2000
DOI: 10.1006/bbrc.2000.2902
|View full text |Cite
|
Sign up to set email alerts
|

Induction of Cytochrome P450 (CYP)1A1, CYP1A2, and CYP3A4 but Not of CYP2C9, CYP2C19, Multidrug Resistance (MDR-1) and Multidrug Resistance Associated Protein (MRP-1) by Prototypical Inducers in Human Hepatocytes

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

4
58
2

Year Published

2002
2002
2009
2009

Publication Types

Select...
7
2

Relationship

0
9

Authors

Journals

citations
Cited by 105 publications
(67 citation statements)
references
References 32 publications
4
58
2
Order By: Relevance
“…Yet in human primary hepatocytes, PB treatment had no effect on MDR1 (Runge et al, 2000). Results presented here also show no significant changes in rat mdr1a or mdr1b mRNA levels upon in vivo treatment with PB.…”
Section: Brady Et Alcontrasting
confidence: 43%
See 1 more Smart Citation
“…Yet in human primary hepatocytes, PB treatment had no effect on MDR1 (Runge et al, 2000). Results presented here also show no significant changes in rat mdr1a or mdr1b mRNA levels upon in vivo treatment with PB.…”
Section: Brady Et Alcontrasting
confidence: 43%
“…However, in primary human hepatocytes from two donors, Runge et al (2000) did not see an increase in MDR1 protein with rifampin treatment. Whereas the report of Synold et al (2001) indicates that rifampicin causes a moderate induction of hepatic MDR1 gene expression in primary human hepatocytes.…”
Section: Brady Et Almentioning
confidence: 70%
“…Human AE cells also expressed genes involved in drug metabolism, such as CYP 2C9, CYP 2D6, and CYP 3A4. It is necessary to investigate whether hAE cells possess drug metabolizing activity (e.g., testosterone-6β-hydroxylase activity of CYP3A4-expressing cells (Runge et al, 2000)). …”
Section: Discussionmentioning
confidence: 99%
“…A major disadvantage is the lack of available material, which is mainly donated by patients with liver resections due to cancer. to counter this deficiency the long-term and serum-free cultivation of human hepatocytes was improved, mainly by adaptation of the culture medium (Runge et al, 1999;Runge et al, 2000;Ferrini et al, 1997). the generated HHMM (Human Hepatocyte Maintenance Medium) maintains human hepatocytes in a dif-of CYP450 proteins and other liver specific functions depend more on cell-cell than on cell-matrix contacts (Hamilton et al, 2001;Isom et al, 1984).…”
Section: Introductionmentioning
confidence: 99%