Excretion of F2‐isoprostanes in bile: A novel index of hepatic lipid peroxidation

Joseph A. Awad, Jason D. Morrow – 1 September 1995 – Lipid peroxidation is believed to be an important mechanism of liver injury caused by some xenobiotics. However, it has been difficult to demonstrate and quantify this process in vivo. Moreover, little is known about the disposition of lipids oxidized in the liver. F2‐isoprostanes are prostanoids produced by nonenzymatic free radical‐catalyzed peroxidation of arachidonic acid esterified to phospholipids. Hydrolysis of F2‐isoprostanes from phospholipids by phospholipases yields free F2‐isoprostanes.

Coexpression of liver‐specific and growth‐induced genes in perinatal and regenerating liver: Attainment and maintenance of the differentiated state during rapid proliferation

Barbara Haber, Leyla Naji, Drew Chessman, Rebecca Taub – 1 September 1995 – The liver shows maximal cellular growth during fetal development and after partial hepatectomy. Exploring overlaps in gene expression patterns in these two types of hepatic growth may provide insight into common regulatory pathways. The expression of a large number of growth‐induced and liver‐specific genes induced in liver regeneration has been examined in the perinatal liver from several days prenatal to 4 weeks postnatal when the major growth phase of the liver ceases.

N‐ethyl‐tauroursodeoxycholic acid, a novel deconjugation‐resistant bile salt analogue: Effects of acute feeding in the rat

Mario Angelico, Andrea Mangiameli, Alessandra Nistri, Leonardo Baiocchi, Mara Sofia, Mario Maina, Mario Di Martino, Adriano Blasi – 1 September 1995 – The purpose of this study was to investigate the physicochemical/biological properties and the effects of acute administration of N‐ethyl‐tauroursodeoxycholic acid in bile‐fistula rats. In vitro determination of high‐performance liquid chromatography mobility, octanol/water partitioning, cholesterol solubilizing capacity, and sensitivity to enzyme deconjugation by bacteria and cholylglycine‐hydroxylase were performed.

A randomized, double‐blind, placebo‐controlled trial of ursodeoxycholic acid in primary biliary cirrhosis

Burton Combes, Robert L. Carithers, Willis C. Maddrey, Danyu Lin, Mary F. McDonald, Donald E. Wheeler, Edwin H. Eigenbrodt, Santiago J. Muñoz, Raphael Rubin, Guadalupe Garcia‐Tsao, Gregory F. Bonner, Alexander B. West, James L. Boyer, Velimir A. Luketic, Mitchell L. Shiffman, A. Scott Mills, Marion G. Peters, Heather M. White, Rowen K. Zetterman, Stephen S. Rossi, Alan F. Hofmann, Rodney S. Markin – 1 September 1995 – One hundred fifty‐one patients with primary biliary cirrhosis (PBC) grouped into four strata based on entry serum bilirubin (<2 mg/dL vs.

Hepatic ischemia‐reperfusion injury modification during liver surgery in rats: Pretreatment with nifedipine or misoprostol

Kenneth J. Hardy, Somsit Tancheroen, Arthur Shulkes – 1 September 1995 – The aim of the study was to determine if pretreatment with misoprostol (a prostaglandin analogue) or nifedipine (a calcium antagonist), known protectants of the whole liver, would ameliorate the ischemia‐reperfusion injury (IRI) of resected liver associated with vascular occlusion.

Centrilobular necrosis after orthotopic liver transplantation: A longitudinal clinicopathologic study in 71 patients

Bruno Turlin, Gabriella I. Slapak, Karen M. Hayllar, Nigel Heaton, Roger Williams, Bernard Portmann – 1 September 1995 – Centrilobular necrosis (CLN) is a histological finding often encountered after orthotopic liver transplantation, but its pathogenesis is still unknown. In this study, the significance of CLN was assessed in a series of 227 consecutive liver transplantations performed between January 1989, and December 1991. Seventy‐one patients (30.9%) showed CLN on at least one biopsy result, which were obtained because of an increase of aspartate aminotransferase activity.

Processing of endoplasmic reticulum luminal antigens associated with halothane hepatitis in rat hepatocytes

Hamid R. Amouzadeh, Lance R. Pohl – 1 September 1995 – In this study we have investigated the mechanism of the processing of trifluoroacetylated liver microsomal protein antigens associated with halothane hepatitis to learn how the immune system might come in contact with these proteins to form antibodies directed against them. Rats were treated with halothane and parenchymal (PC) and non‐parenchymal cells (NPC) were isolated 16 hours later.

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