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The isolated perfused porcine liver: assessment of viability during and after six hours of perfusion
Authors:M. Adham  Simone Peyrol  Michèle Chevallier  Christian Ducerf  Michèle Vernet  Christine Barakat  Eric De La Roche  Abderrahmane Taibi  Thierry Bizollon  Dominic Rigal  Michel Pouyet  Jacques Baulieux
Affiliation:Department of Gastrointestinal Surgery and Liver Transplantation, H?pital de la Croix Rousse, 93, gde rue de la Croix Rousse, F-69317 Lyon Cedex 04, France Fax: + 33 4 72 07 18 97, FR
Department of Pathology, Institut Pasteur Lyon, France, FR
Department of Biochemistry, H?pital de la Croix Rousse, 93, gde rue de la Croix Rousse, F-69317 Lyon Cedex 04, France, FR
Department of Hematology, H?pital de la Croix Rousse, 93, gde rue de la Croix Rousse, F-69317 Lyon Cedex 04, France, FR
Department of Hepatology, H?pital de l'Hotel Dieu, Lyon, France, FR
établissement de Transfusion Sanguine de Lyon, France, FR
Abstract:
Isolated liver perfusion was developed for the study of liver physiology and preservation. The recent development of new perfusion devices and appropriate liver preservation solutions prompted us to reconsider liver perfusion for the specific purpose of evaluating viability in terms of biochemical changes, paying special attention to modifications in the histological ultrastructure. Twenty-two isolated pig livers were perfused with autologous blood. Arterio-portal perfusions were carried out using an extracorporeal perfusion circuit with a hollow fibre membrane oxygenator. Four groups of pig livers were studied using three different liver flushing solutions [Ringer's lactate, ELOHES, and University of Wisconsin (UW)] and two different oxygenation modalities. Liver function tests and histological studies were done. Our results revealed that a high partial oxygen pressure (PO2) level was deleterious to the ultrastructural elements of hepatocytes, in particular to the mitochondria. It was also associated with deficient metabolic performance, i. e., poor bile production and lack of aerobic metabolism. Normal blood gas values could be obtained with the use of air for liver oxygenation. Flushing of the liver with Ringer's lactate or a macromolecular solution such as ELOHES was associated with severe liver cell injuries, as reflected by a marked rise in liver enzymes and histological lesions. Satisfactory results were obtained when UW solution was used for liver harvesting. We conclude that an appropriate liver preservation solution, normal blood gas values, and normal physiological arterio-portal pressure and blood flow are essential for appropriate liver function with preservation of liver architecture and of hepatocyte ultrastructures. Total bilirubin in bile and Factor V are sensitive indicators of good liver function. Received: 24 January 1997 Received after revision: 18 April 1997 Accepted: 24 April 1997
Keywords:Liver preservation  ex vivo perfusion  Preservation  ex vivo perfusion  liver  Ex vivo perfusion  liver  pig
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