dc.contributor.authorLoo, Sze Jie
dc.date.accessioned2016-05-16T03:18:07Z
dc.date.available2016-05-16T03:18:07Z
dc.date.issued2016
dc.identifier.urihttp://hdl.handle.net/10356/67358
dc.description.abstractAnxiety is an emotion that encompasses anxiousness and nervousness which can develop into neurological disorders caused by chronic stressors. Anxiety is mainly mediated by the amygdala that positively regulates the HPA axis, resulting in elevated levels of stress hormones in a person. A heightened HPA axis can further promote neuronal growth and increase spine density in the amygdala, forming a vicious cycle. One of the growth factors that modulate this development is Brain-Derived Neurotrophic Factor (BDNF). In this study, it was hypothesized that over-expression of BDNF in the BLA can lead to anxiety disorders. To prove this, the aim of the study was to clone BDNF gene into AAV vector, allowing co-transfection with pRC-AAV and phelper-AAV plasmids into HEK293T cells to generate viral particles. This project has been optimising BDNF gene cloning and viral packaging protocols to allow the continuation of BDNF gene research. Although unsuccessful in gene cloning, solutions were provided to rectify possible issues in the protocol. Future studies such as BDNF gene silencing and anxiety-related behaviour studies will be needed to support the hypothesis that BDNF gene is a major contributor in causing anxiety.en_US
dc.format.extent42 p.en_US
dc.language.isoenen_US
dc.rightsNanyang Technological University
dc.subjectDRNTU::Scienceen_US
dc.titleGene therapy using viral vector against anxietyen_US
dc.typeFinal Year Project (FYP)en_US
dc.contributor.supervisorRupshi Mitraen_US
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.description.degreeBIOLOGICAL SCIENCESen_US


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