Divergent effects of two different doses of intranasal oxytocin on facial affect discrimination in schizophrenic patients with and without polydipsia
Abstract
Rationale Hyponatremia and dexamethasone resistance in polydipsic schizophrenic patients are attributable to changes in hippocampal-modulated antidiuretic and stress hormone activity, respectively. The relationship of the neuroendocrine findings to the psychiatric illness, however, is unknown. An impaired ability to identify facial emotions has been linked to core features of schizophrenia and to diminished levels of the closely related hormone, oxytocin, in the polydipsic subset. Intranasal oxytocin enhances facial affect discrimination in healthy subjects.Objective The aim of this study is to explore if oxytocin reverses impaired facial affect discrimination in schizophrenic patients with, relative to that in patients without, polydipsia.Methods Intranasal oxytocin (10 or 20 IU) and placebo were administered on three occasions to five polydipsic schizophrenic patients, eight nonpolydipsic patients, and 11 healthy controls. Subsequently, subjects rated the presence and intensity of six facial emotions.Results Emotion recognition fell in both patient groups following 10 IU of oxytocin due to an increased propensity to identify all emotions regardless of whether they were displayed. By contrast, emotion recognition improved following 20 IU in polydipsic relative to nonpolydipsic patients due primarily to divergent effects on the bias to identify fear in nonfearful faces.Conclusion The effects of 20 IU oxytocin support the hypothesis that altered neuroendocrine function in polydipsic patients contributes to their psychiatric illness. Further studies are warranted to confirm these findings and assess if oxytocin treatment improves social functioning in this subset. This is the first psychopharmacologic study to compare different doses of oxytocin in the same subject, thus the significance of the opposing responses is unclear.
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Studies that controlled for dose show important dose-dependent variation on physiology or social cognition.
“Studies that have controlled for dose show important dose-dependent variation on physiology (Cardoso et al., 2013) or social cognition (Goldman et al., 2011; Hall et al., 2012).”
From Endogenous peripheral oxytocin measures can give insight into the dynamics of social relationships: a review (2014) · cites this paper as Goldman et al., 2011
Middle doses (20-24 IU) of oxytocin have the greatest positive effects, whereas low (10 IU) or high doses (48 IU) show blunted effects.
“Middle doses (20–24 IU) have the greatest positive effects, whereas low (10 IU) or high doses (48 IU) show blunted effects (Goldman et al., 2011; Hall et al., 2012; Cardoso et al., 2013).”
From Endogenous peripheral oxytocin measures can give insight into the dynamics of social relationships: a review (2014) · cites this paper as Goldman et al., 2011
In schizophrenic patients, intranasal oxytocin increased emotion recognition at 20 IU and decreased it at 10 IU.
“In schizophrenic patients, intranasal OT increased emotion recognition at one dose (20 IU) and decreased emotion recognition at a different dose (10 IU) (23).”
From Chronic intranasal oxytocin causes long-term impairments in partner preference formation in male prairie voles (2013) · cites this paper as [23]
In patients with schizophrenia, 20 IU oxytocin, but not 10 IU oxytocin, ameliorated emotion recognition deficits in a polydipsic group.
“A clinical study with divergent single-dose oxytocin administration in patients with schizophrenia showed that 20 IU oxytocin, but not 10 IU oxytocin, ameliorated emotion recognition deficits in a polydipsic group.18”
From Oxytocin efficacy is modulated by dosage and oxytocin receptor genotype in young adults with high-functioning autism: a 24-week randomized clinical trial (2016) · cites this paper as [18]
Only a few studies have examined the differential effects of higher (24, 40 or 48 IU) and lower (10, 20 or 24 IU) oxytocin doses.
“Only a few studies examined the differential effects of higher (24, 40 or 48 IU) and lower (10, 20 or 24 IU, respectively) oxytocin doses [103-105].”
From Efficacy of oxytocin administration early after psychotrauma in preventing the development of PTSD: study protocol of a randomized controlled trial (2014) · cites this paper as [103]
In studies examining differential oxytocin doses, the dose around 20 IU (24 IU or 20 IU) had more favorable effects compared to the other dose studied (48, 40 or 10 IU).
“In these studies the dose around 20 IU (24 IU or 20 IU) had more favorable effects compared to the other dose studied (48, 40 or 10 IU).”
From Efficacy of oxytocin administration early after psychotrauma in preventing the development of PTSD: study protocol of a randomized controlled trial (2014) · cites this paper as [103]
The studies examining differential oxytocin doses were single administration studies on non-clinical outcome measures.
“However, these studies were single administration studies on non-clinical outcome measures.”
From Efficacy of oxytocin administration early after psychotrauma in preventing the development of PTSD: study protocol of a randomized controlled trial (2014) · cites this paper as [103]
Cites
Baron‐Cohen, S., Wheelwright, S., Hill, J., Raste, Y., & Plumb, I. (2001) · Journal of Child Psychology and Psychiatry · doi:10.1111/1469-7610.00715 · Cited by 4,555 · cited 1× · see citing works
“Pictures were a subset from Ekman and Friesen (1976) previously used to demonstrate altered responses in facial affect discrimination in patients with amygdala pathology (Adolphs et al. 1999), autism ( Baron-Cohen et al. 2001 ), and schizophrenia (Addington et al. 2006).”
MethodEkman, P. (1976) · Medical Entomology and Zoology · Cited by 4,345 · see citing works
Baron‐Cohen, S., Wheelwright, S. J., Hill, J., Raste, Y., & Plumb, I. (2001) · PubMed · Cited by 4,313 · see citing works
Heinrichs, M., Baumgartner, T., Kirschbaum, C., & Ehlert, U. (2003) · Biological Psychiatry · doi:10.1016/s0006-3223(03)00465-7 · Cited by 2,091 · 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
Neuroendocrine perspectives on social attachment and love
Sue Carter, C. (1998) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(98)00055-9 · Cited by 1,425 · see citing works
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 · see citing works
Contributions to Neuropsychological Assessment
Sarazin, F. (1996) · Europe PMC (PubMed Central) · Cited by 1,151 · see citing works
Facial Emotion Perception in Schizophrenia: A Meta-analytic Review
Kohler, C. G., Walker, J. B., Martin, E. A., Healey, K. M., & Moberg, P. J. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn192 · Cited by 933 · see citing works
Contributions to Neuropsychological Assessment
Greene, J. (1995) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.59.3.346 · Cited by 829 · see citing works
Oxytocin, vasopressin, and human social behavior
Heinrichs, M., von Dawans, B., & Domes, G. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.05.005 · Cited by 799 · see citing works
Facial Emotion Recognition in Schizophrenia: Intensity Effects and Error Pattern
Kohler, C. G., Turner, T. H., Bilker, W. B., Brensinger, C. M., Siegel, S. J., Kanes, S., Gur, R. E., & Gur, R. C. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.10.1768 · Cited by 782 · see citing works
Oxytocin attenuates amygdala responses to emotional faces regardless of valence
Domes, G., Heinrichs, M., Gläscher, J., Büchel, C., Braus, D. F., & Herpertz, S. C. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.03.025 · Cited by 774 · cited 5× · see citing works
“…for Marsh et al. (2010), Di Simplicio et al. (2009), and Fisher-Shofty et al. (2010) more closely resembled those of the current study, but all three utilized morphed, not static, stimuli, and FisherShofty et al. subjects, like those in the Domes et al. (2007b) study, viewed only the eye region.”
BackgroundResultInfluentialOxytocin enhances amygdala-dependent, socially reinforced learning and emotional empathy in humans
Hurlemann, R., Patin, A., Onur, O. A., Cohen, M. X., Baumgartner, T., Metzler, S., Dziobek, I., Gallinat, J., Wagner, M., Maier, W., et al. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5538-09.2010 · Cited by 771 · see citing works
Recognition of facial emotion in nine individuals with bilateral amygdala damage
Adolphs, R., Tranel, D., Hamann, S. B., Young, A. W., Calder, A. J., Phelps, E. A., Anderson, A. K., Lee, G. P., & Damásio, A. R. (1999) · Neuropsychologia · doi:10.1016/s0028-3932(99)00039-1 · Cited by 751 · see citing works
Processing of facial emotion expression in major depression: a review
Bourke, C., Douglas, K., & Porter, R. (2010) · Australian & New Zealand Journal of Psychiatry · doi:10.3109/00048674.2010.496359 · Cited by 557 · see citing works
Effects of intranasal oxytocin on emotional face processing in women
Domes, G., Lischke, A., Berger, C., Grossmann, A., Hauenstein, K., Heinrichs, M., & Herpertz, S. C. (2010) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2009.06.016 · Cited by 521 · cited 2× · see citing works
“Furthermore, some oxytocin effects vary markedly by gender (Domes et al. 2010), but our sample was too small to address gender effects.”
BackgroundDifferent amygdala subregions mediate valence-related and attentional effects of oxytocin in humans
Gamer, M., Zurowski, B., & Büchel, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000985107 · Cited by 487 · cited 2× · see citing works
“Intranasal oxytocin enhances facial affect discrimination (Marsh et al. 2007) and specifically reduces detection of fear in nonfearful faces (Fischer-Shofty et al. 2010) perhaps by diminishing amygdala activity (Kirsch et al. 2005; Domes et al. 2007a; Gamer et al. 2010).”
BackgroundFacial affect recognition: A mediator between cognitive and social functioning in psychosis?
ADDINGTON, J., Saeedi, H., & Addington, D. E. (2006) · Schizophrenia Research · doi:10.1016/j.schres.2006.03.028 · Cited by 345 · see citing works
Oxytocin improves specific recognition of positive facial expressions
Marsh, A. A., Yu, H. H., Pine, D. S., & Blair, R. J. R. (2010) · Psychopharmacology · doi:10.1007/s00213-010-1780-4 · Cited by 321 · see citing works
Adjunctive intranasal oxytocin reduces symptoms in schizophrenia patients
Feifel, D., Macdonald, K., Nguyen, A., Cobb, P., Warlan, H., Galangue, B., Minassian, A., Becker, O., Cooper, J., Perry, W., et al. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.04.039 · Cited by 308 · see citing works
de León, J., Verghese, C., Tracy, J. I., Josiassen, R. C., & Simpson, G. M. (1994) · Biological Psychiatry · doi:10.1016/0006-3223(94)90008-6 · Cited by 279 · see citing works
Prenatal stress generates deficits in rat social behavior: Reversal by oxytocin
Lee, P. R., Brady, D. L., Shapiro, R. A., Dorsa, D. M., & Koenig, J. I. (2007) · Brain Research · doi:10.1016/j.brainres.2007.04.042 · Cited by 270 · see citing works
Accurate identification of fear facial expressions predicts prosocial behavior.
