The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
The comparative distribution of forebrain receptors for neurohypophyseal peptides in monogamous and polygamous mice
Abstract
Several recent studies have suggested that the neurohypophyseal peptide oxytocin may have a role within the brain to mediate various forms of affiliative behavior. As the regulation of oxytocin function may be largely determined by the number and distribution of its membrane bound receptor, we investigated oxytocin receptor distribution in two Peromyscus species selected for differences in affiliative behavior. Using in vitro receptor autoradiography with the selective oxytocin receptor ligand [125I]d(CH2)5[Tyr(Me)2,Tyr-NH9(2)]OVT ([125I]OTA), we compared Peromyscus maniculatus, a polygamous species, to Peromyscus californicus, a monogamous species. Marked species differences in the distribution of [125I]OTA were apparent in several brain areas, including olfactory pathways, bed nucleus of the stria terminalis, amygdala, dorsal lateral septum, and several cortical regions. In addition, gender differences in the binding pattern were evident in several regions, mostly due to sexually dimorphic patterns in the polygamous species, P. maniculatus. To further compare these species, the binding of a [3H]arginine-vasopressin antagonist was assessed in alternate sections from those used for [125I]OTA. Relative to oxytocin receptors, binding to arginine-vasopressin receptors showed fewer species differences, although the monogamous species appeared to have more arginine-vasopressin receptors in the neocortex and lateral septum. The striking differences in oxytocin receptor distribution are consistent with earlier studies in other rodents, suggesting that oxytocin may have an important role for mediating species-typical patterns of social affiliation.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“In Peromyscus (P.) maniculatus and P. californicus mice, no sex differences were found for VP receptor binding in any of the brain regions analyzed, except for higher binding in the centromedial thalamic nucleus in females”
From Vasopressin and oxytocin receptor systems in the brain: Sex differences and sex-specific regulation of social behavior (2016) · cites this paper as Insel et al., 1991
In the citing paper
“Interestingly, these sex-specific effects seem to be independent of whether sex differences are found in VP and/or V1aR binding (rats; Figs. 1 and 2) or whether no sex differences are found in VP and/or V1aR binding (prairie voles: Insel et al., 1991; Smeltzer et al., 2006; humans: Loup et al., 1991).”
From Vasopressin and oxytocin receptor systems in the brain: Sex differences and sex-specific regulation of social behavior (2016) · cites this paper as Insel et al., 1991
In the citing paper
“Similar to V1aR, sex differences in OTR binding were found in multiple brain regions in those rodent studies that used a more comprehensive analysis (deer mice: 8 out of 20 brain regions; Insel et al., 1991; rats: 9 out of 15 forebrain regions; Dumais et al., 2013).”
From Vasopressin and oxytocin receptor systems in the brain: Sex differences and sex-specific regulation of social behavior (2016) · cites this paper as Insel et al., 1991
In the citing paper
“There were no sex differences in OTR expression, consistent with previous reports in other species (53, 54).”
From Oxytocin receptors in the anteromedial bed nucleus of the stria terminalis promote stress-induced social avoidance in female California mice (2018) · cites this paper as [54]
Citations
Cites
Pedersen, C. A., & Prange, A. J. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.12.6661 · Cited by 841
Oxytocin induces maternal behavior in virgin female rats
Pedersen, C. A., Ascher, J. A., Monroe, Y. L., & Prange, A. J. (1982) · Science · doi:10.1126/science.7071605 · Cited by 770
Evolution of spatial cognition: sex-specific patterns of spatial behavior predict hippocampal size.
Jacobs, L. F., Gaulin, S. J. C., Sherry, D. F., & Hoffman, G. E. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.16.6349 · Cited by 370
Possible Role for Endogenous Oxytocin in Estrogen-Facilitated Maternal Behavior in Rats
Fahrbach, S. E., Morrell, J. I., & Pfaff, D. W. (2008) · Neuroendocrinology · doi:10.1159/000124125 · Cited by 322
The biparental care system of the California mouse, Peromyscus californicus.
