Corticosterone Impairs Hippocampal Neurogenesis and Behaviors through -Mediated ROS Accumulation.

Stress is known to induce a reduction in adult hippocampal neurogenesis (AHN) and anxiety-like behaviors. Glucocorticoids (GCs) are secreted in response to stress, and the hippocampus possesses the greatest levels of GC receptors, highlighting the potential of GCs in mediating stress-induced hippocampal alterations and behavior deficits. Herein, RNA-sequencing (RNA-seq) analysis of the hippocampus following corticosterone (CORT) exposure revealed the central regulatory role of the gene, which exhibited interactions with oxidative stress-related differentially expressed genes (DEGs), suggesting a potential link between and oxidative stress-related pathways. Remarkably, -overexpression in the hippocampal dentate gyrus partially recapitulated CORT-induced phenotypes, including reactive oxygen species (ROS) accumulation, diminished AHN, dendritic atrophy, and the onset of anxiety-like behaviors. Significantly, inhibiting ROS exhibited a partial rescue of anxiety-like behaviors and hippocampal alterations induced by -overexpression, as well as those induced by CORT, underscoring the therapeutic potential of targeting ROS or in the hippocampus as a promising avenue for mitigating anxiety disorders provoked by chronic stress.