Download e-book for kindle: Hepatotoxicity: From Genomics to In Vitro and In Vivo Models by Saura C. Sahu

By Saura C. Sahu

ISBN-10: 0470057165

ISBN-13: 9780470057162

ISBN-10: 0470516747

ISBN-13: 9780470516744

This publication addresses the entire present, up to date advancements during this clinical self-discipline. Liver is the executive metabolizing web site within the physique, and hence, it's a significant objective organ for drug and chemical toxicity. accordingly, hepatotoxicity is a vital endpoint within the safeguard overview of substances and chemical compounds. Contributions from best investigators in hepatotoxicity learn handle present advancements during this medical self-discipline and talk about use of present leading edge know-how similar to microarrays in hepatotoxicity hence offering a greater knowing of hepatotoxins, their interactions and mechanisms of motion. This useful authoritative resource of data is the 1st e-book to deal with this subject for almost ten years, making it a vital source for readers from a variety of disciplines similar to toxicology, pharmacology, hepatology, drug toxicity and nutrients technology.

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Extra resources for Hepatotoxicity: From Genomics to In Vitro and In Vivo Models

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Ten ml of diluted Percoll (30 vol %) were placed in the bottom of each tube and centrifuged at 1100 × g for 5 min. The pellets were washed with Williams E at 30 × g for 2 min and then resuspended in 20 ml Williams E solution. Viability of the isolated hepatocytes used in these studies was typically greater than 90 %. 35 mg/ml) to a final cell density of 4 × 105 cells/ml and plated in 12 (1 ml) or 6 (2 ml) well plates, as previously indicated for rat hepatocytes (Davila and Morris, 1999). 3 Cell Culture Treatment Hepatocytes were treated for two consecutive days at 24 h and 48 h after initial plating with optimal concentrations of phenobarbital, PB (100 μM), rifampicin, RIF (10 μM), 3-methylcholanthrene, 3MC (1 μM), clofibrate, CLO (50 μM), tamoxifen (TAM, 10 μM), omeprazole (OMZ, 20 μM), pregnenolone-16α-carbonitrile (PCN, 1 μM) and hydrocortisone (HC, 20 μM).

As a result, ultimate in vitro/in vivo correlation of these systems remains a challenge for their widespread use and adoption for assessing hepatotoxicity. 5 Other Cell Lines and Engineered Cellular Systems In addition to the cellular systems mentioned above, several other cell lines have been used, although not as widespread, to address mechanisms of hepatotoxicity. , 1997). Continued evaluation and testing of these cell lines will be a critical step for the acceptance of these as viable reagents to predict toxic events in the liver.

2005). Markers identified were mainly markers of early hepatic differentiation. , 2005). The lack of cytokeratin expression would suggest that the cells remained mesenchymal and did not fully differentiate into an epithelial cell type such as a parenchymal hepatocyte. , 2006). 2 Embryonic Stem Cell-Derived Hepatocytes It might seem that the derivation of hepatocytes from embryonic stem (ES) cells might be the major focus of researchers trying to generate hepatocytes from stem cells. However, this is not the case.

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Hepatotoxicity: From Genomics to In Vitro and In Vivo Models by Saura C. Sahu

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