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dc.contributor.authorLim, Gerard Shing-Wan.
dc.description.abstractDopamine (DA) plays a critical role in cognition and reward. Therefore, dysregulation of DA neurotransmission has been implicated in neurological diseases such as Parkinson’s disease, and psychiatric disorders such as attention-deficit hyperactive disorder. Tyrosine hydroxylase (TH) is the rate-limiting enzyme in DA synthesis and its regulation has been found to be altered in transgenic mice lacking the dopamine transporter (DAT). DAT plays a critical role in the re-uptake of DA release in the synaptic cleft, thus determining the intensity and duration of DA neurotransmission. In this study, we further explored age-dependent regulation of TH in DAT knockout (KO) mice. The DAT mice exhibited a state of hyperactivity in our 10-minute locomotor activity test, a behavioral characteristic consistent in previous studies of such mice. It was found in our research that there were no significant differences in TH and pTH levels between WT and DAT KO mice up to 3 week-old. However, a dramatic and gradual decrease of both TH and pTH levels were observed from 4 week-old to 16 week-old mice. Thus, our findings provide further evidence that DAT not only plays a role in controlling the duration of DA neurotransmission, but also in the regulation of presynaptic TH homeostasis.en_US
dc.format.extent33 p.en_US
dc.rightsNanyang Technological University
dc.subjectDRNTU::Science::Biological sciences::Human anatomy and physiology::Neurobiologyen_US
dc.titleExploring age-dependent regulation of tyrosine hydroxylase in mice lacking the dopamine transporter.en_US
dc.typeFinal Year Project (FYP)en_US
dc.contributor.supervisorZhang Xiaodongen_US
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.description.degreeBachelor of Science in Biological Sciencesen_US
dc.contributor.organizationDuke-NUS Medical Schoolen_US
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Appears in Collections:SBS Student Reports (FYP/IA/PA/PI)
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