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(The FASEB Journal. 2003;17:993-1002.)
© 2003 FASEB

Recovery of hepatocellular ATP and "pericentral apoptosis" after hemorrhage and resuscitation

MARKUS PAXIAN*, INGE BAUER*, HAUKE RENSING*, HARTMUT JAESCHKE{ddagger}, ANGELIKA E. M. MAUTES#, STEFAN A. KOLB{dagger}, BEATE WOLF*, ANDRE STOCKHAUSEN*, SILKE JEBLICK* and MICHAEL BAUER*,1

* Department of Anesthesiology and Critical Care Medicine, University of the Saarland, D-66421 Homburg, Germany;
# Neurosurgical Research Laboratory, University of the Saarland, D-66421 Homburg, Germany;
{ddagger} Department of Pharmacology and Toxicology, University of Arkansas for Medical Science, Little Rock, Arkansas, USA; and
{dagger} Department of Pathology, University Hospital Zürich, Zürich, Switzerland

1Correspondence: Department of Anesthesiology and Critical Care Medicine, University of the Saarland, D-66421 Homburg, Germany. E-mail: aimbau{at}uniklinik-saarland.de

Progressive liver dysfunction contributes significantly to the development of multiple organ failure after trauma/hemorrhage. This study tested the relative impact of necrotic and apoptotic cell death in a graded model of hemorrhagic shock (mean arterial blood pressure=35±5 mmHg for 1, 2, or 3 h, followed by 2 h, 1 h, or no resuscitation, respectively) in rats. Prolonged periods of hemorrhagic hypotension (3 h) were paralleled by a profound decrease of hepatic ATP levels and occurrence of pericentral necrosis. Resuscitation after shorter periods of hemorrhagic hypotension resulted in restoration of tissue ATP whereas hepatocellular function as assessed by indocyanine green clearance remained depressed (49.9±1.6 mL/(min·kg) at baseline, 28.8±1.2 mL/(min·kg) after 2 h of resuscitation; P<0.05). Under these conditions, induction of caspase activity and DNA fragmentation were observed in pericentral hepatocytes that could be prevented by the radical scavenger tempol. Pretreatment with z-Val-Ala-Asp(O-methyl)-flouromethylketone prevented de novo expression of caspase-generated cytokeratin 18, DNA fragmentation, and depression of hepatocellular indocyanine green clearance. These data suggest that prolonged low flow/hypoxia induces ATP depletion and pericentral necrosis and restoration of oxygen supply and ATP levels after shorter periods of low flow ischemia propagate programmed cell death or "pericentral apoptosis."—Paxian, M., Bauer, I., Rensing, H., Jaeschke, H., Mautes, A. E. M., Kolb, S. A., Wolf, B., Stockhausen, A., Jeblick, S., Bauer, M. Recovery of hepatocellular ATP and "pericentral apoptosis" after hemorrhage and resuscitation.


Key Words: necrosis • apoptosis • necrapoptosis • liver • ATP • oxygen free radicals




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