Novel unconditioned prosocial behavior in prairie voles (Microtus ochrogaster) as a model for empathy
In this study, empathy is quantified using a novel social test. Empathy and prosocial behavior are linked to the expression of oxytocin in humans and rodent models. Specifically, prosocial behavior in prairie voles (Microtus ochrogaster) has been linked to the expression of oxytocin in the paraventricular nucleus of the hypothalamus. The animal’s behavior was considered empathic if it spends significantly more time attempting to remove a loos fitting restraint (tether) from the stimulus animal than time in contact with a, simultaneously presented, non-social object similar to the tether. The behavioral data was cross-referenced with the number of neurons expressing oxytocin and arginine vasopressin, as well as the density of dopaminergic neurons (identified by the expression of tyrosine hydroxylase), in the paraventricular nucleus of the hypothalamus. These proteins influence empathic behavior in humans, non-human primates, rats, mice, and prairie voles.
The consistency between neuroanatomical mechanisms linked to empathy, and the durations of time spent engaging in empathic contact, support the prediction that the empathic contact in this test is a distinct prosocial behavior, lacking prior behavioral training or the naturally occurring ethological relevance of other prosocial behaviors, and is a measure of empathy.
KeywordsEmpathy Prosocial Oxytocin Dopamine Rodent model Vole
paraventricular nucleus of the hypothalamus
In humans, observing distress drives signaling between the cingulate cortex, prefrontal cortex, and limbic regions, such as the amygdala and hypothalamus . This correlates with self-reported empathy, an external expression of which is prosocial behavior . Prosocial behaviors have been linked to the expression of oxytocin (OT) in humans [3, 4]. In prairie voles (Microtus ochrogaster), OT regulates prosocial behaviors, such as partner preference formation, alloparental care, and consoling behavior [5, 6, 7, 8]. Specifically, prosocial behavior in prairie voles has been linked to the expression of OT in the paraventricular nucleus of the hypothalamus (PVN) [9, 10]. The PVN signals to the pituitary and the supraoptic nucleus, triggering a cascade of signaling molecules that modulate the regulatory mechanisms of steroid-dependent prosocial behaviors such as pair-bonding and alloparental care, through estrogen receptor alpha (ERα) . It has been hypothesized that OT’s role as an empathogen may have first evolved in the context of kinship relationships, and that the ability to accurately infer others emotions may provide an advantage through the ‘trust-effect’ of OT . The mechanism by which OT influences empathy is currently unknown, but if it is an extension of the mechanism by which it regulates other steroid-dependent prosocial behaviors, it is likely to modulate corticolimbic signaling patterns  through ERα.
In this study, neurons expressing OT, arginine vasopressin (AVP), or tyrosine-hydroxylase (TH) (dopaminergic neurons), were counted in the PVN of prairie voles. While OT, AVP and dopamine in the PVN are linked to social behaviors like exploratory sniffing [14, 15, 16], only OT and AVP in the PVN are linked to empathy [7, 12, 17, 18, 19, 20]. A role for dopaminergic PVN neurons, in the context of empathy, remains unexplored. Dopamine in the anterior cingulate cortex  and nucleus accumbens, however, is important in empathy-like responses to observational fear. In prairie voles, males have more dopaminergic neurons in the PVN than females , but not OT neurons . Here we sought to determine if there is an unconditioned prosocial behavior, distinct from other prosocial behaviors, that is indicative of empathy and linked to PVN OT neurons.
To establish this behavior as empathic, time spent engaging in exploratory sniffing and time spent in contact with a non-social object were quantified. A significant difference in time in empathic contact and time in contact with the non-social object would suggest that the empathic contact is prosocial. The prosocial behavior most similar to empathic contact is exploratory sniffing, and a significant difference in empathic contact and exploratory sniffing would suggest that these are separate prosocial behaviors. If, as predicted, the empathic contact is a distinct prosocial behavior, without training or the ethological relevance of other prosocial behaviors, we conclude that it is a measure of empathy.
Study animals originated from an Urbana, IL wild stock and were used in a prior experiment . The prairie vole is a rodent model for investigating prosocial behavior . Prairie voles differ from traditional laboratory rodents in specific housing, diet and husbandry requirements [30, 31, 32].
Novel social test
Behavioral data recordings were taken for another, previously published experiment with different endpoints and goals . Only the control animals of both sexes from that prior study were used for the work herein. Briefly, on post-natal day 30, the animals were tested for 1 h in a novel social arena as described previously [5, 33] and in Fig. 1, using a gently tethered, unrelated stimulus animal (same sex, size, and age matched). The tether was a restraint loosely fit around the stimulus animal’s neck on one end and fixed to the wall mounted non-social object (represented in Fig. 1 as an elongated grey oval with a red outline) preventing the test animal from entering the non-social chamber or the adjoining tube. Attached to the cage wall was a non-social object of the same material and luster as the tether that was not directly linked to the collar portion of the animal’s tether.
A treatment-blinded observer scored behaviors using Jwatcher v1.0 behavioral scoring software (UCLA) . The measured behaviors included total test time spent in exploratory sniffing, chewing or pulling on tether/collar within 1.3 cm of the stimulus animal (empathic contact), and time spent engaging in contact with non-social object. An observer remained in the room for the duration of the test to monitor potential signs of aggression; no injury to any animals occurred.
Brain collection and preparation for immunohistochemistry
Brains were collected and processed as described in our prior publication . Again, only the control animals were used for the experiments described herein. Briefly, the animals were euthanized between post-natal days 60–90. Each animal was given 0.05-mL buprenorphine ip and then deeply anesthetized 15 min later with 0.05 mL of ketamine–xylazine (at a concentration of 67.7 and 13.33 mg/kg, respectively) mixture administered sc. Brains were collected and immersion fixed for 24 h in 4% paraformaldehyde and transferred to fresh solution at 2 and 4 h. 30% buffered sucrose with 0.1% sodium azide was used to cryoprotect the brains, which were then shipped to the Patisaul Lab, where they were stored in fresh cryoprotectant overnight at 4 °C and then flash frozen and stored at − 80 °C. Brains were sectioned at 35 µm coronally on a frozen sliding microtome. Subsequently, sections for each individual brain corresponding to the regions of interest were collected and processed for immunohistochemistry.
For each test animal, 8 sequential sections of the PVN were collected and processed for immunohistochemical staining of AVP and OT using routine procedures described previously  using 1:12,000 monoclonal mouse anti-OT (catalog number MAB5296; Millipore) and 1:12,000 polyclonal rabbit anti-AVP (catalog number 20069; Immunostar). Sections were then washed and incubated for 120 min in a solution of Alexa Fluor 568 goat anti-mouse and Alexa Fluor 488 goat anti-rabbit secondary antibodies (both at 1:200). Immunohistochemical staining of TH was performed on two consecutive posterior PVN sections as described previously  with the polyclonal rabbit anti-TH (catalog number AB152; Millipore) primary antibody at 1:4000 and Alexa Fluor 488 donkey anti-rabbit secondary antibody at 1:200. These sections were also counterstained via a 45-s incubation with Hoechst (catalog number H3569; Invitrogen Life Technologies). After a final wash in cold KPBS, all PVN sections were mounted on Fisher super frost plus glass slides, coverslipped with a glycerol mountant, and stored at − 20 °C.
Quantification and analysis
The 8 sequential sections selected for OT immunoreactivity (OT-ir) and AVP immunoreactivity (AVP-ir) quantification encompassed the entire PVN, as previously described . For the present study, the PVN subregional counts, established previously , were averaged within animal and then animal specific means were averaged by sex, so that each animal contributed one value to the final mean. The dopaminergic immunoreactive cell counts (TH-ir) are the same as previously reported .
All analyses were done with IBM SPSS Statistic version 21. Novel social results were analyzed by a one-way ANOVA testing for significant (P ≤ 0.05) sex-specific differences (homogeneity of variance was validated using Levene’s test, there were no distribution effects of unequal sample sizes). Paired t tests (2-tailed) were performed within sex testing for significant (P ≤ 0.05) differences in total test time between empathic behavior and non-social object contact, or empathic behavior and exploratory sniffing (males n = 9, females n = 22).
Significant (P ≤ 0.05) sex-specific differences in numbers of OT-ir, AVP-ir and TH-ir neurons in the PVN were determined by a one-way ANOVA. Significant (P ≤ 0.05) within-sex differences in the number of neurons expressing OT, AVP and TH were determined by a one-way ANOVA (OT and AVP males and females n = 11, TH males and females n = 7).
As expected, the immunohistochemistry results revealed that the number of OT-ir and AVP-ir neurons across the PVN are not sexually dimorphic, but that the density of dopaminergic neurons in the posterior PVN is sexually dimorphic (Fig. 2c). Significantly more TH-ir neurons were observed in males than females (ANOVA F(1,12) = 8.76 P ≤ 0.05). Males also had greater numbers of OT-ir neurons than AVP-ir neurons (paired t-test, maleOT-AVP t10 = 30 P ≤ 0.001). Additionally, there were more TH-ir neurons than AVP-ir neurons in males, but there was no significant difference between the number of OT-ir and TH-ir neurons. In the PVN of females, there were significantly fewer AVP-ir neurons and TH-ir neurons than OT-ir neurons (paired t-test, femaleOT-AVP t11 = 12.23 P ≤ 0.001; femaleOT-TH t6 = 4.17 P ≤ 0.05), with no significant difference between AVP-ir and TH-ir neurons. Taken together, the results of this study suggest sex-specific differences in the expression of prosocial behavior, with concordant patterns of sexually dimorphic significance in the underlying neurobiology of the PVN. It is important to note that while region and neuron specific histology provides a broad understand of the underlying mechanisms contributing to prosocial behavior, it is the OT and AVP signaling that guides behavior.
Here we used behaviorally observable exploratory sniffing to measure sexually dimorphic non-empathic prosocial behavior. Males spent significantly more time engaging in empathic contact than non-social object contact, suggesting that empathic contact is prosocial (Fig. 2a). Additionally, the significant difference between exploratory sniffing and empathic contact suggests that empathic contact is distinct from non-empathic prosocial behaviors (Fig. 2a).
Because empathy is regulated by OT and AVP, but not dopaminergic PVN neurons, in humans and voles [7, 12, 17, 18, 19] we hypothesized that if empathic contact is distinct from other prosocial behaviors, then the number of OT-ir, AVP-ir and TH-ir neurons in the PVN would support this difference. Our measure of non-empathic prosocial behavior, exploratory sniffing, was similar across sexes as were the number of TH-ir neurons in the PVN. However, as predicted, the number of TH-ir PVN neurons across sexes was not did not parallel the duration of empathic contact between males and females. This observation is consistent with prior work showing that dopamine expression in the cingulate cortex is linked to empathy, but expression in the PVN is not . Our results support region-specific differences and suggest that dopaminergic neurons in the PVN may regulate exploratory sniffing and possibly other non-empathic prosocial behaviors.
Also consistent with our hypothesis, time spent in empathic contact and the number of AVP-ir and OT-ir neurons in the PVN, followed similar patterns across sexes (Fig. 2c). These data support prior work showing that empathy is regulated by oxytocinergic and vasopressinergic systems in the PVN of humans, rats and prairie voles [7, 8, 18, 19]. The number of PVN neurons expressing AVP and OT is independent of sex and consistent with the time spent in empathic contact versus contact with a non-social object across sexes. Finally, the neuroanatomical mechanisms that regulate empathy in prairie voles , and the time spent in empathic contact, support the prediction that empathic contact is a distinct prosocial behavior, independent of training or known ethological relevance, and is a measure of empathy. All supporting data can be accessed through the Additional file 1.
The cell counts used in this study provide strong correlative evidence for the role of PVN OT, AVP, and TH neurons in empathic behavior, but to demonstrate causal influence of these neuronal populations would require in vivo manipulations of the discussed cell populations. Reduced empathic contact concurrent with optogenetic silencing of PVN OT or AVP neurons using a noninvasive red-shifted microbial rhodopsin  would provide strong evidence for a causal role of these cells in empathy. To a lesser extent the use of pharmacological manipulations, such as OT or AVP antagonists could provide similar support, but could not account for off target effects from the peripheral nervous system, or other brain regions that express OT such as the olfactory tubercle .
LAS: Primary author, empathy assay design and quantification, tissue collection, statistical analysis of behavioral and neuroanatomical data. AWS: Collection of autoradiography data and quantification of neuroanatomy, manuscript revision. HBP: Study design and support, autoradiography/histology training, and manuscript revision. BSC: Study design and support, behavioral testing training, histology training, and manuscript revision. All authors read and approved the final manuscript.
The authors wish to thank Prof. Troy Ghashghaei from NCSU Department of Molecular Biomedical Sciences for providing access to his confocal fluorescence microscope used to image the tissue sections in this study.
Authors declare that there is no conflict of interest, financial interest or otherwise, that could have influenced the objectivity of the observations, results or interpretation of the findings.
Availability of data and materials
All data used in this study is available in the additional supporting documents.
Consent for publication
Ethic approval and consent to participate
Human subjects were not involved in this study, all related declaration statements are non-applicable. All animals were housed in accordance with USDA and NIH guidelines and all procedures were approved by the University of Akron and the Northeast Ohio Medical University Animal Care and Use Committee prior to undertaking any experimental manipulation.
The sources of funding for this study came from institutional funds available at North Carolina State University as well as a grant from the National Institute of Environmental Health Sciences, Award Number: ES021233, awarded to Dr. Heather B. Patisaul.
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- 4.Abu-Akel A, Palgi S, Klein E, Decety J, Shamay-Tsoory S. Oxytocin increases empathy to pain when adopting the other- but not the self-perspective. Soc Neurosci. 2014;10:1–9.Google Scholar
- 6.Perkeybile AM, Delaney-Busch N, Hartman S, Grimm KJ, Bales KL. Intergenerational transmission of alloparental behavior and oxytocin and vasopressin receptor distribution in the prairie vole. Front Behav Neurosci. 2015;9:191. https://doi.org/10.3389/fnbeh.2015.00191/abstract.CrossRefPubMedPubMedCentralGoogle Scholar
- 10.Yamamoto Y, Cushing BS, Kramer KM, Epperson PD, Hoffman GE, Carter CS. Neonatal manipulations of oxytocin alter expression of oxytocin and vasopressin immunoreactive cells in the paraventricular nucleus of the hypothalamus in a gender-specific manner. Neuroscience. 2004;125:947–55.CrossRefPubMedGoogle Scholar
- 11.Cushing BS. The organizational effects of oxytocin and vasopressin: behavioral implications. In: Oxytocin, Vasopressin Relat Pept Regul Behav. E. Choleris M. Kavaliers DWP, editors. Cambridge: Cambridge University Press; 2013. p. 56–66.Google Scholar
- 22.Young KA, Gobrogge KL, Liu Y. Wang Z. Front. Neuroendocrinol: The neurobiology of pair bonding: insights from a socially monogamous rodent; 2011. p. 53–69.Google Scholar
- 24.Lü Y-F, Yang Y, Li C-L, Wang Y, Li Z, Chen J. The locus coeruleus-norepinephrine system mediates empathy for pain through selective up-regulation of P2X3 receptor in dorsal root ganglia in rats. Front Neural Circuits. 2017. https://doi.org/10.3389/fncir.2017.00066/full.CrossRefPubMedPubMedCentralGoogle Scholar
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