Social Threat-Safety Test Uncovers Psychosocial Stress-Related Phenotypes

Sarah Ayash; Marianne M&#252;ller; Ulrich Schmitt

doi:10.3791/65640

JoVE Journal > Behavior

行为学

Social Threat-Safety Test Uncovers Psychosocial Stress-Related Phenotypes

Published: December 15, 2023

doi:

10.3791/65640

Sarah Ayash¹, Marianne Müller^1,2, Ulrich Schmitt¹

¹Leibniz-Institute for Resilience Research, ²Translational Psychiatry, Department of Psychiatry and Psychotherapy,Johannes Gutenberg University Medical Center

Summary

The social threat-safety test allows a simultaneous assessment of social avoidance development as a measurement of aversive conditioned learning and social threat-safety discrimination ability, both utilized to identify stress-susceptible and stress-resilient individuals within a single group of chronically socially defeated male mice.

Abstract

Social stress is a major cause of the development of mental disorders. To enhance the translational value of preclinical studies, social stress experience and its behavioral impact on mice should be comparable to humans. Chronic social defeat (CSD) utilizes a type of social stress involving physical attacks and sensory threats to induce mental dysfunctions resembling human affective disorders. To strengthen the psychosocial component of CSD, a 10-day CSD protocol was applied in which daily physical attacks are standardized to three 10 s episodes followed by a 24 h sensory phase. After the 10^th sensory phase, the CSD protocol is followed by a refined behavioral assay called the social threat-safety test (STST). Post-stress behavioral assays need to determine how and to what extent the social stressor has influenced behavior. The STST allows chronically socially defeated male mice to interact with 2 novel male individuals (social targets): one social target from the attacking strain encountered during the CSD days and the other from a novel strain. Both are presented simultaneously in different compartments of a three-chambered test arena. The test enables a simultaneous assessment of social avoidance development to measure successful aversive conditioned learning and social threat-safety discrimination ability. The development of social avoidance towards both strains reflects a generalized aversive response and thus, a measurement of stress susceptibility. Meanwhile, the development of social avoidance towards only the attacking strain reflects threat-safety discrimination and thus, a measurement of stress resilience. Finally, the absence of social avoidance towards the attacking strain reflects impaired aversive conditioned learning. The protocol aims to refine the currently used mouse models of stress susceptibility/resilience by including translational criteria, specifically threat-safety discrimination and aversive response generalization, to categorize a single group of chronically socially defeated animals into resilient and susceptible subgroups, eventually advancing future translational approaches.

Introduction

Stress is defined as the disruption of homeostasis caused by physical or psychological stimuli¹. Stress is a well-known major risk factor for the development of mental disorders such as post-traumatic stress disorder, depression, and anxiety²^,³. In particular, social stress is considered a major risk factor for the development of stress-related mental disorders⁴. One type of social stress that has gained particular importance in research is social subordination stress⁵. Mice, like humans, are capable of a rich set of social behavior⁶, rendering them suitable for investigations involving social stress. In the laboratory setting, when adult mice are group housed, they establish a social structure involving the formation of ranks⁷. Accordingly, the colony model was designed to study the effects of naturally established social hierarchies in mixed-sex groups of mice⁸. Over the years, variations of the colony model have been developed to utilize social subordination stress, including same-sex group models, the social instability model, and the intruder-colony model. In recent years, however, one particular variant known as the male resident-intruder model has been popularized in literature, simplifying the social complexity to two mice: a resident and an intruder. The animal of interest, known as the intruder, is placed into the cage of a larger, older, and retired breeder, known as the resident or aggressor. The resident then physically attacks the intruder as a method of confrontation, establishing a social hierarchy wherein the resident is dominant and the intruder is subordinate. When confrontations are one-time events, they classify as "acute" (the "acute social defeat model"), whereas repeated confrontations lasting over several days (usually 10) are known as "chronic" (the "chronic social defeat model"). In the chronic social defeat (CSD) model, attacks are intermittent and typically confined to a period of 5-10 min⁹, termed the physical phase. Following the physical phase, the intruder and resident are kept overnight in the same cage, separated in half with a mesh wall, allowing for all forms of interaction except physical contact. This configuration, known as the sensory phase, induces stress through the continuous appearance of threat instead of direct physical confrontation. In 2018, van der Kooji and colleagues introduced a modified chronic social defeat treatment to focus on the psychosocial component of the model by standardizing and strictly limiting the physical phase¹⁰. The modified model limits physical attacks to three 10 s episodes with different residents, occurring in 15 min inter-episode intervals of the sensory phase. Following the third physical episode, the sensory phase lasts overnight. This cycle repeats for 10 consecutive days with new residents per episode. The modified treatment enhances the translational validity of the chronic social defeat model as physical harm of the intruder is minimized, and outcome variability from differential durations of physical attacks is reduced.

