The DOI matches its Crossref record; 74 of the 74 references it cites were found in a registry or an index.
Nonapeptides and the evolutionary patterning of sociality
Open accessAbstract
Neuropeptides of the arginine vastocin (AVT) family, including the mammalian peptides arginine vasopressin (AVP) and oxytocin (OXT), comprise neuroendocrine circuits that range from being evolutionarily conserved to evolutionarily diverse. For instance, the functions and anatomy of the AVT/AVP projections to the pituitary (which arise in the preoptic area and hypothalamus) are strongly conserved, whereas the functions and anatomy of AVT/AVP circuits arising in the medial bed nucleus of the stria terminalis (BSTm) are species-specific and change rapidly over evolutionary time. Circuits arising in the BSTm mediate various affiliative behaviors and exhibit species-specific evolution in relation to mating system in mammals (monogamous vs. non-monogamous) and sociality in songbirds (gregarious vs. relatively asocial). In estrildid songbirds AVT neurons in the BSTm increase their Fos expression only in response to "positively-valenced" social stimuli (stimuli that normally elicit affiliation), whereas "negative" stimuli (which elicit aggression or aversion) produce no response or even suppress Fos expression. Relative to territorial species, gregarious species show: (1) greater social induction of Fos within AVT neurons, (2) a higher baseline of Fos expression in AVT neurons, (3) more AVT neurons in the BSTm and (4) a higher density of V(1a)-like binding sites in the lateral septum. Furthermore, septal AVT infusions inhibit resident-intruder aggression, but facilitate aggression that is motivated by mate competition (an affiliative context). This functional profile of the BSTm AVT neurons is quite distinct from that of hypothalamic AVT/AVP neurons, particularly those of the paraventricular nucleus (PVN), which are classically stress-responsive. This is paradoxical, given that AVT/AVP projections from the PVN and BSTm likely overlap. However, despite this overlap, each AVT/AVP cell group should produce a distinct pattern of modulation across brain regions. Relative weighting of hypothalamic and BSTm nonapeptide circuitries may therefore be an important determinant of approach-avoidance behaviour, and may be a prime target of natural selection related to sociality.
Overview
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
Verification
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?
The cited source says what the claim attributes to it.
In the citing paper
“AVP, OT, and their homologs regulate social behavior across vertebrate taxa (for review, see Goodson 2008; Kelly & Ophir 2015)”
From Quantitative mapping reveals age and sex differences in vasopressin, but not oxytocin, immunoreactivity in the rat social behavior neural network (2017) · cites this paper as Goodson 2008
In the citing paper
“Central OTRs exhibit extraordinarily diverse expression patterns that are associated with individual and species differences in social behavior.”
From Oxytocin receptors modulate a social salience neural network in male prairie voles (2017) · cites this paper as Goodson, 2008
In the citing paper
“Central distribution patterns and region-specific densities of OT receptors (OTRs) have undergone rapid evolutionary divergence between closely related species of birds and mammals that exhibit divergent social behavior”
From Oxytocin receptors modulate a social salience neural network in male prairie voles (2017) · cites this paper as Goodson, 2008
In the citing paper
“comparative analyses have revealed that the effects of OT and AVP on social behavior are as complex and diverse as the differences in reproductive and social strategies found across the animal kingdom (Goodson, 2008; Kelly and Ophir, 2015).”
From Neuropeptide diversity and the regulation of social behavior in New World primates (2016) · cites this paper as Goodson, 2008
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The neurobiology of pair bonding.
Young, L. J., & Wang, Z. (2004) · Nature Neuroscience · doi:10.1038/nn1327 · Cited by 1,523 · cited 10×
“AVT/AVP cells of the BSTm likely contribute to the regulation of multiple affiliative behaviours, including pair bonding in rodents (Young and Wang, 2004; De Vries and Panzica, 2006), but no research had previously determined how different classes of social stimuli elicit responses in these neurons.”
BackgroundInfluentialNeuroendocrine perspectives on social attachment and love
Sue Carter, C. (1998) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(98)00055-9 · Cited by 1,425
NEWMAN, S. W. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09271.x · Cited by 1,189
Landgraf, R., & Neumann, I. D. (2004) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2004.05.001 · Cited by 1,059
Cerebral hemisphere regulation of motivated behavior
Swanson, L. W. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02905-x · Cited by 846
Oxytocin receptor distribution reflects social organization in monogamous and polygamous voles
Insel, T. R., & Shapiro, L. E. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.5981 · Cited by 833
The vertebrate social behavior network: Evolutionary themes and variations
Goodson, J. L. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.02.003 · Cited by 771
Self-citationGoodson, J. L., & Bass, A. H. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00043-1 · Cited by 646
Self-citationLim, M. M., Wang, Z., Olazábal, D. E., Ren, X., Terwilliger, E. F., & Young, L. J. (2004) · Nature · doi:10.1038/nature02539 · Cited by 628
Liu, Y., & Wang, Z. X. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00555-4 · Cited by 580 · cited 1×
“…voles, mice and primates) point toward two brain areas as being relevant for monogamous pair bonding — the nucleus accumbens in the case of OXT receptors, and the ventral pallidum in the case of AVP V1a receptors (Wang et al., 1997; Young et al., 1999; Liu and Wang, 2003; Lim et al., 2004a).”
Background
Research works printed but not linked: 1
- Skead DM. Ecological studies of four Estrildines in the central Transvaal. Ostrich. 1975 11:1–55. [Google Scholar]
Cited by
Sorted by citations
The oxytocin receptor: from intracellular signaling to behavior
Jurek, B., & Neumann, I. D. (2018) · Physiological Reviews · doi:10.1152/physrev.00031.2017 · Cited by 999
The Peptide That Binds: A Systematic Review of Oxytocin and its Prosocial Effects in Humans
MacDonald, K., & MacDonald, T. M. (2010) · Harvard Review of Psychiatry · doi:10.3109/10673220903523615 · Cited by 585
Bosch, O. J., & Neumann, I. D. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.11.002 · Cited by 400
Graustella, A. J., & MacLeod, C. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.01.002 · Cited by 379
Genetics of Human Social Behavior
Ebstein, R. P., Israel, S., Chew, S. H., Zhong, S., & Knafo, A. (2010) · Neuron · doi:10.1016/j.neuron.2010.02.020 · Cited by 323
The contributions of oxytocin and vasopressin pathway genes to human behavior
Ebstein, R. P., Knafo, A., Mankuta, D., Chew, S. H., & Lai, P. S. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.12.014 · Cited by 283
Nonapeptide mechanisms of social cognition, behavior and species-specific social systems
Goodson, J. L., & Thompson, R. R. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.08.020 · Cited by 261
Self-citationMesotocin and nonapeptide receptors promote estrildid flocking behavior
Goodson, J. L., Schrock, S. E., Klatt, J. D., Kabelik, D., & Kingsbury, M. A. (2009) · Science · doi:10.1126/science.1174929 · Cited by 241
Self-citationAggression and anxiety: social context and neurobiological links
Neumann, I. D. (2010) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2010.00012 · Cited by 252
Oxytocin and human social behavior.
Campbell, A. (2010) · Personality and Social Psychology Review · doi:10.1177/1088868310363594 · Cited by 232
Genes, hormones, and circuits: An integrative approach to study the evolution of social behavior
O’Connell, L. A., & Hofmann, H. A. (2010) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.12.004 · Cited by 238
Influence of photoperiod on hormones, behavior, and immune function
Walton, J. C., Weil, Z. M., & Nelson, R. J. (2010) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.12.003 · Cited by 207
Goodson, J. L., & Kabelik, D. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.05.007 · Cited by 209
