY differentially potentiate ATP and adrenergic stimulated vasopressin and oxytocin release

Kapoor, J. R., & Sladek, C. D. (2001) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2001.280.1.r69 · Cited by 46 · see citing works

Oxytocin-induced elevation of ADP-ribosyl cyclase activity, cyclic ADP-riboseor Ca2+ concentrations is involved in autoregulation of oxytocin secretionin the hypothalamus and posterior pituitary in male mice

Lopatina, O. L., Liu, H.-X., Amina, S., Hashii, M., & Higashida, H. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.06.012 · Cited by 45 · see citing works

Neurohypophyseal peptides in aging and Alzheimer’s disease

Ishunina, T. A., & Swaab, D. F. (2002) · Ageing Research Reviews · doi:10.1016/s1568-1637(02)00013-2 · Cited by 44 · see citing works

Synthesis of Stable and Cell-type Selective Analogues of Cyclic ADP−Ribose, a Ca2+-Mobilizing Second Messenger. Structure−Activity Relationship of the N1-Ribose Moiety1

Kudoh, T., Fukuoka, M., Ichikawa, S., et al. (2005) · Journal of the American Chemical Society · doi:10.1021/ja050732x · Cited by 42 · see citing works

Opioidergic Modulation of Voltage-Activated K+Currents in Magnocellular Neurons of the Supraoptic Nucleus in Rat

Müller, W. S., Hallermann, S., & Swandulla, D. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.4.1617 · Cited by 42 · see citing works

Stimulation of Central and Systemic Oxytocin Release by Histamine in the Paraventricular Hypothalamic Nucleus: Evidence for an Interaction with Norepinephrine*

Bealer, S. L., & Crowley, W. R. (1999) · Endocrinology · doi:10.1210/endo.140.3.6601 · Cited by 41 · see citing works

The hypothalamic magnocellular neurosecretory system in developing rats

Lipari, E. F., Lipari, D., Gerbino, A., Liberto, D. D., Bellafiore, M., Catalano, M., & Valentino, B. (2009) · European Journal of Histochemistry · doi:10.4081/1626 · Cited by 40 · see citing works

Targeting of Green Fluorescent Protein to Secretory Granules in Oxytocin Magnocellular Neurons and Its Secretion from Neurohypophysial Nerve Terminals in Transgenic Mice

Zhang, B.-J., Kusano, K., Zerfas, P. M., Iacangelo, A. L., Young, W. S., & Gainer, H. (2002) · Endocrinology · doi:10.1210/endo.143.3.8700 · Cited by 38 · see citing works

CD38 regulates oxytocin secretion and complex social behavior

Bartz, J. A., & McInnes, L. A. (2007) · BioEssays · doi:10.1002/bies.20623 · Cited by 38 · see citing works

Oxytocin: The Neuropeptide of Love Reveals Some of Its Secrets

Neumann, I. D. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.03.008 · Cited by 37 · see citing works

Colocalization of tyrosine hydroxylase with oxytocin or vasopressin in neurons of the human paraventricular and supraoptic nucleus

Panayotacopoulou, M. T., Raadsheer, F. C., & Swaab, D. F. (1994) · Developmental Brain Research · doi:10.1016/0165-3806(94)90179-1 · Cited by 35 · see citing works

Differential Effects of Glutamate Agonists and D-Aspartate on Oxytocin Release from Hypothalamus and Posterior Pituitary of Male Rats

Pampillo, M., Dı́az, M. D. C., Duvilanski, B. H., Rettori, V., Seilicovich, A., & Lasaga, M. (2001) · Endocrine · doi:10.1385/endo:15:3:309 · Cited by 34 · see citing works

Endogenous Cannabinoids Take the Edge off Neuroendocrine Responses to Stress

Tasker, J. G. (2004) · Endocrinology · doi:10.1210/en.2004-1218 · Cited by 34 · see citing works

Uterine Contractile Activity Stimulates Supraoptic Neurons in Term Pregnant Rats Via a Noradrenergic Pathway

Douglas, A. J. (2001) · Endocrinology · doi:10.1210/en.142.2.633 · Cited by 34 · see citing works

Regulating the Social Brain: A New Role for CD38

Young, L. J. (2007) · Neuron · doi:10.1016/j.neuron.2007.04.011 · Cited by 33 · see citing works

Role of Neurokinin 3 Receptors in Supraoptic Vasopressin and Oxytocin Neurons

Howe, H. E., Somponpun, S. J., & Sladek, C. D. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3164-04.2004 · Cited by 33 · see citing works

Mechanisms of glial retraction in the hypothalamo‐neurohypophysial system of the rat

Salm, A. K. (2000) · Experimental Physiology · doi:10.1111/j.1469-445x.2000.tb00024.x · Cited by 31 · see citing works

Melatonin inhibits the substance P-induced secretion of vasopressin and oxytocin from the rat hypothalamo-neurohypophysial system: In vitro studies