Since the CSD model is utilized to study stress-related illness (e.g., depression, anxiety, post-traumatic stress disorder), post-behavioral assays are chosen, including, but not limited to, behavioral assays of aggression, memory, and anhedonia. In recent years, post-CSD behavioral assays in mice often evaluate how and to what extent sociability is affected⁹. Sociability is defined as the innate preference of mice to socially interact rather than socially avoid a conspecific. Since sociability is subject to stress effects, assays that solely assess social avoidance development were established. Stress-induced social avoidance has a translational relevance as it represents one of the main behavioral symptoms of social anxiety and depression in humans¹¹. Similar to humans, not all mice develop social avoidance following CSD treatment, suggesting the presence of individuality in stress responsiveness. Cohen and colleagues have proposed cut-off behavioral criteria to be a promising approach for studying the neurobiology of individuality¹². Selection of animals based on behavior results in group division, underlining the basis for gene-environment studies. Subsequently, different subgroups often show distinct enrichment of specific genetic variants/modifications, which in turn can be investigated under different environmental conditions¹³. Accordingly, individuality in the development of social avoidance was utilized to divide the single group of chronically socially defeated male mice into two subgroups: stress susceptible (socially avoidant) and stress resilient (socially non-avoidant⁹^,¹⁴). However, the interpretation of the social avoidance phenotype in mice as a maladaptive or adaptive behavior should be considered in the overall context of both the treatment (here CSD) and post-treatment behavioral assay. Additionally, the post-treatment behavioral assay of choice would ideally assess other facets of sociability and not solely social avoidance development. Our recent work revealed the involvement of conditioned learning in CSD-induced social avoidance¹⁵. Specifically, CSD-induced social avoidance is an aversive conditioned response towards the characterizing traits of the residents' strain serving as the conditioned stimulus to the unconditioned stimulus, namely the attacks by the residents. Moreover, within the socially avoidant subgroup, some individuals can discriminate between the traits of the aversive residents' strain and those of other safe novel strains, while other individuals show generalized social avoidance to both strains. We propose here a refined behavioral post-CSD assay: the Social Threat-Safety Test (STST)¹⁵. Unlike other social interaction tests⁹, the STST enables a simultaneous assessment of social avoidance development as a measurement of the correct aversive conditioned response (i.e., successful conditioned learning) and social threat-safety discrimination ability, both of which are utilized to identify stress-susceptible and stress-resilient individuals within a single group of chronically socially defeated male mice. The assessment of social threat-safety discrimination versus aversive response generalization extends the translational criteria used to classify the single group of chronically socially defeated animals into resilient and susceptible subgroups.

Protocol

All procedures were performed in accordance with the European Communities Council Directive regarding the care and use of animals for experimental procedures and were approved by local authorities (Landesuntersuchungsamt Rheinland-Pfalz). Figure 1 represents a schematic timeline.

1. Treatment

Animals of interest: Obtain C57BL6/J male mice at 7 weeks of age, and upon arrival, single-house in a temperature- and humidity-controlled facility on a 12 h light-dark cycle (lights on: 8:00; lights off: 20:00; 23 °C; 38% humidity) with food and water ad libitum.
Chronic social defeat (CSD)
1. Treatment group
  1. Following 1 week of habituation, perform CSD treatment for 10 consecutive days using the CD-1 strain as the resident's strain (for a detailed protocol, refer to chronic social defeat⁹ and the modified chronic social defeat treatment¹⁰).
  2. Introduce the C57BL6/J mouse into the cage of the CD-1 mouse and count 10 s of physical attack. Repeat this episode three times, each with a different CD-1 mouse, and separate by 15 min inter-episode intervals.
  3. Place a mesh wall between the C57BL6/J mouse and CD-1 mouse during these intervals, allowing only sensory contact. Following the third episode, house the C57BL6/J mice overnight in the cages of the CD-1 mice, separating both by a mesh wall. Repeat for 10 days.
    NOTE: CD-1 mice number = C57BL6/J mice number + 1. If the number of C57BL6/J treated mice is below 10 then a minimum of 10 CD-1 mice is still needed to ensure that every day the last sensory phase (lasting overnight) is with a new CD-1 mouse throughout the 10 days of treatment.
  4. Carefully assess the physical well-being of the animals throughout the 10 days. If an animal is severely wounded, exclude it from the experiment for ethical and scientific (mobility/activity during the post-treatment test) reasons. Table 1 provides a well-being checklist.
2. Control group
  1. Upon arrival, maintain same-age mice in the same conditions as the treatment group.
  2. Following 1 week of habituation, introduce the control animals for 90 s in an empty cage and then return them to individual cages (single-housed) separated in half by mesh walls identical to those used for the treatment group. Perform this daily in parallel to the 10 treatment days.
    NOTE: It is advisable to keep the control group and the treatment group housed in different rooms.
After the last (10^th) sensory phase, single-house all mice in new cages in similar conditions to those described upon arrival and leave them to rest overnight.
NOTE: The last sensory phase should last 24 h, then animals are single-housed.

2. Post-treatment test: Social threat-safety test (Figure 2)

Following CSD treatment, single-house all mice (treated and control groups) in new cages in similar conditions to those described upon arrival and leave them to rest overnight.
During the morning hours (8:00-13:30), clean the three-chambered arena (rectangle in shape with a total size of 60 cm x 40 cm, made of transparent acrylic walls and smooth floors) with 5% ethanol and place it under the camera with light conditions of 37 lux. Ensure that the entire arena is visible.
Clean the mesh enclosures (cage-like made from metal or acrylic) with 5% ethanol and position them as shown in the corners in Figure 1A.
Habituation phase: Introduce the animal of interest at the center of the arena, allow for exploration for 6 min, and then return them to their home cage.
Place the novel (unknown) CD-1 social target (conspecific) under one mesh enclosure and the novel 129/Sv social target under the other mesh enclosure.
NOTE: It is important to use an unknown 129/Sv conspecific to avoid a familiarity bias. Preferably have 4 mesh enclosures per arena: 2 attributed to the habituation phase and 2 to the testing phase.
Testing phase: Immediately re-introduce the animal of interest at the center of the arena and allow exploration for 6 min.
Return all animals to their home. Clean the arena and mesh enclosures with 5% ethanol between tests of different animals, but never during the observation of the same animal, i.e., never between habituation and testing phases.
Alternate the location of the mesh enclosures between animals (and never between the two phases within the same animal) to control for possible location preferential bias.

3. Scoring and analysis

NOTE: Only the post-stress treatment test, i.e., the STST is scored and analyzed (and not the CSD stress treatment).

Define the interaction zone as 2 cm around the mesh enclosures' boundaries.
Score the duration spent exploring the mesh enclosures during the habituation phase when the animal's nose is within the interaction zone.
Score the duration spent interacting with the social targets during the testing phase when the animal's nose is within the interaction zone.
NOTE: Detection can be achieved either manually (using a timer or software for manual scoring) or automatically. Regardless of the detection method, take the nose point for exploration and social interaction measurements and the center point of the body for activity-related measurements (e.g., distance moved).
Calculate the social interaction index as follows: time spent exploring each social target during the testing phase / average time spent exploring the two empty mesh enclosures during the habituation phase (Figure 2B).
Divide the treatment group into 3 subgroups as follows: Animals with a social interaction index ≥1 with the CD-1 social target are non-avoiders, animals with a social interaction index <1 with both social targets are indiscriminate-avoiders, animals with a social interaction index ≥1 only with the 129/Sv social target are discriminating-avoiders (Figure 2C-D).
NOTE: The number of animals within each of the three subgroups can differ between different animal batches (about 1/3 of all animals that undergo the CSD treatment will display the phenotypic characteristics of one of the three subgroups).
Assess the stress effect by statistically analyzing the social interaction index with the CD-1 social target between the treatment and control groups (either parametric two-sample t-test or nonparametric Mann-Whitney test).

Representative Results

Social interaction index as a measurement of aversive conditioned response
A social interaction index ≥1 reflects greater social interaction with the respective social target compared to the exploration of the empty mesh enclosures. Under baseline conditions, defined here as having neither appetitive nor aversive experience with the characterizing traits of a specific strain (here both social targets to the control group and the 129/Sv social target to the treatment group), intact sociability levels are reflected in a social interaction index ≥1 with that same strain. Meanwhile, following a socially aversive conditioning experience (here CSD treatment) with a specific strain (here the resident's strain, i.e., CD-1 strain) and thus, with its characterizing traits serving as a conditioned stimulus, social avoidance development as a measurement of a correct aversive conditioned response is reflected in a social interaction index <1 with that same strain. CSD stress effect is the first to be assessed and on an overall treatment group level (see step 3.6 in the protocol). Specifically, the stress effect is reflected in the treatment group having a social interaction index <1 with the CD-1 social target as a measurement of social avoidance development towards the CD-1 strain. Meanwhile, intact baseline sociability levels of the control group are reflected in having a social interaction index ≥1 with the same social target. This results in a significant difference (p < 0.05) in the social interaction index with the CD-1 social target between both groups (Figure 2C).

Identification of three distinct phenotypic subgroups within a single chronically socially defeated group by the social threat-safety test
After dividing the animals based on their social interaction index, as explained in steps 3.4 and 3.5 in the protocol, a significant difference (p < 0.05) in the index within a single subgroup between both social targets, will only be found within the discriminating-avoiders subgroup (Figure 2D,E). The discriminating-avoiders subgroup and the indiscriminate-avoiders subgroup have a social interaction index <1 with the CD-1 social target, a measurement of social avoidance development towards the conditioned stimulus (CD-1 strain), thereby reflecting the development of a correct aversive conditioned response and of successful aversive conditioned learning. In contrast, the social interaction index (≥1) of the non-avoiders subgroup reflects impaired aversive conditioned learning with the same social target (CD-1 strain). Meanwhile, threat-safety discrimination ability is reflected in the discriminating-avoiders subgroup having a social interaction index ≥1 with the 129/Sv social target as a measurement of intact sociability levels towards a safe/neutral stimulus (129/Sv strain). In contrast, the aversive response generalization of the indiscriminate-avoiders subgroup is reflected in having a social interaction index <1 with the same social target as a measurement of social avoidance and thus, an aversive conditioned response towards a safe/neutral stimulus. The percentage of mice within each subgroup is about 33%; however, this is unpredictable as some batches of animals have more or less in each subgroup. Finally, the absence of social preferential bias as a potential confounding factor is reflected in social interaction indices of ≥1 (i.e., p>0.05) with both social targets within the control group.

Interpretation of the social threat-safety test results
The characteristics of the discriminating-avoiders subgroup, including successful conditioned learning of threat-associated cues and threat-safety discrimination, are discussed as characteristics of stress resilient individuals¹⁶^,¹⁷^,¹⁸^,¹⁹^,²⁰^,²¹^,²². In contrast, generalized aversive conditioned responses after traumatic events, as seen by the Indiscriminate-avoiders subgroup, are a key symptom of stress-related mental disorders such as post-traumatic stress disorder and anxiety disorders¹⁶^,¹⁷^,²³^,²⁴^,²⁵^,²⁶ and thus, are characteristic of stress-susceptible individuals. Finally, the non-avoiders subgroup represents a phenotype of impaired learning¹⁶.

Figure 1: Schematic timeline. Upon arriving at the facility, single-house all mice for 7 days then designate to the treatments: CSD stress treated group or handled control treated group. The treatments last for 10 days after which the animals are single-housed for 1 day. Set up the arenas to perform the STST (which takes place after the single-housing of the animals by 1 day). Start with the habituation phase for 6 min. Follow the habituation phase immediately with the testing phase for another 6 min. Finally, return the animals to their home cages. Please click here to view a larger version of this figure.

Figure 2: Social threat-safety test. (A) Test design. The test is performed in a three-chambered arena divided into three equal parts separated by transparent walls with openings, allowing the animal of interest (C57BL6/J, black) to move in-between. At each of the peripheries, one mesh enclosure is placed. One enclosure contains a novel social target from the residents' strain encountered earlier during the CSD treatment (CD-1, white); the other contains a novel social target from a novel strain matched in age, size, and sex to the novel mouse from the residents' strain but of different fur color (129/Sv, brown). Both social targets are older and larger than the animal of interest. The animal of interest is introduced in the middle of the arena and is allowed to explore the arena for 6 min during the habituation phase when the mesh enclosures are empty and again during the testing phase when the social targets are placed inside the mesh enclosures as depicted. (B) Social interaction index. Score the time spent exploring the mesh enclosures during the habituation phase when the animal's nose is within the interaction zone (2 cm around the mesh enclosures' boundaries). Subsequently, score the time spent interacting with the social targets during the testing phase when the nose is within the interaction zone. Calculate the social interaction index as shown. (C) Chronic social defeat stress effect: The treatment group has a social interaction index <1 with the CD-1 social target as a measurement of social avoidance development towards the CD-1 strain. Meanwhile, intact baseline sociability levels of the control group are reflected in having a social interaction index ≥1 with the same social target. This results in a significant difference (p < 0.05) in the social interaction index with the CD-1 social target between both groups. Results presented as mean ± standard error of the mean (SEM), n=16 per group, Mann-Whitney test. (D) Social threat-safety test representative results following chronic social defeat treatment. The treatment group is divided into three subgroups based on the animals' social interaction indices with the social targets. Mice with a social interaction index ≥1 with the CD-1 social target are termed non-avoiders, mice with a social interaction index <1 with both social targets are termed indiscriminate-avoiders, and mice with a social interaction index ≥1 only with the 129/Sv social target are termed discriminating-avoiders. The control group has similar indices with both social targets. Results presented as mean ± SEM, n = 55 per sub/group. (E) Representative heatmaps of each sub/group during the testing phase of STST. Darker colors indicate more time spent in the area. Please click here to view a larger version of this figure.

Table 1: Abort criteria for chronic social defeat procedure. The table presents a total of four families of observations, each with several sub-observations²⁷. Each observation has a score. Depending on the sum of the score, measures to take are indicated. Please click here to download this Table.

Discussion

The behavioral protocol here describes the Social Threat-Safety Test, used to divide a single group post-CSD treatment into three different subgroups, serving as a method to investigate the underlying biology of stress susceptibility and resilience and to test potential therapies. The biological context and technical details need to be carefully considered to guide a thorough experimental design.

