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Journal ArticleDOI

Studies on the mechanism of secretion of corticosteroids by the isolated perfused adrenal of the rat.

Sibley Cp, +4 more
- 01 Nov 1981 - 
- Vol. 91, Iss: 2, pp 313-323
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TLDR
The results are consistent with those obtained in previous in-vitro studies and have been interpreted as suggesting that the main mechanism of corticosterone secretion is simple diffusion, while 18-hydroxy-DOC secretion, at least at sub-maximal levels of stimulation, appears to require a more complex process.
Abstract
A technique for the perfusion of the rat adrenal cortex is described. With tissue culture Medium 199 the preparation was responsive in terms of steroid production of both ACTH and K+ ions. Production of corticosterone and 18-hydroxydeoxycorticosterone (18-hydroxy-DOC) was stimulated by ACTH when it was administered at rates between 5 uu.'/min and 5 mu./min. Increasing the K+ ion concentration of the perfusate from 3.6 to 5.4 and 8.9 mmol/l stimulated the production of aldosterone, 18-hydroxycorticosterone and deoxycorticosterone, although not of corticosterone or 18-hydroxy-DOC. This preparation has been used to study further the mechanism of secretion of corticosterone and 18-hydroxy-DOC. Thus, production of these two steroids was measured at different perfusion flows, varying between 0.1 and 0.6ml/min, with different levels of ACTH stimulation. Corticosterone production was significantly (P less than 0.001) increased by increasing flows both under control conditions and with ACTH was administered at constant rates of 50 uu./min or 1 mu./min. Production of 18-hydroxy-DOC was not affected by flow either under control conditions or with 50 uu. ACTH/min. However, when ACTH was administered at 1 mu./min. 18-hydroxy-DOC production was also significantly (P less than 0.001) increased by flow. The results are consistent with those obtained in previous in-vitro studies and have been interpreted as suggesting that the main mechanism of corticosterone secretion is simple diffusion. In contrast, 18-hydroxy-DOC secretion, at least at sub-maximal levels of stimulation, appears to require a more complex process.

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Citations
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Journal ArticleDOI

Intraadrenal Interactions in the Regulation of Adrenocortical Steroidogenesis

TL;DR: The splanchnic nerve in regulating adrenocortical neural function and the influence of adrenal innervation on adrenOCortical function are studied.
Journal ArticleDOI

The neuroendocrinology of the adrenal cortex

TL;DR: The view is offered that neural inputs may provide fine tuning of the responses to systemic factors such as ACTH, through direct actions on specific adrenocortical cells, and neural regulation also provides an integrative function, through actions on the flow of blood through the gland, which itself exerts a powerful influence on adrenoc Cortical function.
Journal ArticleDOI

P-glycoprotein transports corticosterone and is photoaffinity-labeled by the steroid.

TL;DR: It is shown that 3H‐corticosterone can specifically photoaffinity label P‐glycoprotein and that corticosterone is effluxed from multidrug‐resistant cells by P‐ Glycoprotein, suggesting that cortiosterone may be an endogenous substrate for P‐ glycoprotein.
Journal ArticleDOI

Physiological role of corticotropin-releasing factor in the control of adrenocorticotropin-mediated corticosterone release from the rat adrenal gland.

TL;DR: The findings suggest that immunoneutralization of endogenous CRF results in a 3-fold reduction of the adrenal sensitivity to ACTH.
Journal ArticleDOI

Identification of the rat adrenal zona fasciculata/reticularis specific protein, inner zone antigen (IZAg), as the putative membrane progesterone receptor.

TL;DR: More detailed examination of the distribution of this protein, not only in the zona fasciculata/reticularis of the rat adrenal cortex, but also in the Leydig cell, kidney and liver, suggest it may have a role in steroid hormone synthesis and/or metabolism.
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