Literature DB >> 8597037

Cultured hepatocytes as investigational models for hepatic toxicity: practical applications in drug discovery and development.

R G Ulrich1, J A Bacon, C T Cramer, G W Peng, D K Petrella, R P Stryd, E L Sun.   

Abstract

Drugs can fail at any phase during discovery, preclinical or clinical development due to unacceptable levels of toxicity, and liver is commonly the principle target organ. Investigational toxicology methods, using appropriate models and hypotheses, can often resolve problems, identify toxic chemical substituents and salvage therapeutic discovery programs. While in vivo models are used to investigate hepatic drug effects in the context of toxicokinetics and systemic influences, cell culture models provide in vitro systems for investigating specific mechanisms in a precisely controlled environment. Using primary hepatocytes isolated from laboratory animals, we have explored several drug-induced hepatic disorders that surfaced during different phases of drug discovery and development. Additionally, the use of human hepatocytes has allowed us to address concerns for human exposure, examine human relevance of animal data, and provide perspective on problems encountered in clinical trials.

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Year:  1995        PMID: 8597037     DOI: 10.1016/0378-4274(95)03547-8

Source DB:  PubMed          Journal:  Toxicol Lett        ISSN: 0378-4274            Impact factor:   4.372


  5 in total

1.  Gene expression profiling of extracellular matrix as an effector of human hepatocyte phenotype in primary cell culture.

Authors:  Jeanine L Page; Mary C Johnson; Katy M Olsavsky; Steven C Strom; Helmut Zarbl; Curtis J Omiecinski
Journal:  Toxicol Sci       Date:  2007-02-27       Impact factor: 4.849

2.  Gene expression profiling and its practice in drug development.

Authors:  Murty V Chengalvala; Vargheese M Chennathukuzhi; Daniel S Johnston; Panayiotis E Stevis; Gregory S Kopf
Journal:  Curr Genomics       Date:  2007-06       Impact factor: 2.236

3.  A strategy for primary high throughput cytotoxicity screening in pharmaceutical toxicology.

Authors:  P J Bugelski; U Atif; S Molton; I Toeg; P G Lord; D G Morgan
Journal:  Pharm Res       Date:  2000-10       Impact factor: 4.200

4.  Harnessing endogenous signals from hepatocytes using a low volume multi-well plate.

Authors:  Pantea Gheibi; Kyung Jin Son; Gulnaz Stybayeva; Alexander Revzin
Journal:  Integr Biol (Camb)       Date:  2017-05-22       Impact factor: 2.192

5.  Induction of lacZ mutations in MutaMouse primary hepatocytes.

Authors:  Guosheng Chen; John Gingerich; Lynda Soper; George R Douglas; Paul A White
Journal:  Environ Mol Mutagen       Date:  2010-05       Impact factor: 3.216

  5 in total

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