Influence of paraesophageal venous collaterals on efficacy of endoscopic sclerotherapy for esophageal varices

Ching‐Yih Lin, Pin‐Wen Lin, Hong‐Ming Tsai, Xi‐Zhang Lin, Ting‐Tsung Chang, Jeng‐Shiann Shin – 1 March 1994 – To determine the diagnostic accuracy of computer tomography in the detection of venous collaterals surrounding the esophagus in patients with portal hypertension, preoperative computer tomography interpretations of these veins in 15 patients who were candidates for the Sugiura procedure for treatment of esophageal varices were correlated with those of the intraoperative assessment.

Just say “no” to viral hepatitis?

Raymond T. Chung – 1 March 1994 – Interferons (IFNs) induce antiviral activity in many cell types. The ability of IFN‐γ to inhibit replication of ectromelia, vaccinia, and herpes simplex‐1 viruses in mouse macrophages correlated with the cells' production of nitric oxide (NO). Viral replication was restored in IFN‐γ–treated macrophages exposed to inhibitors of NO synthase. Conversely, epithelial cells with no detectable NO synthesis restricted viral replication when transfected with a complementary DNA encoding inducible NO synthase or treated with organic compounds that generate NO.

Activin A and hepatocyte growth regulation

Raymond N. Dubois – 1 March 1994 – The present study was conducted to examine the effect of activin A on growth of rat hepatocytes. EGF induced a 10‐fold increase in DNA synthesis as assessed by [3H]thymidine incorporation in cultured hepatocytes. When activin A was added together with EGF, DNA synthesis induced by EGF was markedly inhibited. Inhibition was detected at a concentration of 10−10 M, and 5×10−9 M activin A almost completely blocked EGF‐mediated DNA synthesis. Similarly, activin A completely blocked DNA synthesis induced by hepatocyte growth factor/scatter factor.

Immunohistochemical study of hepatic fibrosis induced in rats by multiple galactosamine injections

A. Mieke Jonker, Freke W. J. Dijkhuis, Machiel J. Hardonk, Peter Moerkerk, Joop Ten Kate, Joris Grond – 1 March 1994 – Multiple injections of D‐galactosamine induce liver fibrosis and cirrhosis in rats. The purpose of this immunopathological study was to correlate inflammation and hepatic extracellular matrix remodeling after repeated administration of galactosamine. Rats were given 10, 20, 30, 40, 60, 80, 100 and 140 intraperitoneal injections of D‐galactosamine (500 mg/kg body wt, three times weekly). Controls received injections of saline solution.

Structure and localization of the IGFBP‐1 gene and its expression during liver regeneration

Jehyuk Lee, Linda Greenbaum, Barbara A. Haber, Deborah Nagle, Victoria Lee, Vashti Miles, Kenneth L. Mohn, Maja Bucan, Rebecca Taub – 1 March 1994 – Insulin‐like growth factor–binding protein‐1s are important modulators of the insulin‐like growth factors that may have both positive and negative effects on the ability of insulin‐like growth factors to stimulate cell growth. The IGFBP‐1 gene is one of the most highly induced immediate‐early genes after partial hepatectomy.

Predictive factors in ursodeoxycholic acid‐treated patients with primary biliary Cirrhosis: Role of serum markers of connective tissue

Renée E. Poupon, Beverley Balkau, Jérôme Guéchot, François Heintzmann – 1 March 1994 – The aim of this study was to define factors predictive of the onset of the terminal phase, defined by hyperbilirubinemia or the occurrence of a severe clinical complication, in patients with primary biliary cirrhosis treated with ursodeoxycholic acid. The 97 primary biliary cirrhosis patients in this study participated in a 2‐yr clinical trial.

Enhanced hepatic collagen type I mRNA expression into fat‐storing cells in a rodent model of hemochromatosis

Antonello Pietrangelo, Rossana Gualdi, Giovanna Casalgrandi, Albert Geerts, Pieter de Bleser, Giuliana Montosi, Ezio Ventura – 1 March 1994 – In recent years, identifying the hepatic cell type responsible for collagen synthesis in experimental models of postnecrotic or inflammatory fibrosis has been the subject of active investigation. In primary iron overload states, however, hepatic fibrosis and cirrhosis occur without accompanying necroinflammatory phenomena.

Fibrinogen assembly: Insights from chicken hepatocytes

Carole Oddoux, Gerd Grieninger – 1 March 1994 – In all vertebrate species studied, the complex, disulfide‐linked structure of fibrinogen is essentially the same: a hexamer assembled from three different subunits (Aα, Bß,γ)2. This study utilized species differences in fibrinogen subunit monomer pools to address the question of how these surplus subunit pools may affect the assembly process. We used a chicken model system in which Bß and γ‐subunits are present in excess, in contrast to the Aα and γ‐subunit surplus found in human model systems.

Inflammatory cytokines up‐regulate intercellular adhesion molecule‐1 expression on primary cultured mouse hepatocytes and T‐lymphocyte adhesion

Masahiko Morita, Yoshifumi Watanabe, Toshihiro Akaike – 1 February 1994 – We investigated the effect of inflammatory cytokines on the intercellular adhesion molecule‐1 expression on primary cultured murine hepatocytes. Tumor necrosis factor‐α, interferon‐γ and interleukin‐1α up‐regulated the intercellular adhesion molecule‐1 expression on hepatocytes in a dose‐dependent fashion; however, interleukin‐6 did not. On the basis of kinetic analysis, the expression level reached a peak 24 hr after stimulation, and both cycloheximide and actinomycin D inhibited the expression.

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