Marsh, A. A., Kozak, M. N., & Ambady, N. (2007) · Emotion · doi:10.1037/1528-3542.7.2.239 · Cited by 265 · see citing works
Di Simplicio, M., Massey-Chase, R., Cowen, P., & Harmer, C. (2009) · Journal of Psychopharmacology · doi:10.1177/0269881108095705 · Cited by 229 · see citing works
Gur, R. E., Loughead, J., Kohler, C. G., Elliott, M. A., Lesko, K., Ruparel, K., Wolf, D. H., Bilker, W. B., & Gur, R. C. (2007) · Archives of General Psychiatry · doi:10.1001/archpsyc.64.12.1356 · Cited by 229 · see citing works
Salonia, A., Nappi, R. E., Pontillo, M., Daverio, R., Smeraldi, A., Briganti, A., Fabbri, F., Zanni, G. E., Rigatti, P., & Montorsi, F. (2004) · Hormones and Behavior · doi:10.1016/j.yhbeh.2004.10.002 · Cited by 229 · see citing works
Peripheral oxytocin is associated with reduced symptom severity in schizophrenia
Rubin, L. H., Carter, C. S., Drogos, L. L., Pournajafi‐Nazarloo, H., Sweeney, J. A., & Maki, P. M. (2010) · Schizophrenia Research · doi:10.1016/j.schres.2010.09.014 · Cited by 228 · see citing works
Impairment in the Specificity of Emotion Processing in Schizophrenia
Schneider, F. W., Gur, R. C., Koch, K., Backes, V., Amunts, K., Shah, N. J., Bilker, W. B., Gur, R. E., & Habel, U. (2006) · American Journal of Psychiatry · doi:10.1176/appi.ajp.163.3.442 · Cited by 215 · see citing works
Social cognition in schizophrenia: a review of face processing
Marwick, K., & Hall, J. (2008) · British Medical Bulletin · doi:10.1093/bmb/ldn035 · Cited by 214 · see citing works
Kucharska‐Pietura, K., David, A. S., Masiak, M., & Phillips, M. L. (2005) · The British Journal of Psychiatry · doi:10.1192/bjp.187.6.523 · Cited by 213 · see citing works
Goldman, M. B., Marlow-O’Connor, M., Torres, I. J., & Carter, C. S. (2007) · Schizophrenia Research · doi:10.1016/j.schres.2007.09.019 · Cited by 211 · see citing works
Overactivation of Fear Systems to Neutral Faces in Schizophrenia
Hall, J., Whalley, H. C., McKirdy, J. W., Romaniuk, L., McGonigle, D. J., McIntosh, A. M., Baig, B. J., Gountouna, V., Job, D. E., Donaldson, D. I., et al. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.12.014 · Cited by 195 · see citing works
The effect of intranasal administration of oxytocin on fear recognition
Fischer-Shofty, M., Shamay-Tsoory, S. G., Harari, H., & Levkovitz, Y. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.09.003 · Cited by 184 · see citing works
Sharing secrets: oxytocin and trust in schizophrenia
Kéri, S., Kiss, I., & Kelemen, O. (2009) · Social Neuroscience · doi:10.1080/17470910802319710 · Cited by 167 · see citing works
Sustained activation of the hippocampus in response to fearful faces in schizophrenia
Holt, D. J., Weiss, A. P., Rauch, S. L., Wright, C. I., Zalesak, M., GOFF, D. C., Ditman, T., Welsh, R. C., & Heckers, S. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.01.033 · Cited by 139 · see citing works
Intranasal drug targeting of hypocretin-1 (orexin-A) to the central nervous system
Dhuria, S. V., Hanson, L. R., & Frey, W. H. (2008) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.21604 · Cited by 135 · see citing works
Oxytocin modulates psychotomimetic-induced deficits in sensorimotor gating
Feifel, D., & Reza, T. L. (1999) · Psychopharmacology · doi:10.1007/s002130050811 · Cited by 121 · see citing works
Oxytocin Links Mothering Received, Mothering Bestowed and Adult Stress Responses
Pedersen, C. A., & Boccia, M. L. (2002) · Stress · doi:10.1080/1025389021000037586 · Cited by 116 · see citing works
Oxytocin as a natural antipsychotic: a study using oxytocin knockout mice
Caldwell, H. K., Stephens, S. L., & Young, W. S. (2008) · Molecular Psychiatry · doi:10.1038/sj.mp.4002150 · Cited by 108 · see citing works
Addington, J., Girard, T. A., Christensen, B. K., & Addington, D. E. (2010) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.080039 · Cited by 100 · see citing works
Goldman, M. B. (1997) · Archives of General Psychiatry · doi:10.1001/archpsyc.1997.01830170069010 · Cited by 99 · see citing works
Tsoi, D. T., Lee, K.-H., Khokhar, W. A., Mir, N. U., Swalli, J. S., Gee, K. A., Pluck, G., & Woodruff, P. W. R. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2007.11.006 · Cited by 92 · see citing works
Goghari, V. M., MacDonald, A. W., & Sponheim, S. R. (2010) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq046 · Cited by 90 · see citing works
Intranasal oxytocin in obsessive-compulsive disorder
Epperson, C. N., McDougle, C. J., & Price, L. H. (1996) · Biological Psychiatry · doi:10.1016/0006-3223(96)00120-5 · Cited by 88 · see citing works
Impaired facial emotion recognition and reduced amygdalar volume in schizophrenia
Namiki, C., Hirao, K., Yamada, M., Hanakawa, T., Fukuyama, H., Hayashi, T., & Murai, T. (2007) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2007.03.004 · Cited by 78 · see citing works
ORGANIC FUNCTIONS IN SCHIZOPHRENIA
Hoskins, R. G. (1933) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1933.02240130131008 · Cited by 75 · see citing works
Goldman, M. B. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.06.004 · Cited by 60 · see citing works
Hawken, E. R., Crookall, J. M., Reddick, D., Millson, R. C., Milev, R. V., & Delva, N. J. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2008.09.029 · Cited by 56 · see citing works
