Skip to main content
Log in

Effect of cyclosporine on hepatic cytosolic estrogen and androgen receptor levels before and after partial hepatectomy

  • Original Articles
  • Published:
Digestive Diseases and Sciences Aims and scope Submit manuscript

Abstract

Estrogen and androgen receptors within the liver have been reported to modulate the hepatic regenerative response to partial hepatectomy. Moreover, cyclosporine has several untoward effects that might occur as a consequence of alterations in sex hormone activity. To evaluate these questions the following experiments were performed. Estrogen and androgen receptors in cytosol were quantitated in livers of rats treated with cyclosporine or olive oil vehicle before and after partial hepatectomy or a sham operation. Ornithine decarboxylase activity and thymidine kinase activity were assessed as indices of hepatic regeneration. Preoperative levels of estrogen receptor activity in the hepatic cytosol were significantly greater in rats treated with cyclosporine as compared to vehicle treated controls (P<0.01). In contrast, preoperative levels of androgen receptor activity in the cyclosporine-treated and vehicle-treated animals were similar. Following partial hepatectomy, a reduction in the activity of both sex hormone receptors in the hepatic cytosol was observed and was compatible with results described previously in normal animals. Unexpectedly the preoperative levels of ornithine decarboxylase (P<0.01) and thymidine kinase activity (P<0.01) were significantly greater in the rats treated with cyclosporine as compared to the vehicle treated controls. As expected, ornithine decarboxylase activity (at 6 hr) and thymidine kinase activity (at 24 hr) rose and peaked in response to a partial hepatectomy but were significantly greater (P<0.05) in the rats treated with cyclosporine as compared to the vehicle. These results show that cyclosporine treatment causes an increase in the hepatic content of estrogen receptor activity that is associated with an enhanced potential for a regenerative response. These effects of cyclosporine treatment on the sex hormone receptor levels in liver may explain the mechanisms responsible for some of the untoward effects of treatment with this agent.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Eagon PK, Porter LE, Francavilla A, Di Leo A, Van Thiel DH: Estrogen and androgen receptors in the liver: Their role in liver disease and regeneration. Semin Liver Dis 5:59–69, 1985

    PubMed  Google Scholar 

  2. Bardin CW, Catteral JS: Testosterone: A major determinant of extragenital sexual dimorphism. Science 211:1285–1294, 1981

    PubMed  Google Scholar 

  3. Gustafsson JA, Mode A, Norstedt G, Skett P: Sex steroid induced changes in hepatic enzymes. Annu Rev Physiol 45:51–60, 1983

    PubMed  Google Scholar 

  4. Roy AK, Chatterjee B: Sexual dimorphism in the liver. Annu Rev Physiol 45:37–50, 1983

    PubMed  Google Scholar 

  5. Francavilla A, Eagon PK, DiLeo A, Polimeno L, Panella C, Aquilino AM, Ingrosso M, Van Thiel DH, Starzl TE: Sex hormone related functions in regenerating male rat liver. Gastroenterology 91:1263–1270, 1986

    PubMed  Google Scholar 

  6. Starzl TE, Iwatsuki S, Van Thiel DH, et al: Evolution of liver transplantation. Hepatology 2:614–636, 1982

    PubMed  Google Scholar 

  7. Kahn D, Makowka L, Gavaler JS, Starzl TE, Van Thiel DH: The outcome after clinical liver transplantation is influenced by the gender of the donor. Hepatology (in press)

  8. Calne RY, White DJ, Thisu S, et al: Cyclosporin A in patients receiving renal allografts from cadaver donors. Lancet ii:1323–1327, 1978

    Google Scholar 

  9. Higgins GM, Anderson RM: Experimental pathology of the liver: Restoration of the liver of the white rat following surgical removal. Arch Pathol 12:186–201, 1931

    Google Scholar 

  10. Eagon PK, Fisher SE, Imhoff AF, et al: Estrogen-binding proteins of male rat liver: Influences of hormonal changes. Arch Biochem Biophys 201:486–499, 1980

