The first report on increased production of 17-ketosteroids in healthy children before puberty was published by N. Talbot et al. in 1943. F. Albrigth et al. introduced the concept of "adrenarch", which everyone has used for the past 50 years. Later, with the advent of more advanced methods, it was shown that increased excretion of 17-ketosteroids during this development period is due to increased secretion of the adrenal cortex of dehydroepiandrosterone (DHEA) and dehydroepiandrosterone sulfate (DHEAS). It must be emphasized that the content of other adrenal androgens - androstenedione and lip-hydroxyandrostenedione - does not increase during the adrenarche period. An increase in their secretion is recorded at the age of 6-8 years, that is, it is somewhat behind the activation of DHEA secretion. It must be remembered that androstenedione is also a product of DHEA metabolism in peripheral tissues. In contrast, lip-hydroxyandrostenedione can form only in the cortical layer of the adrenal gland, which is due to the presence of the corresponding enzyme system, which is localized in the adrenal tissue.
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http://dx.doi.org/10.14341/probl200652216-21 | DOI Listing |
Dev Cogn Neurosci
January 2025
Institute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, USA; Center for Pediatric Brain Health, Boys Town National Research Hospital, Boys Town, NE, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, USA.
The pituitary gland (PG) plays a central role in the production and secretion of pubertal hormones, with documented links to the increase in mental health symptoms during adolescence. Although literature has largely focused on examining whole PG volume, recent findings have demonstrated associations among pubertal hormone levels, including dehydroepiandrosterone (DHEA), PG subregions, and mental health symptoms during adolescence. Despite the anterior PG's role in DHEA production, studies have not yet examined potential links with transdiagnostic symptomology (i.
View Article and Find Full Text PDFEur J Endocrinol
November 2024
Faculty of Biology, Technion-Israel Institute of Technology, Haifa 32000, Israel.
Objective: High concentrations of dehydroepiandrosterone sulfate (DHEAS) often precede premature puberty and sometimes polycystic ovary syndrome (PCOS). We hypothesized that the underlying mechanisms might involve DNA methylation. As an indicator of the downstream effects of DHEAS, we looked for associations between prepubertal DHEAS concentration, pubertal progression, and DNA methylation at puberty-related genes in blood cells.
View Article and Find Full Text PDFMol Cell Endocrinol
October 2024
Pediatric Endocrinology, Diabetology, and Metabolism, Inselspital, Bern University Hospital, Bern, Switzerland; Department of BioMedical Research (DBMR), University of Bern, Bern, Switzerland. Electronic address:
Context: Adrenarche is a normal developmental event in mid-childhood characterized by increasing adrenal androgen secretion. The role of the classic androgen pathway has been well described in adrenarche, but the role of newer active androgens and additional androgen pathways is less clear.
Objective: To study the contribution of novel androgens and related steroid biosynthesis pathways to the development of adrenarche, and to identify additional steroid biomarkers of adrenarche.
The pituitary gland (PG) plays a central role in the production and secretion of pubertal hormones, with documented links to the emergence and increase in mental health symptoms known to occur during adolescence. Although much of the literature has focused on examining whole PG volume, recent findings suggest that there are associations among pubertal hormone levels, including dehydroepiandrosterone (DHEA), subregions of the PG, and elevated mental health symptoms (e.g.
View Article and Find Full Text PDFEnviron Epidemiol
April 2024
Department of Epidemiology, Brown University, Providence, Rhode Island.
Background: Triclosan is an endocrine-disrupting chemical, but associations with pubertal outcomes remain unclear. We examined associations of gestational and childhood triclosan with adolescent hormone concentrations and pubertal stage.
Methods: We quantified urinary triclosan concentrations twice during pregnancy and seven times between birth and 12 years in participants recruited from Cincinnati, OH (2003-2006).
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