PUBLICATION
Protective effects of 24-epibrassinolide against the 6-OHDA zebrafish model of Parkinson's disease
- Authors
- Gomes, A., Monteiro, S.M., Venâncio, C., Félix, L.
- ID
- ZDB-PUB-230413-53
- Date
- 2023
- Source
- Comparative biochemistry and physiology. Toxicology & pharmacology : CBP 269: 109630 (Journal)
- Registered Authors
- Keywords
- 6-OHDA, Behaviour, Epibrassinolide, Oxidative stress, Parkinson's disease, Zebrafish
- MeSH Terms
-
- Animals
- Brassinosteroids/pharmacology
- Oxidative Stress
- Oxidopamine/toxicity
- Parkinson Disease*/drug therapy
- Zebrafish/metabolism
- PubMed
- 37044365 Full text @ Comp. Biochem. Physiol. C Toxicol. Pharmacol.
Citation
Gomes, A., Monteiro, S.M., Venâncio, C., Félix, L. (2023) Protective effects of 24-epibrassinolide against the 6-OHDA zebrafish model of Parkinson's disease. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 269:109630.
Abstract
The molecular processes behind Parkinson's disease (PD) remain under debate although mitochondrial oxidative stress generation has been proposed as a fundamental contributor. In this context, different brassinosteroids have shown neuroprotective action hampering oxidative stress. This study determined the effects of 24-Epibrassinolide (24-EPI) against 6-hydroxydopamine- (6-OHDA-) induced toxicity using the zebrafish embryonic model. Embryos were exposed to 250 μM 6-OHDA or co-exposed to 24-EPI (0.01, 0.1, and 1 μM) for 3 days, starting at 48 h post-fertilization (hpf). During the experimental period, developmental parameters were assessed. At 120 hpf, larvae were tested for behavioural phenotypes with different biochemical biomarkers and tyrosine hydroxylase- (TH-) reactive neurons being also assessed. Exposure to 6-OHDA induced a decrease in body length while no other morphological phenotypes were noticed. A significant decrease in TH-neurons immunofluorescence, a decreased locomotion (speed and distance moved), and an increased absolute angle were found in 6-OHDA-exposed embryos. These outcomes were rescuable by the co-exposure with 24-EPI. Surprisingly, the direct effects of 6-OHDA on reactive oxygen species (ROS) were not observed in the present study supporting the involvement of other molecular pathways in the 6-OHDA-induced effects during embryonic development. Overall, the results obtained confirm PD-like symptoms induced by 6-OHDA during embryonic development which were reverted by 24-EPI. Although antioxidative signalling pathways deserve further scrutiny, the findings support the further investigation of 24-EPI neuroprotective effects.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping