α‐Melanocyte‐Stimulating Hormone and Oxytocin: A Peptide Signalling Cascade in the Hypothalamus

Leptin activates anorexigenic POMC neurons through a neural network in the arcuate nucleus

Cowley, M. A., Smart, J. L., Rubinstein, M., Cerdán, M. G., Diano, S., Horvath, T. L., Cone, R. D., & Low, M. J. (2001) · Nature · doi:10.1038/35078085 · Cited by 2,356 · see citing works

Anatomy and regulation of the central melanocortin system

Cone, R. D. (2005) · Nature Neuroscience · doi:10.1038/nn1455 · Cited by 1,583 · see citing works

Localization of the melanocortin-4 receptor (MC4-R) in neuroendocrine and autonomic control circuits in the brain

Mountjoy, K. G., Mortrud, M. T., Low, M. J., Simerly, R. B., & Cone, R. D. (1994) · Molecular Endocrinology · doi:10.1210/mend.8.10.7854347 · Cited by 1,157 · 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

Leptin Increases Hypothalamic Pro-opiomelanocortin mRNA Expression in the Rostral Arcuate Nucleus

Schwartz, M. W., Seeley, R. J., Woods, S. C., Weigle, D. S., Campfield, L. A., Burn, P., & Baskin, D. G. (1997) · Diabetes · doi:10.2337/diab.46.12.2119 · Cited by 879 · see citing works

Agouti-related peptide–expressing neurons are mandatory for feeding

Gropp, E., Shanabrough, M., Borók, E., Xu, A. W., Janoschek, R., Buch, T., Plum, L., Balthasar, N., Hampel, B., Waisman, A., et al. (2005) · Nature Neuroscience · doi:10.1038/nn1548 · Cited by 800 · see citing works

Enhanced partner preference in a promiscuous species by manipulating the expression of a single gene.

Lim, M. M., Wang, Z., Olazábal, D. E., Ren, X., Terwilliger, E. F., & Young, L. J. (2004) · Nature · doi:10.1038/nature02539 · Cited by 628 · see citing works

The origin of the vasopressinergic and oxytocinergic innervation of the rat brain with special reference to the lateral septum

de Vries, G. J., & Buijs, R. M. (1983) · Brain Research · doi:10.1016/0006-8993(83)90855-7 · Cited by 524 · see citing works

Vasopressin and oxytocin receptors in the central nervous system

Tribollet, E., & Barberis, C. (1996) · Critical Reviews™ in Neurobiology · doi:10.1615/critrevneurobiol.v10.i1.60 · Cited by 399 · 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

Dendritic Release of Vasopressin and Oxytocin

Ludwig (1998) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1998.00279.x · Cited by 342 · see citing works

Evidence that paraventricular nucleus oxytocin neurons link hypothalamic leptin action to caudal brain stem nuclei controlling meal size

Blevins, J. E., Schwartz, M. W., & Baskin, D. G. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00604.2003 · Cited by 332 · see citing works

Central Administration of Glucagon-Like Peptide-1 Activates Hypothalamic Neuroendocrine Neurons in the Rat

Larsen, P. J., Tang‐Christensen, M., & Jessop, D. S. (1997) · Endocrinology · doi:10.1210/endo.138.10.5270 · Cited by 316 · see citing works

Cholecystokinin-mediated suppression of feeding involves the brainstem melanocortin system

Fan, W., Ellacott, K. L. J., Halatchev, I. G., Takahashi, K. A., Yu, P., & Cone, R. D. (2004) · Nature Neuroscience · doi:10.1038/nn1214 · Cited by 306 · see citing works

A role for the melanocortin 4 receptor in sexual function

der Ploeg, L. H. T. V., Martin, W. J., Howard, A. D., Nargund, R. P., Austin, C. P., Guan, X.-M., Drisko, J. E., Cashen, D. E., Sebhat, I. K., Patchett, A. A., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.172378699 · Cited by 303 · see citing works

Pro-opiomelanocortin processing in the hypothalamus: impact on melanocortin signalling and obesity

Pritchard, L. E., Turnbull, A. V., & White, A. E. (2002) · Journal of Endocrinology · doi:10.1677/joe.0.1720411 · Cited by 298 · see citing works

Oxytocin and an oxytocin agonist administered centrally decrease food intake in rats

Olson, B. R., Drutarosky, M. D., Chow, M.-S., Hruby, V. J., Stricker, E. M., & Verbalis, J. G. (1991) · Peptides · doi:10.1016/0196-9781(91)90176-p · Cited by 283 · see citing works

Anatomical Markers of Activity in Neuroendocrine Systems: Are we all ‘Fos‐ed out’?

