Abstract

In recent years, a growing body of research has shown sex differences in the prevalence and symptomatology of psychopathologies, such as depression, anxiety, and fear-related disorders, all of which show high incidence rates in early life. This has highlighted the importance of including female subjects in animal studies, as well as delineating sex differences in neural processing across development. Of particular interest is the corticolimbic system, comprising the hippocampus, amygdala, and medial prefrontal cortex. In rodents, these corticolimbic regions undergo dynamic changes in early life, and disruption to their normative development is believed to underlie the age and sex-dependent effects of stress on affective processing. In this review, we consolidate research on sex differences in the hippocampus, amygdala, and medial prefrontal cortex across early development. First, we briefly introduce current principles on sexual differentiation of the rodent brain. We then showcase corticolimbic regional sex differences in volume, morphology, synaptic organization, cell proliferation, microglia, and GABAergic signaling, and explain how these differences are influenced by perinatal and pubertal gonadal hormones. In compiling this research, we outline evidence of what and when sex differences emerge in the developing corticolimbic system, and illustrate how temporal dynamics of its maturational trajectory may differ in male and female rodents. This will help provide insight into potential neural mechanisms underlying sex-specific critical windows for stress susceptibility and behavioral emergence.

Highlights

  • The corticolimbic system plays a critical role in the regulation of affective behaviors and is highly conserved across mammalian species (LeDoux, 2012)

  • There are no sex differences in miniature excitatory postsynaptic current (mEPSC) amplitude or inhibitory synaptic transmission (Cooke and Woolley, 2005). Given that these effects are seen prior to puberty, Cooke and Woolley (2005) postulate that these sex differences in the MeApd of juvenile rats may arise from the organizational effects of perinatal gonadal hormones, consistent with what is seen in overall MeA synapse number (Nishizuka and Arai, 1981)

  • It appears that postpubertal changes to neuron number are more prominent in females, suggesting a stronger influence of gonadal hormones on PL/IL neuronal count. When it comes to medial prefrontal cortex (mPFC) dendritic morphology, studies point to layer-specific sex differences in early life

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Summary

Frontiers in Neuroscience

A growing body of research has shown sex differences in the prevalence and symptomatology of psychopathologies, such as depression, anxiety, and fearrelated disorders, all of which show high incidence rates in early life This has highlighted the importance of including female subjects in animal studies, as well as delineating sex differences in neural processing across development. We outline evidence of what and when sex differences emerge in the developing corticolimbic system, and illustrate how temporal dynamics of its maturational trajectory may differ in male and female rodents This will help provide insight into potential neural mechanisms underlying sex-specific critical windows for stress susceptibility and behavioral emergence

INTRODUCTION
Sexual Differentiation of the Rodent Brain
Anatomy and Hormonal Receptor Distribution
Volume and Morphology
Cell Proliferation and Cell Death
GABAergic Signaling
Sprague Dawley
Summary and Implications of Sex Differences in the Developing Hippocampus
THE AMYGDALA
Summary and Implications of Sex Differences in the Developing Amygdala
THE MEDIAL PREFRONTAL CORTEX
Summary of Sex Differences in the Developing Medial Prefrontal Cortex
Findings
CONCLUDING REMARKS
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