Interplay between Oxytocin and Sensory Systems in the Orchestration of Socio-Emotional Behaviors
Open accessAbstract
The neuropeptide oxytocin (OT) attracts the interest of neuroscientists, psychologists, and psychiatrists due to its capacity to modulate emotional and social behavior. Although much has been published on the effects of OT on brain regions and mechanisms at the core of these processes, its role in sensory processing, so important for detecting social context with sufficient accuracy and sensitivity, has been much less studied. In the present review, we summarize evidence for OT modulation of sensory processing and, conversely, effects of sensory input on endogenous OT signaling. We concentrate on mammals, aiming to provide a systematic analysis of the current knowledge on this reciprocal regulation and the role it may play in social and emotional behaviors.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
PVN oxytocin cells receive projections from many areas of the brain.
“PVN oxytocin cells receive projections from many areas of the brain”
From Neural circuitry for maternal oxytocin release induced by infant cries (2023) · cites this paper as [10]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
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
The Retinal Pigment Epithelium in Visual Function
Strauss, O. (2005) · Physiological Reviews · doi:10.1152/physrev.00021.2004 · Cited by 2,828 · see citing works
Hypothalamic integration: organization of the paraventricular and supraoptic nuclei
Swanson, L. W., & Sawchenko, P. E. (1983) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.06.030183.001413 · Cited by 1,991 · see citing works
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 · see citing works
Oxytocin Modulates Neural Circuitry for Social Cognition and Fear in Humans
Kirsch, P., Esslinger, C., Chen, Q., Mier, D., Lis, S., Siddhanti, S., Gruppe, H., Mattay, V. S., Gallhofer, B., & Meyer-Lindenberg, A. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3984-05.2005 · Cited by 1,639 · see citing works
Social effects of oxytocin in humans: context and person matter
Bartz, J. A., Zaki, J., Bolger, N., & Ochsner, K. N. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.05.002 · Cited by 1,572 · cited 2× · see citing works
“of OT can stimulate eye contact, increase face recognition and potentiate communicative behaviors (Bartz et al., 2011).”
Swanson, L. W., & Kuypers, H. G. J. M. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901940306 · Cited by 1,413 · see citing works
Social reward requires coordinated activity of nucleus accumbens oxytocin and serotonin
Dölen, G., Darvishzadeh, A., Huang, K. W., & Malenka, R. C. (2013) · Nature · doi:10.1038/nature12518 · Cited by 1,161 · see citing works
Sensory Processing in Autism: A Review of Neurophysiologic Findings
MARCO, E. J., HINKLEY, L. B. N., HILL, S. S., & NAGARAJAN, S. S. (2011) · Pediatric Research · doi:10.1203/pdr.0b013e3182130c54 · Cited by 1,112 · see citing works
Landgraf, R., & Neumann, I. D. (2004) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2004.05.001 · Cited by 1,059 · see citing works
Energy limitation as a selective pressure on the evolution of sensory systems
Niven, J. E., & Laughlin, S. B. (2008) · Journal of Experimental Biology · doi:10.1242/jeb.017574 · Cited by 1,056 · see citing works
Evoked axonal oxytocin release in the central amygdala attenuates fear response
Knobloch, H. S., Charlet, A., Hoffmann, L. C., Eliava, M., Khrulev, S., Cetin, A. H., Osten, P., Schwarz, M. K., Seeburg, P. H., Stoop, R., et al. (2012) · Neuron · doi:10.1016/j.neuron.2011.11.030 · Cited by 1,049 · see citing works
Self-citationInsel, T. R. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.005 · Cited by 1,044 · see citing works
Oxytocin: The Great Facilitator of Life
Lee, H.-J., Macbeth, A. H., Pagani, J., & Young, W. S. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.04.001 · Cited by 1,037 · see citing works
Paraventricular Nucleus:A Site for the Integration of Neuroendocrine and Autonomic Mechanisms
Swanson, L. W., & Sawchenko, P. E. (2008) · Neuroendocrinology · doi:10.1159/000123111 · Cited by 1,001 · see citing works
Deconstruction of a neural circuit for hunger
Atasoy, D., Betley, J. N., Su, H. H., & Sternson, S. M. (2012) · Nature · doi:10.1038/nature11270 · Cited by 969 · see citing works
Megı́as, M., Emri, Z., Freund, T. F., & Gulyás, A. I. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00496-6 · Cited by 950 · 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
The antidepressant fluoxetine restores plasticity in the adult visual cortex
Vetencourt, J. F. M., Sale, A., Viegi, A., Baroncelli, L., De Pasquale, R., F. O'Leary, O., Castrén, E., & Maffei, L. (2008) · Science · doi:10.1126/science.1150516 · Cited by 890 · see citing works
The neuroscience of placebo effects: connecting context, learning and health
Wager, T. D., & Atlas, L. Y. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3976 · Cited by 844 · see citing works
Pervasive social deficits, but normal parturition, in oxytocin receptor-deficient mice
Takayanagi, Y., Yoshida, M., Bielsky, I. F., Ross, H. E., Kawamata, M., Onaka, T., Yanagisawa, T., Kimura, T., Matzuk, M. M., Young, L. J., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505312102 · Cited by 806 · see citing works
Vasopressin and Oxytocin Excite Distinct Neuronal Populations in the Central Amygdala
Huber, D., Veinante, P., & Stoop, R. (2005) · Science · doi:10.1126/science.1105636 · Cited by 804 · see citing works
Self-citationOxytocin-gaze positive loop and the coevolution of human-dog bonds
Nagasawa, M., Mitsui, S., En, S., Ohtani, N., Ohta, M., Sakuma, Y., Onaka, T., Mogi, K., & Kikusui, T. (2015) · Science · doi:10.1126/science.1261022 · Cited by 753 · see citing works
Oxytocin enables maternal behaviour by balancing cortical inhibition
Marlin, B. J., Mitre, M., D’amour, J. A., Chao, M. V., & Froemke, R. C. (2015) · Nature · doi:10.1038/nature14402 · Cited by 744 · see citing works
Refinement of odor molecule tuning by dendrodendritic synaptic inhibition in the olfactory bulb.
Yokoi, M., Mori, K., & Nakanishi, S. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.8.3371 · Cited by 614 · see citing works
Oxytocin-Mediated GABA Inhibition During Delivery Attenuates Autism Pathogenesis in Rodent Offspring
Tyzio, R., Nardou, R., Ferrari, D. C., Tsintsadze, T., Shahrokhi, A., Eftekhari, S., Khalilov, I., Tsintsadze, V., Brouchoud, C., Chazal, G., et al. (2014) · Science · doi:10.1126/science.1247190 · Cited by 601 · see citing works
Map Plasticity in Somatosensory Cortex
Feldman, D. E., & Brecht, M. (2005) · Science · doi:10.1126/science.1115807 · Cited by 587 · see citing works
Gating of social reward by oxytocin in the ventral tegmental area
Hung, L. W., Neuner, S., Polepalli, J. S., Beier, K. T., Wright, M., Walsh, J. J., Lewis, E. M., Luo, L., Deisseroth, K., Dölen, G., et al. (2017) · Science · doi:10.1126/science.aan4994 · Cited by 578 · see citing works
Taste buds: cells, signals and synapses
Roper, S. D., & Chaudhari, N. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.68 · Cited by 575 · see citing works
GABA: A dominant neurotransmitter in the hypothalamus
Decavel, C., & van den Pol, A. N. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903020423 · Cited by 571 · see citing works
Mammalian social odours: attraction and individual recognition
Brennan, P., & Kendrick, K. M. (2006) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2006.1931 · Cited by 510 · see citing works
Neuromodulation by Oxytocin and Vasopressin
Stoop, R. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.025 · Cited by 506 · see citing works
Self-citationMolecular interrogation of hypothalamic organization reveals distinct dopamine neuronal subtypes
Romanov, R. A., Zeisel, A., Bakker, J., Girach, F., Hellysaz, A., Tomer, R., Alpár, A., Mulder, J., Clotman, F., Keimpema, E., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4462 · Cited by 502 · see citing works
Tyzio, R., Cossart, R., Khalilov, I., Minlebaev, M., Hübner, C. A., Represa, A., Ben-Ari, Y., & Khazipov, R. (2006) · Science · doi:10.1126/science.1133212 · Cited by 485 · see citing works
Oxytocin in general anxiety and social fear: a translational approach
Neumann, I. D., & Slattery, D. A. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.06.004 · Cited by 468 · see citing works
Overlapping activity in anterior insula during interoception and emotional experience
Zaki, J., Davis, J. I., & Ochsner, K. N. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.05.012 · Cited by 462 · see citing works
Elucidating an Affective Pain Circuit that Creates a Threat Memory
Han, S., Soleiman, M. T., Soden, M. E., Zweifel, L. S., & Palmiter, R. D. (2015) · Cell · doi:10.1016/j.cell.2015.05.057 · Cited by 447 · see citing works
A neural basis for melanocortin-4 receptor–regulated appetite
Garfield, A. S., Li, C., Madara, J. C., Shah, B. P., Webber, E. S., Steger, J. S., Campbell, J. N., Gavrilova, O., Lee, C. E., Olson, D. P., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4011 · Cited by 438 · see citing works
Oxytocin Attenuates Affective Evaluations of Conditioned Faces and Amygdala Activity
Petrovic, P., Kalisch, R., Singer, T., & Dolan, R. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4572-07.2008 · Cited by 424 · cited 1× · see citing works
“have emerged during evolution (Hodos and Butler, 1997; Kaas, 1989, 2008; Niven and Laughlin, 2008) and a number of recent break-through studies reported modulatory effects of OT visual and auditory signals in different orders of mammals (Domes et al., 2013; Freeman and Young, 2016; Kirsch et al., 2005; Marlin et al.,…”
Eliava, M., Melchior, M., Knobloch-Bollmann, H. S., Wahis, J., da Silva Gouveia, M., Tang, Y., Ciobanu, A. C., Triana del Rio, R., Roth, L. C., Althammer, F., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.041 · Cited by 409 · see citing works
Self-citationAutism, oxytocin and interoception
Quattrocki, E., & Friston, K. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.09.012 · Cited by 393 · see citing works
Tessmar-Raible, K., Raible, F., Christodoulou, F., Guy, K., Rembold, M., Hausen, H., & Arendt, D. (2007) · Cell · doi:10.1016/j.cell.2007.04.041 · Cited by 384 · see citing works
Loup, F., Tribollet, E., Dubois-Dauphin, M., & Dreifuss, J. J. (1991) · Brain Research · doi:10.1016/0006-8993(91)90345-v · Cited by 378 · see citing works
Oxytocin, motivation and the role of dopamine
Love, T. M. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.06.011 · Cited by 369 · see citing works
Oxytocin enhances social recognition by modulating cortical control of early olfactory processing
Oettl, L.-L., Ravi, N., Schneider, M., Scheller, M. F., Schneider, P., Mitre, M., da Silva Gouveia, M., Froemke, R. C., Chao, M. V., Young, W. S., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.03.033 · Cited by 359 · see citing works
Self-citationNeugebauer, V., Galhardo, V., Maione, S., & Mackey, S. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2008.12.014 · Cited by 353 · see citing works
Uvnäs-Moberg, K., Handlin, L., & Petersson, M. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.01529 · Cited by 351 · see citing works
Brain structures mediating cardiovascular arousal and interoceptive awareness
Pollatos, O., Schandry, R., Auer, D. P., & Kaufmann, C. (2007) · Brain Research · doi:10.1016/j.brainres.2007.01.026 · Cited by 351 · see citing works
Infant vocalization, adult aggression, and fear behavior of an oxytocin null mutant mouse
Winslow, J. T., Hearn, E. F., Ferguson, J., Young, L. J., Matzuk, M. M., & Insel, T. R. (2000) · Hormones and Behavior · doi:10.1006/hbeh.1999.1566 · Cited by 348 · see citing works
Oxytocin enhances hippocampal spike transmission by modulating fast-spiking interneurons