Goldman, M. B., Gnerlich, J. L., & Hussain, N. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301282 · Cited by 40 · see citing works
Poirier, S., Legris, G., Tremblay, P., Michea, R., Viau-Guay, L., Mérette, C., Bouchard, R.-H., Maziade, M., & Roy, M. (2010) · Schizophrenia Research · doi:10.1016/j.schres.2009.12.036 · Cited by 32 · see citing works
Goldman, M. B., Blake, L., Marks, R., Hedeker, D., & Luchins, D. J. (1993) · American Journal of Psychiatry · doi:10.1176/ajp.150.4.653 · Cited by 32 · see citing works
Goldman, H. H. (1993) · American Journal of Psychiatry · doi:10.1176/ajp.150.10.1535 · Cited by 31 · see citing works
Bralet, M., Ton, T., & Falissard, B. (2007) · Psychiatry Research · doi:10.1016/j.psychres.2006.11.009 · Cited by 24 · see citing works
Structural pathology underlying neuroendocrine dysfunction in schizophrenia
Goldman, M. B., Wang, L., Wachi, C., Daudi, S., Csernansky, J. G., Marlow-O’Connor, M., Keedy, S., & Torres, I. J. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.11.025 · Cited by 24 · see citing works
Attribution Biases in Schizophrenia: Relationship to Clinical and Functional Impairments
Cohen, A. S., Nienow, T. M., Dinzeo, T. J., & Docherty, N. M. (2008) · Psychopathology · doi:10.1159/000173702 · Cited by 23 · see citing works
Olfactory deficits in patients with schizophrenia and severe polydipsia
Kopala, L. C., Good, K. P., Koczapski, A. B., & Honer, W. G. (1998) · Biological Psychiatry · doi:10.1016/s0006-3223(97)00436-8 · Cited by 21 · see citing works
Seifer, D. B., Sandberg, E. C., Ueland, K., & Sladen, R. N. (1985) · PubMed · Cited by 20 · see citing works
Association between stereotypic behavior and polydipsia in chronic schizophrenic patients
Shutty, M. S., Mcculley, K., & Pigott, B. (1995) · Journal of Behavior Therapy and Experimental Psychiatry · doi:10.1016/0005-7916(95)00049-6 · Cited by 19 · see citing works
Torres, I., Keedy, S., Marlow-O’Connor, M., Beenken, B., & Goldman, M. (2009) · Neuropsychology · doi:10.1037/a0014481 · Cited by 17 · see citing works
Estimating daily urine volume in psychiatric patients: Empiric confirmation
Goldman, M. B., Marks, R., Blake, L. M., Petkovic, M., Hedeker, D., & Luchins, D. J. (1992) · Biological Psychiatry · doi:10.1016/0006-3223(92)90343-x · Cited by 12 · see citing works
Vieweg, W. V. R., Godleski, L., Hundley, P. L., & Yan, G. R. (1989) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/0278-5846(89)90059-6 · Cited by 3 · see citing works
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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
Is oxytocin “nature’s medicine”
Carter, C. S., Kenkel, W. M., MacLean, E. L., Wilson, S. R., Perkeybile, A. M., Yee, J. R., Ferris, C. F., Nazarloo, H. P., Porges, S. W., Davis, J. M., et al. (2020) · Pharmacological Reviews · doi:10.1124/pr.120.019398 · Cited by 394 · see citing works
Bakermans-Kranenburg, M. J., & van IJzendoorn, M. H. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.34 · Cited by 383 · see citing works
Shahrestani, S., Kemp, A. H., & Guastella, A. J. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.86 · Cited by 283 · see citing works
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
Bales, K. L., Perkeybile, A. M., Conley, O. G., Lee, M. H., Guoynes, C. D., Downing, G. M., Yun, C. R., Solomon, M., Jacob, S., & Mendoza, S. P. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.08.025 · Cited by 265 · see citing works
Kinetics and dose dependency of intranasal oxytocin effects on amygdala reactivity
Spengler, F. B., Schultz, J., Scheele, D., Essel, M., Maier, W., Heinrichs, M., & Hurlemann, R. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.04.015 · Cited by 229 · see citing works
Intranasal oxytocin attenuates the cortisol response to physical stress: a dose-response study
Cardoso, C., Ellenbogen, M. A., Orlando, M. A., Bacon, S. L., & Joober, R. (2013) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.07.013 · Cited by 187 · see citing works
Crockford, C., Deschner, T., Ziegler, T. E., & Wittig, R. M. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00068 · Cited by 187 · 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
MacDonald, K., & Feifel, D. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00035 · Cited by 181 · see citing works
Intranasal administration of oxytocin: behavioral and clinical effects, a review
Veening, J. G., & Olivier, B. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.04.012 · Cited by 169 · see citing works
The Oxytocin–Vasopressin Pathway in the Context of Love and Fear
Carter, C. S. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00356 · Cited by 162 · see citing works
Oxytocin-Augmented Social Cognitive Skills Training in Schizophrenia
Davis, M. C., Green, M. F., Lee, J., Horan, W. P., Senturk, D., Clarke, A. D., & Marder, S. R. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.68 · Cited by 149 · see citing works
Yamasue, H., Yee, J. R., Hurlemann, R., Rilling, J. K., Chen, F. S., Meyer-Lindenberg, A., & Tost, H. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3327-12.2012 · Cited by 149 · see citing works
Blevins, J. E., & Baskin, D. G. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.05.023 · Cited by 132 · see citing works
