Abstract

Following adverse childhood experiences, high quality maternal care can protect against accelerated telomere shortening in peripheral cells. It is less clear, however, how telomere length in the brain is influenced by early caregiving experiences. Using rats, we investigated if quality of care (i.e., aversive or nurturing care outside of the homecage) during the first seven days of postnatal (PN) life affected telomere length in the adult brain (PN90) of male and female rats. At PN90, we found that nurturing care outside of the homecage was associated with longer telomeres in the medial prefrontal cortex relative to nurturing care inside the homecage (i.e., normal maternal care) and aversive care outside of the homecage. Further, pups exposed to aversive care outside of the homecage demonstrated longer telomeres in the amygdala relative to pups exposed to nurturing care inside the homecage. These effects were specific to females. No differences in telomere length between caregiving conditions were observed in the ventral hippocampus. Thus, positive and negative early-life experiences result in long-term, sex-specific changes of telomeres in the brain.

Highlights

  • Maltreatment and chronic stress in childhood are associated with numerous impairments to future physical and mental health, such as anxiety and depression [1,2]

  • Normal care and maltreated females did not differ in medial prefrontal cortex (mPFC) telomere length

  • This study demonstrates for the first time that exposure to nurturing or aversive caregiving environments outside the homecage in infancy result in long-term changes in telomere length within the brain

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Summary

Introduction

Maltreatment and chronic stress in childhood are associated with numerous impairments to future physical and mental health, such as anxiety and depression [1,2]. There is an increasing urgency to discover biomarkers that can discriminate between increased risk susceptibility and resiliency following early-life stress. Telomere length in peripheral cells has emerged as a biomarker of the impact of early-life and chronic stress [3]. Telomeres are long stretches of TTAGGG nucleotide repeats that cap the ends of DNA [4]. Telomere length plays a role in cellular aging with both biological and psychological environmental factors influencing the rate of their attrition in peripheral cells [3,5,6]. The pattern of changes to telomere length differs across gender, cells, organs, and disease-states [7,8,9,10,11,12]

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