PUBLICATION
Maternal Chronic Ethanol Exposure Decreases Stress Responses in Zebrafish Offspring
- Authors
- Kitson, J.E., Ord, J., Watt, P.J.
- ID
- ZDB-PUB-220827-6
- Date
- 2022
- Source
- Biomolecules 12(8): (Journal)
- Registered Authors
- Keywords
- alcohol, cortisol, development, stress, transgenerational, zebrafish
- MeSH Terms
-
- Animals
- Child
- Disease Models, Animal
- Ethanol/toxicity
- Female
- Fetal Alcohol Spectrum Disorders*
- Humans
- Larva
- Pregnancy
- Prenatal Exposure Delayed Effects*
- Zebrafish/physiology
- PubMed
- 36009037 Full text @ Biomolecules
Citation
Kitson, J.E., Ord, J., Watt, P.J. (2022) Maternal Chronic Ethanol Exposure Decreases Stress Responses in Zebrafish Offspring. Biomolecules. 12(8).
Abstract
In humans, prenatal alcohol exposure can cause serious health issues in children, known collectively as Foetal Alcohol Spectrum Disorders (FASD). Despite the high prevalence of FASD and a lack of effective treatments, the underlying mechanisms causing the teratogenic action of ethanol are still obscure. The limitations of human studies necessitate the use of animal models for identifying the underlying processes, but few studies have investigated the effects of alcohol in the female germline. Here, we used the zebrafish Danio rerio to investigate the effects of chronic (repeated for seven days) exposure to alcohol. Specifically, we tested whether the offspring of females chronically exposed to ethanol during oogenesis exhibited hormonal abnormalities when subjected to a stressor (alarm cue) as larvae, and if they exhibited anxiety-like behaviours as adults. Exposure to alarm cue increased whole-body cortisol in control larvae but not in those of ethanol-treated females. Furthermore, adult offspring of ethanol-treated females showed some reduced anxiety-like behaviours. These findings suggest that the offspring of ethanol-treated females had reduced stress responses. This study is the first to investigate how maternal chronic ethanol exposure prior to fertilisation influences hormonal and behavioural effects in a non-rodent model.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping