PUBLICATION
Toxicity and cardiac effects of acute exposure to tryptophan metabolites on the kynurenine pathway in early developing zebrafish (Danio rerio) embryos
- Authors
- Majewski, M., Kasica, N., Jakimiuk, A., Podlasz, P.
- ID
- ZDB-PUB-180111-4
- Date
- 2018
- Source
- Toxicology and applied pharmacology 341: 16-29 (Journal)
- Registered Authors
- Jakimiuk, Anna, Kasica, Natalia, Podlasz, Piotr
- Keywords
- Anthranilic acid, Cinnabarinic acid, Kynurenic acid, Nicotinic acid, Picolinic acid, Xanthurenic acid
- MeSH Terms
-
- Animals
- Dose-Response Relationship, Drug
- Embryonic Development/drug effects*
- Embryonic Development/physiology*
- Heart Rate/drug effects*
- Heart Rate/physiology*
- Kynurenine/metabolism*
- Kynurenine/toxicity
- Signal Transduction/physiology
- Tryptophan/metabolism*
- Tryptophan/toxicity
- Zebrafish
- PubMed
- 29317240 Full text @ Tox. App. Pharmacol.
Citation
Majewski, M., Kasica, N., Jakimiuk, A., Podlasz, P. (2018) Toxicity and cardiac effects of acute exposure to tryptophan metabolites on the kynurenine pathway in early developing zebrafish (Danio rerio) embryos. Toxicology and applied pharmacology. 341:16-29.
Abstract
Defects in tryptophan metabolism on the l-kynurenine pathway (KP) are implicated in a number of human diseases, including chronic kidney disease, brain edema or injury, tuberculosis and malaria - as well as cancer, neurodegenerative and autoimmune disorders. However, it is unclear to what extent detrimental effects of exposure to tryptophan metabolites might impact the early development of organism. Thus, this study examined the effects of KP exposure in zebrafish embryos starting at the blastula period (4hpf) and the segmentation stage (24hpf). 24-hour EC50 and LC50 values were determined in 4hpf embryos as: 26.74 and 331.6μM for anthranilic acid (AA), 62.88 and 616.4μM for quinolinic acid (QUIN), and EC50 - 96.10μM for picolinic acid (PA) and LC50 - 400μM in kynurenic acid (KYNA). In addition, treatment with nanomolar concentrations of KYNA (50nM, 48 and 72hpf embryos) caused a dose-dependent increase in heartbeat. The increase was also seen with l-kyn treatment (50μM, 72hpf), which was the opposite of other applied l-kyn metabolites. A significant drop in heartbeat was observed after a 20-min acute exposure to 626μM PA, 594μM XA and 499μM QUIN, and complete recovery was seen only when PA had been removed. Concentrations of KP metabolites reached in people with different pathological conditions did not exert toxicity to zebrafish embryos and seems to be safe for developing embryos and therefore, the risk of developing impairments in pregnancy of women carrying KP-associated pathologies is initially low.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping