Multiple‐dose pharmacokinetics of rufloxacin in patients with cirrhosis

David R. Triger, Fernando Granai, Jocelyn Woodcock, Richard Wise, Bruno P. Imbimbo – 1 October 1993 – The multiple‐dose pharmacokinetics of rufloxacin were investigated in 13 patients with biopsy‐proven cirrhosis and in 5 healthy controls. Rufloxacin was administered once a day for 5 consecutive days, starting with a loading dose of 400 mg on day 1 and 200 mg on the subsequent days. Plasma and urinary drug concentrations were determined by high‐performance liquid chromatography and a microbiological assay.

Zonal distribution of protein‐acetaldehyde adducts in the liver of rats fed alcohol for long periods

Renee C. Lin, Feng C. Zhou, Michael J. Fillenwarth, Lawrence Lumeng – 1 October 1993 – Acetaldehyde, a highly reactive intermediate of alcohol metabolism, has been shown to form adducts with liver proteins in rats fed alcohol for long periods. In this report, the zonal distribution of liver proteinacetaldehyde adducts that formed in vivo was studied by means of histoimmunostaining. Rats were pair‐fed alcohol‐containing and alcohol‐free AIN'76 liquid diets for 2 or 11 wk before they were killed and subjected to whole body perfusion with paraformaldehyde.

Endothelins 1 and 3: Potent cholestatic agents secreted and excreted by the liver that interact with cyclosporine

Renata E. Bluhm, Marshall G. Frazer, Mary Vore, C. Wright Pinson, Kamal F. Badr – 1 October 1993 – Autoradiographic studies have shown that the liver accumulates endothelin. High‐affinity binding sites for endothelin have been identified on rat liver plasma membranes. We investigated the role of endothelin isopeptides as mediators of cholestasis with isolated rat liver perfused by a recirculating solution of buffer and blood.

Role of newly synthesized cholesterol or its metabolites on the regulation of bile acid biosynthesis after short‐term biliary diversion in the rat

Z. Reno Vlahcevic, William M. Pandak, Philip B. Hylemon, Douglas M. Heuman – 1 September 1993 – Cholesterol 7αhydroxylase, the rate‐limiting enzyme in the bile acid biosynthetic pathway, is thought to be regulated by hydrophobic bile acids through negative feedback control. The role of cholesterol in the regulation of cholesterol 7αhydroxylase is more controversial, in part because of incomplete understanding of the relationship between the pathways of cholesterol synthesis and degradation.

Amino acid transport and glutathione homeostasis: What is the mechanism for cysteine uptake from bile?

Mark E. Mailliard – 1 September 1993 – Transport of L‐cysteine and a cysteine S‐conjugate, S‐(1,2‐dichlorovinyl)‐L‐cysteine (DCVC) was investigated in rat liver canalicular plasma membrane (cLPM) vesicles. Cysteine uptake into an osmotically active intravesicular space was temperature sensitive and further enhanced by an inwardly directed Na+ gradient.

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