Accumulating evidence from both the human and animal literature indicates that exercise reduces the negative consequences of stress. The neurobiological etiology for this stress protection, however, is not completely understood. Our lab reported that voluntary wheel running protects rats from expressing depression-like instrumental learning deficits on the shuttle box escape task after exposure to unpredictable and inescapable tail shocks (uncontrollable stress). Impaired escape behavior is a result of stress-sensitized serotonin (5-HT) neuron activity in the dorsal raphe (DRN) and subsequent excessive release of 5-HT into the dorsal striatum following exposure to a comparatively mild stressor. However, the possible mechanisms by which exercise prevents stress-induced escape deficits are not well characterized. The purpose of this experiment was to test the hypothesis that exercise blunts the stress-evoked release of 5-HT in the dorsal striatum. Changes to dopamine (DA) levels were also examined, since striatal DA signaling is critical for instrumental learning and can be influenced by changes to 5-HT activity. Adult male F344 rats, housed with or without running wheels for 6 weeks, were either exposed to tail shock or remained undisturbed in laboratory cages. Twenty-four hours later, microdialysis was performed in the medial (DMS) and lateral (DLS) dorsal striatum to collect extracellular 5-HT and DA before, during, and following 2 mild foot shocks. We report wheel running prevents foot shock-induced elevation of extracellular 5-HT and potentiates DA concentrations in both the DMS and DLS approximately 24 h following exposure to uncontrollable stress. These data may provide a possible mechanism by which exercise prevents depression-like instrumental learning deficits following exposure to acute stress.
Citation: Clark PJ, Amat J, McConnell SO, Ghasem PR, Greenwood BN, Maier SF, et al. (2015) Running Reduces Uncontrollable Stress-Evoked Serotonin and Potentiates Stress-Evoked Dopamine Concentrations in the Rat Dorsal Striatum. PLoS ONE 10(11): e0141898. https://doi.org/10.1371/journal.pone.0141898
Editor: Alexandra Kavushansky, Technion - Israel Institute of Technology, ISRAEL
Received: April 28, 2015; Accepted: October 3, 2015; Published: November 10, 2015
Copyright: © 2015 Clark et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are available via Figshare (http://dx.doi.org/10.6084/m9.figshare.1508569).
Funding: Experiments completed in this manuscript were funded by NIH RO1MH068283.
Competing interests: The authors have declared that no competing interests exist.
The stress response is an adaptive physiological reaction to challenges that functions to promote survival. Protracted or exaggerated responses to chronic or severe stress, however, can become maladaptive to brain function, playing a well-documented role in the development of stress-related disorders like anxiety and depression. Mounting evidence indicates abnormal levels of monoamine neurotransmitters contribute to the expression of symptoms associated with anxiety and depression, however the neurobiological mechanisms involved are not well understood (for review see [1–4]). On the other hand, regular mild to moderate physical activity can be beneficial for cognitive function and mental health [5, 6]. For instance, it is clear that physically active organisms are stress robust. Indeed, accumulating evidence in human and rodent studies indicates that a physically active lifestyle promotes stress-resistance and resilience, or respectively, the capability to endure and rapidly recover from the damaging consequences of stress [5, 7–13]. While the specific mechanisms are unclear, exercise may buffer stress, in part, by altering the signaling of brain monoamines . Indeed, acute bouts of exercise have been shown to enhance the activity of monoamines including serotonin (5-HT) and dopamine (DA) in a number of stress sensitive rodent brain regions [14–18]. Moreover, data from rodent models suggest engaging in long-term exercise induces plasticity in 5-HT and DA systems within stress responsive areas that may influence the activity of these neurotransmitters in ways that promote stress-resistance [10, 19–22]. A better understanding of the mechanisms by which physical activity promotes stress robustness could lead to the discovery of novel targets to treat or prevent stress related disorders.
Insight into the neural mechanisms by which physical activity promotes stress resistance has come from rodent models where physical activity status is manipulated by providing access to running wheels before exposure to a potent stressor; 100 inescapable and unpredictable tail shocks (acute stress) [5, 7, 8]. Animals with access to running wheels are protected from the development of several anxiety- and depression-like behaviors following exposure to this acute stressor, including exaggerated fear, increased drug seeking behavior, reduced social exploration, and shuttle box learning deficits [10, 23, 24]. In particular, shuttle box escape deficits following acute stress are thought to be a consequence of impaired goal directed instrumental behavior, a common symptom of depression [25, 26]. The circuitry underlying impaired acquisition of shuttle box task has been well characterized. Exposure to tail shocks hyper-activates 5-HT neurons in the dorsal raphe nucleus (DRN) [27, 28] desensitizing the inhibitory 5-HT1A autoreceptors (5-HT1AR) [29, 30], thereby removing an important source of inhibition over the activity of these neurons. 5-HT activity, thus, becomes sensitized in areas innervated by the DRN during subsequent exposure to a comparatively mild stressor [25, 28, 31, 32]. Impaired escape behavior following acute stress is related to a potent rise in extracellular 5-HT concentrations in DRN projection site the dorsal striatum, and can be prevented by pharmacological blockade of 5-HT2C receptors (5-HT2CR) located in the same striatal region . These data specifically highlight the significance of a stress-sensitized DRN 5-HT response acting in the dorsal striatum to produce depression-like escape deficits. While much is known about the neurobiology underlying the development of escape deficits following exposure to this stressor, comparatively less is understood about how exercise prevents such impairments.
Wheel running may prevent the development of acute stress-induced escape deficits by constraining the activity of DRN 5-HT neurons. Indeed, evidence from our lab suggests rats that engage in 6 wk (but not 3 wk) voluntary running display reduced expression of neural activity marker c-Fos in DRN 5-HT neurons during exposure to tail shocks [10, 19]. Reduced 5-HT neuron activity in wheel running rats is paralleled by an up regulation in 5-HT1AR in the DRN [10, 19]. A potentially stronger 5-HT1AR-mediated inhibition of DRN 5-HT neurons in running rats during acute stress may be sufficient to attenuate or eliminate the subsequent stress-induced sensitization of 5-HT activity in the dorsal striatum, thereby conferring protection against depression-like escape deficits . However, it is currently unknown if exercise prevents or attenuates stress-sensitized 5HT activity in the dorsal striatum following exposure to acute stress.
The purpose of this experiment was to test the hypothesis that 6 weeks of running prevents stress-sensitized 5-HT levels in the rat dorsal striatum using in vivo microdialysis, given the previously reported increases of 5-HT1AR expression and reduced neural activity in the DRN [10, 19]. The dorsal striatum was selectively targeted because previous work from our lab suggests acute stress-sensitized 5-HT response in this brain region is necessary for shuttle box escape deficits , while the contributions of other striatal sub-structures to this paradigm remains unknown. In addition, DA signaling in the striatum is critical for goal-directed processes including instrumental learning and can be modulated by excessive 5-HT activity [33–37]. Therefore, we also explored the possibility that exercise alters DA release in the dorsal striatum following stress exposure in a manner consistent with protection against impaired shuttle box behavior. Sampling was performed in both the medial (DMS) and lateral (DLS) dorsal striatum, as evidence suggests these regions each modulate a distinct aspect of the instrumental behavior, such as shuttle box escape. Indeed, DMS is necessary for the initial acquisition of instrumental behaviors, whereas the DLS then becomes selectively recruited to maintain an instrumental process once it is acquired [38–46]. Therefore, stress induced changes to 5-HT or DA concentrations that are consistent with development of, or protection against, impaired escape behavior may be present in only one sub-region such as the DMS, since rats fail in the acquisition stage of the shuttle box task following acute stress exposure. Moreover, contrasting responses to unpredictable stress have been reported in sub regions of the rat dorsal striatum, whereby DMS displayed atrophy and the DLS displayed hypertrophy , suggesting these areas may react differently to stressors. We report that long-term wheel running attenuates acute stress-induced sensitization of 5-HT, but potentiates DA concentrations in both the DMS and DLS following subsequent exposure to foot shock. These data may provide insight into possible neural adaptations from exercise that contribute to the prevention of depression-like instrumental learning deficits following stress.
Materials and Methods
Subjects and husbandry
Upon arrival, 70 male Fischer344 rats (obtained from Harlan SPF, Indianapolis, IN, USA) weighing approximately 148g were individually housed in standard laboratory cages (45×25.2×14.7 cm) or cages with locked running wheels (45×25.2×14.7 cm). After 1 week, running wheels were unlocked and rats received free access to wheels for the remainder of the study (6–7 weeks). The time course of wheel access was chosen because 6, but not 3, weeks of running is sufficient to prevent shuttle box escape deficits following exposure to 100 unpredictable and inescapable tail shocks [10, 48]. Daily wheel revolutions were recorded digitally using Vital View software (Mini Mitter, Bend, OR, USA). A total of 12 rats were removed from analysis during the experiment due to surgical complications, improper cannula placement, or damage to dialysis probe during sampling. Group sample sizes used for statistical analysis are reported below. Rooms were controlled for temperature (21 ± 1°C) and photo-period (12:12 L:D) for the entire study. Food (Harlan Teklad 7012) and water were provided ad libitum. All procedures were approved by the University of Colorado Institutional Animal Care and Use Committee and adhered to NIH guidelines. Special care was taken to minimize animal discomfort during all procedures.
During the 3rd or 4th week of voluntary wheel running or sedentary conditions rats underwent stereotaxic surgery for microdialysis guide cannulae implantation. Cannulae implantation was performed during the 3rd and 4th week of running because previous work from our lab indicates exercising rats that undergo surgery during this period are still protected from behavioral deficits dependent that follow unpredictable and inescapable tail shock . Rats were anesthetized with a cocktail of ketamine (0.75 mg/kg i.p.; Vedco, St. Joseph, MO, USA) and medetomidine (0.5 mg/kg i.p.; Pfizer, New York, NY, USA). Guide cannulae were implanted unilaterally in the right or left DMS (-0.2 A/P, ± 2 M/L, -3.8 D/V from bregma) or DLS (-0.2 A/P, ± 4.3 M/L, -4.5 D/V from bregma), based on the Paxinos and Watson atlas. Rats were immunized with a single subcutaneous injection of penicillin (0.25mL/Kg; of Combi-Pen, Agrilbas, St. Joseph, Missouri, USA). Atipamezole (0.5 mg/kg i.p.; Pfizer, New York, NY, USA) was administered following surgery to reverse the effects of medetomidine.
Tail shock procedure (acute stress).
Approximately 3–4 weeks after surgery, rats were randomly assigned to either receive tail shock stress (DMS: n = 8 Sedentary Stress, n = 8 Running Stress; DLS: n = 7 Sedentary Stress, n = 8 Running Stress) or no stress (DMS: n = 7 Sedentary Control, n = 7 Running Control; DLS: n = 7 Sedentary Control, n = 6 Running Control). Rats that received tail shock were restrained in a Plexiglas box with the tail protruding from the back of the box where electrodes were placed to deliver 100 tail shocks (5 s, 1.5 mA, 1 min ISI). This uncontrollable stress procedure is necessary for hyperactivation of the DRN, and a sensitized 5-HT response following subsequent mild stress exposure. Control rats were left undisturbed in home cages during tail shocks.
Approximately 4 h following tail shocks, microdialysis probes (CMA 12, 2mm) were inserted into guide cannulae and rats were placed in separate Plexiglas dialysis bowls (Bioanalytical Systems) with access to food and water overnight. Artificial cerebral spinal fluid was perfused through probes using an infusion pump at a follow rate of 0.2 ul/min overnight. The next morning flow rate was increased to 1.5 ul/min and after 90 min of equilibration sampling began. Infusion rate remained constant throughout the sample collecting. Samples were collected every 20 mins. The first two samples (B1-B2) were collected in dialysis bowls. Rats were then carefully moved from dialysis bowls to conditioning chambers where remaining samples were collected before (B3-B4), and immediately following (FS-P4) 2 foot shocks (5s, 0.8 mA, 1min ISI).
Dialysates containing extracellular 5-HT and DA were measured by high-performance liquid chromatography (HPLC) with electrochemical detection. The system consisted of an ESA 5600A Coularray detector with an ESA 5014B analytical cell and an ESA 5020 guard cell. The column was an ESA MD-150 (C-18, 3 m, 150 3.2 mm) maintained at 38°C, and the mobile phase was the ESA buffer MD-TM. The analytical cell potentials were kept at -100 mV and +200 mV and the guard cell at +220mV. Dialysate (25 μl) was injected with an ESA 542 autosampler that kept the dialysates at 6°C. External standards (Sigma) were run for each daily analysis to quantify 5-HT and DA. Samples that contained low volumes of dialysate or were lost during collection were not included for analysis.
Following completion of microdialysis rats were euthanized by rapid decapitation. Brains were rapidly extracted and froze in isopentane (-20C). Brains were coronal sectioned at 40 μm and Nissl stained to verify cannulae placement. Misplaced cannulae were excluded from analysis. Fig 1 displays approximate locations of dialysis probes for the rats included in data analysis.
Overall distance run was compared between Running Stress and Running Control rats using Student’s t-test. Average baseline (B1-B4) values of 5HT and DA in the DMS and DLS were compared by 2-way ANOVAs with exercise condition (Sedentary vs. Running) and acute stress treatment (Control vs. Stress) as factors. Samples containing outlier values were removed from analysis, as determined by Grubbs test. The remaining data are presented as a percentage of baseline mean, as completed by dividing a sampling period (B1-P4) by the mean of the 4 baseline samples (B1-B4) for each rat (as previously reported in [25, 31, 32]). Data were analyzed using a 3-way repeated measure ANOVA with exercise condition, stress treatment, and individual sampling periods (B1-P4) as factors. In addition, average concentrations of 5HT and DA over the entire sampling period following foot shock (FS-P4) were compared using a 2-way ANOVA with exercise condition and stress treatment as factors. One group t-tests were performed to determine if the mean percentage change in extracellular 5HT or DA concentrations following foot shock (FS-P4) differed from baseline. Post hoc analyses with Tukey-Kramer corrections were completed when appropriate. In all analyses, P < 0.05 was considered statistically significant.
Average distance traveled on wheels for the entire time course of this experiment was 3.33 km/day (± 0.24 SE). During the week of surgery (weeks 3 or 4), running distance fell to an average of 1.36 km/day (± 0.36 SE). However, daily running distance recovered during weeks 5 and 6 to 3.99 (± 0.64 SE) and 3.77 km/day (± 0.57 SE) respectively. No differences in running distance were observed between Control and Stress groups.
Baseline values of 5HT & DA
Table 1 shows the average basal (B1—B4) values of 5-HT and DA. No significant differences were found between groups for 5HT or DA concentrations in the DMS and DLS.
Dorsal medial striatum.
For individual sampling periods, a significant 3-way interaction between exercise condition, stress, and sample period was found [F(25, 213) = 2.14, P = 0.002] (Fig 2A and 2B). Within groups, post hoc analysis revealed Sedentary Stress rats had greater concentrations of 5HT during FS, P1, and P4 than all baseline (B1, B2, B3, or B4) sampling periods (all P<0.01). No other within group sampling points differed. Post hoc analysis also revealed no differences between groups during B1-B4 sampling periods. However, Sedentary Stress maintained greater concentrations of 5HT compared to Sedentary Control at FS (P = 0.03) and P1 (P = 0.005) sampling periods. Exercise prevented the sensitized 5HT efflux following foot shock in rats that received tail shock, as Running Stress maintained lower concentrations of 5-HT than Sedentary Stress rats during the FS sample period (P = 0.01).
A) Mean extracellular 5-HT levels expressed as a percentage of baseline samples in the dorsal medial striatum (DMS) of control rats during each 20 min sampling period. B) same as A but for rats exposed to uncontrollable stress (Stress). C) Combined mean post-shock (FS-P4) extracellular 5-HT levels expressed as a percentage of baseline samples (grey dashed line) in the DMS for each group. D) Mean extracellular 5-HT levels expressed as a percentage of baseline samples in the dorsal lateral striatum (DLS) of control rats during each 20 min sampling period. E) same as D but for rats exposed to uncontrollable stress (Stress). F) Combined mean post-shock (FS-P4) extracellular 5-HT levels expressed as a percentage of baseline samples (grey dashed line) in the DLS for each group. aP<0.01 different from B1, B2, B3, or B4 in Sedentary Stress; bP<0.05 Sedentary Stress from Sedentary Control at FS and P1 sampling periods; cP<0.05 Sedentary Stress from Running Stress at FS sampling period; dP<0.05 P3 from B1 or B4 in Sedentary Stress group; e P<0.05 Sedentary Stress from Sedentary Control, Running Control, and Running Stress; fP<0.05 from Running Control and Running Stress; gP<0.05 from baseline (grey dashed line)
Averaging across the post-foot shock sampling periods, a significant 2-way interaction was found between exercise and stress conditions [F(1,26) = 4.23, P<0.05] (Fig 2C). Post hoc analysis revealed that Sedentary Stress group had greater post-shock concentrations of 5-HT than Sedentary Control (P = 0.03), Running Control (P = 0.03), and Running Stress (P<0.05) groups. One group t-tests revealed that extracellular 5-HT concentrations tended to be greater during post-foot shock periods than baseline for Sedentary Stress [t(7) = 3.92, P = 0.006], Running Control [t(6) = 2.94, P = 0.03], and Running Stress [t(7) = 2.71, P = 0.03] groups, however a non-significant trend was also observed for Sedentary Control (P = 0.08) (Fig 2C).
