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Despite extensive research on the impact of emotional stressors on brain function using immediate-early genes (e.g., c- fos ), there are still important questions that remain unanswered such as the reason for the progressive decline of c- fos  expression in response to prolonged stress and the neuronal populations activated by different stressors. This study tackles these 2 questions by evaluating c- fos  expression in response to 2 different emotional stressors applied sequentially, and performing a fluorescent double labeling of c-Fos protein and c- fos  mRNA on stress-related brain areas. Results were complemented with the assessment of the hypothalamic–pituitary–adrenal axis activation. We showed that the progressive decline of c- fos  expression could be related to 2 differing mechanisms involving either transcriptional repression or changes in stimulatory inputs. Moreover, the neuronal populations that respond to the different stressors appear to be predominantly separated in high-level processing areas (e.g., medial prefrontal cortex). However, in low-hierarchy areas (e.g., paraventricular nucleus of the hypothalamus) neuronal populations appear to respond unspecifically. The data suggest that the distinct physiological and behavioral consequences of emotional stressors, and their implication in the development of psychopathologies, are likely to be closely associated with neuronal populations specifically activated by each stressor.

Neuronal Activation After Prolonged Immobilization: Do the Same or Different Neurons Respond to a Novel Stressor?