Prolactin Stimulates and Potentiates Adrenal Steroid Secretion in vitro

1984 ◽  
Vol 20 (4) ◽  
pp. 252-260 ◽  
Author(s):  
Charles Eldridge ◽  
John R. Lymangrover
1963 ◽  
Vol 41 (1) ◽  
pp. 1147-1153
Author(s):  
J. S. Willmer ◽  
O. Héroux

The in vitro adrenal steroid secretion of wild Norway rats (Rattus norvegicus) captured during the winter differed in quantity, but not in quality, from that of similar rats captured during the summer. Whereas there was no evident seasonal effect on adrenal weight either in males or in females, adrenals of both sexes secreted at a faster rate during the winter than during the summer, this increase involving the four groups of steroids characterized chromatographically during both seasons and in both sexes; the predominant steroid secreted was corticosterone. This seasonal adjustment in adrenal activity is similar to that observed in white rats kept in group cages exposed outdoors to the natural summer and winter environmental conditions, but it differs from that found in white rats cold-acclimated in the laboratory, in which adrenal activity is lower than normal after cold acclimation.


1963 ◽  
Vol 41 (5) ◽  
pp. 1147-1153 ◽  
Author(s):  
J. S. Willmer ◽  
O. Héroux

The in vitro adrenal steroid secretion of wild Norway rats (Rattus norvegicus) captured during the winter differed in quantity, but not in quality, from that of similar rats captured during the summer. Whereas there was no evident seasonal effect on adrenal weight either in males or in females, adrenals of both sexes secreted at a faster rate during the winter than during the summer, this increase involving the four groups of steroids characterized chromatographically during both seasons and in both sexes; the predominant steroid secreted was corticosterone. This seasonal adjustment in adrenal activity is similar to that observed in white rats kept in group cages exposed outdoors to the natural summer and winter environmental conditions, but it differs from that found in white rats cold-acclimated in the laboratory, in which adrenal activity is lower than normal after cold acclimation.


1991 ◽  
Vol 44 (3) ◽  
pp. 461-468 ◽  
Author(s):  
Gregor Westhof ◽  
Karin F. Westhof ◽  
Wilhelm L. Braendle ◽  
Gere S. diZerega

1985 ◽  
Vol 106 (1) ◽  
pp. 137-142 ◽  
Author(s):  
Jorg Winterer ◽  
George P. Chrousos ◽  
D. Lynn Loriaux ◽  
Gordon B. Cutler

Endocrinology ◽  
2011 ◽  
Vol 152 (9) ◽  
pp. 3461-3470 ◽  
Author(s):  
Nicolette L. McGuire ◽  
Kristina Kangas ◽  
George E. Bentley

Study of seasonal reproduction has focused on the brain. Here, we show that the inhibition of sex steroid secretion can be seasonally mediated at the level of the gonad. We investigate the direct effects of melatonin on sex steroid secretion and gonadal neuropeptide expression in European starlings (Sturnus vulgaris). PCR reveals starling gonads express mRNA for gonadotropin inhibitory hormone (GnIH) and its receptor (GnIHR) and melatonin receptors 1B (Mel 1B) and 1C (Mel 1C). We demonstrate that the gonadal GnIH system is regulated seasonally, possibly via a mechanism involving melatonin. GnIH/ GnIHR expression in the testes is relatively low during breeding compared with outside the breeding season. The expression patterns of Mel 1B and Mel 1C are correlated with this expression, and melatonin up-regulates the expression of GnIH mRNA in starling gonads before breeding. In vitro, GnIH and melatonin significantly decrease testosterone secretion from LH/FSH-stimulated testes before, but not during, breeding. Thus local inhibition of sex steroid secretion appears to be regulated seasonally at the level of the gonad, by a mechanism involving melatonin and the gonadal GnIH system.


1991 ◽  
Vol 6 (3) ◽  
pp. 249-255 ◽  
Author(s):  
P. Netchitailo ◽  
A. Larcher ◽  
F. Leboulenger ◽  
M. Feuilloley ◽  
D. Philibert ◽  
...  

ABSTRACT To investigate a possible direct action of glucocorticoids on adrenal steroidogenesis, the effect of corticosterone on the conversion of pregnenolone into various metabolites by frog adrenal tissue was examined. Frog interrenal slices were incubated with [3H]pregnenolone (1 mCi/ml) and the various labelled metabolites analysed by reverse-phase high-performance liquid chromatography. With the methanol gradient used, five identified steroids were resolved: progesterone, 11-deoxycorticosterone, corticosterone, 18-hydroxycorticosterone and aldosterone. Corticosterone (10 μg/ml) induced a 45–80% decrease in all steroids synthesized from [3H]pregnenolone. In contrast, the glucocorticoid agonist dexamethasone did not reduce the rate of conversion of pregnenolone into its metabolites. In addition, the inhibitory effect of corticosterone was not reversed by the specific glucocorticoid antagonist RU 43044. These results show that corticosterone exerts a direct inhibitory effect on adrenal steroid secretion. In addition, our data indicate that the ultra-short regulation induced by corticosterone is not mediated through glucocorticoid receptors.


2000 ◽  
Vol 78 (6) ◽  
pp. 1591 ◽  
Author(s):  
E L Zanella ◽  
D D Lunstra ◽  
T H Wise ◽  
J E Kinder ◽  
J J Ford

1990 ◽  
Vol 259 (3) ◽  
pp. E405 ◽  
Author(s):  
A H Miller ◽  
R L Spencer ◽  
M Stein ◽  
B S McEwen

Type I and II adrenal steroid receptor binding was measured in spleen and thymus of adrenalectomized (ADX) rats and intact rats at basal levels of corticosterone after 1 h of restraint stress or after exogenous administration of dexamethasone (DEX). Concurrent receptor determinations were made in the hippocampus and pituitary. Receptor binding measures in immune tissues and pituitary were less responsive to varying levels of endogenous hormones than binding measures in hippocampus. Compared with ADX rats, type I binding in spleen and pituitary of intact rats at basal levels of corticosterone was unchanged, whereas type I binding in the hippocampus was significantly decreased. Furthermore, despite peak levels of corticosterone, type II binding in spleen, thymus, and pituitary of stressed rats was also unchanged, whereas type II binding in the hippocampus of stressed animals was significantly lower. In contrast, DEX, a well-known immunosuppressant, reduced type II binding in immune tissues more than in the hippocampus. Because a decrease in receptor binding measured in vitro may reflect receptor activation in vivo, these results suggest that there may be considerable heterogeneity in the degree of activation of adrenal steroid receptor subtypes in immune, pituitary, and hippocampal tissue by endogenous and exogenous glucocorticoids.


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