    PubMed  Google Scholar 

  11. McGowan JA, Fausto A: Ornithine decarboxylase activity and the onset of deoxyribonucleic acid synthesis in regenerating liver. Biochem J 170:123–127, 1978

    PubMed  Google Scholar 

  12. Kahn D, Stadler J, Terblanche J, Van Hoorn-Hickman R: Thymidine kinase: An inexpensive index of liver regeneration in a large animal model. Gastroenterology 79:907–911, 1980

    PubMed  Google Scholar 

  13. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ: Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275, 1951

    PubMed  Google Scholar 

  14. Fisher B, Gunduz N, Saffer EA, Zheng S: Relation of estrogen and its receptor to rat liver growth and regeneration. Cancer Res 44:2410–2415, 1984

    PubMed  Google Scholar 

  15. Van Thiel DH, Gavaler JS, Kam I, et al: Rapid growth of an intact human liver transplant into a recipient larger than the donor. Gastroenterology 93:1414–1419, 1987

    PubMed  Google Scholar 

  16. Kam I, Lynch S, Svanas G, et al: Evidence that host size determines liver size: Studies in dogs receiving orthotopic liver transplants. Hepatology 7:362–366, 1987

    PubMed  Google Scholar 

  17. Salizzori M, Yandza T, Goyet JV, Tan KC, Kestens PJ, Otte JB: Indication, technique and results of liver graft volume reduction before orthotopic liver transplantation in children. Transplant Proc 5:3549–3551, 1987

    Google Scholar 

  18. Francavilla A, DiLeo A, Eagon PK, Wu SA, Ove R, Van Thiel DH, Starzl TE: Regenerating rat liver: Correlations between estrogen receptor localization and deoxyribonucleic acid synthesis. Gastroenterology 86:552–557, 1984

    PubMed  Google Scholar 

  19. Baum JK, Holtz F, Bookstein JJ, Klein EW: Possible association between benign hepatomas and oral contraceptives. Lancet ii:926–929, 1973

    Google Scholar 

  20. Klatskin G: Hepatic tumors: Possible relationship to use of oral contraceptives. Gastroenterology 73:386–394, 1977

    PubMed  Google Scholar 

  21. Stoll BA, Andrews JT, Matterun R: Liver damage from oral contraceptives. Br Med J 1:960–961, 1966

    Google Scholar 

  22. Kern F Jr: Effect of estrogens on the liver. Gastroenterology 75:512–522, 1978

    Google Scholar 

  23. Bennion LJ, Ginsberg RL, Garnick MB, Bennett PH: Effects of oral contraceptives on the gallbladder bile of normal women. N Engl J Med 294:189–192, 1976

    PubMed  Google Scholar 

  24. Hoyumpa AM, Schiff L, Helfman EL: Budd-Chiari syndrome in women taking oral contraceptives. Am J Med 50:137–140, 1971

    PubMed  Google Scholar 

  25. Porter LE, Elm MS, Van Thiel DH, Eagon PK: Estrogen receptor in human liver nuclei. Hepatology 4:1085, 1984

    Google Scholar 

  26. Chamness GC, Castlow ME, McGuire WL: Estrogen receptor in rat liver and its dependence on prolactin. Steroids 26:363–371, 1975

    PubMed  Google Scholar 

  27. Cardon SB, Larson DF, Russell DH: Rapid elevation of rat serum prolactin concentration by cyclosporine, a novel immunosuppressive drug. Biochem Biophys Res Commun 120:614, 1984

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported by research grants from the Veterans Administration project grant AM 29961, and from the NIDDK AM 32556, and from the NIAAA AA06601.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kahn, D., Gavaler, J.S., Lai, H. et al. Effect of cyclosporine on hepatic cytosolic estrogen and androgen receptor levels before and after partial hepatectomy. Digest Dis Sci 35, 6–11 (1990). https://doi.org/10.1007/BF01537215

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01537215

Key words

Navigation