» Articles » PMID: 38563163

Developmental and Adult Stress: Effects of Steroids and Neurosteroids

Overview
Journal Stress
Publisher Informa Healthcare
Specialties Biology
Neurology
Date 2024 Apr 2
PMID 38563163
Authors
Affiliations
Soon will be listed here.
Abstract

In humans, exposure to early life adversity has profound implications for susceptibility to developing neuropsychiatric disorders later in life. Studies in rodents have shown that stress experienced during early postnatal life can have lasting effects on brain development. Glucocorticoids and sex steroids are produced in endocrine glands and the brain from cholesterol; these molecules bind to nuclear and membrane-associated steroid receptors. Unlike other steroids that can also be made in the brain, neurosteroids bind specifically to neurotransmitter receptors, not steroid receptors. The relationships among steroids, neurosteroids, and stress are multifaceted and not yet fully understood. However, studies demonstrating altered levels of progestogens, androgens, estrogens, glucocorticoids, and their neuroactive metabolites in both developmental and adult stress paradigms strongly suggest that these molecules may be important players in stress effects on brain circuits and behavior. In this review, we discuss the influence of developmental and adult stress on various components of the brain, including neurons, glia, and perineuronal nets, with a focus on sex steroids and neurosteroids. Gaining an enhanced understanding of how early adversity impacts the intricate systems of brain steroid and neurosteroid regulation could prove instrumental in identifying novel therapeutic targets for stress-related conditions.

Citing Articles

Modulation of stress-, pain-, and alcohol-related behaviors by perineuronal nets.

Aguilar J, Lasek A Neurobiol Stress. 2024; 33:100692.

PMID: 39691634 PMC: 11650882. DOI: 10.1016/j.ynstr.2024.100692.


Editorial: Steroid receptors in neuron and glia.

Le Menuet D, Charalampopoulos I, Cunningham R, Kalafatakis K, Nalvarte I Front Endocrinol (Lausanne). 2024; 15:1472908.

PMID: 39205689 PMC: 11349705. DOI: 10.3389/fendo.2024.1472908.

References
1.
Pallares M, Llido A, Modol L, Vallee M, Darbra S . Finasteride administration potentiates the disruption of prepulse inhibition induced by forced swim stress. Behav Brain Res. 2015; 289:55-60. DOI: 10.1016/j.bbr.2015.04.023. View

2.
Bortolato M, Devoto P, Roncada P, Frau R, Flore G, Saba P . Isolation rearing-induced reduction of brain 5α-reductase expression: relevance to dopaminergic impairments. Neuropharmacology. 2011; 60(7-8):1301-8. DOI: 10.1016/j.neuropharm.2011.01.013. View

3.
Gillies G, McArthur S . Estrogen actions in the brain and the basis for differential action in men and women: a case for sex-specific medicines. Pharmacol Rev. 2010; 62(2):155-98. PMC: 2879914. DOI: 10.1124/pr.109.002071. View

4.
Schiavone S, Sorce S, Dubois-Dauphin M, Jaquet V, Colaianna M, Zotti M . Involvement of NOX2 in the development of behavioral and pathologic alterations in isolated rats. Biol Psychiatry. 2009; 66(4):384-92. DOI: 10.1016/j.biopsych.2009.04.033. View

5.
Katahira T, Miyazaki N, Motoyama J . Immediate effects of maternal separation on the development of interneurons derived from medial ganglionic eminence in the neonatal mouse hippocampus. Dev Growth Differ. 2018; 60(5):278-290. DOI: 10.1111/dgd.12540. View