Abstract

Steroids have an important role in growth, development, sexual differentiation and reproduction. All four classes of steroids, androgens, oestrogens, progestogens and glucocorticoids, have varying effects on the brain. Androgens and oestrogens are involved in the sexual differentiation of the brain, and also influence cognition. Progestogens such as progesterone and its metabolites have been shown to be involved in neuroprotection, although their protective effects are timing‐dependent. Glucocorticoids are linked with stress and memory performance, also in a dose‐ and time‐dependent manner. Importantly, dysfunction in steroid function has been implicated in the pathogenesis of disease. Moreover, regulating steroid‐signalling has been suggested as potential therapeutic avenue for the treatment of a number of neurodevelopmental, psychiatric and neurodegenerative disorders. Therefore, clarifying the role of steroids in typical and atypical brain function is essential for understanding typical brain functions, as well as determining their potential use for pharmacological intervention in the atypical brain. However, the majority of studies have thus far have been conducted using animal models, with limited work using native human tissue or cells. Here, we review the effect of steroids in the typical and atypical brain, focusing on the cellular, molecular functions of these molecules determined from animal models, and the therapeutic potential as highlighted by human studies. We further discuss the promise of human‐induced pluripotent stem cells, including advantages of using three‐dimensional neuronal cultures (organoids) in high‐throughput screens, in accelerating our understanding of the role of steroids in the typical brain, and also with respect to their therapeutic value in the understanding and treatment of the atypical brain.

Highlights

  • Steroid hormones are cyclical chemical compounds made up of rings of carbon atoms that play an essential role in a wide range of physiological functions, including growth, development, energy metabolism, homeostasis and reproduction

  • We have reviewed the important role steroids play in development and sexual differentiation of the brain through a nuclear receptor mediated mechanism

  • One well-­characterised mechanism of action is through differential modulation of apoptosis in neurons depending on biological sex

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Summary

| INTRODUCTION

Steroid hormones are cyclical chemical compounds made up of rings of carbon atoms that play an essential role in a wide range of physiological functions, including growth, development, energy metabolism, homeostasis and reproduction. Testosterone and oestrogen signalling through AR and ERs interact with histone-­modifying factors such as histone acetyl transferases to bring about profound gene regulatory effects.[6,48,49] ERα demonstrates high promoter methylation in both sexes corresponding to reduced ERα gene expression in the cortex,[50,51] and a study using rats has shown that greater ERα promoter methylation is associated with higher neonatal maternal grooming and early oestradiol exposure.[52] Another study in mice showed that testosterone administration in neonatal females altered brain DNA methylation 20-­fold in adulthood to shift towards a male methylation pattern,[53] whereas short-­term effects of testosterone were relatively modest This late-­emerging effect provides insight into the vital role of steroids in long-­term sexually dimorphic molecular changes in the brain, and shows the importance of the effect of steroids on DNA methylation in bringing about brain sex-­specific organisation. Immediate effects of testosterone and oestrogens have been reported in human studies, such as in one study from our group where a single sublingual dose of testosterone administered to young women significantly impaired empathy and

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| CONCLUSIONS
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