Juszczak, M., & Stempniak, B. (2002) · Brain Research Bulletin · doi:10.1016/s0361-9230(02)00942-5 · Cited by 30 · see citing works

Sustained stimulation of vasopressin and oxytocin release by ATP and phenylephrine requires recruitment of desensitization-resistant P2X purinergic receptors

Gomes, D. A., Song, Z., Stevens, W., & Sladek, C. D. (2009) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00358.2009 · Cited by 30 · see citing works

Steroid Hormone Action in the Brain: Cross‐Talk Between Signalling Pathways

Mani, S. K., Portillo, W., & Reyna, A. J. (2009) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2009.01844.x · Cited by 29 · see citing works

Differential sensitivity of intranuclear and systemic oxytocin release to central noradrenergic receptor stimulation during mid- and late gestation in rats

Lipschitz, D. L., Crowley, W. R., & Bealer, S. L. (2004) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00572.2003 · Cited by 29 · see citing works

Correlation between electrophysiological and morphological characteristics during maturation of rat supraoptic neurons

Chevaleyre, V., Moos, F., & Desarménien, M. G. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01489.x · Cited by 29 · see citing works

Differential effects of various opioid peptides on vasopressin and oxytocin release from the rat pituitary in vitro

Maysinger, D., Vermes, I., Tilders, F. J. H., Seizinger, B. R., Gramsch, C., H�llt, V., & Herz, A. (1984) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/bf00512071 · Cited by 28 · see citing works

cADPR stimulates SERCA activity in Xenopus oocytes

Yamasaki-Mann, M., Demuro, A., & Parker, I. (2009) · Cell Calcium · doi:10.1016/j.ceca.2008.11.008 · Cited by 28 · see citing works

Role of metabotropic glutamate receptors in vasopressin and oxytocin release

Morsette, D. J., Sidorowicz, H., & Sladek, C. D. (2001) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2001.281.2.r452 · Cited by 27 · see citing works

Extracellular Synthesis of cADP-Ribose from Nicotinamide-Adenine Dinucleotide by Rat Cortical Astrocytes in Culture

Pawlikowska, L., Cottrell, S. E., Harms, M. B., Li, Y., & Rosenberg, P. A. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-17-05372.1996 · Cited by 25 · see citing works

Insulin-Like Growth Factor-1 Inhibits Adult Supraoptic Neurons via Complementary Modulation of Mechanoreceptors and Glycine Receptors

Ster, J., Colomer, C., Monzo, C., Duvoid, A., Moos, F., Alonso, G., & Hussy, N. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4053-04.2005 · Cited by 23 · see citing works

Mechanisms of transmitter release from astrocytes

Malarkey, E. B., & Parpura, V. (2008) · Springer eBooks · doi:10.1007/978-0-387-79492-1_12 · Cited by 19 · see citing works

Fast Delivery

Douglas, A. J., & Meddle, S. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-374285-8.00014-7 · Cited by 19 · see citing works

Neuropeptide Y2 receptors on nerve endings from the rat neurohypophysis regulate vasopressin and oxytocin release

Sheikh, S. P., Feldthus, N., Orkild, H., et al. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00256-x · Cited by 19 · see citing works

Functional switching of GABAergic synapses by ryanodine receptor activation

Sun, M., Nelson, T. J., & Alkon, D. L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.210396697 · Cited by 19 · see citing works

Stimulation of Central and Systemic Oxytocin Release by Histamine in the Paraventricular Hypothalamic Nucleus: Evidence for an Interaction with Norepinephrine

Bealer, S. L. (1999) · Endocrinology · doi:10.1210/en.140.3.1158 · Cited by 18 · see citing works

Postnatal developmental changes in Ca2+ homeostasis in supraoptic magnocellular neurons

Lee, S. H., Park, K. H., Ho, W., & Lee, S. (2006) · Cell Calcium · doi:10.1016/j.ceca.2006.08.003 · Cited by 17 · see citing works

Naloxone Increases the Angiotensin II Stimulated Rise of Arginine Vasopressin and Oxytocin Secretion in Man

Coiro, V., & Chiodera, P. (2008) · Neuroendocrinology · doi:10.1159/000125720 · Cited by 16 · see citing works

Role of Estrogen Receptor- in Regulation of Vasopressin and Oxytocin Release in Vitro

Somponpun, S. J. (2002) · Endocrinology · doi:10.1210/en.143.8.2899 · Cited by 16 · see citing works

Expression of GABAB Receptors in Magnocellular Neurosecretory Cells of Male, Virgin Female and Lactating Rats

Richards, D. S., Villalba, R. M., Álvarez, F. J., & Stern, J. E. (2005) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2005.01324.x · Cited by 15 · see citing works

Calbindin D28k and calretinin in oxytocin and vasopressin neurons of the rat supraoptic nucleus

Arai, R., Jacobowitz, D. M., & Hida, T. (1999) · Cell and Tissue Research · doi:10.1007/pl00008808 · Cited by 15 · see citing works

