Chronic Environmental or Genetic Elevation of Galanin in Noradrenergic Neurons Confers Stress Resilience in Mice

Rachel P. Tillage,1 Genevieve E. Wilson,1 L. Cameron Liles,1 Philip V. Holmes,2 and David Weinshenker1 1Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, and 2Department of Psychology, University of Georgia, Athens, Georgia 30602

The neuropeptide galanin has been implicated in stress-related neuropsychiatric disorders in humans and rodent models. While pharmacological treatments for these disorders are ineffective for many individuals, physical activity is beneficial for stress-related symptoms. Galanin is highly expressed in the noradrenergic system, particularly the locus coeruleus (LC), which is dysregulated in stress-related disorders and activated by exercise. Galanin expression is elevated in the LC by chronic exer- cise, and blockade of galanin transmission attenuates exercise-induced stress resilience. However, most research on this topic has been done in rats, so it is unclear whether the relationship between exercise and galanin is species specific. Moreover, use of intracerebroventricular (ICV) galanin receptor antagonists in prior studies precluded defining a causal role for LC- derived galanin specifically. Therefore, the goals of this study were twofold. First, we investigated whether physical activity (chronic wheel running) increases stress resilience and galanin expression in the LC of male and female mice. Next, we used transgenic mice that overexpress galanin in noradrenergic neurons (Gal OX) to determine how chronically elevated noradren- ergic-derived galanin, alone, alters anxiogenic-like responses to stress. We found that three weeks of ad libitum access to a running wheel in their home cage increased galanin mRNA in the LC of mice, which was correlated with and conferred resil- ience to stress. The effects of exercise were phenocopied by galanin overexpression in noradrenergic neurons, and Gal OX mice were resistant to the anxiogenic effect of optogenetic LC activation. These findings support a role for chronically increased noradrenergic galanin in mediating resilience to stress.

Key words: anxiety; exercise; galanin; locus coeruleus; mice; stress

Significance Statement

Understanding the neurobiological mechanisms underlying behavioral responses to stress is necessary to improve treatments for stress-related neuropsychiatric disorders. Increased physical activity is associated with stress resilience in humans, but the neurobiological mechanisms underlying this effect are not clear. Here, we investigate a potential causal mechanism of this effect driven by the neuropeptide galanin from the main noradrenergic nucleus, the locus coeruleus (LC). We show that chronic voluntary wheel running in mice increases stress resilience and increases galanin expression in the LC. Furthermore, we show that genetic overexpression of galanin in noradrenergic neurons causes resilience to a stressor and the anxiogenic effects of optogenetic LC activation. These findings support a role for chronically increased noradrenergic galanin in media- ting resilience to stress.

Introduction Stress-related neuropsychiatric disorders affect ;600 million people worldwide, yet current pharmacological treatments have

limited efficacy and cause adverse side effects for many people (Nestler et al., 2002; Rush et al., 2006; James et al., 2018). Clinical studies have consistently linked physical exercise to improve- ments in a wide array of neuropsychiatric disorders (Herring et al., 2010; Cooney et al., 2013; Ashdown-Franks et al., 2020). Individuals who regularly exercise are less likely to experience stress-related neuropsychiatric disorders, such as depression, anxiety, and posttraumatic stress disorder (Whitworth and Ciccolo, 2016; Chekroud et al., 2018; Harvey et al., 2018), and chronic voluntary wheel running increases resilience to various stressors in rodents (Sciolino et al., 2012; Kingston et al., 2018; Mul et al., 2018; Tanner et al., 2019). A multitude of biological changes occur as a result of chronically increased physical activ- ity which may or may not be causally linked to alterations in

Received Apr. 24, 2020; revised June 16, 2020; accepted July 14, 2020. Author contributions: R.P.T., P.V.H., and D.W. designed research; R.P.T., G.E.W., and L.C.L. performed

research; R.P.T. and G.E.W. analyzed data; R.P.T. and D.W. wrote the paper. This work was supported by the National Institutes of Health Extramural Research Program Grants

MH116622 (to R.P.T.) and DA038453, AG047667, AG061175, and NS102306 (to D.W.). We thank Jason Schroeder for his assistance with the behavioral experiments, John Hepler and Suneela Ramineni for assistance with the in situ hybridization experiment, and Cheryl Strauss for helpful editing of the manuscript. The authors declare no competing financial interests. Correspondence should be addressed to David Weinshenker at

Copyright © 2020 the authors

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stress resilience and mood; however, a promising candidate for mediating these beneficial effects is the neuropeptide galanin.

