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The influence of liver dysfunction on cyclosporine pharmacokinetics —A comparison between 70 per cent hepatectomy and complete bile duct ligation in dogs—

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Abstract

The influence of experimentally induced hepatic dysfunction on the pharmacokinetics of Cyclosporine A (CsA) was determined in dogs. The pharmacokinetics of oral (PO) and intravenous (IV) CsA were studied before and after 70 per cent hepatectomy or complete bile duct ligation (CBDL). Changes in liver function were monitored by serial measurements of serum bilirubin, and by the maximum removal rate (Rmax) and plasma disappearance rate (ICG-K) of indocyanine green (ICG). Concentrations of CsA in whole blood were measured by HPLC. Seventy per cent hepatectomy caused significant liver dysfunction: the ICG-Rmax decreased by 47.7±7.1 per cent (mean±SD) and the ICG-K decreased by 61.3±9.7 per cent during the first week after hepatectomy. At the same time, the systemic clearance (CLs) of IV-CsA decreased by 43.9±8.2 per cent, the area under the concentration curve (AUC) of IV-CsA increased by 35.4±20.8 per cent and the bioavailability of CsA decreased by 26.4±14.8 per cent. CBDL also induced significant liver dysfunction: the ICG-Rmax decreased by 39.1±12.8 per cent and the ICG-K decreased by 65.6±3.6 per cent in the second week after the operation. During the same period, the AUC of PO-CsA decreased by 69.9±10.7 per cent and the bioavailability of CsA also decreased markedly by 73.9±15.6 per cent. These data indicate that hepatic impairment significantly influences the pharmacokinetics of CsA, not only by the changes in intestinal absorption, but also by those in hepatic, metabolism. Dose adjustment is therefore necessary in the presence of hepatic dysfunction in order to maintain an adequate blood concentration of CsA without causing side effects.

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References

  1. Kahan BD. Individualization of cyclosporine therapy using pharmacokinetic and pharmacodynamic parameters. Transplantation 1985; 40: 457–476.

    PubMed  CAS  Google Scholar 

  2. Sigel B. Partial hepatectomy in the dog. Arch Surg 1963; 87: 788–791.

    PubMed  CAS  Google Scholar 

  3. Price JB, Voorhees AB, Britton RC. Partial hepatic autotransplantation with complete revascularization in the dog. Arch Surg 1967; 95: 59–64.

    PubMed  Google Scholar 

  4. Sawchuk RJ, Cartier LL. Liquid-chromatographic determination of cyclosporine A in blood and plasma. Clin Chem 1981; 27: 1368–1371.

    PubMed  CAS  Google Scholar 

  5. Rikkers LF, Moody FG. Estimation of functional reserve of normal and regenerating dog livers. Surgery 1974; 75: 421–429.

    PubMed  CAS  Google Scholar 

  6. Mizumoto R, Kawarada Y, Yamawaki T, Noguchi T, Nishida S. Resectability and functional reserve of the liver with obstructive jaundice in dogs. Am J Surg 1979; 137: 768–772.

    Article  PubMed  CAS  Google Scholar 

  7. Paumgartner G, Probst P, Kraines R, Leevy CM. Kinetics of indocyanine green removal from the blood. Ann NY Acad Sci 1970; 170: 134–146.

    CAS  Google Scholar 

  8. Venkataramanan R, Starzl TE, Yang S, Burckart GJ, Ptachcinski RJ, Shaw BW, Iwatsuki S, Van Thiel DH, Sanghvi A, Seltman H. Transplant Proc 1985; 17: 286–289.

    Google Scholar 

  9. Follath F, Wenk M, Vozeh S, Thiel G, Brunner F, Loertscher R, Lemaire M, Nussbaumer K, Niederberger W, Wood. A Intravenous cyclosporine kinetics in renal failure. Clin Pharmaco Ther 1983; 34: 638–643.

    Article  CAS  Google Scholar 

  10. Burckart G, Starzl TE, Williams L, Sanghvi A, Gartner C, Venkataramanan R, Zitelli B, Malatack J, Urbach A, Diven W, Ptachcinski R, Shaw B, Iwatsuki S. Cyclosporine monitoring and pharmacokinetics in pediatric liver transplant patients. Transplant Proc 1985; 17: 1172–1175.

    PubMed  Google Scholar 

  11. Starzl TE, Iwatsuki S, Shaw BW, Gordon RD. Orthotopic liver transplantation in 1984. Transplant Proc 1985; 17: 250–259.

    Google Scholar 

  12. Yee GC, Kennedy MS, Storb R, Thomas ED. Pharmacokinetics of intravenous cyclosporine in bone marrow transplant patients. Transplantation 1984; 38: 511–513.

    PubMed  CAS  Google Scholar 

  13. Hows JM, Chipping PM, Smith SF, Baughan SA, Gordon-Smith EC. Nephrotoxicity in bone marrow transplant recipients treated with cyclosporine A. Br J Hematol 1983; 54: 69–78.

    CAS  Google Scholar 

  14. Teranaka M, Schenk WG. Hepatic blood flow measurement and electromagnetic techniques in normal and abnormal flow states in the dog. Ann Surg 1977; 185: 58–63.

    PubMed  CAS  Google Scholar 

  15. Cherrick GR, Stein SW, Leevy CM, Davidson CS. Indocyanine green: Observations on its physical properties, plasma decay, and hepatic extraction. J Clin Invest 1959; 39: 592–600.

    Article  Google Scholar 

  16. Barbier F, Weerdt GA. Chromatography and I.R. spectrography of indocyanine green. Clin Chem Acta 1964; 10: 549–554.

    Article  CAS  Google Scholar 

  17. Sendama I, Hemptinne B, Lambotte L. Recovery of liver function in partially hepatectomized rats evaluated by aminopyrine demethylation capacity. Hepatology 1985; 5: 629–633.

    PubMed  CAS  Google Scholar 

  18. Buice RG, Gurley BJ, Stentz FB, Sidhu P, McClellan T, Williams JW. Cyclosporine disposition in the dog. Transplantation 1985; 40: 483–488.

    PubMed  CAS  Google Scholar 

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This research was performed in the Department of Surgery, University of Pittsburgh Health Center, University of Pittsburgh, USA

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Takaya, S., Iwatsuki, S., Noguchi, T. et al. The influence of liver dysfunction on cyclosporine pharmacokinetics —A comparison between 70 per cent hepatectomy and complete bile duct ligation in dogs—. The Japanese Journal of Surgery 19, 49–56 (1989). https://doi.org/10.1007/BF02471566

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