Plasma carnitine kinetics during orthotopic liver transplantation.

BACKGROUND Carnitine is synthesized mainly in the liver and plays an essential role in the transport of fatty acids in liver mitochondria for subsequent oxidation and energy production. METHODS The plasma concentrations of free carnitine, acylcarnitine, total ketone bodies, lactate, pyruvate, and hepatocyte growth factor (HGF) were measured during liver transplantation. RESULTS The plasma free carnitine and acylcarnitine concentrations and the lactate to pyruvate ratio in patients with compromised grafts (group A) were significantly higher than those in patients with well-functioning grafts (group B) after reperfusion. The acylcarnitine concentration in group B decreased after incision, but it remained at a high level in group A. Significant correlations were found between the concentrations of HGF and free and acylcarnitine after reperfusion. CONCLUSION The accelerated flux of carnitine in the graft may be associated with deterioration of energy metabolism in the graft. An increased acylcarnitine concentration may reflect impaired liver regeneration.

[1]  S. Hirono,et al.  Clinical significance of serum hepatocyte growth factor in orthotopic liver transplantation. , 1996, Surgery.

[2]  H. Lai,et al.  Alterations of remnant liver carnitine palmitoyltransferase I activity and serum carnitine concentration after partial hepatectomy in rats. , 1995, The Journal of surgical research.

[3]  S. Lindstedt,et al.  Impaired ketogenesis in carnitine depletion caused by short-term administration of pivalic acid prodrug. , 1994, Biochemical medicine and metabolic biology.

[4]  J. Farber,et al.  Cyclosporin and carnitine prevent the anoxic death of cultured hepatocytes by inhibiting the mitochondrial permeability transition. , 1993, The Journal of biological chemistry.

[5]  Y. Yamaoka,et al.  ARTERIAL KETONE BODY RATIO AND GLUCOSE ADMINISTRATION AS AN ENERGY SUBSTRATE IN RELATION TO CHANGES IN KETONE BODY CONCENTRATION AFTER LIVING‐RELATED LIVER TRANSPLANTATION IN CHILDREN , 1993, Transplantation.

[6]  Y. Yamaoka,et al.  Changes in energy substrates in relation to arterial ketone body ratio after human orthotopic liver transplantation. , 1993, Surgery.

[7]  H. Bismuth,et al.  Impact of glycogen content of the donor liver in clinical liver transplantation. , 1993, Transplantation proceedings.

[8]  S. Hirono,et al.  Prediction of outcome in fulminant hepatic failure by serum human hepatocyte growth factor , 1992, The Lancet.

[9]  Y. Yamaoka,et al.  Evaluation of ketogenesis in seriously reduced hepatic mitochondrial redox state. An analysis of survivors and non-survivors in critically ill hepatectomized patients. , 1992, Scandinavian journal of gastroenterology.

[10]  Cooper Cs The met oncogene: from detection by transfection to transmembrane receptor for hepatocyte growth factor. , 1992, Oncogene.

[11]  Z. Zadák,et al.  Liver regeneration in partially hepatectomized rats infused with carnitine and lipids. , 1992, Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie.

[12]  J. Larsson,et al.  Availability of energy substrates during liver regeneration in malnourished rats. , 1991, Scandinavian journal of gastroenterology.

[13]  M. Castagneto,et al.  Intraoperative trends of oxygen consumption and blood lactate as predictors of primary dysfunction after liver transplantation. , 1991, Transplantation proceedings.

[14]  T. Starzl,et al.  The clinical significance of the arterial ketone body ratio as an early indicator of graft viability in human liver transplantation. , 1991, Transplantation.

[15]  G. Kispál,et al.  Surplus acylcarnitines in the plasma of starved rats derive from the liver. , 1990, The Journal of biological chemistry.

[16]  T. Sugimoto,et al.  Effect of L-carnitine on glycogen synthesis and ATP production in cultured hepatocytes of the newborn rat. , 1989, The Journal of nutrition.

[17]  E. Lebenthal,et al.  Quantitation of urinary carnitine esters in a patient with medium-chain acyl-coenzyme A dehydrogenase deficiency: effect of metabolic state and L-carnitine therapy. , 1989, The Journal of pediatrics.

[18]  S. Grisolía,et al.  Effect of L-carnitine on ketone bodies, redox state and free amino acids in the liver of hyperammonemic mice. , 1987, Biochemical pharmacology.

[19]  O. Stenqvist,et al.  Rapid indication of allograft function in liver transplantation. , 1987, Transplantation proceedings.

[20]  Z. Akcetin,et al.  Ketogenic effects of low and high levels of carnitine during total parenteral nutrition in the rat. , 1987, The American journal of clinical nutrition.

[21]  C. Stanley New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency. , 1987, Advances in pediatrics.

[22]  C. Rebouche,et al.  Kinetic compartmental analysis of carnitine metabolism in the human carnitine deficiency syndromes. Evidence for alterations in tissue carnitine transport. , 1984, The Journal of clinical investigation.

[23]  T. Nakatani Changes in the energy substrate after hepatectomy--preferential utilization of fatty acids and its effect on hepatic regeneration after major hepatectomy. , 1982, Nihon geka hokan. Archiv fur japanische Chirurgie.

[24]  Y. Kamiyama,et al.  Changes in predominant energy substrate after hepatectomy. , 1981, Life sciences.

[25]  C. Rebouche,et al.  Tissue distribution of carnitine biosynthetic enzymes in man. , 1980, Biochimica et biophysica acta.

[26]  J. Holm,et al.  γ‐Butyrobetaine hydroxylase activity in human and ovine liver and skeletal muscle tissue , 1979 .

[27]  J. McIntosh,et al.  Turnover of carnitine by rat tissues. , 1975, The Biochemical journal.

[28]  T. Bøhmer Conversion of butyrobetaine to carnitine in the rat in vivo. , 1974, Biochimica et biophysica acta.

[29]  S. Lindstedt,et al.  A method for the determination of carnitine in the picomole range. , 1972, Clinica chimica acta; international journal of clinical chemistry.

[30]  J. Šimek,et al.  Effect of Glucose administered in vivo or in vitro on the Respiratory Quotient of Rat Liver Tissue after Partial Hepatectomy , 1965, Nature.