Gender‐related differences in bile acid and sterol metabolism in outbred CD‐1 mice fed low‐ and high‐cholesterol diets

Stephen D. Turley, Margrit Schwarz, David K. Spady, John M. Dietschy – 30 December 2003 – These studies were undertaken to determine whether in young adult outbred CD‐1 mice there were any gender‐related differences in basal bile acid metabolism that might be important in determining how males and females in this species responded to a dietary cholesterol challenge. When fed a plain cereal‐based rodent diet without added cholesterol, 3‐month‐old females, compared with age‐matched males, manifested a significantly larger bile acid pool (89.1 vs.

Increased risk of chronic liver failure in adults with heterozygous α‐antitrypsin deficiency

Ivo W. Graziadei, Jacob J. Joseph, Russell H. Wiesner, Terry M. Therneau, Kenneth P. Batts, Michael K. Porayko – 30 December 2003 – Controversy exists whether patients who are genetically heterozygous for α1 ‐antitrypsin deficiency (α1 ATD), carrying a single PI*Z allele, are at increased risk of developing chronic liver disease. In these investigations, we determined the prevalence of heterozygous α1 AT phenotypes (PI MZ, PI SZ) in a well‐characterized cohort of patients presenting with chronic liver failure before orthotopic liver transplantation (OLT).

Effects of propranolol on the hepatic hemodynamic response to physical exercise in patients with cirrhosis

Juan‐Carlos Bandi, Joan Carles García‐Pagán, Angels Escorsell, Erik François, Eduardo Moitinho, Joan Rodés, Jaume Bosch – 30 December 2003 – Physical exercise increases portal pressure (hepatic venous pressure gradient [HVPG]) in patients with cirrhosis. It is unknown if this deleterious effect is associated with changes in gastroesophageal collateral blood flow and if these can be prevented by propranolol administration. The aim of this study was to characterize the effects of propranolol on the splanchnic hemodynamic response to exercise in patients with cirrhosis.

Regulation of cyclin G1 during murine hepatic regeneration following dipin‐induced DNA damage

Michael Rugaard Jensen, Valentina M. Factor, Snorri S. Thorgeirsson – 30 December 2003 – Cyclin G1 has been linked to both positive and negative growth regulation. The expression of cyclin G1 is induced by transforming growth factor β1and p53, as well as by multiple mitogenic stimuli in mammalian cells in culture. However, the physiological role of cyclin G1 remains unclear. To examine the cell‐cycle regulation of cyclin G1 in vivo, two models of coordinated cell proliferation induced by partial hepatectomy (PH) in the presence or absence of DNA damage were used.

Transformation‐dependent susceptibility of rat hepatic stellate cells to apoptosis induced by soluble fas ligand

WenRong Gong, Adali Pecci, Sylke Roth, Birgit Lahme, Miguel Beato, Axel M. Gressner – 30 December 2003 – Cytokine‐driven activation of hepatic stellate cells (HSC) in tissue injury and inflammation is a key pathogenetic event in liver fibrogenesis leading to an expanded pool of matrix producing myofibroblasts (MFB) which represent the transformed counterpart of HSC. We hypothesize that expansion of the pool of MFB might also be accomplished by modulation of apoptosis, which plays an opposite and complementary role to mitosis in the cellular homeostasis.

Infiltrating CD45RC− T cells are associated with immunologic unresponsiveness induced by donor class I major histocompatibility complex antigens in rats

Yasuo Yamaguchi, Nobutomo Miyanari, Osamu Ichiguchi, Eiji Akizuki, Fujio Matsumura, Teishi Matsuda, Kazutoshi Okabe, Jian Liang, Hajime Ohshiro, Katsutaka Mori, Michio Ogawa – 30 December 2003 – It has previously been shown that a single intravenous injection of freshly heparinized donor‐specific blood transfusion (DST) before transplantation significantly prolongs the survival of fully allogeneic ACI (RT1a)‐to‐LEW(RT11) rat hepatic allografts.

Flumazenil for hepatic encephalopathy grade III and IVa in patients with cirrhosis: An italian multicenter double‐blind, placebo‐controlled, cross‐over study

Giuseppe Barbaro, Gabriella Di Lorenzo, Maurizio Soldini, Giuseppe Giancaspro, Giorgio Bellomo, Giancarlo Belloni, Benvenuto Grisorio, Mauro Annese, Donato Bacca, Ruggiero Francavilla, Giorgio Barbarini – 30 December 2003 – The rationale for use of benzodiazepine receptor antagonists is based on the so‐called benzodiazepine pathogenetic hypothesis of hepatic encephalopathy (HE).

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