Our ultimate goal is to understand the neural circuits underlying neuropsychiatric disorder. There is a strong heritable (genetic) component to neuropsychiatric disorders, but the likelihood of developing the disorders is also affected by environmental challenges, such as stress. We exploit the range of benefits of using zebrafish as a model, including the genetic tools and recent improvements in zebrafish automated behavioural analysis. Adopting this approach allows us to characterise discrete components of neuropsychiatric disorders in terms of their underlying biology and help us to develop more effective treatments in the future.
Animals held in captivity often display range of repetitive, morphologically invariant, habitual behavioural patterns, often referred to as stereotypies, or stereotypic behaviour. There are a few projects on stereotypic behaviour currently in the lab. Kirsty Roberts' PhD is examining neurocognitive endophenotypes of stereotypic and repetitive behaviour in horses. She has been characterising environmental (living conditions) and personality-based (frustration, impulsivity) risk factors in a large scale survey, and recently developed a new method for testing impulsivity in horses. I am interested in the causes of these behaviours, both in terms of their potential as indicators of poor welfare, but also in the sense that they may be very useful in helping us to understand habitual behaviours and compulsions in humans (e.g., addiction).
Prenatal exposure to alcohol causes a range of physical and neurological disabilities, collectively referred to as Foetal Alcohol Spectrum Disorders (FASD). At the extreme end Foetal Alcohol
Syndrome (FAS) causes significant physical and neurological disability. At the lower end, more subtle differences in behaviour result. Genetic differences in the foetus may be crucial in
ameliorating or exacerbating the severity of the symptoms suffered as a result of exposure. For example, monozygotic twins (who share 100% of their genes and environment) that are exposed to
alcohol during their mother's pregnancy are both affected 100% of the time; however, dizygotic twins (who share environment but 50% of their genes) are only both affected 63% of the time. Animal
studies have been critical in increasing our understanding of this mechanism. We have been examining the effects of low/moderate alcohol exposure on zebrafish neurodevelopment.