نتایج جستجو برای: cholestatic rat

تعداد نتایج: 277745  

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2015
Takeshi Susukida Shuichi Sekine Mayuka Nozaki Mayuko Tokizono Kousei Ito

Drug-induced liver injury (DILI) is of concern to the pharmaceutical industry, and reliable preclinical screens are required. Previously, we established an in vitro bile acid-dependent hepatotoxicity assay that mimics cholestatic DILI in vivo. Here, we confirmed that this assay can predict cholestatic DILI in clinical situations by comparing in vitro cytotoxicity data with in vivo risk. For 38 ...

Journal: :Journal of lipid research 1991
R J Sokol M Devereaux R A Khandwala

To assess whether lipid peroxidation of hepatic mitochondria is associated with cholestatic hepatic injury we examined the effect of bile duct ligation (BDL) versus sham surgery on mitochondrial lipids of rats maintained on one of seven diets. Diets included vitamin E-deficient (E-) and vitamin E-sufficient (E+) combined with normal lipid (11.9% calories as stripped corn oil), high lipid (35% c...

Journal: :Gastroenterology 1995
C M Rodríguez-Ortigosa I Vesperinas C Qian J Quiroga J F Medina J Prieto

BACKGROUND/AIMS Cysteinyl-containing leukotrienes seem to exert a cholestatic effect. However, leukotriene inhibitors were found to reduce bile salt efflux in isolated rat hepatocytes, suggesting a role for leukotrienes in bile flow formation. METHODS In the isolated rat liver, the effects of two different concentrations of leukotriene C4 on bile flow and bile salt excretion are analyzed, as ...

2013
Monika Szabo Zsuzsa Veres Zsolt Baranyai Ferenc Jakab Katalin Jemnitz

Human hepatocytes are the gold standard for toxicological studies but they have several drawbacks, like scarce availability, high inter-individual variability, a short lifetime, which limits their applicability. The aim of our investigations was to determine, whether HepaRG cells could replace human hepatocytes in uptake experiments for toxicity studies. HepaRG is a hepatoma cell line with most...

2017
Yun Bin Lee Jong Ho Choi Eun Nam Kim Jin Seok Hyun-Jung Lee Jung-Hwan Yoon Gi Jin Kim

In cholestatic liver diseases, impaired bile excretion disrupts lipid homeostasis. We investigated changes of lipid metabolism, including mitochondrial β-oxidation, in a rat model of bile duct ligation (BDL) in which chorionic plate-derived mesenchymal stem cells (CP-MSCs) were transplanted. Serum cholesterol level, which was elevated after BDL, was significantly decreased following CP-MSC tran...

Journal: :The Journal of clinical investigation 1989
G Fricker L Landmann P J Meier

To elucidate the consequences of extrahepatic cholestasis on the structure and function of hepatocytes, we studied the effects of bile duct ligation on the turnover, surface distribution, and functional activity of the canalicular 100-kD bile salt transport protein (cBSTP). Basolateral (blLPM) and canalicular (cLPM) liver plasma membrane vesicles were purified to the same degree from normal and...

Journal: :American journal of physiology. Gastrointestinal and liver physiology 2008
Giuseppe Calamita Domenico Ferri Patrizia Gena Flavia I Carreras Giuseppa E Liquori Piero Portincasa Raúl A Marinelli Maria Svelto

Rat hepatocytes express aquaporin-9 (AQP9), a basolateral channel permeable to water, glycerol, and other small neutral solutes. Although liver AQP9 is known for mediating the uptake of sinusoidal blood glycerol, its relevance in bile secretion physiology and pathophysiology remains elusive. Here, we evaluated whether defective expression of AQP9 is associated to secretory dysfunction of rat he...

Journal: :Toxicology and applied pharmacology 2014
Sagnik Chatterjee Lysiane Richert Patrick Augustijns Pieter Annaert

Early detection of drug-induced cholestasis remains a challenge during drug development. We have developed and validated a biorelevant sandwich-cultured hepatocytes- (SCH) based model that can identify compounds causing cholestasis by altering bile acid disposition. Human and rat SCH were exposed (24-48h) to known cholestatic and/or hepatotoxic compounds, in the presence or in the absence of a ...

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