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Published on: May 29, 2020
Fipronil induces CYP isoforms and cytotoxicity in human hepatocytes
Parikshit C Das1, Yan Cao, Nathan Cherrington
1Department of Environmental and Molecular Toxicology, North Carolina State University, Raleigh, NC 27695-7633, USA.
Abstract:
Recent studies have demonstrated the potential of pesticides to either inhibit or induce xenobiotic metabolizing enzymes in humans. Exposure of human hepatocytes to doses of fipronil (5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl) sulfinyl]-1H-pyrazole-3-carbonitrile) ranging from 0.1 to 25 microM resulted in a dose dependent increase in CYP1A1 mRNA expression (3.5 to approximately 55-fold) as measured by the branched DNA assay. In a similar manner, CYP3A4 mRNA expression was also induced (10-30-fold), although at the higher doses induction returned to near control levels. CYP2B6 and 3A5 were also induced by fipronil, although at lower levels (2-3-fold). Confirmation of bDNA results were sought through western blotting and/or enzyme activity assays. Western blots using CYP3A4 antibody demonstrated a dose responsive increase from 0.5 to 1 microM followed by decreasing responses at higher concentrations. Similar increases and decreases were observed in CYP3A4-specific activity levels as measured using 6beta-hydroxytestosterone formation following incubation with testosterone. Likewise, activity levels for a CYP1A1-specific substrate, luciferin CEE, demonstrated that CYP1A1 enzyme activities were maximally induced by 1 microM fipronil followed by dramatically declining activity measurements at 10 and 25 microM. Cytotoxic effects of fipronil and fipronil sulfone were examined using the adenylate kinase and the trypan blue exclusion assays in HepG2 cells and human hepatocytes. The results indicate both that HepG2 cells and primary human hepatocytes are sensitive to the cytotoxic effects of fipronil. The maximum induction of adenylate kinase was ca. 3-fold greater than the respective controls in HepG2 and 6-10-fold in the case of primary hepatocytes. A significant time- and dose-dependent induction of adenylate kinase activity in HepG2 cells was noted from 0.1 to 12.5 microM fipronil followed by decreasing activities at 25 and 50 microM. For fipronil sulfone, cytotoxic effects increased throughout the dose range. The trypan blue assay indicated that cytotoxic effects contributing to an increase of greater than 10% of control values was indicated at doses above 12.5 microM. However, fipronil sulfone induced cytotoxic effects at lower doses. The possibility that cytotoxic effects were due to apoptosis was indicated by significant time- and dose-dependent induction of caspase-3/7 activity in both HepG2 cells and human hepatocytes. Fipronil mediated activation of caspase-3/7 in concurrence with compromised ATP production and viability are attributed to apoptotic cell death.
Insights
Fipronil pesticide exposure significantly increases human CYP1A1 and CYP3A4 enzyme expression, but can also cause cytotoxic and apoptotic effects in liver cells. Further research is needed to understand fipronil
Area of Science:
- Toxicology
- Enzymology
- Cell Biology
Background:
- Pesticides can modulate human xenobiotic metabolizing enzymes.
- Fipronil is a widely used insecticide with potential human health implications.
Purpose of the Study:
- To investigate the effects of fipronil on xenobiotic metabolizing enzymes in human hepatocytes.
- To assess the cytotoxic effects of fipronil and its metabolite, fipronil sulfone, in liver cells.
Main Methods:
- Human hepatocytes and HepG2 cells were exposed to varying doses of fipronil.
- Enzyme expression and activity were measured using branched DNA assays, Western blotting, and enzyme activity assays.
- Cytotoxicity was assessed using adenylate kinase and trypan blue exclusion assays.
- Apoptosis was evaluated by measuring caspase-3/7 activity.
Main Results:
- Fipronil dose-dependently induced CYP1A1, CYP3A4, CYP2B6, and CYP3A5 mRNA expression.
- Enzyme activity assays confirmed increased CYP1A1 and CYP3A4 activity at lower fipronil concentrations, with decreased activity at higher doses.
- Fipronil and fipronil sulfone exhibited cytotoxic effects in both HepG2 cells and primary human hepatocytes.
- Apoptosis was indicated by the induction of caspase-3/7 activity.
Conclusions:
- Fipronil can induce key drug-metabolizing enzymes in human liver cells, potentially altering drug metabolism.
- Fipronil and its metabolite demonstrate significant cytotoxicity and induce apoptosis in hepatocytes.
- The findings highlight the need for further investigation into the toxicological risks associated with fipronil exposure.
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