Use of laser auto-fluorescence for evaluating liver grafts

✍ Scribed by A. K. Sankarankutty; O. Castro e Silva Jr.; J. Ferreira; M. E. J. Souza; M. C. Gomes; C. Kurachi; V. S. Bagnato

• Publisher: John Wiley and Sons
• Year: 2006
• Tongue: English
• Weight: 182 KB
• Volume: 3
• Category: Article
• ISSN: 1612-2011
• DOI: 10.1002/lapl.200610051

✦ Synopsis

There has been an increasing demand for liver transplantation, while the supply of liver grafts remains limited. Strategies to augment the donor pool include "liver-splitting", "domino" procedure, Living-related liver transplantation and the use of marginal donors. Simultaneously, there has been growing interest in Laser-induced fluorescence (LIF) as a diagnostic tool, mainly in oncology. The basis of all optical spectroscopic techniques is that physiological, morphological or biochemical changes associated with physical disorders, affect the interaction between light and tissue. The aim of this experimental study was to analyze the applicability of LIF in evaluating liver grafts, in rats. In this experiment, the animals were divided into two groups according to the temperature of the perfusion medium. The perfusion medium used was saline solution between 0-4 • C in one group (CS group) and the same solution, between 22-26 • C, in the other group (RT group). Mitochondrial respiratory capacity, swelling and membrane potential along with the cellular ATP content were used as the functional and metabolic indicators of viability. The Cluster-Russia fluorescence spectroscopy system was used to analyze the LIF. Deterioration of mitochondrial function and ATP content occurred progressively and relatively rapidly. LIF reflected the findings of the mitochondrial respiratory control ratio in the CS group, but not in the RT group. The ratio of the intensity of fluorescence detected at 636 nm and 600 nm showed rapid change 5 to 6 hours after perfusion in the CS group. Therefore LIF shows great potential as an auxiliary tool in the analysis of liver grafts, for transplantation.

12