Ziv Ben‐Ari, Amar P. Dhillon, Redwan Moqbel, Linda Garwood, David Booth, Keith Rolles, Brian Davidson, Andrew K. Burroughs – 1 January 1996 – There has been recent interest in eosinophils as a histological diagnostic marker of liver allograft rejection. However, the reliability of counting eosinophils in sections stained with hematoxylin and eosin (H&E) has not been evaluated previously. We quantified eosinophils in 10 day‐5 protocol liver biopsy specimens in 10 patients.

Eelco F. M. Wijdicks, Paola R. Blue, Jeffery L. Steers, Russell H. Wiesner – 1 January 1996 – Central pontine myelinolysis (CPM) after orthotopic liver transplantation is frequently diagnosed at autopsy. Its actual prevalence is unknown. We reviewed 386 orthotopic liver transplantations performed at the Mayo Clinic, Rochester, MN, including 39 with autopsy reports. CPM developed in four patients (1%) (found using magnetic resonance imaging in two, at autopsy in two).

Joél Pitre, Olivier Soubrane, Bertrand Dousset, Yves Ozier, François Baudin, Denis Devictor, Olivier Bernard, Didier Houssin, Yves Chapuis – 1 January 1996 – Multiple‐organ failure (MOF), defined as the failure of initially uninvolved organs, is the final step of definitive and massive liver necrosis. Emergency liver transplantation (ELT) has radically modified the outcome of acute liver failure and early primary graft failure, but the results of ELT in cases of MOF are unknown. From May 1988 to June 1993, 243 patients underwent a liver transplantation (LT).

T F Baumert, T J Liang – 1 January 1996

V Arroyo, P Ginès, A L Gerbes, F J Dudley, P Gentilini, G Laffi, T B Reynolds, H Ring‐Larsen, J Schölmerich – 1 January 1996

J Geraldo, P Ferraz, J L Wallace – 1 January 1996 – Cirrhotic rats have an increased susceptibility to ethanol‐induced gastric injury, related to an inability to mount a defensive gastric hyperemic response to luminal irritants, and associated with an impaired reactivity of the gastric microcirculation to nitric oxide (NO)/cyclic guanosine monophosphate (cGMP)‐dependent vasodilators. Whether this hyporesponsiveness is in some way related to depressed prostaglandin synthesis by the stomach of cirrhotic rats is not clear.

F B Kasravi, L Wang, X Wang, G Molin, S Bengmark, B Jeppsson – 1 January 1996 – Acute liver injury is associated with a high rate of infectious and septic complications. Most of these infections are produced by gram negative enteric bacteria. We evaluated bacterial translocation, intestinal permeability, blood flow, portal pressure, and intestinal microflora after induction of liver injury and 70% liver resection in the rat.

A Y Howe, M J Robins, J S Wilson, D L Tyrrell – 1 January 1996 – Hepatitis B virus (HBV) replication is mediated by the viral polymerase that possesses three functional domains: primer, DNA polymerase/reverse transcriptase, and RNase H. Using the Pekin duck as an animal model, we demonstrate a novel mechanism of inhibition of duck hepatitis B virus (DHBV) by 2,6‐diaminopurine 2′,3′‐dideoxyriboside (ddDAPR), a prodrug of 2′,3′‐dideoxyguanosine (ddG).

L Frost, J Mahoney, J Field, G C Farrell – 1 January 1996 – To characterize the early events in liver injury produced by halothane, experiments were performed in genetically susceptible guinea pigs 19 hours after halothane exposure. Serum bile acid concentrations were fourfold increased in halothane‐exposed animals compared with controls. In isolated perfused liver experiments, livers from halothane‐exposed animals did not differ in hepatic oxygen uptake or in perfusion pressure at the end of experiments, but bile flow and biliary bile salt concentrations were reduced.

F Lin, C M Noyer, Q Ye, J Courvalin, H J Worman – 1 January 1996 – Autoantibodies from rare patients with primary biliary cirrhosis (PBC) recognize LBR, or lamin B receptor, an integral membrane protein of the inner nuclear membrane. Human LBR has a nucleoplasmic, amino‐terminal domain of 208 amino acids followed by a carboxyl‐terminal domain with eight putative transmembrane segments. Autoantibodies against LBR from four patients with PBC recognized the nucleoplasmic, amino‐terminal domain but not the carboxyl‐terminal domain.