Journal
NEUROPSYCHOPHARMACOLOGY
Volume 42, Issue 12, Pages 2398-2406Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/npp.2017.64
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Funding
- Shire Pharmaceuticals
- Sage Therapeutics
- Epperson [P50 MH099910]
- Penn PROMOTES Research on Sex and Gender in Health (Epperson) [R01MH107703, F30AG055256]
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Many healthy women with no history of cognitive dysfunction experience subjective executive difficulties during menopause. Preclinical literature suggests latent effects of early life adversity on serotonin function may play a role in this phenomenon. However, evidence in human participants regarding the mechanisms by which loss of estradiol contributes to this vulnerability is lacking. Here we examined the impact of tryptophan depletion (TD) and adverse childhood experiences (ACE) on brain activation during a working memory task in menopausal women. We hypothesized that an interactive effect between ACE and TD would be observed when women were hypogonadal, and that treatment with estradiol would attenuate this effect. Thirty-three women underwent functional imaging at four time points (123 total scans) in this double-blind, placebo controlled, cross-over study. The effects of TD, ACE, and TD x ACE were evaluated using a voxel-wise, mixed-effects, 2 x 2 ANOVA. In the absence of exogenous estradiol, a TD by ACE interaction was observed on BOLD signal in the right DLPFC such that TD increased activation in high ACE subjects but decreased activation in low ACE subjects. While a similar interaction was observed with placebo treatment, treatment with estradiol attenuated the effects of ACE and TD such that no between or within group differences were observed. Together, these results suggest that early life adversity may have a lasting impact on serotonergic circuits underlying executive function that are unmasked by loss of estradiol during menopause.
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