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dc.contributor.authorLawal, AOen_US
dc.contributor.authorMarnewick, Jeanine Len_US
dc.contributor.authorEllis, EMen_US
dc.identifier.citationLawal, AO, Marnewick JL & Ellis EM. 2015. Heme oxygenase-1 attenuates cadmiuminduced mitochondrial-caspase 3- dependent apoptosis in human hepatoma cell line. BMC Pharmacology and Toxicology, 16:41 DOI 10.1186/s40360-015-0040-yen_US
dc.description.abstractBackground: Cadmium (Cd) is a well known environmental and industrial toxicant causing damaging effects in numerous organs. In this study, we examined the role of heme oxygenase-1 (HO-1) in modulating the Cd-induced apoptosis in human hepatoma (HepG2) cells after 24 h exposure. Methods: HepG2 cells were exposed to 5 and 10 μM Cd as CdCl2 for 24 h while other sets of cells weren pre-treated with either 10 μM Cobalt protoporphyrin (CoPPIX) or 10 μM Tin protoporphyrin (SnPPIX) for 24 h, or 50 μM Z-DEVD-FMK for 1 h before exposure to 5 and 10 μM CdCl2 for 24 h. Expressions of caspase 3, cytosolic cytochrome c, mitochondrial Bax and anti-apoptotic BCL-xl proteins were assessed by western blot. Intracellular reactive oxygen species (ROS) production was determined using the dihydrofluorescein diacetate (H2DFA) method. Cell viability was assessed by MTT assay, while a flow cytometry method was used to assess the level of apoptosis in the cell populations. Results: Our results show that there were a significant increase in the expression of cytosolic cytochrome c, mitochondrial Bax protein, and caspase 3 at 5 and 10 μM compared to the control, but these increases were attenuated by the presence of CoPPIX. The presence of SnPPIX significantly enhanced Cd-induced caspase 3 activities. CoPPIX significantly decreased the level of ROS production by 24.6 and 22.2 % in 5 and 10 μM CdCl2, respectively, but SnPPIX caused a significant increase in ROS production in the presence of CdCl2. HepG2 cell viability was also significantly impaired by 13.89 and 32.53 % in the presence of 5 and 10 μM CdCl2, respectively, but the presence of CoPPIX and Z-DEVD-FMK significantly enhanced cell survival, while SnPPIX enhanced Cd-impaired cell viability. The presence of CoPPIX and Z-DEVD-FMK also significantly decreased the population of apoptotic and necrotic cells compared with Cd. Conclusion: In summary, the present study showed that HO-1 attenuates the Cd-induced caspase 3 dependent pathway of apoptosis in HepG2 cells, probably by modulating Cd-induced oxidative stress.en_US
dc.description.sponsorshipCommonwealth Scholarship, UK.en_US
dc.relation.ispartofBMC Pharmacology and Toxicologyen_US
dc.subjectHeme oxygenase-1en_US
dc.subjectCytochrome cen_US
dc.subjectHuman hepatoma cellsen_US
dc.titleHeme oxygenase-1 attenuates cadmiuminduced mitochondrial-caspase 3- dependent apoptosis in human hepatoma cell lineen_US
Appears in Collections:HWSci - Journal Articles (DHET subsidised)
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