The University of Southampton
University of Southampton Institutional Repository

Age-specific changes in sex steroid biosynthesis and sex development

Age-specific changes in sex steroid biosynthesis and sex development
Age-specific changes in sex steroid biosynthesis and sex development
Normal male sex development requires the SRY gene on the Y chromosome, the regression of Mullerian structures via anti-Mullerian hormone (AMH) signalling, the development of the Wolffian duct system into normal male internal genital structures consequent to testosterone secretion by the testicular Leydig cells, and finally, sufficient activation of testosterone to dihydrotestosterone by 5alpha-reductase. All these events take place during weeks 8-12 of gestation, a narrow window of sexual differentiation. Recent studies in human fetal development have demonstrated the early fetal expression of the adrenocorticotrophic hormone (ACTH) receptor and all steroidogenic components necessary for the biosynthesis of cortisol. These findings provide compelling evidence for the assumed pathogenesis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, diminished feedback to the pituitary due to glucocorticoid deficiency, subsequent ACTH excess, and up-regulation of adrenal androgen production with subsequent virilization. Another CAH variant, P450 oxidoreductase deficiency, manifests with 46,XX disorder of sex development (DSD), i.e., virilized female genitalia, despite concurrently low circulating androgens. This CAH variant illustrates the existence of an alternative pathway toward the biosynthesis of active androgens in humans which is active in human fetal life only. Thus CAH teaches important lessons from nature, providing privileged insights into the window of human sexual differentiation, and particularly highlighting the importance of steroidogenesis in the process of human sexual differentiation
biomedical research, secretion, hypothalamo-hypophyseal system, classification, hormones, fetal, biosynthesis, congenital, sex, animals, fetal development, male, differentiation, 46, genetics, metabolism, embryology, nadph-ferrihemoprotein reductase, research, up-regulation, steroid 21-hydroxylase, cortisol, human, gonadal dysgenesis, deficiency, physiology, pituitary-adrenal system, female, xx, feedback, expression, sexual development, humans, biochemical, adrenal hyperplasia, review, aging, gonadal steroid hormones
1521-690X
393-401
Krone, Nils
770eb3c0-dff2-4f01-b679-6746fe4c44bb
Hanley, Neil A.
bf03f7bb-f377-44fb-8344-0bb1ca8b2ef9
Arlt, Wiebke
fcf7aa71-468a-4097-b2cc-a04b283e53c7
Krone, Nils
770eb3c0-dff2-4f01-b679-6746fe4c44bb
Hanley, Neil A.
bf03f7bb-f377-44fb-8344-0bb1ca8b2ef9
Arlt, Wiebke
fcf7aa71-468a-4097-b2cc-a04b283e53c7

Krone, Nils, Hanley, Neil A. and Arlt, Wiebke (2007) Age-specific changes in sex steroid biosynthesis and sex development. Best Practice & Research Clinical Endocrinology & Metabolism, 21 (3), 393-401. (doi:10.1016/j.beem.2007.06.001).

Record type: Article

Abstract

Normal male sex development requires the SRY gene on the Y chromosome, the regression of Mullerian structures via anti-Mullerian hormone (AMH) signalling, the development of the Wolffian duct system into normal male internal genital structures consequent to testosterone secretion by the testicular Leydig cells, and finally, sufficient activation of testosterone to dihydrotestosterone by 5alpha-reductase. All these events take place during weeks 8-12 of gestation, a narrow window of sexual differentiation. Recent studies in human fetal development have demonstrated the early fetal expression of the adrenocorticotrophic hormone (ACTH) receptor and all steroidogenic components necessary for the biosynthesis of cortisol. These findings provide compelling evidence for the assumed pathogenesis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, diminished feedback to the pituitary due to glucocorticoid deficiency, subsequent ACTH excess, and up-regulation of adrenal androgen production with subsequent virilization. Another CAH variant, P450 oxidoreductase deficiency, manifests with 46,XX disorder of sex development (DSD), i.e., virilized female genitalia, despite concurrently low circulating androgens. This CAH variant illustrates the existence of an alternative pathway toward the biosynthesis of active androgens in humans which is active in human fetal life only. Thus CAH teaches important lessons from nature, providing privileged insights into the window of human sexual differentiation, and particularly highlighting the importance of steroidogenesis in the process of human sexual differentiation

This record has no associated files available for download.

More information

Published date: September 2007
Keywords: biomedical research, secretion, hypothalamo-hypophyseal system, classification, hormones, fetal, biosynthesis, congenital, sex, animals, fetal development, male, differentiation, 46, genetics, metabolism, embryology, nadph-ferrihemoprotein reductase, research, up-regulation, steroid 21-hydroxylase, cortisol, human, gonadal dysgenesis, deficiency, physiology, pituitary-adrenal system, female, xx, feedback, expression, sexual development, humans, biochemical, adrenal hyperplasia, review, aging, gonadal steroid hormones

Identifiers

Local EPrints ID: 59953
URI: http://eprints.soton.ac.uk/id/eprint/59953
ISSN: 1521-690X
PURE UUID: abe2c87c-5cb0-467c-b696-8c24d44c4450

Catalogue record

Date deposited: 05 Sep 2008
Last modified: 15 Mar 2024 11:18

Export record

Altmetrics

Contributors

Author: Nils Krone
Author: Neil A. Hanley
Author: Wiebke Arlt

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×