Inhaled black carbon induces depressive-like behavior and enhances stress-related blood–brain molecular vulnerability in mice

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Abstract

Black carbon (BC), a combustion-derived component of fine particulate matter, has been linked to depressive symptoms, but controlled experimental evidence remains limited. We established a controlled BC inhalation model combined with chronic restraint stress (CRS) to determine whether inhaled BC alone induces depressive-like behavior and whether concurrent stress enhances behavioral and molecular vulnerability. Male C57BL/6J mice were assigned to Control, CRS, BC, or BC+CRS groups and exposed for 21 consecutive days, followed by behavioral testing and molecular analyses of plasma-depleted whole blood and stress-related brain regions. BC exposure alone induced depressive-like behavior, and the combined BC+CRS condition showed the most pronounced phenotype. These findings indicate that inhaled BC is sufficient to influence stress-relevant behavior and may heighten vulnerability under chronic stress. At the molecular level, BC shifted peripheral responses toward a stress- and inflammation-associated state with reduced plasticity-related signaling, whereas CRS preferentially engaged glucocorticoid-responsive regulation. Combined BC+CRS exposure further altered plasticity- and transcription-related regulatory programs in blood and stress-related brain regions, with prominent changes in the nucleus accumbens. These condition-dependent molecular patterns suggest that BC engages blood–brain stress-related pathways in a context- and region-specific manner. Together, these findings identify inhaled BC as a neurobehaviorally relevant environmental hazard.

Abstract Figure

Graphical summary.

Effects of black carbon exposure and chronic restraint stress on depressive-like behavior and blood–brain molecular responses.

Inhaled black carbon (BC) exposure induced depressive-like behavioral alterations and reshaped molecular profiles in plasma-depleted whole blood and stress-related brain regions. Molecular changes were classified as BC-associated, CRS-associated, shared BC/CRS-associated, or most evident in the BC+CRS condition. mPFC, medial prefrontal cortex; NAc, nucleus accumbens.

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