Dorsal lateral striatum.
For individual sampling periods, a significant 3-way interaction between exercise condition, stress, and sample period was found (Fig 2E and 2F) [F(25, 192) = 2.00, P = 0.005]. Within groups, post hoc analysis revealed Sedentary Stress rats had greater concentrations of 5HT during FS than all baseline (B1, B2, B3, or B4) sampling periods (All P<0.002). Moreover, Sedentary Stress rats had greater concentrations of 5HT during P3 than B1 (P<0.05) and B4 (P = 0.03) sampling periods. No other within group sampling points differed significantly. Post hoc analysis revealed no differences between groups during B1-B4 sampling periods. However, exercise prevented the elevated 5-HT efflux following foot shock in rats that received tail shock, as Running Stress maintained lower concentrations of 5-HT than Sedentary Stress rats during the FS sample period (P<0.05).
Averaging across the post-foot shock sampling periods, significant main effects of exercise [F(1, 24) = 6.68, P = 0.02] and stress [F(1, 24) = 5.38, P = 0.03], but no significant interaction between exercise and stress (P = 0.1) was found (Fig 2F). Post hoc analysis revealed that Sedentary Stress group maintained greater post-shock concentrations of 5-HT than Running Control (P = 0.02), Running Stress (P<0.05), and a non-significant trend towards increased levels compared to Sedentary Control (P = 0.07) groups. One group t-tests revealed that extracellular 5-HT concentrations tended to be greater during post-foot shock periods than baseline in Sedentary Control [t(7) = 2.68, P = 0.04] and Sedentary Stress [t(7) = 2.64,P = 0.04] groups (Fig 2F).
Dorsal medial striatum.
For individual sampling periods, the 3-way interaction between exercise condition, stress, and sample period was marginally not significant (Fig 3A and 3B [F(25, 206) = 1.54, P = 0.06]. However, a main effect of sampling period was found [F(8, 214 = 7.53, P < 0.0001]. Moreover, a significant 2-way interaction was found between exercise condition and stress [F(1, 214) = 5.47, P = 0.02]. Post hoc analysis on this interaction revealed the Running Stress group maintained overall greater concentrations of DA than Running Control (P = 0.001), Sedentary Control (P = 0.004), and Sedentary Stress (P = 0.01). These group differences are primarily due to the varying degree of increased DA concentrations during the post-foot shock period.
A) Mean extracellular DA levels expressed as a percentage of baseline samples in the dorsal medial striatum (DMS) of control rats during each 20 min sampling period. B) same as A but for rats exposed to uncontrollable stress (Stress). C) Combined mean post-shock (FS-P4) extracellular DA levels expressed as a percentage of baseline samples (grey dashed line) in the DMS for each group. D) Mean extracellular DA levels expressed as a percentage of baseline samples in the dorsal lateral striatum (DLS) of control rats during each 20 min sampling period. E) same as D but for rats exposed to uncontrollable stress (Stress). F) Combined mean post-shock (FS-P4) extracellular DA levels expressed as a percentage of baseline samples (grey dashed line) in the DLS for each group. aP<0.05 at P1 from P4 within Running Control; bP<0.05 FS from B2 or B3 within Running Stress; cP<0.05 P1 from B3 within Running Stress; DP<0.05 P2 from B1, B2, or B3 within Running Stress; eP<0.05 at Running Stress from Sedentary Stress for respective sampling period; fP<0.01 from Sedentary Control, Sedentary Stress, Running Control; gP<0.001 main effect of exercise condition; hP<0.01 from baseline (grey dashed line)
Averaging across the entire post-foot shock sampling periods, a significant 2-way interaction was found between exercise and stress conditions [F(1,26) = 5.46, P = 0.03] (Fig 3C). Post hoc analysis revealed that Running Stress group maintained greater post-shock concentrations of DA than Sedentary Control (P = 0.009), Sedentary Stress (P = 0.03), and Running Control (P = 0.005) groups. One group t-tests revealed that extracellular DA concentrations tended to be greater during post-foot shock periods than baseline in Sedentary Stress [t(7) = 7.06, P = 0.0002] and Running Stress [t(7) = 4.78,P = 0.002] groups (Fig 3C).
Dorsal lateral striatum.
For individual sampling periods, a significant 3-way interaction between exercise condition, stress, and sample number was found [F(25, 195 = 1.62, P = 0.04) (Fig 3D and 3E). Within groups, Running Stress rats had greater DA concentrations at FS compared to B2 (P = 0.03) and B3 (P = 0.01). Moreover, Running Stress rats had greater DA concentrations at P1 than B3 (P = 0.02). Finally, DA concentrations were higher for Running Stress rats at P2 than at B1 (P = 0.03), B2 (P = 0.02), and B3 (P = 0.005). Running Control group had greater DA concentrations at P1 than B4 (P = 0.02). Post hoc analysis revealed no differences between groups during B1-B4 sampling periods. However, exercise potentiated dopamine efflux following foot shocks in rats that received tail shock, as Running Stress maintained greater concentrations of DA than Sedentary Stress during FS (P = 0.04), P2 (P = 0.05), P3 (P = 0.02), and P4 (P = 0.006) sampling periods.