Gubernick, D. J., & Alberts, J. R. (1987) · Journal of comparative psychology · doi:10.1037/0735-7036.101.2.169 · Cited by 274
Oxytocin facilitates the sexual receptivity of estrogen-treated female rats
Caldwell, J. D., Prange, A. J., & Pedersen, C. A. (1986) · Neuropeptides · doi:10.1016/0143-4179(86)90093-4 · Cited by 229
Sex Differences in Neurotransmitter Systems
Vries, G. J. D. (1990) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1990.tb00385.x · Cited by 226
Gonadal hormone actions on the morphology of the vasopressinergic innervation of the adult rat brain
De Vries, G. J., Buijs, R. M., & Sluiter, A. A. (1984) · Brain Research · doi:10.1016/0006-8993(84)91157-0 · Cited by 224
Tribollet, E., Audigier, S., Dubois-Dauphin, M., & Dreifuss, J. J. (1990) · Brain Research · doi:10.1016/0006-8993(90)90232-z · Cited by 203
Birdsall, D. A., & Nash, D. (1973) · Evolution · doi:10.1111/j.1558-5646.1973.tb05922.x · Cited by 175
Research works printed but not linked: 4
- Archer, 1974, Chemistry of the neurohypophyseal hormones: an example of molecular evolution, Handbook Physiol., 4, 119
- Dewsbury, 1981, An exercise in the prediction of monogamy in the field from laboratory data on 42 species of muroid rodents, The Biologist, 63, 138
- Insel, 1989, The development of the oxytocin receptor in rat forebrain: chemical neuroanatomy and behavioral correlations, Soc. Neurosci. Abstr., 15, 118.11
- Shapiro, 1990, Oxytocin receptor distribution reflects species-typical patterns of social behavior, Soc. Neurosci. Abstr., 16, 186.6
Cited by
Sorted by citations
Items 101–200 of 210
Olazábal, D. E. (2014) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2014.10.002 · Cited by 35
Anxiety or Nervousness Disturbs the Progress of Birth Based on Human Behavioral Evolutionary Biology
Hishikawa, K., Kusaka, T., Fukuda, T., Kohata, Y., & Hiromi, I. (2019) · The Journal of Perinatal Education · doi:10.1891/1058-1243.28.4.218 · Cited by 35
Pultorak, J. D., Alger, S. J., Loria, S. O., Johnson, A. M., & Marler, C. A. (2018) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2018.00125 · Cited by 37
Ophir, A. G., Sorochman, G., Evans, B. L., & Prounis, G. S. (2013) · Journal of Neuroendocrinology · doi:10.1111/jne.12049 · Cited by 32
Mooney, S. J., Coen, C. W., Holmes, M. M., & Beery, A. K. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.06.043 · Cited by 30
Postweaning, forebrain-specific perturbation of the oxytocin system impairs fear conditioning
Pagani, J. H., Lee, H.-J., & Young, W. S. (2011) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2011.00709.x · Cited by 30
Peromyscus as a model system for understanding the regulation of maternal behavior
Bester‐Meredith, J. K., Burns, J. N., Conley, M. F., Mammarella, G. E., & Ng, N. D. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.07.001 · Cited by 29
Pharmacology of Economic and Social Decision Making
Crockett, M. J., & Fehr, E. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-416008-8.00014-0 · Cited by 29
Dubois‐Dauphin, M., Theler, J., Ouarour, A., Pévet, P., Barberis, C., & Dreifuss, J. J. (1994) · Brain Research · doi:10.1016/0006-8993(94)90659-9 · Cited by 28
Oldfield, R. G., Harris, R. M., & Hofmann, H. A. (2015) · Frontiers in Zoology · doi:10.1186/1742-9994-12-s1-s16 · Cited by 28
BAXTER, A. B., Anderson, M., Seelke, A. M. H., Kinnally, E. L., Freeman, S. M., & Bales, K. L. (2020) · Scientific Reports · doi:10.1038/s41598-020-74243-1 · Cited by 26
Laredo, S. A., Orr, V. N., McMackin, M. Z., & Trainor, B. C. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.01.039 · Cited by 26
Behavioral relevance of species-specific vasotocin anatomy in gregarious finches
Kelly, A. M., & Goodson, J. L. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00242 · Cited by 24
Olszewski, P. K., Ulrich, C., Ling, N., Allen, K. L., & Levine, A. S. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2014.07.007 · Cited by 24
Becker, R. O., Lazzari, V. M., Menezes, I. C., Morris, M., Rigatto, K., Lucion, A. B., Rasia‐Filho, A. A., & Giovenardi, M. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.07.034 · Cited by 22
DiBenedictis, B. T., Cheung, H. K., Nussbaum, E. R., & Veenema, A. H. (2019) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2019.104462 · Cited by 21
Oxytocin, vasopressin and their interplay with gonadal steroids
Dhakar, M. B., Stevenson, E. L., & Caldwell, H. K. (2013) · Oxytocin, Vasopressin and Related Peptides in the Regulation of Behavior · doi:10.1017/cbo9781139017855.003 · Cited by 20
Oxytocin, vasopressin, and the evolution of mating systems in mammals
Freeman, S. M., & Young, L. J. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139017855.011 · Cited by 19
Freeman, A. R., Aulino, E. A., Caldwell, H. K., & Ophir, A. G. (2020) · Journal of Neuroendocrinology · doi:10.1111/jne.12828 · Cited by 18
Using transgenic mouse models to study oxytocin's role in the facilitation of species propagation
Lee, H., Pagani, J. H., & Young, W. S. (2010) · Brain Research · doi:10.1016/j.brainres.2010.08.042 · Cited by 21
Towards meeting Tinbergen's challenge
Ophir, A. G. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.03.012 · Cited by 18
Dong, N., Du, P., Hao, X., He, Z., Hou, W., Wang, L., Yuan, W., Yang, J., Jia, R., & Tai, F. (2017) · Neuropeptides · doi:10.1016/j.npep.2017.07.006 · Cited by 20
Keller, M., Pawluski, J. L., Brock, O., Douhard, Q., & Bakker, J. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.01.013 · Cited by 18
Estrogen receptor α and vasopressin in the paraventricular nucleus of the hypothalamus in Peromyscus
Kramer, K. M., Yamamoto, Y., Hoffman, G. E., & Cushing, B. S. (2004) · Brain Research · doi:10.1016/j.brainres.2004.10.070 · Cited by 17
Liu, H., Wang, Y., Crofton, J. T., Funyu, T., & Share, L. (1996) · Brain Research · doi:10.1016/0006-8993(96)00054-6 · Cited by 18
Chappell, A., Freeman, S. M., Lin, Y.-C., LaPrairie, J. L., Inoue, K., Young, L. J., & Hayes, L. D. (2016) · Journal of Zoology · doi:10.1111/jzo.12332 · Cited by 18
Froemke, R. C., & Carcea, I. (2017) · Principles of Gender-Specific Medicine · doi:10.1016/b978-0-12-803506-1.00037-1 · Cited by 20
The Bold, Silent Type: Predictors of Ultrasonic Vocalizations in the Genus Peromyscus
Kalcounis‐Rueppell, M. C., Petric, R., & Marler, C. A. (2018) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2018.00198 · Cited by 17
Potretzke, S., Zhang, Y., Li, J., Fecteau, K. M., Erikson, D. W., Hibert, M., & Ryabinin, A. E. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01490-3 · Cited by 17
Alone, in the dark: The extraordinary neuroethology of the solitary blind mole rat
Kashash, Y., Smarsh, G. C., Zilkha, N., Yovel, Y., & Kimchi, T. (2022) · eLife · doi:10.7554/elife.78295 · Cited by 16
Mechanisms underlying sexual and affiliative behaviors of mice: relation to generalized CNS arousal
