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Nevirapine induces apoptosis in liver (HepG2) cells
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Document Title
Nevirapine induces apoptosis in liver (HepG2) cells
Author
Wongtrakul J, Paemanee A, Wintachai P, Thepparit C, Roytrakul S, Thongtan T, Janphen K, Supparatpinyo K, Smith DR
Name from Authors Collection
Affiliations
Chiang Mai University; Mahidol University; National Science & Technology Development Agency - Thailand; National Center Genetic Engineering & Biotechnology (BIOTEC); Chulalongkorn University; Chiang Mai University
Type
Article
Source Title
ASIAN PACIFIC JOURNAL OF TROPICAL MEDICINE
Year
2016
Volume
9
Issue
6
Page
547-553
Open Access
gold
Publisher
ELSEVIER SCI LTD
DOI
10.1016/j.apjtm.2016.04.015
Format
Abstract
Objective: To generate insights into the mechanism of NVP induced hepatotoxicity. Methods: Liver (HepG2) cells were cultured with various concentrations of NVP. This cell line was chosen because it has low expression of cytochrome P450, allowing evaluation of the effects of NVP rather than specific metabolites. Cytotoxicity was determined using a proliferation assay and cell numbers were monitored using trypan blue exclusion assay for long term culture experiments and apoptosis induction was determined by morphological and biochemical investigation. Results: HepG2 cells treated with the highest concentration of NVP tested (819 mu M) initially showed a rounded morphology and all cells had died by week three of exposure. Nuclear condensation and fragmentation, increased Annexin V/propidium iodide staining and caspase 9 activation all supported the induction of apoptosis in HepG2 cells in response to NVP treatment. Conclusions: There is a clear induction of apoptosis in response to NVP which suggests that NVP has significant cytotoxicity, over and above any cytotoxicity of metabolites and may contribute directly to patient hepatotoxicity.
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Knowledge Taxonomy Level 1
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Knowledge Taxonomy Level 3
Funding Sponsor
National Research Council of Thailand (NRCT); Office of the Higher Education Commission; Chiang Mai University under the National Research Universities Initiative
License
CC-BY-NC-ND
Rights
Publisher
Publication Source
WOS