Cited by 1,059Neuroendocrine regulation and behaviorNeuropeptides and Animal PhysiologyNeuroscience and Neuropharmacology Research

The DOI matches its Crossref record; 295 of the 295 references it cites were found in a registry or an index.

Vasopressin and oxytocin release within the brain: a dynamic concept of multiple and variable modes of neuropeptide communication

Landgraf, Rainer, Neumann, Inga D.·2004·Frontiers in Neuroendocrinology

DOI 10.1016/j.yfrne.2004.05.001

Open this paper in CoChat — free account

Abstract

As exemplified particularly with vasopressin and oxytocin, release of neuropeptides within the brain occurs from dendrites, somata, and axons of neurosecretory neurons; mechanisms include activation of intracellular Ca2+ stores, changed strength of synaptic input and altered interaction between transcription factors and gene promoters. Upon demand, both diffuse spread of neuropeptides in the extracellular fluid following dendritic release and focal release from axonal terminals may contribute to regionally and temporally varying combinations of neuromodulator and neurotransmitter actions, thus providing a theoretically unlimited variability in interneuronal signaling. Thus, instead of favoring volume or synaptic transmission following central neuropeptide release, a more dynamic concept is presented with multiple and variable modes of release and communication. This concept considers neuropeptides in the extracellular fluid of the brain rather than those in the cerebrospinal fluid or plasma as primary signals, triggering a variety of receptor-mediated effects, including those underlying behavioral and neuroendocrine regulation and psychopathology.

Integrity signals

Registry

Crossref · 10.1016/j.yfrne.2004.05.001

Cites

295 of 295 references verified0 citation errors · 0 not checkable

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?

Items 201–295 of 295

Developmental Regulation of a Local Positive Autocontrol of Supraoptic Neurons
Chevaleyre, V., Dayanithi, G., Moos, F., & Desarménien, M. G. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-15-05813.2000 · Cited by 62
Vasopressin from hypothalamic magnocellular neurons has opposite actions at the adenohypophysis and in the supraoptic nucleus on ACTH secretion
Wotjak, C. T., Ludwig, M., Ebner, K., Russell, J. A., Singewald, N., Landgraf, R., & Engelmann, M. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02101.x · Cited by 61
Self-citation
Oxytocin and vasopressin release in discrete brain areas after naloxone in morphine-tolerant and -dependent anesthetized rats: push-pull perfusion study
Russell, J., Neumann, I. D., & Landgraf, R. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-03-01024.1992 · Cited by 61
Self-citation
Extracellular oxytocin in the paraventricular nucleus: hyperosmotic stimulation by in vivo microdialysis
Hattori, T., Morris, M., Alexander, N., & Sundberg, D. K. (1990) · Brain Research · doi:10.1016/0006-8993(90)91216-4 · Cited by 60
Targeting of Peptidergic Vesicles in Cotransmitting Terminals
Karhunen, T., Vilim, F. S., Alexeeva, V., Weiss, K. R., & Church, P. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-03-j0005.2001 · Cited by 60
Simultaneous comparison of cerebral dialysis and push–pull perfusion in the brain of rats: a critical review
Myers, R. D., Adell, A., & Lankford, M. F. (1998) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(97)00025-0 · Cited by 56
Differential subcellular mRNA targeting: deletion of a single nucleotide prevents the transport to axons but not to dendrites of rat hypothalamic magnocellular neurons.
Mohr, E., Morris, J. F., & Richter, D. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.10.4377 · Cited by 55
Central and systemic oxytocin release: A study of the paraventricular nucleus by in vivo microdialysis
Hattori, T., Sundberg, D. K., & Morris, M. (1992) · Brain Research Bulletin · doi:10.1016/0361-9230(92)90187-3 · Cited by 55
Corticotropin-releasing factor release from the mediobasal hypothalamus of the rat as measured by microdialysis
Pich, E. M., Koob, G. F., Heilig, M. A., Menzaghi, F., Vale, W., & Weiss, F. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90435-i · Cited by 55
Differential regulation of central vasopressin in transgenic rats harboring the mouse Ren-2 gene
Moriguchi, A., Ferrario, C. M., Brosnihan, K. B., et al. (1994) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1994.267.3.r786 · Cited by 55
New Aspects of Firing Pattern Autocontrol in Oxytocin and Vasopressin Neurones
Moos, F., Gouzènes, L., Brown, D., Dayanithi, G., Sabatier, N., Boissin‐Agasse, L., Rabié, A., & Richard, P. (1998) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4871-3_18 · Cited by 54
Vasopressin induction of long‐lasting potentiation of synaptic transmission in the dentate gyrus
Chen, C., Brinton, R. D., Shors, T. J., & Thompson, R. F. (1993) · Hippocampus · doi:10.1002/hipo.450030211 · Cited by 54
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 54
Effects of Tetrodotoxin on Osmotically Stimulated Central and Peripheral Vasopressin and Oxytocin Release
Ludwig, M., Callahan, M. F., & Morris, M. (2008) · Neuroendocrinology · doi:10.1159/000127058 · Cited by 52
Osmotic responsiveness and cross talk involving oxytocin, but not vasopressin or amino acids, between the supraoptic nuclei in virgin and lactating rats
Neumann, I. D., Landgraf, R., Bauce, L., & Pittman, Q. J. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-05-03408.1995 · Cited by 51
Self-citation
Autosomal Dominant Neurohypophyseal Diabetes Insipidus due to Substitution of Histidine for Tyrosine2 in the Vasopressin Moiety of the Hormone Precursor
Rittig, S., Siggaard, C., Özata, M., Yetkin, İ., Gregersen, N., Pedersen, E. B., & Robertson, G. L. (2002) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.87.7.8677 · Cited by 51
NMDA and non-NMDA receptors on rat supraoptic nucleus neurons activated monosynaptically by olfactory afferents
Yang, Q. Z., Smithson, K. G., & Hatton, G. I. (1995) · Brain Research · doi:10.1016/0006-8993(95)00153-h · Cited by 50
Vasopressin in the lateral septum promotes elemental conditioning to the detriment of contextual fear conditioning in mice
Desmedt, A., Garcia, R., & Jaffard, R. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00815.x · Cited by 49
Chapter 6: Central release of vasopressin: stimuli, dynamics, consequences
Landgraf, R. (1992) · Progress in brain research · doi:10.1016/s0079-6123(08)62313-4 · Cited by 47
Self-citation
Stimulation of oxytocin release within the supraoptic nucleus and into blood by CCK-8
Neumann, I., Landgraf, R., Takahashi, Y., Pittman, Q. J., & Russell, J. A. (1994) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1994.267.6.r1626 · Cited by 44
Self-citation
Anxiety Profiles of Mice Selectively Bred for Intermale Aggression
Nyberg, J. M., Vekovischeva, O. Y., & Sandnabba, N. K. (2003) · Behavior Genetics · doi:10.1023/a:1025718531997 · Cited by 43
The stress-vulnerability hypothesis in psychotic disorders: Focus on the stress response systems
Wied, C. C. G., & Jansen, L. M. C. (2002) · Current Psychiatry Reports · doi:10.1007/s11920-002-0022-9 · Cited by 43
Regulation of gene promoters of hypothalamic peptides
Burbach, J. P. H. (2002) · Frontiers in Neuroendocrinology · doi:10.1016/s0091-3022(02)00005-5 · Cited by 43
Facilitative role of endogenous oxytocin in noradrenaline release in the rat supraoptic nucleus
Onaka, T., Ikeda, K., Yamashita, T., & Honda, K. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.03037.x · Cited by 43
Supraoptic nucleus afferents from the accessory olfactory bulb: Evidence from anterograde and retrograde tract tracing in the rat
Smithson, K. G., Weiss, M. L., & Hatton, G. I. (1992) · Brain Research Bulletin · doi:10.1016/0361-9230(92)90028-v · Cited by 43
No Stress Response of the Hypothalamo-Pituitary-Adrenal Axis in Parturient Rats: Lack of Involvement of Brain Oxytocin
Neumann, I. D., Bosch, O. J., Toschi, N., Torner, L., & Douglas, A. J. (2003) · Endocrinology · doi:10.1210/en.2003-0037 · Cited by 43
Self-citation
Neurosteroid regulation of oxytocin and vasopressin release from the rat supraoptic nucleus
Widmer, H., Ludwig, M., Bancel, F., Leng, G., & Dayanithi, G. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.036863 · Cited by 43
Distribution of neurohypophysial peptides in the guinea pig brain. II. An immunocytochemical study of oxytocin
Dubois‐Dauphin, M., Tribollet, E., & Dreifuss, J. J. (1989) · Brain Research · doi:10.1016/0006-8993(89)91052-4 · Cited by 42
A Subset of Neurons Containing Immunoreactive Prolactin Is a Target for Estrogen Regulation of Gene Expression in Rat Hypothalamus
Shivers, B. D., Harlan, R. E., & Pfaff, D. W. (2008) · Neuroendocrinology · doi:10.1159/000125086 · Cited by 42
Neuropeptides in Anxiety Modulation
Landgraf, R. (2005) · Handbook of experimental pharmacology · doi:10.1007/3-540-28082-0_12 · Cited by 41
Self-citation
The History of Neuropeptides III
Klavdieva, M. M. (1996) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1996.0004 · Cited by 41
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
Studies of vasopressin in the human cerebrospinal fluid
Sørensen, P. S. (1986) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.1986.tb04633.x · Cited by 41
Modulation of GABAergic transmission by endogenous glutamate in the rat supraoptic nucleus
Piet, R., Bonhomme, R., Theodosis, D. T., Poulain, D. A., & Oliet, S. H. R. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02611.x · Cited by 40
Differential impact of predator or immobilization stressors on central corticotropin-releasing hormone and bombesin-like peptides in Fast and Slow seizing rat
Merali, Z., Kent, P., Michaud, D. S., McIntyre, D., & Anisman, H. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02556-2 · Cited by 40
Neuropathological findings after intracerebral implantation of microdialysis catheters
Whittle, I. R., Glasby, M. A., Lammie, A., et al. (1998) · Neuroreport · doi:10.1097/00001756-199808240-00025 · Cited by 40
Measuring of extracellular cortisol and corticotropin-releasing hormone in the amygdala using immunosensor coupled microdialysis
Cook, C. J. (2001) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(01)00421-6 · Cited by 39
Cardiac, neuroendocrine, and behavioral effects of central amygdaloid vasopressinergic and oxytocinergic mechanisms under stress-free conditions in rats
Roozendaal, B., Schoorlemmer, G. H. M., Koolhaas, J. M., & Bohus, B. (1993) · Brain Research Bulletin · doi:10.1016/0361-9230(93)90157-7 · Cited by 39