Galanin is abundant in the brain (Tatemoto et al., 1983; Kofler et al., 2004; Fang et al., 2015), and modulates stress, mood, cogni- tion, food intake, nociception, and seizures (Mitsukawa et al., 2008; Lang et al., 2015). Human studies have implicated genetic variants in the genes encoding the galanin gene and its receptors (GalR1, GalR2, and GalR3) in conferring an increased risk of depression and anxiety, especially in the context of environmental stress expo- sure, and postmortem studies have similarly revealed galaninergic dysregulation in people with major depressive disorder (Barde et al., 2016).

While the pattern of galanin expression in the brain can vary from species to species, it is particularly rich in the noradrenergic locus coeruleus (LC) of both humans and rodents (Skofitsch and Jacobowitz, 1985; Melander et al., 1986; Holets et al., 1988; Chan-Palay et al., 1990; Pérez et al., 2001; Le Maître et al., 2013). The LC is activated by stress, and norepinephrine (NE) release plays a crucial role in the stress response, coordinating a host of downstream effects via broad axonal projections required for the “fight-or-flight” response (Valentino and Van Bockstaele, 2008). Consistent with this role, the LC-NE system is dysregulated in stress-related neuropsychiatric disorders, such as anxiety, depres- sion, and posttraumatic stress disorder (Roy et al., 1988, 2017; Ordway et al., 1994; Wong et al., 2000; Bissette et al., 2003; Ehnvall et al., 2003; Naegeli et al., 2018). In rats, galanin expres- sion increases in the LC following chronic wheel running or treadmill exercise and correlates with running distance (O’Neal et al., 2001; Van Hoomissen et al., 2004; Holmes et al., 2006; Sciolino et al., 2012, 2015; Epps et al., 2013), and in Sciolino et al. (2015), we found that wheel running confers resilience to a stres- sor. Galanin has both acute neuromodulatory and chronic neu- rotrophic properties, and the beneficial effects of exercise in rats were blocked by chronic, but not acute, intracerebroventricular (ICV) infusion of a galanin antagonist and recapitulated by chronic ICV infusion of galanin alone, suggesting a neurotrophic mechanism of action (Sciolino et al., 2015). However, it is not known whether these phenomena can be extrapolated to other species or attributed to LC-derived galanin.

To investigate the contribution of chronically elevated noradren- ergic galanin to stress resilience in mice, we investigated behavioral responses to foot shock in both an environmental (voluntary wheel running) and genetic (dopamine b -hydroxylase-galanin transgene; Gal OX) model of LC galanin overexpression. To isolate anxiety- like responses mediated specifically by the LC, we also examined the behavior of Gal OX mice following optogenetic LC activation. Our findings support a causal role for chronically elevated norad- renergic-derived galanin in promoting stress resilience.

Materials and Methods Animals All procedures related to the use of animals were approved by the Institutional Animal Care and Use Committee of Emory University and were in accordance with the National Institutes of Health guidelines for the care and use of laboratory animals. All mice were group housed and maintained on a 12/12 h light/dark cycle with access to food and water ad libitum, unless noted otherwise. All manipulations and behavioral tests occurred during the light cycle. Adult male and female mice (three to ninemonths), with equal numbers of both sexes, were used for all experiments. The Gal OXmice were generated with a transgene contain- ing the mouse galanin gene driven by the human dopamine b -hydroxy- lase (Dbh) promoter, resulting in an ;fivefold increase in galanin mRNA in noradrenergic and adrenergic neurons and a twofold increase in galanin protein in LC-innervated forebrain regions compared with

wild-type (WT) littermates (The Jackson Laboratory stock #004996; Steiner et al., 2001). All mice used in this study were on a C57BL/6J background.