Shelley, D. N., Choleris, E., Kavaliers, M., & Pfaff, D. W. (2006) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsl032 · Cited by 17
Coen, C. W., Bennett, N. C., Holmes, M. M., & Faulkes, C. G. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-65943-1_3 · Cited by 16
Valesky, E. M., Burda, H., Kaufmann, R., & Oelschläger, H. (2012) · The Anatomical Record · doi:10.1002/ar.22414 · Cited by 15
Rabhi, M., Stoeckel, M. E., Calas, A., & Freund‐Mercier, M. J. (1999) · Brain Research Bulletin · doi:10.1016/s0361-9230(98)00158-0 · Cited by 15
Oxytocin and the neurobiology of attachment
Insel, T. R. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069818 · Cited by 15
Self-citationClarke, L., Zyga, O., Pineo-Cavanaugh, P. L., Jeng, M., Fischbein, N. J., Partap, S., Katznelson, L. J., & Parker, K. J. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104770 · Cited by 13
Vasopressin as Possible Treatment Option in Autism Spectrum Disorder
László, K., Vörös, D., Correia, P., Fazekas, C. L., Török, B., Plangár, I., & Zelena, D. (2023) · Biomedicines · doi:10.3390/biomedicines11102603 · Cited by 13
The role of oxytocin on peaceful associations and sociality in mammals
Romero, T., Onishi, K., & Hasegawa, T. (2016) · Behaviour · doi:10.1163/1568539x-00003358 · Cited by 13
Powell, J. M., Inoue, K., Wallace, K. J., Seifert, A. W., Young, L. J., & Kelly, A. M. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02581-z · Cited by 13
Vallet, P. G., Bouras, C., Barberis, C., Dreifuss, J. J., & Dubois‐Dauphin, M. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903620206 · Cited by 12
Dumais, K. M., & Veenema, A. H. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-802114-9.00011-1 · Cited by 11
Oxytocin and the Neuroendocrine Basis of Affiliation
Insel, T. R. (1993) · Elsevier eBooks · doi:10.1016/b978-0-12-631330-7.50016-2 · Cited by 11
Self-citationFreeman, A. R., Hare, J. F., & Caldwell, H. K. (2019) · Journal of Neuroscience Research · doi:10.1002/jnr.24400 · Cited by 10
Reese, M. A., Bryant, D. J., & Ethridge, L. E. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.03.009 · Cited by 14
Comparative neurobiology and genetics of mammalian social behavior
Beery, A. K., Kamal, Y., Sobrero, R., & Hayes, L. D. (2016) · Wiley eBooks · doi:10.1002/9781118846506.ch3 · Cited by 9
PVN-mPFC OT projections modulate pup-directed pup care or attacking in virgin mandarin volesPreprint
Li, L., Li, Y., Huang, C., Hou, W., Lv, Z., Zhang, L., Qu, Y., Sun, Y., Huang, K., Han, X., et al. (2024) · eLife · doi:10.7554/elife.96543 · Cited by 10
What do attachment objects afford?
Capitanio, J. P. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069776 · Cited by 8
Oxytocin Receptor Binding Sites in the Periphery of the Neonatal Prairie Vole
Greenwood, M. A., & Hammock, E. A. D. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00474 · Cited by 7
Psychobiological attachment theory (PAT) and psychopathology
Kraemer, G. W. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069922 · Cited by 7
Freeman, S. M. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1759-5_7 · Cited by 7
The interface between the psychobiological and cognitive models of attachment
Sigman, M., & Siegel, D. J. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069892 · Cited by 6
Wunsch, S. (2007) · HAL · Cited by 6
[Fibroma and pregnancy. Apropos of 51 case reports surveyed from April 1976 to December 1984].
