JOE Society for Endocrinology Archive
HOME HELP CONTACT US SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


DOI: 10.1677/joe.0.1680475

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (16)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Simmonds, P.
Right arrow Articles by Canny, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Simmonds, P.
Right arrow Articles by Canny, B.
Journal of Endocrinology, Vol 168, Issue 3, 475-485
Copyright © 2001 by Society for Endocrinology


Articles

The role of the pituitary gland and ACTH in the regulation of mRNAs encoding proteins essential for adrenal steroidogenesis in the late-gestation ovine fetus

PJ Simmonds, ID Phillips, KR Poore, ID Coghill, IR Young, and BJ Canny


To further understand the relative roles of the pituitary gland and ACTH in the regulation of mRNAs encoding proteins that are essential for adrenal development, we investigated the effects of, first, an ACTH infusion and labour in intact fetuses and, secondly, the effect of an ACTH infusion to fetuses with and without a pituitary gland, on the relative abundance of the mRNA encoding for the ACTH receptor (MC2R), steroidogenic factor 1 (SF-1), cholesterol side-chain cleavage enzyme (P450(scc)), 3beta-hydroxysteroid dehydrogenase (3betaHSD) and 17alpha-hydroxylase (P450(C17)) in the fetal adrenal gland. ACTH(1-24) infusion (14.7 pmol/kg per h) to intact fetuses was without effect on the abundance of mRNA encoding MC2R and SF-1, irrespective of whether the infusion was given for 18 (115-132 days of gestation) or 32 days (115 days to term (147 days of gestation)). Hypophysectomy (HX) did not alter the expression of MC2R mRNA; however, the abundance of SF-1 mRNA fell by approximately 50% following the removal of the pituitary gland. ACTH(1-24) infusion to HX fetuses failed to restore levels of SF-1 mRNA to that seen in intact animals. P450(scc) and 3betaHSD mRNAs were increased by ACTH(1-24) infusion for 18 days in intact animals, although no effects of the infusion were seen on P450(C17) mRNA levels. For all three of these mRNAs, there was a significant increase in their abundance between 132 days of gestation and term in intact fetuses. By term, ACTH(1-24) infusion was without any additional effect on their abundance. HX decreased the expression of P450(scc), 3betaHSD and P450(C17) mRNAs, while ACTH(1-24) infusion to HX fetuses increased the expression of these mRNAs to levels seen in intact animals. There were significant correlations between the abundance of the mRNA for P450(scc), 3betaHSD and P450(C17), but not MC2R and SF-1, and premortem plasma cortisol concentrations. These results emphasise the importance of the pituitary gland and ACTH in the regulation of the enzymes involved in adrenal steroidogenesis. Factors in addition to ACTH may also play some role, as the infusion was not always effective in increasing the abundance of the mRNAs. Surprisingly, the mRNA for MC2R and SF-1 did not appear to be regulated by ACTH in the late-gestation ovine fetus, though a pituitary-dependent factor may be involved in the regulation of SF-1 mRNA abundance.


This article has been cited by other articles:


Home page
EndocrinologyHome page
J. Gersting, C. E. Schaub, M. Keller-Wood, and C. E. Wood
Inhibition of Brain Prostaglandin Endoperoxide Synthase-2 Prevents the Preparturient Increase in Fetal Adrenocorticotropin Secretion in the Sheep Fetus
Endocrinology, August 1, 2008; 149(8): 4128 - 4136.
[Abstract] [Full Text] [PDF]


Home page
Reproductive SciencesHome page
Yixin Su and J. C. Rose
The Impact of ACTH Receptor Knockdown on Fetal and Adult Ovine Adrenocortical Cell Function
Reproductive Sciences, March 1, 2008; 15(3): 253 - 262.
[Abstract] [PDF]


Home page
Reproductive SciencesHome page
K. S. Rehman, R. Sirianni, C. R. Parker JR, W. E. Rainey, and B. R. Carr
The Regulation of Adrenocorticotrophic Hormone Receptor by Corticotropin-Releasing Hormone in Human Fetal Adrenal Definitive/Transitional Zone Cells
Reproductive Sciences, September 1, 2007; 14(6): 578 - 587.
[Abstract] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
L. C. Carey, Y. Su, N. K. Valego, and J. C. Rose
Infusion of ACTH stimulates expression of adrenal ACTH receptor and steroidogenic acute regulatory protein mRNA in fetal sheep
Am J Physiol Endocrinol Metab, August 1, 2006; 291(2): E214 - E220.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
D. A. Myers, K. Hyatt, M. Mlynarczyk, I. M. Bird, and C. A. Ducsay
Long-term hypoxia represses the expression of key genes regulating cortisol biosynthesis in the near-term ovine fetus
Am J Physiol Regulatory Integrative Comp Physiol, December 1, 2005; 289(6): R1707 - R1714.
[Abstract] [Full Text] [PDF]


Home page
Reproductive SciencesHome page
Y. Su, L. C. Carey, N. K. Valego, and J. C. Rose
Developmental Changes in Adrenocorticotrophin (ACTH)-Induced Expression of ACTH Receptor and Steroid Acute Regulatory Protein mRNA in Ovine Fetal Adrenal Cells
Reproductive Sciences, September 1, 2005; 12(6): 416 - 420.
[Abstract] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
N. K. Valego, Y. Su, L. C. Carey, S. F. Young, S. B. Tatter, J. Wang, and J. C. Rose
Hypothalamic-pituitary disconnection in fetal sheep blocks the peripartum increases in adrenal responsiveness and adrenal ACTH receptor expression
Am J Physiol Regulatory Integrative Comp Physiol, August 1, 2005; 289(2): R410 - R417.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
M. E. Bell, T. J. McDonald, and D. A. Myers
Proopiomelanocortin Processing in the Anterior Pituitary of the Ovine Fetus after Lesion of the Hypothalamic Paraventricular Nucleus
Endocrinology, June 1, 2005; 146(6): 2665 - 2673.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
M. Thomas, M. Keramidas, E. Monchaux, and J.-J. Feige
Dual Hormonal Regulation of Endocrine Tissue Mass and Vasculature by Adrenocorticotropin in the Adrenal Cortex
Endocrinology, September 1, 2004; 145(9): 4320 - 4329.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
K.E. Warnes, I.C. McMillen, J.S. Robinson, and C.L. Coulter
Differential Actions of Metyrapone on the Fetal Pituitary-Adrenal Axis in the Sheep Fetus in Late Gestation
Biol Reprod, August 1, 2004; 71(2): 620 - 628.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
A. J. W. Fletcher, X. H. Ma, W. X. Wu, P. W. Nathanielsz, H. H. G. McGarrigle, A. L. Fowden, and D. A. Giussani
Antenatal glucocorticoids reset the level of baseline and hypoxemia-induced pituitary-adrenal activity in the sheep fetus during late gestation
Am J Physiol Endocrinol Metab, February 1, 2004; 286(2): E311 - E319.
[Abstract] [Full Text] [PDF]


Home page
Reproductive SciencesHome page
J. J. Wang, N. K. Valego, Y. Su, J. Smith, and J. C. Rose
Developmental Aspects of Ovine Adrenal Adrenocorticotropic Hormone Receptor Expression
Reproductive Sciences, January 1, 2004; 11(1): 27 - 35.
[Abstract] [PDF]


Home page
EndocrinologyHome page
R. AEsoy, G. Mellgren, K.-I. Morohashi, and J. Lund
Activation of cAMP-Dependent Protein Kinase Increases the Protein Level of Steroidogenic Factor-1
Endocrinology, January 1, 2002; 143(1): 295 - 303.
[Abstract] [Full Text] [PDF]




HOME HELP CONTACT US SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2001 by the Society for Endocrinology.