Exercise Both exercise and sedentary mice were singly housed for one week before the start of running wheel experiments. On the first day of the experiment, low-profile wireless running wheels (Med Associates) were placed in the cage of the exercise mice. Sedentary animals had no additions to their home cages, consistent with our previous studies in rats (Sciolino et al., 2012, 2015). All mice were monitored daily for threeweeks.

Behavioral assays For the behavioral battery following exercise, assays were conducted 24– 48 h after foot shock stress, with at least 2–3 h between tests, in order of least stressful to most stressful to minimize effects from the previous tests. Baseline behavioral assays [open field (OF), elevated plus maze (EPM), forced swim test (FST), fear conditioning, nestlet shredding, ele- vated zero maze (EZM), marble burying (MB), novelty-suppressed feed- ing (NSF), locomotor activity, and shock-probe defensive burying (SPDB)] were conducted as previously described (Tillage et al., 2020) with at least 4–5 d between tests.

Stress paradigm The foot shock stress protocol was modified from a previously published paradigm (Lecca et al., 2016). Mice were individually exposed to 20min of foot shock exposure consisting of 19 shocks randomly interspaced by 30, 60, or 90 s (0.5-ms shocks, 1mA) in chambers (Coulbourn Instruments) equipped with a house light, a ceiling-mounted camera, and an electric grid shock floor. Control animals were placed in the chamber for 20min but were not administered shocks. Chambers were cleaned with MB-10 between animals.

Corticosterone (CORT) measurement Mice used for CORT measurement went through the foot shock stress paradigm described above and were anesthetized with isoflurane 15min after the end of the stress. Mice were rapidly decapitated, and trunk

Table 1. Antibodies used

Antibody Species Dilution Source Catalog #

TH Chicken 1:1000 Abcam AB76442 c-fos Rabbit 1:5000 Millipore ABE457 DsRed Rabbit 1:1000 Takara 632496 Alexa Fluor 488 anti-rabbit Goat 1:500 Invitrogen A-11008 Alexa Fluor 568 anti-rabbit Goat 1:500 Invitrogen A-11011 Alexa Fluor 488 anti-chicken Goat 1:500 Abcam AB150169 Alexa Fluor 568 anti-chicken Goat 1:500 Invitrogen A-11041

Figure 1. Distance traveled by mice with access to running wheels. WT C57Bl6/J mice were given ad libitum access to running wheels in their home cage for three weeks; n= 7 per group, mixed males and females (for breakdown by sex, see Extended Data Fig. 1-1). Error bars show SEM.

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blood was collected in EDTA-coated tubes (Sarstedt Inc.) and chilled on ice. Blood was centrifuged for 20min at 3000 rpm at 4°C, and the result- ing plasma was collected and stored at �80°C. CORT was measured using the Enzo Life Sciences kit following the manufacturer’s small vol- ume protocol for blood plasma, including diluting samples 1:40 with a steroid displacement reagent solution.

Galanin in situ hybridization and densitometry To measure galanin mRNA in the LC following exercise, mice were deeply anesthetized with isoflurane and rapidly decapitated for

brain extraction. Brains were collected, flash frozen in Tissue Freezing Medium, and stored at �80°C until processing. Brains were sectioned at 12 mm and collected on gelatin-coated slides (SouthernBiotech). Slides were stored at �80°C. Galanin in situ hybridization was conducted and images were acquired as previ- ously described (Sciolino et al., 2015). For quantification, images were converted to 16-bit in NIH ImageJ (, and the mean grayscale value was measured in three to four LC sec- tions per animal using a standardized region of interest to obtain an average measurement per animal. The mean grayscale value of the

Figure 2. Exercise increases resilience to foot shock stress-induced anxiety-like behavior. WT C57Bl6/J mice were given ad libitum access to running wheels in their home cage (“Exercise”) or no running wheel (“Sedentary”) for three weeks, then were tested in behavioral assays 24–48 h following foot shock (“Stress”) or no foot shock (“No stress”). A, Exercise paradigm timeline. B, Sedentary mice show decreased time spent in the open arms of the EZM after stress, but exercise mice do not. C, No significant differences were seen in the MB assay. D, In the SPDB assay, sedentary stressed mice showed increased freezing compared with sedentary non-stressed mice, but there was no difference between stressed and non-stress exercise mice. Exercise mice showed an overall increase in both rearing (E) and number of probe touches compared with sedentary mice (F), with no effect of stress. G, There were no differences as a result of exercise or stress on grooming or (H) digging in the SPDB assay. I, In the NSF test, sedentary mice took significantly longer to eat after stress compared with non-stressed sedentary mice, with no differ- ence between stressed and non-stressed exercise mice. J, Exercise mice tended to consume more food during the hour after the NSF test, but it was not significant; n= 7–8 mice per group, mixed males and females (for breakdown by sex, see Extended Data Figure 2-1). Error bars show SEM; *p, 0.05, ***p, 0.001.

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background was subtracted out for each measurement. The experi- menter was blind to treatment during image analysis.

Stereotaxic surgery For optogenetic experiments, mice were anesthetized with isoflurane and given the analgesic meloxicam at the start of the surgery (5mg/kg, s.c.). A lentiviral vector containing the channel-rhodopsin-2 (ChR2) con- struct with an mCherry tag under control of the noradrenergic-specific PRSx8 promoter (Hwang et al., 2001) was infused unilaterally into the LC (�5.4 AP; 11.2 ML; �4.0 DV) with a 5-ml Hamilton syringe and Quintessential Stereotaxic Injector (Stoelting) pump at a rate of 0.15ml/min. Unilateral LC stimulation is sufficient to produce behavioral effects in mice that are indistinguishable from bilateral stimulation (Carter et al., 2010; McCall et al., 2015). Control mice received a lentivirus containing mCherry alone under the PRSx8 promoter. Each animal received a 0.7-ml infusion, and the infusion needle was left in place for 5min after infusion to allow for viral diffusion. An optic fiber ferrule (ThorLabs) was implanted 0.5 mm dorsal to the viral injection site (�5.4 AP;11.2 ML; �3.5 DV) and perma- nently attached to the skull with screws and dental acrylic. Mice were singly housed after this surgery to prevent cage mates from damaging the headcap and given at least threeweeks to recover and allow for full viral expression before testing.

Optogenetic stimulation Mice were habituated to handling and connection of the optic patch cable to the implanted optic fer- rule for at least one week before testing. The LC optogenetic stimulation was based on a previ- ously published paradigm (McCall et al., 2015). Photostimulation was delivered to the LC for 30min (5-Hz tonic stimulation, 10-ms light pulses, 473nm) in 3min on/off bins in the home cage.

Histology To assess correct targeting of the LC in mice used for optogenetic experiments, all animals were exposed to 5-Hz LC photostimulation for 15min in the home cage, then anesthetized 90min later with isoflurane and transcardially perfused with potassium PBS (KPBS), followed by 4% paraformaldehyde (PFA) in PBS. Brains were postfixed overnight by immersion in 4% PFA at 4°C and then transferred to 30% sucrose in KPBS for 48 h at 4°C. Brains were flash fro- zen in isopentane on dry ice and embedded in Tissue Freezing Medium. Tissue was cryosec- tioned at 40 mm for immunohistochemistry. Viral expression and correct optic fiber tar- geting were assessed by immunostaining for the mCherry tag using rabbit anti-DsRed primary antibody (1:1000) and goat anti- rabbit 568 secondary (1:500). Sections were co-stained for the noradrenergic marker tyrosine hydroxylase (TH) with chicken anti-TH (1:1000) and goat anti-chicken 488 secondary (1:500). In adjacent LC sections, activated LC neurons were detected with rabbit anti c-Fos primary antibody (1:5000) with goat anti-rabbit 488 secondary (1:500) and TH-expressing cells were co-stained using chicken anti-TH (1:1000) with goat anti-chicken 568 secondary (1:500). After staining, all sections were mounted on slides and coverslipped with Fluoromount plus DAPI (Southern Biotech). Images were col- lected on a Leica DM6000B epifluorescent upright microscope at 10� or 20�. Mice were excluded from analyses if they did not show viral expression in the LC, correct optic fiber targeting, and increased c-Fos

expression in the LC compared with the control animals of the same cohort. Antibodies are summarized in Table 1.

Statistical analysis Data were found to be normally distributed using the D’Agostino– Pearson test. Data were analyzed via unpaired t test or two-way ANOVA with Sidak’s correction for multiple comparisons, where appropriate. Significance was set at p, 0.05, and two-tailed variants of tests were used throughout. Data are presented as mean 6 SEM. Calculations were performed and figures created using Prism Version 8 (GraphPad Software).

Results Wheel running characteristics Singly housed WT C57BL6/J mice were given unrestricted access to a running wheel in their home cage for 21 d. Mice steadily increased their running distance over the first week, after which they ran;10–16 km/d, which is comparable to distances reported for C57BL/6J mice in previous studies using similar running wheels (De Bono et al., 2006; Goh and Ladiges, 2015; Fig. 1).

Figure 3. Exercise increases galanin mRNA in the LC of mice. Galanin mRNA levels in the LC were measured via in situ hybridization in WT C57Bl6/J mice following three weeks of ad libitum access to running wheels in their home cage (Exercise) or no running wheels (Sedentary), foot shock (Stress) or no foot shock (No stress), and behavioral testing. A, Representative images of galanin in situ hybridization. B, Quantitative densitometry analysis revealed that exercise mice showed significantly elevated galanin mRNA in the LC compared with sedentary mice, with no effect of foot shock stress exposure. C, Correlation analysis showed that the average distance ran per day during the third week for each mouse showed a significant positive correlation with the level of galanin mRNA expression in the LC. The average dis- tance ran per day during the first (D) and second (E) weeks did not correlate with the level of galanin mRNA expres- sion in the LC; n= 5–8 mice per group, mixed males and females (for breakdown by sex, see Extended Data Fig. 3-1). Error bars show SEM; ****p, 0.0001.

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Female mice ran significantly more than males (F(1,12) = 9.101, p=0.0107; Extended Data Fig. 1-1).

Exercise increases resilience to foot shock stress-induced anxiety-like behavior At the end of the threeweeks, half of the mice were subjected to a foot shock stressor. The fol- lowing day, mice were put through a battery of behavioral tasks consisting of EZM, MB, and SPDB. Mice were then food-deprived overnight and tested in an NSF assay the next day before euthanasia and tissue collection (Fig. 2A). These behavioral assays were chosen to cover a range of both active (e.g., digging in MB and SPDB) and passive (e.g., freezing in SPDB, decreased exploration in EZM, longer latency to feed in NSF) anxiety-like behaviors displayed by mice, as well as to align with the behavioral assays previously used in our studies on the anxiolytic effects of exercise in rats (Sciolino et al., 2012, 2015). For the EZM, a two-way ANOVA showed a significant exercise � stress interaction (F(1,25) = 5.718, p=0.0246), and post hoc tests revealed that sedentary mice had a significant decrease in the time spent in the open arms of the EZM after stress (p=0.0294), while stress had no effect on the exer- cise animals (p=0.6810; Fig. 2B). No differences were seen in the MB test as a result of exercise (F(1,25) = 2.265, p=0.1448) or stress (F(1,25) = 0.06874, p=0.7953; Fig. 2C).

In the SPDB assay, a two-way ANOVA showed a main effect of exercise (F(1,19) = 9.133, p=0.007) and stress (F(1,19) = 4.759, p= 0.0419) on freezing behavior, with the stressed sedentary animals spending significantly more time freezing com- pared with non-stressed sedentary animals (p= 0.021). The effects of stress were abrogated by exercise (p= 0.9489; Fig. 2D). There was a main effect of exercise on rearing behavior, showing that regardless of stress exposure (F(1,19) = 0.09776, p= 0.7579), exercise mice displayed more rearing bouts in the SPDB task (F(1,19) = 16.24, p=0.0007; Fig. 2E). Exercise mice also had a slight, but significant increase in the number of shock probe touches from the electrified probe compared with sedentary mice (F(1,19) = 6.004, p=0.0241), regardless of stress exposure (F(1,19) = 0.01144, p=0.9160; Fig. 2F). There was no effect of exercise or stress on the amount of time mice spent grooming (exercise: F(1,19) = 3.917, p= 0.0625; stress: F(1,19) = 0.9914, p=0.3319) or digging (exercise: F(1,19) = 0.08843, p=0.7694; stress: F(1,19) = 0.02293, p= 0.8812) in the SPDB test (Fig. 2G,H).

In the NSF task, there was a main effect of exercise on the latency to eat the food in the novel environment (F(1,25) = 78.94, p, 0.0001) but no main effect of stress (F(1,25) = 3.092, p = 0.0909). Post hoc testing revealed that stressed sedentary animals had a significantly longer latency to eat compared with non-stressed sedentary animals (p = 0.0243), with no effect of stress on the exercise animals (p = 0.9825; Fig. 2I). As a control, the amount of food consumed by each mouse in 1 h immediately after the NSF test was recorded. There were no significant differences because of exercise (F(1,25) = 2.371, p = 0.1361) or stress (F(1,25) = 0.003919, p=0.9506; Fig. 2J). There were no differences between males and females in any behavioral

measures (Extended Data Fig. 2-1). Together, these results demon- strate that chronic wheel running affords protection from the anx- iogenic-like effects of foot shock stress.

Exercise increases gal mRNA in the LC Several previous studies have shown that chronic voluntary exer- cise increases prepro-galanin mRNA in the LC of rats (Van Hoomissen et al., 2004; Holmes et al., 2006; Sciolino et al., 2012, 2015), but this change has never been examined in mice. We measured prepro-galanin mRNA in the LC of exercise and sed- entary mice using in situ hybridization and found a robust and significant increase in galanin mRNA in exercise mice compared with their sedentary counterparts (F(1,23) = 58.24, p, 0.0001), with no difference according to stress exposure (F(1,23) = 0.08014, p= 0.7796; Fig. 3A,B). Furthermore, we found a positive correla- tion between the average distance each mouse ran per day in the third week and the level of galanin mRNA in the LC (r2 = 0.4196, p= 0.0312; Fig. 3C), but not in week 1 (r2 = 0.08,222, p=0.3926) or week 2 (r2 = 0.2234, p=0.142; Fig. 3D,E). There were no sig- nificant differences between male and females in galanin mRNA level in the LC at baseline (sedentary) or after exercise (Extended

Figure 4. Galanin mRNA levels in the LC correlate with exercise-induced stress resilience. There was no signifi- cant correlation between galanin mRNA levels in the LC and percentage time spent in the open arms of the EZM for non-stressed mice, but there was a significant positive correlation for stressed mice (A, B). There were signifi- cant negative correlations between galanin mRNA levels in the LC and latency to eat in the NSF assay for both non-stressed and stressed animals (C, D). There was no significant correlation between LC galanin mRNA expres- sion and freezing during the SPDB assay for non-stressed mice, but there was a significant negative correlation for stressed mice (E, F); n= 5–8 mice per group.

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Data Fig. 3-1). These results indicate that elevation of galanin expression in the LC occurs as a result of chronic physical activ- ity in mice, similar to what is observed in rats.

Galanin mRNA levels in the LC correlate with exercise- induced stress resilience To further determine the relationship between galanin abun- dance in the LC and stress resilience, we examined whether the

magnitude of galanin mRNA expression correlated with the exercise-induced stress resilience behavioral changes seen in the EZM, NSF, and SPDB assays. Strikingly, there was a non-signifi- cant trend toward a negative correlation between LC galanin expression and amount of time spent in the open arms of the EZM for non-stressed mice (r2 = 0.1036, p=0.2553), but a strong, significant positive correlation for stressed mice between these two measures (r2 = 0.7058, p=0.0152; Fig. 4A,B). There

Figure 5. Gal OX mice display normal behavior at baseline. A battery of behavioral tests was conducted on Gal OX mice compared with their WT littermates. A, Timeline showing order of tests. B, EPM. C, EZM. D, OF. E, TST, tail suspension test. F, FST. G, NS, nestlet shredding. H, MB. I, NSF. J–L, FC, fear conditioning. M, LA, locomotor activity. SPDB. Gal OX mice were normal in all measures; n= 8–11 mice per group, mixed males and females (for breakdown by sex, see Extended Data Fig. 5-1). Error bars show SEM.

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were significant negative correlations between galanin mRNA levels in the LC and latency to eat in the NSF assay for both non- stressed (r2 = 0.4873, p=0.0055) and stressed animals (r2 = 0.6279, p=0.0036; Fig. 4C,D). Finally, there was not a significant correlation between LC galanin mRNA levels and freezing dur- ing the SPDB assay for non-stressed mice (r2 = 0.2638, p= 0.0876), but there was a significant negative correlation between these measures for stressed mice (r2 = 0.4981, p= 0.0217; Fig. 4E, F). For all three behaviors, the correlations with LC galanin mRNA levels were stronger (and in the case of EZM, opposite) in the stressed mice compared with non-stressed mice. Together, these data support the idea that LC-derived galanin is less impor- tant for anxiety-like behavior at baseline but becomes preferen- tially engaged by stress to confer resilience.

Gal OX mice show normal baseline behavior Gal OX mice are reported to have normal performance in several canonical tests for anxiety-like behavior, including the EPM and OF test, but are resistant to yohimbine-induced anxiety-like behavior in a light-dark exploration task (Holmes et al., 2002). To confirm and expand on previous baseline behavioral studies conducted with the Gal OX mice, we conducted an extensive bat- tery of anxiety-, depression-, learning-, and motor-related behav- ioral tasks (Fig. 5A). We observed no differences between Gal OX and littermate WT control mice in canonical tests of anxiety- like behavior (EPM, t(17) = 0.1641, p=0.8717; zero maze, t(17) = 0.6739, p=0.5095; OF, t(17) = 0.3211, p= 0.7521) or depressive- like behavior (tail suspension test, t(17) = 1.578, p= 0.1331; FST, t(17) = 0.4564, p=0.6539; Fig. 5B–F). They showed no difference from WT littermates in compulsive behaviors during the nestlet shredding task (t(7) = 0.07,861, p=0.9395) or MB task (t(17) = 0.8051, p= 0.4319; Fig. 5G,H). Additionally, Gal OX behavior was comparable to WT in the NSF task (t(17) = 1.355, p=0.1933; Fig. 5I). Gal OX mice exhibited normal cognitive responses in contextual (F(1,17) = 0.2773, p=0.6053) and cued fear condition- ing (F(1,17) = 0.5667, p=0.4619; Fig. 5J–L). The locomotor activ- ity of Gal OX mice was normal (F(1,17) = 0.6486, p=0.4317; Fig. 5M). In the SPDB task, Gal OXmice were normal in most behav- iors, including digging (t(12) = 0.7124, p=0.4899), freezing (t(12) = 0.7015, p= 0.4964), rearing (t(12) = 0.4402, p=0.6676), and a number of probe touches (t(12) = 0.6455, p=0.5308; Fig. 6A–D). The only exception was that Gal OX mice spent significantly less time grooming during the task than their WT counterparts (t(12) = 3.152, p= 0.0084; Fig. 6E). There were no differences between males and females in any behavioral measures (Extended Data Figs. 5-1, 6-1).

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