Monnier, J. C., Bernardi, C., Lanciaux, B., Vinatier, D., & Lefebvre, C. (1986) · PubMed · Cited by 6
Effects of mesotocin manipulation on the behavior of male and female common waxbills
Trigo, S., Silva, P. A., Cardoso, G. C., & Soares, M. C. (2023) · Physiology & Behavior · doi:10.1016/j.physbeh.2023.114226 · Cited by 5
Mooney, S. J., Forger, N. G., & Holmes, M. M. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-65943-1_4 · Cited by 7
Guoynes, C. D., & Marler, C. A. (2022) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2023.114230 · Cited by 5
The Role of Oxytocin in Neuropsychiatric Disorders: Concepts and Mechanisms
Levin, R., Edelman, S., Shalev, I., Ebstein, R. P., & Heresco‐Levy, U. (2010) · Springer eBooks · doi:10.1007/978-90-481-8553-5_20 · Cited by 5
A wise child: Face perception by human neonates
Ellis, H. D. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0006979x · Cited by 4
Malone, C. L., Li, J., Luebke, E. M., Carreras-Simons, L., Treis, W. W., Hammond, E. R., Monari, P. K., & Marler, C. A. (2025) · Biology of Sex Differences · doi:10.1186/s13293-025-00741-4 · Cited by 4
Chlorpyrifos and neuroendocrine function: Concerns for research with free-living mammal populations
Mitzel, K. M., & Freeman, A. R. (2025) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2025.114807 · Cited by 3
Taylor, J. H., Campbell, N., Powell, J. M., Albers, H. E., & Kelly, A. M. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.05.004 · Cited by 3
Does function imply structure?
Mason, W. A. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069855 · Cited by 3
Kagan, J. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069831 · Cited by 3
Stoehr, M. C., Martin, E. M., Babalola, J. T., Xue, J., Kern, M., Li, N. Y., Winters, M. F., Bhagwagar, S., & Smith, C. J. (2026) · Journal of Neuroendocrinology · doi:10.1111/jne.70151 · Cited by 2
Freeman, A. R., Arenas, S., Lee, D. N., Singh, B., & Ophir, A. G. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1390203 · Cited by 3
Brain Mechanisms Related to Social and Reproductive Behavior
Freed, W. J. (2022) · Springer eBooks · doi:10.1007/978-3-031-10477-0_16 · Cited by 2
Emotions of human infants and mothers and development of the brain
Trevarthen, C. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069910 · Cited by 2
Münz, F., Abele, N., Zink, F., Wolfschmitt, E.-M., Hogg, M., Barck, C., Anetzberger, J., Hoffmann, A., Gröger, M., Calzia, E., et al. (2024) · Biomolecules · doi:10.3390/biom14111385 · Cited by 1
Altered Patterns of Growth Hormone Secretion in Somatostatin Knockout Mice
Low, M. J., Rubinstein, M., & Otero-Corchón, V. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/1-4020-8033-6_5 · Cited by 2
Prepulse Inhibition of the Startle Reflex in Forebrain Oxytocin Receptor Knockout Mice
Swonger, J. M. (2011) · OhioLink ETD Center (Ohio Library and Information Network) · Cited by 1
Olazábal, D. E., Pillay, N., Sandberg, N. Y., & Hartman, K.-J. (2023) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2023.114224 · Cited by 1
Teruyama, R., & Govar, A. A. (2024) · Peptides · doi:10.1016/j.peptides.2024.171283 · Cited by 1
Attachment: How early, how far?
Jacobs, B., & Raleigh, M. J. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0006982x · Cited by 1
Levels of explanation in theories of infant attachment
Eiserer, L. A. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069788 · Cited by 1
A psychopharmacologist's view of attachment
Svensson, T. H. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069909 · Cited by 1
Attachment and the sources of behavioral pathology
Kovach, J. K. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069843 · Cited by 1
Attachment: A view from evolutionary biology and behavior genetics
Pérusse, D. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069879 · Cited by 1
Genetic Variation in Neurotransmitter Receptors Generates Behavioral Diversity
Bendesky, A. (2025) · Digital Commons - RU (Rockefeller University) · doi:10.48496/3y0n-tx90 · Cited by 1
The Role of Oxytocin in the Stress and Anxiety Response.