Swim stress triggers the release of vasopressin within the suprachiasmatic nucleus of male rats
Engelmann, M., Ebner, K., Landgraf, R., & Wotjak, C. T. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00243-1 · Cited by 39
Self-citation
Peptidergic Modulation of Synaptic Transmission in the Parabrachial NucleusIn Vitro: Importance of Degradative Enzymes in Regulating Synaptic Efficacy
Saleh, T. M., Kombian, S. B., Zidichouski, J. A., et al. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-19-06046.1996 · Cited by 38
Domperidone induces a probenecid-sensitive rise in immunoreactive prolactin in cerebroventricular perfusates in female rats
Felício, L. F., & Bridges, R. S. (1992) · Brain Research · doi:10.1016/0006-8993(92)90122-p · Cited by 38
Hemorrhage-induced vasopressin release in the paraventricular nucleus measured by in vivo microdialysis
Ota, M., Crofton, J. T., & Share, L. (1994) · Brain Research · doi:10.1016/s0006-8993(09)90009-9 · Cited by 38
Signal Transduction of Physiological Concentrations of Vasopressin in A7r5 Vascular Smooth Muscle Cells
Byron, K. L., & Lucchesi, P. A. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m104726200 · Cited by 36
Salt loading abolishes osmotically stimulated vasopressin release within the supraoptic nucleus
Ludwig, M., Williams, K., Callahan, M. F., & Morris, M. (1996) · Neuroscience Letters · doi:10.1016/s0304-3940(96)12956-6 · Cited by 35
Functional role of intrahypothalamic release of oxytocin and vasopressin: consequences and controversies
Ludwig, M. (1995) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1995.268.4.e537 · Cited by 34
Naloxone increases the release of oxytocin, but not vasopressin, within limbic brain areas of conscious parturient rats: A push-pull perfusion study
Neumann, I., Russell, J. A., Wolff, B., & Landgraf, R. (2008) · Neuroendocrinology · doi:10.1159/000125958 · Cited by 33
Self-citation
Substance P Release in the Rat Periaqueductal Gray and Preoptic Anterior Hypothalamus after Noxious Cold Stimulation: Effect of Selective Mu and Kappa Opioid Agonists
Li, X., Geller, E. B., Liu‐Chen, L., et al. (1997) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)36834-x · Cited by 33
Calcium-dependent translocation of synaptotagmin to the plasma membrane in the dendrites of developing neurones
Schwab, Y., Mouton, J., Chasserot‐Golaz, S., Marty, I., Maulet, Y., & Jover, E. (2001) · Molecular Brain Research · doi:10.1016/s0169-328x(01)00244-3 · Cited by 32
Prospects for antidepressant drug discovery
Holsboer, F. (2001) · Biological Psychology · doi:10.1016/s0301-0511(01)00089-8 · Cited by 32
Effects of vasopressin and related peptides on neurons of the rat lateral septum and ventral hippocampus
Urban, I. J. A. (1999) · Progress in brain research · doi:10.1016/s0079-6123(08)61576-9 · Cited by 31
Vasopressin-induced motor effects: Localization of a sensitive site in the amygdala
Willcox, B. J., Poulin, P., Veale, W. L., & Pittman, Q. J. (1992) · Brain Research · doi:10.1016/0006-8993(92)91532-j · Cited by 31
GABA selectively controls the secretory activity of oxytocin neurons in the rat supraoptic nucleus
Engelmann, M., Bull, P. M., Brown, C. H., Landgraf, R., Horn, T. F. W., Singewald, N., Ludwig, M., & Wotjak, C. T. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03151.x · Cited by 31
Self-citation
Histaminergic Control of Oxytocin Release in the Paraventricular Nucleus during Lactation in Rats
Bealer, S. L., & Crowley, W. R. (2001) · Experimental Neurology · doi:10.1006/exnr.2001.7770 · Cited by 31
The Neuropeptide Saga
Scharrer, B. (1990) · American Zoologist · doi:10.1093/icb/30.4.887 · Cited by 31
Taurine selectively modulates the secretory activity of vasopressin neurons in conscious rats
Engelmann, M., Ludwig, M., Singewald, N., Ebner, K., Sabatier, N., Lübec, G., Landgraf, R., & Wotjak, C. T. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01729.x · Cited by 30
Self-citation
Protein synthetic machinery in the dendrites of the magnocellular neurosecretory neurons of wild-type Long-Evans and homozygous Brattleboro rats
Ma, D., & Morris, J. F. (2002) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(01)00158-2 · Cited by 30
Expression of the Genes Encoding the Vasopressin‐Activated Calcium‐Mobilizing Receptor and the Dual Angiotensin II/Vasopressin Receptor in the Rat Central Nervous System