Averaging across the entire post-foot shock sampling periods, a significant main effect of exercise was observed [F(1, 24) = 15.73, P = 0.0006] (see Fig 3F). No significant main effect of stress or interaction between exercise condition and stress treatment was observed. One group t-tests revealed that extracellular DA concentrations tended to be greater during post-foot shock periods than baseline in Running Control [t(5) = 6.25, P = 0.0015] and Running Stress [t(7) = 3.54,P = 0.009] groups (Fig 3F).
Results of this study support the conclusion that 6 weeks of wheel running both prevents acute stress induced sensitization of extracellular 5-HT and potentiates extracellular DA in the dorsal striatum following subsequent exposure to foot shocks. Previous work has demonstrated the development of impaired escape behavior 24 h following tail shocks is dependent upon excessive 5-HT activity in the dorsal striatum [30, 49]. Consistent with previous reports, exposure to acute stress potently increased extracellular 5-HT levels in the dorsal striatum of escape deficit vulnerable sedentary rats following exposure to foot shocks [10, 25, 48]. Interestingly, the stress-sensitized 5-HT response was eliminated in wheel running rats, which are also protected from developing escape deficits [10, 23, 48]. Thus, the capacity of wheel running to prevent the sensitized 5-HT response elicited by two foot shocks 24 h following acute stress may provide key insight into the mechanism by which exercise protects against the development of depression-like shuttle box escape deficits.
The exact mechanism by which wheel running prevents acute stress-sensitized 5-HT response following subsequent comparatively mild stress exposure is unknown, but may involve constraining the activation of 5-HT neurons located in the DRN, thereby suppressing the release of 5-HT to projection sites like the dorsal striatum. In support of this hypothesis, our lab has identified a number of targets for plasticity in DRN of wheel running rats that may have influence on the activity of 5-HT neurons, including changes to the expression of 5-HT transporters, 5-HT1BR, and 5-HT1AR . A potential functional increase of the inhibitory 5-HT1A autoreceptors in the DRN following wheel running is a particularly attractive candidate, since previous work has identified these receptors as a source contributing to the stress-evoked 5-HT response [29, 30, 49]. Moreover, the parallel by which 6 weeks (but not 3 weeks) of wheel access is required to both an increase of 5-HT1AR expression in the DRN, and protection against escape deficits that are dependent upon a stress-sensitized 5HT response [19, 48] further suggests increased 5-HT1AR from running may contribute to preventing acute stress-evoked 5-HT response [7, 8]. Consistent with this idea, our lab has found 6 weeks of running attenuates acute stress-induced expression of neural activity marker c-Fos in 5-HT neurons in areas of the DRN known to project to the dorsal striatum [10, 48]. However, whether or not functional increases of 5-HT1A autoreceptors contribute to constrained activation of 5-HT neurons in the DRN and subsequent prevention of stress-sensitized 5-HT activity in projection sites, including the dorsal striatum, should be topics for future investigation.
If the mechanism by which wheel running prevents sensitized 5-HT activity in the dorsal striatum is through decreasing the activity of 5-HT neurons across the DRN, it could have broader implications for several behavioral correlates of depression and anxiety related to or dependent upon excessive DRN 5-HT activity including exaggerated fear, reduced social interaction, decreased sucrose preference, and enhanced drug seeking [24, 30, 50, 51]. For instance, the expression of exaggerated fear and reduced social exploration, following exposure to tail shocks, are related to an elevation of extracellular 5-HT in the basolateral amygdala (BLA) and can be prevented by intra-BLA blockade of 5-HT2CR or intra-DRN agonism of 5-HT1A autoreceptors [31, 51]. These data indicate acute stress-sensitized activation of 5-HT neurons in the DRN; and excessive 5-HT release in the BLA, a DRN projection site, is responsible for the development of anxiety-like behavior in rats. Therefore, constrained activity of 5-HT neurons in the DRN following wheel running could broadly buffer other stress-evoked depression and anxiety-like behaviors. Whether or not wheel running prevents stress-sensitized extracellular 5-HT concentrations in other DRN projection sites should be topics for further investigation, as it could provide further insight into neural mechanisms of exercise-induced stress robustness.
While the role of acute stress-stimulated 5-HT activity in the development of shuttle box escape deficits is well established, comparatively few studies have explored how excessive 5-HT release may interact with the signaling of other neurotransmitter systems to promote the development of depression-like behavior. Neuroanatomical evidence supports dorsal raphe 5-HT modulation of DA signaling in the dorsal striatum. Indeed, neurons from the DRN are the primary source of 5-HT in the nigrostriatal pathway, which includes DA projections from the substantia nigra to dorsal striatum . DA signaling in the dorsal striatum is critical for the acquisition of goal-directed instrumental processes (as reviewed in ), thus altered DA function, as a result of stress-sensitized 5-HT activity, could contribute to shuttle box escape deficits. While some disagreement exists in literature, this hypothesis is generally supported by several lines of evidence indicating augmented DRN 5-HT activity can oppose nigrostriatal DAergic function [36, 37]. Indeed, electrical stimulation of 5-HT neurons in DRN has been reported to inhibit the majority of DA neurons in the substantia nigra  and decrease extracellular DA content in the dorsal striatum . In fact, electrical stimulation of dorsal raphe 5-HT neurons at the highest frequency examined (20Hz) decreased extracellular DA levels in the dorsal striatum while lower frequencies (3-10Hz) had no effect , suggesting excessive increases in 5-HT levels may be particularly effective at interfering with dorsal striatum DA transmission. Interestingly, evidence suggests activation of 5-HT2CR in the dorsal striatum, which are involved in the development of escape deficits following tail shock , may also suppress DA release in the nigrostriatal pathway , although the circuitry involved is not well established. Therefore, the observed 2–2.5 fold increase of dorsal striatum extracellular 5-HT levels could contribute to a dampening of the DA response in acute stressed sedentary rats following foot shock. Conversely, wheel running prevented stress-sensitized 5-HT activity, which may have eliminated a source of constraint over nigrostriatal DA activity allowing for elevated DA levels following exposure to foot shocks. While it is difficult to conclude that the control of DA transmission following foot shock and during the shuttle box paradigm are similar, given the central role of DA signaling in striatum-involved motor and instrumental learning, the capacity of DA levels to become elevated following subsequent stress exposure may be critical for unhindered escape behavior following stress.
