Gastrin-releasing peptide is essential for generalization of auditory conditioned fear under stress.

Abstract

Fear generalization, which allows animals to respond adaptively to cues similar to original threatening ones, is generally beneficial for survival. However, an inability to distinguish between threat and safety, leading to the overgeneralization of fear to non-threatening stimuli, is maladaptive and is implicated in anxiety disorders such as post-traumatic stress disorder (PTSD). The neuropeptide gastrin-releasing peptide (GRP) is known to modulate fear memory under stress, yet its role in response to intense aversive stimuli remains less understood. In this study, we used GRP knockout (Grp^-/-) mice to examine the role of GRP in enhancing fear responses to conditioned stimulus (10 kHz tone, CS+) and non-conditioned stimulus (2 kHz tone, CS-) in a model of auditory fear conditioning with high-intensity footshocks following single acute restraint stress (RS). Our findings reveal that GRP is required not only for enhanced response to CS+ but also for generalized fear responses to CS-. Furthermore, we observed that infusion of GRP into the auditory cortex (AC) of Grp^-/- mice restores freezing behavior in response to CS- and fear generalization. Additionally, GRP in the AC is essential for the generalization of CS+ responsive neurons to respond to CS- during fear memory retrieval. These results highlight a novel role for GRP in the mechanisms underlying maladaptive fear in highly stressful situations, offering potential new targets for treating anxiety-related disorders.