Long-term exposure to intranasal oxytocin in a mouse autism model
Bales, K. L., Solomon, M., Jacob, S., Crawley, J. N., Silverman, J. L., Larke, R. H., Sahagún, E., Puhger, K. R., Pride, M. C., & Mendoza, S. P. (2014) · Translational Psychiatry · doi:10.1038/tp.2014.117 · Cited by 131 · see citing works
Reduced levels of vasopressin and reduced behavioral modulation of oxytocin in psychotic disorders
Rubin, L. H., Carter, C. S., Bishop, J. R., Pournajafi-Nazarloo, H., Drogos, L. L., Hill, S. K., Ruocco, A. C., Keedy, S. K., Reilly, J. L., Keshavan, M. S., et al. (2014) · Schizophrenia Bulletin · doi:10.1093/schbul/sbu027 · Cited by 127 · see citing works
Effects of single dose intranasal oxytocin on social cognition in schizophrenia
Davis, M. C., Lee, J., Horan, W. P., Clarke, A. D., McGee, M. R., Green, M. F., & Marder, S. R. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.04.023 · Cited by 124 · see citing works
Montag, C., Brockmann, E.-M., Lehmann, A. I., Müller, D. J., Rujescu, D., & Gallinat, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051882 · Cited by 123 · see citing works
Cacciotti-Saija, C., Langdon, R., Ward, P. B., Hickie, I. B., Scott, E. M., Naismith, S. L., Moore, L., Alvares, G. A., Redoblado Hodge, M. A., & Guastella, A. J. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbu094 · Cited by 119 · see citing works
Millan, M. J., & Bales, K. L. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.09.012 · Cited by 116 · see citing works
Kosaka, H., Okamoto, Y., Munesue, T., Yamasue, H., Inohara, K., Fujioka, T., Anme, T., Orisaka, M., Ishitobi, M., Jung, M., et al. (2016) · Translational Psychiatry · doi:10.1038/tp.2016.152 · Cited by 117 · see citing works
Oxytocin administration enhances controlled social cognition in patients with schizophrenia
Woolley, J. D., Chuang, B., Lam, O., Lai, W., O’Donovan, A., Rankin, K. P., Mathalon, D. H., & Vinogradov, S. (2014) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2014.04.024 · Cited by 116 · see citing works
Oxytocin in schizophrenia: a review of evidence for its therapeutic effects
MacDonald, K. S., & Feifel, D. (2011) · Acta Neuropsychiatrica · doi:10.1111/j.1601-5215.2011.00634.x · Cited by 111 · see citing works
A Review of Oxytocin’s Effects on the Positive, Negative, and Cognitive Domains of Schizophrenia
Feifel, D., Shilling, P. D., & MacDonald, K. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.07.025 · Cited by 110 · see citing works
Role of oxytocin signaling in the regulation of body weight
Blevins, J. E., & Ho, J. M. (2013) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-013-9260-x · Cited by 108 · see citing works
Intranasal Oxytocin as an Adjunct to Risperidone in Patients with Schizophrenia
Modabbernia, A., Rezaei, F., Salehi, B., Jafarinia, M., Ashrafi, M., Tabrizi, M. H., Hosseini, S. M. R., Tajdini, M., Ghaleiha, A., & Akhondzadeh, S. (2012) · CNS Drugs · doi:10.1007/s40263-012-0022-1 · Cited by 107 · see citing works
Oxytocin and oxytocin receptor gene polymorphisms and risk for schizophrenia: A case–control study
Montag, C., Brockmann, E.-M., Bayerl, M., Rujescu, D., Müller, D. J., & Gallinat, J. (2012) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2012.677547 · Cited by 104 · see citing works
From Autism to Eating Disorders and More: The Role of Oxytocin in Neuropsychiatric Disorders
Romano, A., Tempesta, B., Bonaventura, M. V. M. D., & Gaetani, S. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00497 · Cited by 102 · see citing works
Intranasal oxytocin effects on social cognition: A critique
Evans, S. L., Dal Monte, O., Noble, P., & Averbeck, B. B. (2014) · Brain Research · doi:10.1016/j.brainres.2013.11.008 · Cited by 97 · see citing works
Oxytocin and stress-related disorders: neurobiological mechanisms and treatment opportunities
Sippel, L. M., Allington, C. E., Pietrzak, R. H., Harpaz-Rotem, I., Mayes, L. C., & Olff, M. (2017) · Chronic Stress · doi:10.1177/2470547016687996 · Cited by 99 · see citing works
Social cognitive interventions for people with schizophrenia: A systematic review
Tan, B., Lee, S.-A., & Lee, J. (2016) · Asian Journal of Psychiatry · doi:10.1016/j.ajp.2016.06.013 · Cited by 97 · see citing works
Sex-specific associations between peripheral oxytocin and emotion perception in schizophrenia
Rubin, L. H., Carter, C. S., Drogos, L. L., Jamadar, R., Pournajafi‐Nazarloo, H., Sweeney, J. A., & Maki, P. M. (2011) · Schizophrenia Research · doi:10.1016/j.schres.2011.06.002 · Cited by 91 · see citing works
Oxytocin and vasopressin levels are decreased in the plasma of male schizophrenia patients
Jobst, A., Dehning, S., Ruf, S., Notz, T., Buchheim, A., Henning-Fast, K., Meißner, D., Meyer, S., Bondy, B., Müller, N., et al. (2014) · Acta Neuropsychiatrica · doi:10.1017/neu.2014.20 · Cited by 89 · see citing works
Oxytocin effects in schizophrenia: Reconciling mixed findings and moving forward
Bradley, E., & Woolley, J. D. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.05.007 · Cited by 88 · see citing works
Gibson, C. M., Penn, D. L., Smedley, K. L., Leserman, J., Elliott, T., & Pedersen, C. A. (2014) · Schizophrenia Research · doi:10.1016/j.schres.2014.04.009 · Cited by 88 · see citing works