Different housing conditions can alter aggression sociability levels, potentially influencing results obtained from the post-treatment test²⁸^,²⁹^,³⁰. Such conditions include single-housing all animals upon arrival and 24 h prior to the post-treatment test as well as single-housing the control group during the 10 days of treatment. Moreover, the CSD stress effect can be compromised if the control group is accidentally stressed. This can result from exposing the control group to stress-induced odors and vocalizations of the treatment group during the 10 days of treatment as well as the control group witnessing the treatment³¹. Thus, it is advisable to keep the control group and the treatment group housed in different rooms. Furthermore, due to the involvement of conditioned learning¹⁵, certain steps are critical for obtaining post-treatment test results similar to those described here. This includes performing the treatment on young adults for 10 days as well as performing the post-treatment test 24 h following rest (see step 2.1 in the protocol). Conditioned learning can be different in younger (or older) mice. Similarly, performing the treatment for more or less than 10 days means more or less conditioning of the animal, respectively. Changes in treatment duration can result in different subgroup sizes. Additionally, it is advisable that within the same experiment, either the same experimenter performs the treatment and the post-treatment test on all animals or there is a separation between experimenters performing the treatment and those performing the post-treatment test that is similar on all animals. This is because the experimenter/s represents part of the overall conditioning (CSD treatment) and testing (social threat-safety post-treatment test) context for the animal; thus, all animals within the same experiment should be exposed to the same context throughout the experiment. Additionally, animals' behavior during the post-treatment test can be confounded by odor cues³². Cleaning with 5% ethanol between animals standardizes the odor cues. However, avoid cleaning between the two phases of the post-treatment test (habituation and testing) among the same animal. This is because the habituation phase is partially intended to familiarize the animal with the arena so that during the testing phase, the animal's behavior is mainly driven by the new presence of the novel social targets. Thus, cleaning between the two phases can compromise the odor cues marked by the animal during the habituation phase, rendering the arena less familiar during the testing phase of the post-treatment test³³. Furthermore, it is preferable to have four mesh enclosures per arena, two of which are attributed to the habituation phase (always used empty) and two to the testing phase (always used with the social targets), in order to extinguish the potential residual smell of the CD-1 and 129/Sv social targets in the mesh enclosures from the testing phase to the habituation phase. The elimination of residual smell in the mesh enclosures is critical because it can influence the animal's exploration of the mesh enclosures during the habituation phase, changing the social interaction index results and thus, the division of the treatment group into three subgroups³³. Similarly, attributing specific social targets for the post-treatment test and maintaining them in similar conditions when not in use is advisable. This is because involving one social target in other treatments and tests can influence the behavior of the respective target in the mesh enclosure during the post-treatment test. For example, using the CD-1 social target in other experiments as a resident for CSD treatment can change its aggression levels relative to the 129/Sv when used in the social threat-safety post-treatment test. Differences in aggression levels can signal different cues to the animal of interest during the post-treatment test, creating a preferential bias that is not attributed to conditioned learning from the 10 days of treatment. Thus, both social targets having similar experiences before use in the post-treatment test can help standardize the behavior and cues of both while being in the mesh enclosure. Another measure to avoid the implication of a preferential bias includes the use of older and larger social targets than the animal of interest¹⁵, affirming the main cue as the characterizing traits of the strain, not the age or size. For this purpose, the post-treatment test employs the 129/Sv strain to contrast the CD-1 and C57BL6/J strains. The 129/Sv strain has a different fur color from both. It would be of interest to test different strains of different fur colors and see how the results in the post-treatment test are influenced¹⁵.

Chronic Social Defeat is one of the most robust models for post-traumatic stress disorder, depression, and other stress-related illnesses³⁴. It has excellent etiological-³⁵, predictive-, discriminative-, pharmacological- and face validity⁸^,³⁶. Here, a modified CSD protocol in male mice introduced by van Der Kooji and colleagues that aims to strengthen the psychosocial component of the induced stress is described¹⁰. The social avoidance phenotype is robust, reliable, and easily testable and possesses ethological relevance and strong face validity³⁴. Unlike other social interaction tests⁹, the STST enables simultaneous assessment of social avoidance development and social threat-safety discrimination ability¹⁶. The results from the STST are utilized to identify stress-susceptible and stress-resilient subgroups within a single group of chronically socially defeated mice, which aligns with the evidence in humans characterizing resilient individuals with threat-safety discrimination and susceptible individuals with aversive response generalization¹⁶. This classification can be followed by experimental manipulations to help unravel the neural basis of stress resilience and susceptibility in general and specific to threat-safety discrimination versus aversive response generalization¹⁶^,³⁷. Despite decades of research and certain improvements in treatment, stress-related mental disorders remain prevalent in humans. However, by focusing on heterogeneity across different individuals in response to the same stressor, there is a paradigm shift from conducting disease-oriented research alone to conducting disease- and health-oriented research simultaneously. This paradigm shift might help develop novel prevention³⁸^,³⁹ approaches and identify improved targeted treatment strategies.