Self-citationMaternal aggression in rodents: brain oxytocin and vasopressin mediate pup defence
Bosch, O. J. (2013) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2013.0085 · Cited by 194
Albers, H. E. (2015) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.07.001 · Cited by 200
Johnson, Z. V., Walum, H., Jamal, Y. A., Xiao, Y., Keebaugh, A. C., Inoue, K., & Young, L. J. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.11.011 · Cited by 190
Lukas, M., Bredewold, R., Neumann, I. D., & Veenema, A. H. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.06.020 · Cited by 183
Gobrogge, K. L., Liu, Y., Young, L. J., & Wang, Z. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908620106 · Cited by 178
Neumann, I. D. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.04.012 · Cited by 162
Effects of Adverse Early‐Life Events on Aggression and Anti‐Social Behaviours in Animals and Humans
Haller, J., Harold, G. T., Sandi, C., & Neumann, I. D. (2014) · Journal of Neuroendocrinology · doi:10.1111/jne.12182 · Cited by 186
Veenema, A. H. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.12.002 · Cited by 172
Evolving nonapeptide mechanisms of gregariousness and social diversity in birds
Goodson, J. L., Kelly, A. M., & Kingsbury, M. A. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.01.005 · Cited by 139
Self-citationBrain serotonin receptors and transporters: initiation vs. termination of escalated aggression
Takahashi, A., Quadros, I. M., de Almeida, R. M. M., & Miczek, K. A. (2010) · Psychopharmacology · doi:10.1007/s00213-010-2000-y · Cited by 140
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 140
Self-citationBehavioral and Pharmacogenetics of Aggressive Behavior
Takahashi, A., Quadros, I. M., de Almeida, R. M. M., & Miczek, K. A. (2011) · Current topics in behavioral neurosciences · doi:10.1007/7854_2011_191 · Cited by 123
Oxytocin receptors modulate a social salience neural network in male prairie voles
Johnson, Z. V., Walum, H., Xiao, Y., Riefkohl, P. C., & Young, L. J. (2017) · Hormones and Behavior · doi:10.1016/j.yhbeh.2016.10.009 · Cited by 113
Goodson, J., Kabelik, D., Kelly, A. M., Rinaldi, J. M., & Klatt, J. D. (2009) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0811821106 · Cited by 115
Self-citationZhang, L., & Hernández, V. S. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2012.10.010 · Cited by 96
Slattery, D. A., & Neumann, I. D. (2010) · Pharmaceuticals · doi:10.3390/ph3030702 · Cited by 94
Rotondo, F., Butz, H., Syro, L. V., Yousef, G. M., Di Ieva, A., Restrepo, L. M., Quintanar-Stephano, A., Berczi, I., & Kovacs, K. (2016) · Pituitary · doi:10.1007/s11102-015-0703-0 · Cited by 93
Effects of isotocin on social responses in a cooperatively breeding fish
Reddon, A. R., O’Connor, C. M., Marsh‐Rollo, S. E., & Balshine, S. (2012) · Animal Behaviour · doi:10.1016/j.anbehav.2012.07.021 · Cited by 93
Taylor, P. V., Veenema, A. H., Paul, M. J., Bredewold, R., Isaacs, S., & de Vries, G. J. (2012) · Biology of Sex Differences · doi:10.1186/2042-6410-3-15 · Cited by 86
Charvet, C. J., Striedter, G. F., & Finlay, B. L. (2011) · Brain Behavior and Evolution · doi:10.1159/000329851 · Cited by 89
Brain levels of arginine–vasotocin and isotocin in dominant and subordinate males of a cichlid fish
Almeida, O., Gozdowska, M., Kulczykowska, E., & Oliveira, R. F. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.12.008 · Cited by 85
Ho, J. M., Murray, J. H., Demas, G. E., & Goodson, J. L. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.03.021 · Cited by 76
Self-citationDifferences in inhibitory avoidance, cortisol and brain gene expression in TL and AB zebrafish
Gorissen, M., Manuel, R., Pelgrim, T. N. M., Mes, W., de Wolf, M. J. S., Zethof, J., Flik, G., & van den Bos, R. (2015) · Genes Brain & Behavior · doi:10.1111/gbb.12220 · Cited by 77
Neural Distribution of Vasotocin Receptor mRNA in Two Species of Songbird
Leung, C. H., Abebe, D. F., Earp, S. E., Goode, C. T., Grozhik, A. V., Mididoddi, P., & Maney, D. L. (2011) · Endocrinology · doi:10.1210/en.2011-1394 · Cited by 82
DiBenedictis, B. T., Nussbaum, E. R., Cheung, H. K., & Veenema, A. H. (2017) · Journal of Comparative Neurology · doi:10.1002/cne.24216 · Cited by 74
“Because AVP, OT, and their homologs regulate social behavior across vertebrate taxa (for review, see Goodson 2008; Kelly & Ophir 2015), further research should explore whether there are similar age and sex differences in AVP-ir (or a similar lack of age and sex differences in OT-ir) in other…”
BackgroundAntisocial oxytocin: Complex effects on social behavior
Beery, A. K. (2015) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2015.11.006 · Cited by 74
Arginine vasotocin regulates social ascent in the African cichlid fish Astatotilapia burtoni
Huffman, L. S., Hinz, F. I., Wojcik, S., Aubin‐Horth, N., & Hofmann, H. A. (2014) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2014.03.004 · Cited by 76
The Control of Calcium Metabolism in Zebrafish (Danio rerio)
Lin, C.-H., & Hwang, P. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17111783 · Cited by 77
da Silva, A. C. R., Perrone, R., Zubizarreta, L., Batista, G., & Stoddard, P. K. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.082180 · Cited by 73
Huffman, L. S., O’Connell, L. A., Kenkel, C. D., Kline, R. J., Khan, I. A., & Hofmann, H. A. (2012) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2012.05.002 · Cited by 75
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
Kabelik, D., Klatt, J. D., Kingsbury, M. A., & Goodson, J. L. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.03.017 · Cited by 70
Self-citationChou, M., Hung, J.-C., Wu, L.-C., Hwang, S. L., & Hwang, P. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0593-2 · Cited by 67
Neuropeptide diversity and the regulation of social behavior in New World primates
French, J. A., Taylor, J. H., Mustoe, A. C., & Cavanaugh, J. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.03.004 · Cited by 66
Goodson, J. L., Kabelik, D., & Schrock, S. E. (2009) · Biology Letters · doi:10.1098/rsbl.2009.0316 · Cited by 65
Self-citationRamallo, M. R., Grober, M. S., Cánepa, M. M., Morandini, L., & Pandolfi, M. (2012) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2012.08.015 · Cited by 65
Shalev, I., Israel, S., Uzefovsky, F., Gritsenko, I., Kaitz, M., & Ebstein, R. P. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.04.005 · Cited by 65
Kawabata, Y., Hiraki‐Kajiyama, T., Takeuchi, A., & Okubo, K. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.05.021 · Cited by 68
Goodson, J. L., Rinaldi, J., & Kelly, A. M. (2008) · Hormones and Behavior · doi:10.1016/j.yhbeh.2008.10.007 · Cited by 62
Self-citationReddon, A. R., O’Connor, C. M., Marsh‐Rollo, S. E., Balshine, S., Gozdowska, M., & Kulczykowska, E. (2015) · Royal Society Open Science · doi:10.1098/rsos.140072 · Cited by 62
Ophir, A. G. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00397 · Cited by 66
Insights into the molecular evolution of oxytocin receptor ligand binding
Koehbach, J., Stockner, T., Bergmayr, C., Muttenthaler, M., & Gruber, C. W. (2013) · Biochemical Society Transactions · doi:10.1042/bst20120256 · Cited by 61
Arginine Vasotocin Regulation of Interspecific Cooperative Behaviour in a Cleaner Fish
Soares, M. C., Bshary, R., Mendonça, R., Grutter, A. S., & Oliveira, R. F. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039583 · Cited by 60
Hypothalamic vasopressin system regulation by maternal separation: Its impact on anxiety in rats
Zhang, L., Hernández, V. S., Liu, B., Medina‐Pizarro, M., Nava-Kopp, A. T., Irles, C., & Morales, M. A. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.03.046 · Cited by 60
The role of oxytocin and vasopressin in emotional and social behaviors
Bachner‐Melman, R., & Ebstein, R. P. (2014) · Handbook of clinical neurology · doi:10.1016/b978-0-444-59602-4.00004-6 · Cited by 65
Kelly, A. M., & Vitousek, M. N. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0243 · Cited by 57
Nonapeptides and the Evolution of Social Group Sizes in Birds
Goodson, J. L., & Kingsbury, M. A. (2011) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2011.00013 · Cited by 59
Self-citationMitochondria, Oxytocin, and Vasopressin: Unfolding the Inflammatory Protein Response
Bordt, E. A., Smith, C. J., Demarest, T. G., Bilbo, S. D., & Kingsbury, M. A. (2019) · Neurotoxicity Research · doi:10.1007/s12640-018-9962-7 · Cited by 58
Fernández‐Juricic, E., Gall, M. D., Dolan, T., O'Rourke, C. T., Thomas, S., & Lynch, J. R. (2011) · Animal Behaviour · doi:10.1016/j.anbehav.2010.11.014 · Cited by 56
Hormones and neuroplasticity: A lifetime of adaptive responses
Been, L. E., Sheppard, P. A. S., Galea, L. A. M., & Glasper, E. R. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.11.029 · Cited by 58
The zebra finch neuropeptidome: prediction, detection and expression
Xie, F., London, S. E., Southey, B. R., Annangudi, S. P., Amare, A., Rodriguez‐Zas, S. L., Clayton, D. F., & Sweedler, J. V. (2010) · BMC Biology · doi:10.1186/1741-7007-8-28 · Cited by 54
Lema, S. C., Slane, M. A., Salvesen, K. E., & Godwin, J. (2012) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2012.10.001 · Cited by 57
Isotocin and sociality in the cooperatively breeding cichlid fish, Neolamprologus pulcher
Reddon, A. R., Voisin, M. R., O’Connor, C. M., & Balshine, S. (2014) · Behaviour · doi:10.1163/1568539x-00003190 · Cited by 53
Global map of oxytocin/vasopressin-like neuropeptide signalling in insects
Liutkevičiūtė, Z., Koehbach, J., Eder, T., Gil‐Mansilla, E., & Gruber, C. W. (2016) · Scientific Reports · doi:10.1038/srep39177 · Cited by 49
DeAngelis, R., Gogola, J. V., Dodd, L., & Rhodes, J. S. (2017) · Hormones and Behavior · doi:10.1016/j.yhbeh.2017.02.013 · Cited by 50
Exploring bioactive peptides from natural sources for oxytocin and vasopressin drug discovery
Gruber, C. W., Koehbach, J., & Muttenthaler, M. (2012) · Future Medicinal Chemistry · doi:10.4155/fmc.12.108 · Cited by 49
Banerjee, P., Joy, K. P., & Chaube, R. (2016) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2016.04.025 · Cited by 55
Parreiras‐e‐Silva, L. T., Vargas‐Pinilla, P., Duarte, D. Â., Longo, D., Pardo, G. V. E., Finkler, A. D., Paixão‐Côrtes, V. R., Paré, P., Rovaris, D. L., Oliveira, E. B., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1711687114 · Cited by 48
DeAngelis, R., Dodd, L., Snyder, A., & Rhodes, J. S. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2018.06.006 · Cited by 47
Zheng, D., Larsson, B., Phelps, S. M., & Ophir, A. G. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.02.024 · Cited by 51
Dewan, A., & Tricas, T. C. (2011) · Brain Research · doi:10.1016/j.brainres.2011.05.029 · Cited by 48
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
Brain vasopressin signaling modulates aspects of maternal behavior in lactating rats
Bayerl, D. S., & Bosch, O. J. (2019) · Genes, Brain and Behavior · doi:10.1111/gbb.12517 · Cited by 46
Sexual dimorphism of oxytocin and vasopressin in social cognition and behavior
Lu, Q., Lai, J., Du, Y., Huang, T., Prukpitikul, P., Xu, Y., & Hu, S. (2019) · Psychology Research and Behavior Management · doi:10.2147/prbm.s192951 · Cited by 47
Santangelo, N., & Bass, A. H. (2010) · Brain Behavior and Evolution · doi:10.1159/000316867 · Cited by 46
Oxytocin has ‘tend-and-defend’ functionality in group conflict across social vertebrates
Triki, Z., Daughters, K., & Dreu, C. K. W. D. (2022) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2021.0137 · Cited by 45
Comparative Neurobiology of Sound Production in Fishes
Bass, A. H., Chagnaud, B. P., & Feng, N. Y. (2015) · Animal signals and communication · doi:10.1007/978-3-7091-1846-7_2 · Cited by 42
Kelly, A. M., & Goodson, J. L. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.09.006 · Cited by 38
Self-citationAggression- and sex-induced neural activity across vasotocin populations in the brown anole
Kabelik, D., Alix, V. C., Burford, E. R., & Singh, L. J. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.11.016 · Cited by 38