Hurbin, A., Orcel, Ferraz, Moos, & Rabié (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00499.x · Cited by 30
Oxytocin neurone autoexcitation during morphine withdrawal in anaesthetized rats
Brown, C. H., Munro, G., Johnstone, L. E., Robson, A. C., Landgraf, R., & Russell, J. A. (1997) · Neuroreport · doi:10.1097/00001756-199703030-00027 · Cited by 29
Self-citation
Central carbachol stimulates vasopressin release into interstitial fluid adjacent to the paraventricular nucleus
Ota, M., Crofton, J. T., Festavan, G. T., & Share, L. (1992) · Brain Research · doi:10.1016/0006-8993(92)91682-5 · Cited by 29
Probing the Brain and Spinal Cord with Neuropeptides in Pathways Related to Pain and Other Functions
Duggan, A. W., & Furmidge, L. J. (1994) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1994.1011 · Cited by 29
Heterogeneity of expression of neuropeptide genes by astrocytes: functional implications.
Schwartz, J. P., & Taniwaki, T. (1994) · PubMed · Cited by 28
Chapter 1 The magnocellular neuronal phenotype: cell-specific gene expression in the hypothalamo-neurohypophysial system
Gainer, H., Yamashita, M., Fields, R. L., House, S. B., & Rusnák, M. (2002) · Progress in brain research · doi:10.1016/s0079-6123(02)39003-4 · Cited by 27
Antidepressant effect of the calcium-activated tyrosine kinase Pyk2 in the lateral septum
Sheehan, T. P., Neve, R. L., Duman, R. S., & Russell, D. (2003) · Biological Psychiatry · doi:10.1016/s0006-3223(02)01815-2 · Cited by 26
Fear and power-dominance motivation: proposed contributions of peptide hormones present in cerebrospinal fluid and plasma
Sewards, T. V., & Sewards, M. A. (2003) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(03)00034-4 · Cited by 26
Vasopressin and Oxytocin Decrease Excitatory Amino Acid Release in Adult Rat Supraoptic Nucleus
Currás‐Collazo, M., Gillard, E. R., Jin, J., & Pandika, J. (2003) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2003.00976.x · Cited by 26
Vasopressin metabolites: A link between vasopressin and memory?
Reijmers, L. G. J. E., van Ree, J. M., Spraijt, B. M., Burbach, J. P. H., & de Wied, D. (1999) · Progress in brain research · doi:10.1016/s0079-6123(08)61591-5 · Cited by 25
Central interleukin‐1 beta stimulation of vasopressin release into the rat brain: activation of an antipyretic pathway.
Wilkinson, M. F., Horn, T. F. W., Kasting, N. W., & Pittman, Q. J. (1994) · The Journal of Physiology · doi:10.1113/jphysiol.1994.sp020470 · Cited by 25
Effects of arginine-vasopressin (AVP) on long-term potentiation in intact anesthetized rats
Dubrovsky, B. O., Tatarinov, A. L., Gijsbers, K., Harris, J., & Tsiodras, A. (2003) · Brain Research Bulletin · doi:10.1016/s0361-9230(02)00961-9 · Cited by 25
Got milk? Oxytocin triggers hippocampal plasticity
Monks, D. A., Lonstein, J. S., & Breedlove, S. M. (2003) · Nature Neuroscience · doi:10.1038/nn0403-327 · Cited by 25
In vivo release of somatostatin from rat hippocampus and striatum
Mathé, A. A., Nomikos, G. G., & Svensson, T. H. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90771-c · Cited by 25
Immunoreactive Prolactin in the Hypothalamus and Cerebrospinal Fluid of Male and Female Rats
DeVito, W. J. (2008) · Neuroendocrinology · doi:10.1159/000125219 · Cited by 24
Characterization of Spontaneous and N-Methyl-D-Aspartate-Induced Calcium Rise in Rat Cultured Hypothalamic Neurons
Dayanithi, G., Rage, F., Richard, P., et al. (2008) · Neuroendocrinology · doi:10.1159/000126846 · Cited by 24
Chronic corticotropin-releasing hormone and vasopressin regulate corticosteroid receptors in rat hippocampus and anterior pituitary
Hügin-Flores, M. E., Steimer, T. J., Schulz, P., Vallotton, M. B., & Aubert, M. L. (2003) · Brain Research · doi:10.1016/s0006-8993(03)02585-x · Cited by 23
C‐fos and c‐jun in the paraventricular nucleus play a role in regulating peptide gene expression, oxytocin and glutamate release, and maternal behaviour
Costa, A. P. C., de la Riva, C., Guevara‐Guzmán, R., & Kendrick, K. M. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00637.x · Cited by 21
In vivo microdialysis of corticotropin releasing factor (CRF): Calcium dependence of depolarization-induced neurosecretion of CRF
