Abstract

Our ability to develop the cognitive strategies required to deal with daily-life stress is regulated by region-specific neuronal networks. Experimental evidence suggests that prolonged stress in mice induces depressive-like behaviors via morphological, functional and molecular changes affecting the mesolimbic and mesocortical dopaminergic pathways. Yet, the molecular interactions underlying these changes are still poorly understood, and whether they affect males and females similarly is unknown. Here, we used chronic social defeat stress (CSDS) to induce depressive-like behaviors in male and female mice. Density of the mesolimbic and mesocortical projections was assessed via immuno-histochemistry combined with Sholl analysis along with the staining of activity-dependent markers pERK and c-fos in the ventral tegmental area (VTA), nucleus accumbens (NAc) and medial prefrontal cortex (mPFC). Our results show that social stress decreases the density of TH+ dopaminergic axonal projections in the deep layers of the mPFC in susceptible but not resilient male and female mice. Consistently, our analyses suggest that pERK expression is decreased in the mPFC but increased in the NAc following CSDS in males and females, with no change in c-fos expression in both sexes. Overall, our findings indicate that social defeat stress impacts the mesolimbic and mesocortical pathways by altering the molecular interactions regulating somatic and axonal plasticity in males and females.

Highlights

  • Our ability to develop the cognitive strategies required to deal with daily-life stress is regulated by region-specific neuronal networks

  • We compared the impact of chronic social defeat stress (CSDS) on the morphological and molecular properties of the mesolimbic and mesocortical dopaminergic pathways in male and female mice (Fig. 1A)

  • We first combined IHC staining with 2D Sholl ­analysis[35] to quantify variations in the axonal arborization of ventral tegmental area (VTA) DA neurons projecting to the different layers of the medial prefrontal cortex in males and females after CSDS

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Summary

Introduction

Our ability to develop the cognitive strategies required to deal with daily-life stress is regulated by region-specific neuronal networks. DA neurons from the VTA project to several parts of the brain to modulate a wide spectrum of emotionally-relevant behavioral processes such as reward, salience, fear, aversion and ­memory[25,26,27]: many of which have been shown to be impaired in MDD patients and mouse models of chronic s­ tress[28,29,30] Amongst these different DA circuits, the mesolimbic and mesocortical pathways have been consistently associated with the expression of stress responses in m­ ice[31,32,33]. A study revealed opposite dopamine metabolism responses between mesocortical and mesolimbic pathways in mice undergoing the forced swim t­est[33] While these results support the distinct contribution of both pathways in mediating the impact of social stress, their contribution in males and females remains unclear

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