Stress-sensitized 5-HT and -dampened DA levels in sedentary rats, as well as the prevention of these responses by running, were similar in both striatum sub-regions, making it difficult to identify if region specific changes to 5-HT or DA signaling that may underlie the stress-induced development of instrumental learning deficits. However, instrumental learning is now thought to be mediated by two functionally and anatomically distinct modalities, which include goal-directed and habit processes that are under the control of neural substrates comprising the DMS and DLS respectively [38–46]. A growing body of evidence suggests stress exposure mediates instrumental action in a manner that favors the use of well-rehearsed habits over goal-directed strategies (for review see ). Consistent with these observations, stress-induced shuttle box escape deficits occur rapidly in rats that have no prior experience with the task (i.e. not rehearsed), suggesting impaired escape behavior may be related to altered signaling in neural circuits responsible for processing goal directed action. Therefore, the possibility remains that stress-sensitized 5-HT or -restricted DA response could be acting in a dorsal striatum region-specific manner to impair shuttle box escape, despite a similar response observed in both the DMS and DLS. Future studies could be aimed at identifying potential dorsal striatum region specific contributions of stress-evoked 5-HT or attenuated DA response to the development of impaired escape behavior.
In conclusion, the current data indicate that 6 weeks of access to running wheels prevents acute stress-induced sensitization of extracellular 5-HT, but potentiates DA concentrations in the dorsal striatum following subsequent mild stress exposure. The ability of physical activity to constrain excessive 5-HT activity from the DRN following stress exposure may allow for the capacity of DA to become elevated in the dorsal striatum. These data may provide key insight into the mechanism by which wheel running protects against shuttle box escape deficits, and may have broader implications for impaired goal-directed processes associated with stress-related disorders like depression.
Conceived and designed the experiments: PJC JA BNG SFM MF. Performed the experiments: PJC JA SOM PRG. Analyzed the data: PJC JA SOM PRG. Contributed reagents/materials/analysis tools: JA SFM. Wrote the paper: PJC MF.
- 1. Heninger GR, Delgado PL, Charney DS. The revised monoamine theory of depression: a modulatory role for monoamines, based on new findings from monoamine depletion experiments in humans. Pharmacopsychiatry. 1996;29(1):2–11. pmid:8852528.
- 2. Lacasse JR, Leo J. Serotonin and depression: a disconnect between the advertisements and the scientific literature. PLoS medicine. 2005;2(12):e392. pmid:16268734; PubMed Central PMCID: PMC1277931.
- 3. Nutt DJ. The role of dopamine and norepinephrine in depression and antidepressant treatment. The Journal of clinical psychiatry. 2006;67 Suppl 6:3–8. pmid:16848670.
- 4. Nutt DJ. Overview of diagnosis and drug treatments of anxiety disorders. CNS spectrums. 2005;10(1):49–56. pmid:15618947.
- 5. van Praag H, Fleshner M, Schwartz MW, Mattson MP. Exercise, energy intake, glucose homeostasis, and the brain. The Journal of neuroscience: the official journal of the Society for Neuroscience. 2014;34(46):15139–49. pmid:25392482; PubMed Central PMCID: PMC4228123.
- 6. Dishman RK, Berthoud HR, Booth FW, Cotman CW, Edgerton VR, Fleshner MR, et al. Neurobiology of exercise. Obesity. 2006;14(3):345–56. pmid:16648603.
- 7. Greenwood BN, Fleshner M. Exercise, learned helplessness, and the stress-resistant brain. Neuromolecular medicine. 2008;10(2):81–98. pmid:18300002.
- 8. Greenwood BN, Fleshner M. Exercise, stress resistance, and central serotonergic systems. Exercise and sport sciences reviews. 2011;39(3):140–9. pmid:21508844.
- 9. Dishman RK, Bunnell BN, Youngstedt SD, Yoo HS, Mougey EH, Meyerhoff JL. Activity wheel running blunts increased plasma adrenocorticotrophin (ACTH) after footshock and cage-switch stress. Physiology & behavior. 1998;63(5):911–7.
- 10. Greenwood BN, Foley TE, Day HE, Campisi J, Hammack SH, Campeau S, et al. Freewheel running prevents learned helplessness/behavioral depression: role of dorsal raphe serotonergic neurons. The Journal of neuroscience: the official journal of the Society for Neuroscience. 2003;23(7):2889–98. pmid:12684476.
- 11. Sinyor D, Schwartz SG, Peronnet F, Brisson G, Seraganian P. Aerobic fitness level and reactivity to psychosocial stress: physiological, biochemical, and subjective measures. Psychosomatic medicine. 1983;45(3):205–17. pmid:6611800.
- 12. Rimmele U, Zellweger BC, Marti B, Seiler R, Mohiyeddini C, Ehlert U, et al. Trained men show lower cortisol, heart rate and psychological responses to psychosocial stress compared with untrained men. Psychoneuroendocrinology. 2007;32(6):627–35. pmid:17560731.
- 13. Crews DJ, Landers DM. A meta-analytic review of aerobic fitness and reactivity to psychosocial stressors. Medicine and science in sports and exercise. 1987;19(5 Suppl):S114–20. pmid:3316910.
- 14. Chaouloff F. Physical exercise and brain monoamines: a review. Acta physiologica Scandinavica. 1989;137(1):1–13. pmid:2678895.
- 15. Blomstrand E, Perrett D, Parry-Billings M, Newsholme EA. Effect of sustained exercise on plasma amino acid concentrations and on 5-hydroxytryptamine metabolism in six different brain regions in the rat. Acta physiologica Scandinavica. 1989;136(3):473–81. pmid:2473602.
- 16. Goekint M, Bos I, Heyman E, Meeusen R, Michotte Y, Sarre S. Acute running stimulates hippocampal dopaminergic neurotransmission in rats, but has no influence on brain-derived neurotrophic factor. Journal of applied physiology. 2012;112(4):535–41. pmid:22134693; PubMed Central PMCID: PMC3289437.
- 17. Chaouloff F, Laude D, Merino D, Serrurrier B, Guezennec Y, Elghozi JL. Amphetamine and alpha-methyl-p-tyrosine affect the exercise-induced imbalance between the availability of tryptophan and synthesis of serotonin in the brain of the rat. Neuropharmacology. 1987;26(8):1099–106. pmid:2443870.
- 18. Davis JM, Alderson NL, Welsh RS. Serotonin and central nervous system fatigue: nutritional considerations. The American journal of clinical nutrition. 2000;72(2 Suppl):573S–8S. pmid:10919962.
- 19. Greenwood BN, Foley TE, Day HE, Burhans D, Brooks L, Campeau S, et al. Wheel running alters serotonin (5-HT) transporter, 5-HT1A, 5-HT1B, and alpha 1b-adrenergic receptor mRNA in the rat raphe nuclei. Biological psychiatry. 2005;57(5):559–68. pmid:15737672.
- 20. Greenwood BN, Foley TE, Le TV, Strong PV, Loughridge AB, Day HE, et al. Long-term voluntary wheel running is rewarding and produces plasticity in the mesolimbic reward pathway. Behavioural brain research. 2011;217(2):354–62. pmid:21070820; PubMed Central PMCID: PMC3021978.
- 21. Greenwood BN, Strong PV, Loughridge AB, Day HE, Clark PJ, Mika A, et al. 5-HT2C receptors in the basolateral amygdala and dorsal striatum are a novel target for the anxiolytic and antidepressant effects of exercise. PloS one. 2012;7(9):e46118. pmid:23049953; PubMed Central PMCID: PMC3458100.
- 22. Foley TE, Fleshner M. Neuroplasticity of dopamine circuits after exercise: implications for central fatigue. Neuromolecular medicine. 2008;10(2):67–80. pmid:18274707.
- 23. Greenwood BN, Loughridge AB, Sadaoui N, Christianson JP, Fleshner M. The protective effects of voluntary exercise against the behavioral consequences of uncontrollable stress persist despite an increase in anxiety following forced cessation of exercise. Behavioural brain research. 2012;233(2):314–21. pmid:22610051; PubMed Central PMCID: PMC3402647.
- 24. Rozeske RR, Greenwood BN, Fleshner M, Watkins LR, Maier SF. Voluntary wheel running produces resistance to inescapable stress-induced potentiation of morphine conditioned place preference. Behavioural brain research. 2011;219(2):378–81. pmid:21262267; PubMed Central PMCID: PMC3062637.
- 25. Strong PV, Christianson JP, Loughridge AB, Amat J, Maier SF, Fleshner M, et al. 5-hydroxytryptamine 2C receptors in the dorsal striatum mediate stress-induced interference with negatively reinforced instrumental escape behavior. Neuroscience. 2011;197:132–44. pmid:21958863; PubMed Central PMCID: PMC3235414.
- 26. Schwabe L, Wolf OT. Stress-induced modulation of instrumental behavior: from goal-directed to habitual control of action. Behavioural brain research. 2011;219(2):321–8. pmid:21219935.
- 27. Grahn RE, Will MJ, Hammack SE, Maswood S, McQueen MB, Watkins LR, et al. Activation of serotonin-immunoreactive cells in the dorsal raphe nucleus in rats exposed to an uncontrollable stressor. Brain research. 1999;826(1):35–43. pmid:10216194.
- 28. Maswood S, Barter JE, Watkins LR, Maier SF. Exposure to inescapable but not escapable shock increases extracellular levels of 5-HT in the dorsal raphe nucleus of the rat. Brain research. 1998;783(1):115–20. pmid:9479059.
- 29. Rozeske RR, Evans AK, Frank MG, Watkins LR, Lowry CA, Maier SF. Uncontrollable, but not controllable, stress desensitizes 5-HT1A receptors in the dorsal raphe nucleus. The Journal of neuroscience: the official journal of the Society for Neuroscience. 2011;31(40):14107–15. pmid:21976495; PubMed Central PMCID: PMC3207271.
- 30. Maier SF, Grahn RE, Watkins LR. 8-OH-DPAT microinjected in the region of the dorsal raphe nucleus blocks and reverses the enhancement of fear conditioning and interference with escape produced by exposure to inescapable shock. Behavioral neuroscience. 1995;109(3):404–12. pmid:7662151.
- 31. Amat J, Matus-Amat P, Watkins LR, Maier SF. Escapable and inescapable stress differentially alter extracellular levels of 5-HT in the basolateral amygdala of the rat. Brain research. 1998;812(1–2):113–20. pmid:9813270.
- 32. Amat J, Matus-Amat P, Watkins LR, Maier SF. Escapable and inescapable stress differentially and selectively alter extracellular levels of 5-HT in the ventral hippocampus and dorsal periaqueductal gray of the rat. Brain research. 1998;797(1):12–22. pmid:9630480.
- 33. Gervais J, Rouillard C. Dorsal raphe stimulation differentially modulates dopaminergic neurons in the ventral tegmental area and substantia nigra. Synapse. 2000;35(4):281–91. pmid:10657038.
- 34. De Deurwaerdere P, Stinus L, Spampinato U. Opposite change of in vivo dopamine release in the rat nucleus accumbens and striatum that follows electrical stimulation of dorsal raphe nucleus: role of 5-HT3 receptors. The Journal of neuroscience: the official journal of the Society for Neuroscience. 1998;18(16):6528–38. pmid:9698340.
- 35. Olvera-Cortes ME, Anguiano-Rodriguez P, Lopez-Vazquez MA, Alfaro JM. Serotonin/dopamine interaction in learning. Progress in brain research. 2008;172:567–602. pmid:18772051.
- 36. Di Giovanni G, Di Matteo V, Pierucci M, Esposito E. Serotonin-dopamine interaction: electrophysiological evidence. Progress in brain research. 2008;172:45–71.
- 37. Di Giovanni G, Esposito E, Di Matteo V. Role of serotonin in central dopamine dysfunction. CNS neuroscience & therapeutics. 2010;16(3):179–94. pmid:20557570.
- 38. Balleine BW, Liljeholm M, Ostlund SB. The integrative function of the basal ganglia in instrumental conditioning. Behavioural brain research. 2009;199(1):43–52. pmid:19027797.
- 39. Maroteaux M, Valjent E, Longueville S, Topilko P, Girault JA, Herve D. Role of the plasticity-associated transcription factor zif268 in the early phase of instrumental learning. PloS one. 2014;9(1):e81868. pmid:24465372; PubMed Central PMCID: PMC3900405.
- 40. Shiflett MW, Brown RA, Balleine BW. Acquisition and performance of goal-directed instrumental actions depends on ERK signaling in distinct regions of dorsal striatum in rats. The Journal of neuroscience: the official journal of the Society for Neuroscience. 2010;30(8):2951–9. pmid:20181592; PubMed Central PMCID: PMC2844638.
- 41. Lex B, Hauber W. The role of dopamine in the prelimbic cortex and the dorsomedial striatum in instrumental conditioning. Cerebral cortex. 2010;20(4):873–83. pmid:19605519.
- 42. Yin HH, Knowlton BJ, Balleine BW. Lesions of dorsolateral striatum preserve outcome expectancy but disrupt habit formation in instrumental learning. Eur J Neurosci. 2004;19(1):181–9. WOS:000188462400019. pmid:14750976
- 43. Faure A, Haberland U, Conde F, El Massioui N. Lesion to the nigrostriatal dopamine system disrupts stimulus-response habit formation. The Journal of neuroscience: the official journal of the Society for Neuroscience. 2005;25(11):2771–80. pmid:15772337.
- 44. Wickens JR, Horvitz JC, Costa RM, Killcross S. Dopaminergic mechanisms in actions and habits. The Journal of neuroscience: the official journal of the Society for Neuroscience. 2007;27(31):8181–3. pmid:17670964.
- 45. Yin HH, Ostlund SB, Knowlton BJ, Balleine BW. The role of the dorsomedial striatum in instrumental conditioning. Eur J Neurosci. 2005;22(2):513–23. pmid:16045504.
- 46. Yin HH, Knowlton BJ, Balleine BW. Lesions of dorsolateral striatum preserve outcome expectancy but disrupt habit formation in instrumental learning. Eur J Neurosci. 2004;19(1):181–9. pmid:14750976.
- 47. Dias-Ferreira E, Sousa JC, Melo I, Morgado P, Mesquita AR, Cerqueira JJ, et al. Chronic stress causes frontostriatal reorganization and affects decision-making. Science. 2009;325(5940):621–5. pmid:19644122.
- 48. Greenwood BN, Foley TE, Burhans D, Maier SF, Fleshner M. The consequences of uncontrollable stress are sensitive to duration of prior wheel running. Brain research. 2005;1033(2):164–78. pmid:15694921.
- 49. Maier SF, Watkins LR. Stressor controllability and learned helplessness: the roles of the dorsal raphe nucleus, serotonin, and corticotropin-releasing factor. Neuroscience and biobehavioral reviews. 2005;29(4–5):829–41. pmid:15893820.
- 50. Christianson JP, Paul ED, Irani M, Thompson BM, Kubala KH, Yirmiya R, et al. The role of prior stressor controllability and the dorsal raphe nucleus in sucrose preference and social exploration. Behavioural brain research. 2008;193(1):87–93. pmid:18554730; PubMed Central PMCID: PMC2583404.
- 51. Christianson JP, Ragole T, Amat J, Greenwood BN, Strong PV, Paul ED, et al. 5-hydroxytryptamine 2C receptors in the basolateral amygdala are involved in the expression of anxiety after uncontrollable traumatic stress. Biological psychiatry. 2010;67(4):339–45. pmid:19914601; PubMed Central PMCID: PMC3278236.
- 52. Azmitia EC, Segal M. An autoradiographic analysis of the differential ascending projections of the dorsal and median raphe nuclei in the rat. The Journal of comparative neurology. 1978;179(3):641–67. pmid:565370.
- 53. Alex KD, Yavanian GJ, McFarlane HG, Pluto CP, Pehek EA. Modulation of dopamine release by striatal 5-HT2C receptors. Synapse. 2005;55(4):242–51. pmid:15668911.