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Role of Amygdala-Infralimbic Cortex Circuitry in Glucocorticoid-induced Facilitation of Auditory Fear Memory Extinction.
Vafaei, Abbas Ali; Rashidy-Pour, Ali; Trahomi, Parnia; Omoumi, Samira; Dadkhah, Masoomeh.
Affiliation
  • Vafaei AA; Research Center of Physiology, Department of Physiology, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran.
  • Rashidy-Pour A; Research Center of Physiology, Department of Physiology, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran.
  • Trahomi P; Student Research Committee, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran.
  • Omoumi S; Student Research Committee, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran.
  • Dadkhah M; Pharmaceutical Sciences Research Center, Ardabil University of Medical Sciences, Ardabil, Iran.
Basic Clin Neurosci ; 13(2): 193-205, 2022.
Article in En | MEDLINE | ID: mdl-36425953
ABSTRACT

Introduction:

The basolateral amygdala (BLA) and infralimbic area (IL) of the medial prefrontal cortex (mPFC) are two interconnected brain structures that mediate both fear memory expression and extinction. Besides the well-known role of the BLA in the acquisition and expression of fear memory, projections from IL to BLA inhibit fear expression and have a critical role in fear extinction. However, the details of IL-BLA interaction have remained unclear. Here, we investigated the role of functional reciprocal interactions between BLA and IL in mediating fear memory extinction.

Methods:

Using lidocaine (LID), male rats underwent unilateral or bilateral inactivation of the BLA and then unilateral intra-IL infusion of corticosterone (CORT) prior to extinction training of the auditory fear conditioning paradigm. Freezing behavior was reported as an index for conditioned fear. Infusions were performed before the extinction training, allowing us to examine the effects on fear expression and further extinction memory. Experiments 1-3 investigated the effects of left or right infusion of CORT into IL and LID unilaterally into BLA on fear memory extinction.

Results:

Intra-IL infusion of CORT in the right hemisphere reduced freezing behavior when administrated before the extinction training. Auditory fear memory extinction was impaired by asymmetric inactivation of BLA and CORT infusion in the right IL; however, the same effect was not observed with symmetric inactivation of BLA.

Conclusion:

IL-BLA neural circuit may provide additional evidence for the contribution of this circuit to auditory fear extinction. This study demonstrates dissociable roles for right or left BLA in subserving the auditory fear extinction. Our finding also raises the possibility that left BLA-IL circuitry may mediate auditory fear memory extinction via underlying mechanisms. However, further research is required in this area. Highlights Corticosterone infusion in the right (but not the left) infralimbic area facilitates auditory fear memory extinction.Corticosterone infusion in the right infralimbic area following symmetric basolateral amygdala inactivation has no effect on auditory fear memory extinction.Asymmetric basolateral amygdala inactivation prior to corticosterone infusion into the right infralimbic area impairs auditory fear memory extinction. Plain Language

Summary:

Previous studies have established that glucocorticoids, which are released in stressful conditions, enhance fear memory extinction. In this study, we found that corticosterone infusion into the right infralimbic area, but not the left one, facilitates auditory fear memory extinction. The effect of corticosterone infusion in the infralimbic area was not blocked by the intra-basolateral amygdala injections of lidocaine when administrated in the ipsilateral hemisphere. However, asymmetric basolateral amygdala inactivation and corticosterone infusion into the right infralimbic area impairs auditory fear memory extinction.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Basic Clin Neurosci Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Basic Clin Neurosci Year: 2022 Document type: Article