Mantella, R. C. (2005) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 1
Nowicki, J. P., Pratchett, M. S., Walker, S. P. W., Coker, D. J., & O’Connell, L. A. (2017) · King Abdullah University of Science and Technology Repository (King Abdullah University of Science and Technology) · doi:10.1101/214759 · Cited by 1
Neuropeptides in mental health: CRF, AVP, and OXT
Hammock, E. A. D. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91497-0.00211-3 · Cited by 1
Denney, K. A., Wu, M. V., Sun, S. D., Moon, S., & Tollkühn, J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.12.540606 · Cited by 1
Effects of central neuropeptides on social preference and social recognition in male rats
Lukas, M. (2011) · University of Regensburg Publication Server (University of Regensburg) · doi:10.5283/epub.22540
A new psychobiological theory of attachment:Primum non nocere
Nemeroff, C. B., & Goodman, S. H. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069867
Boccia, M. L. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069764
Neuropeptides in Mental Health: CRF, AVP, and OXT
Hammock, E. A. D. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-397045-9.00137-3
The Effect of U-50488H, on Vasopressin Receptor Expression in Immature Ovine Kidney and Brainstem
Mutardi, M. (2014) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/28092
Freedman, D. G. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069806
Behavioural, aminergic and neural systems in attachment
Salzen, E. A. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069880
Effects of Oxytocin in the Medial Prefrontal Cortex: Anxiety, Maternal Care, and Maternal Aggression
Sabihi, S. (2013) · OhioLink ETD Center (Ohio Library and Information Network)
On oxytocin and social behavior
Hovey, D. (2018) · Gothenburg University Publications Electronic Archive (Gothenburg University)
The Other Face of Oxytocin : Role of Oxytocin in Neuropsychiatric Disorders
Chetcuti, S., Sammut, E., Sammut, M., & Calleja‐Agius, J. (2019) · doi:10.24946/ijpls.20.18.00.00.040605
Sharma, K. (2020) · Louisiana State University · doi:10.31390/gradschool_dissertations.5408
Benedetti, F. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780198843177.003.0005
Guoynes, C. D., & Marler, C. A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.12.507587
ROLE OF NEUROHYPOPHYSIS IN VARIOUS PATHOLOGICAL CONDITIONS
(2024) · International Journal of Biology Pharmacy and Allied Sciences · doi:10.31032/ijbpas/2024/13.3.7899
Reciprocal interactions between the oxytocin and somatosensory systems
Küppers, S., Lefèvre, A., & Grinevich, V. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00085-1
PVN-mPFC OT projections modulates pup-directed pup care or attacking in virgin mandarin volesPreprint
Li, L., He, Z., Yin, L., Huang, C., Hou, W., Lv, Z., Zhang, L., Qu, Y., Sun, Y., Huang, K., et al. (2024) · eLife · doi:10.7554/elife.96543.1
PVN-mPFC OT projections modulates pup-directed pup care or attacking in virgin mandarin volesPreprint
Li, L., Li, Y., Huang, C., Hou, W., Lv, Z., Zhang, L., Qu, Y., Sun, Y., Huang, K., Han, X., et al. (2024) · eLife · doi:10.7554/elife.96543.2
Metadata
- Authors
- Insel, T. R., Gelhard, R., & Shapiro, L. E.
- Affiliations
- National Institute of Mental Health (US)
- Corresponding author
- Insel, T.R.
- ORCID
- Insel, T.R.
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 1991-01
- Volume
- 43
- Issue
- 2-3
- Pages
- 623-630
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W1992791641
- Cited by
- 209
- References
- 28
- Citations by year
- 2026: 6 · 2025: 3 · 2024: 10 · 2023: 6 · 2022: 7 · 2021: 4 · 2020: 5 · 2019: 9 · 2018: 11 · 2017: 7 · 2016: 6 · 2015: 11 · 2014: 7 · 2013: 14 · 2012: 5
- FWCI
- 20.03
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Keywords
- oxytocin receptor, arginine vasopressin receptor, neurohypophyseal peptides, monogamy, polygamy, deer mouse, Peromyscus californicus, affiliative behavior, social behavior, sexual dimorphism, species differences, bed nucleus of the stria terminalis, amygdala, lateral septum, olfactory pathway, neocortex, receptor autoradiography
- MeSH terms
- Animals, Autoradiography, Oxytocin, Peromyscus, Receptors, Angiotensin, Sexual Behavior, Animal, Sex Characteristics, Tissue Distribution, Vasopressins, Prosencephalon, Receptors, Oxytocin, Mice
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