bioRxiv Science⌕ Search

Biology subjects

Touretsky, K.

Publications and source records attributed to Touretsky, K..

2 recordsLinked to original sources

Androgen depletion increases sensitivity to effort-related costs and alters mesoaccumbal circuit function in male mice

BackgroundAndrogen deficiency in males is associated with reduced motivation, fatigue, and decreased goal-directed behavior, yet the neural mechanisms underlying these changes remain poorly understood. Dopamine signaling within the nucleus accumbens (NAc) plays a central role in regulating effort-based decision making. Here, we tested the hypothesis that loss of testicular hormones alters mesoaccumbal dopamine function to increase sensitivity to effort-related costs. MethodsMale mice underwent orchiectomy (ORX) either before puberty onset or in adulthood. Effort-based decision making was assessed using a progressive ratio 1 closed economy (PR1-CE) task. Dopamine-related function was assessed using systemic haloperidol administration and high-performance liquid chromatography to measure dopamine and metabolites, while whole-cell recordings were used to assess intrinsic excitability of NAc spiny projection neurons (SPNs). ResultsORX increased sensitivity to effort costs, reflected by a shift toward energy-efficient responding while maintaining overall food intake. These behavioral changes were accompanied by reduced responsiveness to haloperidol. Postpubertal ORX increased dopamine content and reduced metabolite-to-dopamine ratios in the NAc, consistent with reduced dopamine turnover, whereas prepubertal ORX did not affect dopamine measures. Prepubertal ORX selectively reduced excitability of NAc core D1R+ SPNs, while postpubertal ORX increased excitability across both D1R+ and D1R- populations. ConclusionsAndrogen depletion increases effort cost sensitivity and is associated with alterations in mesoaccumbal circuit function. Although behavioral effects were similar following pre- or postpubertal ORX, distinct neurochemical and cellular adaptations were observed, suggesting developmental timing influences neural adaptations to androgen depletion. These findings provide insight into neural mechanisms linking androgen deficiency to motivational deficits.

neuroscience↗

Cell Type-Specific Changes in Dendritic Spines Across Adolescence Within Mouse Medial Prefrontal Cortex

Across species, cognitive capacities that rely on the frontal cortex do not fully mature until adulthood. Adolescent circuit refinement, including structural remodeling of dendritic spines, is believed to underlie this protracted maturation. Understanding cell type-dependent patterns of structural maturation would provide important insight into frontal cortex development. Here, we leveraged retrograde adeno-associated viruses to quantify dendritic spines on pyramidal tract (PT) vs. intratelencephalic (IT) neuronal populations in parallel within the mouse medial prefrontal cortex (mPFC) across adolescence. IT-type neurons showed opposing changes in mushroom and thin spines that were: 1) consistent with increasing synaptic maturity and 2) largely absent in PT-type neurons. We next probed the function of brain-resident immune cells, microglia, by transiently ablating them within the mPFC at mid-adolescence. This led to cell type-dependent changes in dendritic spines in late adolescence, with thin spine proportion increasing on both cell types but total spine density increasing on IT-type neurons only. Meanwhile, there was no effect on performance in an mPFC-dependent task of cognitive flexibility at either late adolescent or adult time points following microglia ablation. These findings provide evidence that mPFC IT-type neurons undergo greater spine remodeling during adolescence compared to PT-type neurons and implicate microglia as potential mediators.

neuroscience↗