Abstract

The links between early life stress (ELS) and the emergence of psychopathology such as increased anxiety and depression are now well established, although the specific neurobiological and developmental mechanisms that translate ELS into poor health outcomes are still unclear. The consequences of ELS are complex because they depend on the form and severity of early stress, duration, and age of exposure as well as co-occurrence with other forms of physical or psychological trauma. The long term effects of ELS on the corticolimbic circuit underlying emotional and social behavior are particularly salient because ELS occurs during critical developmental periods in the establishment of this circuit, its local balance of inhibition:excitation and its connections with other neuronal pathways. Using examples drawn from the human and rodent literature, we review some of the consequences of ELS on the development of the corticolimbic circuit and how it might impact fear regulation in a sex- and hemispheric-dependent manner in both humans and rodents. We explore the effects of ELS on local inhibitory neurons and the formation of perineuronal nets (PNNs) that terminate critical periods of plasticity and promote the formation of stable local networks. Overall, the bulk of ELS studies report transient and/or long lasting alterations in both glutamatergic circuits and local inhibitory interneurons (INs) and their associated PNNs. Since the activity of INs plays a key role in the maturation of cortical regions and the formation of local field potentials, alterations in these INs triggered by ELS might critically participate in the development of psychiatric disorders in adulthood, including impaired fear extinction and anxiety behavior.

Highlights

  • Numerous human epidemiological and observational studies have strongly linked adverse early life experiences with consequences on cognitive and emotional health (Bremne and Vermetten, 2001; Pechtel and Pizzagalli, 2011; Gould et al, 2012)

  • Increased synaptic plasticity found in the right BLA of juvenile male rats exposed previously to early-life stress (ELS) (Guadagno et al, 2020) might constitute one of the mechanisms leading to amygdala hyperexcitability after ELS, seeing as chronic stress in adulthood increases LTP formation in the amygdala (Dalton et al, 2012; Suvrathan et al, 2014)

  • There is some discrepancy about sex differences in amygdala growth, some reports showing that the female amygdala volume peak in pre-adolescence, 18 months earlier than in males, regardless of hemisphere (Uematsu et al, 2012) while others found that amygdala gray matter volume (GMV) is increased in males compared to females, only on the left side, and varies according to pubertal stage and circulating testosterone levels (Neufang et al, 2009). These findings suggest that gonadal steroid levels might play an important role in governing sexually dimorphic amygdala development

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Summary

INTRODUCTION

Numerous human epidemiological and observational studies have strongly linked adverse early life experiences with consequences on cognitive and emotional health (Bremne and Vermetten, 2001; Pechtel and Pizzagalli, 2011; Gould et al, 2012). Accelerated maturation of an adult-like type of corticolimbic connectivity has been documented in individuals subjected to early life adversity (Gee et al, 2013a) even though a consistent association of ELS with amygdala-PFC connectivity was not detected in a recent large meta-analysis (Colich et al, 2020). Studies across species have revealed that amygdala development is protracted, with many changes in morphology and function of the BLA occurring postnatally in both humans and rodents. Environmental insults, such as ELS, during critical periods of amygdala neurodevelopment could lead to deviations in the normal maturational trajectory and subsequently affect the integrity of the amygdala. Inactivation of the amygdala [BLA, lateral amygdala (LA), central amygdala (CeA)] disrupts extinction on PND17 but not on PND24 (Kim and Richardson, 2008), suggesting that extinction becomes more dependent on the mPFC once reciprocal connections between the BLA and mPFC are established (Kim and Richardson, 2008; Sotres-Bayon and Quirk, 2010; Jovanovic et al, 2013)

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