A limitation of the model is that only males were investigated. Because the STST is based on the CSD model, which was developed based on male mice' behavior in nature⁴⁰, the test was not assessed for its compatibility with female mice. A compatible test with female mice would be one that follows a stress treatment created either on both sexes or on females only. Further studies are needed to extend these findings reported from male to female mice. Moreover, the expected results reported here are from young adult mice. It would add to our understanding to know how (if) the findings change by using different ages. Of note, a recent study found that social avoidance behavior following CSD is similar between mice of different age groups⁴¹. Similarly, other variables to be considered are treatment duration, if different than 10 days, and time of behavioral assay, if conducted more than 24 h following rest. Overall, the model substantially refines the currently used mice models of stress susceptibility/resilience and contributes to advancing future translational approaches.

Disclosures

The authors have nothing to disclose.

Acknowledgements

This research is supported by the Collaborative Research Center 1193, Subproject Z02, funded by the German National Research Foundation (SFB1193, Neurobiology of Resilience) and the Boehringer Ingelheim Foundation (grant to Leibniz Institute for Resilience Research and Individual Phenotyping and High-Resolution Automated Behavioural Analysis). We would like to thank Dr. Konstantin Radyushkin and Mrs. Sandra Reichel for their technical assistance as well as Mrs. Hanna Kim for her English language support. The funding sources had no involvement in the model design; collection, analysis, and interpretation of data; in the writing of the protocol; and in the decision to submit the protocol for publication.

Materials

Arenas	Noldus, Sociability cage, Wageningen, the Netherlands	https://www.noldus.com/applications/sociability-cage	Three-chambered, rectangle in shape with a total size of 60 cm x 40 cm, made of acrylic transparent walls and smooth floors
Camera for video recording	Basler AG, Germany An der Strusbek 60-62 22926 Ahrensburg	ace Classic acA1300-60gc	If using automatic detection program, make sure cameras are compatible
Camera objective	KOWA Kowa Optimed Deutschland GmbH Fichtenstr. 123 40233 Duesseldorf: LMVZ4411 \| 1/1.8" 4.4~11mm Varifokal Objektiv	Part-No. 10504
Detection program/Timer	Noldus, EthoVision-XT, Wageningen, the Netherlands	https://www.noldus.com/ethovision-xt	Detection can be achieved either manually (using a timer or a software for manual scoring) or automatically
Housing cages	ZOONLAB GmbH, Hermannstraße 6, 44579 Castrop-Rauxel	3010010	Type 2 cages: 265 mm x 205 mm x 140 mm (l x w x h) i.e. 360 cm² bottom area. Made of Polycarbonate (Makrolone©) and Polysulfone. Lids are made of stainless steel. European standard cages for up to 5 mice (20–25 g). Autoclavable up to 134 °C
Mesh enclosures	Part of the Arena Package: Noldus, Sociability cage, Wageningen, the Netherlands	https://www.noldus.com/applications/sociability-cage	Small acrylic or metal cage-like with a diameter of 100 mm and a height of 200 mm with openings of a 10 mm in size. Two mesh enclosures per arena would work but four is preferable (see point 2.5 in protocol)
Mesh wall	selfmade	N/A	Acrylic or metal, one for each cage. Size depends on cages used. The walls must not allow the two animals to have a physical contact
Social targets: Mice of the strains CD-1 and 129/Sv; retired male breeders	Mice provided by Charles River: Strain name: CD-1®IGS Mouse 129S2/SvPasCrl	Crl:CD1(ICR); 129S2/SvPasCrl	CD-1 and 129/Sv retired male breeders, single-housed, novel (unknown) conspecifics to the animals of interest. If retired male breeders are not available then males older than 1 year from both strains would suffice

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Ayash, S., Müller, M., Schmitt, U. Social Threat-Safety Test Uncovers Psychosocial Stress-Related Phenotypes. J. Vis. Exp. (202), e65640, doi:10.3791/65640 (2023).