Effects of prolonged ACTH-stimulation on adrenocortical cholesterol reserve and apolipoprotein E concentration in young and aged Fischer 344 male rats

• Published in: The Journal of steroid biochemistry and molecular biology Vol. 66; no. 5; pp. 335 - 345
• Main Authors: Cheng, Behling, Chou, Shui-Chou, Abraham, Susamma, Kowal, Jerome
• Format: Journal Article
• Language: English
• Published: Oxford Elsevier Ltd 01.09.1998; Elsevier Science
• Subjects: adrenal cortex; Adrenal Cortex - growth & development; Adrenal Cortex - metabolism; Adrenals. Interrenals; Adrenocortical hormones. Regulation; Adrenocorticotropic Hormone - pharmacology; aging; Aging - physiology; Animals; apolioprotein E; Apolipoproteins E - metabolism; Biological and medical sciences; cholesterol; Cholesterol Esters - metabolism; Corticosterone - urine; Fundamental and applied biological sciences. Psychology; Male; Organ Size; Rats; Rats, Inbred F344; Vertebrates: endocrinology; apolioprotein E; cholesterol; aging; adrenal cortex; Rat; Rodentia; Adrenal cortex; ACTH; Lipids; Cholesterol; Vertebrata; Mammalia; Adenohypophyseal hormone; Apolipoprotein E; Steroidogenesis; Storage lipid; Age
• ISSN: 0960-0760; 1879-1220
• DOI: 10.1016/S0960-0760(98)00062-4

Changes in the morphology of rat adrenal cortex with age include increased accumulations of lipid droplets and lipofuscin granules. Because glandular concentrations of cholesteryl esters (CE) and apolipoprotein (apo) E are also increased in parallel, the utilization or metabolism of lipid-droplet stored CE for steroidogenesis might be altered in aging cells. To explore this possibility, adrenocortical cholesterol storage and utilization were studied in 3–6 months-old (mo) (Y) rats and 20–23 mo (O) Fischer 344 male rats. Both groups received either adrenocorticotropin (ACTH1-39, Acthar gel) or gelatin alone daily for seven consecutive days. We found that: (a) the CE concentration in O rats, but not Y animals, was diminished by ACTH. The depleted CE in stimulated-O rats was replenished within five days post stimulation. Failure to deplete CE in stimulated-Y rats was not associated with an insufficient dose of the hormone, since stimulation of Y animals with higher doses of ACTH actually increased the CE concentration. In contrast, adrenocortical free cholesterol concentration remained constant during stimulation regardless of age. (b) The depleted CE in stimulated-O rats was principally comprised of cholesteryl adrenate, cholesteryl arachidonate and cholesteryl cervonate. The accumulated CE in stimulated-Y animals was primarily comprised of cholesteryl adrenate, cholesteryl arachidonate and cholesteryl oleate. (c) Whereas in stimulated-Y rats adrenal apoE concentration declined, the concentration in stimulated O animals was well maintained. (d) In vitro, adrenal homogenate or cytosolic fraction from stimulated-O rats displayed a higher capacity to hydrolyze exogenous CE than its Y counterpart. However, cholesterol esterification with external fatty acid substrates in adrenal homogenate or microsomal fraction was comparable in the two age-groups. Our findings revealed altered adrenocortical cholesterol reserve in O rats to cope with prolonged ACTH-stimulation. Changes in apoE levels and CE hydrolysis activity may be factors associated with this alteration. Depletion and accumulation of adrenocortical CE are reflected in parallel changes in cholesteryl adrenate and cholesteryl arachidonate, suggesting physiologic importance of these polyunsaturated fatty acids during sustained steroidogenesis.