The many faces of oxytocin: Implications for psychiatry
Zik, J. B., & Roberts, D. L. (2014) · Psychiatry Research · doi:10.1016/j.psychres.2014.11.048 · Cited by 85 · see citing works
Potential of Oxytocin in the Treatment of Schizophrenia
Shilling, P. D., & Feifel, D. (2016) · CNS Drugs · doi:10.1007/s40263-016-0315-x · Cited by 82 · see citing works
Improving social perception in schizophrenia: The role of oxytocin
Fischer-Shofty, M., Brüne, M., Ebert, A., Shefet, D., Levkovitz, Y., & Shamay‐Tsoory, S. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.01.006 · Cited by 83 · see citing works
Inhaled oxytocin increases positive social behaviors in newborn macaques
Simpson, E. A., Sclafani, V., Paukner, A., Hamel, A. F., Novak, M. A., Meyer, J. S., Suomi, S. J., & Ferrari, P. F. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402471111 · Cited by 82 · see citing works
Oxytocin enhances attention to the eye region in rhesus monkeys
Dal Monte, O., Noble, P. L., Costa, V. D., & Averbeck, B. B. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00041 · Cited by 80 · see citing works
Self-reported empathy deficits are uniquely associated with poor functioning in schizophrenia
Smith, M. J., Horan, W. P., Karpouzian‐Rogers, T., Abram, S. V., Cobia, D. J., & Csernansky, J. G. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.01.012 · Cited by 81 · see citing works
Bürkner, P., Williams, D. R., Simmons, T. C., & Woolley, J. D. (2017) · Schizophrenia Bulletin · doi:10.1093/schbul/sbx053 · Cited by 80 · see citing works
Oxytocin in Schizophrenia: Pathophysiology and Implications for Future Treatment
Goh, K. K., Chen, C.-H., & Lane, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22042146 · Cited by 78 · see citing works
Peled‐Avron, L., Abu-Akel, A. M., & Shamay‐Tsoory, S. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.023 · Cited by 73 · see citing works
Oxytocin administration alters HPA reactivity in the context of parent–infant interaction
Weisman, O., Zagoory-Sharon, O., & Feldman, R. (2013) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2013.06.006 · Cited by 70 · see citing works
A single dose of oxytocin nasal spray improves higher-order social cognition in schizophrenia
Guastella, A. J., Ward, P. B., Hickie, I. B., Shahrestani, S., Hodge, M. A., Scott, E. M., & Langdon, R. A. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2015.06.005 · Cited by 66 · see citing works
Rubin, L. H., Carter, C. S., Bishop, J. R., Pournajafi‐Nazarloo, H., Harris, M. S. H., Hill, S. K., Reilly, J. L., & Sweeney, J. A. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.01.019 · Cited by 65 · see citing works
Cardoso, C., Linnen, A.-M., Joober, R., & Ellenbogen, M. A. (2012) · Experimental and Clinical Psychopharmacology · doi:10.1037/a0025763 · Cited by 60 · see citing works
Frijling, J. L., van Zuiden, M., Koch, S. B., Nawijn, L., Goslings, J. C., Luitse, J. S., Biesheuvel, T. H., Honig, A., Bakker, F. C., Denys, D., et al. (2014) · BMC Psychiatry · doi:10.1186/1471-244x-14-92 · Cited by 59 · see citing works
A Role for Oxytocin in the Etiology and Treatment of Schizophrenia
Rich, M. E., & Caldwell, H. K. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00090 · Cited by 55 · see citing works
Jarskog, L. F., Pedersen, C. A., Johnson, J. L., Hamer, R. M., Rau, S. W., Elliott, T., & Penn, D. L. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.01.008 · Cited by 55 · see citing works
Strauss, G. P., Keller, W. R., Koenig, J. I., Gold, J. M., Ossenfort, K. L., & Buchanan, R. W. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2014.12.023 · Cited by 54 · see citing works
Bartholomeusz, C. F., Ganella, E. P., Labuschagne, I., Bousman, C., & Pantelis, C. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2015.06.007 · Cited by 54 · see citing works
Oxytocin and social cognition in affective and psychotic disorders
Pérez-Rodríguez, M. M., Mahon, K., Russo, M., Ungar, A. K., & Burdick, K. E. (2014) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2014.07.012 · Cited by 52 · see citing works
Oya, K., Matsuda, Y., Matsunaga, S., Kishi, T., & Iwata, N. (2015) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-015-0634-9 · Cited by 51 · see citing works
Plasma oxytocin levels predict social cue recognition in individuals with schizophrenia
Strauss, G. P., Keller, W. R., Koenig, J. I., Gold, J. M., Frost, K. H., & Buchanan, R. W. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2015.01.034 · Cited by 51 · see citing works
Strauss, G. P., Chapman, H. C., Keller, W. R., Koenig, J. I., Gold, J. M., Carpenter, W. T., & Buchanan, R. W. (2019) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2019.02.017 · Cited by 49 · see citing works
Strauss, G. P., Keller, W. R., Koenig, J. I., Sullivan, S. K., Gold, J. M., & Buchanan, R. W. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2015.01.022 · Cited by 46 · see citing works
Bose, M., Quipildor, G. F., Ehrlich, M. E., & Salton, S. R. (2022) · Cells · doi:10.3390/cells11223629 · Cited by 44 · see citing works
Fischer-Shofty, M., Shamay‐Tsoory, S., & Levkovitz, Y. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00127 · Cited by 41 · see citing works
Comparative and developmental perspectives on oxytocin and vasopressin.
Bales, K. L. (2013) · American Psychological Association eBooks · doi:10.1037/14250-002 · Cited by 40 · see citing works
Buchanan, R. W., Kelly, D. L., Weiner, E., Gold, J. M., Strauss, G. P., Koola, M. M., McMahon, R. P., & Carpenter, W. T. (2017) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0000000000000720 · Cited by 40 · see citing works
Sabé, M., Zhao, N., Crippa, A., Strauss, G. P., & Kaiser, S. (2021) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyab020 · Cited by 40 · see citing works
The Role of Intranasal Oxytocin in the Treatment of Patients with Schizophrenia: A Systematic Review
Berardis, D. D., Marini, S., Iasevoli, F., Tomasetti, C., de Bartolomeis, A., Mazza, M., Valchera, A., Fornaro, M., Cavuto, M., Srinivasan, V., et al. (2013) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527311312020012 · Cited by 38 · see citing works
Oxytocin Signaling Pathway: From Cell Biology to Clinical Implications
Iovino, M., Messana, T., Tortora, A., Giusti, C., Lisco, G., Giagulli, V. A., Guastamacchia, E., Pergola, G. D., & Triggiani, V. (2020) · Endocrine Metabolic & Immune Disorders - Drug Targets · doi:10.2174/1871530320666200520093730 · Cited by 39 · see citing works
Cardoso, C., Orlando, M. A., Brown, C. A., & Ellenbogen, M. A. (2014) · Social Neuroscience · doi:10.1080/17470919.2013.873079 · Cited by 37 · see citing works
Horta de Macedo, L. R., Zuardi, A. W., Machado-de-Sousa, J. P., Chagas, M. H. N., & Hallak, J. E. C. (2014) · Psychiatry Research · doi:10.1016/j.psychres.2014.07.082 · Cited by 35 · see citing works
Gumley, A. I., Braehler, C., & MacBeth, A. M. (2014) · British Journal of Clinical Psychology · doi:10.1111/bjc.12041 · Cited by 34 · see citing works
RetractedThe Potential of Nasal Oxytocin Administration for Remediation of Autism Spectrum Disorders
Okamoto, Y., Ishitobi, M., Wada, Y., & Kosaka, H. (2016) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527315666160413120845 · Cited by 33 · see citing works
Green, M. F., Lee, J., & Ochsner, K. N. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt131 · Cited by 33 · see citing works
Oxytocin and interpersonal relationships
Patin, A., Scheele, D., & Hurlemann, R. (2017) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2017_22 · Cited by 32 · see citing works
Schwartz, S. S., Gallagher, R. J., & Berkson, G. (1986) · PubMed · Cited by 32 · see citing works
Patin, A., & Hurlemann, R. (2015) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-16522-6_10 · Cited by 32 · see citing works
Oxytozin: Evidenz für ein therapeutisches Potenzial des sozialen Neuromodulators
Eckstein, M., & Hurlemann, R. (2013) · Der Nervenarzt · doi:10.1007/s00115-013-3832-6 · Cited by 28 · see citing works
Canty, A. L., Cao, Y., Neumann, D. L., & Shum, D. (2021) · Psychiatry Research · doi:10.1016/j.psychres.2021.113852 · Cited by 26 · see citing works
Oxytocin improves probabilistic reversal learning but not effortful motivation in Brown Norway rats
Roberts, B. Z., Young, J. W., He, Y. V., Cope, Z. A., Shilling, P. D., & Feifel, D. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.02.028 · Cited by 24 · see citing works
Are We There Yet? The Clinical Potential of Intranasal Oxytocin in Psychiatry
Liu, J. C., McErlean, R. A., & Dadds, M. R. (2012) · Current Psychiatry Reviews · doi:10.2174/157340012798994902 · Cited by 24 · see citing works
Strauss, G. P., Granholm, E. L., Holden, J. L., Ruiz, I., Gold, J. M., Kelly, D. L., & Buchanan, R. W. (2018) · Psychological Medicine · doi:10.1017/s0033291718002465 · Cited by 25 · see citing works
Oxytocin and Social Cognitions in Schizophrenia: A Systematic Review
Bukovskaya, O., & Shmukler, A. B. (2015) · Psychiatric Quarterly · doi:10.1007/s11126-015-9407-x · Cited by 22 · see citing works
Skinner, J. A., Garg, M. L., Dayas, C. V., Fenton, S., & Burrows, T. L. (2018) · Nutrition Reviews · doi:10.1093/nutrit/nux078 · Cited by 22 · see citing works
Brain circuit dysfunction in a distinct subset of chronic psychotic patients
Goldman, M. B. (2014) · Schizophrenia Research · doi:10.1016/j.schres.2014.06.001 · Cited by 21 · see citing works
Increased Serum and Urinary Oxytocin Concentrations after Nasal Administration in Beagle Dogs
Temesi, A., Thuróczy, J., Balogh, L., & Miklósi, Á. (2017) · Frontiers in Veterinary Science · doi:10.3389/fvets.2017.00147 · Cited by 18 · see citing works
Nance, M. G., Sullivan, K. M., & Puglia, M. H. (2024) · Pediatric Research · doi:10.1038/s41390-024-03563-z · Cited by 18 · see citing works
Romero‐Martínez, Á., Sarrate‐Costa, C., & Moya‐Albiol, L. (2021) · Biology · doi:10.3390/biology10121334 · Cited by 18 · see citing works
Reproductive experiential regulation of cognitive and emotional resilience
Kinsley, C. H., Bales, K. L., Bardi, M., & Stolzenberg, D. S. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.05.015 · Cited by 17 · see citing works
Güzel, D., Yazıcı, A. B., Pek, T. M., Doğanay, S., Saykan, A. B., Sağlam, K., Turan, Ç., & Yazıcı, E. (2018) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s169619 · Cited by 16 · see citing works
Marazziti, D., Diep, P.-T., Carter, C. S., & Carbone, M. G. (2022) · Current Medicinal Chemistry · doi:10.2174/0929867329666220727120646 · Cited by 16 · see citing works
Oxytocin and Schizophrenia Spectrum Disorders
Ettinger, U., Hurlemann, R., & Chan, R. C. K. (2017) · Current topics in behavioral neurosciences · doi:10.1007/7854_2017_27 · Cited by 16 · see citing works
Pedersen, C. A. (2014) · Brain Research · doi:10.1016/j.brainres.2014.01.050 · Cited by 12 · see citing works
Spilka, M. J., Keller, W. R., Buchanan, R. W., Gold, J. M., Koenig, J. I., & Strauss, G. P. (2022) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.13421 · Cited by 12 · see citing works
Exploring a Possible Interplay between Schizophrenia, Oxytocin, and Estrogens: A Narrative Review
Papadea, D., Dalla, C., & Tata, D. Α. (2023) · Brain Sciences · doi:10.3390/brainsci13030461 · Cited by 11 · see citing works
Personality Disorders, Attachment and Psychodynamic Psychotherapy
Weinstein, L., Pérez-Rodríguez, M. M., & Siever, L. J. (2014) · Psychopathology · doi:10.1159/000366135 · Cited by 8 · see citing works
The Use of Oxytocin in Personality Disorders: Rationale and Current Status
Pérez-Rodríguez, M. M., Derish, N. E., & New, A. S. (2014) · Current Treatment Options in Psychiatry · doi:10.1007/s40501-014-0026-1 · Cited by 7 · see citing works
Schepisi, C., Cianci, S., Bedse, G., Fu, J., Gaetani, S., & Nencini, P. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3527-0 · Cited by 6 · see citing works
Massey, S. H., Estabrook, R., Lapping-Carr, L. R., Newmark, R. L., Jean Decety, A., Wisner, K. L., & Wakschlag, L. S. (2022) · Social Science & Medicine · doi:10.1016/j.socscimed.2022.115071 · Cited by 5 · see citing works
Oxytocin in Prevention of Schizophrenia
Tadjibaev, A. (2013) · International Journal of Prevention and Treatment of Substance Use Disorders · Cited by 4 · see citing works
Heinrichs, M., Chen, F. S., & Domes, G. (2012) · Wiley eBooks · doi:10.1002/9781119945901.ch8 · Cited by 4 · see citing works
Doshi, G., Bhatia, N. Y., Ved, H. S., Pandya, A., Kulkarni, D., Naik, J., Bandiwadekar, T., Godad, A. P., & Kale, P. P. (2022) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527321666220817161035 · Cited by 3 · see citing works
- Authors
- Goldman, M. B., Gomes, A. M., Carter, C. S., & Lee, R.
- Affiliations
- Northwestern University (US)
- University of Illinois Chicago (US)
- University of Chicago (US)
- Corresponding author
- Goldman, Morris B.
- Venue
- Psychopharmacology
- Published
- 2011-02-09
- Volume
- 216
- Issue
- 1
- Pages
- 101-110
- ISSN
- 0033-3158 (ISSN-L)
- 1432-2072
- OpenAlex
- W2071486937
- Cited by
- 112
- References
- 62
- Citations by year
- 2024: 1 · 2023: 1 · 2022: 5 · 2021: 5 · 2020: 4 · 2019: 5 · 2018: 3 · 2017: 11 · 2016: 6 · 2015: 12 · 2014: 24 · 2013: 20 · 2012: 10
- FWCI
- 25.20
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Psychopharmacology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Chicago
- National Institutes of Health
- National Institute of Mental Health (R21MH082295)
- Topics
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
- Keywords
- intranasal oxytocin, polydipsia, schizophrenia, facial emotion recognition, dose-dependent effects, hyponatremia, dexamethasone resistance, neuroendocrine dysfunction, vasopressin, stress hormones
- MeSH terms
- Administration, Intranasal, Adult, Dose-Response Relationship, Drug, Double-Blind Method, Emotions, Facial Expression, Female, Humans, Male, Middle Aged, Oxytocin, Pilot Projects, Schizophrenia, Schizophrenic Psychology, Thirst, Linear Models
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