PUBLICATION
Simvastatin effects on detoxification mechanisms in Danio rerio embryos
- Authors
- Cunha, V., Santos, M.M., Moradas-Ferreira, P., Ferreira, M.
- ID
- ZDB-PUB-160405-5
- Date
- 2016
- Source
- Environmental science and pollution research international 23(11): 10615-29 (Journal)
- Registered Authors
- Ferreira, Miguel Godinho, Santos, Manuel
- Keywords
- ABC transporters, Antioxidant enzymes, Biotransformation, Phase I and II, Simvastatin, Zebrafish embryos
- MeSH Terms
-
- ATP-Binding Cassette Transporters/metabolism*
- Animals
- Embryo, Nonmammalian/drug effects*
- Inactivation, Metabolic/drug effects*
- Oxidative Stress/drug effects*
- Simvastatin/toxicity*
- Zebrafish
- PubMed
- 27040680 Full text @ Environ. Sci. Pollut. Res. Int.
Citation
Cunha, V., Santos, M.M., Moradas-Ferreira, P., Ferreira, M. (2016) Simvastatin effects on detoxification mechanisms in Danio rerio embryos. Environmental science and pollution research international. 23(11):10615-29.
Abstract
The transcription and protein activity of defence mechanisms such as ABC transporters, phase I and II of cellular detoxification and antioxidant enzymes can be altered in the presence of emerging contaminants such as pharmaceuticals impacting the overall detoxification mechanism. The present work aimed to characterise the effects of simvastatin on the detoxification mechanisms of embryonic stages of Danio rerio. In a first approach, constitutive transcription of key genes involved in detoxification was determined. Embryos were collected at different developmental stages, and transcription patterns of genes coding for ABC transporters, phase I and II and oxidative stress were analysed. With exception of abcc2, all genes seem to be from maternal transfer (0-2 hpf). Embryos were then exposed to different concentrations of simvastatin (5 and 50 μg/L), verapamil and MK571 (10 μM; ABC protein inhibitors) and a combination of simvastatin and ABC inhibitors. mRNA expression levels of abcb4, abcc1, abcc2, abcg2, cyp1a, cyp3a65, gst, sod, cat was evaluated. Accumulation assays to measure ABC proteins activity and activity of EROD, GST, CAT and Cu/ZnSOD, were also undertaken. Simvastatin acted as a weak inhibitor of ABC proteins and increased EROD and GST activity, whereas Cu/ZnSOD and CAT activity were decreased. Simvastatin up-regulated abcb4 and cyp3a65 transcription (both concentrations), as well as abcc1 and abcc2 at 50 μg/L, and down-regulated gst, sod, cat at 5 μg/L. In conclusion, our data revealed the interaction of simvastatin with detoxification mechanisms highlighting the importance of monitoring the presence of this emerging contaminant in aquatic environments.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping