Can adenine nucleotides predict primary nonfunction of the human liver homograft?

Transpl Int. 1994;7(2):89-95. doi: 10.1007/BF00336468.

Abstract

Sixty-eight primary liver grafts were analyzed to see whether adenine nucleotides (AN: ATP, ADP, and AMP) or purine catabolites (PC: adenosine, inosine, hypoxanthine, and xanthine) of tissue or effluent can predict primary graft nonfunction. AN, PC, and nicotinamide adenine dinucleotide, oxidized form (NAD+) of the tissue before (pretransplant) and after graft reperfusion (post-transplant) and of the effluent were analyzed. The graft outcome was classified into two groups (group A: successful, n = 64; group B: primary nonfunctioning, n = 4). No significant differences were observed in pretransplant measurements between groups A and B, whereas ATP, ADP, total AN, total AN + total PC (T) and NAD+, in post-transplant tissues, were significantly higher in group A. Xanthine in the effluent was significantly higher in group B than in group A. ATP, ADP, total AN, T, and NAD+ in post-transplant tissue were significantly associated with primary graft nonfunction by logistic regression analysis.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenine Nucleotides / metabolism*
  • Adolescent
  • Adult
  • Aged
  • Chromatography, High Pressure Liquid
  • Female
  • Graft Rejection / diagnosis*
  • Graft Rejection / physiopathology
  • Graft Survival
  • Humans
  • Liver Transplantation / physiology*
  • Male
  • Middle Aged
  • NAD / metabolism
  • Purines / metabolism
  • Transplantation, Homologous

Substances

  • Adenine Nucleotides
  • Purines
  • NAD