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Am J Physiol Endocrinol Metab 290: E199-E203, 2006. First published August 16, 2005; doi:10.1152/ajpendo.00337.2005
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TRANSLATIONAL PHYSIOLOGY

Steroidogenesis in human aldosterone-secreting adenomas and adrenal hyperplasias: effects of hypoxia in vitro

Hershel Raff, Eric D. Bruder the St. Luke's Medical Center Adrenal Tumor Study Group

Endocrine Research Laboratory, St. Luke's Medical Center, Medical College of Wisconsin, Milwaukee, Wisconsin

Submitted 25 July 2005 ; accepted in final form 13 August 2005

The synthesis of adrenal steroids requires molecular oxygen. Because arterial hypoxemia is a common clinical condition, the purpose of the present study was to examine steroidogenesis in vitro under physiological changes in O2 tension (PO2) in cells from human adrenal glands with aldosterone-secreting adenomas (ASA; n = 3) or with bilateral adrenal hyperplasia causing Cushing's syndrome (n = 4). A decrease in PO2 from 150 mmHg (mild hyperoxia) to 80 mmHg had minimal effect on steroid production. A reduction to 40 mmHg (still well within the physiological range) significantly inhibited cAMP- and ACTH-stimulated aldosterone, cortisol, and dehydroepiandrosterone (DHEA) production from ASA. Furthermore, cortisol and DHEA production in cells from histologically normal tissue, adjacent to ASA and from bilateral adrenal hyperplasias, was also inhibited under a PO2 of 40 mmHg. We conclude that physiological decreases in PO2 to levels typical for adrenal venous PO2 under mild hypoxia inhibit steroidogenesis. These studies may have implications for oxygen therapy in critically ill patients with functional adrenal insufficiency, as well as for therapeutic options in patients with adrenal neoplasms.

oxygen; cortisol; dehydroepiandrosterone; adrenal cortex



Address for reprint requests and other correspondence: H. Raff, St. Luke's Physician's Office Bldg., 2801 W KK River Pkwy, Suite 245, Milwaukee, WI 53215 (e-mail: hraff{at}mcw.edu)




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Effects of hypoxia on testosterone release in rat Leydig cells
Am J Physiol Endocrinol Metab, November 1, 2009; 297(5): E1039 - E1045.
[Abstract] [Full Text] [PDF]




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