Hoffman, G. E., & Lyo, D. (2002) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2002.00775.x · Cited by 242 · see citing works

Orexins (hypocretins) directly interact with neuropeptide Y, POMC and glucose‐responsive neurons to regulate Ca2+ signaling in a reciprocal manner to leptin: orexigenic neuronal pathways in the mediobasal hypothalamus

Muroya, S., Funahashi, H., Yamanaka, A., Kohno, D., Uramura, K., Nambu, T., Shibahara, M., Kuramochi, M., Takigawa, M., Yanagisawa, M., et al. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03255.x · Cited by 241 · see citing works

Species and individual differences in juvenile female alloparental care are associated with oxytocin receptor density in the striatum and the lateral septum

Olazábal, D. E., & Young, L. J. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.12.010 · Cited by 230 · see citing works

Microvascular specializations promoting rapid interstitial solute dispersion in nucleus tractus solitarius

Gross, P. M., Wall, K. M., Pang, J. J., Shaver, S. W., & Wainman, D. S. (1990) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1990.259.6.r1131 · Cited by 206 · see citing works

Proopiomelanocortin Neurons in Nucleus Tractus Solitarius Are Activated by Visceral Afferents: Regulation by Cholecystokinin and Opioids

Appleyard, S. M., Bailey, T. W., Doyle, M. W., Jin, Y., Smart, J. L., Low, M. J., & Andresen, M. C. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4177-04.2005 · Cited by 195 · see citing works

α-Melanocyte-Stimulating Hormone Stimulates Oxytocin Release from the Dendrites of Hypothalamic Neurons While Inhibiting Oxytocin Release from Their Terminals in the Neurohypophysis

Sabatier, N., Caquineau, C., Dayanithi, G., Bull, P., Douglas, A. J., Guan, X. M. M., Jiang, M., Van der Ploeg, L., & Leng, G. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10351.2003 · Cited by 190 · see citing works

Cholecystokinin and gastric distension activate oxytocinergic cells in rat hypothalamus

Renaud, L. P., Tang, M., McCann, M. J., Stricker, E. M., & Verbalis, J. G. (1987) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1987.253.4.r661 · Cited by 190 · see citing works

Dendritically Released Peptides Act as Retrograde Modulators of Afferent Excitation in the Supraoptic Nucleus In Vitro

Kombian, S. B., Mouginot, D., & Pittman, Q. J. (1997) · Neuron · doi:10.1016/s0896-6273(00)80971-x · Cited by 186 · see citing works

Brain oxytocin receptor antagonism blunts the effects of anorexigenic treatments in rats: evidence for central oxytocin inhibition of food intake

OLSON, B. R., DRUTAROSKY, M. D., STRICKER, E. M., & VERBALIS, J. G. (1991) · Endocrinology · doi:10.1210/endo-129-2-785 · Cited by 180 · see citing works

The role of oxytocin and the paraventricular nucleus in the sexual behaviour of male mammals

Argiolas, A., & Melis, M. R. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.08.019 · Cited by 177 · see citing works

Oxytocin and vasopressin secretion in response to stimuli producing learned taste aversions in rats.

Verbalis, J. G., McHale, C. M., Gardiner, T. W., & Stricker, E. M. (1986) · Behavioral Neuroscience · doi:10.1037//0735-7044.100.4.466 · Cited by 171 · see citing works

Oxytocin innervation of caudal brainstem nuclei activated by cholecystokinin

Blevins, J. E., Eakin, T. J., Murphy, J. A., Schwartz, M. W., & Baskin, D. G. (2003) · Brain Research · doi:10.1016/j.brainres.2003.08.036 · Cited by 164 · see citing works

Neuropeptides and sexual behaviour

Argiolas, A. (1999) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(99)00068-8 · Cited by 148 · see citing works

The distribution and cells of origin of ACTH(1–39)-stained varicosities in the paraventricular and supraoptic nuclei

Sawchenko, P. E., Swanson, L. W., & Joseph, S. (1982) · Brain Research · doi:10.1016/0006-8993(82)90280-3 · Cited by 146 · see citing works

Oxytocin and vasopressin secretion in response to stimuli producing learned taste aversions in rats.

Verbalis, J. G., McHale, C. M., Gardiner, T. W., et al. (1986) · Behavioral Neuroscience · doi:10.1037/0735-7044.100.4.466 · Cited by 146 · see citing works

Dendritically released transmitters cooperate via autocrine and retrograde actions to inhibit afferent excitation in rat brain

Hirasawa, M., Schwab, Y., Natah, S. S., Hillard, C. J., Mackie, K., Sharkey, K. A., & Pittman, Q. J. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.066159 · Cited by 143 · see citing works

Oxytocin in the central nervous system and sexual behaviour in male rats

Hughes, A. M., Everitt, B. J., Lightman, S. L., & Todd, K. (1987) · Brain Research · doi:10.1016/0006-8993(87)91333-3 · Cited by 140 · see citing works

Divergent Regulation of Proopiomelanocortin Neurons by Leptin in the Nucleus of the Solitary Tract and in the Arcuate Hypothalamic Nucleus

Huo, L., Grill, H. J., & Bjørbæk, C. (2006) · Diabetes · doi:10.2337/diabetes.55.03.06.db05-1143 · Cited by 128 · see citing works

Role of melanocortins in the central control of feeding

Vergoni, A. V., & Bertolini, A. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00538-0 · Cited by 125 · see citing works

PT‐141: A Melanocortin Agonist for the Treatment of Sexual Dysfunction

Molinoff, P. B., Shadiack, A. M., Earle, D. C., Diamond, L. E., & Quon, C. Y. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb03167.x · Cited by 106 · see citing works

Oxytocin and Male Reproductive Function

Ivell, R., Balvers, M., Rust, W., Bathgate, R. A. D., & Einspanier, A. (1997) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-5913-9_47 · Cited by 97 · see citing works

Electrical stimulations of perifused magnocellular nuclei in vitro elicit Ca2+-dependent, tetrodotoxin-insensitive release of oxytocin and vasopressin

Scala-Guenot, D. D., Strosser, M. T., & Richard, P. (1987) · Neuroscience Letters · doi:10.1016/0304-3940(87)90717-8 · Cited by 87 · see citing works

Activation of melanocortin MC4 receptors increases erectile activity in rats ex copula

Martin, W. J., McGowan, E., Cashen, D. E., Gantert, L. T., Drisko, J. E., Hom, G. J., Nargund, R. P., Sebhat, I. K., Howard, A. D., der Ploeg, L. H. T. V., et al. (2002) · European Journal of Pharmacology · doi:10.1016/s0014-2999(02)02479-2 · Cited by 83 · see citing works

Discovery that a melanocortin regulates sexual functions in male and female humans

Hadley, M. E. (2005) · Peptides · doi:10.1016/j.peptides.2005.01.023 · Cited by 78 · see citing works

N-acetylation of hypothalamic α-melanocyte-stimulating hormone and regulation by leptin

Guo, L., Münzberg, H., Stuart, R. C., Nillni, E. A., & Bjørbæk, C. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0403165101 · Cited by 71 · see citing works

Leptin Regulates Growth Hormone-Releasing Factor, Somatostatin, and α-Melanocyte-Stimulating Hormone But Not Neuropeptide Y Release in Rat HypothalamusIn Vivo: Relation with Growth Hormone Secretion

Watanobe, H., & Habu, S. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-14-06265.2002 · Cited by 70 · see citing works

β‐Endorphin Cells in the Arcuate Nucleus: Projections to the Supraoptic Nucleus and Changes in Expression During Pregnancy and Parturition

Douglas, A. J., Bicknell, R. J., Leng, G., Russell, J. A., & Meddle, S. (2002) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2002.00837.x · Cited by 65 · see citing works

Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatment

Assereto, S., Stringara, S., Sotgia, F., Bonuccelli, G., Broccolini, A., Pedemonte, M., Traverso, M., Biancheri, R., Zara, F., Bruno, C., et al. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00434.2005 · Cited by 65 · see citing works

Proopiomelanocortin-Derived Peptides in Rat Cerebrospinal Fluid and Hypothalamic Extracts: Evidence that Secretion Is Regulated with Respect to Energy Balance

Pritchard, L. E., Oliver, R. L., McLoughlin, J. D., Birtles, S., Lawrence, C. B., Turnbull, A. V., & White, A. E. (2003) · Endocrinology · doi:10.1210/en.2002-220866 · Cited by 65 · see citing works

Regulation of Oxytocin Secretion

Leng, G., Caquineau, C., & Sabatier, N. (2005) · Vitamins and hormones · doi:10.1016/s0083-6729(05)71002-5 · Cited by 64 · see citing works

Central Oxytocin Mediates Inhibition of Sodium Appetite by Naloxone in Hypovolemic Rats

Blackburn, R. E., Stricker, E. M., & Verbalis, J. G. (2008) · Neuroendocrinology · doi:10.1159/000126236 · Cited by 63 · see citing works

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 · see citing works

Afferents originating from the dorsal penile nerve excite oxytocin cells in the hypothalamic paraventricular nucleus of the rat

Yanagimoto, M., Honda, K., Goto, Y., & Negoro, H. (1996) · Brain Research · doi:10.1016/0006-8993(96)00800-1 · Cited by 58 · see citing works

Role of α-MSH in the regulation of consummatory behavior: immunohistochemical evidence

Olszewski, P. K., Wirth, M. M., Shaw, T. J., Grace, M. K., Billington, C. J., Giraudo, S. Q., & Levine, A. S. (2001) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2001.281.2.r673 · Cited by 55 · see citing works

Thapsigargin‐induced mobilization of dendritic dense‐cored vesicles in rat supraoptic neurons

Tobin, V. A., Hurst, G., Norrie, L., Rio, F. P. D., Bull, P. M., & Ludwig, M. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03388.x · Cited by 53 · see citing works

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 · see citing works

Early response genes as markers of neuronal activity and growth factor action.

Sagar, S. M., & Sharp, F. R. (1993) · PubMed · Cited by 50 · see citing works

Dehydration anorexia is attenuated in oxytocin-deficient mice

Rinaman, L., Vollmer, R. R., Karam, J. R., Phillips, D., Li, X., & Amico, J. A. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00860.2004 · Cited by 48 · see citing works

Sexual Motivation Promotes Oxytocin Secretion in Male Rats

Hillegaart, V., Alster, P., Uvnäs‐Moberg, K., & Ahlénius, S. (1998) · Peptides · doi:10.1016/s0196-9781(97)00250-7 · Cited by 43 · see citing works

Identification, localization and functional in vitro and in vivo activity of oxytocin receptor in the rat penis

ZHANG, X. H., Filippi, S., Vignozzi, L., Morelli, A., Mancina, R., Luconi, M., Donati, S., Marini, M., Vannelli, G. B., Forti, G., et al. (2005) · Journal of Endocrinology · doi:10.1677/joe.1.05885 · Cited by 42 · see citing works

Differential regulation of somatodendritic and nerve terminal dopamine release by serotonergic innervation of substantia nigra

Cobb, W. S., & Abercrombie, E. D. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01546.x · Cited by 39 · see citing works

Effect of feeding on Fos protein expression in sheep hypothalamus with special reference to the supraoptic and paraventricular nuclei: an immunohistochemical study

Chaillou, É., Baumont, R., Tramu, G., & Tillet, Y. (2000) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2000.01338.x · Cited by 38 · see citing works

Oxytocin Released from Magnocellular Dendrites

Sabatier, N., Caquineau, C., Douglas, A. J., & Leng, G. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb03183.x · Cited by 34 · see citing works

Quantitative Expression Analysis of Genes Regulated by Both Obesity and Leptin Reveals a Regulatory Loop between Leptin and Pituitary-derived ACTH

Renz, M. E., Tomlinson, E., Hultgren, B., Levin, N., Gu, Q., Shimkets, R. A., Lewin, D. A., & Stewart, T. A. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.14.10429 · Cited by 29 · see citing works

Characterisation of the Pro Opiocortin Family of Peptides in Human Cerebrospinal Fluid

McLoughlin, L., Lowry, P. J., Ratter, S. J., Hope, J. E., BESSER, G. M., & REES, L. H. (2008) · Neuroendocrinology · doi:10.1159/000123160 · Cited by 28 · see citing works

Excitation of oxytocin cells in the hypothalamic supraoptic nucleus by electrical stimulation of the dorsal penile nerve and tactile stimulation of the penis in the rat

Honda, K., Yanagimoto, M., Negoro, H., Narita, K., Murata, T., & Higuchi, T. (1999) · Brain Research Bulletin · doi:10.1016/s0361-9230(98)00180-4 · Cited by 27 · see citing works

Neuronal Activation of the Hypothalamic Magnocellular System in Response to Oropharyngeal Stimuli in the Rat

Naïmi, N., Rivest, S., Racotta, I. S., & Richard, D. (1997) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1997.00573.x · Cited by 24 · see citing works

Pro-opiocortin peptides in rat cerebrospinal fluid

Jackson, S., Kiser, S., Corder, R., & Lowry, P. J. (1985) · Regulatory Peptides · doi:10.1016/0167-0115(85)90076-x · Cited by 19 · see citing works

Long-term retention of 207Bi in the human body after injection of 206Bi.

Wc, B., Fh, C., & Lb, B. (1985) · PubMed · Cited by 6 · see citing works

[Immunocytologic analysis, in rat hypothalamus, of neurons producing peptides related to endorphin, ACTH, MSH and beta-LPH. Comparison with other peptidergic and monoaminergic neurons].

Bloch, B., Lenys, D., Gouget, A., FELLMANN, D., & Bugnon, C. (1979) · PubMed · Cited by 2 · see citing works

Oxytocin and the Neural Mechanisms Regulating Social Cognition and Affiliative Behavior

Ross, H. E., & Young, L. J. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.05.004 · Cited by 856 · see citing works

Exogenous and evoked oxytocin restores social behavior in the <i>Cntnap2</i> mouse model of autism

Peñagarikano, O., Lázaro, M. T., Lu, X.-H., Gordon, A., Dong, H., Lam, H. A., Peles, E., Maidment, N. T., Murphy, N. P., Yang, X. W., et al. (2015) · Science Translational Medicine · doi:10.1126/scitranslmed.3010257 · Cited by 378 · see citing works

Nesfatin-1-Regulated Oxytocinergic Signaling in the Paraventricular Nucleus Causes Anorexia through a Leptin-Independent Melanocortin Pathway

Maejima, Y., Sedbazar, U., Suyama, S., Kohno, D., Onaka, T., Takano, E., Yoshida, N., Koike, M., Uchiyama, Y., Fujiwara, K., et al. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.09.002 · Cited by 317 · see citing works

Functional consequences of neuropeptide and small-molecule co-transmission

Nusbaum, M. P., Blitz, D. M., & Marder, E. E. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.56 · Cited by 304 · see citing works

The contribution of brain reward circuits to the obesity epidemic

Stice, E., Figlewicz, D. P., Gosnell, B. A., Levine, A. S., & Pratt, W. E. (2013) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.12.001 · Cited by 274 · see citing works

The Role of Oxytocin in Psychiatric Disorders: A Review of Biological and Therapeutic Research Findings

Cochran, D. M., Fallon, D., Hill, M., & Frazier, J. A. (2013) · Harvard Review of Psychiatry · doi:10.1097/hrp.0b013e3182a75b7d · Cited by 267 · see citing works

Nesfatin-1 Neurons in Paraventricular and Supraoptic Nuclei of the Rat Hypothalamus Coexpress Oxytocin and Vasopressin and Are Activated by Refeeding

Kohno, D., Nakata, M., Maejima, Y., Shimizu, H., Sedbazar, U., Yoshida, N., Dezaki, K., Onaka, T., Mori, M., & Yada, T. (2007) · Endocrinology · doi:10.1210/en.2007-1276 · Cited by 258 · see citing works

Cross-talk among oxytocin and arginine-vasopressin receptors: Relevance for basic and clinical studies of the brain and periphery

Song, Z., & Albers, H. E. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.10.004 · Cited by 244 · see citing works

Oxytocin Deficiency Mediates Hyperphagic Obesity of Sim1 Haploinsufficient Mice

Kublaoui, B. M., Gemelli, T., Tolson, K. P., Wang, Y., & Zinn, A. R. (2008) · Molecular Endocrinology · doi:10.1210/me.2008-0067 · Cited by 239 · see citing works

The oxytocin system in drug discovery for autism: Animal models and novel therapeutic strategies

Modi, M. E., & Young, L. J. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.12.010 · Cited by 218 · see citing works

Species, sex and individual differences in the vasotocin/vasopressin system: relationship to neurochemical signaling in the social behavior neural network

Albers, H. E. (2015) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.07.001 · Cited by 200 · see citing works

Helping oxytocin deliver: considerations in the development of oxytocin-based therapeutics for brain disorders

MacDonald, K., & Feifel, D. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00035 · Cited by 181 · see citing works

Reward systems and food intake: role of opioids

Gosnell, B. A., & Levine, A. S. (2009) · International Journal of Obesity · doi:10.1038/ijo.2009.73 · Cited by 173 · see citing works

Nesfatin-1, a unique regulatory neuropeptide of the brain

Pałasz, A., Krzystanek, M., Worthington, J. J., Czajkowska, B. I., Kostro, K., Wiaderkiewicz, R., & Bajor, G. (2012) · Neuropeptides · doi:10.1016/j.npep.2011.12.002 · Cited by 126 · see citing works

Oxytocin Secretion Is Associated with Severity of Disordered Eating Psychopathology and Insular Cortex Hypoactivation in Anorexia Nervosa

Lawson, E. A., Holsen, L. M., Santin, M., Meenaghan, E. M., Eddy, K. T., Becker, A. E., Herzog, D. B., Goldstein, J. M., & Klibanski, A. (2012) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2012-1702 · Cited by 121 · see citing works

Oxytocin and appetite

LENG, G., ONAKA, T., CAQUINEAU, C., SABATIER, N., TOBIN, V, & TAKAYANAGI, Y. (2008) · Progress in brain research · doi:10.1016/s0079-6123(08)00413-5 · Cited by 112 · see citing works

Neuroendocrine mechanisms of change in food intake during pregnancy: A potential role for brain oxytocin

Douglas, A. J., Johnstone, L. E., & Leng, G. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.04.012 · Cited by 108 · see citing works

The role of oxytocin in mating and pregnancy

Borrow, A. P., & Cameron, N. M. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.11.001 · Cited by 101 · see citing works

Role of oxytocin in the control of stress and food intake

Onaka, T., & Takayanagi, Y. (2019) · Journal of Neuroendocrinology · doi:10.1111/jne.12700 · Cited by 98 · see citing works

Oxytocin – The Sweet Hormone?

Leng, G., & Sabatier, N. (2017) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2017.02.007 · Cited by 89 · see citing works

Rebalancing the Addicted Brain: Oxytocin Interference with the Neural Substrates of Addiction

Bowen, M. T., & Neumann, I. D. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.10.003 · Cited by 83 · see citing works

Somato‐dendritic vasopressin and oxytocin secretion in endocrine and autonomic regulation

Brown, C. H., Ludwig, M., Tasker, J. G., & Stern, J. E. (2020) · Journal of Neuroendocrinology · doi:10.1111/jne.12856 · Cited by 65 · see citing works

CCK-8S activates c-Fos in a dose-dependent manner in nesfatin-1 immunoreactive neurons in the paraventricular nucleus of the hypothalamus and in the nucleus of the solitary tract of the brainstem

Noetzel, S., Stengel, A., Inhoff, T., Goebel, M., Wisser, A.-S., Bannert, N., Wiedenmann, B. J., Klapp, B. F., Taché, Y., Mönnikes, H., et al. (2009) · Regulatory Peptides · doi:10.1016/j.regpep.2009.06.009 · Cited by 67 · see citing works

FMRFamide-Like Neuropeptides and Mechanosensory Touch Receptor Neurons Regulate Male Sexual Turning Behavior inCaenorhabditis elegans

Liu, T., Kim, K., Li, C., & Barr, M. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1405-07.2007 · Cited by 67 · see citing works

Targets for Drug Therapy for Autism Spectrum Disorder: Challenges and Future Directions

Lacivita, E., Perrone, R., Margari, L., & Leopoldo, M. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b00965 · Cited by 66 · see citing works

Targeting the Oxytocin System: New Pharmacotherapeutic Approaches

Gulliver, D. W., Werry, E. L., Reekie, T. A., Katte, T. A., Jorgensen, W. T., & Kassiou, M. (2018) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2018.11.001 · Cited by 63 · see citing works

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 · see citing works

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

Salmina, A. B., Lopatina, O., Ekimova, M. V., Mikhutkina, S. V., & Higashida, H. (2010) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2010.01970.x · Cited by 36 · see citing works

Neonatal melanocortin receptor agonist treatment reduces play fighting and promotes adult attachment in prairie voles in a sex-dependent manner

Barrett, C. E., Modi, M. E., Zhang, B. C., Walum, H., Inoue, K., & Young, L. J. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.05.041 · Cited by 34 · see citing works

Systemic Leptin Increases the Electrical Activity of Supraoptic Nucleus Oxytocin Neurones in Virgin and Late Pregnant Rats

Velmurugan, S., Russell, J. A., & Leng, G. (2013) · Journal of Neuroendocrinology · doi:10.1111/jne.12016 · Cited by 29 · see citing works

Neurotransmitter regulation of c-fos and vasopressin gene expression in the rat supraoptic nucleus

Kawasaki, M., Ponzio, T. A., Yue, C., Fields, R. L., & Gainer, H. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.05.019 · Cited by 29 · see citing works

Attenuated hypothalamic responses to α‐melanocyte stimulating hormone during pregnancy in the rat

Ladyman, S. R., Augustine, R. A., Scherf, E., Phillipps, H. R., Brown, C. H., & Grattan, D. R. (2015) · The Journal of Physiology · doi:10.1113/jp271605 · Cited by 26 · see citing works

Endogenous modulators of synaptic transmission: cannabinoid regulation in the supraoptic nucleus

MCDONALD, N., Kuzmiski, J. B., Naderi, N., Schwab, Y., & Pittman, Q. J. (2008) · Progress in brain research · doi:10.1016/s0079-6123(08)00412-3 · Cited by 23 · see citing works

Anxiolytic drug discovery: What are the novel approaches and how can we improve them?

Stewart, A. M., & Kalueff, A. V. (2014) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2014.857309 · Cited by 22 · see citing works

Effects of Cholecystokinin in the Supraoptic Nucleus and Paraventricular Nucleus are Negatively Modulated by Leptin in 24‐h Fasted Lean Male Rats

Caquineau, C., Douglas, A. J., & Leng, G. (2010) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2010.01982.x · Cited by 19 · see citing works

The promiscuity of the oxytocin–vasopressin systems and their involvement in autism spectrum disorder

Borie, A. M., Theofanopoulou, C., & Andari, E. (2021) · Handbook of clinical neurology · doi:10.1016/b978-0-12-819973-2.00009-5 · Cited by 18 · see citing works

Ventromedial hypothalamic nucleus in regulation of stress-induced gastric mucosal injury in rats

Sun, H., Zhao, P., Liu, W., Li, L., Hong-bin, A., & Ma, X. (2018) · Scientific Reports · doi:10.1038/s41598-018-28456-0 · Cited by 17 · see citing works

The Role of the Oxytocin/Arginine Vasopressin System in Animal Models of Autism Spectrum Disorder

Zhang, R., Xu, X., Zhang, H.-F., Han, S., & Han, J. (2017) · Advances in anatomy, embryology and cell biology · doi:10.1007/978-3-319-52498-6_8 · Cited by 16 · see citing works

Leu8 and Pro8 oxytocin agonism differs across human, macaque, and marmoset vasopressin 1a receptors

Mustoe, A. C., Schulte, N. A., Taylor, J. H., French, J. A., & Toews, M. L. (2019) · Scientific Reports · doi:10.1038/s41598-019-52024-9 · Cited by 15 · see citing works

Detection of neuropeptides in vivo and open questions for current and upcoming fluorescent sensors for neuropeptides

Inutsuka, A., Ino, D., & Onaka, T. (2020) · Peptides · doi:10.1016/j.peptides.2020.170456 · Cited by 15 · see citing works

Mate Selection, Sexual Orientation, and Pair Bonding

Balthazart, J., & Young, L. J. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397175-3.00048-x · Cited by 12 · see citing works

Annexin A1 Complex Mediates Oxytocin Vesicle Transport

Makani, V. S., Rukhsana Sultana, A., Sie, K. S., Orjiako, D., Tatangelo, M. D., Dowling, A., Cai, J., Pierce, W. M. J., Butterfield, D. A., Hill, J. W., et al. (2013) · Journal of Neuroendocrinology · doi:10.1111/jne.12112 · Cited by 12 · see citing works

The central effects of alpha-melanocyte stimulating hormone (α-MSH) in chicks involve changes in gene expression of neuropeptide Y and other factors in distinct hypothalamic nuclei

Delp, M. S., Cline, M. A., & Gilbert, E. R. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.04.064 · Cited by 11 · see citing works

Oestrogen-dependent hypothalamic oxytocin expression with changes in feeding and body weight in female rats

Nishimura, K., Yoshino, K., Ikeda, N., Baba, K., Sanada, K., Akiyama, Y., Nishimura, H., Tanaka, K., Sonoda, S., Ueno, H., et al. (2022) · Communications Biology · doi:10.1038/s42003-022-03889-6 · Cited by 11 · see citing works

Elevated Neuropeptides in Dry Eye Disease and Their Clinical Correlations

Yang, T., Zhou, Y., Ma, B., Duan, H., Liu, R., Zhao, L., & Qi, H. (2022) · Cornea · doi:10.1097/ico.0000000000003069 · Cited by 9 · see citing works

Dendritic osmosensors modulate activity-induced calcium influx in oxytocinergic magnocellular neurons of the mouse PVN

Sheng, W., Harden, S. W., Tan, Y., Krause, E. G., & Frazier, C. J. (2021) · eLife · doi:10.7554/elife.63486 · Cited by 7 · see citing works

Oxytocin treatment rescues irritability-like behavior in Cc2d1a conditional knockout mice

Cheng, K., Hung, Y.-C., Ling, P., & Hsu, K. (2024) · Neuropsychopharmacology · doi:10.1038/s41386-024-01920-4 · Cited by 5 · see citing works

Melanocortin agonism in a social context selectively activates nucleus accumbens in an oxytocin-dependent manner

Ford, C. L., McDonough, A. A., Horie, K., & Young, L. J. (2024) · Neuropharmacology · doi:10.1016/j.neuropharm.2024.109848 · Cited by 4 · see citing works

Rol Modulador de la Oxitocina en la Interacción Social y el Estrés Social

Flórez-Acevedo, S., & Cárdenas, F. P. (2017) · Universitas Psychologica · doi:10.11144/javeriana.upsy15-5.rmoi · Cited by 1 · see citing works

The neurohypophysis

Ball, S. G. (2011) · doi:10.1093/med/9780199235292.003.2018 · Cited by 1 · see citing works

Genetic modulation of oxytocin's effects in social functioning.

Huang, H., & Papaleo, F. (2015) · PubMed Central · doi:10.3978/j.issn.2305-5839.2015.09.36

Oxytocin and Appetite

Caquineau, C., & Leng, G. (2011) · Springer eBooks · doi:10.1007/978-0-387-92271-3_20

Oxytocin receptors in neurodevelopmental disorders : innovative approaches for the quantification of sopramolecular receptor complexes

Santini, F. (2021) · theses.fr (ABES) · doi:10.70675/c00b0393z4da7z42caz9cd8z609df0efd23c

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

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

BindingDB Entry 50000440: Targets for Drug Therapy for Autism Spectrum Disorder: Challenges and Future Directions.

BindingDB (2019) · UC San Diego · doi:10.7270/q2377c5d

α-Melanocyte-Stimulating Hormone Stimulates Oxytocin Release from the Dendrites of Hypothalamic Neurons While Inhibiting Oxytocin Release from Their Terminals in the Neurohypophysis

Sabatier, N., Caquineau, C., Dayanithi, G., Bull, P., Douglas, A. J., Guan, X. M. M., Jiang, M., Van der Ploeg, L., & Leng, G. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10351.2003 · Cited by 190 · see citing works

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 55 · see citing works

�-Melanocyte-Stimulating Hormone Stimulates Oxytocin Release from the Dendrites of Hypothalamic Neurons While Inhibiting Oxytocin Release from Their Terminals

Neurohypophysis, I. T., Sabatier, N., Caquineau, C., Dayanithi, G., Bull, P. M., Douglas, A. J., Guan, X. M. M., Jiang, M., der Ploeg, L. H. T. V., & Leng, G. (2013)

Oxytocin Released from Magnocellular Dendrites

Sabatier, N., Caquineau, C., Douglas, A. J., & Leng, G. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb03183.x · Cited by 34 · see citing works

Multiple signalling modalities mediated by dendritic exocytosis of oxytocin and vasopressin

Ludwig, M., & Stern, J. E. (2015) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2014.0182 · Cited by 66 · see citing works