PUBLICATION
            Micromolar Valproic Acid Doses Preserve Survival and Induce Molecular Alterations in Neurodevelopmental Genes in Two Strains of Zebrafish Larvae
- Authors
 - Messina, A., Boiti, A., Sovrano, V.A., Sgadò, P.
 - ID
 - ZDB-PUB-201002-198
 - Date
 - 2020
 - Source
 - Biomolecules 10(10): (Journal)
 - Registered Authors
 - Keywords
 - AB inbred zebrafish strain, TU inbred zebrafish strain, VPA, ascl1a/b, dopamine, serotonin
 - MeSH Terms
 - 
    
        
        
            
                
- Animals
 - Zebrafish/genetics*
 - Zebrafish/growth & development
 - Female
 - Larva/drug effects
 - Larva/genetics
 - Anticonvulsants/adverse effects
 - Anticonvulsants/pharmacology
 - Autism Spectrum Disorder/chemically induced
 - Autism Spectrum Disorder/drug therapy*
 - Autism Spectrum Disorder/genetics
 - Autism Spectrum Disorder/pathology
 - Disease Models, Animal
 - Valproic Acid/adverse effects*
 - Valproic Acid/pharmacology
 - Valproic Acid/toxicity
 - Metabolic Networks and Pathways/drug effects
 - Metabolic Networks and Pathways/genetics
 - Anxiety/chemically induced
 - Anxiety/drug therapy*
 - Anxiety/genetics
 - Anxiety/pathology
 
 - PubMed
 - 32987891 Full text @ Biomolecules
 
            Citation
        
        
            Messina, A., Boiti, A., Sovrano, V.A., Sgadò, P. (2020) Micromolar Valproic Acid Doses Preserve Survival and Induce Molecular Alterations in Neurodevelopmental Genes in Two Strains of Zebrafish Larvae. Biomolecules. 10(10):.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Autism spectrum disorders (ASDs) comprise a genetically heterogeneous group of conditions characterized by a multifaceted range of impairments and multifactorial etiology. Epidemiological studies have identified valproic acid (VPA), an anticonvulsant used to treat epilepsy, as an environmental factor for ASDs. Based on these observations, studies using embryonic exposure to VPA have been conducted in many vertebrate species to model ASD. The zebrafish is emerging as a popular model in biomedical research to study the molecular pathways involved in nervous system disorders. VPA exposure in zebrafish larvae has been shown to produce a plethora of effects on social, motor and anxiety behavior, and several genetic pathways altered by VPA have been described. However, the doses and regimen of administration reported in the literature are very heterogenous, creating contradictory results and posing serious limits to the interpretation of VPA action on neurodevelopment. To shed light on the toxic effect of VPA, we tested micromolar concentrations of VPA, using exposure for 24 and 48 h in two different zebrafish strains. Our results show that micromolar doses of VPA mildly affect embryo survival but are sufficient to induce molecular alterations in neurodevelopmental genes previously shown to be influenced by VPA, with substantial differences between strains.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping