A tale of two steroids: the importance of the androgens DHEA and DHEAS for early neurodevelopment

RF Greaves, SA Wudy, E Badoer, M Zacharin… - The Journal of steroid …, 2019 - Elsevier
RF Greaves, SA Wudy, E Badoer, M Zacharin, JJ Hirst, T Quinn, DW Walker
The Journal of steroid biochemistry and molecular biology, 2019Elsevier
DHEA and DHEAS are neuroactive neurosteroids that interact with several major receptor
systems in the brain, including sigma (σ), glutamate, and GABA-A receptors. It has been
recognized as early as 1952, that the loss of DHEA/DHEAS in adult life is associated with
neuropsychiatric disorders (eg schizophrenia, depression). However, the mechanistic role
for DHEA/DHEAS in any of these domains remains speculative, not the least because the
presence of these androgens in the adrenal gland and brain is largely confined to humans …
Abstract
DHEA and DHEAS are neuroactive neurosteroids that interact with several major receptor systems in the brain, including sigma (σ), glutamate, and GABA-A receptors. It has been recognized as early as 1952, that the loss of DHEA/DHEAS in adult life is associated with neuropsychiatric disorders (eg schizophrenia, depression). However, the mechanistic role for DHEA/DHEAS in any of these domains remains speculative, not the least because the presence of these androgens in the adrenal gland and brain is largely confined to humans and only some non-human primates. DHEA and DHEAS are dynamically regulated from before birth and before the onset of puberty, and therefore an understanding of the synthesis, regulation, and functions of this important androgen pathway warrants attention. Here, we draw attention to the possible modulating influence of DHEA/DHEAS in early brain development from fetal life to the remarkable increase of these steroids in early childhood - the adrenarche. We propose that the pre-pubertal DHEA/DHEAS surge plays a key role in modulating early brain development, perhaps by prolonging brain plasticity during childhood to allow the pre-adolescent brain to adapt and re-wire in response to new, and ever-changing social challenges. Nonetheless, the aetiology of neurodevelopmental phenomena in relation to DHEA/DHEAS synthesis and action cannot be easily studied in humans due to the obvious ethical restrictions on mechanistic studies, the uncertainty of predicting the future mental characteristics of individuals, and the difficulty of conducting retrospective investigations based on pre-birth and/or neonatal complications. We discuss new opportunities for animal studies to resolve these important questions.
Elsevier