Adrenal steroidogenic actions of cyclic nucleotide derivatives in the rat

• Published in: Endocrinology (Philadelphia) Vol. 100; no. 5; p. 1287
• Main Authors: Free, C A, Paik, V S
• Format: Journal Article
• Language: English
• Published: United States 01.05.1977
• Subjects: Adrenal Glands - drug effects; Adrenal Glands - metabolism; Adrenocorticotropic Hormone - pharmacology; Animals; Betamethasone - pharmacology; Blood Glucose - metabolism; Corticosterone - biosynthesis; Cyclic AMP - analogs & derivatives; Cyclic AMP - pharmacology; Cyclic GMP - analogs & derivatives; Cyclic GMP - pharmacology; Glycerol - blood; Hypophysectomy; Male; Nucleotides, Cyclic - pharmacology; Protein Kinases - metabolism; Rats
• ISSN: 0013-7227
• DOI: 10.1210/endo-100-5-1287

Fifteen 3',5'-cyclic nucleotides and related compounds were studied for ability to mimic the steroidogenic action of ACTH in rats in which secretion of ACTH and corticosterone were suppressed by treatment with betamethasone, or by hypophysectomy. Subcutaneous administration of 8-chloro-cAMP, at doses of 40 mg/kg or greater, elicited the secretion of corticosterone to normal plasma levels in both betamethasone-treated and hypophysectomized animals. Cyclic AMP, dbcAMP, 8-methylthio-cAMP, 8-hydroxy-cAMP and the 6-chloro-8-aminopurine cyclic ribotide analog of cAMP also displayed steroidogenic activity in the betamethasone-treated rat; cGMP, 8-bromo-cGMP and 8-benzylthio-cGMP were inactive. Each of the steroidogenic derivatives of cAMP also displayed ability to activate steroidogenesis in isolated rat adrenal cells. These experiments demonstrate that various derivatives of cAMP mimic the adrenal steroidogenic action of ACTH, in vivo. Structure-activity comparisons support a steroidogenic mechanism involving direct activation by the nucleotides of cAMP-dependent protein kinase of the adrenal cortex.