Gabr, R. W., Gladfelter, W. E., Birkle, D. L., et al. (1994) · Neuroscience Letters · doi:10.1016/0304-3940(94)90357-3 · Cited by 20
Peptidergic transmission in the brain. II. Mediation by a vasopressin-like peptide
Smock, T., Albeck, D. S., McMechen, P., & Purves, D. (1990) · Brain Research · doi:10.1016/0006-8993(90)90220-6 · Cited by 18
Characterization of CArG-binding protein A initially identified by differential display
Rushlow, W. J., Rajakumar, N., Flumerfelt, B. A., et al. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00342-5 · Cited by 17
Hippocampal vasopressin release evoked by N-methyl D-aspartate (NMDA) microdialysis
Orłowska-Majdak, M., Wz, T., & Szymański, D. (2003) · Physiological Research · doi:10.33549/physiolres.930283 · Cited by 14
Chapter 8: Endogenous opioids regulate intracerebral oxytocin release during parturition in a region-specific manner
Neumann, I. D., Russell, J. A., & Landgraf, R. (1992) · Progress in brain research · doi:10.1016/s0079-6123(08)62315-8 · Cited by 13
Self-citation
Oxytocin modulates oxytocin neurons in the paraventricular nuclei of female rats throughout pregnancy and parturition
Kawarabayashi, T., Kuriyama, K., Nakashima, T., Kiyohara, T., & Sugimori, H. (1993) · American Journal of Obstetrics and Gynecology · doi:10.1016/s0002-9378(12)90854-6 · Cited by 13
Arginine Vasopressin Fragment AVP4-9 Facilitates Induction of Long-Term Potentiation in the Hippocampus
Chepkova, A. N., Kapai, N. A., & Skrebitskii, V. G. (2001) · Bulletin of Experimental Biology and Medicine · doi:10.1023/a:1017583626625 · Cited by 13
Characterization of prolactin immunoreactivity in human cerebrospinal fluid
Nyberg, F., Isacson, C.-A. ̊., Brostedt, E., et al. (1990) · Brain Research · doi:10.1016/0006-8993(90)91208-x · Cited by 11
Immunocytochemical detection of oxytocin in the supraependymal neuronal complex of the golden hamster
Cloft, H. J., & Mitchell, J. A. (1994) · Brain Research · doi:10.1016/0006-8993(94)91735-3 · Cited by 9
What is special about peptides as neuronal messengers?
JOOSSE, J. (1988) · Cambridge University Press eBooks · doi:10.1017/cbo9780511752230.002 · Cited by 9
Action at a distance: The extracellular spread of chemicals in the nervous system
Routtenberg, A. (1991) · Cited by 9
Local synthesis of the rat Vasopressin precursor in dendrites of in vitro cultured nerve cells
Mohr, E., & Richter, D. (2003) · Molecular Brain Research · doi:10.1016/s0169-328x(03)00137-2 · Cited by 8
Intermittent Footshock Facilitates Dendritic Vasopressin Release but Suppresses Vasopressin Synthesis within the Rat Supraoptic Nucleus
Onaka, T., Serino, R., & Ueta, Y. (2003) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2003.01053.x · Cited by 7
Spatial, cellular and temporal basis of vasopressin potentiation of norepinephrine-induced cAMP formation
Brinton, R. D., Thompson, R. H., & Brownson, E. A. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00543-4 · Cited by 6
Transgenic studies in rats and mice on the osmotic regulation of vasopressin gene expression
Murphy, D., Xu, J., & Waller, S. J. (2000) · Experimental Physiology · doi:10.1111/j.1469-445x.2000.tb00026.x · Cited by 6
Vasopressin differentially modulates noradrenaline release in the rat supraoptic nucleus
Yamashita, T., Liu, X., Onaka, T., Honda, K., Saito, T., & Yagi, K. (2001) · Neuroreport · doi:10.1097/00001756-200111160-00027 · Cited by 5
Opioids influence neurohypophysial but not central oxytocin release following direct hyperosmotic stimulation of the supraoptic nucleus in urethane-anaesthetised rats
Munro, G., Ludwig, M., Landgraf, R., & Russell, J. A. (1994) · Neuropeptides · doi:10.1016/0143-4179(94)90052-3 · Cited by 5
Self-citation
Effects of advancing age on cerebrospinal fluid concentrations of prolactin in the female rat
Simpkins, J. W. (1992) · Brain Research · doi:10.1016/0006-8993(92)90157-5 · Cited by 5
Oxytocin, Norepinephrine and Olfactory Bulb Mediated Recognition
Dluzen, D. E., Shang, Y., & Landgraf, R. (2001) · Springer eBooks · doi:10.1007/978-1-4615-0671-3_14 · Cited by 5
Self-citation
Breast-feeding and stress : evidence for psychoendocrine stress protective effects in women
Heinrichs, M., Ehlert, U., Neumann, I., et al. (2001) · Cited by 2
Self-citation
The broad autism phenotype: A complementary strategy for molecular genetic studies of autism
(2001) · doi:10.1002/1096-8628(20010108)105:1

