Using a triple neural tagging technique, the team applied visual markers to engram neurons active during the training, neurons activated in response to the shock-paired tone, and those activated when the second tone was presented alone. They found that a 3 mL/mg dose of corticosterone activated increased neurons during the threat discrimination task, thus increasing the size of the engram. The bigger the engram, the more salient the fear memory, making the mouse more likely to fear a non-threatening stimulus. These findings are consistent with how humans react to traumatic stimuli that trigger a high release of cortisol.

Upon further investigation, investigators were able to determine the mechanism through which corticosterone induces fear generalization. When corticosterone was injected directly into the amygdala of mice, Lesius observed a decrease in activity of inhibitory neurons during the threat conditioning experiment. Reduced inhibition of neurons not associated with a specific engram memory seems to be what leads to fear generalization.

Will what was found in mice translate to humans? Additional research is needed to determine how lifestyle factors and genetics influence stress and memory in humans. Reducing cortisol levels alone may not be the most effective way to reduce fear generalization and other chronic anxiety symptoms. Cortisol has numerous roles throughout the body that keep us alert and healthy. When accompanied with psychotherapy, it may be possible that weakening the activity of glucocorticoid receptors in select areas of the brain could alleviate symptoms among those experiencing extreme anxiety disorders, such as PTSD. With this study, we are one step closer to providing relief for the millions of people that struggle with these conditions.