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Species, sex and individual differences in the vasotocin/vasopressin system: Relationship to neurochemical signaling in the social behavior neural network
Open accessAbstract
Arginine-vasotocin (AVT)/arginine vasopressin (AVP) are members of the AVP/oxytocin (OT) superfamily of peptides that are involved in the regulation of social behavior, social cognition and emotion. Comparative studies have revealed that AVT/AVP and their receptors are found throughout the "social behavior neural network (SBNN)" and display the properties expected from a signaling system that controls social behavior (i.e., species, sex and individual differences and modulation by gonadal hormones and social factors). Neurochemical signaling within the SBNN likely involves a complex combination of synaptic mechanisms that co-release multiple chemical signals (e.g., classical neurotransmitters and AVT/AVP as well as other peptides) and non-synaptic mechanisms (i.e., volume transmission). Crosstalk between AVP/OT peptides and receptors within the SBNN is likely. A better understanding of the functional properties of neurochemical signaling in the SBNN will allow for a more refined examination of the relationships between this peptide system and species, sex and individual differences in sociality.
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In the citing paper
“ERβ has also been identified as one component of a “four-gene micronet” regulating social recognition (7, 131) via the PVN, amygdala, and olfactory system.”
From Endocrine Disruption of Vasopressin Systems and Related Behaviors (2017) · cites this paper as [7]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Although no animal model can fully capture the sophisticated complexity of human social behavior, the neuroendocrine pathways coordinating numerous social traits are highly conserved (7, 42), including the coordinating roles of AVP and OT.”
From Endocrine Disruption of Vasopressin Systems and Related Behaviors (2017) · cites this paper as [7]
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In the citing paper
“By this model, estradiol simultaneously acts through ERβ in the PVN to increase OT, and ERα in the amygdala to increase OTR expression.”
From Endocrine Disruption of Vasopressin Systems and Related Behaviors (2017) · cites this paper as [7]
Experimental — accuracy not yet measuredIn the citing paper
“Different patterns of OT and AVP receptor activation across structures within these networks could contribute to the regulation of the complex behaviors and physiological processes under their control (see [8] for a review).”
From Cross-talk among oxytocin and arginine-vasopressin receptors: Relevance for basic and clinical studies of the brain and periphery (2018) · cites this paper as [8]
In the citing paper
“Vasopressin modulates social communication, social investigation, territorial behavior, and aggression, predominantly in males.”
From Oxytocin, Vasopressin, and Social Behavior: From Neural Circuits to Clinical Opportunities (2022) · cites this paper as [16]
In the citing paper
“whereas central AVP has been shown to regulate social communication, territorial aggression, pair bonding, and mate guarding, especially in males (9,15,16).”
From Oxytocin, Vasopressin, and Social Behavior: From Neural Circuits to Clinical Opportunities (2022) · cites this paper as [16]
In the citing paper
“Vasopressin modulates social communication, social investigation, territorial behavior, and aggression, predominantly in males.”
From Oxytocin, Vasopressin, and Social Behavior: From Neural Circuits to Clinical Opportunities (2022) · cites this paper as [16]
In the citing paper
“Vasopressin modulates social communication, social investigation, territorial behavior, and aggression, predominantly in males.”
From Oxytocin, Vasopressin, and Social Behavior: From Neural Circuits to Clinical Opportunities (2022) · cites this paper as [16]
In the citing paper
“The behavioral effects of AVP are mediated primarily by V1aR (or Avpr1a) and V1bR (16,37,38,49,68), while AVP acts on V2 to regulate fluid homeostasis in the kidney (69).”
From Oxytocin, Vasopressin, and Social Behavior: From Neural Circuits to Clinical Opportunities (2022) · cites this paper as [16]
In the citing paper
“AVP also plays a role in aggression in prairie voles and Syrian hamsters, sometimes in a sex-specific manner.”
From Oxytocin, Vasopressin, and Social Behavior: From Neural Circuits to Clinical Opportunities (2022) · cites this paper as [16]
In the citing paper
“For example, pharmacological studies revealed that AVP in the anterior hypothalamus facilitates intermale aggression both in prairie voles and hamsters (16,43,116), while the opposite effect was found in female hamsters (117).”
From Oxytocin, Vasopressin, and Social Behavior: From Neural Circuits to Clinical Opportunities (2022) · cites this paper as [16]
In the citing paper
“There is also a growing interest in OT and the related neurohypophyseal nonapetide arginine vasopressin (AVP) and their analogues in the regulation of social behavior beyond the maternal context, including social attachments among adults, social cognition, and aggression”
From Neuropeptide diversity and the regulation of social behavior in New World primates (2016) · cites this paper as Albers, 2015
In the citing paper
“V1a-like receptors are the most common and widely distributed vasopressin receptor in the vertebrate brain (Albers, 2015)”
From Neuropeptide diversity and the regulation of social behavior in New World primates (2016) · cites this paper as Albers, 2015
In the citing paper
“The distribution of OT-ergic and AVP-ergic neurons, and cellular receptors for OT (OTR) and AVP (V1aR, V1bR, V2R) have been well characterized in rodents (Albers, 2015; Johnson and Young, 2015) and other vertebrates (Goodson and Kabelik, 2009; O’Connell and Hofmann, 2012, 2011), and this distribution includes substantial overlap with the social behavior network (SBN; Newman, 1999).”
From Neuropeptide diversity and the regulation of social behavior in New World primates (2016) · cites this paper as Albers, 2015
In the citing paper
“The important role of neuropeptide signaling in regulating a host of behavioral processes in invertebrate and especially vertebrate animals, especially in the social realm, has been firmly established (Albers, 2015; Caldwell and Young III, 2006; Donaldson and Young, 2008; Taghert and Nitabach, 2012; Wircer et al., 2015).”
From Neuropeptide diversity and the regulation of social behavior in New World primates (2016) · cites this paper as Albers, 2015
In the citing paper
“What is particularly interesting about the aforementioned brain nuclei is that many of them are a part of the “social behavioral network,” which is comprised of neuroanatomical areas or “nodes” that are interconnected, express gonadal hormone receptors, appear to be influenced by Oxt, and are important in the regulation of many types of social behaviors (92, 93).”
From Oxytocin during Development: Possible Organizational Effects on Behavior (2015) · cites this paper as [93]
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Citations
Cites
Wingfield, J. C., Hegner, R. E., Dufty, & Ball, G. F. (1990) · The American Naturalist · doi:10.1086/285134 · Cited by 2,330
The neurobiology of pair bonding.
Young, L. J., & Wang, Z. (2004) · Nature Neuroscience · doi:10.1038/nn1327 · Cited by 1,523 · cited 1×
“Because of this difference in V1a receptor binding and because the ventral pallidum is involved in reward systems, it was hypothesized that V1a receptors facilitate pairbonding (Winslow et al., 1993; Young et al., 1997; Pitkow et al., 2001; Lim et al., 2004; Young and Wang, 2004).”
BackgroundKleiman, D. G. (1977) · The Quarterly Review of Biology · doi:10.1086/409721 · Cited by 1,436
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
Sawchenko, P. E., & Swanson, L. W. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902050306 · Cited by 1,150
Microsatellites Within Genes: Structure, Function, and Evolution
Li, Y. (2004) · Molecular Biology and Evolution · doi:10.1093/molbev/msh073 · Cited by 1,132
Landgraf, R., & Neumann, I. D. (2004) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2004.05.001 · Cited by 1,059
Evoked axonal oxytocin release in the central amygdala attenuates fear response
Knobloch, H. S., Charlet, A., Hoffmann, L. C., Eliava, M., Khrulev, S., Cetin, A. H., Osten, P., Schwarz, M. K., Seeburg, P. H., Stoop, R., et al. (2012) · Neuron · doi:10.1016/j.neuron.2011.11.030 · Cited by 1,049
Insel, T. R. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.005 · Cited by 1,044
Intra- and extrahypothalamic vasopressin and oxytocin pathways in the rat
Buijs, R. M., Swaab, D. F., Dogterom, J., & van Leeuwen, F. W. (1978) · Cell and Tissue Research · doi:10.1007/bf00224932 · Cited by 1,029
Research works printed but not linked: 1
- Huhman, 1998, Vasopressin (AVP) dose-dependently increases flank marking but not aggressive behavior in Syrian hamsters, Soc. Neurosci. Abs.
Cited by
Sorted by citations
Dumais, K. M., & Veenema, A. H. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2015.04.003 · Cited by 520
“…neuropeptides vasopressin (VP) and oxytocin (OT) are involved in the regulation of diverse social behaviors such as social recognition, pair-bonding, and social cognition in mammals, including humans (Veenema & Neumann, 2008; Ross & Young, 2009; MeyerLindenberg et al., 2011; Albers, 2014).”
BackgroundInfluentialIs 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
Song, Z., & Albers, H. E. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.10.004 · Cited by 244
Self-citationJohnson, Z. V., & Young, L. J. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.01.034 · Cited by 242
Oxytocin and vasopressin: powerful regulators of social behavior
Caldwell, H. K. (2017) · The Neuroscientist · doi:10.1177/1073858417708284 · Cited by 216
Amygdala, neuropeptides, and chronic pain-related affective behaviors
Neugebauer, V., Mazzitelli, M., Cragg, B., Ji, G., Navratilova, E., & Porreca, F. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108052 · Cited by 220
Perrone, R., & da Silva, A. C. R. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00001 · Cited by 212
Oxytocin, Vasopressin, and Social Behavior: From Neural Circuits to Clinical Opportunities
Rigney, N., de Vries, G. J., Petrulis, A., & Young, L. J. (2022) · Endocrinology · doi:10.1210/endocr/bqac111 · Cited by 191
Neurobiological mechanisms of social attachment and pair bonding
Johnson, Z. V., & Young, L. J. (2015) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2015.01.009 · Cited by 169
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 170
Oxytocin signaling in the medial amygdala is required for sex discrimination of social cues
Yao, S., Bergan, J., Lanjuin, A., & Dulac, C. (2017) · eLife · doi:10.7554/elife.31373 · Cited by 151
Smith, C. J. W., Poehlmann, M. L., Li, S., Ratnaseelan, A. M., Bredewold, R., & Veenema, A. H. (2017) · Brain Structure and Function · doi:10.1007/s00429-016-1260-7 · Cited by 143
The neuroscience of social feelings: mechanisms of adaptive social functioning
Eslinger, P. J., Anders, S., Ballarini, T., Boutros, S., Krach, S., Mayer, A. V., Moll, J., Newton, T. L., Schroeter, M. L., de Oliveira-Souza, R., et al. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.05.028 · Cited by 130
Oxytocin, vasopressin, and the motivational forces that drive social behaviors
Caldwell, H. K., & Albers, H. E. (2015) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2015_390 · Cited by 129
Self-citationTerranova, J. I., Song, Z., Larkin, T. E., Hardcastle, N., Norvelle, A., Riaz, A., & Albers, H. E. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1610446113 · Cited by 123
Self-citationSex-dependent regulation of social reward by oxytocin: an inverted U hypothesis
Borland, J. M., Rilling, J. K., Frantz, K. J., & Albers, H. E. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-018-0129-2 · Cited by 116
Self-citationAlbers, H. E., Walton, J. C., Gamble, K. L., McNeill, J. K., & Hummer, D. L. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.11.003 · Cited by 117
Self-citationde Almeida, R. M. M., Cabral, J. C. C., & Narvaes, R. F. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.02.053 · Cited by 116
The Role of Oxytocin and Vasopressin in Attachment
Carter, C. S. (2017) · Psychodynamic Psychiatry · doi:10.1521/pdps.2017.45.4.499 · Cited by 105
Song, Z., Borland, J. M., Larkin, T. E., O’Malley, M., & Albers, H. E. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.09.001 · Cited by 101
Self-citationRotondo, 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
Zuloaga, D. G., Heck, A., Guzman, R. M. D., & Handa, R. J. (2020) · Biology of Sex Differences · doi:10.1186/s13293-020-00319-2 · Cited by 99
Sex differences in the regulation of offensive aggression and dominance by arginine-vasopressin
Terranova, J. I., Ferris, C. F., & Albers, H. E. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00308 · Cited by 85
Self-citationThe Monogamy Paradox: What Do Love and Sex Have to Do With It?
Carter, C. S., & Perkeybile, A. M. (2018) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2018.00202 · Cited by 87
Oxytocin and behavior: lessons from knockout mice
Caldwell, H. K., Aulino, E. A., Freeman, A. R., Miller, T. V., & Witchey, S. K. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22431 · Cited by 79
Oxytocin during Development: Possible Organizational Effects on Behavior
Miller, T. V., & Caldwell, H. K. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00076 · Cited by 79
Social Novelty Investigation in the Juvenile Rat: Modulation by the μ‐Opioid System
Smith, C. J. W., Wilkins, K. B., Mogavero, J. N., & Veenema, A. H. (2015) · Journal of Neuroendocrinology · doi:10.1111/jne.12301 · Cited by 77
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
“Vasopressin (AVP) and oxytocin (OT) have garnered considerable attention for their essential role in the regulation of various social behaviors in humans, rodents, and other animals (reviewed in Veenema & Neumann, 2008; Ross & Young, 2009; Heinrichs, von Dawans, & Domes, 2009; Albers, 2015; Caldwell & Albers, 2015).”
BackgroundNeuropeptide 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
Sparapani, S., Millet-Boureima, C., Oliver, J., Mu, K., Hadavi, P., Kalostian, T., Ali, N., Avelar, C. M., Bardies, M., Barrow, B., et al. (2021) · Biomedicines · doi:10.3390/biomedicines9010089 · Cited by 64
Ophir, A. G. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00397 · Cited by 66
Modulation of social behavior by distinct vasopressin sources
Rigney, N., Vries, G. J. D., & Petrulis, A. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1127792 · Cited by 64
Smith, C. J. W., DiBenedictis, B. T., & Veenema, A. H. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.02.001 · Cited by 59
Eastman, G., Valiño, G., Radío, S., Young, R. L., Quintana, L., Zakon, H. H., Hofmann, H. A., Sotelo-Silveira, J. R., & da Silva, A. C. R. (2020) · Scientific Reports · doi:10.1038/s41598-020-66494-9 · Cited by 61
Ross, A. P., McCann, K. E., Larkin, T. E., Song, Z., Grieb, Z. A., Huhman, K. L., & Albers, H. E. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.104578 · Cited by 57
Self-citationHodges, T. E., Baumbach, J. L., Marcolin, M. L., Bredewold, R., Veenema, A. H., & McCormick, C. M. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.07.032 · Cited by 61
Animal models of endocrine disruption
Patisaul, H. B., Fenton, S. E., & Aylor, D. L. (2018) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2018.03.011 · Cited by 62
Endocrine Disruption of Vasopressin Systems and Related Behaviors
Patisaul, H. B. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00134 · Cited by 54
“The anatomical and functional features of AVP/ OT neuronal subpopulations are beyond the scope of this review and detailed elsewhere (6, 7).”
BackgroundRilling, J. K., Li, T., Chen, X., Gautam, P., Haroon, E., & Thompson, R. R. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00200 · Cited by 52
Comparative Assessment of Familiarity/Novelty Preferences in Rodents
Beery, A. K., & Shambaugh, K. L. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.648830 · Cited by 50
Flattery, C. N. R., Ross, A. P., Sahu, S. P., Siegel, E. R., Dooyema, J. M., Cree, M. A., Stopa, E. G., Young, L. J., Rilling, J. K., Albers, H. E., et al. (2018) · American Journal of Primatology · doi:10.1002/ajp.22875 · Cited by 53
Self-citationRigney, N., Beaumont, R., & Petrulis, A. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104715 · Cited by 49
Endogenous Oxytocin, Vasopressin, and Aggression in Domestic Dogs
MacLean, E. L., Gesquiere, L. R., Gruen, M. E., Sherman, B. L., Martin, W. L., & Carter, C. S. (2017) · Frontiers in Psychology · doi:10.3389/fpsyg.2017.01613 · Cited by 52
Song, Z., Larkin, T. E., Malley, M. O., & Albers, H. E. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2016.02.004 · Cited by 47
Self-citationNeuropeptide Regulation of Social Attachment: The Prairie Vole Model
Tabbaa, M., Paedae, B., Liu, Y., & Wang, Z. (2016) · Comprehensive physiology · doi:10.1002/cphy.c150055 · Cited by 53
Schulte, L. M., & Summers, K. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2017.03.005 · Cited by 43
Rigney, N., Whylings, J., de Vries, G. J., & Petrulis, A. (2021) · Neuroendocrinology · doi:10.1159/000509421 · Cited by 42
Differential activation of vasotocin neurons in contexts that elicit aggression and courtship
Loveland, J. L., & Fernald, R. D. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.09.008 · Cited by 42
Grieb, Z. A., Ross, A. P., McCann, K. E., Lee, S. D., Welch, M., Gomez, M. G., Norvelle, A., Michopoulos, V., Huhman, K. L., & Albers, H. E. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104878 · Cited by 42
Self-citationDonovan, M. L., Liu, Y., & Wang, Z. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.01.015 · Cited by 45
Prounis, G. S., Thomas, K., & Ophir, A. G. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24450 · Cited by 38
Hormonal and neural correlates of care in active versus observing poison frog parents
Fischer, E. K., & O’Connell, L. A. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104696 · Cited by 37
Cid-Jofré, V., Moreno, M., Reyes-Parada, M. I., & Renard, G. M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222112077 · Cited by 40
Guoynes, C. D., Simmons, T. C., Downing, G., Jacob, S., Solomon, M., & Bales, K. L. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.11.037 · Cited by 38
Taylor, J. H., Walton, J. C., McCann, K. E., Norvelle, A., Liu, Q., Vander Velden, J. W., Borland, J. M., Hart, M., Jin, C., Huhman, K. L., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2121037119 · Cited by 35
Self-citationThe role of vasopressin in olfactory and visual processing
Wacker, D. W., & Ludwig, M. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2867-1 · Cited by 37
Bruce, M. R., Couch, A. C. M., Grant, S. E., McLellan, J., Ku, K. M., Chang, C. C., Bachman, A. M., Matson, M., Berman, R. F., Maddock, R. J., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02020-3 · Cited by 35
Kabelik, D., Weitekamp, C. A., Choudhury, S. C., Hartline, J. T., Smith, A. N., & Hofmann, H. A. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2018.06.013 · Cited by 32
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Massey, S. H., Schuette, S., Pournajafi‐Nazarloo, H., Wisner, K. L., & Carter, C. S. (2016) · Archives of Women s Mental Health · doi:10.1007/s00737-016-0616-6 · Cited by 34
Female HPA axis displays heightened sensitivity to pre-pubertal stress
Brydges, N. M., Best, C., & Thomas, K. L. (2019) · Stress · doi:10.1080/10253890.2019.1658738 · Cited by 30
Scarola, S. J., Trejo, J. R. P., Granger, M., Gerecke, K. M., & Bardi, M. (2019) · Comparative Medicine · doi:10.30802/aalas-cm-18-000025 · Cited by 30
Kinley, B. L., Kyne, R. F., Lawton‐Stone, T. S., Walker, D. M., & Paul, M. J. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15520 · Cited by 28
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Reddon, A. R., O’Connor, C. M., Nesjan, E., Cameron, J., Hellmann, J. K., Ligocki, I. Y., Marsh‐Rollo, S. E., Hamilton, I. M., WYLIE, D. R. W., Hurd, P. L., et al. (2017) · Royal Society Open Science · doi:10.1098/rsos.170350 · Cited by 25
Nonapeptides mediate trade-offs in parental care strategy
DeAngelis, R., Dodd, L., & Rhodes, J. S. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104717 · Cited by 24
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Tong, W. H., Abdulai-Saiku, S., & Vyas, A. (2020) · Neuroendocrinology · doi:10.1159/000508862 · Cited by 26
Carter, C. S. (2017) · Current topics in behavioral neurosciences · doi:10.1007/7854_2017_18 · Cited by 27
Pitra, S., Zhang, M., Cauley, E. S., & Stern, J. E. (2019) · The Journal of Physiology · doi:10.1113/jp277167 · Cited by 25
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Zimmermann-Peruzatto, J. M., Lazzari, V. M., de Moura, A. C., Almeida, S., & Giovenardi, M. (2015) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00130 · Cited by 23
Petersen, C. L., & Hurley, L. M. (2017) · Integrative and Comparative Biology · doi:10.1093/icb/icx055 · Cited by 25
Perkins, A. E., Varlinskaya, E. I., & Deak, T. (2019) · International review of neurobiology · doi:10.1016/bs.irn.2019.08.001 · Cited by 23
Satoh, K., Oti, T., Katoh, A., Ueta, Y., Morris, J. F., Sakamoto, T., & Sakamoto, H. (2015) · FEBS Journal · doi:10.1111/febs.13291 · Cited by 21
Vasopressinergic control of stress-related behavior: studies in Brattleboro rats
Csikota, P., Fodor, A., Balázsfi, D., Pintér, O., Mizukami, H., Weger, S., Heilbronn, R., Engelmann, M., & Zelena, D. (2016) · Stress · doi:10.1080/10253890.2016.1183117 · Cited by 21
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Metadata
- Authors
- Albers, H. E.
- Affiliations
- Georgia State University (US)
- Corresponding author
- Albers, H. Elliott
- ORCID
- Albers, H. Elliott
- Venue
- Frontiers in Neuroendocrinology
- Publisher
- Elsevier BV
- Published
- 2015-01
- Volume
- 36
- Pages
- 49-71
- ISSN
- 0091-3022 (ISSN-L)
- PMC
- PMC4317378
- OpenAlex
- W2007630334
- Cited by
- 200
- References
- 334
- Citations by year
- 2026: 17 · 2025: 11 · 2024: 12 · 2023: 8 · 2022: 12 · 2021: 14 · 2020: 19 · 2019: 13 · 2018: 33 · 2017: 26 · 2016: 24 · 2015: 11
- FWCI
- 2.91
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Frontiers in Neuroendocrinology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH
- NSF (IOS-092330)
- 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
- arginine vasotocin, vasopressin, oxytocin, social behavior, species differences, sex differences, individual differences, volume transmission, CO release, peptide receptors, gonadal hormones, sociality
- MeSH terms
- Animals, Brain, Humans, Individuality, Nerve Net, Sex Characteristics, Social Behavior, Species Specificity, Vasopressins, Vasotocin, Signal Transduction
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