Individual Calcium Syntillas Do Not Trigger Spontaneous Exocytosis from Nerve Terminals of the Neurohypophysis

McNally, J. M., Crescenzo, V. D., Fogarty, K. E., Walsh, J. V., & Lémos, J. R. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1726-09.2009 · Cited by 13 · see citing works

Morphological plasticity of astroglial/neuronal interactions: functional implications

Hatton, G. I. (2004) · Springer eBooks · doi:10.1007/978-1-4020-7937-5_4 · Cited by 13 · see citing works

Noradrenergic regulation in mouse supraoptic nucleus involves a nitric oxide pathway only to regulate arginine‐vasopressin expression and not oxytocin expression

Maolood, N., Grange‐Messent, V., Raison, D., et al. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21394 · Cited by 11 · see citing works

Role of purinergic P2Y1 receptors in regulation of vasopressin and oxytocin secretion

Song, Z., Gomes, D. A., & Stevens, W. (2009) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00163.2009 · Cited by 11 · see citing works

Detection of a Novel Pattern of Connexin 43 Immunoreactivity Responsive to Dehydration in Rat Hypothalamic Magnocellular Nuclei

Eisner, I., & Colombo, J. A. (2002) · Experimental Neurology · doi:10.1006/exnr.2002.7953 · Cited by 11 · see citing works

Catecholaminergic input to the oxytocin neurosecretory system in the human hypothalamus

Semeniken, K., Merchenthaler, I. J., Hu, W., & Dudás, B. (2009) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2009.01.004 · Cited by 7 · see citing works

The actin filament and dendritic peptide release

Tobin, V. A., & Ludwig, M. (2007) · Biochemical Society Transactions · doi:10.1042/bst0351243 · Cited by 7 · see citing works

Social Memory, Maternal Care, and Oxytocin Secretion, But not Vasopressin Release, Require CD38 In Mice

Higashida, H., Jin, D., Liu, H.-X., Lopatina, O. L., Yokoyama, S., Koizumi, K., Hashii, M., Islam, M. S., Hayashi, K., & Munesue, T. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-374285-8.00023-8 · Cited by 2 · see citing works

Neuroendocrine regulation of maternal behavior

Bridges, R. S. (2015) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.11.007 · Cited by 346 · see citing works

The contributions of oxytocin and vasopressin pathway genes to human behavior

Ebstein, R. P., Knafo, A., Mankuta, D., Chew, S. H., & Lai, P. S. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.12.014 · Cited by 283 · see citing works

CD38 and its role in oxytocin secretion and social behavior

Higashida, H., Yokoyama, S., Kikuchi, M., & Munesue, T. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.12.011 · Cited by 98 · see citing works

Communication Impairment in Ultrasonic Vocal Repertoire during the Suckling Period of Cd157 Knockout Mice: Transient Improvement by Oxytocin

Lopatina, O. L., Furuhara, K., Ishihara, K., Salmina, A. B., & Higashida, H. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00266 · Cited by 30 · see citing works

The role of genetic variants in genes regulating the oxytocin–vasopressin neurohumoral system in childhood-onset aggression

Malik, A. I., Zai, C. C., Berall, L., Abu, Z., Din, F., Nowrouzi, B., Chen, S., & Beitchman, J. H. (2014) · Psychiatric Genetics · doi:10.1097/ypg.0000000000000044 · Cited by 29 · see citing works

Exogenous Glucocorticoids and a High-Fat Diet Cause Severe Hyperglycemia and Hyperinsulinemia and Limit Islet Glucose Responsiveness in Young Male Sprague-Dawley Rats

Beaudry, J. L., D'souza, A. M., Teich, T., Tsushima, R. G., & Riddell, M. C. (2013) · Endocrinology · doi:10.1210/en.2012-2114 · Cited by 44 · see citing works

The Effect of Fasting on Tissue Cyclic cAMP and Plasma Glucagon in the Obese Hyperglycemic Mouse

VINE, R. L. L., Voyles, N. R., Perrino, P. V., & Recant, L. (1975) · Endocrinology · doi:10.1210/endo-97-3-615 · Cited by 38 · see citing works

Modulation of Adipoinsular Axis in Prediabetic Zucker Diabetic Fatty Rats by Diazoxide

Alemzadeh, R., & Tushaus, K. (2004) · Endocrinology · doi:10.1210/en.2003-1523 · Cited by 38 · see citing works

Mechanisms of Impaired Growth Hormone Secretion in Genetically Obese Zucker Rats: Roles of Growth Hormone-Releasing Factor and Somatostatin*

TANNENBAUMt, G. S., Lapointe, M., Gurd, W., & Finkelstein, J. A. (1990) · Endocrinology · doi:10.1210/endo-127-6-3087 · Cited by 72 · see citing works

Growth hormone binding protein in the rat: effects of gonadal steroids

Carmignac, D. F., Gabrielsson, B. G., & Robinson, I. C. A. F. (1993) · Endocrinology · doi:10.1210/endo.133.6.8243263 · Cited by 68 · see citing works