Lindeyer, C. M., Langen, E. M. A., Swaney, W. T., & Reader, S. M. (2015) · Behaviour · doi:10.1163/1568539x-00003261 · Cited by 40
Klatt, J. D., & Goodson, J. L. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.10.001 · Cited by 38
Self-citationLudwig, M., Tobin, V. A., Callahan, M. F., Papadaki, E., Becker, A., Engelmann, M., & Leng, G. (2013) · Journal of Neuroendocrinology · doi:10.1111/jne.12046 · Cited by 37
Caffrey, M. K., Nephew, B. C., & Febo, M. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.06.023 · Cited by 37
Kabelik, D., Weiss, S. L., & Moore, M. C. (2008) · Brain Behavior and Evolution · doi:10.1159/000174248 · Cited by 36
Evolutionary themes in the neurobiology of social cognition
Weitekamp, C. A., & Hofmann, H. A. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.06.005 · Cited by 39
Migliaro, A., & da Silva, A. C. R. (2016) · Brain Behavior and Evolution · doi:10.1159/000445494 · Cited by 36
Kabelik, D., Morrison, J. A., & Goodson, J. L. (2010) · Brain Behavior and Evolution · doi:10.1159/000297522 · Cited by 33
Self-citationPerrone, R. (2010) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2010.00052 · Cited by 33
Roles of arginine vasotocin receptors in the brain and pituitary of submammalian vertebrates
(2013) · International Review of Cell and Molecular Biology · doi:10.1016/b978-0-12-407696-9.00004-x · Cited by 30
Tinbergen’s challenge for the neuroscience of behavior
Pfaff, D. W., Tabansky, I., & Haubensak, W. E. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1903589116 · Cited by 33
Panzica, G., Bo, E., Martini, M., Miceli, D., Mura, E., Viglietti‐Panzica, C., & Gotti, S. (2011) · Journal of Toxicology and Environmental Health Part B · doi:10.1080/10937404.2011.578562 · Cited by 33
Are retinoids potential therapeutic agents in disorders of social cognition including autism?
Ebstein, R. P., Mankuta, D., Yirmiya, N., & Malavasi, F. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.05.004 · Cited by 32
Arginine vasotocin reduces levels of cooperative behaviour in a cleaner fish
Cardoso, S. C., Paitio, J. R., Oliveira, R. F., Bshary, R., & Soares, M. C. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.11.052 · Cited by 31
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
Agonistic interactions elicit rapid changes in brain nonapeptide levels in zebrafish
Teles, M. C., Gozdowska, M., Kalamarz‐Kubiak, H., Kulczykowska, E., & Oliveira, R. F. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2016.05.020 · Cited by 30
Applying gene regulatory network logic to the evolution of social behavior
Baran, N. M., McGrath, P. T., & Streelman, J. T. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1610621114 · Cited by 30
Metadata
- Authors
- GOODSON, J.
- Affiliations
- Indiana University Bloomington (US)
- Corresponding author
- GOODSON, J
- Venue
- Progress in brain research
- Publisher
- Elsevier
- Published
- 2008
- Volume
- 170
- Pages
- 3-15
- ISSN
- 0079-6123 (ISSN-L)
- PMC
- PMC2570786
- OpenAlex
- W1538837544
- Cited by
- 228
- References
- 74
- Citations by year
- 2026: 3 · 2025: 6 · 2024: 7 · 2023: 8 · 2022: 9 · 2021: 10 · 2020: 5 · 2019: 12 · 2018: 12 · 2017: 14 · 2016: 14 · 2015: 15 · 2014: 14 · 2013: 20 · 2012: 20
- FWCI
- 49.24
- Type
- book chapter
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Progress in brain research (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Mental Health (R01MH062656, MH62656)
- 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 › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Animal Behavior and Reproduction
- Keywords
- arginine vasotocin, vasopressin, oxytocin, nonapeptide, evolution of social behavior, Fos expression, songbirds, aggression, mate competition, approach-avoidance behavior, paraventricular nucleus, lateral septum, V1a receptor, affiliative behavior
- MeSH terms
- Animals, Annelida, Arginine Vasopressin, Brain, Fishes, Genetics, Behavioral, Humans, Neurons, Oligopeptides, Social Behavior, Vertebrates, Evolution, Molecular, MicroRNAs
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