Owen, S. F., Tuncdemir, S. N., Bader, P. L., Tirko, N. N., Fishell, G., & Tsien, R. W. (2013) · Nature · doi:10.1038/nature12330 · Cited by 339 · cited 8× · see citing works
“A C1 C2 AON piriform cortex MC MC GC OSN = OTR expression B CA1 CA3 entorhinal cortex + oxytocin = GABA Figure 4 B Auditory system IC Aud Ctx MG DC Tz SOc inner year IO A Visual system SC LGThalamus Visual cortex pigment epitheliumretina Figure 3 trigeminal ganglion SpTN STN Somatosensory system SS Ctx PAG Cg Ctx NTS…”
InfluentialSwanson, L. W., & McKellar, S. (1979) · Journal of Comparative Neurology · doi:10.1002/cne.901880108 · Cited by 336 · see citing works
Assembling the puzzle: pathways of oxytocin signaling in the brain
Grinevich, V., Knobloch-Bollmann, H. S., Eliava, M., Busnelli, M., & Chini, B. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.04.013 · Cited by 309 · see citing works
Vaccari, C., Lolait, S. J., & Ostrowski, N. L. (1998) · Endocrinology · doi:10.1210/endo.139.12.6382 · Cited by 308 · see citing works
A distributed network for social cognition enriched for oxytocin receptors
Mitre, M., Marlin, B. J., Schiavo, J. K., Morina, E., Norden, S. E., Hackett, T. A., Aoki, C. J., Chao, M. V., & Froemke, R. C. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2409-15.2016 · Cited by 305 · see citing works
Beyond the Tripartite Cognition–Emotion–Interoception Model of the Human Insular Cortex
Uddin, L. Q., Kinnison, J., Pessoa, L., & Anderson, M. L. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00462 · Cited by 275 · see citing works
Dabrowska, J., Hazra, R., Ahern, T. H., Guo, J.-D., McDonald, A. J., Mascagni, F., Muller, J. F., Young, L. J., & Rainnie, D. G. (2011) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.03.003 · Cited by 274 · see citing works
Nucleoside triphosphate diphosphohydrolase‐2 is the ecto‐ATPase of type I cells in taste buds
Bartel, D. L., Sullivan, S. L., Lavoie, É. G., et al. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20954 · Cited by 274 · see citing works
Nociceptors: a phylogenetic view
Smith, E. S. J., & Lewin, G. R. (2009) · Journal of Comparative Physiology A · doi:10.1007/s00359-009-0482-z · Cited by 271 · see citing works
Oxytocin/vasopressin-related peptides have an ancient role in reproductive behavior
Garrison, J. L., Macosko, E. Z., Bernstein, S., Pokala, N., Albrecht, D. R., & Bargmann, C. I. (2012) · Science · doi:10.1126/science.1226201 · Cited by 266 · see citing works
Evolution of oxytocin pathways in the brain of vertebrates
Knobloch, H. S., & Grinevich, V. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00031 · Cited by 259 · see citing works
Self-citationThe human cortex responds to an interoceptive challenge
Critchley, H. D. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401510101 · Cited by 251 · see citing works
Cytoarchitecture and Probabilistic Maps of the Human Posterior Insular Cortex
Kurth, F., Eickhoff, S. B., Schleicher, A., Hömke, L., Zilles, K., & Amunts, K. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp208 · Cited by 241 · see citing works
Shah, B. P., Vong, L., Olson, D. P., Koda, S., Krashes, M. J., Ye, C., Yang, Z., Fuller, P. M., Elmquist, J. K., & Lowell, B. B. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1407843111 · Cited by 240 · see citing works
Lee, M. R., Scheidweiler, K. B., Diao, X. X., Akhlaghi, F., Cummins, A., Huestis, M. A., Leggio, L., & Averbeck, B. B. (2018) · Molecular Psychiatry · doi:10.1038/mp.2017.27 · Cited by 235 · see citing works
A rapidly acting glutamatergic ARC→PVH satiety circuit postsynaptically regulated by α-MSH
Fenselau, H., Campbell, J. N., Verstegen, A. M. J., Madara, J. C., Xu, J., Shah, B. P., Resch, J. M., Yang, Z., Mandelblat-Cerf, Y., Livneh, Y., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4442 · Cited by 233 · see citing works
Tribollet, E., Charpak, S., Schmidt, A., Dubois-Dauphin, M., & Dreifuss, J. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-05-01764.1989 · Cited by 228 · see citing works
Tracey, I. (2008) · British Journal of Anaesthesia · doi:10.1093/bja/aen102 · Cited by 223 · see citing works
Cortical Sulcal Maps in Autism
Levitt, J. G. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.7.728 · Cited by 220 · see citing works
An intrinsic vasopressin system in the olfactory bulb is involved in social recognition
Tobin, V. A., Hashimoto, H., Wacker, D. W., Takayanagi, Y., Langnaese, K., Caquineau, C., Noack, J., Landgraf, R., Onaka, T., Leng, G., et al. (2010) · Nature · doi:10.1038/nature08826 · Cited by 213 · see citing works
Lukas, M., Toth, I., Veenema, A. H., & Neumann, I. D. (2013) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.09.018 · Cited by 211 · see citing works
Oxytocin signaling in the lateral septum prevents social fear during lactation
Menon, R., Grund, T., Zoicas, I., Althammer, F., Fiedler, D., Biermeier, V., Bosch, O. J., Hiraoka, Y., Nishimori, K., Eliava, M., et al. (2018) · Current Biology · doi:10.1016/j.cub.2018.02.044 · Cited by 211 · see citing works
Self-citationOxytocin mediates early experience-dependent cross-modal plasticity in the sensory cortices
Zheng, J.-J., Li, S.-J., Zhang, X.-D., Miao, W.-Y., Zhang, D., Yao, H., & Yu, X. (2014) · Nature Neuroscience · doi:10.1038/nn.3634 · Cited by 206 · see citing works
Gauriau, C., & Bernard, J. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10873 · Cited by 205 · see citing works
Young, L. J., & Barrett, C. E. (2015) · Science · doi:10.1126/science.aaa8120 · Cited by 200 · see citing works
Freeman, S. M., & Young, L. J. (2016) · Journal of Neuroendocrinology · doi:10.1111/jne.12382 · Cited by 196 · cited 2× · see citing works
“visual system is a major target of OT in these mammals ((Freeman and Young, 2016).”
