Horm Metab Res 1983; 15(10): 508-512
DOI: 10.1055/s-2007-1018770
© Georg Thieme Verlag, Stuttgart · New York

Cortisol 21-Mesylate Exerts Glucocorticoid Action on the Induction of Milk Protein Synthesis in Cultured Mammary Gland

N. Terada, T. Oka
  • Section on Intermediary Metabolism, Laboratory of Biochemistry and Metabolism, NIADDK, National Institute of Health, Bethesda, Maryland, U.S.A.
Further Information

Publication History

1982

1982

Publication Date:
14 March 2008 (online)

Summary

Cortisol 21-mesylate, an alkylating derivative of cortisol, was previously shown to exert an anti-glucocorticoid action in rat hepatoma cell culture (Simons, Thompson and Johnson 1980). In this study the effect of cortisol 21-mesylate on milk protein synthesis induced in cultured mouse mammary gland by glucocorticoid, insulin, and prolactin was investigated. Addition of cortisol 21-mesylate at concentrations ranging from 10-8M to 10-6M produced no inhibition of casein synthesis that was induced by glucocorticoid, insulin and prolactin in mammary explants from midpregnant mice. On the other hand, cortisol 21-mesylate in combination with insulin and prolactin stimulated casein synthesis in cultured tissue. The potency of cortisol mesylate was about 1/10 to 1/30th of that of cortisol. Cortisol 21-mesylate, like cortisol, also augmented the accumulation of α-lactalbumin in midpregnant rat mammary tissue cultured in the presence of insulin and prolactin. A cell-free competition study of glucocorticoid receptors using cytoplasmic extracts from mouse mammary tissue showed that cortisol 21-mesylate competitively inhibited the binding of dexamethasone to glucocorticoid receptors. The apparent affinity of cortisol 21-mesylate for glucocorticoid receptors is about 1/10th of that of cortisol. These results indicate that cortisol 21-mesylate acts as a glucocorticoid but not as an antiglucocorticoid in the mammary gland.