Abstract

BackgroundFindings about sex differences in the field of fear conditioning and fear extinction have been mixed. At the psychophysiological level, sex differences emerge only when taking estradiol levels of women into consideration. This suggests that this hormone may also influence sex differences with regards to activations of brain regions involved in fear conditioning and its extinction. Importantly, the neurobiological correlates associated with the use of hormonal oral contraceptives in women have not been fully contrasted against men and against naturally cycling women with different levels of estradiol. In this study, we begin to fill these scientific gaps.MethodsWe recruited 37 healthy men and 48 healthy women. Of these women, 16 were using oral contraceptives (OC) and 32 were naturally cycling. For these naturally cycling women, a median split was performed on their serum estradiol levels to create a high estradiol (HE) group (n = 16) and a low estradiol (LE) group (n = 16). All participants underwent a 2-day fear conditioning and extinction paradigm in a 3 T MR scanner. Using the 4 groups (men, HE women, LE women, and OC users) and controlling for age and coil type, one-way ANCOVAs were performed to look at significant activations within the nodes of the fear circuit. Using post-hoc analyses, beta-weights were extracted in brain regions showing significant effects in order to unveil the differences based on hormonal status (men, HE, LE, OC).ResultsSignificant main effect of hormonal status group was found across the different phases of the experiment and in different sub-regions of the insular and cingulate cortices, amygdala, hippocampus, and hypothalamus. During conditioning, extinction and recall, most of the observed differences suggested higher activations among HE women relative to men. During the unconditioned response, however, a different pattern was observed with men showing significantly higher brain activations.ConclusionsOur data further support the important contribution of estradiol levels in the activation of brain regions underlying fear learning and extinction. The results highlight the need to document gonadal hormonal levels, menstrual cycle phase as well as oral contraceptive use in women in order to avoid overlooking sex differences when investigating the neurobiology of emotional regulation.

Highlights

  • Findings about sex differences in the field of fear conditioning and fear extinction have been mixed

  • We focused our attention on 4 different contrasts of interest: 1) the unconditioned response during the fear conditioning phase (UCR: Shock vs. Conditioned stimulus (CS)- offset) in order to examine activations associated with the sensation of the shock; 2) the conditioned response during the fear conditioning phase (Conditioning: CS+ vs. CS-) in order to examine fear conditioninginduced activations; 3) the late extinction phase in order to examine fear extinction learning–induced activation towards the end of extinction learning; and 4) the early extinction recall phase in order to examine extinction memory-induced brain activation during the early phase of recall

  • During the unconditioned response of the fearconditioning phase, significant effects were revealed in the hippocampus and the insular cortex

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Summary

Introduction

Findings about sex differences in the field of fear conditioning and fear extinction have been mixed. Sex differences emerge only when taking estradiol levels of women into consideration This suggests that this hormone may influence sex differences with regards to activations of brain regions involved in fear conditioning and its extinction. Reports related to sex differences during fear learning and extinction are often inconsistent, highlighting the need to examine biological factors that may contribute to this inconsistency [22,23,24,25,26,27] These studies call for a better understanding of how sex differences may emerge during fear conditioning and extinction, as well as how sex hormones may mediate some of these differences [23,24,25,26,27,28,29,30]. Estradiol is the predominant and most potent circulating estrogen during the reproductive years in non-pregnant women

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