Ketamine attenuates cytochrome p450 aromatase gene expression and estradiol-17beta levels in zebrafish early life stages
- Authors
- Trickler, W.J., Guo, X., Cuevas, E., Ali, S.F., Paule, M.G., and Kanungo, J.
- ID
- ZDB-PUB-130703-4
- Date
- 2014
- Source
- Journal of applied toxicology : JAT 34(5): 480-8 (Journal)
- Registered Authors
- Keywords
- ketamine, zebrafish, estradiol-17β, CYP aromatase, gene expression, testosterone
- MeSH Terms
-
- Animals
- Aromatase/genetics*
- Chromatography, High Pressure Liquid
- Embryo, Nonmammalian/drug effects*
- Embryo, Nonmammalian/enzymology
- Embryo, Nonmammalian/metabolism
- Estradiol/analysis*
- Gene Expression/drug effects*
- Ketamine/toxicity*
- Zebrafish/blood
- Zebrafish/embryology*
- Zebrafish/genetics
- Zebrafish Proteins/genetics*
- PubMed
- 23696345 Full text @ J. Appl. Toxicol.
- CTD
- 23696345
Ketamine, a dissociative anesthetic, is a noncompetitive antagonist of N-methyl-D-aspartate-type glutamate receptors. In rodents and non-human primates as well as in zebrafish embryos, ketamine has been shown to be neurotoxic. In cyclic female rats, ketamine has been shown to decrease serum estradiol-17β (E2) levels. E2 plays critical roles in neurodevelopment and neuroprotection. Cytochrome p450 (CYP) aromatase catalyzes E2 synthesis from androgens. Although ketamine down-regulates a number of CYP enzymes in rodents, its effect on the CYP aromatase (CYP19) is not known. Zebrafish have been used as a model system for examining mechanisms underlying drug effects. Here, using wild-type (WT) zebrafish (Danio rerio) embryos, we demonstrate that ketamine significantly reduced E2 levels compared with the control. However, the testosterone level was elevated in ketamine-treated embryos. These results are concordant with data from mammalian studies. Ketamine also attenuated the expression of the ovary form of CYP aromatase (cyp19a1a) at the transcriptional level but not the brain form of aromatase, cyp19a1b. Exogenous E2 potently induced the expression of cyp19a1b and vtg 1, both validated biomarkers of estrogenicity and endocrine disruption, but not cyp19a1a expression. Attenuation of activated ERK/MAPK levels, reportedly responsible for reduced human cyp19 transcription, was also observed in ketamine-treated embryos. These results suggest that reduced E2 levels in ketamine-treated embryos may have resulted from the suppression of cyp19a1a transcription. Published 2013. This article is a U.S. Government work and is in the public domain in the USA.