Busnelli, M., Saulière, A., Manning, M., Bouvier, M., Galès, C., & Chini, B. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.277178 · Cited by 195 · see citing works
Olfactory projections to the hypothalamus
Price, J. L., Slotnick, B. M., & Revial, M. ‐. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903060309 · Cited by 191 · see citing works
Leonzino, M., Busnelli, M., Antonucci, F., Verderio, C., Mazzanti, M., & Chini, B. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.03.013 · Cited by 191 · see citing works
Central administration of oxytocin modulates the infant rats response to social isolation
Insel, T. R., & Winslow, J. (1991) · European Journal of Pharmacology · doi:10.1016/0014-2999(91)90806-2 · Cited by 185 · see citing works
Perspectives on sensory processing disorder: a call for translational research
Miller, L. (2009) · Frontiers in Integrative Neuroscience · doi:10.3389/neuro.07.022.2009 · Cited by 183 · see citing works
Cloning and identification of an oxytocin/vasopressin-like receptor and its ligand from insects
Stafflinger, E., Hansen, K. K., Hauser, F., Schneider, M., Cazzamali, G., Williamson, M. P., & Grimmelikhuijzen, C. J. P. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710897105 · Cited by 180 · see citing works
Convergence of olfactory and vomeronasal projections in the rat basal telencephalon
Pró-Sistiaga, P., Mohedano‐Moriano, A., Úbeda‐Bañón, I., Jiménez, M. D. M. A., Marcos, P., Artacho‐Pérula, E., Crespo, C., Insausti, R., & Martı́nez-Marcos, A. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21455 · Cited by 177 · see citing works
Developmental Perspectives on Oxytocin and Vasopressin
Hammock, E. A. D. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.120 · Cited by 177 · see citing works
Vasopressin/Oxytocin-Related Signaling Regulates Gustatory Associative Learning in C. elegans
Beets, I., Janssen, T. A. H., Meelkop, E., Temmerman, L., Suetens, N., Rademakers, S., Jansen, G., & Schoofs, L. (2012) · Science · doi:10.1126/science.1226860 · Cited by 177 · see citing works
Evolution of nociception in vertebrates: comparative analysis of lower vertebrates
Sneddon, L. U. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.07.007 · Cited by 174 · see citing works
The evolution of the complex sensory and motor systems of the human brain
Kaas, J. H. (2007) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2007.10.009 · Cited by 174 · see citing works
Morphological aspects of the teleostean visual system: A review
Vanegas, H., & Ito, H. (1983) · Brain Research Reviews · doi:10.1016/0165-0173(83)90036-x · Cited by 171 · see citing works
Localization of oxytocin receptor messenger ribonucleic acid in the rat brain.
Yoshimura, R., Kiyama, H., Kimura, T., Araki, T., Maeno, H., Tanizawa, O., & Tohyama, M. (1993) · Endocrinology · doi:10.1210/endo.133.3.8396014 · Cited by 161 · see citing works
Ueta, Y., Fujihara, H., Serino, R., Dayanithi, G., Ozawa, H., Matsuda, K., Kawata, M., Yamada, J., Ueno, S., Fukuda, A., et al. (2004) · Endocrinology · doi:10.1210/en.2004-0830 · Cited by 160 · see citing works
Localization of the glutamate–aspartate transporter, GLAST, in rat taste buds
Lawton, D. M., Furness, D. N., Lindemann, B., et al. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00207.x · Cited by 159 · see citing works
Toyoizumi, T., Miyamoto, H., Yazaki-Sugiyama, Y., Atapour, N., Hensch, T. K., & Miller, K. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.022 · Cited by 158 · see citing works
A retinohypothalamic pathway in man: Light mediation of circadian rhythms
Sadun, A. A., Schaechter, J. D., & Smith, L. E. H. (1984) · Brain Research · doi:10.1016/0006-8993(84)90252-x · Cited by 157 · see citing works
Freeman, S. M., Walum, H., Inoue, K., Smith, A. L., Goodman, M. M., Bales, K. L., & Young, L. J. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.04.055 · Cited by 153 · see citing works
Structure, function, and phylogeny of [Arg8]vasotocinreceptors from teleost fish and toad.
Mahlmann, S., Meyerhof, W., Hausmann, H., Heierhorst, J., Schönrock, C., Zwiers, H., Lederis, K. P., & Richter, D. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.4.1342 · Cited by 151 · see citing works
Oxytocin signaling in the medial amygdala is required for sex discrimination of social cues
Yao, S., Bergan, J., Lanjuin, A., & Dulac, C. (2017) · eLife · doi:10.7554/elife.31373 · Cited by 151 · see citing works
Chang, Y.-S., Owen, J. P., Desai, S. S., Hill, S. S., Arnett, A. B., Harris, J., Marco, E. J., & Mukherjee, P. (2014) · PLoS ONE · doi:10.1371/journal.pone.0103038 · Cited by 149 · see citing works
Oxytocin, feeding, and satiety
Sabatier, N., Leng, G., & Menzies, J. (2013) · Frontiers in Endocrinology · doi:10.3389/fendo.2013.00035 · Cited by 149 · see citing works
Development of order in the rat trigeminal system
Erzurumlu, R. S., & Killackey, H. P. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902130402 · Cited by 145 · see citing works
Gur, R., Tendler, A., & Wagner, S. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.03.022 · Cited by 144 · see citing works
The action radius of oxytocin release in the mammalian CNS: from single vesicles to behavior
Chini, B., Verhage, M., & Grinevich, V. (2017) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2017.08.005 · Cited by 141 · cited 2× · see citing works
“This led us to an alternative hypothesis that OT released from single axons activates micro-ensembles of OT-sensitive neurons and modulates brain-region specific behaviors (Chini et al., 2017).”
Gould, B. R., & Zingg, H. H. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00283-5 · Cited by 138 · see citing works
Diversity of oxytocin neurones: Beyond magno‐ and parvocellular cell types?
Althammer, F., & Grinevich, V. (2018) · Journal of Neuroendocrinology · doi:10.1111/jne.12549 · Cited by 138 · see citing works
Self-citationOxytocin and Pain Perception: From Animal Models to Human Research
Boll, S., de Minas, A. C. A., Raftogianni, A., Herpertz, S. C., & Grinevich, V. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.09.041 · Cited by 137 · see citing works
Self-citationWullimann, M. F., & Northcutt, R. G. (2008) · Brain Behavior and Evolution · doi:10.1159/000116558 · Cited by 133 · see citing works
Welch, M. G., Tamir, H., Gross, K. J., Chen, J. C., Anwar, M., & Gershon, M. D. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21872 · Cited by 132 · see citing works
Paraventricular oxytocin neurons are involved in neural modulation of breathing
Mack, S. O., Kc, P., Wu, M., Coleman, B. R., Tolentino-Silva, F. P., & Haxhiu, M. A. (2002) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00839.2001 · Cited by 132 · see citing works
Oxytocin-like receptors mediate pair bonding in a socially monogamous songbird
Klatt, J. D., & Goodson, J. L. (2012) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2012.2396 · Cited by 132 · see citing works
Miranda-Cardenas, Y., Rojas‐Piloni, G., Martı́nez-Lorenzana, G., Rodríguez-Jiménez, J., López-Hidalgo, M. A., Freund‐Mercier, M. J., & Condés‐Lara, M. (2006) · Pain · doi:10.1016/j.pain.2006.01.029 · Cited by 131 · see citing works
Ontogeny of oxytocin receptors in rat forebrain: A quantitative study
Shapiro, L. E., & Insel, T. R. (1989) · Synapse · doi:10.1002/syn.890040312 · Cited by 131 · see citing works
Oxytocin knockout mice demonstrate enhanced intake of sweet and nonsweet carbohydrate solutions
Sclafani, A. J., Rinaman, L., Vollmer, R. R., & Amico, J. A. (2007) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00826.2006 · Cited by 131 · see citing works
Intranasal oxytocin increases covert attention to positive social cues
Domes, G., Sibold, M., Schulze, L., Lischke, A., Herpertz, S. C., & Heinrichs, M. (2013) · Psychological Medicine · doi:10.1017/s0033291712002565 · Cited by 130 · see citing works
Yu, G.-Z., Kaba, H., Okutani, F., Takahashi, S., & Higuchi, T. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00600-1 · Cited by 129 · see citing works
Central vasopressin and oxytocin receptor distributions in two species of singing mice
Polly Campbell, A., Ophir, A. G., & Phelps, S. M. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22116 · Cited by 128 · see citing works
Newborn Analgesia Mediated by Oxytocin during Delivery
Mazzuca, M., Minlebaev, M., Shakirzyanova, A., Tyzio, R., Taccola, G., Janáčková, S., Gataullina, S., Ben‐Ari, Y., Giniatullin, R. A., & Khazipov, R. (2011) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2011.00003 · Cited by 127 · see citing works
Putative isotocin distributions in sonic fish: Relation to vasotocin and vocal–acoustic circuitry
Goodson, J. L., Evans, A. K., & Bass, A. H. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10679 · Cited by 126 · see citing works
Agonist selectivity in the oxytocin/vasopressin receptor family: new insights and challenges
Chini, B., & Manning, M. (2007) · Biochemical Society Transactions · doi:10.1042/bst0350737 · Cited by 123 · see citing works
Sexually dimorphic expression of oxytocin binding sites in forebrain and spinal cord of the rat
Uhl-Bronner, S., Waltisperger, E., Martínez-Lorenzana, G., Condes Lara, M., & Freund-Mercier, M. J. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.05.025 · Cited by 123 · see citing works
Oxytocin action in the ventral tegmental area affects sucrose intake
Mullis, K., Kay, K., & Williams, D. L. (2013) · Brain Research · doi:10.1016/j.brainres.2013.03.026 · Cited by 122 · see citing works
Jankowski, M., Danalache, B. A., Wang, D., Bhat, P. V., Hajjar, F., Marcinkiewicz, M. M., Paquin, J., McCann, S. M., & Gutkowska, J. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0405324101 · Cited by 120 · see citing works
Lagman, D., Daza, D. O., Widmark, J., Abalo, X. M., Sundström, G., & Larhammar, D. (2013) · BMC Evolutionary Biology · doi:10.1186/1471-2148-13-238 · Cited by 120 · see citing works
Rault, J., van den Munkhof, M. H., & Buisman‐Pijlman, F. T. A. (2017) · Frontiers in Psychology · doi:10.3389/fpsyg.2017.01521 · Cited by 118 · see citing works
Neural Connections of Hypothalamic Neuroendocrine Nuclei in the Rat
Saeb‐Parsy, K., Lombardelli, Khan, McDowall, Au‐Yong, & Dyball (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00503.x · Cited by 116 · see citing works
Hammock, E. A. D. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00195 · Cited by 115 · see citing works
Schorscher-Petcu, A., Dupré, A., & Tribollet, E. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.06.016 · Cited by 111 · see citing works
Antagonistic sensory cues generate gustatory plasticity in Caenorhabditis elegans
Hukema, R. K., Rademakers, S., Dekkers, M. P., Burghoorn, J., & Jansen, G. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7600940 · Cited by 111 · see citing works
Physiology of invertebrate oxytocin and vasopressin neuropeptides
Gruber, C. W. (2014) · Experimental Physiology · doi:10.1113/expphysiol.2013.072561 · Cited by 110 · see citing works
Retinal projections in the goldfish: A study using cobaltous‐lysine
Springer, A. D., & Gaffney, J. S. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.902030306 · Cited by 109 · see citing works
Sex Differences in Vasopressin and Other Neurotransmitter Systems in the Brain
De Vries, G. J., Buijs, R. M., & Van Leeuwen, F. W. (1984) · Progress in Brain Research · doi:10.1016/s0079-6123(08)64435-0 · Cited by 106 · see citing works
Oxytocin Acting in the Nucleus Accumbens Core Decreases Food Intake
Herisson, F. M., Waas, J. R., Fredriksson, R., Schiöth, H. B., Levine, A. S., & Olszewski, P. K. (2016) · Journal of Neuroendocrinology · doi:10.1111/jne.12381 · Cited by 104 · see citing works
Maternal oxytocin response predicts mother-to-infant gaze
Kim, S., Fonagy, P., Koos, O., Dorsett, K., & Strathearn, L. (2014) · Brain Research · doi:10.1016/j.brainres.2013.10.050 · Cited by 102 · see citing works
Figueira, R. J., Peabody, M. F., & Lonstein, J. S. (2008) · Behavioral Neuroscience · doi:10.1037/0735-7044.122.3.618 · Cited by 101 · see citing works
Juif, P.-E., & Poisbeau, P. (2013) · Pain · doi:10.1016/j.pain.2013.05.003 · Cited by 101 · see citing works
Central oxytocin inhibition of angiotensin-induced salt appetite in rats
Blackburn, R. E., Demko, A. D., Hoffman, G. E., Stricker, E. M., & Verbalis, J. G. (1992) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1992.263.6.r1347 · Cited by 97 · see citing works
Schoenen, J. E., Lotstra, F., Vierendeels, G., Reznik, M., & Vanderhaeghen, J. J. (1985) · Neurology · doi:10.1212/wnl.35.6.881 · Cited by 90 · see citing works
Design-based estimation of neuronal number and individual neuronal volume in the rat hippocampus
Sharifabad, M. H., & Nyengaard, J. R. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.01.009 · Cited by 90 · see citing works
Egli, M., Bertram, R., Sellix, M. T., & Freeman, M. E. (2004) · Endocrinology · doi:10.1210/en.2003-1710 · Cited by 88 · see citing works
The evolution of complex sensory systems in mammals
Kaas, J. H. (1989) · Journal of Experimental Biology · doi:10.1242/jeb.146.1.165 · Cited by 87 · see citing works
Excitatory Synaptic Transmission in the Lateral and Central Amygdala
Sah, P., & de Armentia, M. L. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07072.x · Cited by 86 · see citing works
Ancient neuromodulation by vasopressin/oxytocin-related peptides
Beets, I., Temmerman, L., Janssen, T. A. H., & Schoofs, L. (2013) · Worm · doi:10.4161/worm.24246 · Cited by 85 · see citing works
Dvoryanchikov, G. A., Sinclair, M. S., Perea‐Martinez, I., et al. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22152 · Cited by 84 · see citing works
Kojima, S., Stewart, R., Demas, G. E., & Alberts, J. R. (2012) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2012.02280.x · Cited by 83 · see citing works
Teleost isotocin receptor: structure, functional expression, mRNA distribution and phylogeny
Hausmann, H., Meyerhof, W., Zwiers, H., Lederis, K. P., & Richter, D. (1995) · FEBS Letters · doi:10.1016/0014-5793(95)00832-t · Cited by 83 · see citing works
Mbiene, J., & Mistretta, C. M. (1997) · Cells Tissues Organs · doi:10.1159/000148006 · Cited by 83 · see citing works
Yu, G.-Z., Kaba, H., Okutani, F., Takahashi, S., Higuchi, T., & Seto, K. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00599-4 · Cited by 83 · see citing works
eSabatier, N., eLeng, G., & eMenzies, J. (2013) · Frontiers in Endocrinology · Cited by 83 · see citing works
Editorial comment: Oxytocin, vasopressin and social behavior
Young, L. J., & Flanagan-Cato, L. M. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.02.019 · Cited by 81 · see citing works
Retinofugal projections to the hypothalamus, anterior thalamus and basal forebrain in hamsters
Youngstrom, T. G., Weiss, M. L., & Nunez, A. A. (1991) · Brain Research Bulletin · doi:10.1016/0361-9230(91)90014-b · Cited by 80 · see citing works
Identification of oxytocin receptor in the dorsal horn and nociceptive dorsal root ganglion neurons
Moreno-López, Y., Martı́nez-Lorenzana, G., Condés‐Lara, M., & Rojas‐Piloni, G. (2012) · Neuropeptides · doi:10.1016/j.npep.2012.09.008 · Cited by 80 · see citing works
Oliva, J. L., Rault, J., Appleton, B., & Lill, A. (2015) · Animal Cognition · doi:10.1007/s10071-015-0843-7 · Cited by 80 · see citing works
Synaptogenesis in the developing mouse visual cortex
Ming-shan, L., Cui, Z., Niu, Y., Liu, B., Fan, W., Yu, D., & Deng, J. (2009) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2009.08.028 · Cited by 80 · see citing works
Oxytocin during Development: Possible Organizational Effects on Behavior
Miller, T. V., & Caldwell, H. K. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00076 · Cited by 79 · see citing works
Kubo, A., Shinoda, M., Katagiri, A., Takeda, M., Suzuki, T., Asaka, J., Yeomans, D. C., & Iwata, K. (2017) · Pain · doi:10.1097/j.pain.0000000000000808 · Cited by 79 · see citing works
Smithson, K. G., Weiss, M. L., & Hatton, G. I. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90373-4 · Cited by 74 · see citing works
Ho, J. M., Anekonda, V. T., Thompson, B. W., Zhu, M., Curry, R. W., Hwang, B. H., Morton, G. J., Schwartz, M. W., Baskin, D. G., Appleyard, S. M., et al. (2014) · Endocrinology · doi:10.1210/en.2014-1148 · Cited by 74 · see citing works
DelaTorre, S., Rojas‐Piloni, G., Martı́nez-Lorenzana, G., Rodríguez-Jiménez, J., Villanueva, L., & Condés‐Lara, M. (2009) · Pain · doi:10.1016/j.pain.2009.05.002 · Cited by 74 · see citing works
Tzabazis, A., Mechanic, J., Miller, J. T., Klukinov, M., Pascual, C., Manering, N. A., Carson, D. S., Jacobs, A., Qiao, Y., Cuéllar, J. M., et al. (2015) · Cephalalgia · doi:10.1177/0333102415618615 · Cited by 73 · see citing works
Cell‐Type Specific Expression of Oxytocin and Vasopressin Genes: An Experimental Odyssey
Gainer, H. (2011) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2011.02236.x · Cited by 71 · see citing works
Oxytocin increases locus coeruleus alpha 2-adrenoreceptor responsiveness in rats
Petersson, M., Uvnäs-Moberg, K., Erhardt, S., & Engberg, G. (1998) · Neuroscience Letters · doi:10.1016/s0304-3940(98)00729-0 · Cited by 71 · see citing works
Discovery of Defense- and Neuropeptides in Social Ants by Genome-Mining
Gruber, C. W., & Muttenthaler, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032559 · Cited by 70 · see citing works
Concentrations and origin of oxytocin in breast milk.
