Korean J Intern Med.  2011 Sep;26(3):314-319. 10.3904/kjim.2011.26.3.314.

Cyclosporin A Inhibits Albumin Synthesis in Huh7 Cells

Affiliations
  • 1Bupyoung Internal Medicine Clinic, Incheon, Korea.
  • 2Division of Nephrology, Department of Internal Medicine, The Catholic University of Korea School of Medicine, Seoul, Korea. kimcmc@catholic.ac.kr

Abstract

BACKGROUND/AIMS
Hypoalbuminemia occurs frequently in renal transplant recipients immediately after renal transplantation. We studied the regulation of hepatic albumin synthesis by cyclosporin A (CsA) in Huh7 cells.
METHODS
Huh7 cells were incubated with various concentrations of CsA for 4, 8, 16, and 24 hours. Albumin was measured in Huh7 cell-conditioned medium by sandwich enzyme-linked immunosorbent assay and Western blot. Albumin mRNA expression was analyzed by Northern blotting in CsA-treated cells.
RESULTS
CsA (10(-7)-10(-4) M) inhibited albumin synthesis in Huh7 cells in a dose- dependent manner. A Western blot analysis for albumin in the conditioned medium released from CsA-treated (10(-7)-10(-5) M) cells also showed significant inhibition of albumin synthesis in a dose-dependent manner. Vehicle (olive oil) did not affect albumin synthesis. In contrast, a Northern blot analysis revealed no inhibition of albumin mRNA expression by CsA at any time point from 1-24 hours, indicating that the inhibition of albumin synthesis occurred at the translational level.
CONCLUSIONS
Our results suggest that inhibition of hepatic albumin synthesis by high dose CsA contributes to the hypoalbuminemia in renal transplant recipients.

Keyword

Cyclosporin A; Albumins; Kidney transplantation; Hypoalbuminemia

MeSH Terms

Blotting, Northern
Blotting, Western
Carcinoma, Hepatocellular/genetics/*metabolism
Cell Line, Tumor
Cell Survival/drug effects
Culture Media, Conditioned/metabolism
Cyclosporine/*pharmacology/toxicity
Dose-Response Relationship, Drug
Enzyme-Linked Immunosorbent Assay
Gene Expression Regulation, Neoplastic/drug effects
Humans
Hypoalbuminemia/chemically induced/metabolism
Immunosuppressive Agents/*pharmacology/toxicity
Liver Neoplasms/genetics/*metabolism
RNA, Messenger/metabolism
Serum Albumin/genetics/*metabolism
Time Factors
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