PUBLICATION
Effects of acetyl L-carnitine on zebrafish embryos: Phenotypic and gene expression studies
- Authors
- Gu, Q., Ali, S.F., Kanungo, J.
- ID
- ZDB-PUB-200722-3
- Date
- 2020
- Source
- Journal of applied toxicology : JAT 41(2): 256-264 (Journal)
- Registered Authors
- Keywords
- PCR array, acetyl L-carnitine, developmental toxicity, reactive oxygen species (ROS), zebrafish
- MeSH Terms
-
- Acetylcarnitine/toxicity*
- Animals
- Antioxidants/toxicity*
- Embryo, Nonmammalian/drug effects*
- Embryonic Development/drug effects*
- Genetic Variation
- Genotype
- Phenotype
- Zebrafish/genetics*
- Zebrafish/growth & development*
- PubMed
- 32691447 Full text @ J. Appl. Toxicol.
Citation
Gu, Q., Ali, S.F., Kanungo, J. (2020) Effects of acetyl L-carnitine on zebrafish embryos: Phenotypic and gene expression studies. Journal of applied toxicology : JAT. 41(2):256-264.
Abstract
Acetyl L-carnitine (ALCAR), a dietary supplement and an antioxidant, plays a vital role in the bioenergetic process that produces ATP. Although there are reports on antioxidant toxicity, there is no information on the potential toxicity of ALCAR. Here, using zebrafish embryos, we explored whether ALCAR modulated ATP synthesis, generation of reactive oxygen species (ROS) and expression of specific genes related to major signaling pathways that control metabolism, growth, differentiation, apoptosis and oxidative stress. First, we show that ALCAR elicits a physiologic response, as ATP levels increased after ALCAR treatment. Simultaneously, an increase in the expression of ROS, a by-product of ATP synthesis, was observed in the ALCAR-treated embryos. Consistent with higher ROS expression, the level of cysteine, a precursor of glutathione, was significantly reduced. ALCAR did not have any drastic effect on overall development and heart rate. Polymerase chain reaction-based gene expression array analyses showed no significant change in the expression of 83 genes related to 10 major signaling pathways including: the transforming growth factor β (TGFβ), Wingless and Int-1 (Wnt), nuclear factor κ-light-chain-enhancer of activated B cells (NF-κB), Janus kinase/signal transducers and activators of transcription (JAK/STAT), p53, Notch, Hedgehog, Peroxisome proliferator-activated receptor (PPAR), oxidative stress, and hypoxia pathways. Our results show that the expression of 83 genes related to these major signaling pathways did not change significantly.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping