Abstract

Reduced capacity to experience pleasure, also known as anhedonia, is a key feature of the depressive state and is associated with poor disease prognosis and treatment outcome. Various behavioral readouts (e.g., reduced sucrose intake) have been employed in animal models of depression as a measure of anhedonia. However, several aspects of anhedonia are poorly represented within the repertoire of current preclinical assessments. We recently adopted the social defeat-induced persistent stress (SDPS) paradigm that models a maintained depressive-like state in the rat, including social withdrawal and deficits in short-term spatial memory. Here we investigated whether SDPS elicited persistent deficits in natural reward evaluation, as part of anhedonia. We examined cue-paired operant sucrose self-administration, enabling us to study acquisition, motivation, extinction, and relapse to sucrose seeking following SDPS. Furthermore, we addressed whether guanfacine, an α2-adrenergic agonist that reduces stress-triggered maladaptive behavioral responses to drugs of abuse, could relief from SDPS-induced anhedonia. SDPS, consisting of five social defeat episodes followed by prolonged (≥8 weeks) social isolation, did not affect sucrose consumption during acquisition of self-administration. However, it strongly enhanced the motivational drive to acquire a sucrose reward in progressive ratio training. Moreover, SDPS induced initial resilience to extinction and rendered animals more sensitive to cue-induced reinstatement of sucrose-seeking. Guanfacine treatment attenuated SDPS-induced motivational overdrive and limited reinstatement of sucrose seeking, normalizing behavior to control levels. Together, our data indicate that long after the termination of stress exposure, SDPS induces guanfacine-reversible deficits in evaluation of a natural reward. Importantly, the SDPS-triggered anhedonia reflects many aspects of the human phenotype, including impaired motivation and goal-directed conduct.

Highlights

  • One of the most prominent characteristics of depressive disorders is a diminished ability to experience pleasure, a mental state traditionally termed as anhedonia

  • Cognitive performance was impaired in the social defeat-induced persistent stress (SDPS) group, as assessed using the object place recognition (OPR) test (Figure 1C)

  • The depressive state is characterized by multifaceted behavioral manifestations that span from negative mood and suicidality to indecisiveness, cognitive confusion, and blunted emotional reactivity (Leistedt and Linkowski, 2013)

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Summary

Introduction

One of the most prominent characteristics of depressive disorders is a diminished ability to experience pleasure, a mental state traditionally termed as anhedonia. Anhedonia falls in the category of pathologies of the affective domain, and might be largely explained by effects of dysfunctional processing of reinforcing information on mood and cognition. Depressed individuals suffer cognitive deficits predominantly related to the affective domain (Eshel and Roiser, 2010). As a result, depressed patients show defective decision-making and inappropriate behavioral adjustments in face of emotionally charged events (Cella et al, 2010). These deficits are linked to dysfunctional brain circuitry responsible for decision-making, attribution of incentive salience, behavioral reinforcement and expression of motivated behavior (e.g., via the prefrontal cortex and striatum) (Russo and Nestler, 2013)

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