Flagged first, then by citations

Sorted by citations

Oxytocin increases trust in humans
Kosfeld, M., Heinrichs, M., Zak, P. J., Fischbacher, U., & Fehr, E. (2005) · Nature · doi:10.1038/nature03701 · Cited by 3,690
Oxytocin and vasopressin in the human brain: social neuropeptides for translational medicine
Meyer-Lindenberg, A., Domes, G., Kirsch, P., & Heinrichs, M. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3044 · Cited by 1,688
The neuro-symphony of stress
Joëls, M., & Baram, T. Z. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2632 · Cited by 1,521
Oxytocin improves “mind-reading” in humans
Domes, G., Heinrichs, M., Michel, A., Berger, C., & Herpertz, S. C. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.07.015 · Cited by 1,298
Oxytocin shapes the neural circuitry of trust and trust adaptation in humans
Baumgartner, T., Heinrichs, M., Vonlanthen, A., Fischbacher, U., & Fehr, E. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.009 · Cited by 1,258

See all 1,059

Authors: Landgraf, R., & Neumann, I. D.
Affiliations: Max Planck Society (DE)
University of Regensburg (DE)
Corresponding author: Landgraf, Rainer
ORCID: Neumann, Inga D.
Venue: Frontiers in Neuroendocrinology
Publisher: Elsevier BV
Published: 2004-09
Volume: 25
Issue: 3-4
Pages: 150-176
ISSN: 0091-3022 (ISSN-L)
DOI: 10.1016/j.yfrne.2004.05.001
OpenAlex: W1996368170
Cited by: 1,059
References: 295
Citations by year: 2026: 24 · 2025: 25 · 2024: 38 · 2023: 38 · 2022: 48 · 2021: 52 · 2020: 61 · 2019: 47 · 2018: 54 · 2017: 59 · 2016: 60 · 2015: 54 · 2014: 61 · 2013: 66 · 2012: 61
FWCI: 43.49
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Frontiers in Neuroendocrinology (publishedVersion)
PubMed (publishedVersion)
Max Planck Institute for Plasma Physics (submittedVersion)
University of Regensburg Publication Server (University of Regensburg) (submittedVersion)
MPG.PuRe (Max Planck Society) (submittedVersion)
Topics: Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: vasopressin, oxytocin, neuropeptide release, dendritic release, neurosecretory cells, intracellular calcium stores, synaptic input, transcription factors, neuromodulation, neuroendocrine regulation, psychopathology
MeSH terms: Animals, Brain, Cell Communication, Humans, Nerve Net, Neurons, Oxytocin, Vasopressins, Feedback, Physiological

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 release within the brain: a dynamic concept of multiple and variable modes of neuropeptide communication

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