Literature DB >> 6291918

Studies on corticotropin-induced desensitization of normal rat adrenocortical cells.

C S Rani, G Keri, J Ramachandran.   

Abstract

The effects of prior exposure of normal rat adrenocortical cells to ACTH on the responsiveness of the cells to subsequent stimulation with the hormone have been studied. ACTH induces a time- and concentration-dependent refractoriness of both cAMP formation and steroidogenesis. Desensitization of either response was observed only upon activation of the response. Thus, both ACTH and 8-Br-cAMP caused desensitization of the steroidogenic response. The ACTH-induced desensitization of steroidogenesis, however, was completely prevented by blocking the steroidogenic action of ACTH with aminoglutethimide during exposure of cells to the hormone. Aminoglutethimide had no effect on ACTH-induced desensitization of the cAMP response. Studies with analogs of the hormone also confirmed that induction of desensitization of the steroidogenic response is independent of the desensitization of the cAMP response. Binding studies showed that the insignificant decrease in ACTH receptors could not account for the large changes in the responsiveness induced by prior exposure of cells to ACTH. Desensitization of the steroidogenic response appears to result from a defect in the rate-limiting first step of the steroidogenic pathway, namely conversion of cholesterol to pregnenolone.

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Year:  1983        PMID: 6291918     DOI: 10.1210/endo-112-1-315

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  7 in total

1.  Stereological and functional investigations on isolated adrenocortical cells: zona fasciculata/reticularis cells of chronically ACTH-treated rats.

Authors:  P G Andreis; P Rebuffat; A S Belloni; G Neri; L Cavallini; G Gottardo; G Mazzocchi; A Coi; L K Malendowicz; G G Nussdorfer
Journal:  Cell Tissue Res       Date:  1989-10       Impact factor: 5.249

2.  Dose-response downregulation within the span of single interpulse intervals.

Authors:  Daniel M Keenan; Ferdinand Roelfsema; Johannes D Veldhuis
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2010-04-21       Impact factor: 3.619

3.  Tripartite control of dynamic ACTH-cortisol dose responsiveness by age, body mass index, and gender in 111 healthy adults.

Authors:  Johannes D Veldhuis; Ali Iranmanesh; Ferdinand Roelfsema; Paul Aoun; Paul Takahashi; John M Miles; Daniel M Keenan
Journal:  J Clin Endocrinol Metab       Date:  2011-07-13       Impact factor: 5.958

4.  Corticotropin positively regulates its own receptors and cAMP response in cultured bovine adrenal cells.

Authors:  A Penhoat; C Jaillard; J M Saez
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

5.  Regulation of corticotropin receptor number and messenger RNA in cultured human adrenocortical cells by corticotropin and angiotensin II.

Authors:  M C Lebrethon; D Naville; M Begeot; J M Saez
Journal:  J Clin Invest       Date:  1994-04       Impact factor: 14.808

Review 6.  Proopiomelanocortin production by epidermal cells: evidence for an immune neuroendocrine network in the epidermis.

Authors:  R S Bhardwaj; T A Luger
Journal:  Arch Dermatol Res       Date:  1994       Impact factor: 3.017

7.  Modulation of adrenal cell functions by cadmium salts: 3. Sites affected by CdCl2 during stimulated steroid synthesis.

Authors:  O P Mgbonyebi; C T Smothers; J J Mrotek
Journal:  Cell Biol Toxicol       Date:  1994-02       Impact factor: 6.691

  7 in total

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