Takeda, S., Kuwabara, Y., & Mizuno, M. (1986) · Endocrinologia Japonica · doi:10.1507/endocrj1954.33.821 · Cited by 69 · see citing works
Caba, M., Rovirosa-Hernández, M. D. J., & Silver, R. (2003) · Developmental Brain Research · doi:10.1016/s0165-3806(03)00064-6 · Cited by 65 · 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
Bilateral Descending Hypothalamic Projections to the Spinal Trigeminal Nucleus Caudalis in Rats
Abdallah, K., Artola, A., Monconduit, L., Dallel, R., & Luccarini, P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073022 · Cited by 62 · see citing works
González‐Hernández, A., Manzano‐García, A., Martı́nez-Lorenzana, G., Tello-García, I. A., Carranza, M., Arámburo, C., & Condés‐Lara, M. (2017) · Pain · doi:10.1097/j.pain.0000000000001024 · Cited by 62 · see citing works
Wircer, E., Blechman, J., Borodovsky, N., Tsoory, M., Nunes, A. R., Oliveira, R. F., & Levkowitz, G. (2017) · eLife · doi:10.7554/elife.22170 · Cited by 60 · see citing works
Enhanced Salt Intake in Oxytocin Deficient Mice
Puryear, R., Rigatto, K., Amico, J. A., & Morris, M. (2001) · Experimental Neurology · doi:10.1006/exnr.2001.7776 · Cited by 58 · 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
Oxytocin Signaling in Mouse Taste Buds
Sinclair, M. S., Perea‐Martinez, I., Dvoryanchikov, G. A., Yoshida, M., Nishimori, K., Roper, S. D., & Chaudhari, N. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011980 · Cited by 57 · see citing works
Oxytocin facilitates the induction of long-term potentiation in the accessory olfactory bulb
Fang, L.-Y., Quan, R.-D., & Kaba, H. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2007.12.070 · Cited by 57 · see citing works
Oxytocin receptors and cholesterol: interaction and regulation
Gimpl, G., Bürger, K., Politowskat, E., Ciarkowski, J., & Fahrenholz, F. (2000) · Experimental Physiology · doi:10.1111/j.1469-445x.2000.tb00006.x · Cited by 56 · see citing works
New opportunities in vasopressin and oxytocin research: a perspective from the amygdala.
Stoop, R., Hegoburu, C., & van den Burg, E. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-033904 · Cited by 56 · see citing works
Self-citationAmico, J. A., Morris, M., & Vollmer, R. R. (2001) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2001.281.5.r1368 · Cited by 55 · see citing works
Wang, Z., & Young, L. J. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00138-7 · Cited by 54 · see citing works
Somppi, S., Törnqvist, H., Topál, J., Koskela, A., Hänninen, L. T., Krause, C. M., & Vainio, O. (2017) · Frontiers in Psychology · doi:10.3389/fpsyg.2017.01854 · Cited by 53 · see citing works
The Role of Serotonin, Vasopressin, and Serotonin/Vasopressin Interactions in Aggressive Behavior
Morrison, T. R., & Melloni, R. H. (2014) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_283 · Cited by 51 · see citing works
Dubois‐Dauphin, M., Armstrong, W. E., Tribollet, E., & Dreifuss, J. J. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90257-x · Cited by 51 · see citing works
Oxytocin antagonist disrupts male mouse medial amygdala response to chemical-communication signals
Samuelsen, C. L., & Meredith, M. J. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.02.030 · Cited by 51 · see citing works
Selective localization of oxytocin receptors and vasopressin 1a receptors in the human brainstem
Freeman, S. M., Smith, A. L., Goodman, M. M., & Bales, K. L. (2017) · Social Neuroscience · doi:10.1080/17470919.2016.1156570 · Cited by 51 · see citing works
Oxytocin in the Circadian Timing of Birth
Roizen, J. D., Luedke, C. E., Herzog, E. D., & Muglia, L. J. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000922 · Cited by 50 · see citing works
Distribution and identity of neurons expressing the oxytocin receptor in the mouse spinal cord
Wrobel, L. J., Schorscher-Petcu, A., Dupré, A., Yoshida, M., Nishimori, K., & Tribollet, E. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.03.033 · Cited by 49 · see citing works
Vargas-Martínez, F., Uvnás-Moberg, K., Petersson, M., Olausson, H., & Jiménez-Estrada, I. (2014) · Progress in neurobiology · doi:10.1016/j.pneurobio.2014.10.001 · Cited by 49 · see citing works
Broser, P. J., Grinevich, V., Osten, P., Sakmann, B. J., & Wallace, D. J. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm189 · Cited by 48 · see citing works
Self-citationOng, Z. Y., Bongiorno, D. M., Hernando, M. A., & Grill, H. J. (2017) · Endocrinology · doi:10.1210/en.2017-00200 · Cited by 48 · see citing works
Bitter taste receptors as targets for tocolytics in preterm labor therapy
Zheng, K., Lü, P., Delpapa, E. H., Bellve, K. D., Deng, R., Condon, J. C., Fogarty, K. E., Lifshitz, L. M., Simas, T. A. M., Shi, F., et al. (2017) · The FASEB Journal · doi:10.1096/fj.201601323rr · Cited by 48 · see citing works
Oxytocin in the periaqueductal grey regulates nociception in the rat
Yang, J., Li, P., Liang, J., Pan, Y.-J., Yan, X.-Q., Yan, F., Hao, F., Zhang, X.-Y., Zhang, J., Qiu, P.-Y., et al. (2011) · Regulatory Peptides · doi:10.1016/j.regpep.2011.04.007 · Cited by 47 · see citing works
Vasopressin and oxytocin receptor mRNAs are expressed in the rat inner ear
Kitano, H., Takeda, T., Suzuki, M., et al. (1997) · Neuroreport · doi:10.1097/00001756-199707070-00038 · Cited by 46 · see citing works
Caba, M., Silver, R., González‐Mariscal, G., Jiménez, A., & Beyer, C. (1996) · Brain Research · doi:10.1016/0006-8993(96)00036-4 · Cited by 46 · see citing works
Mangiamele, L. A., Gomez, J. R., Curtis, N. J., et al. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24056 · Cited by 46 · see citing works
Higashida, H., Furuhara, K., Yamauchi, A.-M., Deguchi, K., Harashima, A., Munesue, S., Lopatina, O. L., Gerasimenko, M., Salmina, A. B., Zhang, J., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-07949-4 · Cited by 46 · see citing works
Lee, S. K., Ryu, P. D., & Lee, S. Y. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.09.070 · Cited by 45 · see citing works
The Emerging Role of Nucleus Accumbens Oxytocin in Social Cognition
Dölen, G., & Malenka, R. C. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.06.009 · Cited by 44 · see citing works
Evolution of Sensory Pathways in Vertebrates
Hodos, W., & Butler, A. B. (2008) · Brain Behavior and Evolution · doi:10.1159/000113333 · Cited by 43 · see citing works
Oxytocin decreases sweet taste sensitivity in mice
Sinclair, M. S., Perea‐Martinez, I., Abouyared, M., John, S. J. S., & Chaudhari, N. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.12.048 · Cited by 43 · see citing works
Vasopressin casts light on the suprachiasmatic nucleus
Tsuji, T., Allchorne, A. J., Zhang, M., Tsuji, C., Tobin, V. A., Pineda, R., Raftogianni, A., Stern, J. E., Grinevich, V., Leng, G., et al. (2017) · The Journal of Physiology · doi:10.1113/jp274025 · Cited by 42 · see citing works
Self-citationCRTH2, a prostaglandin D2 receptor, mediates depression-related behavior in mice
Onaka, Y., Shintani, N., Nakazawa, T., Haba, R., Ago, Y., Wang, H., Kanoh, T., Hayata‐Takano, A., Hirai, H., Nagata, K., et al. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.02.013 · Cited by 40 · see citing works
Boccia, M. M., & Baratti, C. M. (2000) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1999.3954 · Cited by 39 · see citing works
Bader, A., Klein, B., Breer, H., & Strotmann, J. M. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00084 · Cited by 39 · see citing works
Pajkossy, P., Szöllősi, Á., Demeter, G., & Racsmány, M. (2017) · Psychophysiology · doi:10.1111/psyp.12964 · Cited by 38 · see citing works
Gerendai, I., Tóth, I. E., Kocsis, K., Boldogkői, Z., Medveczky, I., & Halász, B. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00399-2 · Cited by 37 · see citing works
Olszewski, P. K., Waas, J. R., Brooks, L. L., Herisson, F. M., & Levine, A. S. (2013) · Peptides · doi:10.1016/j.peptides.2013.09.008 · Cited by 36 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Veening, J.G., and Olivier, B. (2013). Intranasal administration of oxytocin: behavioral and clinical effects, a review. Neurosci Biobehav Rev 37 , 14451465.
Cited by
Sorted by citations
Social touch promotes interfemale communication via activation of parvocellular oxytocin neurons
Tang, Y., Benusiglio, D., Lefevre, A., Hilfiger, L., Althammer, F., Bludau, A., Hagiwara, D., Baudon, A., Darbon, P., Schimmer, J., et al. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0674-y · Cited by 249 · see citing works
Self-citationOxytocin Signaling in the Central Amygdala Modulates Emotion Discrimination in Mice
Ferretti, V., Maltese, F., Contarini, G., Nigro, M., Bonavia, A., Huang, H., Gigliucci, V., Morelli, G., Scheggia, D., Managò, F., et al. (2019) · Current Biology · doi:10.1016/j.cub.2019.04.070 · Cited by 212 · see citing works
Self-citationYu, H., Miao, W., Ji, E., Huang, S., Jin, S., Zhu, X., Liu, M.-Z., Sun, Y.-G., Xu, F., & Yu, X. (2022) · Neuron · doi:10.1016/j.neuron.2021.12.022 · Cited by 144 · see citing works
Whole-brain wiring diagram of oxytocin system in adult mice
Son, S., Manjila, S. B., Newmaster, K. T., Wu, Y.-T., Vanselow, D. J., Ciarletta, M., Anthony, T. E., Cheng, K. C., & Kim, Y. (2022) · The Journal of Neuroscience · doi:10.1523/jneurosci.0307-22.2022 · Cited by 125 · see citing works
Neural circuitry for maternal oxytocin release induced by infant cries
Valtcheva, S., Issa, H. A., Bair-Marshall, C. J., Martin, K. A., Jung, K., Zhang, Y., Kwon, H.-B., & Froemke, R. C. (2023) · Nature · doi:10.1038/s41586-023-06540-4 · Cited by 115 · see citing works
Links between the neurobiology of oxytocin and human musicality
Harvey, A. R. (2020) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2020.00350 · Cited by 85 · see citing works
Oxytocin and love: myths, metaphors and mysteries.
Carter, C. S. (2022) · Comprehensive Psychoneuroendocrinology · doi:10.1016/j.cpnec.2021.100107 · Cited by 57 · see citing works
Developmental effects of oxytocin neurons on social affiliation and processing of social information
Nunes, A. R., Gliksberg, M., Varela, S. A. M., Teles, M., Wircer, E., Blechman, J., Petri, G., Levkowitz, G., & Oliveira, R. F. (2021) · The Journal of Neuroscience · doi:10.1523/jneurosci.2939-20.2021 · Cited by 47 · see citing works
Neural effects of oxytocin and mimicry in frontotemporal dementia: A randomized crossover study
Oliver, L. D., Stewart, C., Coleman, K., Kryklywy, J. H., Bartha, R., Mitchell, D. G. V., & Finger, E. C. (2020) · Neurology · doi:10.1212/wnl.0000000000010933 · Cited by 26 · see citing works
- Authors
- Grinevich, V., & Stoop, R.
- Affiliations
- German Cancer Research Center (DE)
- Centre Hospitalier Universitaire Vaudois (CH)
- Corresponding author
- Grinevich, Valery
- Stoop, Ron
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2018-09
- Volume
- 99
- Issue
- 5
- Pages
- 887-904
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2891353824
- Cited by
- 139
- References
- 233
- Citations by year
- 2026: 16 · 2025: 13 · 2024: 13 · 2023: 14 · 2022: 27 · 2021: 25 · 2020: 18 · 2019: 12 · 2018: 1
- FWCI
- 2.12
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- SERVAL (Université de Lausanne) (acceptedVersion, cc-by-nc-nd)
- IRIS (submittedVersion, cc-by-nc-nd)
- Funders
- Chica and Heinz Schaller Research Foundation
- German Research Foundation (DFG) within the Collaborative Research Center (1134, 1158)
- Human Frontiers Science Program (RGP0019/2015)
- DFG-ANR GR (3619/7-1)
- DFG-SNF GR (3619/8-1)
- Topics
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- oxytocin, sensory processing, social behavior, emotional behavior, neuropeptides, mammals
- MeSH terms
- Animals, Brain, Emotions, Humans, Nerve Net, Oxytocin, Sensation, Social Behavior
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