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Growth hormone stimulates adrenal steroidogenesis in the fetus
The ‘surge’ of corticosteroid in fetal plasma during late gestation has been implicated in the initiation of parturition and the maturation of enzyme systems in organs such as the lung, liver, adrenal medulla and thyroid 1–5 . But in all species studied, the mechanism responsible for increased secre...
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Published in: | Nature (London) 1981-04, Vol.290 (5805), p.404-405 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The ‘surge’ of corticosteroid in fetal plasma during late gestation has been implicated in the initiation of parturition and the maturation of enzyme systems in organs such as the lung, liver, adrenal medulla and thyroid
1–5
. But in all species studied, the mechanism responsible for increased secretion in the fetus remains unclear. The hormone adrenocorticotropin (ACTH) is well established as the primary regulator of adrenocortical cellular growth and secretory function during fetal and adult life
6
. However, no increase in fetal plasma ACTH has been observed before the corticosteroid surge in sheep or humans
7,8
, although differential responsiveness of the fetal adrenal cortex to ACTH at various gestational ages and a possible role of extra-adrenal inhibitory factors have been proposed
9–12
. The possible steroidogenic effect of α-melanocyte-stimulating hormone (αMSH) on fetal adrenocortical function is controversial
13–16
, and we could not demonstrate any such action in fetal lamb or rabbit
17,18
. Prolactin and growth hormone (GH) potentiate the steroidogenic effect of ACTH in adult rats
19–22
but prolactin had no such effect in fetal lamb
17
. We have investigated the steroidogenic properties of GH, and report here that it stimulates adrenal steroidogenesis in the fetal but not maternal rabbit
in vitro
and in fetal but not maternal sheep
in vitro
as well as
in vivo
. |
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ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/290404a0 |